Biomedical Engineering Technology: Health Technology Management

ISTUDY Introduction to Biomedical Engineering Technology This updated fourth edition provides current information on devices and is divided into diagnostic and treatment sections. Devices are described with the theory of operation and relevant anatomical and physiological considerations. Aspects of BMET work including test equipment, standards, and information technology are also discussed. The text covers a wide variety of diagnostic and treatment devices currently used in hospitals that students will likely encounter in their career. Principles of operation and examples of use are provided. This book is unique in that it is written by an experienced biomed tech with 30 years’ experience in hospitals rather than by engineers with little frontline experience. It is also unique in that it provides ancillary materials on the web and is the only guide divided into diagnostic and treatment device sections. This new edition also includes two new chapters on computers, information technology, and networking as well as health technology management. From the previous edition: “The book presents a comfortable balance between clinical applications, basic technical information, and various pictures of medical technologies one will encounter in the field. Additionally, related anatomy and physiology principles and essential technical terms are a nice complement to the technologies presented. The everyday duties and responsibilities of a biomed are captured by the various ‘true-to-life’ scenarios introduced throughout the book.” —Joey Jones, Madisonville Community College, Kentucky, USA This book is intended for students in biomedical engineering technology and healthcare technology management (BMET/HTM) programs as well as biomedical engineering students. Field service representatives, medical device designers, and medical device sales representatives will also find it useful. Introduction to Biomedical Engineering Technology Health Technology Management Fourth Edition Laurence J. Street Fourth edition published 2023 by CRC Press 6000 Broken Sound Parkway NW, Suite 300, Boca Raton, FL 33487-2742 and by CRC Press 4 Park Square, Milton Park, Abingdon, Oxon, OX14 4RN CRC Press is an imprint of Taylor & Francis Group, LLC © 2023 Laurence J. Street First edition published by CRC Press 2008 Second edition published by CRC Press 2011 Third edition published by CRC Press 2017 Reasonable efforts have been made to publish reliable data and information, but the author and publisher cannot assume responsibility for the validity of all materials or the consequences of their use. The authors and publishers have attempted to trace the copyright holders of all material reproduced in this publication and apologize to copyright holders if permission to publish in this form has not been obtained. If any copyright material has not been acknowledged please write and let us know so we may rectify in any future reprint. Except as permitted under U.S. Copyright Law, no part of this book may be reprinted, reproduced, transmitted, or utilized in any form by any electronic, mechanical, or other means, now known or hereafter invented, including photocopying, microfilming, and recording, or in any information storage or retrieval system, without written permission from the publishers. For permission to photocopy or use material electronically from this work, access www.copyright. com or contact the Copyright Clearance Center, Inc. (CCC), 222 Rosewood Drive, Danvers, MA 01923, 978-750-8400. For works that are not available on CCC please contact m pkbookspermissions@ tandf.co.uk Trademark notice: Product or corporate names may be trademarks or registered trademarks and are used only for identification and explanation without intent to infringe. ISBN: 978-0-367-68700-7 (hbk) ISBN: 978-0-367-69154-7 (pbk) ISBN: 978-1-003-14060-3 (ebk) DOI: 10.1201/9781003140603 Typeset in Times by codeMantra Access the companion website: www.routledge.com/cw/street Contents Preface...................................................................................................................... xv Acknowledgments...................................................................................................xvii Author......................................................................................................................xix Scope of This Book..................................................................................................xxi Chapter 1 Introduction...........................................................................................1 History of Medical Devices..................................................................1 Stethoscopes..........................................................................................5 Microscopes..........................................................................................7 Surgery..................................................................................................8 Defibrillators....................................................................................... 11 Typical Course Outline for an HTM Program.................................... 13 Characteristics of Human Anatomy and Physiology That Relate to Medical Devices................................................................... 18 Electrical Signals and Conductivity.................................................... 18 Circulation...........................................................................................20 Blood................................................................................................... 27 Respiration..........................................................................................28 Chemical Balances.............................................................................. 29 Densities.............................................................................................. 30 Tissue Densities................................................................................... 31 Temperature......................................................................................... 31 Hypothermia........................................................................................ 32 Hyperthermia...................................................................................... 33 Summary.............................................................................................34 Questions.............................................................................................34 Chapter 2 Diagnostic Devices: Part One............................................................. 35 Physiological Monitoring Systems...................................................... 35 Overview........................................................................................ 35 Integration and Connectivity...............................................................40 Central Stations................................................................................... 41 Telemetry............................................................................................. 43 The Heart............................................................................................ 47 Amplifiers............................................................................................ 51 Interference......................................................................................... 52 Internally Generated Artifacts............................................................ 52 Externally Generated Artifacts........................................................... 53 Filters................................................................................................... 53 Alarms................................................................................................. 54 Lead Arrangements............................................................................. 55 vi Contents Patient Isolation................................................................................... 58 Digital Systems................................................................................... 58 Waveform Analysis and Measurements.............................................. 59 Waveform/Event Storage..................................................................... 59 Arrhythmia Analysis...........................................................................60 Types of Arrhythmias......................................................................... 61 Stress Testing....................................................................................... 63 Exercise Component............................................................................ 63 Interface............................................................................................... 65 Controller............................................................................................ 67 ECG Monitor....................................................................................... 68 Ambulatory ECG Recorders/Analysis Systems.................................. 68 Cardiac Output.................................................................................... 70 Summary............................................................................................. 71 Questions............................................................................................. 71 Chapter 3 Diagnostic Devices: Part Two............................................................. 73 Circulatory System and Blood............................................................ 73 Introduction.................................................................................... 73 Hypertension....................................................................................... 74 Hypotension......................................................................................... 75 Blood Pressure Measurement.............................................................. 75 Invasive Blood Pressure Monitors.................................................. 75 Pressure Transducers........................................................................... 75 Noninvasive Blood Pressure Monitors................................................ 76 Pressure Measurement Cycle.............................................................. 78 Further Notes....................................................................................... 79 New Developments in NBP Measurements........................................80 Pulse Oximeters.................................................................................. 81 Transcutaneous CO2 Analyzers........................................................... 86 Blood Chemistry Analyzers................................................................ 86 Glucometers......................................................................................... 87 Doppler Blood Flow Detectors............................................................90 Respiratory System............................................................................. 91 Pulmonary Function Analyzers...................................................... 91 Incentive Spirometer...........................................................................94 Graphing Spirometer........................................................................... 95 Pulmonary Function Analyzer............................................................ 95 Respiration Monitors........................................................................... 95 Capnography Monitors........................................................................97 Oxygen Analyzers............................................................................... 98 Bronchoscopy Systems...................................................................... 100 Nervous System................................................................................. 102 EEG Monitors and Machines............................................................ 103 BIS Monitors..................................................................................... 106 Contents vii Muscle/Nerve Stimulators................................................................. 106 Summary........................................................................................... 107 Questions........................................................................................... 108 Chapter 4 Diagnostic Devices: Part Three........................................................ 109 Digestive System............................................................................... 109 Endoscopes................................................................................... 109 General.................................................................................... 109 Types of Endoscopes......................................................................... 109 Rigid Endoscopes.............................................................................. 111 Flexible Endoscopes.......................................................................... 112 Other System Components................................................................ 113 Light Source................................................................................. 113 Camera.............................................................................................. 116 Video Recorder/Storage.................................................................... 118 Video Monitor................................................................................... 118 Insufflator.......................................................................................... 119 Irrigation and Suction........................................................................ 119 Tools.................................................................................................. 120 Sensory Organs................................................................................. 121 Oto/Laryngo/Ophthalmoscopes........................................................ 121 Otoscope............................................................................................ 122 Laryngoscope.................................................................................... 122 Ophthalmoscope................................................................................ 123 Slit Lamps......................................................................................... 124 Reproduction..................................................................................... 126 Fetal Heart Detectors................................................................... 126 Fetal Monitors................................................................................... 128 Infant Scales...................................................................................... 132 Apgar Timers..................................................................................... 134 Skin, Bone, Muscle, and Miscellaneous........................................... 135 Thermometers............................................................................... 135 Electronic Probe Thermometers....................................................... 135 Tympanic Thermometers.................................................................. 136 Temporal Artery Thermometers....................................................... 138 Densitometers.................................................................................... 138 Arthroscopy Systems........................................................................ 139 Summary........................................................................................... 139 Questions........................................................................................... 140 Chapter 5 Diagnostic Imaging........................................................................... 141 Introduction....................................................................................... 141 X-Rays............................................................................................... 141 History.......................................................................................... 141 viii Contents Physics............................................................................................... 141 Definitions of Units........................................................................... 142 Detectors........................................................................................... 143 Effects and Dosage Limits................................................................ 143 X-Ray Safety..................................................................................... 144 X-Ray Procedures............................................................................. 144 Dental X-Rays................................................................................... 144 General Purpose X-Ray Rooms........................................................ 145 Mammography.................................................................................. 149 Computerized (Axial) Tomography Scanners................................... 149 Magnetic Resonance Imaging Scanners........................................... 152 Positron Emission Tomography......................................................... 155 Diagnostic Ultrasound....................................................................... 157 Picture Archiving and Communication System................................ 157 Summary........................................................................................... 160 Questions........................................................................................... 160 Chapter 6 Treatment Devices: Part One............................................................ 161 Heart.................................................................................................. 161 Defibrillators..................................................................................... 161 History............................................................................................... 162 Theory of Operation.......................................................................... 162 Function............................................................................................. 163 Energy Source................................................................................... 164 Voltage Multiplier.............................................................................. 164 Charge Storage.................................................................................. 164 Waveforms......................................................................................... 165 Discharge Relay................................................................................. 165 Wave Shaping.................................................................................... 165 Paddles and Electrodes...................................................................... 165 Defibrillator Types............................................................................ 170 Internal (Implantable) Defibrillators................................................. 170 External Manual Defibrillators......................................................... 171 ECG Measurement and Analysis...................................................... 172 Recorders........................................................................................... 172 Additional Components..................................................................... 172 Displays............................................................................................. 173 Audio................................................................................................. 173 Ergonomics........................................................................................ 174 Testing and Maintenance.................................................................. 174 Automatic External Defibrillators..................................................... 175 Pacemakers........................................................................................ 176 History............................................................................................... 176 Theory of Operation.......................................................................... 177 Construction...................................................................................... 178 Contents ix Application........................................................................................ 179 External Pacemakers......................................................................... 179 Circulatory System and Blood.......................................................... 180 Artificial Hearts............................................................................ 180 Ventricular Assist Devices................................................................ 181 Intra-Aortic Balloon Pumps.............................................................. 181 Heart–Lung Machines....................................................................... 181 Sequential Compression Devices...................................................... 183 Automatic Tourniquets...................................................................... 184 Blood Warmers.................................................................................. 184 Intravenous Fluid Administration Pumps......................................... 187 Pressure Infusers............................................................................... 187 Fluid Controllers............................................................................... 187 Syringe Pumps.................................................................................. 188 Piston Pumps..................................................................................... 190 Peristaltic Pumps............................................................................... 190 Patient-Controlled Analgesia Pumps................................................ 193 Safety Features of IV Pumps............................................................ 197 Respiratory System........................................................................... 198 Ventilators..................................................................................... 198 CPAP/BiPAP Units...........................................................................207 Oxygen Concentrators.......................................................................208 Humidifiers........................................................................................209 Summary...........................................................................................209 Questions........................................................................................... 210 Chapter 7 Treatment Devices: Part Two............................................................ 211 Nervous System................................................................................. 211 Anesthesia.................................................................................... 211 Anesthetic Agents............................................................................. 211 Anesthetic Machines......................................................................... 213 Anesthesia Vaporizers....................................................................... 219 Anesthetic Gas Monitors................................................................... 221 Electroconvulsive Therapy Machines............................................... 222 Digestive System............................................................................... 223 Feeding Pumps..................................................................................224 Renal System..................................................................................... 226 Hemodialysis..................................................................................... 226 Water Purification System................................................................. 228 Access Point...................................................................................... 228 Monitoring Components................................................................... 230 Dialyzer............................................................................................. 230 Peritoneal Dialysis............................................................................. 232 Lithotriptors....................................................................................... 233 Sensory Organs................................................................................. 237 x Contents Phacoemulsifiers........................................................................... 237 Ophthalmic Lasers............................................................................ 239 Summary........................................................................................... 243 Questions........................................................................................... 243 Chapter 8 Treatment Devices: Part Three......................................................... 245 Reproduction..................................................................................... 245 Bilirubin Therapy Systems........................................................... 245 Infant Incubators...............................................................................246 Infant Resuscitators........................................................................ 251 N2O Units...................................................................................... 255 Skin, Bone, Muscle, and Miscellaneous........................................... 256 Electrosurgery Machines.............................................................. 256 Monopolar Electrosurgery................................................................ 258 Bipolar Electrosurgery...................................................................... 263 Surgical Lasers..................................................................................264 Carbon Dioxide Lasers.................................................................... 264 Neodymium-Doped Yttrium Aluminum Garnet Lasers................... 265 Argon Lasers.....................................................................................266 Excimer Lasers..................................................................................266 Laser Safety.......................................................................................266 Surgical Ultrasound...........................................................................266 Cryosurgery Units............................................................................. 267 Microscopes...................................................................................... 268 Sterilizers........................................................................................ 272 Gas Sterilizers................................................................................... 272 Heat Sterilizers.................................................................................. 272 Liquid Sterilizers............................................................................... 272 Physiotherapy Equipment.................................................................. 274 Continuous Passive Motion............................................................... 274 Pain Relief......................................................................................... 274 Direct Heat........................................................................................ 274 Induced Heat..................................................................................... 276 Interferential Therapy....................................................................... 277 Laser Therapy........................................................................................... 278 Transcutaneous Electrical Nerve Stimulators................................... 278 Promotion of Healing........................................................................ 279 Ultraviolet Light Therapy............................................................. 279 Sequential Compression Devices...................................................... 279 Percussors.......................................................................................... 281 Summary........................................................................................... 281 Questions........................................................................................... 282 Contents xi Chapter 9 HTMT Work..................................................................................... 283 Overview........................................................................................... 283 Electrical Safety................................................................................ 283 Rationale............................................................................................284 Testing Methods................................................................................ 285 Other Safety Considerations.............................................................. 291 Fire Safety......................................................................................... 291 Chemical Safety................................................................................ 291 Mechanical Safety............................................................................. 292 Infection Control............................................................................... 293 Sharps Safety..................................................................................... 295 Performance Assurance.................................................................... 295 Troubleshooting Techniques.............................................................300 Electrostatic Discharge...................................................................... 305 Summary...........................................................................................306 Questions...........................................................................................306 Chapter 10 Testers and Tools...............................................................................307 Introduction.......................................................................................307 General Test Equipment....................................................................307 Digital Multimeters...........................................................................307 Oscilloscopes.....................................................................................308 Other Test Equipment........................................................................ 312 Specialized Biomedical Test Equipment........................................... 312 ESU Analyzers.................................................................................. 314 Infusion Device Analyzers................................................................ 317 Physiological Simulators................................................................... 319 NIBP Analyzers................................................................................ 321 Ventilator Analyzers.......................................................................... 323 Incubator Analyzers.......................................................................... 325 SpO2 Analyzers................................................................................. 327 Pacemaker Analyzers........................................................................ 330 Specialized Calibration and Testing Devices.................................... 331 Tools.................................................................................................. 332 General.............................................................................................. 332 Specialized Tools and Components.................................................. 335 Power Tools....................................................................................... 335 Soldering........................................................................................... 337 Other.................................................................................................. 339 Summary........................................................................................... 341 Questions........................................................................................... 342 xii Contents Chapter 11 Radiation and IT................................................................................ 343 Electromagnetic Radiation................................................................ 343 Digital Electronics.............................................................................344 Introduction.......................................................................................344 Digital Signals...................................................................................344 Binary Numbers................................................................................ 345 Analog-to-Digital Conversion........................................................... 345 Microprocessors................................................................................346 Computers and Networks..................................................................346 Summary........................................................................................... 347 Questions........................................................................................... 347 Chapter 12 Health Technology Management....................................................... 349 Introduction....................................................................................... 349 General Considerations..................................................................... 349 Planning............................................................................................ 349 Technology Management Software................................................... 350 Equipment Management Systems..................................................... 351 Test Automation................................................................................ 352 Ansur by Fluke Biomedical.......................................................... 352 Summary........................................................................................... 352 Chapter 13 Regulations and Standards................................................................ 353 Introduction....................................................................................... 353 Standards and Regulations Organizations........................................ 354 International Electrotechnical Commission................................. 354 IEC 60601......................................................................................... 354 IEC 62353.......................................................................................... 355 National Fire Protection Association................................................ 355 International Organization for Standardization................................ 356 About ISO.......................................................................................... 356 What Are Standards?........................................................................ 356 ISO 9000—Quality Management..................................................... 356 ISO 31000—Risk Management........................................................ 357 CSA................................................................................................... 357 About CSA Group............................................................................. 357 Electro-Medical Equipment.............................................................. 358 Testing and Certification................................................................... 358 CSA Standards.................................................................................. 358 UL and ULC..................................................................................... 359 About UL........................................................................................... 359 About Underwriters Laboratories of Canada.................................... 359 Standards Council of Canada............................................................ 359 Contents xiii About the SCC.................................................................................. 359 About Standardization.......................................................................360 Food and Drug Administration.........................................................360 Products and Medical Procedures.....................................................360 Medical Device Safety......................................................................360 Health Canada...................................................................................360 Medical Devices................................................................................360 Health Canada’s Role........................................................................ 361 Association for the Advancement of Medical Instrumentation........ 361 American National Standards Institute............................................. 361 Institute of Electrical and Electronics Engineers.............................. 361 IEEE Quick Facts.............................................................................. 361 Therapeutic Goods Administration................................................... 362 BSI Group.......................................................................................... 362 Summary........................................................................................... 363 Chapter 14 A Gallery of Real-Life Problems...................................................... 365 Chapter 15 Anatomy Color Insert........................................................................ 379 Appendix A: Normal Values................................................................................ 391 Appendix B: Image Credits................................................................................. 397 Index....................................................................................................................... 401 Preface This new edition of Introduction to Biomedical Engineering incorporates updates and revisions to most chapters, and in response to user feedback, additional material on HTM Tech (BMET) certification, regulations, and standards have been added. The book still includes the adventures of “Joe Biomed” and his colleagues. Joe is a fictional character, but the descriptions of his work are real. Joe has his own Facebook page, and readers are welcome to send him friend requests. Images, unless otherwise noted, are from my own collection. Some older devices have been included because many facilities don’t always have the latest and greatest. This edition of Introduction to Biomedical Engineering Technology includes access to an exclusive website that provides a large amount of additional material that is not practical to include in the print copy. Some of the material has lists that have links to external sources, which are much more accessible when online rather than having to transcribe a long URL from a printed page. Linked topics include: • • • • • Medical device manufacturers HTM/BME test equipment manufacturers Medical and HTM/BME general information HTMT/BMET education programs in the USA and Canada HTM/BME organizations and groups, including some social media links Also included: • Copies of the anatomical illustrations from the book, plus more • A timeline of medical technology The web page will be updated and expanded at times. Access the page with the following QR code: Chapter questions and problems are included at the end of each chapter and on the ancillary web page. Laurence J. Street Acknowledgments Thank you, Marc Gutierrez, for your care and professionalism, Nick Mould for your assistance, and all the rest of the team at Taylor & Francis that helped bring it all together. Thank you to Richard Pisano and his crew at the Academy of Health Technology Management for suggestions and ideas. Thanks also to Dennis Schweers, long-time friend and always an inspiration. Zhouyan Feng translated the third edition of the book into Chinese, and his expert editing skills have helped make this fourth edition better. My pre-retirement work partner, Frank Torok, helped nudge me into the whole project in the first place. Philips Medical has been very generous in allowing me to use images of many of their devices as well as excerpts from various documents, all of which have helped make this edition more current and relevant. Thank you to Fluke Biomedical USA for permission to use many of their images and text passages, this has added greatly to the book. Thank you to Mohit Arora of Philips, Ben Fox of GE Healthcare, Shanta Fisher of Masimo, and Terry Peristerakis of Medit for help in obtaining images of their products. Shutterstock is an invaluable source of royalty-free graphics and is very easy to work with—thanks for a great resource! Finally, thanks again to my family for their constant support. Sheri, Jordan, and Shannon—I couldn’t have done it without you. Author Laurence J. Street earned a diploma in biomedical engineering technology at the British Columbia (BC) Institute of Technology in Vancouver, British Columbia, Canada, in 1979, and has since worked continuously in a variety of hospitals, from the very large Shaughnessy/BC Children’s/Vancouver Women’s complex to a regional hospital in the BC interior to (1991–2010) the Chilliwack General Hospital, a mid-sized community hospital outside Vancouver, and part of the Fraser Health Authority. In the latter two cases, he was solely responsible for setting up and implementing the Biomedical Engineering Department. The author’s hospital work involved the repair and maintenance of all patient care electronic devices in the hospital as well as close involvement in planning for future technological directions and the evaluation and acquisition of equipment. He also provided in-service education to medical staff regarding the safe and effective use of patient care devices. As CGH is a well-equipped acute care and teaching hospital and is also part of a regional medical community, he worked with an extremely wide variety of both older and very modern pieces of equipment. He has taken a large number of factory training courses on the various devices that he services. He is retired from service after working for 30 years in this field. Scope of This Book Medical devices are often very complex, and while there are differences in design from one manufacturer to another, the principles of operation and, more importantly, the physiological and anatomical characteristics on which they operate are universal. In this book, more attention will be paid to the commonalities of equipment than to differences. With many details specific to a given manufacturer, it would be impossible to cover all such material in a text of this nature; it is meant to serve as an overview. As such, the book is not intended as a substitute for service or operator manuals; the specifics of operation of any device are too complex and idiosyncratic for this to be practical. Factory and self-guided training courses, including the study of manuals, are required for individual devices. Details of electronic circuits are not covered because these vary greatly not only from one manufacturer to another but also from one generation of equipment to another. Moving from vacuum tubes to transistors to integrated circuits to microprocessor-based systems, the details of electronic design and function have become less and less relevant to technical support staff, whereas the overall function and integration of equipment into the medical system have become more and more important. With the goal of giving students a clear idea of the function and application of the various medical devices, extensive descriptions of theory have been avoided because these can obscure the overview. Where theory is directly relevant to function and application, an appropriate description has been provided. The main focus of the book is on clinical equipment, devices that are used directly with patients in the course of their care for diagnostic or treatment purposes. Seven chapters are used to describe medical devices: three covering clinical diagnostic equipment, one for diagnostic imaging systems, and three for treatment devices. There is some overlap between diagnostic and treatment devices; for example, a bronchoscope can be used to diagnose respiratory diseases and, in conjunction with an electrosurgery machine, can be used to remove lesions from bronchial passages. In such cases, both functions are described together. Only an overview of the imaging technology is given because of its high degree of complexity; these devices are covered in much more detail in other texts, referenced in the ancillary material online. Many laboratory devices are also very complex, and very manufacturer-specific; because of this and their distance from direct patient care, they are not included in this book. Again, these devices are covered in much more detail in other texts, referenced in the ancillary material online. Regarding photographs in the text, some are from a stock photo company, some were very graciously supplied by equipment manufacturers, and the rest were taken by me in the hospital where I worked. The latter images are not of studio quality. They were taken in the field and so there may be the odd cable or box of paper or telephone in the background, but I trust they are clear enough. This was not a negative in my opinion because Biomeds working in a hospital are much more likely to xxii Scope of This Book find equipment beside a coffee cup or under a stack of papers than on a pedestal in a perfectly lit, perfectly tidy studio. Images from the book, and more, can be found in the ancillary material online. Scan this QR code for access to the ancillary material. 1 Introduction OBJECTIVES FOR THIS CHAPTER • To review the history and development of medical devices, including some specific examples. • To briefly discuss the role of Health Technology Management in today’s health care system. • To look at some of the characteristics of anatomy and physiology that are relevant to medical device design and function, including the role of electrical signals in the body, the operation of the circulatory and respiratory systems, the role of chemical balances, and the importance of body temperature. HISTORY OF MEDICAL DEVICES The history of medicine is a story of humans trying to better understand and treat the various diseases and injuries that befell themselves and their companions. From simply providing comfort and empathy, medical care evolved with ever more effective means of diagnosing and treating illnesses. A quote attributed to the anthropologist Margaret Mead said that a healed human femur was the earliest sign of human civilization, as it showed that the individual was cared for and assisted during the healing process. Pharmacology was likely the first tool to be developed, thousands of years ago, as shaman or medicine women or simply mothers caring for infants found that certain plants had beneficial properties, in part by observing animals and birds utilizing the plants. In The Clan of the Cave Bear (1980), Jean M. Auel describes how a Neanderthal medicine woman treated the wounds of a small Cro-Magnon child (1980): “This destroys the evil spirits that make infection,” Iza motioned, pointing to the antiseptic iris-root solution. “A poultice of the root draws out poisons and helps the wound heal.” She picked up a bone bowl and dipped in a finger to check the temperature. “Clover makes the heart grow strong to fight evil spirits – stimulates it.” … “Alder bark cleans the blood, purifies it, drives out the spirits that poison it.” (p. 21) Even though Iza did not fully understand the true nature of infection, she recognized that there were tools she could use to ward off its symptoms (Figure 1.1). Though many later developments in medicine were fraudulent, generally medical practitioners looked for better and better ways to diagnose and treat their patients. They recognized that there were different, specific maladies and that these maladies caused specific symptoms. The location, type, and degree of pain or tenderness; localized or systemic heating (Figure 1.2); swellings; skin color; eye appearance; the color, texture, and odor of bodily discharges; and heart, lung, and digestive system sounds— all served to help diagnose ailments and guide treatment. DOI: 10.1201/9781003140603-1 2 Introduction to Biomedical Engineering Technology FIGURE 1.1 Aloe vera, an ancient medicinal plant. FIGURE 1.2 Fever. Adept physicians knew that the better they could identify symptoms, the better their chances of curing their patients, and so they searched for better methods of determining symptoms. Just as pharmacology developed from observing the effects of various foods, to trial and error of natural substances (Figure 1.3), through outright quackery, to the scientific research, testing, and analysis used by modern drug companies, so too has medical hardware evolved. 3 Introduction FIGURE 1.3 A mortar and pestle used to prepare medications. A PATIENT FROM THE PAST Robert Smith entered Dr. James Llewelyn’s Surgery in London and collapsed into a chair, moaning and clutching his abdomen. Dr. Llewelyn’s nurse, Mrs Peabody, bustled out to him and managed to get him up from the chair and into the doctor’s examination room, where he lay upon the table, still moaning. Dr. Llewelyn entered and immediately looked the patient over, noting that he was pale, breathing shallowly, and perspiring profusely. “Well, sir, what have we here?” he enquired. “It’s me belly, Doctor, it hurts so!” replied Smith, grimacing. “All right, let’s have a look shall we? Come on, I’ll unbutton your vest and loosen your belt. There. Now I’m going to press on different parts of your belly and you tell me where it hurts most, will you?” Gentle probing revealed extreme tenderness in Mr Smith’s lower right side, and the doctor noted a recently healed wound in the area. “Mrs. Peabody, Laudanum, please,” ordered the Doctor, and his nurse produced a bottle of syrup from which he poured a spoonful and fed it to his patient. Dr. Llewelyn took his stethoscope from a side table and listened intently to Smith’s heart, lungs, and abdomen. He then asked Mrs Peabody to help get Mr Smith into the next room, where they assisted the poor man, now quite groggy from the laudanum but at least not moaning so much, onto another table. 4 Introduction to Biomedical Engineering Technology A strange and marvellous device, called a Crookes tube, was mounted above the table, and it was connected to more machinery that the good doctor referred to as “My lovely Ruhmkorff coil,” though Mr Smith was, by this time, less than impressed. Mrs Peabody brought out a glass photographic plate, which she slid into a space under the tabletop. Dr. Llewelyn implored his long-suffering patient to remain as still as possible, and then he energized his contraption. There was a loud humming sound, which went on for many minutes, and after a while a hot electrical smell filled the room. Finally, the machine was shut off, and Mrs Peabody retrieved the plate from beneath the nearly comatose Smith. Dr. Llewelyn took the plate into a side room and proceeded to develop the image of Smith’s abdomen. Though blurry, the plate confirmed the good doctor’s suspicions—Smith had a lead ball lodged in his belly, the result, no doubt, of a barroom brawl gone too far. “Right then, Mrs. P., let’s get him to the Surgery,” the doctor said cheerily, and they struggled to get Smith onto yet another table in a third room. It hardly seemed necessary, but Llewelyn used ether to render Smith completely unconscious. Then, after bathing the area in carbolic acid and donning thick rubber gloves and a cloth mask, he used a scalpel (Figure 1.4) (which had also been soaked in carbolic acid) to deftly slice through the layers of FIGURE 1.4 Surgical scalpel. Introduction 5 tissue near the wound. Mrs Peabody, masked and gowned, valiantly mopped up blood, and finally Dr. Llewelyn reached into the surgical opening and extracted the lead ball with a cry of victory. More carbolic acid washed out the area and Llewelyn stitched up his patient layer by layer. The Roentgen Rays, the Roentgen Rays, What is this craze? The town’s ablaze With the new phase Of x-ray’s ways. “I’m full of daze, Shock and amaze; For nowadaysI hear they’ll gaze Thro’ cloak and gown – and even stays, These naughty, naughty Roentgen Rays. STETHOSCOPES Perhaps the first medical diagnostic device was the stethoscope. Medicine men knew that the sounds made by a patient’s heart, the noises of breathing, and the gurgling of the intestinal tract all could provide clues as to the patient’s condition. Rapid heartbeats could signal infections, unusual beat sounds could mean a heart structure defect, and wet-sounding inhalations might point to pneumonia or tuberculosis. Laying an ear on the patient provided the first means of detecting such sounds, but this was often inconvenient, inefficient, or messy, and so mechanical means of listening were devised. The first stethoscopes might have been cones of bark, but someone discovered that sounds were carried quite well by wooden sticks, and even better by hollow tubes. A cup on the end of the tube helped to gather more sound, providing more information, and when the tubes were split into a “Y” and brought to both ears at once (Figure 1.5), external sounds were shut out and the important internal ones amplified, allowing even more refined discernment and interpretation of bodily sounds. The shape and size of the cup, or bell, have been improved, a diaphragm added, and better materials used to make the modern stethoscopes a vital tool for physicians and nurses. It is used to listen to not only heart, lung, and intestinal sounds, but also to pick up the Korotkoff sounds made by blood vessels in determining blood pressure (in conjunction with a manometer), and the sounds of a fetal heartbeat within the mother’s abdomen. With the advent of electronics, stethoscope evolution took another large step. Sensitive microphones, acoustically coupled to the skin with special gel, provided signals that could be amplified and filtered and then reproduced with either headphones or larger speakers. Some units can record sounds internally and/or transmit them to nearby devices via Bluetooth™, a valuable feature for teaching. Of course, such devices are more expensive than traditional mechanical stethoscopes, they are more fragile, and they need batteries, so the old style continues in common use except where the additional capabilities of electronic versions are required. 6 Introduction to Biomedical Engineering Technology FIGURE 1.5 A modern stethoscope. DOPPLER FETAL HEART DETECTORS A device related to the stethoscope became available with electronic technology, and it used a principle discovered in 1842 by Christian Andreas Doppler. The “Doppler effect” is that waves produced by a moving object will be compressed or expanded relative to a stationary observer depending on whether the source is moving toward or away from the observer (the classic change in pitch of a train whistle as it passes by is a good example of the Doppler effect). The phenomenon was first used practically with RADAR systems, in which radio waves were bounced off objects such as airplanes. If the returning wave was of a higher frequency than the emitted wave (i.e., it was compressed), the reflective object was moving toward the radar installation; if it was of a lower frequency, the object was moving away. Comparing the values quantitatively allowed a calculation of the speed of the object. In medicine, it was found that this principle could be applied using ultrasonic waves. When sound waves are sent into a patient’s body, they are reflected by the various structures within. If the surface that reflects the waves is moving, such as the components of the heart during each beat, or the walls of blood vessels as they expand and contract when blood pulses through them (Figure 1.6), 7 Introduction FIGURE 1.6 A Doppler fetal heart detector. or blood cells themselves as they flow through vessels, the reflected sound waves will show the Doppler effect. The motions of the internal structures can therefore be determined and represented, as a sound or an image or both. MICROSCOPES Technology was adopted in many other ways as the practice of medicine evolved. Lenses were discovered thousands of years ago, but their magnifying ability was not likely put to use by medical practitioners until perhaps the time of Roger Bacon in the thirteenth century. Hans Jansen, Robert Hooke, and Antonie van Leeuwenhoek contributed to the development and use of microscopes (Figure 1.7). Microscopes evolved with better glass and optical coatings, improved mechanical features, binocular eyepieces (Figure 1.8), and more effective and varied lighting methods, including polarization and ultraviolet light. Adapters have been created to allow a second person to observe the image, or a video camera can be attached so that images can be displayed on video monitors or computer systems. 8 Introduction to Biomedical Engineering Technology FIGURE 1.7 An early microscope. Electronics really entered into the realm of microscopy with the advent of the electron microscope in the 1930s. Using an electron beam instead of visible light waves, these devices enabled greater magnification of images. SURGERY Surgical devices were in use many thousands of years ago, as evidenced by the discovery of human skulls that had been cut open (trepanation) (Figure 1.9) and later healed over. Stone or obsidian scalpels were used to peel back the scalp and then to carve a hole in the patient’s skull. Afterward a section of bone was removed from the skull, so that evil demons (or perhaps pressure from a subdural hematoma) could escape from the person’s head. 9 Introduction FIGURE 1.8 A modern binocular microscope. FIGURE 1.9 Primitive brain surgery. 10 Introduction to Biomedical Engineering Technology FIGURE 1.10 Electrosurgery unit. The age of metals saw the development of scalpels that were easier to be shaped and manufactured than those of stone, and that could also be sharpened when necessary. Steel became the ultimate physical scalpel material, but again electronics entered into the picture. It was found that high-frequency electrical signals could not only cut tissues but cauterize them as well, helping to reduce both bleeding and the chance of infection. These electrosurgery units (ESUs) were at first simply a1qaz power supply and connectors. Cushing and Bovie refined the equipment, creating a “spark-gap” device that became widely used; even today, ESUs are sometimes referred to as “Bovies.” ESUs, since they employed electrical currents to produce cutting and cauterization, required a return path for the current to carry the electricity from the cutting site, through the patient’s body (which is filled with conductive fluids), and back to the ESU or a common ground point. This return path had to be arranged so that the current leaving the patient’s body was spread over a large enough area, thereby avoiding damage because of burning or overheating. The requirement of a return path also meant that safeguards were needed to prevent alternate paths, either through other parts of the patient’s body or through staff members. ESU evolution produced devices with output waveforms optimally shaped to provide the best combinations of cutting and coagulation with minimal collateral tissue damage and minimal risks to both patients and staff (Figure 1.10). Further developments of this technology included the use of beams of ionized gas to provide the contact for cutting and coagulation, rather than a metal blade as in previous units. ESUs are often used in conjunction with laparoscopic procedures since appropriate accessories can carry the surgical current through small tubes and into the patient’s body without the need for large incisions. 11 Introduction Another development in surgical technology involves the use of laser beams instead of electrical current. By controlling the power, wavelength, and width of laser beams, various surgical effects can be achieved, from cutting and/or coagulation to tissue ablation, to “welding” detached retinal tissue to the inner surface of the eye. DEFIBRILLATORS Cardiac arrest is a major cause of death, and as soon as scientists discovered the electrical nature of heart contractions and especially the characteristics of fibrillation, they began to devise means of restarting or re-coordinating the cardiac rhythm. Electrical shocks seemed to be the logical means of accomplishing this, especially since they could induce fibrillation in some circumstances. It was on a dreary night of November that I beheld the accomplishment of my toils. With an anxiety that almost amounted to agony, I collected the instruments of life around me, that I might infuse a spark of being into the lifeless thing that lay at my feet. It was already one in the morning; the rain pattered dismally against the panes, and my candle was nearly burnt out, when, by the glimmer of the half-extinguished light, I saw the dull yellow eye of the creature open; it breathed hard, and a convulsive motion agitated its limbs. Mary Shelley Frankenstein, 1818 Electrically induced fibrillation was discovered in 1849, and 50 years later, it was found that another applied shock could sometimes re-establish a normal cardiac rhythm. Dr. Claude S. Beck from the University Hospitals in Cleveland used a defibrillator to save a human life for the first time in 1947. Since that time, defibrillators have become more sophisticated and effective, using precisely designed waveforms to provide optimal efficacy with minimal electrical current (Figure 1.11). They have integrated electrocardiogram (ECG) circuitry, which allows observation of patient waveforms as well as synchronization to abnormal rhythms. Some include pacemakers or pulse oximeters (Figure 1.12), some have been miniaturized enough to be implanted within a patient’s body so they can provide shocks directly to the heart whenever needed, and some have been automated and simplified in operation sufficiently that they can be placed in public places or private homes to be used by untrained personnel. Drones have been used to quickly deliver defibrillators to isolated or remote locations. As medical technology evolved, a need arose for people to take care of the equipment involved. Devices had to be designed and built, their use had to be demonstrated and explained to the end users, functionality had to be checked and maintained, and these devices had to be repaired when they failed. At first, much of this was done by whoever invented the equipment, but eventually specialization was required and specific individuals were assigned responsibility for the maintenance of medical technological devices. Depending on the equipment, these people might have been electricians, or technicians who would normally operate the devices, or simply someone in the medical facility who had an interest in, and aptitude for, hardware. 12 Introduction to Biomedical Engineering Technology FIGURE 1.11 An older model defibrillator. FIGURE 1.12 Defibrillator. (Courtesy of Philips Medical, Canada.) Further development of equipment made it more complex and varied, and this meant that the people taking care of it had to be more highly trained and experienced. Electronic circuits became critical and powerful components of many medical devices, so an in-depth knowledge of electronics became a necessity. Sometime after World War II, the field of medical equipment support became sufficiently specialized that a title was given to those who practiced it: BMET, or biomedical equipment technician. Gradually the “E” changed to mean first “electronics” and then “engineering,” while the “T” moved from technician to technologist. More recently, the terms “Health Technology Management” and “HTM Technologist” have become more commonly used, all of these changes reflecting the changing roles and responsibilities of HTMTs in the medical community (Figure 1.13). The terms BMET/HTMT and Biomedical Engineering/Health Technology Management are used somewhat interchangeably in the text. Today, most HTMTs receive their initial training in a 2- or 3-year program at a community college, technical school, or university, or through an Armed Forces 13 Introduction FIGURE 1.13 An HTMT at work. training school. A listing of most of these programs in the United States and Canada is provided in the ancillary material at TYPICAL COURSE OUTLINE FOR AN HTM PROGRAM DIPLOMA COURSES: Anatomy and Medical Terminology (3 credit Anatomy and Medical Terminology (3 credit hours/4 weeks) hours/4 weeks) Networking A+ OR Network+ (3 credit Networking A+ OR Network+ (3 credit hours/4 weeks) hours/4 weeks) Healthcare Technology Management (3 credit Healthcare Technology Management (3 credit hours/4 weeks) hours/4 weeks) Biomedical Equipment (3 credit hours/4 weeks) Biomedical Equipment (3 credit hours/4 weeks) Specialized Medical Equipment (3 credit hours/4 weeks) Total of 15 credit hours (20 weeks) Total of 15 credit hours (20 weeks) COURSE ADD-ON OPTIONS: COURSE ADD-ON OPTIONS: Networking A+ (3 credit hours/4 weeks) Networking A+ (3 credit hours/4 weeks) Network+ (3 credit hours/4 weeks) Network+ (3 credit hours/4 weeks) Practical Electronics (3 credit hours/4 weeks) Practical Electronics (3 credit hours/4 weeks) Healthcare Technology Management II (CBET Healthcare Technology Management II (CBET Prep) (3 credit hours/4 weeks) Prep) (3 credit hours/4 weeks) (Continued) 14 Introduction to Biomedical Engineering Technology HANDS-ON TRAINING: HANDS-ON TRAINING: AHTM has set up nationwide partnerships and continues to set up partnerships for students to gain hands-on training when needed. This is usually completed over a period of 8 weeks. DIPLOMA COURSES: DIPLOMA COURSES: Anatomy and Medical Terminology (3 credit Anatomy and Medical Terminology (3 credit hours/4 weeks) hours/4 weeks) Networking A+ OR Network+ (3 credit hours/4 weeks) Healthcare Technology Management (3 credit Healthcare Technology Management (3 credit hours/4 weeks) hours/4 weeks) – Courtesy of the Academy of Health Technology Management, Richard Pisano, Director The evolution of medical technology continues, and this means that HTMTs continue to learn throughout their careers, with on-the-job experience and mentoring, continuing education classes, and factory training courses on specific devices. A DAY IN THE LIFE OF JOE BIOMED 7:30 a.m.—Joe Biomed arrives at work, the Health Technology Management Lab at Hippocrates General Hospital, a mid-sized community hospital in Einthoven, Ohio, a mid-sized semirural town. He greets Angela Jones, one of the two other HTM staff, who had arrived earlier that morning. Joe checks for phone messages and then signs on to the hospital computer intranet to check for e-mail and to see if any work orders have been assigned to him for the day (Figure 1.14). He notes that he is scheduled to do a PM on a defibrillator from the cardiac intensive care unit, or CICU. Then he discusses the previous day events with Angela, and they go over plans for the day. 7:45 a.m.—An IV pump arrived at the lab overnight. It has a note taped to it that says “not working.” Joe looks up the pump in their database and finds that it FIGURE 1.14 Data entry and database access. Introduction came from third-floor nursing unit. He marks that on the pump and retrieves the service manual for that model from their departmental library. Being familiar with the pumps (there are over 60 of them in the hospital), Joe sets it up on the IV pump analyzer and starts it running at 125 mL/h. After a few minutes, the pump stops and an alarm sounds, accompanied by an alarm code on the LCD screen. Joe looks up the code in the service manual. The manual suggests testing the voltage at a particular test point, which Joe does. The voltage is lower than it should be, and the manual indicates that, in that case, the CPU board of the pump needs to be replaced. Joe asks Angela if there are any CPU boards left in stock, and she informs him that the last one got used 2 weeks ago. Joe orders several CPU boards, since they have been a common source of problems with these pumps, and then puts all the parts for the pump in a container and sets it aside, with a note on it explaining that parts were on order and giving the order number. He returns the service manual to the library. 8:15 a.m.—Joe greets Mike Cho, the third member of the team, as he arrives at work. Then he reads over the work order for the defibrillator, noting the equipment number. He takes a small cart and makes his way through various corridors and up an elevator to the CICU, where, after observing the proper infection control protocols, he chats with the nurses at the central monitoring station. Joe tells them he needs the defibrillator for testing, and after going over the current patients and expected admissions, they tell Joe he can take the unit away, but he has to have it back by the afternoon. Joe unplugs the defibrillator, removes any charts as well as accessories that he will not need, then transfers the unit from the CICU crash cart to his own cart and places a note on the crash cart indicating where the unit has been taken and when it should be back. Returning to the biomed lab, Joe does a thorough visual inspection of the unit and accessories, then connects it to their defibrillator analyzer (Figure 1.15) and runs through a series of pre-programmed performance tests. FIGURE 1.15 Defibrillator analyzer. (Courtesy of Fluke Biomedical.) 15 16 Introduction to Biomedical Engineering Technology These test results are transferred to the equipment control database on the department computer. Joe then uses an automated electrical safety analyzer to check that the unit meets grounding and electrical leakage standards; these tests also feed into the equipment control database. After completion of testing, Joe types a few notes into the work order and then closes it. The program prints out an inspection label, which Joe affixes to the unit. Then he returns it to the CICU, replaces it on the crash cart, reconnects the AC cord, and does a quick operational check, noting especially that the AC indicator is lit. He informs the nursing staff that the unit is back in service, and then returns to the lab. 9:30 a.m.—Coffee break. 9:45 a.m.—Joe answers a phone call from a supplier regarding changes in part numbers for infant resuscitator temperature probes (Figure 1.16). He notes these changes in the database. 9:55 a.m.—Another phone call, this time it’s an ER nurse asking about changing the order of the waveforms on their bedside monitors. Joe describes the procedure for changing the order temporarily and asks if they want this to be their default configuration. He is transferred to the ER manager, who agrees that it should be changed, so he makes a note on his tablet to perform the configuration change when convenient. 10:20 a.m.—A porter brings some boxes, one of which contains parts for a pulse oximeter that Joe was working on last week. He enters the parts in the database, and then completes the repair and does a performance assurance test on the pulse oximeter. Test results are entered in the database and the work order for the unit is signed off and closed, a repair label goes on, and the unit is sent back to its home ward. FIGURE 1.16 Yet another Biomed at work. 17 Introduction FIGURE 1.17 Code Blue! A defibrillator in use on a patient simulator. (no credit) 10:55 a.m.—“Code Blue, CICU” is called over the hospital PA system, and since the defibrillators there are relatively new to the hospital, Joe decides to attend. The primary Code Blue team passed by him in the hallway on the run to the CICU, and by the time he gets there, they are just getting the defibrillator in place (Figure 1.17). The resident doctor in charge recognizes him and asks how many charges they can get from the battery. Joe informs him of the number specified by the manufacturer and adds that they have confirmed that in testing. The patient is resuscitated successfully, so Joe returns to the lab, where he has to fill Angela and Mike in on the excitement. 11:50 a.m.—Lunch break. 12:30 p.m.—Joe attends a meeting as member of the hospital’s equipment acquisition committee, to discuss the replacement program for their IV pumps. Joe will arrange with the purchasing team to have several demo units from different manufacturers brought in for evaluation. He explains some of the new features of the pumps to the other committee members. 1:35 p.m.—Joe’s hospital cell chimes with a notification, indicating the number for the OR. He calls them, and is told that there has been a possible patient burn incident involving an ESU. He asks the OR staff to tag the unit that was involved and to keep all the accessories and cables that had been used during the surgery. He gets a list of the doctors and nurses involved in the case and asks that they call him as soon as possible. He begins the incident report process, and then the ESU and accessories arrive at the lab. Joe performs a visual inspection of the items and then does a detailed performance 18 Introduction to Biomedical Engineering Technology test, especially noting areas that might have been involved in a possible patient burn. He receives a phone call from one of the OR nurses who was working with the patient; she tells him that the burn appeared to be under the return electrode pad. Joe finds no faults with the equipment, so he goes to post-op recovery room where he talks to nurses and asks them if they could put a section of ESU return electrode pad on the patient’s leg. Shortly afterward, Joe has a look at the patient’s leg and finds that there is definite reddening under the electrode pad. He discusses this with the OR staff, and together they conclude that the “burn” was actually a sensitivity reaction to the electrode adhesive. Joe completes the incident report and sends both the paper and e-mail copies to the OR supervisor, the safety committee, and the biomed lab. 4:00 p.m.—End of the day. While the majority of HTM technologists will likely work in a hospital setting, there are many other career paths. Equipment manufacturers and vendors (which are sometimes one and the same) need experienced professionals to help design and test new devices, and to market them. Equipment installation, user training, and hospital HTM staff training is often performed by other HTMTs employed by the equipment manufacturer. Vendors/manufacturers also employ field or bench service technologists. Research facilities may need HTMTs to design, build, and maintain specialized research devices. And finally, because of the increasing need for HTMTs in the medical system as a whole, instructors for training programs are required, and these are often HTMTs with work experience who have the desire and ability to teach. Association for the Advancement of Medical Instrumentation has an excellent section about HTMT jobs on their web page—see the ancillary web site at CHARACTERISTICS OF HUMAN ANATOMY AND PHYSIOLOGY THAT RELATE TO MEDICAL DEVICES A number of anatomical illustrations are provided in the Anatomy Color Insert for greater clarity; these and more are also found on the ancillary web site. ELECTRICAL SIGNALS AND CONDUCTIVITY Much of the function of the human body depends at least in part on electrical signals. Nerves carry signals throughout the body via chemical reactions and electrical impulses, and these impulses can act on muscle tissue to cause muscle contractions, ranging from skeletal muscle action involved in movement to sphincter muscle control to the beating of the heart. Within neurons, signals travel by simple conduction within Introduction 19 FIGURE 1.18 Neuron structures. the ionic solution inside the cells. In order for the signal to move from one nerve cell to another, or between nerve cells and muscle cells, a chemical reaction must occur. This has a number of consequences that are relevant to biomedical devices. The chemicals involved in conveying nerve signals, or action potentials, between cells are called neurotransmitters and include such molecules as acetylcholine, epinephrine (adrenaline), dopamine, and nitric oxide. When an electrical nerve impulse arrives at the junction, or synapse, between the conducting nerve and the next nerve cell in the particular pathway, molecules of neurotransmitters are released into the space between the nerve cells. The neurotransmitter molecules then connect with a receptor structure on the receiving nerve cell, and this causes an electrical signal to be generated in the new cell. Signals thus travel along a chain of nerve cells to their target tissue (Figure 1.18). With the neurotransmitter steps involved, nerve signal transmission is far slower than electrical conduction speed, in the range of 200 m/s as compared to 3 × 108 m/s. Electrical signals are generated by the flow of calcium, sodium, and potassium ions into and out of cells; this flow is controlled or mediated by the neurotransmitters and their receptors. Due to the nature of the receptor mechanisms, nerve cells can become desensitized, that is, transmission can be reduced or blocked after prolonged stimulation. Muscle action also has an electrical component, with a wave of polarization proceeding in one direction through the muscle tissue as it contracts, followed by a wave of depolarization in the opposite direction as the muscle relaxes again. This 20 Introduction to Biomedical Engineering Technology polarization and depolarization involves the movement of calcium ions in a complex process, but relevant to biomedical instrumentation, it produces the flow of electrical current, which in turn causes a voltage signal to be developed in proportion to the muscle contraction. Various conditions can affect nerve and muscle activity, such as exercise levels, blood gas levels (especially oxygen and carbon dioxide), electrolyte levels, hormones, temperature, physical trauma, toxins, and disease processes. An accurate measure of the different signals present in the body followed by effective analysis can give direct or indirect indications of the factors that are affecting these signals, thus aiding in the diagnosis of disease. These topics will be examined in more detail in the sections that describe specific biomedical devices. CIRCULATION The function of the heart is to pump blood throughout the body, from the heart to the lungs and back, and then from the heart to the rest of the body and return. It is made up of four chambers, each of which has muscle tissue, conduction pathways, connecting vessels, and a valve (Figure 1.19). The four chambers, the right and left atria and right and left ventricles, effectively form two pumps, each with an atrium and a ventricle. The two pumps contract simultaneously. FIGURE 1.19 Structure of the heart. Introduction 21 FIGURE 1.20 The electric heart. Blood is pumped from the right atrium into the right ventricle, and from there to the lungs, where excess carbon dioxide is removed and fresh oxygen acquired. Returning from the lungs, the blood passes through the left atrium and then the left ventricle to be distributed to the rest of the body, including the heart itself. Returning from the body, blood is now back at the right atrium. The ventricles do the main work of the heart and are therefore larger and have thicker muscle walls than do the atria. The rate and strength of contractions of the heart are controlled by a number of factors, including the oxygen demands of the body and blood levels of various hormones such as adrenaline (epinephrine). Coordination of contractions is critical for pumping to be effective, and this coordination is brought about by a system of tissues within the heart that initiate and distribute electrical signals, or action potentials, throughout the heart muscle (Figure 1.20). Built-in delay mechanisms allow the various parts of the heart to contract at the correct time. Signals originate in the sinoatrial (SA) node. These signals cause the atria to contract and are also carried to the atrioventricular (AV) node. From the AV node, action potentials travel down a bundle of fibers called the AV bundle or the bundle of His. This splits into left and right bundle branches, which in turn split into Purkinje fibers, or subendocardial fibers, which ultimately deliver the signals to the ventricular muscles. The electrical signals within the heart are of relatively small amplitude, in the range of 100 mV. Since the inside of the human body consists of electrically conductive tissue, a part of the cardiac contraction signals is carried to the skin, where it 22 Introduction to Biomedical Engineering Technology can be detected by an ECG. On the skin, the signals are much lower in amplitude than at the heart, approximately 1 mV. However, these signals at the skin surface can be amplified and filtered sufficiently to provide a clear representation of the original signals from the heart. Special electrodes allow for optimal contact between the skin and the measuring wires, or leads. Depending on the placement of the electrodes on the body, the signals coming from the heart can be viewed in a number of different orientations—for example, from left to right horizontally, from lower left to upper right, and so on. Originally using just the left arm and right leg, to take advantage of the long axis of the heart to maximize signal size, the placement of electrodes has now become standardized in order to allow useful comparisons (Figure 1.21). FIGURE 1.21 Three-lead ECG electrode placement. 23 Introduction The basic ECG electrode placement has electrodes on the left and right shoulders (left arm or LA and right arm or RA), and the left and right lower abdomen (called the left leg or LL and right leg or RL, from earlier times when the electrodes were actually on the legs, or even consisted of a bucket of saline solution into which the feet were placed). The wires for these electrodes have been color coded (LA = black, RA = white, LL = red, RL = green). Depending on which two contact points are used for measurement, various orientations of the ECG signal can be observed. These selections are called “leads,” and the first ones in common use were labeled with Roman numerals. Lead I takes the left arm as positive and the right arm as negative. Since this orientation is across a smaller section of the heart, the lead I signal is usually relatively small. Lead II has right leg positive, right arm negative, and lead III is left leg positive, left arm negative. THE ECG WAVEFORM The P wave is generated by the contraction of the right atrium (the rising part of the P wave) and the left atrium (the falling part of the P wave) (Figure 1.22). If the P wave amplitude is greater than normal, it may indicate right atrial enlargement, while if it is wider than normal, left atrial enlargement may be the cause. Signal blockages at or near the AV node can cause multiple P waves. After the P wave, there is a delay caused by the AV node, which gives blood time to flow from the atria into the ventricles. When the signal reaches the ventricles, they contract powerfully, producing the QRS complex. The Q portion is a result of depolarization of the septa, the walls separating the chambers of the heart. Heart muscle damaged by a heart attack can cause the Q wave to be deeper than normal. The R and S waves represent phases of ventricular depolarization. Finally, the ventricles repolarize, producing the T wave, and the cycle can begin again. A variety of issues can cause deformation of the T wave. FIGURE 1.22 Normal ECG waveform. 24 Introduction to Biomedical Engineering Technology Positive and negative were chosen as such because, with the wave of polarization of cardiac muscle proceeding generally from the top of the heart to the bottom, this will give a waveform that is mostly positive-going. Other ECG leads have been developed, with a chest electrode location (brown) added to make a five-lead system (Figure 1.23). Six-lead and twelve-lead arrangements are also used, with the 12 lead being the standard for complete diagnostic ECG measurements (Figure 1.24). Some manufacturers have developed electrode placement and signal analysis systems whereby near-diagnostic quality 12-lead ECG waveforms can be derived using only five electrodes. FIGURE 1.23 Five-lead ECG electrode placement. 25 Introduction FIGURE 1.24 Twelve-lead ECG electrode placement. ECG lead systems are discussed in more detail in Chapter 2. Since the focus of ECG measurement and analysis is to aid in the diagnosis of cardiac disease, the changes that disease process cause to ECG signals are of critical importance. Many of these changes reflect either a reduced blood supply to some areas of the heart muscle, or damage to the muscle or conduction pathways caused by a partial or complete blockage of blood flow to an area of cardiac tissue. Normally one’s heart rate is controlled by signals from the autonomic nervous system, which are in turn influenced by exercise, hormone levels, drugs, noncardiac disease processes, and other factors. Cardiac muscle cells, however, are unique in the body in that they will contract rhythmically all by themselves. These automatic contractions can be coordinated by an overriding signal, which under normal 26 Introduction to Biomedical Engineering Technology FIGURE 1.25 Ventricular fibrillation waveform. circumstances results in the proper, effective beating of all areas of heart muscle tissue. If conduction pathways are blocked, either temporarily or permanently (usually be inadequate or no blood flow to part of the heart containing the conductive pathway), then individual areas of the heart can begin beating independently of each other. If these areas consist of small sections of heart muscle, the action is called fibrillation, which can occur either in the atria (atrial fibrillation or a-fib) or ventricles (ventricular fibrillation or v-fib). These areas can be resynchronized by an electric shock, a process called defibrillation. In atrial fibrillation, the ventricles are usually beating more or less normally and still pumping blood, though less efficiently than normal (Figure 1.25). A shock at the wrong time could disrupt the ventricular rhythm; therefore, the defibrillation pulse has to be timed to the ventricular contraction signal and delivered at the correct part of the cycle, a procedure commonly called synchronized cardioversion. With ventricular fibrillation, the atria are likely fibrillating as well and so the defibrillating shock can be delivered at any time. There are many other types of abnormal cardiac rhythms, or arrhythmias, each of which reflects blockage to some part of the conduction pathways of the heart. By examining high-quality ECG waveforms, experts can learn a great deal about the condition of the heart, and computerized analysis allows classification of arrhythmias by ECG machines and physiological monitors. Arrhythmias will be discussed in more detail in the sections on these devices. When the heart is beating normally, the rate is controlled by the sinoatrial (SA) node, which has a natural rhythm of about 70–80 beats per minute. If the atrioventricular (AV) node is controlling contractions, there will be a slower rate of 40–60 bpm, while the contractions led by conduction bundles are slower yet at only 15–40 bpm. Some arrhythmias are brought on by chemical, thermal, or electrical disturbances to the heart and will often disappear when the causative factors are resolved. If this process is prolonged or if the problem is caused by permanent damage to part of the heart, it may be necessary to provide continued synchronization of the heart muscle contractions artificially, using a pacemaker. There are three modes of delivering Introduction 27 pacemaker pulses to the heart: with a relatively large signal applied through electrodes placed on the patient’s chest; through wires connected from an external device directly to the heart muscle; or via wires from an implanted pacemaker device to the heart muscle. These devices will be covered in Chapter 6. Besides ECG signal measurement devices, a number of other technologies can be used to help diagnose heart problems. Injecting a radiopaque dye into the patient’s bloodstream and taking X-ray images as the dye passes through the cardiac arteries can show reduced blood flow to parts of the cardiac system. Ultrasound, CT, or MRI scans can provide detailed images of cardiac structures in two or three dimensions. Pressure transducers, introduced to different chambers of the heart by catheters via an artery in the neck, arm, or groin, and sometimes isolated from other areas by a balloon further down on the catheter, can give precise measurements of pressure at different points, which can be clues regarding heart function. Cardiac output (the amount of blood flow per unit of time) can be measured by introducing either dye or cold saline into the heart and measuring dilution at a later point. Technological means of improving cardiac function include the previously mentioned defibrillators and pacemakers as well as angioplasty devices, which enlarge blocked arteries either by expanding them with a balloon or cutting out blockages with a mechanical auger or a laser. Blocked arteries can also be bypassed using a section of vein taken from another part of the body. Faulty valves can be replaced with biological or mechanical implants, and the whole heart can be replaced with either a donor heart or an artificial pump. BLOOD Blood performs a number of functions in the body, including gas and nutrient transport, wound healing, disease resistance, and homeothermy. Some of these functions are more important than others from an engineering perspective, and these will be discussed in this section. Mechanically, blood is a fluid somewhat more viscous than water, made up mostly of water, plus various compounds such as sodium chloride, nutrient and waste molecules, a variety of proteins, and several types of cells. The most numerous of these cells are erythrocytes, or red blood cells (Figure 1.26), whose main function is transporting oxygen and carbon dioxide between the lungs and body tissues. Other cells are involved in immune response and tissue clean-up and repair. Being an ionic solution, blood is a relatively good conductor of electricity. Red blood cells carry various proteins and carbohydrates on their cell membranes, and the type and arrangement of these substances vary between individuals. If the membrane surfaces of two individuals are similar, they are said to have the same blood type. The broadest and most commonly referenced blood types are A, B, AB, and O, each of which can have a particular characteristic (the Rh factor) either present (positive) or absent (negative). If these main blood types are compatible, one individual can accept a blood donation from another. Blood types have a great deal more complexity than this, but the basic descriptions are sufficient for this text. The movement of blood cells within veins and arteries allows the detection of blood flow by means of Doppler ultrasound, which is described in Chapter 3. 28 Introduction to Biomedical Engineering Technology FIGURE 1.26 Red blood cells. Blood is also involved in clotting, which is the means by which the body tries to prevent excessive blood loss following a breach of blood vessels by trauma or disease. A soluble glycoprotein, fibrinogen, is activated in the presence of an opening in a vessel, and it is converted into fibrin, an insoluble protein that polymerizes to form a mesh. Platelet cells in the blood bind to the fibrin to produce a clot, which reduces and hopefully blocks the escape of blood. Blood clotting is of course critical to survival, but can also be a problem when it occurs at the wrong time or place (which can result in the immediate blockage of a blood vessel, or, after becoming detached from its formation point and moving to another location in a narrower vessel, blocking flow there—i.e., an embolism), or when it takes place too slowly, as in a major trauma such as an accident or surgery. RESPIRATION Respiration is the process by which atmospheric oxygen is taken into an organism so that it can be transported to tissues where it is exchanged for carbon dioxide. The carbon dioxide is then transported so that it can be released from the organism, completing the respiration cycle. Some other gaseous metabolic wastes may also be removed from the body during the cycle. Ventilation is a subset of the respiration process, involving only the movement of gases in and out of the lungs. The human respiratory system consists of the airways of the nose and mouth, trachea, bronchi and bronchioles, the lungs, the muscles that power the flow of air into and out of the lungs, and associated nervous system control components (Figure 1.27). Passive gas exchange occurs in the alveoli of the lungs, which are the interfaces between air and blood. Airways provide additional functions of filtering, warming, and humidifying-inspired air. Both a shortage of oxygen and an excess of carbon dioxide are harmful and potentially fatal, thus the vital nature of the respiratory system. The mechanical nature of Introduction 29 FIGURE 1.27 Human respiratory system. the system makes it accessible to medical intervention in case of inadequate function or failure. Air intake (inspiration) is accomplished mainly by the muscles of the diaphragm and the external intercostal muscles of the rib cage. The diaphragm is normally a sheet of muscle domed up at the bottom of the chest cavity. When it contracts, it flattens out, pulling air into the lungs. The intercostal muscles act to “square up” the chest cavity, thus increasing its volume, again drawing air into the lungs. During maximal inspiratory efforts, some other muscles around the chest cavity may also assist the diaphragm and intercostals. Expiration is normally mostly passive due to the elasticity of the lungs, though abdominal muscles and external intercostals can provide forced expiration. Typically, about 500 mL of air is taken in with each resting breath, and about 10–20 breaths are taken per minute, resulting in 250 mL of oxygen uptake and 200 mL of carbon dioxide output per minute. These values can, of course, have a wide range depending on the individual, age, gender, exertion level, and state of health. Given the important roles of oxygen and carbon dioxide in the body, means have been developed to measure their levels in both inspired and expired air as well as in the blood. Instruments to perform these measurements are described in Chapter 3. CHEMICAL BALANCES All physiological functions involve chemicals as part of their processes, and normal health depends on these chemicals remaining in overall balance. Chemicals in the body range from ions of elements such as sodium, chlorine, potassium, and calcium, to simple molecules like carbon dioxide, water, and oxygen, to more complex sugars and carbohydrates, to convoluted proteins, and to the genetic materials of RNA and DNA. 30 Introduction to Biomedical Engineering Technology Gas balances are described in more detail above and in Chapter 3. Most protein and genetic material chemistries are outside the scope of this book, but the balance of ions and relatively simple molecules will be examined more closely. One of the most important organ systems in maintaining chemical balance is the renal system, consisting of the blood supplies to the kidneys, the kidneys themselves, the ureters, bladder and urethra, and associated control components. Kidneys are vital but they are also vulnerable to damage by disease or harmful chemicals, and thus a wide variety of medical equipment is designed to help determine the state of kidney function and to take over some or all function should the kidneys fail. These devices are described in Chapter 7. Membranes within the kidneys selectively pass different molecules and ions, thus maintaining balance. As an example, sodium intake can vary from one-tenth normal to ten times normal, and the kidneys maintain blood plasma sodium concentrations to within just a few percent. Just 10% of kidney function can maintain health. Buffer chemicals in the blood help maintain proper pH balance, which is important since a drop from the normal pH of 7.4 to just 6.8, or a rise to 7.8, can be fatal. These buffers are controlled by both the kidneys and the lungs. Equipment to measure pH and other blood chemicals are described in Chapter 3. The simple sugar, glucose, is the means by which energy is supplied to cells in the body. Glucose is produced by the digestion of most foods or by the utilization of body fat, and its levels are controlled mainly by the pancreas and the insulin it produces; insulin operates by controlling the movement of glucose in and out of cells. Chronic inadequate production and/or control of insulin is known as diabetes, or more properly diabetes mellitus. Glucose is normally maintained at concentrations between 4 and 8 mmol/L (72– 144 mg/dL) of blood. The brain is the first organ to show signs of low blood glucose (hypoglycemia). At levels below 3.6 mM/L, reductions in mental capacity start to become apparent, while levels below 2.2 mM/L cause significant impairment of judgment and performance. Seizures can result if levels drop further, and under 0.55 mM/L produces a coma state and, if not corrected, death. High levels of blood glucose (hyperglycemia) in diabetes can also have severe consequences. Intraocular pressure changes result in blurred vision. Patients may also experience extreme hunger and thirst, fatigue, weight loss, impaired wound healing, dry skin and mouth, and impaired infection handling. Eventually, blindness and also tissue death in the extremities can occur. Blood glucose levels can be measured by a variety of devices (Figure 1.28), as described in Chapter 3, while pumps to help maintain proper insulin levels are discussed in Chapter 6. DENSITIES The densities of various body tissues and fluids are a factor in the function of many biomedical devices. A listing of some tissue and fluid densities is as follows. 31 Introduction FIGURE 1.28 A glucometer. TISSUE DENSITIES Tissue Type Density (g/cm3) Bone marrow Fat Bone White matter Gray matter Skin Eye Muscle Blood CSF Nerve tissue Cartilage Water 1.81 0.92 1.81 1.04 1.04 1.01 1.17 1.04 1.06 1.01 1.04 1.10 1.00 TEMPERATURE Humans are endothermic, or warm-blooded, organisms, which means that internally produced heat as well as various cooling mechanisms help maintain internal body temperature at a constant level of about 37°C. This means that we can continue to be active when external temperatures are significantly above or below body temperature, allowing a wider range of useable habitats. This maintenance of core temperature is called homeothermy; the body has a “set point” temperature, and if core temperature changes significantly from the set point, mechanisms are activated to bring it back in line. 32 Introduction to Biomedical Engineering Technology FIGURE 1.29 The arctic fox has thick fur insulation as well as short limbs and small ears to help keep its internal temperature normal. There is some small variation of “normal” body temperatures both between different individuals and within individuals at different times. Other species can have significantly higher or lower normal body temperatures than humans. Maintaining homeothermy requires a number of adaptations, including a system to monitor temperature and signal any variations, circulatory modifications to reduce or increase blood flow to the skin and extremities, structures to increase or decrease heat loss to the environment (such as sweat glands that excrete water to the skin surface, which evaporates and cools the skin, or layers of body fat and/or hair to provide insulation) (Figure 1.29), and behaviors to assist in the process (such as increasing physical activity and/or shivering to produce extra heat, seeking shelter from temperature extremes, or utilizing clothing). If core body temperature cannot be maintained, severe symptoms will result. Various means of measuring and monitoring body temperature are described in Chapter 4. HYPOTHERMIA Hypothermia results when core temperature drops significantly, and physiological responses are fairly consistent. Below about 35°C, shivering occurs (Figure 1.30), heart and respiration rates increase, and blood pressure rises. Further below this temperature, all of these parameters begin to decline again, and some brain functions may become impaired, resulting in decreased coordination, disorientation, and communication difficulties. Below 32°C, shivering usually ceases and decreased metabolism results in reduced oxygen consumption. Cardiac output drops, arrhythmias may appear, and the patient may be in a stupor. Introduction 33 FIGURE 1.30 Brrr! Shivering—along with adequate clothing—keeps humans warm in cold environments. Further drops to below 28°C produce a complete loss of nervous reflexes and greatly reduced brain function, as well as greatly reduced cardiac output and severe arrhythmias. The patient may appear to be dead, and death will certainly result if conditions worsen and/or continue for any length of time, though some extreme cases of survival have been recorded. Some victims of accidental hypothermia have been successfully revived from core temperatures as low as 14°C, while under controlled conditions of induced hypothermia, core temperatures have been as low as 9°C. Cardiorespiratory function has been seen to stop for as long as an hour under these conditions, with no lasting damage, because metabolic rates have been so low. The key to survival in these circumstances seems to be that brain temperature must drop relatively quickly, which is why small children have survived for long periods of extreme hypothermia. Re-warming extreme hypothermic patients is difficult, as all vital body structures must be warmed quickly and almost simultaneously, but high temperatures of warming materials must be avoided. HYPERTHERMIA Increases in core body temperature can result from a response to disease processes (fever) or from excessive production or absorption of heat. Fever increases the body’s temperature set point by a few degrees, thus initiating responses to bring core temperature up to the new set point. This is why people with fevers may feel chills (their actual core temperature is initially below the new set point) and experience shivering as their body attempts to raise its core temperature. As a benefit, higher temperatures seem to enhance immune system response and also seem to negatively affect some pathogens such as viruses. Excessively high fever temperatures can be harmful or even fatal and must be reduced by medication and/ or external means. 34 Introduction to Biomedical Engineering Technology When body temperature rises due to increased internal heat production and/or increased ambient temperature or incident infrared radiation, a number of responses can occur. Behaviorally, any organism might seek shade or water, while humans can alter their clothing or simply turn up the air conditioner. Physiologically, blood flow may increase to skin areas where excess heat can be radiated away, and (in humans) sweat glands in the skin produce perspiration, which evaporates and cools the body. If human core temperature rises above 39°C or 40°C, behavioral changes such as irritability and confusion (“mad dogs and Englishmen”) start to appear. As well, the skin reddens, blood pressure drops, and heart and respiration rates increase. Further temperature increases produce still lower blood pressure, which may result in a blotchy appearance of the skin. Convulsions may occur, as well as chills and shivering. At 41°C, brain death begins, and at 45°C, death almost always occurs. Recovery from extreme hyperthermia is less likely than from extreme hypothermia, but it is important to cool the victim’s body as soon as possible to prevent excessive core temperatures. Methods of doing this range from simple moistening of the skin, to cold- or ice-water baths, to the use of special cooling devices. SUMMARY This chapter provided a brief look at the history of some medical devices and an outline of some important anatomical and physiological features of the human body, including electrical signals, circulation and blood, respiration, chemical balances, tissue densities, thermoregulation, and sensory systems. QUESTIONS 1. What are some nontechnological means of diagnosing a patient’s condition? What are the modern technological equivalents? 2. How is the Doppler effect used in detecting and measuring a fetal heartbeat? 3. What advantages are there for using electrical current to perform surgery? Disadvantages? 4. Which other devices are sometimes integrated with cardiac defibrillators? 5. What is the main electrolyte involved in generating muscle electrical signals? 6. Describe the path of blood through the body, especially in the heart. 7. Why doesn’t the whole heart contract at once? What would happen if it did? 8. What are the three ways of delivering cardiac pacemaker pulses to the heart? Which requires the largest signal, and which requires the smallest? 9. Describe the movement of air in and out of the lungs, including the structures involved. 10. What is the difference between respiration and ventilation? 11. Why is the average intake volume of oxygen per breath greater than the average output volume of carbon dioxide? 12. Describe at least two functions of the renal system. 13. What is a potential benefit of increased body temperature when an infection is present in the body? 2 Part One Diagnostic Devices OBJECTIVES FOR THIS CHAPTER • To examine the design, function, and features of physiological monitoring systems. • To look in detail at the anatomy and function of the heart, including a full description of ECG signals and how they are measured and analyzed. PHYSIOLOGICAL MONITORING SYSTEMS Overview Various means of examining and measuring the “vital signs” of patients have been developed in the past. Heart rate, electrocardiograph (ECG) waveform, blood pressure, temperature, respiratory rate, blood oxygen content, and other parameters could be determined accurately. As technology advanced, it became apparent that some of the equipment for these monitored parameters could be integrated into a single unit. This made monitoring more convenient and also allowed direct comparison of values and integrated recording of numeric and graphical data. Electronic data storage allowed systems to store parameter values and waveforms for significant periods, with times extending as technology advanced (Figure 2.1). Patient charting became easier and more comprehensive. Data communications gave the capability of displaying information from one patient on to the monitor of another patient, or at a central location, or even off-site. Changing capabilities led to evolving labels for equipment. What was once called simply an ECG monitor became a bedside monitor, a vital signs monitor, and then a physiological monitoring system or multiparameter monitoring system. Monitor design also diverged, due to the differing needs of various clinical areas. Intensive care units, ERs, and ORs require a means of visualizing patient waveforms and need the capability of monitoring a wider variety of parameters, and in more detail (Figure 2.2). General medical/surgical nursing floors need a quick, compact, portable, and reliable means of measuring basic vital signs such as ECG rate, blood pressure, and temperature (Figure 2.3). DOI: 10.1201/9781003140603-2 36 FIGURE 2.1 Introduction to Biomedical Engineering Technology A physiological monitor screen. (Courtesy of Philips.) FIGURE 2.2 Various add-on modules for a multiparameter monitor (M3012A, M3014A, M3015A, M3016A MMS extensions). Some include several additional functions while others are dedicated to one function. (Courtesy of Philips.) Diagnostic Devices: Part One FIGURE 2.3 A modern multiparameter monitor. (Courtesy of Philips.) INCOMING INSPECTION OF A VITAL SIGNS MONITOR Two large boxes—or rather, one large box and one huge box—were sitting in the middle of the floor when Joe arrived for work in the morning. Mike, who started early, swivelled in his workstation chair and waved a greeting. “The VSM arrived this morning, in case you didn’t notice.” “Thanks, Mike—I might have tripped over this stuff if you hadn’t warned me.” “No problem!” Joe hung up his jacket and logged on to the network, quickly checked for e-mail messages, then turned to the two boxes and retrieved the shipping paperwork and purchase order copy that were taped to the side of the smaller box. He grabbed a box cutter from his toolbox and sliced the boxes open. The smaller box had a packing slip inside, which he placed with the other papers. Opening the larger box, he pulled out another box from inside, and then retrieved a shiny metal tube. Underneath was a six-wheeled device set into a Styrofoam form. Joe pulled the six-wheeled unit from the Styrofoam and then opened the box that had been inside the first, large box. Inside this box were a wire basket and a plastic bag with a few items of hardware inside. He located a large hex-head bolt and washer, and then inserted the metal tube into a hole in the six-wheeled base. Flipping the assembly upside down, he threaded the bolt through a hole in the base and into the tube, tightening it with a socket wrench. Then he uprighted the stand and found the hardware to attach the basket to the middle section of the metal tube. He then turned his attention to the smaller of the original two boxes, referring to the packing slip and checking off the contents. The largest item was the vital signs monitor itself, but there was also an AC power cord, a battery, an 37 38 Introduction to Biomedical Engineering Technology FIGURE 2.4 A vital signs monitor with ECG, temperature (left), pulse oximetry, and NIBP. (Courtesy of Philips.) SpO2 cable and sensor, a thermometer probe and several boxes of probe covers, an NIBP hose and one each of three different sizes of BP cuffs, a few rolls of recording paper, a quick-reference card, an operator’s manual, and a service manual on CD. Joe affixed the monitor onto the stand and connected the various cables, then inserted the battery into its compartment, finally plugging in the AC cord. He noted that the AC power indicator and battery indicators both illuminated and that the monitor completed its power on self-test successfully (Figure 2.4). He knew it would take several hours of charging to ensure that the battery was fully charged, but he could complete some of the incoming inspection processes while it was charging. Before beginning the tests, he noted the serial and model numbers of the unit, affixed an equipment control number sticker, and entered the information into the equipment database program. He unplugged the unit, rolled it closer to the test bench, and started the test device interface program on the laptop there. The first test was electrical safety, so he plugged the AC cord into the safety analyzer and clipped the test cable to the ground pin on the back of the monitor. He selected the basic test routine on the laptop, which was connected to the safety analyzer through a serial cable, and started the tests. Relays clicked and the AC LED flickered on and off as the analyzer measured the line cord resistance, and the AC leakage current under several different conditions, including ground open and line/ neutral reversal. The test results were logged automatically by the controlling laptop and then sent over the network to the central server that held the equipment management database. Diagnostic Devices: Part One Once the safety tests were completed with no warnings, Joe went on to the performance tests. First on that list was the SpO2, or pulse oximeter, tests. As with all the testing equipment, the SpO2 analyzer was connected and controlled through the laptop, with test results being fed to the equipment management database. The analyzer consisted of a box with an LCD display and a finger-like projection. Joe fitted the SpO2 sensor over the finger simulator, selected the specific manufacturer of the probe, and started the test process. The unit simulated various SpO2 percentages at several different perfusion levels as well as producing motion artifacts to check the stability of the monitor. Joe entered the readings from the monitor when prompted by the test program. Next up, temperature tests. The temperature tester was one of the few test devices not integrated into the computerized system, being simply a calibrated, temperature-controlled well into which the probe was inserted. Two different temperatures could be selected, though it took several minutes to switch between the two due to thermal inertia. Joe placed a probe cover on the probe to ensure accurate measurements and inserted the probe. While he was waiting for the temperature reading, he connected the NIBP hose to the monitor and attached the normal adult cuff. By then the temperature reading was available, and he entered it manually into the testing program. He switched to the alternate temperature on the unit and went on to the NIBP tests while the temperature tested stabilized at the new setting. A T-fitting went between the cuff and the hose, with one arm of the T connecting to the NIBP analyzer. The cuff was wrapped around a plastic device that was a stand-in for a patient’s arm, and the test initiated. A pump internal to the analyzer inflated the cuff to a pre-set level and then pneumatic circuitry simulated the oscillometric variations of blood pulsing through a patient’s brachial artery while the pressure in the cuff is slowly bled off. Systolic and diastolic waveforms are simulated, and when cuff pressure drops a certain amount below diastolic, all pressures are released. The monitor calculates systolic, diastolic, and mean pressures as well as pulse rate, and Joe enters these values into the program. The test is repeated at several different pressures, checking that high and low alarms are generated at appropriate pressure values. Once the NIBP tests are complete, the temperature tester has stabilized and Joe rechecks the temperature. Joe initiates a recording of measurements and visually checks the recorder for clarity and smooth operation. Testing complete, Joe closes the program and disconnects all the accessories. He then tidies the unit, coiling cords, and hoses carefully, then affixes a sticker indicating that the unit has been tested by HTM and is ready for use. He rolls the unit to the side and plugs it in to AC so it can finish charging the battery overnight. In the morning, he will wheel it up to the ward where it will be used. 39 40 Introduction to Biomedical Engineering Technology INTEGRATION AND CONNECTIVITY The integration of various vital signs monitoring devices into one brought a number of benefits: The monitoring location became much less cluttered, with a single box and power cord, and one set of mounting hardware. The number of connections to the patient was not reduced, but at least they all originated in the same area. Some functions such as determining heart rate could be adapted to use the best source available. For example, if an ECG signal was noisy, pulse information might be gathered from an invasive blood pressure line or an SpO2 waveform. Comparison of waveforms was much easier. Looking at ECG signals on the same timescale as pressure waveforms can provide useful information (Figure 2.5). Connecting the monitoring system to other devices, such as central stations, networks, and so on, is much easier when all components are in one box and designed with common interface and communication standards. The earliest interconnected monitoring systems used proprietary interfaces, different for each manufacturer, and utilizing heavy, multiconductor cables. Newer systems use industry-standard serial communications with CAT-5 or optical cables. This allows the use of standard data switches, amplifiers, connectors, and other components. The systems are actually just computer LANs, making that part of system design much more standard and “off the shelf.” This also allows easier connections to other networks, such as in-hospital LANs/WANs and the Internet. Some systems are now using wireless communication between components of the system, which alleviates a lot of wiring difficulties, especially in upgrades to existing facilities. FIGURE 2.5 A monitor at a patient’s bedside. Diagnostic Devices: Part One FIGURE 2.6 41 Block diagram of a typical multiparameter monitor. (Courtesy of Philips.) In this block diagram (Figure 2.6), you can see that, as with most electronics currently, the CPU is the heart of the system. These blocks indicate individual circuit boards or assemblies. The power supply feeds directly to the CPU board, and all other components then are fed power from the CPU board. The sections on the right side of the diagram are input/output components, including a thermal printer and touchscreen display. The lower left shows two optional boards, one for SpO2 (pulse oximetry) and the other for NIBP (noninvasive blood pressure). CENTRAL STATIONS When more patients were being monitored electronically, special hospital units were developed to have all such patients in the same area, since their medical needs were similar. These areas were called intensive care units, cardiac care units, special care units, and a variety of other descriptive names. With such a concentration of patients, it became increasingly difficult for nursing staff to watch all the monitors, and indeed most patients went for relatively long periods of time without any critical events occurring. Systems were then developed to gather data from each bedside monitor and transmit it to a central location such as a nursing station, where it could be displayed on a monitor—a central station (Figure 2.7). Since there is generally more data from all of the bedside care units than can be simultaneously be displayed on one monitor at the central station, certain data is selected for display. Generally, other data can be selected for individual circum- 42 Introduction to Biomedical Engineering Technology FIGURE 2.7 Intensive care central station displays, with keyboard and mouse for patient data entry and system configuration. (Courtesy of Philips.) FIGURE 2.8 A recording strip showing tracings from two separate ECG leads. Because of its location, it is convenient to be able to enter patient data into the system at the central station when a new patient is admitted, so a keyboard (and perhaps a computer mouse) was added for this function. Hard-copy recordings are often needed for analysis and to use as part of a patient’s record, and the central station arrangement makes this much more convenient. Instead of individual strip chart recorders at each bedside, from which paper strips would have to be collected, the recorders can be located in the central station, printing strips out from whichever bedside originated the request (Figure 2.8). Depending on the amount of recording being requested, two or more recorder modules might be present in the central station. Larger-format recordings are useful as well, and the bulky recorders (such as a laser printer) required for this are located at or near the central station. Multilead ECGs, longerterm waveform recordings, tables of measured values, patient data, and even troubleshooting information can all be conveniently printed on the central printer (Figure 2.9). All of these recordings can be saved digitally as part of the patient record rather than as hard copies, if required. Diagnostic Devices: Part One 43 FIGURE 2.9 Example printout from central station recorder. Multiple screens allow more patients and/or more detailed information to be displayed, though there is a practical limit to the number of patients that can be handled from each central station, so large care units may be divided into groups. Some other features that may be present with a central station include touch screens for ease of response and information selection; an interface to a nurse call or paging system so that staff can be alerted when critical alarms occur; the capability of transferring certain data from one bedside to another so that staff can check information from other patients in the unit without leaving the bedside of the patient they are with; communication with other special care monitoring systems or other areas in the hospital to allow staff to examine patient data from these other areas, including diagnostic images (X-ray, CT, MRI, PET) and lab results; integration with hospital admission, discharge, and transfer systems to coordinate the movement and collection of patient information; and the ability to transmit information to remote locations such as another hospital, a physician’s office, or a hand-held device such as a smartphone or tablet (Figure 2.10). TELEMETRY As patients, particularly cardiac patients, improve, they often come to a point where it would be beneficial to be able to get out of bed and exercise some, but they still require monitoring in case there are problems. Radio technology came into play, combined with ever-smaller electronic circuits, to allow the development of telemetry units, which combine ECG leads, filters, and amplifiers with a radio transmitter in order to pick up the patient’s ECG signal and broadcast it to a central receiver and monitor. These units had to be small enough to be readily portable, have enough battery capacity to transmit for many hours without battery replacement, and have sufficient range to allow adequate freedom of movement to the patient and to supply a 44 Introduction to Biomedical Engineering Technology FIGURE 2.10 Smartphones and tablets can be used to remotely check patient information, including viewing waveforms. clinically useful signal (accurate and free from significant noise or drift) at the monitoring end of the system. As telemetry systems have evolved, they have grown in capability and quality while shrinking in size (Figure 2.11). Current systems may include SpO2 monitoring and even noninvasive blood pressure, though the pumps and other mechanisms needed for the latter make the transmitter heavier. The transmitter portion of a modern “tele” pack includes a set of three or more lead wires (usually not more than five), ECG input and amplification circuitry, sometimes ECG analysis components, components for additional functions such as SpO2 and NIBP if present, a battery compartment and power circuitry including what is needed to generate low battery signals, a nurse call and/or “event” button for patient use, an RF transmitter including antenna, and interface circuitry to go between the ECG and RF portions. Most new telemetry is digital, which means that analog-todigital conversion is also included. Many tele packs have some kind of port to allow direct communication with a computer or other device that allows for programming parameters and troubleshooting. Digital systems have the capability of changing channel frequencies to make the system more flexible, or perhaps to avoid channels that have excess interference. Telemetry receivers are usually mounted in a rack (Figure 2.12), with one module for each transmitter channel. The rack is in a chassis that contains conditioning Diagnostic Devices: Part One FIGURE 2.11 45 A modern telemetry transmitter pack. FIGURE 2.12 Telemetry receiver rack. and interface circuitry to connect to the central monitoring station and/or other networks. Some systems have dedicated monitors with a single-channel telemetry receiver built in, and/or with another interface to the transmitter such as an infrared link, allowing direct observation of the telemetry signals. 46 Introduction to Biomedical Engineering Technology FIGURE 2.13 Telemetry antenna (black rod) mounted in ceiling. Digital telemetry allows for changing channel assignments and frequencies, within a predefined range. A few RF bands have been allocated for medical telemetry in North America: 608–614, 1395–1400, and 1427–1429.5 MHz. Earlier generations used 450–470 MHz; some older systems may still use this band, but all new installations must use the higher bands. A properly designed antenna system is critical for the effective functioning of a telemetry system. Since power output is relatively low and signal integrity is critical, the antennas must be fairly close together and distributed in all areas where telemetry patients will be active (Figure 2.13). Impedance matching at all points in the system is vital, and if some antennas are to be mounted at a considerable distance from the central receiver (e.g., a system might have antennas in the diagnostic imaging and physical therapy departments so that patients can continue to be monitored when they are temporarily in these locations), then adequate RF signal amplifiers must be used. Newer telemetry systems, and monitoring systems in general, are using Wi-Fi for connectivity, which simplifies the process by using industry-standard protocols and hardware. Special attention must be paid to reliability and security. For monitoring systems, doing away with cables for connections reduces installation time, disruptions, and cost and produces a more aesthetically pleasing arrangement as a side benefit, with no clutter of cables leading from monitors to wall plates or from central station cabinets to monitor banks. Fully integrated wireless monitoring of patients is possible as well, with devices such as Sotera’s VISI monitor, which includes ECG, respiration, SpO2, skin temperature, no-cuff NBP*, and posture and activity measurements. The unit has a highresolution display that can show one of three waveforms (ECG, resp, or pleth) as well as numerics for HR, RR, S/M/D pressure, SpO2, and temp. * No-cuff NBP is derived using a PTT (pulse transmit time) protocol, in which systolic pressure is calculated from the time delay between the R wave of the ECG signal and the peak of the plethysmograph wave from the SpO2 signal; diastolic and mean pressure values can also be calculated from the data. This requires a periodic calibration of the unit by doing a manual (auscultatory) blood pressure measurement and entering the values. Diagnostic Devices: Part One 47 No-cuff BP measurement has a number of benefits: • Longer battery life (with no mechanical pump to power). • Continuous BP measurements rather than the periodic measurements done by cuff-based monitors, which allows quicker response to changes in BP. • Fewer encumbrances to the patient, increasing comfort and mobility. • Less patient disturbance, especially during sleep. THE HEART Details of cardiac anatomy (Figure 2.14) and physiology are discussed in Chapter 1. ECG Monitors and Machines The heart being perhaps the “most vital” of the vital organs, it is important to obtain as much information as possible about its function and condition when assessing a patient. Taking a pulse rate manually and listening for heart sounds have been important tools for medical practitioners for centuries, but as the physiology and anatomy of the cardiac system became better understood, it became apparent that electrical signals could provide very useful information about the heart. Investigators found that the signals within the heart that initiated and coordinated contractions, and were produced by these contractions, could be detected at the surface of the patient. By suitably amplifying and filtering these signals, a waveform could be FIGURE 2.14 Heart anatomy. 48 Introduction to Biomedical Engineering Technology FIGURE 2.15 A stylized ECG waveform. produced that provided important information about the heart, without any need for surgery. The signals are different at different points on the skin surface, because they originate in different parts of the heart and travel different pathways to the surface. This means that by placing electrodes at different locations, different types of information about cardiac function can be obtained. ECG systems are a common and powerful tool for medical staff and can be found in a variety of configurations and settings. “ECG monitor” generally refers to a device that provides real-time ECG waveforms, while an “ECG machine” produces a hard-copy version of these waves. As shall be discussed, the lines dividing these two devices are often increasingly blurred as the capabilities of both bedside physiological monitors and ECG machines grow. Any ECG system consists of the same basic components: a means of picking up the ECG signals from the skin (or sometimes other tissue) of the patient, an amplifier/ filter section to boost the signals to more useful levels and remove electrical interference, some means of displaying the resulting waveforms (Figure 2.15), and a power supply. ECG signals are picked up from the skin through a conductive connection, and so for AC-powered devices, an additional feature is necessary for patient safety: a means of preventing potentially harmful electricity (that might be produced by a fault within the circuitry of the device) from flowing back into the patient. A number of techniques were devised for this and will be discussed in more detail. ECG HISTORY—A BRIEF TIMELINE 1838, Italy—Carlo Matteucci demonstrates that an electrical signal is produced each time a frog’s heart beats. He uses a section of frog leg muscle as a detector. 1843, Germany—Emil du Bois-Reymond demonstrates that an “action potential” is produced when muscle contracts. His detector is a galvanometer Diagnostic Devices: Part One FIGURE 2.16 A normal ECG waveform. coil with 24,000 windings. He uses the notations P, Q, R, and S to denote the various parts of the observed waveform. 1856, Germany—Rudolph von Koelliker and Heinrich Müller show that electrical signals are produced with each beat of the heart, and note that the signal is different on diastole and systole. 1869, England—Alexander Muirhead makes the first ECG recording, using an early form of ink-jet printer. (This accomplishment is disputed.) 1878, England—John Burdon Sanderson and Frederick Page record the first (undisputed) ECG, demonstrating the various phases of QRS and T (Figure 2.16). 1887, England—Augustus D. Waller, first human ECG. 1889, Holland—Willem Einthoven, using jars of saline as electrodes and his dog as a subject, demonstrates ECG signals. 1891, England—William Bayliss and Edward Starling refine ECG technique, identifying the P, QRS, and T components of the signal as well as noting the significance of the PR interval. 1893, Holland—Einthoven first uses the term “electrocardiogram.” 1901, Holland—Einthoven develops a 600 lb “string galvanometer,” which is much more sensitive than previous mechanisms. 1905, England—Cambridge Scientific Instruments Company becomes interested in the commercial production of ECG machines. 1905–1906, England and Holland—ECG arrhythmias described. 1906, Germany—First fetal ECG. 1912, England—Einthoven introduces his triangle. 1928, United States—First use of vacuum tubes for ECG signal amplification. 1928, United States—Frank Sanborn builds the first portable ECG machine. 1938, United States and England—V1–V6 chest leads defined. 1942—United States—Emanuel Goldberger developed augmented leads aVR, aVL, and aVF; when included with Einthoven’s three limb leads and the six V leads, this gave the modern 12-lead ECG system. 1949, United States—Norman Jeff Holter builds the first ambulatory ECG recorder, weighing 75 lb—enough to give someone a heart attack! 1963, United States—The first standard (and still used) protocol for cardiac stress testing is developed by Robert Bruce. 49 50 Introduction to Biomedical Engineering Technology FIGURE 2.17 ECG electrodes on patient. FIGURE 2.18 ECG trace showing 60 Hz electrical interference. (Courtesy of Philips Medical, Canada.) The earliest method of making good contact with the patient’s skin in order to pick up ECG signals was to immerse hands and feet in buckets of saline. This was obviously a cumbersome technique, and silver plate electrodes were developed, using a conductive paste to help ensure good contact. A critical part of the conductive pathway for ECG signals is the interface between the skin of the patient and the ECG electrode (Figure 2.17). High impedance at this point can produce increased interference (Figure 2.18), wandering baselines, reduced waveform amplitude, or even a complete loss of signal. The top layer of skin is tough and impervious, which results in higher impedance than is found in underlying tissues. The impedance is significant in all patients, but can be much higher for certain individuals. Dry or oily skin, the use of some skin creams, occupational exposure to insulating oils, and thicker skin layers can all contribute to high impedance. Diagnostic Devices: Part One 51 A coworker once had an uncle who had worked as an auto mechanic for many years. His skin was so impregnated with oil and grease that he could put his finger in a live light socket and feel just a slight tingle. Don’t try this at home! Electrodes are designed to help overcome skin impedance, but for best performance (and sometimes any performance at all), the patient’s skin must be properly prepared before electrodes are applied. This includes removing excess hair, cleaning the site, and gently abrading the skin with a gauze pad, a scraping instrument, or sandpaper. Some ECG electrodes come with a section of sandpaper on the cover, and special abrasive tape is available for this purpose. Note that alcohol can dry skin surfaces, resulting in increased rather than decreased impedance; therefore, alcohol is not recommended for electrode site skin preparation. One of the biggest sources of medical staff complaints about ECG systems is “poor signal,” and this is often a result of inadequate skin prep. Most ECG electrodes use a silver terminal coated with silver chloride, or a terminal of some other conductive material coated with a silver/silver chloride compound. The electrode may have a conductive paste or gel included, or the paste may be applied separately. Most disposable electrodes come in a package including gel and an adhesive ring, with a metal tab or connecting to the ECG leads. ECG paste or gel is a material designed to interface between electrodes and skin, usually containing chloride ions. The interaction between the chloride ions in the gel, the silver chloride, and the silver itself creates a stable, low impedance connection to the leads and then to the ECG input circuitry—as long as the skin is prepared properly. The adhesive and gel are selected to be nonirritating, though some patients will have sensitivity reactions to one or both. These reactions can sometimes be mistaken for burns. AMPLIFIERS ECG signals at the surface of the skin usually have an amplitude in the range of one millivolt. To be analyzed, manipulated, and displayed, the signals need to be about 1000 times larger, so they must be amplified. An amplifier is basically a feedback electronic circuit, in which the applied signal modifies the conductivity of an element in such a way as to allow a large amount of current to flow through the element in proportion to the input voltage. This current can be applied to further circuitry to develop a voltage that is similar in shape but much greater in amplitude than the input signal. Early ECG amplifiers used vacuum tubes, but their bulk, high-power consumption and low reliability encouraged the development of solid-state amplifiers, using transistors. Discrete transistor circuits gave way to integrated circuit amplifiers, though individual transistors may be used for some stages. Modern ECG systems, even though they use microprocessors for some of their signal modification, still rely on discrete transistor or IC analog amplifiers at the “front end,” to amplify the ECG 52 Introduction to Biomedical Engineering Technology signals to a level that they can be converted to digital. Amplifiers at any point in the system must be accurate and free from significant internally generated noise. INTERFERENCE Ending up with a clinically useful ECG signal from the low-level signal present at the patient’s skin requires that all sources of outside interference be reduced to levels much lower than that of the ECG signal itself. There are many potential sources of interference, or artifact. These can be broadly divided into those generated within the patient, and those generated externally. INTERNALLY GENERATED ARTIFACTS The two main sources of internal, or physiological, interference signals are muscles and skin. Skeletal muscles, like cardiac muscles, produce potentials when they contract and relax. These potentials are carried through surrounding tissue to the skin surface, where they are mixed with ECG signals (Figure 2.19). Fortunately, the characteristics of muscle, or EMG, signals are different from those of ECG signals (EMG signals tend to be mostly higher frequency spikes), which allows them to be effectively filtered out. Still, it is best to try to avoid placing ECG electrodes over large muscle groups. Stretching of the epidermis on which electrodes are placed can generate significant low-frequency voltages. This happens when a patient moves or shifts position, and because it is a slowly changing signal it is harder to filter out. Good skin preparation helps, as can placing electrodes in areas where there is minimal skin stretching during movement. FIGURE 2.19 ECG muscle artifact. (Courtesy of Philips Medical, Canada.) Diagnostic Devices: Part One 53 EXTERNALLY GENERATED ARTIFACTS Some early electrode designs formed what was essentially a battery, the electrodes and electrolytes interacting in such a way as to produce a DC voltage. This voltage is known as an offset potential, because it offsets the ECG signal by some amount, possibly even off the screen or chart. It may show up as a rapid shift in the ECG baseline or as a slower drift. Modern silver/silver chloride electrodes are mostly immune to this phenomenon. Most equipment in hospitals operates on 60 Hz AC (50 Hz in some countries). This includes patient monitoring and treatment devices as well as lights, motorized lifts, computers, fax machines, floor cleaners, and more. All of these devices, plus the wiring that feeds them, radiate 60 Hz signals. These signals induce a potential in the body that may be up to a few volts in amplitude, far greater than ECG signals. Some of this 60 Hz artifact can be reduced by removing its sources, but the key to the most effective means of reduction lies in the fact that these 60 Hz signals are contacting all parts of the body equally. ECG systems are designed to measure the differences in signals at different points in the skin. If all ECG electrodes in use on a patient have equally good contact with the skin, then the 60 Hz signal should be equal at all of them. Since the amplifiers in use amplify only the difference in potential between sites, the 60 Hz signal will not be amplified, while the ECG signal will be boosted. Good skin preparation and fresh ECG electrodes are necessary for this method to be effective. Note that ECG electrodes can dry out if they are past their expiry date, if they have been stored improperly (high temperature and/or light levels, torn packages), or if they have been in place on the patient for too long. Electrode manufacturers will have recommendations as to the time intervals for electrode replacement. The 60 Hz artifact can be filtered within the ECG system; however, some useful ECG information may be in the 60 Hz frequency range and will thus be lost by the action of these filters. A trade-off between artifact and signal accuracy is sometimes required. Higher frequency interference can be produced by electrosurgery machines. These devices radiate high-powered signals in the course of their operation, and their power is applied directly to the patient when cutting or coagulating, so the interference is carried throughout the body. Special filters may be used to help reduce such artifacts; also, some ECG lead sets have extra shielding to help block ESU interference. A final source of artifact is the cable system being used. If signal-carrying wires are compromised, or if contacts at various points in the system are contaminated, or if shield wires are broken and ineffective, then ECG signals may be intermittently interrupted or outside interference may enter the system more easily. FILTERS Filters are required within an ECG amplifying system in order to eliminate as much unwanted signal as possible while allowing most of the ECG signal to pass through. How much (Figure 2.20) ECG signal is enough is determined by clinical needs: simple monitoring of rate requires only the basic QRS spike to be available, while 54 Introduction to Biomedical Engineering Technology FIGURE 2.20 Examples of ECG traces showing effects of filtering. (Courtesy of Philips Medical, Canada.) such things as arrhythmia detection and analysis and ST segment analysis require the highest possible quality in the ECG signal. Filters may be simple RC types, or more complex RC or LRC networks. With digital circuitry, algorithms can be applied to the digitized signals to filter out certain artifacts. ALARMS ECG system alarms are generally divided into three levels, corresponding to urgent— life threatening; urgent—nonlife-threatening; and nonurgent. Different alarm tones, display colors, and system responses may be assigned to each level, usually with some degree of configurability for different situations. Diagnostic Devices: Part One 55 LEAD ARRANGEMENTS ECG systems operate on the principle of differential voltages. The electrical signals generated by the heart travel to the skin. The signals are somewhat different depending on which part of the heart they are related to, and therefore by measuring signals at various points on the skin, different information about cardiac function can be determined. The first experimental ECG measurements used buckets of saline solution for electrodes. The subject’s limbs were placed in the buckets and measurements taken. The lead arrangements that evolved from this practice were therefore called the “limb leads,” with reference points being labelled right arm (RA), left arm (LA), right leg (RL), and left leg (LL) (Figure 2.21). The placement of the electrodes on the extremities was abandoned as better electrodes and equipment became available, and standard locations on the chest were adopted for the four points. FIGURE 2.21 Limb lead electrode locations. 56 Introduction to Biomedical Engineering Technology Using LA as a positive reference point and RA as negative is the first standard lead (lead I). Lead II uses LL positive and RA negative, while lead III uses LL positive and LA negative. The three leads together form Einthoven’s triangle. Three additional leads were developed to give more information. These are called the augmented voltage leads and are similar to leads I, II, and III but moved 30° from each other. Instead of a single negative reference point, the augmented leads use pairs of the limb leads as reference. Augmented voltage right arm (aVR) has its positive end toward the right arm and uses lead III as its negative end. aVL is left arm positive, lead II negative, and aVF is left (foot) positive, lead I negative. These six leads (I, II, III, aVR, aVL, and aVF) use only four electrodes—RA, LA, RL, and LL (Figure 2.22). FIGURE 2.22 Five-lead electrode locations. Diagnostic Devices: Part One FIGURE 2.23 57 Twelve-lead electrode locations. Another set of leads provided yet more information, being placed on the chest in front of the heart (precordially). These are the V leads (V1–V6). These leads use LA, RA, and LL connected together as a reference, and require six additional electrodes. All together, this gives 12 ECG leads (using ten electrodes) (Figure 2.23) and has long been considered the ultimate in obtaining ECG information, such that a fullfeatured ECG machine or tracing is still referred to as a 12-lead. Typically, a “12 lead” recording measures a few seconds of ECG activity for all 12 leads simultaneously and then prints them out in a grid (see Figure 2.23). Because of their arrangements, the various leads give different characteristic ECG waveforms. For example, in leads II, III, and aVF, the main P wave is positive-going, while with aVR the P wave is negative-going. 58 Introduction to Biomedical Engineering Technology PATIENT ISOLATION ECG monitoring electrodes must make very good electrical contact with the patient in order that adequate ECG waveforms can be obtained. However, this very characteristic poses potential problems in that the electrical contact could provide a pathway for harmful external electrical currents to enter the body and then the heart, causing severe reactions or even death. These electrical currents might originate from a faulty nonmedical electrical device such as a television, a computer, or an electric shaver; from a fault in one of the many line-powered medical devices in hospitals; or from the normal function of some medical devices such as electrosurgery machines. Although such fault currents are rare, especially with equipment of modern design that has been properly maintained, their consequences are so severe that safeguards must be taken. DIGITAL SYSTEMS Most ECG systems now convert the amplified ECG signal into digital form, using an analog-to-digital converter (Figure 2.24). The conversion system must have adequate conversion speed and bit depth to preserve all significant components of the ECG signal. Typical systems might use a conversion rate of 250 Hz and 10 bits, much lower than in a music system, since ECG signals have a much narrower bandwidth and smaller dynamic range than do music signals. Once the signal is converted into digital form, it can be analyzed and stored for future reference. FIGURE 2.24 Digitized waveform. Diagnostic Devices: Part One 59 WAVEFORM ANALYSIS AND MEASUREMENTS Digitizing ECG signals also opens the possibility of automatic analysis by microprocessor systems. This analysis ranges from simple recognition of QRS complexes for beat counting, to the recognition of the major points in the waveform to allow both time and voltage measurements, to the recognition of abnormal waveforms (arrhythmias) and labelling or triggering alarms based on these results. Arrhythmia analysis is discussed in more detail later in this chapter. As an example of ECG waveform (Figure 2.25) measurement and analysis, one parameter that is often measured is the time between the S and T parts of the ECG wave, referred to as ST segment analysis. This is a relatively straightforward portion of the ECG waveform to detect, and normally, it is curved slightly upward and is about 80 ms in duration. ST segment analysis looks at both the shape and duration of this section (Figure 2.26). If it is flat or sloping downward, or if it is at a lower level than normal, it may mean that blood flow to part of the heart muscles is restricted (cardiac ischemia). If the segment is elevated, it may indicate myocardial infarction (also called cardiac infarction or heart attack, though heart attack can describe other heart problems as well), where part of the heart muscle has necrotized (died) due to loss of blood supply. WAVEFORM/EVENT STORAGE Digital signals can easily be stored in electronic memory or on disks, the amount being dependent only on the storage capacity. Current ECG systems can store a week FIGURE 2.25 ECG waveform. 60 Introduction to Biomedical Engineering Technology FIGURE 2.26 Sample 12-lead ECG print out, including ST segment measurements. (Courtesy of Philips Medical, Canada.) or more of full-quality ECG signals. Single lead or multilead data can be stored, though of course multileads require more storage space. Stored signals can be retrieved later for statistical analysis; for examination by other medical staff either for diagnostic or teaching purposes; to determine the effects of medication, other treatments, or changes in the patient’s condition; or for legal purposes if there is a question about the care given to the patient. Stored data may also be useful for research purposes. Stored signals can be printed out in hard copy, either in strip form, on a sheet with many lines of tracing, or as individual beats or small sections of a signal. The data can be shared over a LAN or wirelessly to a variety of systems and viewing devices. Digitized and stored waveforms can easily be converted into graphical or tabular forms so that trends or responses to medication can be seen more clearly. ARRHYTHMIA ANALYSIS Any variation from a normal ECG rhythm (or normal sinus rhythm) is called an arrhythmia. Arrhythmias range from occasional odd beats that don’t affect the wellbeing of the patient and can be present for years, to critical patterns that, if not corrected immediately, will result in death. Arrhythmias may simply be a normally shaped waveform that, in a patient at rest, is too fast (tachycardia) or too slow (bradycardia). Arrhythmias can arise from a variety of causes: an imbalance in the chemicals that are involved in cardiac function; Diagnostic Devices: Part One 61 damage or interruption to the signal pathways in the heart; faults in the systems that control heart activity; or damage to the myocardium, either through inadequate blood flow (ischemia) or complete loss of blood supply to a particular area of the heart, which results in muscle tissue death (necrosis), called a cardiac infarction. Diagnosis of arrhythmias (or more specifically, their causes) is generally made through a combination of methods. Accurate resting ECG waveforms are examined and analyzed by a cardiologist, perhaps assisted by a computer-based analyzer. Longer-term ECG records are studied (see description of Ambulatory ECG Recorders in this chapter). Stress-test systems take ECGs at various points in an exercise routine. Catheters may be introduced into the heart, to study cardiac output, or to inject radio-opaque dyes for X-ray imaging. Cardiac ultrasound, CT, MRI, and PET scans may also provide information. Finally, analysis of blood samples can provide additional clues. Two of the more common arrhythmias involve loss of coordinated contractions in areas of the heart, a condition called fibrillation. In atrial fibrillation, the atria do not contract in a coordinated manner, with various sections of muscle contracting independently. This makes the heart look as if it is full of wriggling worms and, though it is disturbing to the patient and results in reduced cardiac output, it is generally not life threatening. Atrial fibrillation can be chronic, presenting continuously until treated successfully, or intermittent, coming and going spontaneously, perhaps in association with sleep or exercise. Atrial fibrillation can be reversed and the ECG returned to normal by proper application of a pulse of electrical current, that is, defibrillation. Ventricular fibrillation results in an almost complete cessation of blood flow from the heart, which means certain death if not immediately corrected, either by the administration of certain drugs or by the use of a defibrillator. A sharp blow to the sternum (precordial thump) can sometimes produce defibrillation as well. This technique is used to great dramatic effect on TV and in the movies. Fibrillation and defibrillation are discussed in more detail in the section on defibrillators in Chapter 7. There are a large number of other cardiac arrhythmias, with classifications for general types, though there are often gradations within and between types. Nomenclature is somewhat variable, though, and acronyms abound. A full study of arrhythmias, their origin and treatment, is beyond the scope of this book; however, some knowledge of the basic types is important when working with the diagnostic equipment used. TYPES OF ARRHYTHMIAS There are a large number of different types of arrhythmias, as well as a variety of ways of describing and naming them. Some of the more common types are shown in Figure 2.27. These and some others are described here: • Asystole: Complete cessation of any contractions; “flatline.” No blood flow. Obviously critical, asystole must be treated immediately to prevent death, usually by “defibrillation,” even though the heart is not fibrillating. • Atrial fibrillation (a-fib): Discussed above. Blood clots can form in the heart during atrial fibrillation, leading to an increased incidence of strokes. 62 Introduction to Biomedical Engineering Technology FIGURE 2.27 Recorder strips of various cardiac arrhythmias. • Atrial flutter: Atrial contractions are very rapid and are coordinated within the atria but do not transfer to the ventricles, which continue to contract normally. • Bigeminy: Alternating normal beats and PVCs. • Bradycardia: Significantly lower than normal ECG rate. This is typically considered anything below 60 beats per minute while resting, but this can vary depending on one’s age and physical conditioning. • Premature atrial contractions (PACs): Occasional extra contractions of the atria. These can give the patient the sensation of a missed beat, while actually the opposite is occurring. This is a very common condition, especially in younger people. It is not harmful and often disappears in time without any treatment. Diagnostic Devices: Part One 63 • Premature ventricular contractions (PVCs): These extra beats originate spontaneously within the ventricles and, like PACs, can give the sensation of the heart “skipping” a beat. Also like PACs, PVCs are relatively common, especially in younger people, and often disappear with time. • Right bundle branch block (RBBB): The right ventricle is not triggered to contract as normal (through the right bundle branch), but instead is triggered from the left ventricle contraction. • Sinus tachycardia: A rapid, but otherwise normal, rhythm, usually as a result of exertion or stress. Often simply called tachycardia. • Sick sinus syndrome: An abnormality in the generation of signals from the cardiac sinus, resulting in bradycardia or sometimes alternating bradycardia and tachycardia. • Supraventricular tachycardia (SVT): If a number of PACs occur sequentially, they can induce an increase in overall heart rate, called SVT. This is generally not serious and while it is commonly seen in children, it usually disappears as the patient ages. • Trigeminy: Two normal beats followed by a PVC, in a repeating pattern. • Ventricular fibrillation (v-fib): Discussed above. This is an immediately life-threatening condition which must be treated within minutes. • Ventricular tachycardia (VT or V Tach): A rapid heart rate that is initiated within the ventricles, usually caused by serious heart disease. V Tach is potentially life threatening and must be treated promptly. Usually considered as five or more consecutive premature ventricular contractions (PVCs). • Ventricular couplet: Two PVCs, preceded and followed by normal beats. May also occur in other multiples. STRESS TESTING Many ECG abnormalities that indicate heart disease do not show up when the patient is resting, and so systems were designed to allow monitoring while the patient exercises (Figure 2.28). Such systems require an exercise device, usually a treadmill or stationary bicycle (Figure 2.29), an interface that allows the exercise device to be closely controlled, a controller, and an ECG monitoring and recording component (Figure 2.30). Some systems may incorporate noninvasive blood pressure monitors or pulse oximeters, though these functions may be performed by stand-alone units. Breathing analyzers and other metabolic measurement devices may also be used in conjunction with cardiac stress testing, or independently utilizing the same exercise equipment. EXERCISE COMPONENT This equipment must be robust and reliable enough to be used frequently, often by heavy patients. It must be capable of providing a wide range of exercise loads, and these loads must be accurate and repeatable. It must also have an accessible, easy-tooperate cutoff switch should the patient or staff determine that the exercise session 64 Introduction to Biomedical Engineering Technology FIGURE 2.28 Back on the treadmill again. has to end immediately. The device must stop quickly but in a controlled manner when the cut-off is activated. Finally, the device must have an interface to allow command of its operation by the controller. Treadmills provide a better means of controlling patient effort than do bicycles, but they are bulkier and harder to stop safely (Figure 2.31). Both types must have adequate means of preventing falls should the patient lose their balance. Treadmills have a range of speeds, typically up to about 15 mph (25 km/h), as well as a range of elevation, from level up to about 15°. Speed is controlled by varying the speed of the electric motor that drives the treadmill belt, while elevation is Diagnostic Devices: Part One FIGURE 2.29 65 Patient on stress test treadmill. controlled by a smaller motor that drives a geared vertical shaft mechanism, moving the front of the treadmill up or down. Speed is measured by a tachometer, and this information is fed back to the controller; usually, the controller sends a signal to the main motor to change speeds, and when the tachometer reports that this speed has been attained, the change speed signal is cancelled. Elevation may be monitored and change requests handled in a similar manner, or a simple potentiometer may be used to determine angle. Both speed and elevation components must have reliable safety mechanisms to prevent overactivation. Exercise stationary bicycles may be upright or supine, and their load is usually controlled by means of a magnetic brake. As with a treadmill, speed is measured using a tachometer. INTERFACE Signals originating in the controller are digital, and feedback from the exercise unit must be digital as well, but analog signals are present in the exercise unit, both as 66 Introduction to Biomedical Engineering Technology FIGURE 2.30 Stress test system. FIGURE 2.31 Stress test treadmill. Diagnostic Devices: Part One 67 control and feedback. D/A and A/D conversions may take place in the exercise unit or in the controller. The interface between the exercise component and the controller is a shielded cable that has to be sturdy and reliable. It may carry analog or digital signals depending on which end the conversions take place. Electric motors produce considerable electrical noise, and so both shielding and suppression components must be effective and reliable. CONTROLLER In order to get the most useful information from a cardiac stress test, the exercise program followed must bring the patient’s heart rate up to certain pre-determined levels for specific time intervals. These programs have been refined and defined as protocols, the most common of which is the Bruce protocol, named after its developer, Robert A. Bruce, and published in 1963. There are a number of other protocols available for use, but the Bruce protocol remains at the forefront (Figure 2.32). The Bruce protocol involves seven steps of 3 min each. At each step, the exercise intensity is increased by increasing both speed and slope of the treadmill. The first step has the treadmill inclined slightly. The protocol is designed so that only those who are exceptionally fit can complete all seven steps. All patients are closely monitored, and when their heart rate reaches a specific level (or if problems start to become apparent), the test is ended, usually with a low intensity cool-down period. FIGURE 2.32 Bruce protocol ECG printout. 68 Introduction to Biomedical Engineering Technology Some other common protocols are as follows: • Modified Bruce: Similar to the original Bruce protocol except the treadmill is level on the first step, and only slope, not speed, increases for the first few steps; both are increased in subsequent steps. • Balke or Balke–Ware: The treadmill runs at a constant speed, and the slope is increased in very small, very close steps so that the increase is almost linear. • Ellestad: A six-stage protocol; speed is increased in five of the steps, and the slope is increased in one. • Naughton: A protocol with 2-min steps. Speed stays constant throughout, but the slope is increased in each step. Most controllers have a number of different protocols pre-programmed and can usually accommodate user-designed protocols as well. Protocol selection and treadmill override controls may be via hard keys on the front panel, or through menus on the display screen. ECG MONITOR The ECG monitor of a stress test system is similar to other ECG monitors as discussed previously. A cable, usually 12 lead, attaches to electrodes on the patient. The electrodes may be somewhat different than those used for long-term monitoring. Skin sensitivity issues are not as important, but good adhesion on a moving, perspiring patient is critical. Skin preparation is just as important for obtaining a good signal as for any ECG monitoring situation, but with patient motion and the need for the best possible data, accurate electrode placement is required. A display screen presents ECG waveforms as well as information about protocols, treadmill status, and patient information. Since target heart rates vary with age and gender, this information and more can be entered into the system and used both to help set up testing and in the interpretation of results. The system prints on a large-format chart recorder (8-½ by 11 in. perforated sheets), in a variety of arrangements including 12 lead interval pages, with a few seconds of the 12 leads, continuous ECG, or (if so equipped) summary and analysis (Figure 2.33). AMBULATORY ECG RECORDERS/ANALYSIS SYSTEMS Some cardiac problems occur only occasionally but are critical indicators of further, more serious difficulties that may develop if treatment is not initiated. Some of these initial problems can be triggered by exercise, as in cardiac stress testing, but others may appear more or less randomly. If they are serious enough to require treatment, they will usually show up one or more times within a 24-h period. In 1949 a physician in Montana named Jeff Holter developed a device to record ECG signals over a long time span. The unit worked, but at 75 lb it was not something Diagnostic Devices: Part One 69 FIGURE 2.33 The recorder section of a stress test system. for an elderly person (or anyone, for that matter) to carry around with them for 24 hours. The 24-h ECG recorder was named for its inventor. The first units in use were capable of 24 h of recording, but weight prevented them from being widely used. Advances in both electronics and battery technology allowed the units to shrink in size while expanding in capabilities, such as simultaneous multiple lead recording and longer-term recordings of a week or more. “Wearable” arrangements make the recorders more comfortable and more stable. Mid-generation recorders used standard audiocassette tapes running at a very slow speed to record the ECG signals in an analog format. Current devices digitize signals and record them in flash memory (Figure 2.34) and also may include Bluetooth or other short-range communication systems to allow wireless connection to the base system. Most systems record two leads of information, partly to provide more complete information but also as a backup in case an electrode comes off or develops inadequate contact, or a lead wire breaks. Some record in multilead formats. A button allows patients to insert a signal into the recording when they perceive unusual cardiac events (possible arrhythmias), and they also keep a diary that records physical activities, meal times, and medication times, as well as a further indication of perceived arrhythmias. The ECG signal is handled in much the same way as in other ECG systems, but of course no display or printout mechanism is required to be built into the recorder. When the recorder is first connected to the patient, it is also connected to a display that allows the operator to make sure an adequate signal is being picked up. After the prescribed interval (usually 24 h but sometimes less, and sometimes as long as 48 or even a week), the recorder and electrodes are removed from the patient. 70 FIGURE 2.34 Introduction to Biomedical Engineering Technology A modern Holter ECG recorder. The recorder itself or perhaps just the flash memory card is then plugged into an analyzer, which copies all the data into internal memory. Data is run through a program that measures and tabulates overall and instantaneous beat rates. It also analyzes the waveforms for arrhythmias and counts the numbers of different types, highlighting them in the waveform tracing to enable staff to examine episodes in more detail. Analyzers may be personal computers with good specifications and a card-reader interface, loaded with the analysis software, or specially designed systems just for that purpose. Analysis systems include a high-resolution monitor for waveform examination and display of other data, as well as patient information, archiving parameters, and more. A printer is available for hard-copy information, and a high-capacity storage system allows archiving of information from many patients. Systems may be connected to the hospital network and/or the Internet. CARDIAC OUTPUT When a normal heart beats, the volume of blood pumped is predictable. Damage to any part of the heart, whether it be from ischemia, infarction, or valvular dysfunction, can cause a reduction in blood output, and measurement of this parameter can provide valuable clinical information. There are various means of performing such measurements; until recently, the methods were invasive and uncomfortable, but newer techniques can accomplish the same goal noninvasively. The invasive techniques involve inserting a catheter into the heart circulation (usually the pulmonary artery), releasing a material at one point in the artery, and then measuring its concentration at a point downstream. Applying a formula using the initial and final concentrations as well as the time and distance involved can yield an accurate value for cardiac output. Some systems used a dye, with an optical Diagnostic Devices: Part One 71 sensor to measure downstream concentration; others used a bolus of cold saline with a temperature sensor; still others used a radioactive isotope. These methods all had drawbacks, primarily the discomfort for the patient and the potential for dangerous side effects. Some patients had negative reactions to the dye in use, there is a possibility of physical damage to cardiac structures, and infection at the catheter insertion site could occur. Newer technology has made it possible to determine cardiac output accurately and noninvasively. Specialized devices using magnetic resonance imaging or ultrasound can develop images of the heart and major surrounding vessels as well as blood velocity at specific points. By calculating the area of the vessel being measured with the velocity measurement, cardiac output can be determined. SUMMARY This chapter included descriptions of physiological monitors; central stations; details of cardiac function; some history of the ECG; the generation and meaning of the components of the ECG signal; a description of the various ECG lead systems; and some discussion of digitizing ECGs, arrhythmias, stress testing, Holter monitoring, and cardiac output testing. QUESTIONS 1. Why were various functions integrated in physiological monitoring systems? 2. Why have manufacturers moved toward computer industry standard communications systems for monitoring system interconnections? 3. What benefits might come from connecting a monitoring system to a hospital LAN? 4. What are some benefits of using telemetry systems for patient monitoring? 5. What parameters other than ECG might be included in a telemetry pack? What are the disadvantages of having these features? 6. Why is antenna system design critical for telemetry systems? 7. What are the basic building blocks of any ECG system? 8. What is Einthoven’s triangle? 9. Why would a portable ECG recorder be useful? 10. What are some of the problems associated with high skin impedance? 11. Why is the use of alcohol not recommended in preparing a patient’s skin for ECG electrodes? 12. What are some sources of interference for ECG signals? 13. What might an elevated ST segment of an ECG waveform indicate? 14. What is the term describing a series of premature atrial contractions? 15. Why is ventricular fibrillation more serious than atrial fibrillation? 16. Describe the basic components of an ECG stress test system. 3 Part Two Diagnostic Devices OBJECTIVES FOR THIS CHAPTER • To examine the circulatory system including the relevant characteristics of blood, the physiology and measurement of blood pressure, blood oxygen, blood gases and other components, and blood flow. • To look at the respiratory system and how it is monitored, including the parameters used for measurements, inspired and expired CO2 analysis (capnography), inspired and expired oxygen monitoring, and bronchoscopy. • To discuss the nervous system, including the details of nerve signals, the mechanisms of anesthetics and how they are monitored, the physiology and measurement of EEG signals, and the use of muscle and nerve stimulators. CIRCULATORY SYSTEM AND BLOOD Introduction Blood pressure is a vital sign that can give important information to medical staff and is thus one of the most commonly measured physical parameters. Simply defined, blood pressure is the pressure exerted by blood on the walls of the circulatory system. Due to the structure and function of the system, pressure measurements vary both over time and from one location in the system to another. The circulatory system is under the influence of gravity, so pressure tends to be lower in the highest parts of the body. Due to the cyclic pumping of the heart, blood pressure varies correspondingly, with its highest (systolic) value at the point of maximal cardiac output, falling to a low (diastolic) value between contractions. A shoulder, called the dicrotic notch, occurs when the aortic valve closes. Both systolic and diastolic values, as well as the mean cycle pressure, can provide valuable information about the state of the individual. Blood vessels have a degree of elasticity as well as mechanical resistance to flow. This means that pressure waveforms are reduced at points further away from the heart; both systolic and diastolic values are lower, as is the difference between the two. At the capillaries, pressure is almost constant. Pressure in the venous portion of the circulatory system is also relatively constant at any given point, dropping in response to gravity at higher points in the body. Pressure must be adequate to allow blood to return to the heart. Blood pressure in general is modified by various normal and abnormal physiological conditions. DOI: 10.1201/9781003140603-3 74 Introduction to Biomedical Engineering Technology HYPERTENSION Physical exertion increases blood pressure as the heart pumps harder and more rapidly in order to maintain adequate blood supply to muscles. Various diseases, usually related to the renal system, can cause increases in blood volume, which in turn increases blood pressure (hypertension). Hypertension can also be produced by abnormal responses of the autonomic nervous system. Note: The terms atherosclerosis and arteriosclerosis are sometimes used interchangeably, though arteriosclerosis usually refers specifically to the loss of elasticity in blood vessel walls, while atherosclerosis refers to the build-up of plaque in vessel walls, which in itself reduces elasticity as well as narrowing the vessel. When deposits build up in blood vessel walls (atherosclerosis), the vessel walls become thicker and less elastic, and the interior diameter of the vessels is reduced. Atherosclerosis (Figure 3.1) can be caused by prolonged periods of hypertension or by excess amounts of cholesterol in the blood, or a combination of these factors, and others. The changes of elasticity seen in arteriosclerosis also have an effect on blood pressure waveforms, with a greater difference between systolic and diastolic values. This, combined with the reduced blood flow resulting from narrowed arteries, means that cardiac muscle perfusion is reduced significantly, since cardiac muscle perfusion occurs mainly during diastole. This reduction in cardiac perfusion can produce angina (chest pains) and eventually lead to a heart attack. Persistent hypertension can also cause strokes, aneurysms, and kidney failure. FIGURE 3.1 (a) Atherosclerosis and (b) Illustration of different stages. Diagnostic Devices: Part Two 75 HYPOTENSION Low blood pressure, or hypotension, can also be caused by faulty autonomic nervous system responses, or by blood loss. Some individuals are able to function normally with lower than “normal” blood pressure, and actually may see some health benefits from this situation. Abnormally low blood pressure leads to reduced perfusion of all organs, but most significantly the brain. Reduced cognitive function, dizziness, unconsciousness, and eventually death can result. Some other causes of hypotension include severe infections, toxins, and hormonal imbalances. BLOOD PRESSURE MEASUREMENT Invasive Blood Pressure Monitors The most accurate and timely method of measuring blood pressure is to insert a fine, saline-filled cannula (tube) into the blood vessel or structure of interest. The cannula is connected to a pressure transducer. Alternatively, a small pressure transducer can be mounted on the tip of a catheter, which is then inserted into the target area. This provides a better response than the saline-filled cannula since the transducer is immediately at the site of the pressure being measured, but since it is a somewhat larger diameter, it can’t be used in the very small vessels that are accessible to a cannula. In either case, the pressure transducer produces a signal that can be analyzed to provide a value for pressure. The pressure value can be given as a numeric or charted on a recorder or video display. The response time of the system is faster than any significant temporal features of the actual pressure cycles, and when properly designed and calibrated, is completely adequate to represent the smallest significant amplitude features of the pressure cycle. This technique has a number of disadvantages, however. • It is invasive and thus somewhat difficult to set up and also uncomfortable for the patient. • There is a possibility of infection developing at the insertion site. • Some bleeding may occur at the site. • A blood clot, or thrombus, may form in the vicinity of the cannula. If this breaks free it can cause a blockage in a smaller vessel. The cannula must be flushed regularly if used for an extended time, in order to reduce the formation of clots. PRESSURE TRANSDUCERS Several different technologies can be used in the construction of a pressure transducer. • Resistive elements, which change their impedance when under direct pressure. 76 Introduction to Biomedical Engineering Technology • Strain gauges, which change impedance when deformed. • Piezoelectric crystals, which produce an electrical potential when deformed. Most medical applications use piezo transducers. In order to provide medically useful results, pressure transducers must have adequate performance for a number of characteristics. • Their sensitivity must be suitable for the range of pressures encountered in the human body. Sensitivity is defined as the amount of pressure change required to produce a specific amount of output variation. For example, a transducer might have a sensitivity specification of 20 mV/mmHg, which means that for each millimeter of mercury pressure applied, the transducer produces a potential change of 20 mV. • They must have an adequate range, so that they can produce accurate outputs over the full range of pressures that they will be expected to measure. • They must be sufficiently accurate to be able to measure the smallest pressure variations that are significant to the study. • This accuracy must remain within specified limits over time. This factor also relates to resolution or the smallest changes that the transducer can detect. • Their output must be sufficiently linear over the expected range of values that accurate values can be obtained. Signals can be processed to provide linear outputs, but they must follow a smooth, mathematically predictable curve. • Output must follow positive and negative pressure changes equally well. This parameter is called hysteresis. • The response of the transducer must be rapid enough to capture significant fast changes in pressure. NONINVASIVE BLOOD PRESSURE MONITORS Clinicians saw the need for an accurate, noninvasive method of measuring a patient’s blood pressure. It was known that, if a blood vessel within a limb was compressed, blood flow could be blocked completely. This in turn caused the pulse at the radial artery in the wrist to disappear. If the pulse and pressure were both monitored as pressure was released, the observer could detect when the pulse reappeared. This point corresponded to the systolic blood pressure. Investigators found that, if the pressure applied was between the systolic and diastolic blood pressure, the vessel would open and close as blood pressure rose above the applied pressure and then dropped below it again. This opening and closing of the vessel produced a characteristic sound that could be detected at the brachial/cubital artery at the inner elbow using a stethoscope (auscultation). When the applied pressure was above systolic or below diastolic, the vessel was either fully open or fully closed, and the sounds were not heard. These were named Korotkoff sounds, after one of the early researchers. Diagnostic Devices: Part Two FIGURE 3.2 77 Blood pressure being taken manually. Around 1900, a technique was developed in which a cuff containing an air bladder was placed around the patient’s arm just above the elbow. The cuff/bladder was connected to a manometer (a simple pressure gauge) and to a mechanism for pumping up the pressure and then releasing it slowly. By reducing pressure slowly and noting its values when the Korotkoff sounds first started and when they ended, systolic and diastolic values could be determined (Figure 3.2). This auscultatory method is still in common use, as it gives good results using inexpensive, reliable equipment. Its disadvantages are that it requires human attention, which can make frequent measurements very time-consuming for staff, and that there is some variation in values obtained due to individual difference in technique. Machines were soon developed to duplicate the technique mechanically. Systems used one of two methods to detect blood flow, though both used similar pumping and releasing mechanisms. The first method placed a microphone at the brachial/cubital artery site, which simply picked up the Korotkoff sounds and analyzed the signals to determine systolic and diastolic values. This was more analogous to the manual method but required precise placement of the microphone pickup. The microphone had to stay in place reliably over the time of monitoring. Microphones were sometimes external to the cuff, but more commonly built in to the cuff. Either location required wires to run from the cuff to the chassis along with the pneumatic tubes. A more reliable and convenient method of mechanically detecting the variations in blood flow for pressure determination was developed, using the fact that pressure variations inside the arteries of the arm were transmitted to the skin, especially when constricted by a cuff. These pressure variations were also transferred into the cuff itself, and via the pneumatic tube to the inside of the device chassis. Here, the pressure variations could be measured, processed and analyzed, and used to determine systolic and diastolic values. This oscillometric technique provided reliable, repeatable results, which corresponded well with invasive pressure measurements. Since 78 Introduction to Biomedical Engineering Technology FIGURE 3.3 Comparison graph showing correlation between a monitor’s NBP measurements to direct pressure measurements using a pressure transducer within the artery. (Courtesy of Philips.) the technique is different from the auscultatory method, values obtained may be different, but not incorrect. Both techniques can give values slightly different from invasive measurements (Figure 3.3). Diastolic pressure is more difficult to determine than systolic as the signals are at a lower level; this leads to greater variation in diastolic values between the various measuring techniques. PRESSURE MEASUREMENT CYCLE Once placed in the correct position on the patient’s limb (usually the arm, but measurements can be made on the leg) the cuff is pressurized to a specific value, which is above normal systolic. If oscillations are still detected, the pressure is increased in steps until oscillations are no longer detected. If the pressure required for this is above a threshold value, an alarm sounds and pressure is released, since there is either something wrong with the setup or the patient’s blood pressure is dangerously high. Note that some systems make their determinations as pressure rises rather than as it falls. Diagnostic Devices: Part Two 79 After stabilizing, pressure in the cuff is slowly released. This may be done in a linear manner, in which case the pressure value at the detection of systolic and diastolic points is assigned those values, or the pressure may be reduced in discrete steps. In the latter case, oscillations will likely start and stop at some point between steps, but an interpolation algorithm gives sufficiently accurate values. Once the diastolic point has been passed, cuff pressure is released. Note that, on the first measurement cycle especially, the cuff may “settle in,” adjusting to the patients arm and to the closure mechanism. This may affect measurements; therefore, the second and subsequent readings taken are usually more accurate. Systems may be set to take readings at specific intervals, or only when requested by the operator. Alarm values may be set for systolic, diastolic, and mean readings. Most systems are able to count pulses during the pressure measurement process and thus provide a heart rate value. Values determined are usually displayed with separate numeric readouts or on a video screen. If a video screen is used, graphical trends may be available. Some systems have a paper recorder that can print out values and graphs. NIBP units may be integrated into other devices, such as physiological monitors, defibrillators, or anesthetic machines. In these cases, a shared display is used to present data. FURTHER NOTES For all blood pressure measurement systems, a formula is applied to the systolic and diastolic values to give a mean pressure value. Also for all systems, the effect of gravity must be considered, in that standard blood pressure values are considered to be on the same horizontal plane as the heart. If the measurement site is above the heart, values will be lower; if the site is below the heart, values will be higher. The variation is about 3–4 mmHg for every 5 cm change in vertical position relative to the heart. Using the correct cuff size is important in obtaining the most accurate results. Most cuffs have either a recommended limb circumference or markings to indicate correct sizing, or both. Cuffs that are too large or too small will give incorrect readings; additionally, small cuffs will likely come undone as they are pumped up. Systems may have a means of compensating for the maximum pressure applied. This may be adjusted depending on the previous value of systolic pressure so that the cuff pumps up to an adequate level before readings begin. Care must be taken when applying blood pressure cuffs to avoid a patient’s arm on which other medical devices are being used, since the repeated occlusion of blood flow could affect the efficacy of the other devices (Figure 3.4). For example, intravenous therapy will be interrupted and lines may lose patency when pressure is applied proximally to the insertion site. Pulse oximetry readings will also be altered if blood flow is blocked by the NIBP unit. As a final note, some patients may suffer from “white coat hypertension,” in that they become nervous or agitated when a doctor or nurse approaches, or when undergoing any medical test. The reaction can cause an increase in blood pressure, which is usually temporary. Repeated measurements after the patient relaxes will give more realistic readings. 80 Introduction to Biomedical Engineering Technology FIGURE 3.4 A noninvasive blood pressure monitor (this unit also monitors/measures temperature and SpO2). NEW DEVELOPMENTS IN NBP MEASUREMENTS Although traditional NBP measurement has the advantage over invasive measurement in that it doesn’t require the insertion of a pressure transducer into the patient’s artery, it has drawbacks. The cuff and associated tubes can be cumbersome and restrictive to the patient, and measurements can only take as close together as a minute or two, which means that sudden, clinically critical changes in pressure might not be detected in a timely manner. No-cuff NBP is derived using a PTT (pulse transmit time) protocol, in which systolic pressure is calculated from the time delay between the R wave of the ECG signal and the peak of the plethysmograph wave from the SpO2 signal; diastolic and mean pressure values can also be calculated from the data. This requires a periodic calibration of the unit by doing a manual (auscultatory) blood pressure measurement and entering the values. No-cuff BP measurement has a number of benefits: • Longer battery life (with no mechanical pump to power, making it ideal for ambulatory systems). Diagnostic Devices: Part Two 81 • Continuous BP measurements rather than the periodic measurements done by cuff-based monitors, which allows quicker response to changes in BP. • Fewer encumbrances to the patient. • Less patient disturbance, especially during sleep. PULSE OXIMETERS Traditional vital signs such as pulse, respiration, and temperature required only observation to gather information about a patient. Blood pressure was more difficult to measure but simple mechanisms allowed reasonably accurate determinations to be made. Another basic vital sign had to wait until sophisticated electronic equipment was available before it could be monitored effectively. While a patient may be breathing, and her heart beating, if sufficient oxygen isn’t being transferred into the blood, she could be in critical medical difficulty. Skin tone may provide a small degree of insight into this parameter, but accurate values can only be obtained through blood sample analysis or by the use of a pulse oximeter. Pulse oximetry takes advantage of the physics of hemoglobin, in that this molecule in red blood cells absorbs specific wavelengths of light differently depending on whether or not it is saturated with oxygen (Figure 3.5). The total amount of the saturated form of hemoglobin (oxyhemoglobin) compared to the nonsaturated form (hemoglobin) gives an indication of the effectiveness of ventilation and gas exchange in the lungs. Two precise beams of light are used, with wavelengths of 650 nm (red) and 805– 940 nm (infrared), as determined by lab experimentation. Oxyhemoglobin absorbs less red light than does hemoglobin, but it absorbs more infrared light than its unoxygenated counterpart. By passing beams of both red and infrared light through an area of good blood flow (perfusion) but minimal thickness, such as a fingertip (Figure 3.6) or ear lobe—or toe FIGURE 3.5 Stylized red blood cells. 82 Introduction to Biomedical Engineering Technology FIGURE 3.6 A pulse oximeter sensor in place on a finger. (Courtesy of Philips.) or heel, especially in infants or neonates—and measuring how much light is received by a sensor on the other side, absorbance values can be measured (Figure 3.7). By analyzing these signals with a computer algorithm that adjusts for calibration constants, nonlinearity, and other factors, a numeric value for oxygen concentration can be obtained. This value is shown as a percentage of maximum oxygen saturation. Various factors can reduce the accuracy of oxygen saturation measurement. • Some nail polishes absorb the two wavelengths differentially, introducing errors—sensors should not be used on fingers having nail polish, especially blue, green, or black (Figure 3.8). • Carbon monoxide binds to hemoglobin and can produce false readings. • Some toxins or disease conditions can alter normal hemoglobin, producing methemoglobin, which greatly degrades pulse oximetry performance. • Low perfusion reduces the accuracy of measurements; sensors should always be placed in areas of good perfusion. (Some units give a measure of perfusion, which in itself can be useful diagnostically.) • Some medical dyes such as methylene blue can temporarily reduce displayed saturation values, without affecting actual values. • High levels of ambient light can affect readings. Most current pulse oximeters are accurate to within 1% or 2% at higher saturation levels when compared to measurements made by drawing blood samples and measuring directly. At lower saturation levels, accuracy declines, but when patients are in such conditions they are usually being monitored very closely and saturation is determined by direct blood sampling. Some systems display a value or a bar graph to indicate relative perfusion. Diagnostic Devices: Part Two FIGURE 3.7 A pulse oximeter sensor opened to show sending and receiving sites. FIGURE 3.8 Fingernail polish can interfere with pulse oximeter measurements. 83 84 Introduction to Biomedical Engineering Technology FIGURE 3.9 A modern pulse oximeter. (Courtesy of Masimo.) Some newer systems, such as those from the Masimo Corporation, use sophisticated algorithms to reduce noise interference and improve accuracy at low perfusion levels. Some Masimo models can also measure hemoglobin levels and carbon monoxide levels. Pulse oximeters may be small, hand-held portable units, larger bench- or polemounted devices, or they may be integrated into other devices such as physiological monitors, defibrillators, fetal monitors, anesthetic machines, or telemetry transmitters (Figure 3.9). The integrated oximetry circuitry may be proprietary to the main equipment manufacturer, or it may be licensed from another specialist manufacturer. The pulsatile nature of blood flow through the oximetry monitoring site means that the absorption/transmission of the light beams will vary slightly over the cardiac cycle. At systole, there will be more blood in the area, and less at diastole, so the instantaneous values of light intensity will approximately follow the blood pressure curve. This allows a pulse frequency value to be determined, and in systems so capable, a pulse waveform (plethysmograph) can be displayed. Typically, the displayed waveform amplitude is automatically adjusted to full scale, which means that it doesn’t itself provide information about perfusion levels. Various types of pulse oximetry sensors are available (Figure 3.10). In shorterterm monitoring situations, a finger-, toe-, or ear-clip unit is used, which is springloaded and can be applied and removed easily. For longer-term monitoring, or when the patient is too small for the normal clip type sensors, flexible wrap-around sensors can be used, held in place with an adhesive strip. Some manufacturers provide disposable sensors, intended for single-patient use, to help avoid the possibility of cross-contamination, more important than ever in a pandemic. Newer pulse oximeter systems can differentiate between arterial oxygen saturation (SaO2) and venous oxygen saturation (SvO2), which has clinical significance and adds to the value of these measurements (Figure 3.11). The Masimo Rainbow™ system can, in addition to regular SpO2, measure such values as total hemoglobin (SpHb™), oxygen content (SpOC™), carboxyhemoglobin (SpCO®), and methemoglobin (SpMet®) in real time, giving a more complete picture of the patient’s clinical condition. Diagnostic Devices: Part Two FIGURE 3.10 A variety of pulse oximeter sensors. (Courtesy of Philips.) FIGURE 3.11 Older pulse oximeter. 85 86 Introduction to Biomedical Engineering Technology TRANSCUTANEOUS CO2 ANALYZERS Blood oxygen levels can sometimes be normal while inadequate carbon dioxide removal leads to elevated levels of that gas in the blood. This hypercapnia can cause acidosis, tachycardia, or even coma leading to death. In order to monitor CO2 levels in the blood, the patient’s skin must be heated when in contact with an electrode. Heat increases perfusion and also increases the permeability of the skin, allowing some of the CO2 in the blood to diffuse out through the skin. The electrode consists of an electrolyte-filled cell with a membrane covering. The membrane allows the CO2 from the skin to enter the electrode cell, where chemical reactions with the electrolytes produce a voltage potential proportional to blood CO2 concentration. This signal is processed to provide a numerical value, which can then be displayed and recorded. BLOOD CHEMISTRY ANALYZERS Determining the balance of various chemicals in the blood is critical for both diagnosis and determining courses of treatment. Because imbalances can either cause or be a symptom of life-threatening medical conditions, quick and accurate analysis of blood chemistry is vital. Most blood chemistry analysis is done by drawing a sample of the patient’s blood, taking it to a laboratory, passing it through one or more complex, computerized analyzers, and then reporting the results to staff at the patient’s location. Lab analyzers are outside of the scope of this book and will not be examined. This mode of testing requires careful documentation, special sample handling, and considerable travel, which when combined with the time taken by the analyzers leads to significant delays between when the sample. A technology that is becoming more common is point-of-care (POC) blood analysis. With this type of device, much smaller samples of blood are required and analysis is done, as the name implies, at the “point of care”—the patient’s location. This means that results are obtained much more quickly. With an appropriate interface, measurement values may be able to be copied into the monitoring system being used, to form an integral part of the patient record. Joe Biomed had just finished replacing a recorder module in the CICU central station when he noticed that staff at one of the bedsides was preparing to use their new POC blood analysis unit. Since he had never seen it in operation before, Joe paused to look over the shoulder of one of the resident doctors who was also observing. Normally, one staff member could perform the test by themselves, but everyone wanted to play with the new toy, so there was a small crowd gathered around. A nurse performed a finger-prick on the patient and drew a few drops into a capillary tube. He then transferred the blood to a small cartridge and sealed the cartridge. Diagnostic Devices: Part Two 87 “What can you measure with that one, Sam?” asked a GP who was watching the process with interest. “This is one of the more basic ones,” Sam replied, “It does sodium, potassium, Hematocrit and hemoglobin.” Sam inserted the cartridge into the analyzer, and within a few minutes, values for the four parameters appeared on the LCD screen of the analyzer. Sam passed the unit around for everyone to take a quick look, and then pressed a few buttons to transfer the values to the patient monitor and from there to the central monitoring system. This made it available on the hospital intranet, and, with proper clearance, to users from anywhere in the world through the Internet. Sam removed the cartridge from the analyzer and disposed of it safely, and the test was complete. POC analyzers have different features and technologies depending on manufacturer, and a wide range of parameters can be analyzed. An example of parameters available is given in Table 3.1. As with any device used to determine treatment, the accuracy of POC analyzers is critical. This means that calibrations and cross-checks must be performed and documented as per manufacturer recommendations. With such tools, clinicians can obtain vital information about their patient’s condition quickly, allowing them to initiate or adjust treatments in a timely manner. GLUCOMETERS Diabetes in various forms is a major health issue, and a large part of successfully dealing with the condition depends on regular, reliable measurements of blood glucose levels. Such measurements can be useful in other situations than diabetes, as well, but the overwhelming majority of such tests are done with diabetic patients. The well-being of a diabetic patient is greatly enhanced if they can maintain their blood glucose levels within certain limits on both short-term and long-term bases. Laboratory and POC analyzers can measure blood glucose, but of course this is inconvenient for patients, especially if they need to perform tests several times a day. Such tests also involve the time of health care professionals and are quite expensive. To deal with this situation, small, hand-held glucometers were developed (Figure 3.12). These units can easily be operated by patients or family members and provide quick, accurate results. A typical glucometer “kit” consists of the following: • A set of clean stylets. They are used to puncture the skin. Most stylets are spring-loaded and are designed to provide an optimum skin puncture, neither too shallow nor too deep, with maximum ease of use. 88 Introduction to Biomedical Engineering Technology TABLE 3.1 Some Parameters That Can Be Measured with Point-of-Care Blood Analysis Units CHEM8+ BNP CK-MB Troponin I Creatinine Urea nitrogen (BUN) Glucose (Glu) Chloride (Cl) Sodium (Na) Potassium (K) Ionized calcium (iCa) Hematocrit (Hct) Hemoglobin (Hgb) pH pCO2 pO2 TCO2 HCO3 BEecf sO2 Lactate Anion gap ACT (Celite)® ACT (Kaolin) PT/INR • A set of test strips, onto which a droplet of blood is placed. The blood sample reacts with chemicals in the strip for a specific time, and then the strip is inserted into the reader. • A calibration strip for each batch of test strips. These are used regularly to ensure that the reader is calibrated internally and adjusted to the specifics of the batch of test strips that it came with. • A strip reader, which takes the test strips that have been exposed to blood and performs measurements in order to produce a display of blood glucose level. The reader may also have a timer to prompt the user to insert the strip after the correct reaction time has passed. Some readers have voice messages to guide the user through the steps, and some can communicate with other devices such as smartphones, tablets, or computers to keep more comprehensive records and possibly integrate with diet and exercise applications. Blood glucose levels are measured in milligrams of glucose per deciliter of blood (mg/dL; used mainly in the United States) or millimoles per liter (mmol/L; used in Diagnostic Devices: Part Two 89 FIGURE 3.12 A glucometer kit, with test strips, meter, and stylet. (Courtesy of Abbott.) most other countries, including Canada). The two different standards mean the great care must be taken with new or unfamiliar glucometers to be sure the user knows which units are in use. To convert from mg/dL to mmol/L, readings are multiplied by 0.0555. For example, 100 mg/dL equals 5.55 mmol/L. To perform the reverse calculation, multiply by 18.02. Glucometers may have extra functions such as storage of recent readings, a “diary” function to allow patients to note when insulin was taken and/or when meals were eaten. They may provide an alarm to remind patients to test at specific times of day or at a specific time after meals. Some glucometers may be able to communicate with equipment such as computers or smartphones, and some may interface with insulin pumps so that insulin administration can be triggered when blood glucose levels rise above a set level. Modules that adhere to the skin of the patient and connect to smartphones allow greater mobility and convenience to patients. Normal blood glucose levels can fluctuate considerably depending on when and what the subject has eaten, when and how much exercise has been done, and the time of day. To obtain some kind of standard measurement, patients are asked to avoid food and drinks other than water for a specific time, usually 8–13 h. This allows levels to stabilize before base level measurements are taken. Normal fasting blood glucose levels are below 110 mg/dL or 6.105 mmol/L. If fasting readings are over 126 mg/dL (6.993 mmol/L), the patient is considered to be diabetic, according to the American Diabetes Association. Low blood glucose levels (hypoglycemia) can produce symptoms such as unsteadiness, perspiration, dizziness, rapid heart rate, and confusion. Below 50 mg/ dL (2.775 mmol/L) unconsciousness usually ensues, a condition called insulin shock. This occurs almost only in patients with diabetes. 90 Introduction to Biomedical Engineering Technology High blood glucose levels (hyperglycemia) are any readings over about 180 mg/dL. (9.99 mmol/L). Symptoms of hyperglycemia include excess thirst, headache, blurred vision, and fatigue. Chronic hyperglycemia can lead to impaired nerve function in the lower legs and feet, decreased healing ability, vision problems including possible blindness, and stomach and intestinal malfunctions. Most glucometers have no field serviceable parts; if they fail to operate correctly, they must be replaced. DOPPLER BLOOD FLOW DETECTORS Tissue health throughout the body depends on adequate blood circulation. Circulation can be impaired by various disease conditions or by trauma including surgery (Figure 3.13). If impaired circulation can be detected before damage occurs, preventive measures can be taken. Blood behaves like an ideal fluid in some ways, but not in others, mainly because it contains particles in the form of red blood cells. (White blood cells and others make up an insignificant portion of blood from a hydrodynamic point of view.) Particles moving in flowing blood can provide a target for ultrasound signals, in that the frequency of ultrasound waves reflected back from them is subject to the Doppler effect. This Doppler frequency shift can be detected and analyzed in such a way as to provide information about blood flow, with a non-invasive technique. Ultrasound waves can be beamed into various parts of the body and positioned in such a way that they intersect with blood moving in a target vessel. Some of the ultrasound energy is reflected by the red blood cells, the frequency is altered according to the Doppler effect, and a transducer picks up the reflected waves. By filtering out non-Doppler shifted signals and analyzing the degree of shift, a measure of the blood flow in the target vessel can be derived. Such Doppler blood flow detectors range from relatively simple hand-held devices that provide feedback about blood flow via sound from a speaker or headset (Figure 3.14). Moving blood produces a rushing sound, which varies with the pulsatile flow. This provides a quick means of determining if there is circulation in various parts of the body, usually the limbs. (These devices are very similar to ultrasound fetal heart detectors—see Chapter 4.) Computerized blood flow systems utilize the same principle as the simpler systems, but can provide quantitative and graphical data about blood flow that can be analyzed and stored, along with information about which blood vessels were being targeted, patient parameters, transducers in use, and more (Figures 3.15 and 3.16). FIGURE 3.13 Blood vessels showing narrowing which can cause changes in blood velocities that can be detected with Doppler technology. Diagnostic Devices: Part Two 91 FIGURE 3.14 A simple Doppler blood flow detector. Ultrasound transducers consist of piezoelectric crystals mounted on a probe. When stimulated with an electrical signal, the crystals emit ultrasound waves. The crystals can be arranged in such a way that the beams from the different crystals intersect at a specific depth, or they may use a frequency that penetrates to a specific depth range. Different transducers may be available for blood flow analyzers since lower frequencies penetrate more deeply than higher frequencies (Figure 3.17). As with all ultrasound technology, a gel is used to provide better coupling between the probe and the patient, improving wave transmission in both directions and reducing noise. RESPIRATORY SYSTEM Pulmonary Function Analyzers The respiratory cycle consists simply of breathing in and out; however, there are a number of aspects to this cycle. In normal resting breathing, a relatively constant volume of air is inhaled, with a consistent pattern of flow; exhalation removes the same volume, with somewhat different, but still consistent, flow patterns. An individual 92 Introduction to Biomedical Engineering Technology FIGURE 3.15 A full-body vascular blood flow measurement system. FIGURE 3.16 Vascular blood flow system screenshot. Diagnostic Devices: Part Two 93 FIGURE 3.17 Two vascular blood flow probes. FIGURE 3.18 Human respiratory system. can take in a considerably larger breath than normal if necessary and can also exhale some of the air that normally remains in the lungs after a resting breath. Even after such a forced exhalation, there is some air remaining in the lungs that cannot be expelled (though of course, with mixing, it is not always the same air with each breath) (Figure 3.18). While simply listening to the chest may provide some important information regarding the general health of a patient’s respiratory system, this doesn’t provide any quantitative data and many aspects of system function are not evaluated. As the respiratory or pulmonary system was studied in more detail, different parameters were noted, all of which gave important information about the patient’s condition. 94 Introduction to Biomedical Engineering Technology Some of the parameters of interest are (note that specific terms and abbreviations may vary): • ERV—expiratory reserve volume—The maximum amount of air that can be exhaled starting from the low point of the normal breathing cycle. • FEV1—forced expiratory volume in 1 s—The volume of air exhaled in the first second of a forced vital capacity (FVC) test. • FEV1/FVC—The ratio of these two values, as a percentage. • FRC—functional residual capacity—The amount of air left in the lungs at the end of normal resting breath. • FVC—The maximum amount of air that can be exhaled in a single breath, with full effort. • IC—inspiratory capacity—The maximum volume of air that can be taken into the lungs in a full inhalation, starting from the low point of the breathing cycle; IC is equal to the tidal volume (VT) plus the inspiratory reserve volume (IRV). • IRV—The maximum amount of air that can be inhaled from the end-inspiratory position, starting from the high point of the breathing cycle. • MV—minute ventilation (also called total volume)—The total volume of air exhaled from the lungs per minute. • MVV—maximum voluntary ventilation (maximum breathing capacity)— The greatest volume of air that can be breathed per minute by voluntary effort. • RV—residual volume—The amount of air remaining in the lungs at the end of a maximal exhalation. • TLC—total lung capacity—The amount of air contained in the lung at the end of a maximal inhalation. • VC—vital capacity—The volume of air that can be expelled from the lungs after a maximal inhalation; equal to IC plus ERV. • VT—The volume of gas inhaled and exhaled during one breathing cycle. Respiration or pulmonary function analyzers range from simple devices that simply measure volumes, to complex computerized systems that measure every aspect of respiration and produce charts and tables as well as providing analysis, comparisons with previous tests, archiving, and full information about each patient including medications (Figure 3.19). INCENTIVE SPIROMETER The simplest devices for evaluating respiratory function are tubes containing a ball meter or vane. The patient breathes through the tube, causing a deflection in the measuring component that is proportional to breathing effort. These units are sometimes called incentive spirometers as they are often used to help patients keep up breathing exercises after surgery or for recovery from some respiratory diseases. Diagnostic Devices: Part Two FIGURE 3.19 95 Details of the respiratory system. GRAPHING SPIROMETER Simple spirometers consist of a breathing tube for the patient, and a bellows or piston mechanism that can move when air from the patient’s breathing enters or leaves the system. The movement can be indicated by a pointer and calibrated strip, or by a pen moving against a chart recorder or drum recorder. The spirometer graph may plot volume against time, pressure against time, or pressure against volume. More complex spirometers may have flow transducers that can provide direct rather than calculated flow rates. Some may have digital read-outs, built-in printers, or memory for storing past results. PULMONARY FUNCTION ANALYZER Complete pulmonary function analyzers utilize flow transducers similar to those in spirometers, but the data generated is handled differently. A computer system analyzes the data to provide values for most or all of the parameters described above. Values and flow and volume charts can be displayed on a video screen or printed, and there is extensive analysis and documentation for all relevant information (Figure 3.20). Exercise equipment may be used to provide physical stress while the patient is being tested (Figure 3.21). Oxygen and carbon dioxide levels may be measured within the patient breathing circuit, and pulse oximetry may be integrated into the device. RESPIRATION MONITORS Respiration being one of the basic vital signs, it is important to be able to monitor this parameter automatically. More common mechanisms may detect the variations in 96 Introduction to Biomedical Engineering Technology FIGURE 3.20 Pulmonary function analysis system. FIGURE 3.21 Patient undergoing basic pulmonary function testing. Diagnostic Devices: Part Two FIGURE 3.22 97 Respiration (bottom) and ECG waveforms. impedance of the chest directly, or by placing a band with a sensor around the chest, or by having an air-flow sensor near the patient’s nose or mouth. Some systems apply a magnetic field to the chest; variations in intensity of the field on the opposite side of the chest are indicative of the lung volume. ECG monitors have electrodes placed on the patient’s chest already, so it is relatively easy to derive impedance-based respiration data (Figure 3.22). In impedance pneumography, a constant electrical current is passed through the patient’s chest. By measuring changes in voltage between the contact points (e.g., the ECG electrodes), impedance can be inferred, with increased impedance corresponding to an increased volume of air in the lungs. These values can be analyzed to produce a respiration tracing, usually along with an ECG tracing, as well as a numeric value of breaths per minute. CAPNOGRAPHY MONITORS As described previously (Chapter 3), carbon dioxide levels can be critical in determining the state of a patient’s health and in planning a course of treatment. High carbon dioxide levels are a strong indicator of hypoxia, which if left untreated can lead to brain damage or death. Blood CO2 measurements are important, but determining the amount of CO2 in exhaled breaths provides additional information. Capnographs are designed to measure this parameter, and some designs use the fact that carbon dioxide absorbs certain frequencies of infrared light differently than does room air. Passing a sample of exhaled air from the patient through a sensor with an infrared emitter and receiver and then analyzing the variations in absorbance can provide accurate values of CO2 levels. This type of sensor requires regular user calibration, usually by placing the sensor on a closed cell that contains a known concentration of carbon dioxide. The sensor has to warm up to a certain temperature since measurements vary with temperature. Also, most such systems need to have the infrared signal modulated (turned on and off rapidly) in order to perform analysis; a motor driving a rotating shutter may be used (Figure 3.23). 98 FIGURE 3.23 Introduction to Biomedical Engineering Technology An older capnography sensor and calibration window. Newer sensors use spectroscopy or nanotubes coated with special chemicals for CO2 measurements. These systems allow faster sampling with shorter (or eliminated) warm-up times and smaller sample volumes, and most alleviate the need for user calibration. Most patients for which capnography is beneficial will be on a ventilator, either during anesthesia or in an intensive care situation. Some systems use a sensor mounted directly in the breathing circuit (mainstream sampling), while others draw off a sample from the circuit to an external sensor (sidestream sampling). Mainstream sampling provides more reliable results, but the sensor and attachment apparatus are bulkier than that of sidestream sampling systems. OXYGEN ANALYZERS Although adults can tolerate high oxygen concentrations for breathing, the same is not true for infants. While elevated oxygen levels may be important in caring for neonates, if the levels are too high, blood vessel formation can be significantly altered, especially in the retina and lens. This can result in vision impairment or blindness, and so oxygen must be monitored carefully with these small patients to keep it below 40%. Even with adults, however, oxygen concentrations close to 100% can cause problems such as pulmonary edema, reduced gas exchange in the lungs, and oxidation of some substances within the body. Maintaining delivered oxygen levels at specific values is important in many other situations as well, since levels that are too low may not provide adequate oxygenation in patients with impaired pulmonary or circulatory function, or when undergoing anesthesia. Diagnostic Devices: Part Two FIGURE 3.24 99 An oxygen analyzer. (Courtesy of Fluke Biomedical.) Oxygen analyzers utilize a chemical reaction that occurs between certain chemicals (such as potassium hydroxide) and oxygen that produces an electrical potential (Figure 3.24). When oxygen comes in contact with the chemical in a cell with electrodes, the potential developed will be proportional to the oxygen concentration. This type of device is called an electrogalvanic fuel cell, since oxygen is consumed as the material as the cell oxidizes. Obviously, since the supply of “fuel” in the cell is limited, the chemical reaction will eventually cease, and the generated electrical potential will drop to zero. This means that cells must be kept in very well-sealed containers until they are put into use, and also that they must be replaced when depleted. The exact potential produced within the cell will also vary somewhat over time, as the reactant in the cell is used up, so the system must be calibrated whenever a cell is replaced, and regularly while in use. Most systems will provide an indication when calibration is necessary. Calibration consists of exposing the cell to two known concentrations of oxygen and taking voltage readings at each point. These values can then be used to adjust the compensation required to produce linear results. Room air consists of 20.95% oxygen with almost no significant variation except at high elevations. Room air can thus be used as a convenient calibration point, with the other being 100% oxygen. 100 Introduction to Biomedical Engineering Technology BRONCHOSCOPY SYSTEMS Bronchoscopy systems allow health professionals to see within the upper part of a patient’s respiratory system in order to look for damage, restrictions, or abnormal tissues (Figure 3.25). The systems consist of tubes (the actual bronchoscope) that can be inserted via the mouth or nose, past the larynx and through the epiglottis to the trachea and the left or right bronchi; a light source; a camera; one or more video monitors; possibly a video recorder and/or printer; possibly a mechanism for flushing and suctioning the area being observed; and various associated apparatus. Bronchoscopy systems are similar in many ways to other endoscopic systems, the common components of which are described in detail in Chapter 4. The bronchoscope tube (or “scope”) has optical channels that can deliver light to the end of the scope and also send an image from the end of the scope back to the viewer. Some scopes have one or more hollow sections that can admit instruments or be used for irrigation, suction, and insufflation (Figure 3.26). FIGURE 3.25 Bronchoscopy procedure. Diagnostic Devices: Part Two FIGURE 3.26 101 A few flexible bronchoscopes. Bronchoscopes may be flexible or rigid. Flexible scopes can be made thinner and can thus reach further into the bronchial passages, but rigid scopes can allow certain instruments or lasers to be introduced through the tube to perform procedures such as biopsies, dilations, or burning of small growths. Rigid bronchoscopes are usually used only with general anesthesia and are only introduced through the mouth. Rigid scopes generally use lenses within the tube to transmit illumination and images, while flexible scopes use fiber optics. Cracked or otherwise damaged lenses in rigid scopes and broken optical fibers in flexible scopes will reduce illumination and image quality. Most scopes until recently have used camera sensors at the proximal end, to pick up the visual images transmitted by the fiber-optic channels, but with advances in miniaturization, some newer scopes have imaging chips mounted on the distal end, which can eliminate some transmission problems, since wires can be made smaller and more flexible than optical components. Some manufacturers are providing disposable (single patient use) flexible bronchoscopes, an important consideration for infection control. Any extra costs are offset by reduced cleaning costs and reduced clinical costs related to possible infections from reusable scopes. 102 Introduction to Biomedical Engineering Technology NERVOUS SYSTEM Nerve signals are conducted through the body via two processes. Within nerve cells, the signal is transmitted in long cell extensions called axons. This isn’t as simple as an electrical signal in a wire, as the cell membrane along the axon must be polarized and then depolarized as the signal passes along (Figure 3.27). There is a time lag, or refractory period, that must pass before another signal can be handled in this way. Overall conduction speed within an axon is in the range of 50–200 m/s, far slower than the near-speed-of-light conduction of electrical signals in wires. At various points within the nervous system, signals must be passed from one cell to another through a connection called a synapse. A synapse can connect two nerve cells to simply pass a signal along. Other synapses can actually inhibit signal transmission within the target axon, while some are an interface between nerve axons and muscle cells. This last type, called a neuromuscular junction, uses a chemical called acetylcholine to transmit signals. Acetylcholine must be broken down by an enzyme (acetylcholinesterase) in order for the muscle to relax. Various drugs affect the nervous system in specific ways. Generally, they can either excite the system (agonists) or inhibit it (antagonists). Commonly known agonists include caffeine, cocaine, ecstasy, and amphetamines. Antagonists are drugs such as alcohol, valium, barbiturates, marijuana, and heroin and its derivatives. Some nerve gases (e.g., sarin) as well as pesticides (e.g., DDT and parathion) inhibit the action of acetylcholinesterase. This causes muscles to remain contracted for prolonged periods in spasms, which can lead to a painful death. FIGURE 3.27 A neuron or nerve cell. Diagnostic Devices: Part Two 103 Local anesthetics like procaine, xylocaine, and benzocaine act by blocking motor and sensory synapses in the area of application. General anesthetics such as isoflurane, sevoflurane, and desflurane act by blocking ion channels in the nervous system, thus blocking pain and producing unconsciousness. Anesthetic machines are described in Chapter 7. Various devices are used to test for the effectiveness of anesthetics, such as nerve stimulators and BiSpectral index monitors. EEG MONITORS AND MACHINES Structural abnormalities within the brain can cause many harmful effects, including epilepsy and other seizures, aphasia (impaired ability to communicate), hallucinations, and comas. Various disease processes such as tumors, Parkinson’s disease, and cerebral palsy can lead to extreme difficulties for patients. In the past, an electroencephalogram (EEG) was almost the only tool available, but now diagnosing such problems can involve imaging equipment such as CT, MRI, or PET scanners (see Chapter 6). Still, measurement of the electrical activity of the brain in real time can provide information that other sources cannot, and it can also confirm or expand on the results of other tests. An EEG machine consists of a set of a dozen or more electrodes that are placed in specific locations on the scalp and are connected to an amplifier/digitizer/analyzer/ display/recorder unit that has some similarity to ECG systems. The signals are stored and can be analyzed later and/or printed out on a recorder strip. Some special studies use electrodes that are inserted through the skull and directly into brain tissue (Figure 3.28), allowing precise determination of the location of anomalies. FIGURE 3.28 The human brain. 104 Introduction to Biomedical Engineering Technology FIGURE 3.29 EEG waveforms. The signals recorded from brain electrical activity form recognizable waves that are divided into groups according to their characteristics (Figure 3.29). Alpha waves range from 9 to 14 Hz and are of relatively high amplitude. They are seen in EEG records when the subject is awake but relaxed. Beta waves are lower in amplitude than alpha waves, but higher in frequency, about 15–40 Hz. They indicate that the subject is aroused in some way, angry or frightened or closely involved in a conversation or activity. Theta waves show a variation in amplitude, though usually greater than beta waves, at a low frequency of about 4–8 Hz. Theta waves correspond to periods of inattentive consciousness such as daydreaming (Figure 3.30). Delta waves are the highest in amplitude but lowest in frequency, about 1.5–4 Hz. Periods of sleep show delta wave activity, with frequency corresponding to the depth of sleep—deeper sleep means lower frequencies. Delta waves can be analyzed to indicate the depth of unconsciousness during general anesthesia. An absence of brain wave activity can be a legal indication of brain death in some jurisdictions. EEG activity changes in characteristic ways when various stimuli are applied to the subject, such as flashing and/or colored lights or various sounds. Abnormal responses to these stimuli can indicate various brain abnormalities (Figure 3.31). Also, in studying epilepsy, it is sometimes useful to be able to induce seizures under controlled conditions. This is often done using flashing lights of controlled frequency (usually around 16–25 Hz) and intensity. Only about 5% of patients with epilepsy have such photosensitivity. Diagnostic Devices: Part Two 105 FIGURE 3.30 A young patient with EEG electrodes in place. FIGURE 3.31 EEG recorder output. It has been found that subjects can learn to control some aspects of their brain waves, by using biofeedback training. This can be useful in stress or pain reduction, and in focusing concentration. Some experiments have found that subjects can control external devices by altering their brain waves in a particular manner, with suitable analysis and interface circuitry. 106 Introduction to Biomedical Engineering Technology BIS MONITORS A special application of EEG technology allows clinicians to evaluate the depth of unconsciousness of patients. This can be useful during general anesthesia or when patients are being kept in an induced coma. Under general anesthesia, if the level of consciousness is too high, patients can experience awareness during surgery, which can be very distressing. If the level is too low, recovery from the anesthetic can be prolonged, or in extreme cases, physiological damage can occur. Comas may be induced to help keep a patient immobile when recovering from various traumas, and as with general anesthesia, a balance must be struck between too high and too low depths of unconsciousness. A BiSpectral index monitor (BIS) takes EEG signals from a few specifically placed EEG electrodes and analyzes them with a complex algorithm to produce a “BIS” value, a unitless number that corresponds to the level of consciousness. A BIS value of zero would correspond to brain death, while a value of 100 corresponds to full consciousness and awareness. MUSCLE/NERVE STIMULATORS Under certain circumstances, it is necessary to greatly relax or paralyze a patient’s muscles. During surgical procedures when electrosurgery machines are in use, the signals produced by the ESU action could cause muscle contractions in various areas of the body. Also, some surgeries involving muscles are much easier when the muscles being worked on are relaxed. Patients on ventilators may fight the action of the machine if their breathing muscles are active. Finally, when electroconvulsive therapy (see Chapter 7) is being administered, the ECT pulse can cause extreme contractions in many muscle groups which can result in injuries to patient or staff. As described earlier in this chapter, nerve signals are transmitted to muscles across the neuromuscular junction via acetylcholine. Muscle relaxing agents actually block the action of acetylcholine so that muscle activity is reduced. The degree of inhibition must be sufficient to prevent unwanted muscle activity, but excess dosages are to be avoided. Nerve/muscle stimulators apply calibrated signals to a patient’s skin in a convenient location near a muscle group, for example, the thumb or big toe (Figure 3.32). Normally, once over a certain threshold, the signals will cause muscle contractions to a degree corresponding to the signal amplitude. Once the stimulus reaches a certain high value, muscle contraction is the greatest that is possible. By adding about 10% to this stimulus level (a supramaximal stimulus), maximal muscle contraction is ensured. When muscle relaxants are administered to the patient, supramaximal stimuli can be delivered until such time that muscle action is reduced to a certain percentage of maximum, for example, 20%. At this point, relaxant administration can be leveled or reduced in order to maintain the desired reduction in muscle response. Diagnostic Devices: Part Two 107 FIGURE 3.32 A nerve stimulator. Nerve stimulators can be set to deliver pulses of various amplitudes and durations, and may have settings where pulses are delivered in continuous trains or in bursts of a specific number of pulses. SUMMARY This chapter continued descriptions of diagnostic devices, covering equipment used with the circulatory system and blood, the respiratory system, and the nervous system. Theories of invasive and noninvasive blood pressure measurement were discussed, along with pulse oximetry, capnography, and blood glucose analysis. 108 Introduction to Biomedical Engineering Technology The anatomy and physiology of the respiratory system were described along with methods of analyzing these systems. Nervous system function was examined and EEG and BIS monitors plus nerve stimulators were described. QUESTIONS 1. Describe the effects of hypertension on the heart. 2. At what point during the heartbeat does cardiac muscle perfusion occur? 3. What are some disadvantages of invasive blood pressure monitors? 4. Explain how pulse oximetry uses light to determine the amount of oxygen being absorbed by hemoglobin in the blood. 5. Briefly describe the contents of a typical home glucometer kit and explain the function of each part. 6. Explain how the Doppler effect can measure the blood flow in a target vessel. 7. Define the following: a. FRC b. FVC c. IC d. VC 8. What are the differences between a pulmonary function analyzer and a spirometer? 9. What are the benefits/drawbacks of a flexible bronchoscope and of a rigid bronchoscope? 10. What are the two functions of synapses in the nervous system? 11. Why are BIS monitors used? 4 Part Three Diagnostic Devices OBJECTIVES FOR THIS CHAPTER • To examine diagnostic devices used with, and the relevant anatomy of, various body systems, including the digestive system, sensory organs, the reproductive system related to pregnancy and childbirth, and the musculoskeletal system, with a closer look at arthroscopy. DIGESTIVE SYSTEM Endoscopes General “Endoscope” literally means “inside looking,” and these systems are designed for just that. The general term “endoscope” describes any device that has a tube that can be inserted into an opening in the body, either natural or surgical, for the purpose of viewing structures inside the body. This means that they must have channels both to provide lighting and to transmit visual images back to the user. Endoscopes may also have the capacity to supply fluids such as saline solutions for irrigating sites to provide a clearer view, suction to remove the irrigation and other fluids, an air channel for inflating the space surrounding structures being examined (insufflation), and a channel that can allow the entry of special instruments for doing various procedures inside the body (Figure 4.1). Newer scopes have video camera chips mounted on the distal end, which means that images are carried back along the scope as electronic signals rather than light. This results in better images and more durable scopes. TYPES OF ENDOSCOPES Some types of endoscopes, with their target areas and insertion points, include the following: • • • • • • Arthroscope—joints such as knees; surgical incision Bronchoscopes—trachea and upper bronchial passages; mouth or nose Colonoscopes—colon; anus (Figure 4.2) Colposcope—vagina and uterus; vagina Cystoscope—bladder and urinary tract; urethra Gastroscope—esophagus, stomach, and sometimes upper small intestine (duodenum); mouth • Laparoscope—various abdominal organs; surgical incision DOI: 10.1201/9781003140603-4 110 Introduction to Biomedical Engineering Technology FIGURE 4.1 An endoscopy system. From top: video display, insufflator, camera console, light source, specialized insufflator for gynecologic procedures, video recorder, and video printer. On the right side of the cart are two CO2 cylinders that provide gas for insufflation. • Proctoscope—rectum and lower (sigmoid) colon; anus • Sigmoidoscope—sigmoid colon; anus • Thoracoscope—organs of the thorax, including the pleura (outer covering of the lungs) and pericardium (outer covering of the heart); surgical incision Endoscopy is less invasive and less traumatic than exploratory surgery, and while laparoscopic procedures require one or two small incisions, these are much smaller than open abdominal or thoracic surgery; recovery times are much shorter and the incidence of complications much lower. Endoscopes are divided into rigid or flexible types, the difference being self-explanatory. Diagnostic Devices: Part Three FIGURE 4.2 Colonoscopy procedure. FIGURE 4.3 A rigid endoscope. (Courtesy of Medit.) 111 RIGID ENDOSCOPES Rigid endoscopes consist of a tube, usually made of stainless steel, which contains fiber optics, a series of lenses, and one or more open passages (Figure 4.3). At the distal end of the scope, an objective lens receives light from the object and directs it into the tube. The angle at which the objective lens is set determines the viewing angle of each individual scope, from straight ahead to various angles to the side to partially in reverse. 112 Introduction to Biomedical Engineering Technology FIGURE 4.4 An endoscopic surgical procedure in progress—note the rigid scope on the right, also note abdominal distension due to insufflation. The other lenses, commonly referred to as the telescope, are separated by spacers. They take the light through the tube from the objective lens to the eyepiece. Fiber-optic strands are installed around the lenses to carry illumination light to the subject, and a fitting near the eyepiece allows a light cable to attach to the scope. The open passages in the scope allow for irrigation and suction of the observation site to remove obscuring material such as blood. Also, pieces of tissue that have been cut or otherwise separated from structures such as tumors or polyps can be withdrawn for disposal or examination. The passages can also be used to fill the area around the object of observation with either clear fluid or air in order to allow a clearer view. Finally, the passages can allow the entry of special tools used for such purposes as excising tissue or cauterizing structures (Figure 4.4). FLEXIBLE ENDOSCOPES Flexible endoscopes carry both illumination and visualization light through fiber optics, which allows the flexibility in their name. Flexibility allows the scopes to pass around corners to reach the object of observation; it also means that flexible scopes can be much longer than rigid scopes (Figure 4.5). Flexible endoscopes generally carry markings on the outside to indicate the depth of insertion. Some models have special mechanisms operated by cables that allow the operator to turn the end portion of the scope in different directions (Figures 4.6–4.8). Otherwise, flexible scope function is similar to that of rigid scopes. Some flexible scopes mount directly onto the light source, which makes video and other connections simpler and more effective. Viewing images from such scopes is done via video monitors rather than direct eyepieces. Diagnostic Devices: Part Three 113 FIGURE 4.5 A surgeon during an endoscopic procedure, viewing directly through a flexible endoscope. Some manufacturers are providing disposable (single patient use) flexible endoscopes, an important consideration for infection control. Any extra costs are offset by reduced cleaning costs and reduced clinical costs related to possible infections from reusable scopes. OTHER SYSTEM COMPONENTS Light Source Accurate recognition of normal and abnormal tissues during an endoscopic procedure requires bright illumination with light having a specific spectrum and color temperature. The light also must not impart any significant amount of heat to the tissues in the target area (Figures 4.9 and 4.10). Many endoscopy light sources use quartz halogen bulbs that run in a controlled environment to avoid overheating, with accurate power supplies, since both temperature changes and supply voltage variation can change light characteristics. 114 Introduction to Biomedical Engineering Technology FIGURE 4.6 A flexible endoscope, connector end, showing the connector for a light source and ports for insufflation, irrigation, and suction. Higher intensity bulbs are fitted with heat sinks and fans to help keep them in the correct temperature range. As the technology develops, more light sources are using high-intensity LEDs, which have both lower power consumption and less heat production than incandescent bulbs. They also have a much longer life span. The lower power consumption means that some systems can use battery-powered handles with LEDs to make for a very compact system (figures 4.3 and 4.22). In order to accommodate requirements for different light intensities, a mechanical device may be used to block some portion of the light. Changing voltage to the lamp would also vary intensity, but would also affect light color temperature, which is why mechanical methods are used, allowing the lamp itself to remain in a constant state to provide consistent light quality. Simpler light sources have manual controls for intensity, while more sophisticated units can be controlled by the video portion of the system in order to maintain optimum illumination. Diagnostic Devices: Part Three 115 FIGURE 4.7 Flexible endoscope hand controls allow movement of the tip as well as adjustments to focus and light intensity. FIGURE 4.8 The distal end of an endoscope—note the various channels for light, viewing, irrigation, insufflation, and suction. 116 Introduction to Biomedical Engineering Technology FIGURE 4.9 An older endoscopy light source. The connector at the lower left rotates to allow connection of scopes from different manufacturers. FIGURE 4.10 A current endoscopy light source. The connectors are now dedicated to scopes from the light source manufacturer. (Courtesy of Medit.) Light source units have a connector on the front panel to accommodate the fiber optics for the scope; this may be a simple, single-purpose plug or it may be a more complex connector that can carry optical or electronic images and control signals, as well as air, irrigation, and suction. By using fiber optics to carry light from the source (bulb) to the viewing area, an adequate amount of light is delivered with very little heat. CAMERA Video cameras used in endoscopy systems must be able to generate high-resolution images with accurate color reproduction. In most systems, the camera is in two parts: the image sensor portion and the video-processing portion. Some systems have the Diagnostic Devices: Part Three 117 FIGURE 4.11 An endoscopy camera head, which clips on to the end of the scope and picks up light signals with its image sensor, converting them into electronic video signals that are then carried by cable to the camera console, where they are further processed. FIGURE 4.12 Two pill cameras. image sensor on a head that attaches to the proximal part of the scope, while newer systems mount the sensors at the distal tip of the scope (Figure 4.11). Miniaturization has allowed the development of “pill cams,” devices that look like a (rather large— 27 mm) medication pill that can be swallowed; the unit contains a light source, camera, and transmitter to relay images to an external system (Figure 4.12). The pill cams are single use. Image sensors may consist of a single chip array, or three-chip arrays. With the single chip arrangement, colors are differentiated electronically, while with threechip systems each chip responds to a single primary color. Single chip systems tend to be smaller and less expensive, while three-chip systems tend to provide higher image quality (Figure 4.12). Both single chip and three-chip cameras are available with high-definition resolution; again, higher resolution means higher costs. 118 Introduction to Biomedical Engineering Technology FIGURE 4.13 A three-chip endoscopy camera/video processing unit. FIGURE 4.14 Endoscopy video recorder. In each system, video signals are taken from the sensors to a processing component, usually cabinet mounted (Figure 4.13). This part of the camera handles the video signals to adjust for light intensities and can perform such tasks as white balancing to help ensure color accuracy. The video processor interfaces with light sources as well as video image recorders, printers, and video displays. VIDEO RECORDER/STORAGE Systems may record video as either motion or still pictures, or both, so that clinicians can later examine the images for specific details, or use them for teaching purposes (Figure 4.14). Recorded images from one test on an individual patient may be compared to those from a later test in order to see if changes in tissues or structures have taken place. In the past, endoscopy systems recorded video on videocassette recorders, but new systems use recordable optical disks and/or hard drives, which provide much quicker access to images. VIDEO MONITOR As part of the system, video monitors must have equal capabilities to other links in the imaging chain in terms of resolution and color reproduction. In the past, CRT monitors were used but now all systems use LCD monitors. Diagnostic Devices: Part Three FIGURE 4.15 119 An insufflator front panel. Monitors are mounted to give the person performing the test a clear view, and secondary displays are often used to provide a good view to other staff or students. Capability of connecting to a LAN or the internet may be included. INSUFFLATOR Obtaining a clear view of many internal structures can be difficult when other organs or tissues get in the way; there is normally very little open space inside the body. To alleviate this problem, an inert gas such as carbon dioxide may be introduced to the target area. Obviously, such insufflatory pressures must be carefully limited to avoid damage, and so systems are equipped with regulators and overpressure alarms. Insufflating gas usually comes from pressurized tanks since most facilities don’t have carbon dioxide wall outlets. Room air is not used for insufflation because it isn’t absorbed by tissues as well as carbon dioxide. Excess nonintestinal gas remaining in body cavities after scope procedures can cause pain and discomfort for the patient. Insufflators typically have controls and displays (usually digital) for patient pressure, gas flow rate, and total volume delivered (Figure 4.15). Since there may be some leakage of gas from the scope and also since carbon dioxide can be absorbed quite easily by internal body tissues, some level of continuous flow must be maintained after adequate insufflation is achieved. The insufflating gas may be heated by the unit to help maintain patient body temperature. IRRIGATION AND SUCTION Isotonic saline is usually used for irrigation, and in some circumstances, it is used to distend the viewing area to provide more clearance, when gas insufflation wouldn’t work, such as in the confined spaces of joints when performing arthroscopic procedures. The saline is pumped in through the scope lumen using a low-pressure pump. Removing blood, tissue particles, or the debris from surgical procedures (Figure 4.16) is necessary to maintain good visibility, but as with any body fluid, the evacuated material must be handled using appropriate precautions. A low-suction vacuum pump or line suction is used via the scope lumen. 120 FIGURE 4.16 Introduction to Biomedical Engineering Technology Surgeon with endoscopy system. TOOLS A wide range of procedures can be accomplished with endoscopy, using an equally wide range of tools. For some laparoscopic or thoracoscopic procedures that might require bulkier or multiple tools, a separate tube may be inserted into a second small incision. A common goal of endoscopy, in addition to simple observation, is the removal of small samples of suspect tissue in order to examine the sample in detail to help either diagnose or rule out conditions such as cancer. Special, fine grasping and cutting tools allow such biopsies to be performed quickly and accurately. Larger amounts of tissue can be excised and removed as well, for example, in the removal of tumors or polyps. Since the suction lumen of an endoscope is limited in size, such tissue must be reduced to relatively small pieces before suction is applied. Gall bladder removal is commonly performed in this manner, a procedure called a laparoscopic cholecystectomy. Electrosurgery can be performed laparoscopically, using long, thin electrode probes that are well insulated except for the tips. These tips can be snares or pincers and can be used for such things as polyp ligation or fallopian tube sealing (Figure 4.17). The inner conductor must be insulated from the outer sleeve (Figure 4.18). A flat electrode may be used to cauterize highly vascularized tissue that is causing blood loss, such as in the liver or uterus. Diagnostic Devices: Part Three 121 FIGURE 4.17 A laparoscopic bipolar electrosurgery probe. FIGURE 4.18 The tip of a bipolar ESU probe. In arthroscopy, harder material such as cartilage or bone may need to be removed, in which case rotating grinding tools can be used through the scope. SENSORY ORGANS Of the various human senses, only sight and hearing have a significant amount of medical technology devoted to their study and treatment. Visualization is the primary method of diagnosing problems with the eyes or ears, and specialized devices have been developed to provide effective means of seeing into those organs. Included in this section are tools used to examine the mouth and throat, even though they are not particularly concerned with the mouth as a sensory organ. OTO/LARYNGO/OPHTHALMOSCOPES The eyes, ears, and throat are readily available for examination, but each presents certain difficulties to direct observation. Much of the critical structures of the eye are located behind the iris and can only be seen through the small opening of the pupil (Figure 4.19). The tympanic membrane of the ear is at the end of a narrow passageway, and the tongue and uvula can block the view any further into the throat. 122 FIGURE 4.19 Introduction to Biomedical Engineering Technology Structure of the eye. A set of tools for looking into the eyes, ears, and throat are often grouped together, utilizing the same power source and handle. The device used to examine the eyes is called an ophthalmoscope; for the ears, an otoscope; and for the throat, a laryngoscope. Most of these devices derive power from a battery (rechargeable or disposable) in the handle, though in locations where patients come and many examinations will be performed, the scopes may be line powered. OTOSCOPE The main difficulty in looking into the ear canal is that most light sources that might be used to illuminate the area will also block the view. Otoscopes use fiber optics in a ring around an observing tube to overcome this problem; a low-power lens aids in visualization (Figure 4.20). Different tubes may be attached to various depths, and a disposable cover is used to prevent cross-infection between patients. The intensity of the light source can be varied for different conditions. The lens of the otoscope may be designed to move out of the way to allow small instruments to be inserted, for example, to remove foreign objects or buildups of ear wax. Some units may have an air channel that allows small bursts of air to be directed toward the tympanic membrane to help evaluate its tension. LARYNGOSCOPE Keeping the tongue, and to a lesser extent the uvula, out of the way while providing illumination is the main goal of a laryngoscope. Most consist of a metal or plastic blade that has a very small light bulb or a fiber-optic outlet near the tip. Diagnostic Devices: Part Three 123 FIGURE 4.20 Ear anatomy. Blades are designed to accommodate different depths of observation and different throat sizes. Some have a mechanism to spread the throat passage open, which can be necessary for some visualizations, or for performing minor surgical procedures, or in the process of intubating a patient with an endotracheal tube (Figure 4.21). A specialized type of laryngoscope uses fiber optics for both illumination and visualization. The very thin, flexible line is passed through the nose in order to have a better viewing angle in the throat. OPHTHALMOSCOPE First developed by Welch and Allyn in 1915, the handheld ophthalmoscope has evolved into a powerful device for performing eye examinations; the Welch–Allyn name is still commonly seen on this type of equipment. Ophthalmoscopes have a number of lenses of different magnifications and a light source that can be adjusted in intensity, shape, and color (Figure 4.22). This arrangement allows the clinician to examine the outer surface of the eye and also the inner structures via the pupil. Eye drops to cause pupil dilation are often used to allow a larger opening for observation. The lens and vitreous humor can be examined, but the most important structure viewed by an ophthalmoscope is the retina. By utilizing the different patterns of illumination (including full, slit, and small circle) along with certain color filters, the condition of the retina can be determined. This can aid in the diagnosis of such conditions as increased intracranial pressure, glaucoma, macular degeneration, detached retina, brain tumors, diabetic retinopathy, and hypertension. 124 Introduction to Biomedical Engineering Technology FIGURE 4.21 A laryngoscope and endotracheal tube. FIGURE 4.22 An ophthalmoscope. SLIT LAMPS A slit lamp is a tool commonly used in eye examinations. It provides a stable, adjustable platform for the patient to rest their head, keeping it comfortably but reliably in place during the examination (Figure 4.23). Binocular eyepieces with multiple objective lenses of different magnification allow for a wide variety of examinations. Diagnostic Devices: Part Three FIGURE 4.23 A slit lamp being used to examine a patient’s eyes. FIGURE 4.24 Another view of a slit lamp in use. 125 A high-intensity lamp provides illumination, with the light focused into a narrow line, or slit, which can be turned to various angles and adjusted in position. Various filters can add color to the light, which can aid in identifying certain structures or tissue characteristics (Figure 4.24). 126 Introduction to Biomedical Engineering Technology As with ophthalmoscopes (of which the slit lamp is really just a complex version), eye drops may be administered to the patient to produce pupil dilation, allowing a better view inside the eye. REPRODUCTION Fetal Heart Detectors In utero, a fetus has a rapid heartbeat from a very early stage of development (Figure 4.25). The rate and strength of the heartbeat can give important information about the health of the fetus, and so a simple means of detecting it is very useful. A stethoscope can sometimes pick up the sounds of the fetal heart, but this can be difficult, especially early in pregnancy, since the heart is small and usually quite deep within the mother’s body. Fetal heart detectors utilize the Doppler effect in much the same way as blood flow detectors (Chapter 3), sending a beam of ultrasound in the direction of the fetus and listening for the fluctuations in sound resulting from the ultrasound being reflected by the moving parts of the fetal heart (Figure 4.26). Fetal heartbeats can be detected in this manner as early as 7 or 8 weeks of gestation. FIGURE 4.25 A fetus in utero. Diagnostic Devices: Part Three FIGURE 4.26 127 A fetal heart detector. Ultrasound gel provides good sonic coupling between the detector head and the mother’s abdomen. Some experience is necessary for accurate determination of fetal heart detection, since the pulsing of the mother’s aorta can give a similar signal. Maternal aortic pulse is much slower than the fetal rate, however, and the slower motion produces a distinctive sound. Fetal heart rate is typically between 120 and 160 beats/min, while resting adult rates are usually around 60–80 beats/min. In some circumstances, the maternal rate may be high, and in these cases, care must be taken to differentiate between the two, perhaps by trying different angles to try to avoid the aorta. Because Doppler fetal heart detectors are relatively inexpensive, very portable, and easy to use, they can serve as a vital “early warning system” to potential fetal difficulties. If a problem is suspected, further examination using sophisticated ultrasound machines can be performed. Ultrasound crystals are fragile and can be cracked by a blow. Cracked crystals can sometimes still work, but performance is greatly reduced. Damaged wires for the earpieces, if used, can result in noisy or intermittent signals. 128 Introduction to Biomedical Engineering Technology FETAL MONITORS As mentioned above, fetal heart rate and strength can be a good indicator of fetal health. It may be advantageous to monitor the heart rate for a longer period than is convenient with a fetal heart detector. It is also valuable to be able to determine the correlation of fetal heart rate and uterine contractions, and so a means of quantifying contractions is necessary. Fetal heart monitors, sometimes called antepartum fetal monitors or cardiotocographs, provide these functions (Figures 4.27–4.29). FIGURE 4.27 Fetal monitor in use with telemetry. (Courtesy of Philips.) FIGURE 4.28 Overview of a fetal monitor. Cable connectors at the lower left are for, from the left: SpO2 Diagnostic Devices: Part Three 129 FIGURE 4.29 Details of fetal monitor front panel. (Courtesy of Philips Medical, Canada.) FIGURE 4.30 Fetal monitor ultrasound transducer crystal locations. (Courtesy of Philips Medical, Canada.) Fetal heart detection in these units uses the same principle as the simpler fetal heart detectors described above. However, an array of ultrasound crystals is used, which provides a better signal (Figures 4.30 and 4.31). The crystals are arranged in such a way that the beams from each intersect at a point roughly corresponding to the normal position of the fetus in the mother’s abdomen. This improves the signal and also helps to eliminate signals from other sources, such as the mother’s aorta or the heartbeat of a twin. 130 FIGURE 4.31 Introduction to Biomedical Engineering Technology Fetal monitor ultrasound transducer. These ultrasound transducers are positioned (using ultrasound gel) on the mother’s abdomen to obtain the best possible signal, and a strap is then used to hold the transducer in place. Some monitors have two transducer inputs and are capable of monitoring twins simultaneously. The transducers may have to be adjusted occasionally due to slippage or to the movement of the fetus. Fetal heart signals are amplified and three outputs are derived: a sound signal, much like that of the simple fetal heart detectors; a numeric rate value, displayed on the front panel; and a signal fed to a chart recorder that produces a trace indicating rate. Some systems also can send heart rate data to a central monitoring system. The second part of a fetal monitor is the uterine contraction detector, called a tocograph. This sensor is simply a pressure transducer mounted in a housing and Diagnostic Devices: Part Three 131 FIGURE 4.32 Fetal monitor TOCO transducer. strapped against the mother’s abdomen (Figure 4.32). When a uterine contraction occurs, the abdominal wall becomes more rigid, and this causes the transducer to be compressed. The amount of deflection is translated into a relative, unitless value. The contraction value is displayed on the front panel of the monitor and also produces a recording on the same chart recorder as the fetal heart rate, which allows easy visual correlation (Figures 4.33 and 4.34). Most monitors have a button that can be pressed by the mother to indicate particular events, such as felt fetal movement. This can help in evaluating changes in fetal heart rate. Pressing the button makes a mark on the chart recording. Chart recorders print the time and date at regular intervals along the edge of the paper, which can serve as both a medical and a legal notation. 132 Introduction to Biomedical Engineering Technology FIGURE 4.33 A fetal monitor recording strip test pattern. Fetal heart rate is recorded on the top portion, while contraction strength (TOCO) is recorded on the bottom. INFANT SCALES Infant weight is important in determining growth, fluid balance, and other values, but since babies tend to be quite active at times, the scales used to weigh them must have a means of averaging readings over a short period in order to give a stable weight reading (Figure 4.35). Scales have a “tare” function that allows staff to compensate for the weight of objects other than the baby that may have to be on the scale, such as a diaper or blanket. Scales typically use strain gauges for weight determination. The signals from these units are amplified, digitized and averaged, and a numeric value is then displayed. Diagnostic Devices: Part Three 133 FIGURE 4.34 TOCO/ECG transducer block diagram. Both transducers use the same analog-to-digital conversion, signal processing, and communications circuitry with just the front ends of each being different. (Courtesy of Philips Medical, Canada.) FIGURE 4.35 An infant scale. 134 Introduction to Biomedical Engineering Technology APGAR TIMERS A quick, standardized means of evaluating the health of a neonate is important, and to that end Dr. Virginia Apgar developed the Apgar scoring system in 1952. The scale evaluates five criteria (Table 4.1), giving each a score of zero, one, or two. The scores are totaled, and the resulting value gives a good indication of condition. Acronyms for each criterion have been used as a memory aid, but the name for the test is derived from its originator. The tests are normally done at 1 and 5 min after birth, and possibly later if scores are below normal (Figure 4.36). Generally, total scores under three are considered to be critically low, and seven or above normal. Low scores at the 1-min mark are cause for extra attention but may not indicate major problems, especially if scores improve with time. If the scores are three or less for longer times, up to 30 min, it may indicate that the infant is at significant risk of long-term neurological impairment. A variety of timers are available to signal when to perform the 1 and 3 min tests, since this is usually a busy time for staff who may not be able to watch a clock. Timers may be stand-alone or built into equipment such as infant resuscitators (Chapter 8). TABLE 4.1 Apgar Criteria Criterion Skin color Heart rate Reflex Muscle tone Respiration Acronym Appearance Pulse Grimace Activity Respiration Score 0 Blue all over Absent No response None Absent Score 1 Blue at extremities Less than 100 Grimace/feeble cry Some flexion Weak or irregular FIGURE 4.36 An Apgar timer built in to an infant resuscitator. Score 2 Normal Greater than or equal to 100 Sneeze/cough/pulls away Active movement Strong Diagnostic Devices: Part Three 135 SKIN, BONE, MUSCLE, AND MISCELLANEOUS Thermometers Humans are homeothermic organisms, with most individuals maintaining a core temperature very close to 37°C. Variations from this normal value indicate problems, and so measuring temperature at regular intervals is an important diagnostic procedure. While core temperature is normally maintained within very narrow limits, temperatures of other parts of the body, especially the extremities, can vary considerably. Finding an accessible place to measure temperature that will accurately reflect the core value is vital. Oral (sublingual) temperature, as long as the patient hasn’t consumed food or drink recently, or been breathing through their mouth, is a reasonably good measure of core temperature and is the most commonly used determination point. It is inconvenient for long-term monitoring, however, and is impractical for patients who are unable or unwilling to hold the measuring device under their tongue for the prescribed time. Axillary temperature can be close to core, but significant variations are possible. Rectal temperatures provide very good correlation to core, but can be uncomfortable for the patient and inconvenient for staff. The temperature of the tympanic membrane in the ear is close to core temperature, but measurement is very technique-dependent. Long-term temperature monitoring is most easily done with a probe attached to the patient’s skin, but since this value often doesn’t correspond to core temperature, it is mainly a relative value: if it goes up or down significantly from a previously steady value, it can indicate problems that need further attention. Overall, there is no one method of temperature measurement that will suit all situations, so various methods may have to be employed. The original method of determining temperature was to simply feel the patient’s skin. This method requires no tools and with experience can be a reliable indicator of significant variations in the patient’s temperature. However, it is subjective and doesn’t provide a numerical measurement. Glass tube thermometers were invented in the fifteenth century and used mercury or colored alcohol to indicate temperature (Figure 4.37). These devices continue to be used today, though their use with patients has essentially ceased, due to the possibility of injury and the danger of mercury contamination if the tube was broken. Most hospitals use electronic thermometers, which can be of two basic types. ELECTRONIC PROBE THERMOMETERS Electronic probe thermometers use a resistive element (thermistor) that changes its resistance according to temperature (Figure 4.38). By passing a constant current through the device and measuring voltage drop, and then applying the results to a curve-correcting algorithm, a value for temperature can be determined. Probes can be of various shapes depending on application, but most used in hospitals are either slender rods or flat buttons. 136 FIGURE 4.37 Introduction to Biomedical Engineering Technology Old-style glass tube thermometer. Rod-type probes are used for oral or rectal, or less commonly axillary, measurements, while button probes are used for skin measurements. Rod probes are used with a disposable cover, replaced for each patient to help prevent cross-infection. Systems are designed to make it difficult to take a temperature reading without using a probe cover. They are also designed so that it is impossible to take a second reading without replacing the probe cover. Some models come with two different probes, one for oral and one for rectal measurements; probes are color-coded, usually blue for oral and red for rectal. Single probe units usually use the same color code. Probes are generally replaceable and often are available with various cord lengths. The body of these units has a battery compartment, a probe holder, a holder for a supply of covers, and a display that gives the temperature reading as well as other indicators such as low battery, probe fault, low- or high-temperature alarms, and possibly a timer to indicate when temperature readings should be stabilized. Generally, there is a switch in the probe holder that turns the device off when the probe is inserted and on when it is removed, for battery conservation. Some units may have an internal mechanism such as a magnetic relay or Hall Effect switch that is activated when the unit is placed in a special housing. The unit must be reset by this mechanism after a set number of readings or it will become inoperative. This is to deter theft of the thermometers. Units can usually be changed from Celsius to Fahrenheit depending on application. The control for this is usually hidden, often inside the battery compartment. TYMPANIC THERMOMETERS The tympanic membrane is almost always at core temperature, being well inside the skull at the end of a narrow passage, so in that way it makes an ideal candidate for temperature measurement. Because of its delicate nature, however, direct contact Diagnostic Devices: Part Three 137 FIGURE 4.38 A probe-type thermometer, with oral and rectal probes. with a temperature probe could be harmful. Methods were developed in industrial applications to measure temperature remotely by measuring the infrared radiation emitted by an object. This method was refined and miniaturized to produce the infrared tympanic thermometer (Figure 4.39). Infrared temperature sensors use a semiconductor device called a thermopile, which generates an electrical potential when exposed to infrared radiation. Because there is a delay in response time for thermopile sensors, they must be kept shielded behind a shutter mechanism until the time of temperature measurement. When the unit is pointed in the right direction (in this case, at the tympanic membrane), the shutter is triggered to open for a specific time, during which the temperature of the membrane is determined. Technique is critical when using a tympanic thermometer. If the unit isn’t adjusted and inserted correctly into the ear canal, it may not be pointing at the tympanic membrane when measurement is taken, which will result in erroneous values. Also, the body of the probe should seal against the ear canal, because air currents entering the ear past the unit can cause errors. These devices are designed to use a thin, deformable plastic cover over the probe portion in order to avoid cross-infections. They are designed so that the cover has 138 Introduction to Biomedical Engineering Technology FIGURE 4.39 Tympanic thermometer with lens cover. to be replaced before another reading can be taken. The cover forms part of the optical path, and therefore, accurate readings require that probe covers be in place. Similarly, any dirt or foreign material on the lens or cover will affect readings. IR thermometers tend to drift with time, and so they must be calibrated on a regular basis. TEMPORAL ARTERY THERMOMETERS Temporal artery thermometers rely on the idea that the temperature of blood in the temporal artery, which is one of the arteries nearest to the surface of the skin, is very close to internal body temperature. They use a similar operating principle to tympanic thermometers, with an infrared sensor. Care must be taken to place the unit correctly, as adjacent areas of skin will not have the same temperature as those over the artery. Positioning is not quite as critical as with tympanic thermometers and measurement is quicker and less obtrusive, so this type of thermometer has become much more popular. DENSITOMETERS In the movie, The Pursuit of Happyness, the protagonist tried to make a living in the early 1980s by selling bone densitometers to doctor’s offices and clinics. He had a hard time convincing some of his potential customers of the value of the devices, but now, with the prevalence and awareness of conditions such as osteoporosis, he may have had an easier time. Densitometers use low-level X-rays or ultrasound beams to produce a density reading of the bone tissue through which the exposure is made. Some units are as portable as the ones that Will Smith’s character lugged around in the movie, but most are larger, fixed devices that scan a prone patient from above. Diagnostic Devices: Part Three FIGURE 4.40 139 A knee arthroscopy procedure. ARTHROSCOPY SYSTEMS Arthroscopy systems share a number of characteristics with other endoscopy systems, but because they are working in the confined spaces of joints, some of the hardware is designed differently. Scopes are smaller and shorter, and always rigid. Instruments are passed into the joint via a second (or sometimes third) tube, which also handles irrigation and suction (Figure 4.40). Instead of gas to expand the target area for improved viewing, a clear fluid is used. Since repair of injured joints often involves the removal of torn or damaged cartilage or sometimes calcareous growths on bone, rotating cutting and grinding instruments are used in arthroscopy. Some procedures, such as the repair of tears in the meniscus (the membrane that holds lubricating synovial fluid in the joint) or the repair of torn ligaments, may involve suturing through the tubes. SUMMARY This chapter was concerned with the digestive, sensory, and reproductive systems, as well as miscellaneous topics such as the skin, muscles, and bones. 140 Introduction to Biomedical Engineering Technology Function and application of gastroscopes was covered, as well as equipment used to examine the eyes, ears, and throat. Perinatal monitoring and care were examined, along with various types of thermometers and the principles of thermoregulation. Arthroscopy was briefly discussed. QUESTIONS 1. What channels may be present in an endoscope? 2. What advantages are there to having a camera chip mounted on the tip of an endoscope? 3. How is light transmission different between rigid and flexible endoscopes? 4. Why is light quality important in endoscopy procedures? 5. What factors can influence light quality? 6. Why is a mechanical device used to control light intensity, rather than an electrical/electronic control? 7. What are the advantages and disadvantages of a three-chip camera system? 8. What is the purpose of an insufflator? 9. Why is carbon dioxide used for insufflation? 10. What factors can make it difficult to detect a fetal heartbeat? 11. How is a fetal monitor ultrasound transducer different from that of a simple fetal heart detector? 12. Why might medical staff wish to monitor uterine contractions as well as fetal heart rates? 13. What factors can produce incorrect values for core temperature when measuring temperature orally? 14. What are some advantages and disadvantages of tympanic thermometers? 5 Diagnostic Imaging OBJECTIVES FOR THIS CHAPTER • To briefly describe the history and physics of X-rays, including some of the technology of X-ray detectors. • To discuss X-ray safety, including the units used in the technology. • To describe some of the common X-ray procedures and the equipment used in each. • To briefly discuss the details of CT, MRI, and PET scanners. • To look at the technology and application of diagnostic ultrasound. • To outline the picture archiving and communications system used in managing the images produced in diagnostic imaging procedures. INTRODUCTION As discussed in the preface to this book, diagnostic imaging (DI) is a large, specialized field with mostly very complex, manufacturer-specific equipment. Most DI equipment requires factory training before Health Technology Management Techs can provide effective service. Therefore, it will not be dealt with in depth in this book, but an outline of the various technologies involved is included (Figure 5.1). X-RAYS History Being able to look inside the living human body without cutting it open was a dream of medical workers for most of history. Visible light, no matter how bright, could not provide any significant information about structures beneath the skin. The sense of touch could be used to help diagnose some conditions, but it too was limited. In 1895, Wilhelm Röntgen, in Germany, discovered that some previously unknown rays that were emitted from a vacuum tube across when a high voltage was applied, passed through some materials that were completely opaque to visible light, though not others. The rays, which Röntgen named “X-rays,” were blocked by dense materials such as bone or metal, and so he used them to make an image of his wife’s hand, passing the rays through her hand and onto a photographic plate. For some time, the rays were called Röntgen rays in honor of their discoverer, but the X-ray term has prevailed. PHYSICS Eventual research showed that X-rays were simply very short wavelength emissions in the same spectrum as light and radio waves (see Chapter 11), with wavelengths DOI: 10.1201/9781003140603-5 142 Introduction to Biomedical Engineering Technology from 0.01 to 10 nm. X-rays with wavelengths greater than 0.1 nm are called “soft” X-rays, while those of less than 0.1 nm are “hard” X-rays. The means of producing X-rays were refined, and most current X-ray tubes utilize a beam of electrons accelerated to extreme velocity by high voltage. The beam then collides with a metal target (typically tungsten), and the collision produces X-rays. By angling the target, the X-rays can be directed as desired. Copper is often used as a substrate for the metal target in an X-ray tube because of its high heat conductivity; heat build-up is reduced in the target contact area. With this same heat-reducing end in mind, many modern tubes have a spinning target, first developed by the Philips Company in 1929. X-ray characteristics are determined by the voltage and current used to produce them. Voltages are in the thousands of volts range, and their values are given as the peak voltage, or kVp. Current is in milliamps (mA), but the duration of the current is a factor as well, so the two components are often combined as milliamp-seconds, or mAs. Typical values for voltage, current, exposure time, and radiation dose for different types of X-ray procedures are given below. Dental X-rays 70–90 kVp, 3–10 mA, 0.05–4 s, 20 μSv Mammogram 25–26 kVp, 70–126 mAs, 0.7–1.5 s, up to 2.50 mSv Chest/abdominal/extremity X-rays 60–120 kVp, 1–100 mAs, 0.1–3 mSv Fluoroscopy 40–120 kVp, 1–20 mA, up to a few minutes duration, 20 mSv/min DEFINITIONS OF UNITS • A rad is an older unit, and rad stands for radiation absorbed dose and is defined as 1 W of X-ray power entering 100 kg of tissue. • The rem is also an older unit, and rem stands for “Röntgen equivalent man”; that is, 1 rem is the amount of radiation required to produce the same biological effect as 1 rad (1 rem = 0.01 Sv). FIGURE 5.1 Radiologists examining X-ray films. Diagnostic Imaging 143 • Gray (Gy)—1 Joule of X-ray energy entering 1 kg of tissue (1 Gray = 100 rad). • Sievert (Sv)—The amount of radiation required to produce the same biological effect as 1 Gray (1 Sv = 100 rad). DETECTORS 1. Originally, X-rays were detected by exposing them to a standard (at the time) glass photographic plate. The X-rays caused chemical changes in the silver compounds in much the same way as light did. Since X-rays are blocked to a greater or lesser degree by the tissues they pass through, an X-ray image on a plate is a negative; that is, the lighter areas on the plate correspond to more dense tissue while the darker areas correspond to less dense tissue. 2. Glass plates were replaced by sheets of photographic film, which, since they would be ruined if exposed to light, were held in cassettes that blocked visible light but were transparent to X-rays. The cassettes could be unloaded manually or automatically for processing. 3. Certain materials glow, or fluoresce, when struck by X-rays, so if a sheet of such material is used in place of X-ray film, a continuous (moving) image can be seen. This process is called fluoroscopy and can be very useful when examining situations that involve movement, such as swallowing, or the injection of a radiopaque dye into the patient. 4. Scintillation counters are devices that convert X-ray photons into visible light photons and then use a photomultiplier section to amplify the visible light. This means that acceptable X-ray images can be obtained with lower doses of X-rays. 5. Digital detectors using CCDs (charge-coupled devices) similar to those found in digital cameras (but larger) can be designed to detect X-rays. Due to the sensitivity of these devices, lower X-ray doses can be used to produce adequate results, and resolutions are available that can rival that of X-ray films. Because CCDs produce digital signals, the X-ray images are then available for digital manipulation, storage, or transmission to other areas. EFFECTS AND DOSAGE LIMITS X-radiation is ionizing radiation, that is, it can remove electrons from the atoms of the material it strikes. This has significant effects on living tissue, in that it can cause burns as an immediate effect, or it can cause damage to the chromosomes of some cells, possibly causing or allowing them to become cancerous. For these reasons, dosage limits have been set for X-ray exposure. Some values relating to X-ray exposure (US values; most other jurisdictions are similar): • 1 Msv—The recommended maximum annual dose for individuals in the general public. • 20 Msv—The recommended maximum 5-year-averaged annual dose for workers in radiation industries. • 50 Msv—The recommended maximum single-year dose for workers in radiation industries. 144 Introduction to Biomedical Engineering Technology • 100 Msv—The dose that gives a 0.5% chance of causing cancer later in life. • 1 Sv—The dose that gives a 5% chance of causing cancer later in life. • 10 Sv—The dose that may cause death within days or weeks. People who work in radiation environments, such as X-ray technologists, wear exposure badges that must be read regularly to ensure dose limits are not exceeded. X-RAY SAFETY Great efforts are made to reduce exposures to patients and staff, including the use of lead shields and lead aprons to protect the areas of patient’s bodies that are not being X-rayed; lead aprons for staff when they are in the immediate vicinity of X-rays; leaded glass and walls for staff observation areas; and lead shielding in the outside walls, doors, and windows of X-ray rooms. X-RAY PROCEDURES X-rays are used in a wide variety of situations in health care, with machines that range from simple, inexpensive dental X-ray units to room-filling, multimillion dollar CT scanners (Figure 5.2). DENTAL X-RAYS Dentists are only concerned with teeth, and dental X-ray units are specialized for taking X-rays of teeth, to show root structure, filling and crown placement, and locations of decay and other conditions. The machines are limited to relatively low voltages and currents, often having only a few pre-set exposures available. FIGURE 5.2 Hmmm. Diagnostic Imaging 145 FIGURE 5.3 Dental X-ray unit. They are relatively small and light, and can be mounted on wheeled stands so they can be moved to different areas (Figure 5.3). They generally operate on power from wall outlets. The film for these units is usually held in a device that is placed in the patient’s mouth. Newer units have digital sensors that fit in the patient’s mouth instead of film, giving very rapid results that can be stored easily in a computer system. GENERAL PURPOSE X-RAY ROOMS These are the most common X-ray units in hospitals, and can be used for a variety of applications, from taking X-rays of small structures like hands or feet, to chest and abdomen X-rays, to studies of larger skeletal components. They usually have a table that can be moved in three dimensions as well as a head that can move in three dimensions plus rotate around two axes (Figure 5.4). The table can also tilt, and it contains slots for film cassettes or digital detectors (Figures 5.5 and 5.6). Some units have a second detector section mounted vertically on a wall, for doing studies in which the subject must be standing (Figure 5.7). X-ray heads contain the X-ray tube as well as a collimator, a device that can open or close to limit the area of exposure (Figure 5.8). Collimators usually have lights in them that illuminate the same area that the X-ray exposure will cover, with grids to aid in placement (Figure 5.9). 146 Introduction to Biomedical Engineering Technology FIGURE 5.4 A typical room X-ray system. (Courtesy of GE Medical.) FIGURE 5.5 Room X-ray system showing table. (Courtesy of Philips.) Diagnostic Imaging FIGURE 5.6 X-ray table. (Courtesy of GE Medical.) FIGURE 5.7 A wall X-ray unit. (Courtesy of GE Medical.) 147 148 Introduction to Biomedical Engineering Technology FIGURE 5.8 X-ray head containing the tube and collimator. FIGURE 5.9 View of a collimator from below. Standard X-ray rooms can be used for procedures using radiopaque liquids and dyes. The liquids, usually a barium suspension, can be given to the patient as a drink, for studying the upper digestive system, or as an enema, for studying the lower system. Dyes may be injected into the bloodstream to follow cardiac arteries; some dyes are rapidly excreted by the kidneys and can be used to obtain more details of the renal system. Portable X-ray machines allow the procedures to be taken to the patient rather than vice versa. Units have substantial internal batteries to provide power both to generate X-rays and to mobilize the device. Diagnostic Imaging FIGURE 5.10 149 A portable X-ray machine. (Courtesy of Philips Medical.) MAMMOGRAPHY Mammograms are X-rays specifically designed to detect breast cancer and other breast disorders (Figure 5.10). Since the tissues involved are soft, only low levels of X-rays are needed, with doses around 0.7 mSv (Figure 5.11). Mammography is most effective when the X-rays pass through a wide but thin area, and so the units include a mechanism to compress the breasts horizontally and then vertically while images are taken (Figures 5.12, 5.13 and 5.14). COMPUTERIZED (AXIAL) TOMOGRAPHY SCANNERS CT or CAT scanners evolved from simpler tomography units, which moved the X-ray head in circles while exposures were made to produce a “slice” of image, rather than a “shadow” as do normal X-rays. CT units take this several steps further, with an X-ray tube that can produce a “fan” of X-rays and a large number of detectors arranged in a large ring. Each detector picks up part of the X-ray fan that passes through one axis. Some systems have many detectors (64, 128, or 256 sets) that can process image data separately, producing multiple, higher resolution slices at once (Figure 5.15). 150 Introduction to Biomedical Engineering Technology FIGURE 5.11 A mammogram film—note the large light area indicating a tumor. (Courtesy of GE Medical.) FIGURE 5.12 Mammography compressor. (Courtesy of GE.) Diagnostic Imaging 151 FIGURE 5.13 Mammography system components. (Courtesy of GE.) FIGURE 5.14 Mammography procedure. In a procedure, the patient lies on a table that can move in and out of the ring, stopping at locations where imaging is needed. An exposure is made and each detector feeds its information into a computer, which combines the data from all detectors and constructs a “slice” that represents the structures found transversely through the patient at that location. 152 Introduction to Biomedical Engineering Technology FIGURE 5.15 CT machine. (Courtesy of Philips.) Slices are repeated through the area of interest and can be studied individually, or as a “movie” of a cross-section passing through the body. Newer systems with more computing power can complete more slices, more quickly, and can also combine the data from multiple slices to create a three-dimensional (3D) model of specific structures. The 3D data can also be used to perform virtual dissections, with the operator “removing” different sections or layers of tissue to expose something of interest, such as a tumor. MAGNETIC RESONANCE IMAGING SCANNERS Though images produced by MRI scanners may look similar to those from a CT machine, the principles of operation are quite different. Originally called nuclear magnetic resonance imaging (NMRI) scanners, they operate on the basis of atoms having magnetic properties (Figures 5.16 and 5.17). The details of MRI theory involve complex nuclear physics and a lot of esoteric math, but for our purpose a few basic ideas will hopefully make the technology somewhat understandable. “Spin” is a fundamental property of matter, in the same way as mass or electrical charge are fundamental properties, though not as apparent in everyday experience. Electrons, protons, and neutrons when on their own each have a spin value of ½, and this can be either positive or negative. When particles combine to form atoms or molecules, the spin values of each particle sum together. Thus, the total spin value of an atom or molecule can be various positive or negative multiples of one half, or, if the positive and negative spin particles balance out, the sum can be zero. Diagnostic Imaging FIGURE 5.16 153 MRI scanner. (Courtesy of Philips.) Atoms or molecules with a nonzero spin sum can be affected by a magnetic field. They act something like tiny magnets themselves and align with the applied magnetic field. Hydrogen atoms are an example of a nonzero spin sum material. The magnetic fields in MRI units are generated by superconducting electromagnets. Field strength is usually about 2–4 T. (By comparison, the Earth’s magnetic field has a strength of about 50 μT.) Molecules aligned in a magnetic field can be in a high energy state, as if the north poles of both the magnetic field and the molecule point in the same direction (as do the south poles), or a low energy state in which the field and molecular north poles point in opposite directions. If the various aligned molecules in the magnetic field are hit with a pulse of electromagnetic radiation (EMR; radio waves), some of the low-energy state molecules will absorb the EMR energy and jump up to the high-energy state. Afterward, some of the high-energy state molecules will fall back to the low-energy state and emit EMR of their own. The frequency of radiation is typical of the particle absorbing 154 Introduction to Biomedical Engineering Technology FIGURE 5.17 MRI scanner cut-away. or emitting it, so hydrogen atoms will absorb/emit a different frequency of radiation than, for example, atoms of sodium-23, another nonzero sum particle that is relatively abundant in the human body. By detecting, measuring, and analyzing the radiation emitted in this manner, an image can be developed of the nonzero sum materials in the magnetic field. Since hydrogen atoms constitute a large proportion of the nonzero sum particles in the human body, a map or model of hydrogen distribution can be produced. Further, since different tissues have different amounts of hydrogen in them, tissue structures can be determined. Using a different EMR frequency to pulse the particles in the magnetic field will produce maps of different particles, each of which can provide its own set of useful information. The resonant frequency of the particles to be examined must be known; this is the frequency used to study that particle’s distribution. Other nonzero spin particles include the isotopes carbon-13, oxygen-17, and phosphorus-31. Some of the useful isotopes can be administered to the patient to increase their numbers in the body. For example, water made up of oxygen-17 atoms can be simply ingested and distributed throughout the body just like normal oxygen-16 water. Special isotopes used in MRI studies are generated in research facilities with such equipment as linear accelerators. Functional MRI (fMRI) is a specialized type that detects blood flow in the brain, allowing studies of brain activity in response to various mental activities or disease states. The powerful magnetic fields used in MRI systems will attract any magnetic material in the vicinity, accelerating it toward the center of the field, sometimes with disastrous results. Such materials, therefore, must be completely absent from the imaging vicinity. Diagnostic Imaging 155 The EMR signal is very powerful, as well, and can act like a microwave oven, overheating the patient. Such devices as implanted pacemakers will react very negatively to MRI. POSITRON EMISSION TOMOGRAPHY When a radioactive isotope decays, it emits a positron (an anti-electron, having the same mass as an electron but a positive charge) as radiation. The positron soon collides with an electron and they are mutually annihilated, emitting two photons in exactly opposite directions in the process. These photons can be detected with two scintillation scanners placed opposite each other. If two photons are detected 180° apart from each other and within a few nanoseconds of each other, they are from the same isotope decay event, and the axis of their travel can be determined (Figure 5.16). By averaging thousands of such events, an image of the tissue structure containing the isotope can be formed. Different isotopes are absorbed by different tissues, and so by choosing the appropriate isotope, images of these tissues can be made (Figures 5.18 and 5.19). PET scanners can be integrated with other imaging equipment such as MRI or CT scanners, and when scans using the two different techniques are done simultaneously, FIGURE 5.18 Patient undergoing a PET scan. (Courtesy of GE.) 156 Introduction to Biomedical Engineering Technology FIGURE 5.19 PET scanner. FIGURE 5.20 PET scan of a human brain. the PET image can be placed in context with the more comprehensive but less specific MRI or CT image (Figure 5.20). Isotopes may be taken up by tissues depending on their rate of metabolism, so PET scans can provide information about these rates. Cancer tumors, for example, often have much higher metabolic rates than other, surrounding tissues. Diagnostic Imaging 157 The radioactive isotopes, or radionuclides, have a very short half-life. For example, carbon-11 has a half-life of about 2 min, while fluorine-18 is relatively long-lived with a half-life of about 110 min. The short half-life means that the radionuclides must be produced very near the PET scanner and delivered to the patient immediately after production. The isotopes are produced in a huge device called a cyclotron. DIAGNOSTIC ULTRASOUND X-rays have the potential of causing tissue and genetic damage, especially in a developing fetus. Imaging of the fetus is important in monitoring development, however, so means were explored to accomplish this without using X-rays. Ultrasound proved to be such a technology, and scanners were developed to produce two-dimensional slices of the fetus in utero (Figure 5.21). Technological advances gave higher-quality images and also allowed the data from many two-dimensional scans to be combined to form a 3D image (Figure 5.22). Fetal ultrasound machines use heads with multiple piezoelectric crystals, and different frequencies of heads are used to scan at different depths. Similar machines have been optimized for cardiac imaging as well as for other specialized applications (Figure 5.24). Compact components are used to make hand-held US devices that transmit images to a smartphone or tablet. PICTURE ARCHIVING AND COMMUNICATION SYSTEM With the advent of digital image techniques, powerful and relatively inexpensive computers, and high-speed data networks, it became possible to handle diagnostic images in a coordinated manner. Images could be stored, distributed, and presented FIGURE 5.21 Patient having a prenatal ultrasound examination. 158 Introduction to Biomedical Engineering Technology FIGURE 5.22 3D ultrasound image of a fetus. (Courtesy of GE.) FIGURE 5.23 A portable ultrasound machine. Diagnostic Imaging 159 FIGURE 5.24 Patient having a thyroid ultrasound scan. in a consistent format, allowing various medical personnel to have access to highquality images from many different locations. Such systems came to be called picture archiving and communication systems, or PACS. Any digital image can be handled with a PACS system, including X-rays, and CT, MRI, PET, and ultrasound scans, as well as endoscopy or microsurgery images. Specialists can evaluate images from a distant location where such expertise may not be available, without the delays and inconvenience of having to ship hard-copy images from place to place. Various people can look at the same image simultaneously for collaborative or educational purposes. Digital storage is much more compact and less expensive than the huge archives used in keeping traditional film images. A PACS network consists of a central server connected to various client workstations through a local and/or wide area network. Several PACS systems can be connected together, and the Internet can also be used as a communications channel. Because diagnostic images are large and of high resolution, system data rates must be high enough to allow image transfers in reasonable time periods. Workstations must be capable of displaying images at diagnostic-quality levels and be able to handle them quickly. Two video displays are usually included to allow the comparison of images (Figure 5.25). Smartphones and tablets may have adequate resolution and processing power to be able to handle these images as well. The central server stores images in a database and handles requests for access to existing images or storage of new images. Functions such as database maintenance such as data backup and system upkeep are performed as with any other database. Since images can come from many sources, there must be a very effective means of naming and organizing them. 160 Introduction to Biomedical Engineering Technology FIGURE 5.25 PACS terminal with dual displays, keyboard, and mouse. SUMMARY This chapter covered the field of diagnostic imaging. A history of X-rays was provided along with some of the physics involved. Various X-ray technologies, dose limits, and safety were examined. Specialized scanners like CT, MRI, PET, and diagnostic ultrasound were described. Finally, the PACS was discussed. QUESTIONS 1. Explain the difference between the two types of X-rays. 2. Why is copper often used in X-ray machines? 3. Why is a spinning target used in X-ray tubes? 4. Define: a. Rad b. Rem c. Gray d. Sievert 5. Why are X-ray film images “negatives?” 6. How is a fluoroscopy different from a simple X-ray? 7. What are some methods that can be used to reduce radiation exposure to patients? 8. List four dosage limits for X-ray exposure and the possible effects if each were to be exceeded. 9. Why are radiopaque liquids and dyes used for X-rays and how are they administered? 10. What is a typical dosage for mammograms? Why is it lower than other types of X-rays? 11. Why would an MRI scanner be used rather than a CT scanner? 6 Part One Treatment Devices OBJECTIVES FOR THIS CHAPTER • This chapter examines some of the devices involved in treating patients in relation to the heart, the circulatory system, and the respiratory system, including history, theory, function, and types of the various devices, as well as an overview of relevant anatomy and physiology. • Heart: defibrillators and pacemakers. • Circulatory system: artificial hearts, ventricular assist devices (VADs), intra-aortic balloon pumps, heart–lung machines, sequential compression units, automatic tourniquets, blood warmers, IV pumps, and PCA pumps. • Respiratory system: ventilators, CPAP/BiPAP units, oxygen concentrators, and humidifiers. HEART As the heart is the most intensely monitored organ in the body, it is also the most intensively treated, with a variety of devices used to stabilize or improve the function of a patient’s damaged or diseased heart. DEFIBRILLATORS The defibrillator (or “defib”) is perhaps the most recognized high-tech medical device, thanks to movies and television (Figure 6.1). A doctor holds paddles over a dying patient. She yells “clear” and then places the paddles on the patient’s chest. The patient’s body jerks spasmodically, and the steady beep–beep of monitor resumes— or perhaps a flat line on a screen changes to a familiar waveform. The popular perception is that a defibrillator is used to “restart” a heart that has stopped beating, but its name implies something different. Though occasionally a “flatliner” can be revived with a defib, it is most commonly used to change the uncoordinated contractions of the heart (fibrillation) into a normal sinus rhythm—that is, to defibrillate the heart. In this section, we will briefly review the history of defibrillators and examine the theory of operation and application of a modern device. The various types of defibrillators in use will be surveyed, along with the options and accessories that are available. Finally, we will consider the types of batteries used in defibs and look at the testing and maintenance requirements of the devices. DOI: 10.1201/9781003140603-6 162 FIGURE 6.1 Introduction to Biomedical Engineering Technology A typical portable defibrillator/monitor. (Courtesy of Philips.) HISTORY The history of the defibrillator is closely tied to the history of the electrocardiograph (see Chapter 2). Scientists and physicians first needed to understand how the heart functioned, especially from the perspective of electrical signals and muscle contractions, before they could attempt to devise a means of treating the often-fatal interruptions of normal cardiac contractions. In 1947, after six failed attempts on other patients, Claude Beck, a cardiovascular surgeon in Cleveland, successfully defibrillated the heart of a 14-year-old boy during cardiac surgery. In this case, the impulse from the defibrillation equipment was applied directly to the patient’s heart. In 1956, Paul Zoll, a cardiologist, using a more powerful defibrillator, is able to successfully defibrillate a patient by applying the defibrillator impulse externally— through the chest walls. Research and development of defibrillators took place in Britain and the USSR, as well, including the first mobile unit built in Belfast, to be used in ambulances. THEORY OF OPERATION As discussed in Chapter 1, fibrillation is the rapid, irregular, and unsynchronized contraction of the muscle fibers of the heart. Generally, fibrillation is of one of two types. In atrial fibrillation, the atrial chambers of the heart are not contracting in an effective way, while the ventricles continue to function normally (Figure 6.2). Since the ventricles do most of the work of pumping blood, this is not usually a life-threatening condition, though it is debilitating. Correcting atrial fibrillation, a procedure sometimes called cardioversion or synchronized cardioversion, is not an emergency and is usually done in a calm, controlled clinical situation. Treatment Devices: Part One 163 FIGURE 6.2 Atrial fibrillation waveform. FIGURE 6.3 Ventricular fibrillation waveform. Ventricular fibrillation (or v-fib) results when the ventricles are contracting in a nonsynchronized manner (Figure 6.3). Because ventricular fibrillation results in an almost complete cessation of blood flow from the heart, it is rapidly fatal if not reversed by defibrillation. This is an emergency procedure and is often done after a session of cardiopulmonary resuscitation (CPR). FUNCTION Defibrillators function by delivering a short pulse of electric current to the heart. This pulse of current polarizes all of the muscle and nerve cells in the heart simultaneously 164 Introduction to Biomedical Engineering Technology and (hopefully) allows them to resume normal operation—that is, to produce coordinated contractions in the heart so that blood is pumped through the body. A defibrillator consists of an energy source, circuitry to control the energy, and a means of delivering the energy to the heart. ENERGY SOURCE The first defibrillators in clinical use derived power from AC (line) outlets and were bulky and heavy. This meant that power was available continuously, but units were limited to operation near an outlet, and since defibrillators were often required in locations where outlets were not available, smaller, lighter battery-powered units were soon developed. Batteries used in defibrillators must meet a number of requirements. They must be able to supply an adequate amount of power; they must be reliable and safe; they must be able to be recharged many times; and they must be reasonably lightweight. As battery technology evolved, different battery types were used in defibs. Early units employed nickel–cadmium (NiCad or NiCd) batteries, which had good energy density when new but were prone to developing a “memory,” which prevented them from providing full power. Newer lithium ion battery designs and sophisticated charging circuitry help to alleviate this problem. Sealed lead-acid batteries, which use a gelled electrolyte to prevent spills and allow operation in any orientation, have also been commonly used in defibrillator design. Their high degree of reliability made up for their relatively low energy density. Lead-acid batteries generally do not do well if they are fully discharged and/ or left in a discharged state for prolonged periods, and therefore should be charged immediately after use for best performance. Lithium ion and nickel–metal hydride batteries, having high-energy density and low susceptibility to memory problems, are increasingly being used to power defibrillators; however, they too must be treated carefully to ensure long and reliable operation. VOLTAGE MULTIPLIER The batteries powering defibrillators typically provide 12 V DC, while the discharge to the patient is a specifically shaped wave that may have an amplitude of several thousand volts. The battery voltage must therefore be boosted to around 5000 V. This is applied to a capacitor, which stores the electrical energy until it is delivered to the patient. Circuitry to accomplish this typically chops the DC into a square wave and passes this waveform through a high-ratio step-up transformer. The high-voltage AC waveform is then rectified and used to charge the storage capacitor. CHARGE STORAGE A capacitor with high voltage and capacitance ratings is used to hold the electrical energy until it is delivered to the patient. This capacitor must be of high quality in order to reliably and repeatedly store energy and release it at a high rate. Treatment Devices: Part One 165 WAVEFORMS The first attempts to defibrillate patients used alternating (sinusoidal) current applied through paddles directly to the heart. Appropriate voltage levels had been determined in animal experiments, and further testing indicated that some type of DC waveform was more effective than AC—that is, less energy was required and success was more frequent with DC than with AC, which meant greater patient survival rates and less chance of burns. In the early 1960s, positive-going, pulsed (monophasic) defibrillation waveforms were widely adopted by most defibrillator manufacturers. These waveforms, referred to as Edmark (the most common) or Lown waveforms after their inventors, were used until about 2000, when research showed that a biphasic waveform with both positive and negative components could provide effective results with lower power, thereby increasing patient safety while also reducing demands on batteries and other components. Note that the period of these waveforms is a few milliseconds (biphasic longer than monophasic), while their amplitude may range from a few volts to several hundred volts depending on the application. DISCHARGE RELAY When it is time to deliver the defibrillation shock to the patient, a relay is activated to connect the charge storage capacitor to the wave shaping circuitry and then through the paddles or electrodes to the patient. This relay must meet specific requirements. It has to be fast-acting to make the charge available in a sufficiently short time. The contacts must be carefully designed to be able to withstand many high-current, high voltage surges. Finally, the housing must be airtight to prevent open sparks in case flammable agents are being used in the vicinity. The closing of this relay produces the “thunk” sound when the defib is used. WAVE SHAPING Charge capacitors deliver a simple DC surge. In order to convert this into the required waveform, an array of inductors, resistors, and capacitors are used (an LRC circuit). PADDLES AND ELECTRODES In order to deliver to the patient the large amount of electrical energy required to produce effective defibrillation, a large surface area must be used as the current densities are low enough to prevent burns. External defibrillator paddles typically have a smooth, flat stainless steel face, and most manufacturers have smaller paddles or small slip on attachments to accommodate pediatric patients (Figure 6.4). Conductive (saline) gel is used to help ensure even, low impedance contact between the paddles and the patient’s skin. Conductive electrode pads attached directly to the defib are often used now, reducing the number of movements required and making 166 Introduction to Biomedical Engineering Technology FIGURE 6.4 A BMET testing a defibrillator on an educational manikin. for more reliable contact, with less “clutter” than hand-held paddles with their heavy coiled cords. Defibrillation may also be performed during open-heart surgery, in which case much lower energies are needed. Being able to safely and effectively apply the paddles to a living heart requires that the paddles have relatively small, cupped faces, with long, insulated handles. Defibrillators may have the ability to detect which type of paddle is attached and limit the maximum available energy if pediatric or internal paddles are being used. If repeated defibrillations may be required (e.g., in cases of atrial fibrillation where the patient is subjected to many bouts of fibrillation), it may be more effective and convenient to apply adhesive electrodes to the patient’s chest. If the patient is also undergoing external cardiac pacing, these electrodes may serve to deliver both defibrillating and pacing pulses. Automatic external defibrillators (AEDs), for use in situations where trained medical personnel may not be available, also use adhesive pads in order to simplify procedures. “Code blue, third floor, room 315. Code blue, third floor, room 315. Code blue, third floor, room 315.” The calm but forceful voice rings through the overhead paging system throughout the hospital, and members of the code blue team react instinctively, moving quickly but carefully to the announced location. By the time the ER physician arrives, someone has delivered a crash cart to the patient’s bedside and there is a flurry of activity (Figure 6.5). A nurse is performing CPR while a respiratory therapist waits to intubate the patient with an endotracheal tube should that be necessary. Treatment Devices: Part One 167 FIGURE 6.5 Crash cart with defibrillator (top left), suction (top mid-right), oxygen tank (top far right), sharps container (middle right), and the cart itself with drawers for medications and supplies. Other staff members are monitoring vital signs and preparing to provide a description of the patient, their condition and medications, and the events leading up to the arrest, as far as they are known. Someone gets a suction tube ready and easily accessible, another readies an oxygen supply, while syringes of epinephrine, atropine, and lidocaine are made ready for direct injection or, if there is time, administration via an intravenous line. Other medications are available in the crash cart drawers. A lab tech draws a sample of blood and rushes it to the lab for quick analysis of blood chemistry. Most of the team members perform their tasks quickly and efficiently, with a minimum of confusion, though some of the newer members and students hang back, watching and trying not to get in the way. The patient is a young man who had been in a car accident and who had appeared to be recovering well. His bed covers have been pulled away and 168 Introduction to Biomedical Engineering Technology FIGURE 6.6 Syringe. his hospital pyjamas unceremoniously cut off, so that his chest is exposed. A bandage covers part of his left side where crumpled metal had pierced his skin, breaking three ribs. ECG electrodes have been applied in locations that will not interfere with defibrillation, and they are connected to the defib where a jumbled tracing appears on the display. The ER doctor gets a very quick run-down of the patient and current information and then asks the RT to intubate while she selects a syringe of epinephrine from the crash cart, noting that an intravenous line has now been started (Figure 6.6). Epinephrine is injected into the IV line, and the doctor picks up the defibrillator paddles. A team member applies conductive gel to one paddle surface and the doctor rubs the paddle faces together lightly to distribute the gel evenly, then places the paddles on the patient’s chest. A small diagram on the paddle handles show optimum placement locations, but the physician has done enough codes to know exactly where they go, only having to modify her righthand paddle position in order to avoid the bandages on the patient. “200 joules,” she says, and a nurse turns a knob on the front of the defibrillator to 200. The doctor presses a button on one handle and a whining noise comes from the defib, increasing in pitch along with increasing numbers on the display that show how much energy is being stored in the unit. When the number reach 200, the tone changes to a louder, steady pitch. In a loud, clear voice tinged with tension, the doctor calls out, “I am going to shock on three; One, I am clear; Two, you are clear; Three, everybody is clear,” A glance around shows that everyone is ready. Treatment Devices: Part One 169 FIGURE 6.7 An older defibrillator. “One! Two! Three!” Pressing a button on each paddle handle simultaneously causes a clunking noise to come from the defib, while at the same time the patient’s body jerks spasmodically as a result of some stray defibrillation current stimulating skeletal muscles. A strip of paper starts to stream out of the defib, showing the ECG waveforms from 20 seconds prior to the discharge, with a mark indicating the exact time of the discharge along with a measure of energy delivered and patient impedance (Figure 6.7). The display on the screen has wavered but is still indicating VFib, so the doctor asks for 300 J and the process is repeated, again without success. CPR continues between attempts, the third using the maximum available energy, 360 J. The first attempt at this level fails, but the next one, after an injection of atropine, succeeded in producing a near-normal sinus rhythm. The code blue team relaxes a little and goes about cleaning up the debris from the code, including gathering up the long ribbons of recording paper that will later be entered as part of the patient’s record, so that the process can be analyzed. As one of the nurses moves to the nursing station to begin the process of transferring the patient to the CCU, the ER doctor consults with a cardiologist who arrived just after all the excitement, in order to start planning a course of treatment for the patient and to try to understand why the arrest happened in the first place. 170 Introduction to Biomedical Engineering Technology DEFIBRILLATOR TYPES Defibrillators can be divided into two broad categories, internal and external, while the external type can again be divided into automatic (AED) and manual groups. INTERNAL (IMPLANTABLE) DEFIBRILLATORS Internal defibrillators are implanted into the patient’s body, usually into a pocket made in the tissue just below the patient’s clavicle, with two leads passing through a vein to the heart. Their basic function is the same as all defibrillators, but these units have a number of special requirements. Since they are to be implanted within the body, they must be small and able to withstand fluids (Figure 6.8). They are connected directly to the heart and thus deliver much lower levels of energy than external defibs, but since they are not directly accessible, they must have a battery that will last a very long time. They must contain microprocessor-based circuitry that will accurately recognize ECG waveforms that indicate a need for shock delivery, as well as a radio receiver to allow for programming as well as monitoring function and battery level, and a transmitter so that stored data can be sent to an external system for analysis. Some units have wireless connections that allow real-time monitoring of their function as well as cardiac activity. FIGURE 6.8 Implantable defibrillator. (Courtesy of Philips Medical.) Treatment Devices: Part One 171 Implantable defibrillators must be as inert biologically as possible in order to avoid rejection problems. Cases are usually made from special stainless steel alloys or titanium, and some may be coated with plastic. Leads are plastic coated, and electrode tips are usually stainless steel or some other alloy. Some manufacturers produce units that are both defibrillators and pacemakers (see Section below, Pacemakers), since certain patients require both functions. A number of components are similar in both pacemakers and defibrillators, so these components can be combined in dual-purpose units. EXTERNAL MANUAL DEFIBRILLATORS These are the most common (so far) types of defibrillators, being found on crash carts and in special procedure areas of hospitals and clinics as well as in many emergency response vehicles (Figure 6.9). Originally, external manual defibs were just defibrillators, with no other circuitry. They produced no records of the procedure, and an ECG monitor had to be used in order to be able to see the ECG waveform. As technology evolved, features were added. First came ECG circuitry with a “bouncing ball” CRT display, then a chart recorder (which in early models had to be turned on and off manually), and more recently extra functions such as cardiac pacing, pulse oximetry, noninvasive blood pressure, and capnography. Connectors, or more recently, wireless capability, were included to allow the ECG waveform (and later other parameters) to be transmitted to a bedside monitor or central monitoring system, or to a distant location. Alarm functions, which were non-existent in early versions, began with basic high–low ECG settings. Paddle contact alarms and indicators helped improve patient safety and charge delivery, and low battery warning alarms helped avoid “uh-oh” situations. Defibrillators were able to measure patient impedance and actual delivered energy. FIGURE 6.9 A Philips Intrepid battery-powered defibrillator monitor. Note that this device also has NIBP and pulse oximetry functions. (Courtesy of Philips Medical.) 172 Introduction to Biomedical Engineering Technology ECG MEASUREMENT AND ANALYSIS This topic is discussed in more detail in Chapter 2. Modern defibrillators depend on the accurate automatic processing and evaluation of ECG signals in order to function effectively. Timing discharges to cardioversion (more properly termed “synchronized cardioversion”) requires that the unit be able to detect QRS complexes with a high degree of accuracy, since the relationship of the charge delivery to signal phase is critical if success is to be achieved. Harm can result if discharge timing is incorrect in atrial fibrillation, as ventricular fibrillation can be induced. Charge is ideally delivered between the R wave and the T wave of the patient’s ECG. In addition, proper evaluation of the patient’s condition before and after any defibrillation effort is vital. Many new units perform some degree of automatic ECG analysis and are able to identify a variety of arrhythmias and other signal characteristics. RECORDERS Clinically and, more recently, legally, it is useful and sometimes critical to have a hard-copy record of events around the time of a defibrillation attempt. Strip chart recorders have provided this function since early in the development of portable defibrillators. These units have been developed for a variety of medical and nonmedical purposes and have been adapted to the specific needs of defibrillators. The first recorders used a heated arm that moved vertically as the heat-sensitive paper moved horizontally, while most new designs use a line of tiny elements that can be heated and cooled off very rapidly as the same heat-sensitive paper moves against them, thus producing a dot-matrix-like recording. Recorders must have both a time and an amplitude scale for ECG signals, as well as the capability of printing alphanumerics for rates, time, and date; energy delivered; patient impedance; alarm conditions; and various other parameters, as well as giving a graphic indication of the exact point of charge delivery. Some units print on paper that has a grid on it already, while others print the grid along with the waveforms. The recorders may also be used to print statistical data, either graphically or in a table, as well as device information such as serial number, total number of discharges, last service date, and more. Troubleshooting codes and error logs might also be printable, which can aid greatly in servicing the units. Most recorders can print ECG and other data from several seconds in the past. These recordings start automatically when the defib is discharged in order to provide information about the patient just before as well as after shock delivery. Recorders may be set up to start recording when certain alarm events occur, and they may also be able to draw on stored data to print strips of past events. ADDITIONAL COMPONENTS In order to help caregivers evaluate patients more thoroughly, components other than those directly associated with defibrillation and monitoring were added to defibs. All of these functions add complexity to the physical layout of machines as well as to the Treatment Devices: Part One 173 internal circuitry and display requirements. Displays may be separate from the defib displays, or they may be integrated onto a multifunction graphic display. Pulse oximetry, often using third-party circuit designs and sensors, gives an indication of cardiac pumping and respiration effectiveness, which helps in determining the best direction for treatment. It also is very useful in monitoring patients after a code, or when the unit is being used to transport a patient who has a significant risk of requiring resuscitation. A pulse oximeter must have a connector for the sensor as well as controls for setup and alarms, and displays of measured values and alarms settings. Pulse oximetry is discussed in more detail in Chapter 3. Cardiac patients may need to have a pacemaker as part of their initial treatment regimen, and since much of the ECG signal processing that is needed for effective pacing is already in modern defibrillators as part of their basic design, it was relatively straightforward to add the components necessary to have pacing functions available. Pacing cables are often attached to the same port as the defib paddles since both functions are not often used simultaneously, but the pacemaker does need its own set of controls and displays. Pacemakers are discussed later in this chapter. In addition to pulse oximetry, a measure of exhaled carbon dioxide is useful in diagnosis. Capnography, like pulse oximetry, is usually performed by a separate device installed in the chassis of the defibrillator, though they may share some components such as power supplies. DISPLAYS Most modern manual defibrillators have either an LCD or plasma display. CRTs are still in use, though the CRT is bulkier and requires high voltage circuitry. More and more defibs have color displays, and the graphic displays show waveforms of various parameters as well as alphanumerics for certain measurements and alarms settings. The displays also show prompts and error codes, setup information, time and date, and a variety of other data. Color helps make increasingly cluttered screens easier to read, allowing differentiation of parameters according to hue. Displays must be large enough to be readable yet small enough to fit into the overall compact design of defibrillators. They must be durable and bright enough to be visible in all lighting conditions. AUDIO From near the beginning of defibrillator evolution, sound has been an important design component. It is often a confusing emergency situation when the devices are used, and employing sounds to convey important information allowed code responders to better focus on the task at hand. A specialized circuit usually handles all audio signals. High-voltage circuits such as those that are required to charge the storage capacitor in a defib often produced a high pitched, rising tone as a by-product of their design, and this characteristic was capitalized upon to allow staff to hear when the unit was charging, so they would know that a discharge was imminent. Even when newer designs no longer produced their own intrinsic sounds, engineers added audio 174 Introduction to Biomedical Engineering Technology circuitry to mimic the rising tones so this same vital information was available. A louder, steady tone was added to indicate that the set charge had been reached, and often a warbling or otherwise different tone indicates the actual discharge. Chargeand discharge-related sounds can usually be turned down but not off. ECG beats have beeps or clicks associated with them to provide a nonvisual indication of heart function, though these sounds can often be turned right off as defibs are often used for long periods of time for monitoring patients. Alarm conditions obviously require staff attention and are therefore usually indicated by both visual and audible signals, varying in intensity according to the urgency of the alarm condition. Alarm signals can generally be turned up or down, but again not off completely. Some manufacturers use voice prompts to assist users in device operation, or to notify them of alarms or other conditions. ERGONOMICS Given the kinds of situations in which they are used, ergonomics plays a critical role in the design of defibrillators. Units must be as compact and lightweight as possible and still deliver adequate performance. They must be easily transportable, free of components that might hinder portability. Units have to be tough enough to withstand the drops and bumps that are inevitable in emergencies. Staff using defibrillators are often in an extremely stressful and busy situation, and therefore defibrillator design must allow them to use the unit effectively with minimal concentration or distractions. The operation should be as intuitive as possible, and the device should have clear, logical, and easily accessible controls and displays. Ideally, a staff member should be able to use a new defibrillator without any hesitation or unit-specific training. TESTING AND MAINTENANCE Defibrillators, being critical life support devices, require careful care if they are to provide reliable, effective performance. Most units include a self-test function that checks most of their basic operations. This self-test feature is normally used by clinical staff on a regular basis, such as once a week, and the results noted in a log. Users also need to check the overall condition of the unit, that power is being delivered, and that all necessary accessories are available and in good condition. Part of the self-test routine usually includes charging the unit to a specified level and then discharging through test terminals built in to the paddle holders. This allows the unit to check for continuity of the conductive pathways, and to measure the output and compare it to what was set. Any abnormalities, whether indicated by self-test results or otherwise, must be recorded and reported to service personnel. Testing by trained technical staff (BMET/HTMT) should be done on a schedule as recommended by the manufacturer, and results recorded. This testing includes a thorough physical examination of the unit, as well as the use of extended self-test Treatment Devices: Part One 175 functions. Units usually have a number of error codes that may be generated to aid in troubleshooting, and various performance logs may be accessible during testing. Defib performance is tested using commercial test equipment, which allows precise measurement of delivered energy, waveform duration, and other parameters. Time to reach full charge will be measured and compared to manufacturer specifications. Most test devices include an oscilloscope output port so that waveforms can be examined. Manufacturers may recommend replacing batteries regularly, perhaps every 2–4 years, or when testing indicates substandard characteristics. AUTOMATIC EXTERNAL DEFIBRILLATORS Survival rates for victims of heart attacks are much greater when resuscitation efforts, especially defibrillation, start within a few minutes of the attack. According to the American Heart Association, a sudden cardiac arrest victim’s chances of survival fall 7%–10% for every minute of delay until defibrillation. Personnel trained in CPR, and especially defibrillator operation, are often unavailable when a cardiac arrest occurs, and full-featured defibrillators are generally only found in hospitals or emergency response vehicles. Because of these factors, manufacturers have developed defibrillators that are very simple to operate, performing many functions automatically, so that almost anyone can use them, and use can commence quickly. AEDs are comprised of all the basic components of a standard manual defibrillator (Figure 6.10). They have a power supply, a means of generating and storing high voltage, wave-shaping and delivery components, and ECG detection and analysis circuitry. AEDs typically deliver lower energy levels than full-blown defibs, usually around 150 J maximum. This amount of energy is sufficient to produce good results in most FIGURE 6.10 A HeartStart automatic external defibrillator (AED). (Courtesy of Philips.) 176 Introduction to Biomedical Engineering Technology cardiac arrest situations in which a positive outcome is likely. Also, higher energies are more likely to cause injury to the patient or the persons using the defibrillator. For AEDs to be widely distributed and used, they must be relatively simple in both construction (to minimize costs) and operation (to maximize the number of individuals who can use them). Units have very clear instructions printed on their cases, with numbered pictures showing the various steps to be performed. Many units also include voice prompts to help even completely inexperienced users through the process. More powerful drones and lighter AEDs have combined to make remote delivery of the devices possible. Conductive adhesive pads are used instead of paddles to make application safer and more positive. These pads have pictures to show correct placement on the patient’s body. These units may sit unused for long periods of time, so their batteries must maintain a reliable charge for several years. Lithium chemistries currently provide the best performance in this regard, though manufacturers use lead-acid batteries. All these devices require a charging circuit connected to reliable AC power. Regular inspection and testing of AEDs is important. Someone must ensure that charging power is being delivered at all times, and most units include a self-test function that should be used regularly, for example, once a week. Inspection and testing dates should be recorded. Batteries in AEDs must be replaced at intervals specified by the manufacturer to ensure optimum performance, typically every 2 years. Because defibrillator performance depends on good pad contact, the pads must be sealed in airtight packages, and still they must be replaced at regular intervals to ensure quality. PACEMAKERS Cardiology researchers recognized that some patients with irregular ECGs were suffering from some kind of failure in the natural pacemaking system of the heart. If an electrical signal could be injected into the heart tissue at the correct location and at the right time, more normal cardiac function might be restored. Cardiac function is discussed in more detail in Chapter 2. HISTORY In 1950, Canadians Hopps, Bigelow, and Callaghan developed the first successful cardiac pacemaker. The large unit used vacuum tubes, and the signals it delivered through the patient’s chest wall were crude and often painful to the patient. External pacemakers were developed further in the 1950s by Zoll and others, but these external units still had the disadvantages of being bulky, requiring the use of external electrodes, and being dependent on continuous AC power. Lillehei developed a method of inserting pacing electrodes directly into the heart, greatly reducing the power required. Lillehei’s technique involved making an incision into the chest, but Furman developed a method of inserting electrode wires Treatment Devices: Part One 177 FIGURE 6.11 Diagram showing pacemaker insertion. into a vein and threading them into the heart, where the tips could be embedded in cardiac tissue (Figure 6.11). This had the benefit of reduced trauma to the patient as well as further reducing the power required. In 1958, Swedes Elmqvist and Senning were the first to implant a pacemaker in a human. Despite numerous problems and a large number of different models, the patient survived 43 years and died of causes unrelated to his pacemakers. Some manufacturers have used thermoelectric generators to power pacemakers. These units contain tiny amounts of plutonium; its decay heats components and produces electrical power. Fewer than 100 patients have such nuclear pacemakers, and when the units are removed, they must be transported to Los Alamos, New Mexico, for disposal. Pacemakers now are extremely reliable and versatile, and are implanted in as many as 600,000 patients every year. As well, advanced external pacemakers are used frequently, as a bridge until an internal device can be implanted or when natural pacing can be restored at a later time. THEORY OF OPERATION Pacemakers rely on much of the same design principles as defibrillators. They must be able to recognize ECG waveforms (or lack thereof), and then deliver accurately timed and shaped electrical impulses to the heart (Figure 6.12). Internal pacing signals are several orders of magnitude lower in energy than internal defibrillation pulses, in the range of 25 µJ as compared to up to 35 J for 178 Introduction to Biomedical Engineering Technology FIGURE 6.12 An implantable pacemaker. implantable defibs, and therefore battery voltage can be boosted to provide these levels much more easily. Batteries must be very reliable and long lasting, typically only requiring replacement after at least 4 or 5 years of operation. Implantable pacemakers consume very little power, in the range of 10–40 µW, but they are often in place for 7 years or more, so battery durability is critical. Newer designs can operate on only 240 nW, and even further reductions in power requirements are planned. Sensing of cardiac operation is done by picking up and amplifying ECG signals, which are analyzed by a microprocessor. The results of this analysis combined with programming parameters determine the timing and size of the pulse to be delivered, and then these parameters are fed to a wave-shaping and delivery circuit, which in turn delivers a specific pacing pulse to the heart. Pacing may be used to “fill in the gaps” for patients with certain arrhythmias, or to increase the rate for patients with bradycardia. Patient physical activity may be estimated by the use of an accelerometer, a microelectromechanical device within the pacemaker that detects patient motion. Increased physical activity can be taken as a signal for the pacemaker to increase the heart rate in order to increase blood flow as will be required by the activity. Implantable pacemakers have transceivers so that their programming can be modified to suit patient requirements. Programmers use an antenna placed over the pacemaker site to communicate with the device, and a terminal allows users to see current programming parameters and enter new ones (Figure 6.13). CONSTRUCTION The mechanical construction of implantable pacemakers is very much like that of implantable defibrillators, as described earlier. Nuclear-powered devices require very robust cases that can withstand extreme trauma and even cremation, in order to minimize the risk of escape of nuclear material. Treatment Devices: Part One 179 FIGURE 6.13 A pacemaker programmer. The “lollipop”-shaped section is the electromagnetic wand that carries programming signals to the pacemaker. APPLICATION Pacemakers are usually installed in a pocket made in the tissue of the patient’s upper chest (see Figure 6.11). Electrodes are introduced via the left subclavian vein to the appropriate area of the heart, and the leads routed under the skin to connect to the implanted pacemaker. The axillary or cephalic veins may also be used. Electrode placement locations may include the right atrium and/or ventricle, two different areas of the right atrium and the right ventricle, or each of the right and left ventricles, as well as some other specialized locations. Internal pacemaker signals are generally a few volts (or a few milliamps, depending on the calculation method) in amplitude, and from 0.2 to 0.5 s in duration. EXTERNAL PACEMAKERS Some patients may need cardiac pacing urgently and/or for a relatively short duration, in which cases an external pacemaker may be used. These units utilize similar ECG pickup and analysis systems to implantable defibrillators, but physical construction and power considerations are much different. External devices can be larger, with 180 Introduction to Biomedical Engineering Technology less robust cases. Controls can be manually accessible, and power can come from AC line, or rechargeable or disposable batteries. Some external pacers can deliver pacing signals directly to the heart via introduced (endocardial) electrodes, but most rely on external (transcutaneous) electrodes, which are less traumatic and faster and easier to apply. However, since pacing signals in the latter case are delivered through the patient’s chest wall, they have to be of considerably greater amplitude than those delivered by internal devices, usually about 10 times greater. Usual electrode placement for external pacers is at the top of the sternum and near the bottom of the ribcage along the left axilla. Since transcutaneous pacing signals travel through various surrounding muscles before they reach the heart, these muscles may contract at the set pacing rate. This may cause patient discomfort, and sensitivity reactions to the electrodes or conductive gel may also be seen. External pacemakers may be standalone units or they may be integrated into other devices, mainly defibrillators. CIRCULATORY SYSTEM AND BLOOD Artificial Hearts As the field of cardiology developed, the replacement of diseased hearts moved from imagination to reality (Figure 6.14). The first human heart transplant was performed in South Africa in 1967. The patient survived for 18 days, mainly because rejection problems had not been successfully solved. Currently, over 100,000 patients have received heart transplants, 60,000 of these in the United States. The record for survival is 28 years and counting. FIGURE 6.14 A human heart in the hand of a surgeon. Treatment Devices: Part One 181 The number of patients needing new hearts exceeds the number of donors, however, and artificial hearts were developed to try to meet this need. The first was implanted in 1982, with the patient surviving 112 days. So far, artificial hearts have been used with only a few patients, and many of the devices required large external components in order to function. There are trials underway of totally implantable devices, with one patient having survived 17 months. Though many hurdles remain, the day is getting nearer when hearts like that of Star Trek’s Captain Picard will be available to any patient in need. VENTRICULAR ASSIST DEVICES More immediately useful than artificial hearts are VADs, which are simple pumps that take blood from the left ventricle and pass it into the aorta. These devices are much simpler in operation than artificial hearts and are generally used as a “bridge” while patients wait for a suitable human heart transplant. INTRA-AORTIC BALLOON PUMPS Another device that is used to provide temporary assistance to the patient’s heart is the intraaortic balloon pump. As its name implies, it consists of a balloon that is inserted with a catheter into the descending aorta. The balloon is designed so that when it is inflated, it pushes blood along the aorta in the normal direction of flow, thus decreasing the demands on the heart and increasing perfusion to the patient’s tissues, including the myocardium. The cycling of the balloon must be synchronized to the patient’s heartbeat so that inflation occurs during diastole; otherwise, it would be working in opposition to the heart. It must then deflate before systole. ECG signal detection and simple analysis allow the pump control circuitry to function in this synchronized manner. HEART–LUNG MACHINES During some cardiac surgery, the patient’s heart must be stopped so that surgeons can perform their work. Blood flow and oxygenation must be continued for this time, which may be several hours, and heart–lung machines perform this function. The first successful use of a heart–lung machine in human surgery was in 1953 in Philadelphia, using a machine developed by John Gibbon. Because they are used for relatively short terms in high-acuity environments, there is no need for these units to be small or portable (Figure 6.15). The majority of total blood flow is drawn from the patient’s venous system, usually the superior vena cava or the right atrium. It is then pumped into a membrane system that allows the escape of carbon dioxide from the blood and the intake of oxygen to the blood. The blood is then pumped into the aortic arch where it continues to circulate through the patient’s body. The heart and lungs are bypassed, and the heart can be made to stop to allow surgical procedures to take place. 182 FIGURE 6.15 Introduction to Biomedical Engineering Technology A heart–lung machine, operated by a perfusionist. A number of factors must be considered in the design of heart–lung machines: • The system must have adequate and adjustable pumping capacity to maintain appropriate blood flow through the patient. • The gas exchange system must be sufficiently effective in both removing carbon dioxide to keep blood levels below harmful levels, and in adding oxygen to simulate normal ventilation. Membranes are made of materials such as polypropylene or silicone. • Pumping systems must cause minimal mechanical damage to blood cells. Pumps may be of the roller peristaltic type, or of a centrifugal type in which rotation of blood within the pump head produces flow. Centrifugal pumps tend to cause less damage to cells. • An anti-clotting agent, usually heparin, must be added to the blood to prevent clots forming in the system and passing to the patient. This agent must be neutralized immediately following surgery so that normal clotting can take place. • Temperature of the blood must be controllable in order to maintain, raise, or lower patient body temperature as required by specific circumstances. It may be advantageous to induce hypothermia in order to minimize tissue damage during certain procedures. Heart–lung machines are operated by perfusionists, specially trained technologists who monitor and control system functions working in coordination with anesthetists, surgeons, and the rest of the surgical team (Figure 6.16). Treatment Devices: Part One FIGURE 6.16 183 Heart anatomy. FIGURE 6.17 A sequential compression device. SEQUENTIAL COMPRESSION DEVICES Patients who have recently had surgery on their legs or are otherwise susceptible to the formation of blood clots in the veins of their legs (usually referred to as deep vein thrombosis, or DVT) can benefit from the use of sequential compression devices (SCDs). Lymphedema, a condition resulting from the reduction of flow in 184 Introduction to Biomedical Engineering Technology the patient’s lymphatic system that produces swelling of the extremities, can also be alleviated with SCDs. SCDs consist simply of a pump that feeds a rotating valve with a number of outlet ports (Figure 6.17). The ports are connected to a multichambered sleeve, which fits snugly over the patient’s limb. The chambers inflate in sequence, with higher pressures in the distal chambers and lower pressures in each of the following chambers, thus producing a peristaltic wave of compression that moves from the distal end of the limb toward the proximal end. Typical pressures range from about 45 mmHg distally to about 30 mmHg proximally. Inflation is maintained for several seconds, and then all chambers deflate for a minute or so before the next cycle begins. This process induces the flow of blood and/or lymphatic fluid away from the limb and toward the torso, reducing swelling and its associated problems. It is thought that the SCD action may also reduce the formation of clots in limb veins. AUTOMATIC TOURNIQUETS When surgery is performed on limbs, blood flow to the surgical area can be problematic, both obscuring the field of view and contributing to patient blood loss. A tourniquet placed proximally to the site can be inflated to block blood flow, but if this goes on for too long, tissue damage can occur. Automatic tourniquets incorporate pumps and timing mechanisms that can be programmed for inflation pressure and inflation/deflation cycle timing. Many systems have two independent mechanisms to allow for placement in two different locations (Figure 6.18). BLOOD WARMERS Blood is stored in refrigerated cabinets in order to prolong its usefulness by slowing biological and chemical reactions that can damage blood cells and alter blood chemistry. Normally, blood bags can be allowed to warm to near room temperature before infusion; however, in some emergency situations, there may not be time for this. Also, when the patient is suffering from hypothermia or is otherwise sensitive to body temperature fluctuations, room temperature infusion of blood products may not be acceptable. In such circumstances, fluids may be passed through a blood warmer before being infused into the patient. Most blood warmers are one of two different types: dry heat or water bath. Dry heat blood warmers use a thin plastic pad with many small channels for blood flow. This pad is placed between two metal plates that are heated to constant temperature, and the blood flows through the channels and is warmed as it goes, until it is close to body temperature at the exit. It is then carried by a short tube to the patient. Water bath blood warmers use a double-walled tube to accomplish the same end (Figure 6.19). Blood flows through a small, inner passage while warm water is pumped in the opposite direction through a larger, outer tube (Figure 6.20). This results in a gradual but thorough warming of the blood as it passes through the tubing. The distal end of the double-walled tubing is near the infusion site so that there is minimal cooling before the blood enters the body. Treatment Devices: Part One FIGURE 6.18 185 An automatic two channel tourniquet. All blood warming systems must have very precise temperature control mechanisms, as over-heating blood can cause very rapid degradation. Most units include a temperature display as well as an over temperature alarm system. Some units may have a low-temperature warning indicator. Regular testing and calibration of both the control and alarm systems are important for continued patient safety. 186 FIGURE 6.19 Introduction to Biomedical Engineering Technology Water bath blood warmer. FIGURE 6.20 Female connector for the blood warmer—note the two openings, one for warming fluid to flow out of the machine and into the delivery tubing, and the other for cooled fluid to return to the machine. Treatment Devices: Part One 187 INTRAVENOUS FLUID ADMINISTRATION PUMPS Fluids sometimes must be administered to patients when it is impractical or impossible to deliver them orally. This may be for hydration, medication delivery, blood transfusions, or meeting nutritional needs. In such cases, the fluids can be delivered into the patient’s bloodstream using a needle or catheter connected to a reservoir of the fluid. Veins are used for this purpose rather than arteries because blood pressure is much lower inside them, so the fluids being administered don’t have to overcome a significant pressure gradient. Veins are also usually closer to the surface and so easier to locate, and they have thinner walls, which makes penetration easier. The pressure needed to push intravenous fluids into the body can be supplied simply by gravity, but in some circumstances this can be problematic. If even somewhat accurate delivery rates are important, gravity feed lines must be carefully controlled by measuring drop rates and calculating flow rates from that. They must be closely monitored as flow rates can vary with time. If a specific volume is to be delivered, this must be calculated and timed. Gravity feed may not be able to deliver fluids rapidly enough in some circumstances. For all of the above reasons, intravenous fluids are often administered using a pump. There are a number of different types of IV pumps, depending on manufacturer preferences and delivery parameters. They can range from simple devices that can be used by patients at home, with one type of fluid only at a fixed rate, to sophisticated multichannel units that can deliver several different fluids, each at different rates. Pumps can be grouped according to their mechanism of delivery and control. PRESSURE INFUSERS These units simply apply pressure to a flexible infusion bag, and it is assumed that constant pressure equals constant flow. The pressure may be developed using a mechanical bladder and bulb pump, or some type of electrical pump may be used. Pressure infusers are used when accurate flow rates are not critical. In some circumstances, this is because large amounts of fluid need to be delivered in a short time, such as during some surgical procedures requiring quick blood pressure boosts. Other systems are found in some home-therapy applications where high accuracy is less important than ease of use and simplicity. FLUID CONTROLLERS While not strictly pumps, these devices can be used to provide controlled delivery of intravenous fluids. They operate by simply blocking or opening the fluid pathway, while at the same time detecting and counting drops of fluid as they pass through a drip chamber. Droplets are fairly consistent in volume for a given fluid, and by controlling the number of drops that are allowed through in a given time, flow rate can be controlled. 188 Introduction to Biomedical Engineering Technology SYRINGE PUMPS As the name implies, these devices take a standard injection syringe fitted with an intravenous catheter or needle and depress the plunger with a gear drive mechanism (Figure 6.21). Obviously, these systems deal with relatively low volumes and are used in such situations as when delivering narcotics, spinal anesthetic agents, certain other high-potency drugs, or for administering insulin at intervals over long periods. Because syringes are precisely manufactured and mechanical systems to depress the syringe plunger are relatively easy to control, syringe pumps offer high accuracy but are limited to low flow rates and volumes. Some pumps may have the capacity to handle various sized syringes, while others take only one type. FIGURE 6.21 Syringe pump. Treatment Devices: Part One 189 FIGURE 6.22 Syringe pump with drug (propofol) template. Pumps have been designed so that they can be pre-programmed for specific drugs, with flow rates, volume limits, and alarm settings adjusted for each. Programming may be via selection from a list programmed into the pump, or by the fitting of a template to the face of the pump, which shows the name of the drug and interfaces with the pump to adjust settings (Figure 6.22). General-purpose syringe pumps can be set for different flow rates, though total volume delivered is usually determined by the initial filling of the syringe. Syringe pumps usually have a display that can show the various settings as well as volume delivered and alarm notifications. These pumps are usually battery powered. 190 Introduction to Biomedical Engineering Technology FIGURE 6.23 A multichannel piston cassette pump. PISTON PUMPS High accuracy can be obtained by passing the fluid to be administered through a precise chamber that can be compressed by a plunger. One-way valves control the direction of flow, and the system works like a small piston, delivering discrete pulses of a specific volume (Figure 6.23). Flow rate can then be set by varying the frequency of the pulses. These pumps provide high accuracy, but the complexity and precision of the piston and valve mechanism mean that the costs per patient use are high. Some systems have cassettes with multiple channels, each of which can be controlled separately by the pump. PERISTALTIC PUMPS Peristalsis is a means of moving fluids through a tube by sequentially compressing segments of the tube, pushing the fluid from one section to another in the desired direction of flow. Food is moved through the intestine by peristalsis; rings of muscle in the intestinal walls contract in a wave-like pattern to squeeze food along. Peristaltic pumps use this method to pump IV fluids. An external mechanism compresses a section of tubing at one location, closing it off. The next section along is then compressed, pushing the fluid forward until this section is also closed off. A further section takes over, and then the first section can open up again to admit the next unit of fluid. There are two general methods of generating peristaltic action: rotary and linear. In rotary pumps, a flexible section of tubing is fixed tightly around a wheel that has three or four compression points around its perimeter. The compression points may have a spinning sleeve on them to reduce friction on the tubing, or they may simply be coated with a low-friction material such as Teflon. As the wheel rotates, the tubing Treatment Devices: Part One 191 FIGURE 6.24 Rotary peristaltic pump head. is squeezed along and the fluid between each compression point is moved forward until it reaches the distal end where it is released to flow to the patient (Figure 6.24). Higher pressure can be generated if there is a rim around the outside edge of the pump against which the tubing can be compressed. Without such a rim, if backpressure was great enough it could simply stretch the tubing outward until either backflow occurred or pumping became ineffective. These pumps must use an infusion set that has a section of very flexible, durable material such as silicone rubber, with structures to hold each end of this flexible section in place on the pump. This means that set costs are relatively high. Flow rates are determined simply by the speed of rotation of the pump head. This depends on the inside diameter of the tubing being constant; since tubing will likely stretch with time, sets must be replaced at intervals specified by the manufacturer in order to maintain adequate volume delivery accuracy. Linear peristaltic pumps use a set of “fingers” or bars that are moved in a wave pattern (Figure 6.25). Either a special section of rubber tubing or standard IV tubing is passed over the bars and compressed against a backing such that when a bar is extended, it occludes the tubing and when it is retracted, the tubing is relaxed and completely open (Figure 6.26). The wave pattern of compression and relaxation moves the fluid in the desired direction. Peristaltic compression fingers in an IV pump. The bars are moved by a cam mechanism driven by a rotating motor. 192 FIGURE 6.25 Introduction to Biomedical Engineering Technology A peristaltic-type IV pump. FIGURE 6.26 IV pump open door showing pump head, occlusion sensors (white circles on right), and air sensor (below lower occlusion sensor). Treatment Devices: Part One FIGURE 6.27 193 A newer model three-channel IV pump. As with the rotary-type pumps, volume accuracy depends on the inside diameter of the tubing being constant. Since regular IV tubing is not as elastic as silicone rubber tubing, it must be replaced even more frequently. If there is enough excess tubing in a line, simply moving the line along so that a new section of tubing is in the pump head will maintain accuracy (Figure 6.27). Wireless connectivity is increasing for IV pumps, allowing for central monitoring and control of the pumps, which can help eliminate programming errors and allows for quicker response to alarm situations. Medication/fluid delivery data can be incorporated into the overall patient record. PATIENT-CONTROLLED ANALGESIA PUMPS In the administration of analgesic medications, the patient is usually the best one to determine the level of pain being felt. To this end, pumps were developed that could be controlled to some degree by the patient (Figure 6.28). By pressing a button, the patient could request an extra bolus of pain medication (Figure 6.29). Obviously, there had to be limits to such pumps, otherwise 194 FIGURE 6.28 Introduction to Biomedical Engineering Technology PCA pump. FIGURE 6.29 PCA pump showing patient control pushbutton. Treatment Devices: Part One 195 some patients would simply keep pressing the button until an overdose was delivered. Patient-controlled analgesia pumps, or PCA pumps, have a number of safeguards built in to their design. They are programmable for rate and total volume as with most other IV pumps, but they can also be programmed to set a specific volume that will be delivered with each patient request, as well as the minimum interval between allowed requests and the maximum number of request that will be permitted within a given time. To prevent tampering, most PCA pumps have a cover that can be locked after programming, allowing access to only the stop and start controls. Most PCA pumps have a memory function that allows clinicians to look at how many requests have been made by the patient and how many have been allowed. PCA PUMP PURCHASE EVALUATION “Equipment Acquisition Committee meeting, Room 321, 1400 Monday” read the memo in Joe’s inbox Monday morning. “Wow, talk about giving me time to prepare!” he grumbled to Mike. “At least we have a voice in the process, in a lot of hospitals the on-site Biomeds just have to take what is sent down to them from high above.” “Not to worry, Angela and I are both here today and we’re mostly caught up on critical things, so you should be able to spend all morning on the project. Sounds like fun!” Mike said with a grin. Nobody was fond of meetings. Joe gave Mike a dirty look and opened his files on the evaluations that had been done on PCA pumps. Three different manufacturers had brought their latest and greatest models in over the last 2 months, giving in-service sessions for nursing and pharmacy staff. Field engineers from two of the companies had come out to go over technical details with the three biomed techs. The third company had not bothered with this, a factor that was duly noted in Joe’s assessment. The pumps were put into service on one of the surgical wards, and after using them for a couple of weeks, staff had been asked to complete a survey form that had been designed by a nursing supervisor in collaboration with Joe and one of the senior purchasing agents. Joe was the lucky one who got to go through the survey forms and compile results. He also was responsible for researching service and support issues for the pumps, by going over online information as well as contacting a number of other biomeds from hospitals around the country that he had met on various service courses and at events such as AAMI’s annual Conference and Expo, and the RSNA annual meeting. Joe, Mike, and Angela had examined the pumps in detail in their lab, opening the cases to have a look at design and assembly quality as well as evaluating ease of service. A call to each vendor’s tech support department helped give a more complete picture of how support would go if the pump in question were to be purchased. 196 Introduction to Biomedical Engineering Technology At the meeting, the project leader gave a quick outline of the three pumps, then asked the various committee members to report on their views of each device. First to speak was the head of Pharmacy. “There is a big difference in how easily drug libraries are implemented in the different units, and how well the related safeguards were designed. I have serious misgivings about manufacturer X, but Y and Z were, in my opinion, adequate and about equal. Neither were perfect, but I would be OK with either one.” Next was one of the senior nursing supervisors, who reported that, through informal discussions and coffee break chatter, staff seemed to have found all three pumps fairly easy to use, with most favoring Y. Some people complained that the screens on pump Z were hard to see, but Joe pointed out that there was a brightness control on the back of the unit, though in a rather obscure location. He also took this opportunity to report that analysis of the written surveys confirmed the supervisor’s impressions. “From our perspective in purchasing,” said the rep from that department, “All the pumps have an initial capital cost of zero, since all the vendors will provide as many pumps as we need on signing a consumables purchase contract. I’ve gone over those contract prices and the estimated rate of use of patient sets, and pump X is a clear winner on the bottom line. With budgets the way they are, this has to be a critical consideration.” Attention then shifted to Joe. “We found that all three pumps had technical shortcomings, but that might just mean we’re picky. But pump X has some serious problems. There are a large number of connecting cables, and cable junctions are often a source of problems. Taking the unit apart is difficult and time-consuming, and the circuit boards use less than state-of-the-art components, at least as compared to the other two models.” Joe knew that, with the long development time for medical technology, coupled with arduous approval processes, it was impossible to have really current technology in the newest devices. However, all manufacturers were in the same boat, so it was a question of relative advancement. “I have also talked to a number of colleagues who almost universally reported reliability issues with X, including major battery problems. Again, Y and Z seemed to be about equal. On the basis of our overall evaluation combined with the survey results, Biomed recommends pump Y.” The purchasing agent voiced his budgetary concerns again, but the nursing supervisor and Joe volleyed back and forth about the importance of staff satisfaction both with daily device use and up-time. Joe commented that biomed caught the flak when equipment failed. Finally, the project leader interrupted. “Sorry, but I have another meeting that I’m almost late for, so we have to wrap up. Thank you all for your input. I’ll be thinking things over tomorrow, but as things stand, I think I will be recommending vendor Y.” The meeting adjourned, but the nursing supervisor and Joe hung back for a while, discussing some configuration issues with the new ICU bedside monitors. Treatment Devices: Part One FIGURE 6.30 197 PCA pump showing medication cartridge. Since dosages are critical with analgesic medications, a high degree of accuracy is needed for PCA pumps, and therefore the syringe mechanism is most commonly used, often with a special syringe that has been pre-filled and labelled by pharmacy (Figure 6.30). Wireless connectivity of PCA pumps has potential benefits: • Allowing the integration of medication information into the overall patient record. • Reducing the chances of medication errors. • Improving alarm response time. • Allowing interactions between PCA functions and other monitored parameters, for example, a monitoring system might detect a depression of respiration with the patient, which could communicate with the PCA pumps to prevent further, otherwise permissible, requests for additional deliveries. SAFETY FEATURES OF IV PUMPS Many IV pumps have similar safety features. Most have a mechanism that will generate an alarm if a blockage is detected downstream from the pump. This can occur 198 Introduction to Biomedical Engineering Technology if the IV line in the patient is no longer patent (no longer in the vein), if the tubing has become kinked, if the patient moves in such a way as to block the flow, or if clots form around the tip of the delivery needle or catheter. Alarms may be audible and/or visual, and they may also trigger a nurse call system. Occlusion detectors often rely on the fact that tubing will become more turgid when pressure rises. This increased turgidity causes the outer wall of the tubing to bulge outward and press on a sensor such as a slug moving inside a coil, or a microswitch. Such sensors may require occasional calibration. Most pumps signal when the set volume has been delivered, but most will keep pumping at a very low rate in order to help avoid clot formation at the end of the needle or catheter, keeping the vein open (KVA mode). Some pumps can detect upstream occlusions as well, using the reverse mechanism of downstream occlusion detection. Tubing will tend to collapse if more fluid is being pumped out than is coming in, and a sensor can detect this reduction in diameter. Again, calibration may be required. Since it can be harmful or fatal if air is pumped into a patient’s vein, pumps often have air-in-line detectors. These typically consist of an ultrasound transmitter– receiver pair situated on opposite sides of the IV tubing. When an air bubble greater than a certain size enters the section of tubing between the emitter and sensor, the amount of ultrasound transmitted will drop, triggering an alarm. Calibration of this component is important since small, harmless bubbles are often present in regular IV delivery and these should not trigger an alarm, while bubbles over a certain size should always trigger an alarm. An air alarm will shut the pump off immediately. Most IV pumps use batteries either as their sole source of power or as temporary power for when the patient is being moved from one area of the hospital to another or between facilities. Low battery alarms are generally designed so that they give attendants time to make other arrangements for infusion before the battery fails completely. Rechargeable IV pump batteries should be replaced at regular intervals as specified by the manufacturer in order to help avoid unexpected failures. RESPIRATORY SYSTEM Ventilators Second only to cardiac function, adequate ventilation is critical to physiological survival, and therefore machines that provide artificial ventilation are of the highest importance. When patients suffer paralysis or other trauma or disease that renders their breathing mechanisms ineffective, some form of mechanical ventilation is required if they are to live. This may be in the form of simple and direct application of air pressure to the patient’s lungs by mouth-to-mouth resuscitation or by the use of a simple pressure bag, or it may be accomplished using a large, very complex, and sophisticated electromechanical ventilator. Longer-term life support necessitates the use of mechanical systems. Developments in anesthesia techniques allowed physicians to administer muscle- paralyzing agents. This made some aspects of surgery easier, especially when using electrosurgery units, but this method resulted in the paralysis of breathing muscles as well, which meant that artificial ventilation was required while patients were anesthetized. Treatment Devices: Part One 199 A patient’s natural breathing function may be impaired or blocked by a high-level spinal cord injury or from brain injuries or various diseases. Poliomyelitis epidemics in the mid-twentieth century provided the impetus to develop the first widely used artificial breathing apparatus, commonly referred to as the “iron lung.” These devices enclosed all of the patient’s body below the neck in a steel cylinder. Air pressure within the cylinder was then raised and lowered, causing air to be expelled or drawn into the patient’s lungs. This had the advantage of being noninvasive but was very bulky and extremely limiting to the patient, as well as making personal care of the patient difficult. Devices such as these are referred to as negative pressure ventilators, since they rely on decreasing air pressure around the patient in order to produce inspiration. Newer ventilator designs used compressors and tubes to supply pressurized air to the patient’s trachea, either through a tight-fitting face mask, through a tube inserted into the trachea via the mouth, or, for longer-term situations, directly through a tracheostomy. These are the most commonly used types of ventilator today. They are referred to as positive pressure ventilators. Because “ventilator” can cover such a wide range of devices, from simple handcompressed rubber bellows to large, complex machines with many controllable parameters, alarm and backup systems, monitoring circuitry, display and recording components, and various communications capabilities, it would be impossible in the scope of this text to describe all of the range in great detail. Most hospital ventilators require intensive factory training on the proper use and maintenance of the devices, and much of this information is model-specific. In general terms, a ventilator requires a source of gas suitable for inspiration, a means of pressurizing this gas, tubing and fittings to deliver the compressed gas to the patient’s lungs, and a means of removing gas from the lungs after each breath (Figure 6.31). FIGURE 6.31 Philips Respironics V60 bedside ventilator. (Courtesy of Philips.) 200 FIGURE 6.32 Introduction to Biomedical Engineering Technology A full-featured ventilator. Gas supply may simply be room air at atmospheric pressure but is more commonly filtered, compressed air as well as oxygen. Air and oxygen may be supplied by local tanks or piped in through a building system, or air may be compressed by a built-in compressor. The two gases can be blended in the ventilator, in proportions determined by the state of the patient (Figure 6.32). Researchers tried using electric motors to power some of the first mechanical ventilators; however, sparks produced during the operation of these motors could cause fires when they came in contact with some of the very flammable anesthetic gases used at the time, such as cyclopropane and ether. Ventilators using only compressed gas to power their operation soon came into use, bypassing the fire hazard issue and providing simple, reliable devices (Figure 6.33). Compressed gas caused bellows to rise, and then a simple mechanism allowed the bellows to fall by gravity, thus pushing air into the patient’s lungs. The natural elasticity of the lungs expelled the air at the end of the inspiratory phase. An adjustable mechanical stop controlled the volume of each breath, and varying the flow rate of the operating gas determined the breathing rate. Treatment Devices: Part One 201 FIGURE 6.33 Ventilator controls and connections. Lower left is the expiratory filter; lower right is the inspiratory filter. EXTENDED SELF-TEST FOR THE PURITAN BENNETT 840 PATIENT VENTILATOR EST DESCRIPTION EST verifies the integrity of the Puritan Bennett™ 840 Ventilator System’s subsystems using operator participation. EST requires a “gold standard” test circuit. All test resources, including the software code to run EST, are in the ventilator. EST testing, excluding tests of optional equipment (such as the compressor), takes about 15 minutes. A single test feature allows individual EST tests to be run in any order, but the full suite of EST tests must have successfully passed before the ventilator can be used on a patient. EST checks the pneumatics system (including the compressor), memory, safety system, front panel controls and indicators, digital and analog electronics, power supplies, analog out system, transducers, and options. EST can run only when the ventilator is in service mode. Air and oxygen supplies are required (the compressor can supply the air source). EST is a comprehensive ventilator test designed to be run by qualified service personnel for periodic and corrective maintenance. The main characteristics of EST include • EST fully tests the ventilator’s electrical system, including nonmajor electronic functions (e.g., battery power) and electronics subsystems that require operator intervention (e.g., display/keyboard verification, and calibration). 202 Introduction to Biomedical Engineering Technology • EST checks the pneumatics subsystem, including gas supplies, proportional solenoid (PSOL) valves, flow sensors, circuit pressure accuracy, safety valve, and exhalation valve. • EST tests available options, including the compressor. • Ventilator safe state tests (both GUI and BDU can force the ventilator into a ventilator inoperative state). EST Results The ventilator displays the current test name, automatically runs tests that do not require operator action, prompts the operator to run tests that do require operator action, and displays test results. Once a test begins, it runs to completion. If an EST failure or alert occurs, the test name and results are displayed, and you can choose to rerun the test (for a FAILURE or an ALERT), skip to the next test (for an ALERT only), or quit EST (Figure 6.34). At the end of EST, one of these overall results is displayed: • Passed: All tests passed; normal ventilation can begin. • Alert: A fault was detected. If it can be determined with certainty this cannot create a hazard for the patient, or add to the risk which may arise from other hazards, the technician can choose to override the ALERT status and authorize ventilation. • Overridden: An ALERT status was overridden, and ventilation is authorized. FIGURE 6.34 A ventilator being tested. Note the “gold standard” tubing connecting the ventilator and the tester on the left. 203 Treatment Devices: Part One FIGURE 6.35 Ventilator screen showing “INOP” condition, meaning that a critical test has failed and it is no longer considered safe to continue/begin patient ventilation. • Failure: One or more critical problems were detected. The ventilator does not allow normal ventilation until EST runs without failing any tests. • Never run: After new ventilator software has been downloaded or a single test EST was run, this message appears in the ventilator test summary. • Outcome: All EST tests required. After any single test EST test is run, in order to ventilate a patient, service personnel must perform and successfully pass the full suite of EST tests. This message appears in the diagnostic code log. The technician must switch the ventilator to service mode, then choose to invoke EST. If the ventilator is powered down in EST after detecting one or more EST failures or alerts, the technician must run EST without a failure or nonoverridden alert before the ventilator can begin normal ventilation (Figure 6.35). If EST is interrupted and ventilation was allowed before you started EST, normal ventilation is allowed if EST did not detect any failures or alerts before the interruption, and no other errors occurred that would prevent ventilation. Source: Covidien/Nellcor-Puritan Bennett. 204 Introduction to Biomedical Engineering Technology As medical science continued to advance, it became apparent that it would be beneficial to be able to control more aspects of the ventilatory cycle and also to be able to monitor various parameters associated with ventilation. These features gradually became integrated into ventilator design, and the range of ventilators expanded as some applications required more complexity than others. Following are some of the parameters that can be controlled and/or monitored on a modern ventilator: Airway pressure—The instantaneous pressure within the patient airway of the ventilator system. Continuous positive airway pressure (CPAP)—Pressure within the airway is always maintained at least at this set pressure. End inspiratory pressure—Pressure in the airway at the end of the inspiratory phase. Expiratory pause—Period of time (usually about 1–3 s) of constant pressure and no airflow at the end of the expiratory phase. I:E Ratio—The ratio of inspiratory time to expiratory time. Inspiratory pause—As above, for the inspiratory phase. Minute volume or minute ventilation (MV)—Total volume delivered to the patient over a 1 minute time period. Mean airway pressure (MAP)—Self-explanatory. Tidal volume inspired—Total volume delivered to the patient in one inspiratory phase. Tidal volume expired—As above, for the expiratory phase. Peak inspiratory pressure (PIP)—Maximum airway pressure during the inspiratory phase. Names and abbreviations of parameters may vary from one manufacturer to another, and by region. Various modes of ventilation may be used with a patient depending on their needs. These modes may be different for different ventilators, or a single ventilator may be able to provide different modes depending on the set-up. Volume control—Tidal volume of ventilation is determined by a preset volume value. The ventilator will continue to deliver gas to the patient until this volume has been delivered, using whatever pressure is required (within limits). Pressure control—Tidal volume of ventilation is determined by a preset pressure value. The ventilator will continue to deliver gas to the patient until this pressure has been reached, no matter what volume has been delivered (within limits). Positive end expiratory pressure (PEEP)—In this mode, airway pressure at the end of expiration is kept above atmospheric pressure. This has been found to prevent too-rapid movement of blood through the lungs, thus allowing better gas exchange. Airway pressure release ventilation (APRV)—The ventilator cycles between two different CPAP values, thus allowing residual gases to escape from the lungs during the lower value part of the cycle. Treatment Devices: Part One 205 Bilevel—Bilevel refers to the two levels of PEEP or CPAP that are used in this mode of ventilation. The ventilator may alternate between the two levels on a set schedule, or it may switch depending on the patient’s spontaneous breathing efforts. This mode is easier on patients, so they do not need to be as heavily sedated as in some other modes of ventilation. Synchronized intermittent mandatory ventilation (SIMV)—Ventilator operation is synchronized to the patient’s breathing efforts, that is, breath cycles are initiated by the patient and assisted by the ventilator so that adequate tidal volumes are maintained. Pressure assist (PA)—Similar to SIMV. Breathing rate is entirely set by the patient. Pressure support (PS)—The ventilator simply provides positive pressure during inspiration, which is initiated by the patient. Pressure is supplied up to a preset limit. Proportional assist ventilation (PAV)—Pressure assist ventilation in which the pressure supplied by the ventilator varies according to the inspiratory effort of the patient. Inverse ratio ventilation (IRV)—In normal ventilation, the ratio of inspiratory to expiratory times is about 8 or 9 to 1. With IRV, the ratio is reduced to about 4 to 1, and most of the inspiratory flow occurs in the first third of the inspiratory phase. This mode improves gas exchange and cardiac output. High-frequency oscillation ventilation (HFOV)—“Normal” ventilation modes can sometimes lead to decreased cardiac output, decreased urine output, and lung tissue damage. HFOV delivers much smaller volumes per breath— in the range of 150 mL—at much higher rates—about 4–5 breaths/s. This method has been found to alleviate many of the problems associated with other modes of ventilation. HFOV is usually done with a completely different ventilator, specifically designed for this application. All modern patient ventilators have monitoring and alarm systems for patientrelated parameters such as pressure, flow, oxygen concentration, and expired CO2 concentration (Figure 6.36). Ventilator systems thus include oxygen analyzers and capnographs. Additional alarms might include air leak, power failure, backup gas supply tank pressures, and backup battery capacity. A communications interface may handle such things as measured and set parameters as well as alarm conditions. This interface may connect to nurse call systems, physiological monitors, external recorders, remote monitoring systems, or in-hospital computer networks or the Internet. Patients on long-term ventilation often have a tracheostomy through which the ventilator is attached, allowing the patient to eat and perhaps speak using their mouth, which would otherwise be blocked by an endotracheal tube (Figure 6.37). In order to handle all the complex functions of a ventilator, complete microprocessor systems are employed, often with hard disks and/or optical drives and flat-screen monitors. These systems may be Microsoft Windows based. 206 FIGURE 6.36 Introduction to Biomedical Engineering Technology A compact multiparameter ventilator. FIGURE 6.37 Tracheostomy. The primary design parameters of a ventilator system are physiological function adequacy and reliability. Systems use multiple failsafe designs so that ventilation can continue even after one or more failures have occurred. For example, many systems can operate with an external gas supply, with self-contained tanks, with a built-in compressor, or even with manual actuation. They may be line powered but with battery back-up and a gas pressure activated mode. Since ventilators are often used for long periods of time, they are usually designed to work as quietly and unobtrusively as possible, given their function. 207 Treatment Devices: Part One SUPERMAN Christopher Reeve was an actor, a sportsman, and a family man. He played Superman on the big screen, but he was also a pianist and environmentalist. He participated in a wide variety of sports, including horseback riding. In 1995, at age 42, he was thrown from his horse and suffered a high-level spinal cord injury, which meant that he would be dependent on a mechanical ventilator. Through his amazing will and with the help of his loving family and friends, he was able to achieve many remarkable successes, and he inspired many people who had similar accidents. His ventilator was usually unobtrusive when he made his many public appearances, but still it made millions of people aware of the vital role played by ventilators in many people’s lives. They saw that one could live a rewarding, loving life after such severe injuries. Christopher Reeve passed away on October 10, 2004, but his legacy lives on. CPAP/BiPAP UNITS Continuous positive airway pressure (CPAP) units are very simple versions of pressure support ventilators. They provide air at a pressure somewhat above atmospheric, which is delivered to the patient through a nasal mask. This helps keep airways open during inspiration, which in turn helps prevent snoring or, more seriously, obstructive sleep apnea and other conditions (Figure 6.38). Oxygen may be added to the air before delivery to the patient. Bilevel positive airway pressure (BiPAP) devices are somewhat more complex, in that they sense inspiratory effort and provide slightly higher pressure at that time. After flow stops, the pressure drops to a level more like that used with CPAP units. FIGURE 6.38 CPAP machine. 208 Introduction to Biomedical Engineering Technology Because both of these types of devices are used when the patient is sleeping, they are designed to operate as quietly as possible. OXYGEN CONCENTRATORS Many patients require supplementary oxygen on a long-term basis, but when living at home or in a long-term care facility, a central oxygen supply may not be available, and relying on heavy, bulky oxygen tanks is less than ideal. Oxygen concentrators fill this need, supplying high oxygen percentages at high enough flow rates for almost all patient requirements (Figure 6.39). These devices rely on the properties of a material called zeolite for their function. Zeolite has the capacity to selectively absorb nitrogen while bypassing oxygen. Oxygen concentrators consist of two pressure tanks containing zeolite, a compressor, and a valve system. Room air is compressed and then passed through one of the zeolite tanks, where most of the nitrogen is removed, leaving oxygen at up to 95% concentration. This is delivered to the patient through a flowmeter. Once the zeolite FIGURE 6.39 Oxygen concentrator. Treatment Devices: Part One 209 in the first tank is mostly saturated with nitrogen, the valves switch the airflow to the second tank, so that oxygen is delivered to the patient continuously. While the second tank is being used, the first tank is pumped down to very low pressure, which draws the nitrogen out of the zeolite and passes it back into the room. Once the second tank is saturated and the first purged completely, the airflow is then switched back, so that the first tank absorbs nitrogen and the second tank is purged. Cycles typically take about 20 s/tank. Oxygen concentrators are designed to operate as quietly as possible, since they usually sit close to the patient 24 hours a day. The pumps are powerful, so there has to be effective sound insulation in the unit’s cabinet. Some units have an oxygen analyzer built in to give an alarm if oxygen concentration drops too low. All devices have power fail and airflow alarms. HUMIDIFIERS When gases are delivered to a patient, either via an anesthetic machine during surgery, by a ventilator, or simply as auxiliary oxygen, it is very low in water vapor content. This can cause the patient’s airways to dry out, which can lead to discomfort as well as increased susceptibility to infections and tissue damage. If the gases are to be delivered for any significant length of time, it is important that they have water vapor added by a humidifier. There are a number of different mechanisms of humidifier function. The most basic is to simply bubble the gas through a reservoir of water. The water must be distilled to avoid contamination. Other humidifiers use heat to vaporize water in a tank, and the gas flow passes over the surface of the water, picking up water vapor as it goes. A third method of vaporizing water is with the use of ultrasonic crystals. Highfrequency sound waves passing through water break some of it up into tiny droplets, which can then be passed into the patient breathing circuit. The droplets may pass to the patient directly or they may, due to their small size, evaporate along the way. Ultrasonic humidifiers, or nebulizers, have the advantage of not heating the water, which can help avoid patient hyperthermia problems. SUMMARY This chapter was wide ranging. The heart and its treatment were covered, including a history of defibrillators, the theory and designs of defibs, a Code Blue scenario, types of defibs, and some history and theory behind pacemakers, both implanted and exterior. Circulation and blood were next, with topics of artificial hearts, heart–lung machines, tourniquets, and blood warmers. IV and feeding pumps were covered, plus PCA pumps. The respiratory system discussion included ventilator theory and function, CPAP/ BiPAP units, oxygen concentrators, and humidifiers. 210 Introduction to Biomedical Engineering Technology QUESTIONS 1. Which is more dangerous to the patient, atrial or ventricular fibrillation? Why? 2. What are the three basic components of a defibrillator? 3. Why is a high voltage required for external defibrillation pulses? 4. What are the advantages of biphasic defibrillator waveforms over monophasic waveforms? 5. Why is it important to keep defibrillator electrodes insulated from each other during operation? 6. What allows an implantable pacemaker to have a much smaller battery than an external defibrillator? 7. What are some of the “extra” functions that may be found on an external manual defibrillator? 8. When should the charge be delivered in a cardioversion procedure? 9. What are some of the details printed on a defibrillator chart recorder? 10. Why is it important to record data from the time before a defibrillation attempt? 11. How are implanted pacemakers programmed? 12. Why is it important to warm blood before it is infused into a patient? 13. List three types of infusion pumps. 14. Why do PCA pumps have a locking door covering the control panel? 15. What are some of the benefits of positive pressure ventilators as compared to negative pressure units? 16. What might cause reduced output in an oxygen concentrator? 7 Part Two Treatment Devices OBJECTIVES FOR THIS CHAPTER • This chapter examines some of the devices involved in treating patients in relation to the nervous system, digestive system, sensory system, and renal system, including history, theory, function, and types of the various devices, as well as an overview of relevant anatomy and physiology. • Nervous system: Anesthesia, anesthetic machines, anesthetic gas monitors, and ECT machines. • Digestive system: Feeding pumps. • Renal system: Hemodialysis systems, peritoneal dialysis units, lithotripters. • Sensory systems: Phacoemulsifiers, ophthalmic lasers. NERVOUS SYSTEM Anesthesia From the first time any kind of surgery was attempted on humans, it was obvious that it was extremely painful for the patient; the shock alone could easily be enough to cause death. In addition to this problem, the reaction of the patient to the trauma of surgery made it difficult for the surgeon to perform their tasks. Various means were used to help alleviate the suffering of surgical patients, such as the administration of numbing drugs like laudanum (a tincture of opium) or alcohol (“Gimme a shot of that whiskey before you take the arrow out, doc!”). Patients usually had to be restrained and were often given something to bite on to help deal with the pain (“Biting the bullet”). But surgery under these conditions was still excruciating, prompting surgeons to work as quickly as possible. This, of course, often led to serious or even fatal errors, and sometimes, apocryphally, to the surgeon cutting off his own finger in his haste to complete a procedure. Despite the claims by some that pain was natural and something that should simply be endured, most physicians and patients wished for pain-free procedures. Dentistry, too, was advancing in both use and technique, and this helped drive the search for pain relieving agents. ANESTHETIC AGENTS In the mid-1800s, certain volatile liquids were found to produce temporary unconsciousness when administered carefully. Ether (CH3–CH2–O–CH2–CH3) (Figure 7.1) and chloroform (CHCl3) were used, at first simply by wetting a cloth with the liquid and having the patient breath through the material. Later designs had the cloth held DOI: 10.1201/9781003140603-7 212 Introduction to Biomedical Engineering Technology FIGURE 7.1 Ether molecular structure. FIGURE 7.2 Sevoflurane molecule. on a wire framework placed over the patient’s face, with a regulated amount of ether being dripped onto the cloth. Further refinements reduced the escape of vaporized gases by the use of cooling water jackets that kept the liquid below its boiling point until it was applied at the patient. Ether had some advantages in addition to its anesthetic effect, in that it stimulated respiration and cardiac output and promoted abdominal relaxation. It didn’t cause uterine relaxation, which made it useful for Caesarian sections. However, it was extremely flammable; it caused bronchial irritation, which could lead to coughing fits; and the onset of its effect was slow, as was recovery from its effects. By the mid-twentieth century, ether in anesthesia had mostly been displaced by cyclopropane (C3H6, arranged in a triangle of carbons), trichloroethylene (ClCH=CCl2), and halothane (C2HBrClF3). Currently, the most commonly used anesthetic agents are more complex compounds such as sevoflurane (2,2,2-trifluoro1-(trifluoromethyl) ethyl ether), (Figure 7.2) desflurane (2-(difluoromethoxy)-1,1,1,2tetrafluoroethane), and isoflurane (chloro-2-(difluoromethoxy)-1,1,1-trifluoroethane), which have the advantage of both rapid onset and rapid recovery, with minimal side effects, as well as being nonflammable. Treatment Devices: Part Two 213 ANESTHETIC MACHINES All of the anesthetic agents must be administered in a controlled manner in order to attain anesthesia that is adequate without being excessive (Figures 7.3 and 7.4). Anesthetic machines were developed for this purpose, with a basic component being a vaporizer assembly to convert stored liquid anesthetic agent to a vapor form suitable for delivery to the patient (Figures 7.5–7.8). FIGURE 7.3 A modern anesthetic machine. FIGURE 7.4 A typical operating room, with the anesthetic machine at the center rear. 214 Introduction to Biomedical Engineering Technology FIGURE 7.5 Another view of an OR with the anesthetic machine on the left. (Courtesy of Philips Medical.) FIGURE 7.6 Anesthetic machine controls. In order to conserve anesthetic agents, they can be recirculated to the patient after exhalation, but this requires a means of absorbing the carbon dioxide exhaled. A canister containing soda lime or similar materials is included in the breathing circuit of anesthetic machines using this technique. The soda lime absorbs carbon dioxide and changes color from off-white to violet as it becomes saturated, allowing replacement before it becomes ineffective (Figure 7.9). Surgery often involves paralyzing the patient’s muscles as well as inducing anesthesia, and so a mechanism to provide artificial ventilation was required and was incorporated into anesthetic machines (Figure 7.10). Treatment Devices: Part Two FIGURE 7.7 215 Anesthetic machine screens. FIGURE 7.8 The face mask is used for short procedures or to initially deliver anesthetic agents until intubation can be arranged. 216 Introduction to Biomedical Engineering Technology FIGURE 7.9 Anesthetic machine CO2 absorber. FIGURE 7.10 Anesthetic machine bellows, providing ventilation for the patient. Treatment Devices: Part Two 217 Oxygen, medical air, and nitrous oxide are used in the course of anesthesia, so supply and control systems for these gases are also included. A monitor for analyzing the concentration of the anesthetic agent in use may form part of the system, either as a built-in component or as an add-on. Monitors for patient parameters such as ECG, SpO2, temperature, and blood pressure are included in some machines, though most utilize a separate physiological monitor. There may be a means of communication between the anesthetic machine and the patient monitor, allowing anesthetic information to be included in the data being stored by the monitor (Figures 7.11–7.13). Hypothermia is a serious side effect of surgery under general anesthesia, and it can be extremely dangerous if it advances into the malignant stage. Heated humidifiers that inject warm moisture into the breathing circuit can help prevent hypothermia, as well as alleviating the desiccation that can also be a problem. FIGURE 7.11 Anesthetic machine screens. The upper screen is for patient vital signs, while the lower is for ventilator operations. 218 Introduction to Biomedical Engineering Technology FIGURE 7.12 Closer view of anesthetic machine screens. FIGURE 7.13 Part of the controls of an anesthetic machine. Treatment Devices: Part Two 219 Other components of a typical anesthetic machine include backup gas supplies in cylinders, gauges for measuring flow and volume, backup battery power supplies to allow continued function should line power fail, alarm systems to detect leaks, pressure loss and other malfunctions, and a scavenging system to remove excess anesthetic agents from the operating room. A suction mechanism may be present to allow removal of fluids from the patient’s airways. The details of design and operation of anesthetic machines vary from one manufacturer to another and from one model to another. Manufacturer training on these specifics, and direct experience with the units, are necessary for support personnel. ANESTHESIA VAPORIZERS As described above, the vaporizer used with anesthetic machines converts liquid anesthetic agents into a gaseous form suitable for delivery to the patient for inhalation. There are two main types of vaporizers found in most current hospital anesthetic machines; the characteristics of the agents determine which is used. Most machines can have two or more vaporizers installed at the same time, though interlock mechanisms must be used to prevent the delivery of two different agents simultaneously. Vaporizers are designed to work with only one anesthetic agent and are always clearly marked to indicate which agent they take. Systems are designed to make it physically difficult to fill a vaporizer with the wrong agent. Some agents have relatively high boiling points (isoflurane 48°C, sevoflurane 58.5°C), which allows them to be used in a specific type of vaporizer called a plenum vaporizer (Figures 7.14 and 7.15). Boiling points well above room temperature mean that vapor pressures of these agents in a closed chamber, or plenum, are constant (but of course different for each agent). Medical air under pressure is applied to the vaporizer from the anesthetic machine and is split into two channels. One channel bypasses the agent chamber while the FIGURE 7.14 Sevoflurane vaporizer. 220 Introduction to Biomedical Engineering Technology FIGURE 7.15 Another sevo vaporizer. other passes through the chamber, and is then mixed back into the bypass channel. This chamber has an open space (plenum) into which some of the agent vaporizes. If the agent is kept at a constant temperature (usually room temperature; this is maintained in part by constructing the vaporizer with heavy metal walls which serve as a heat stabilizer), then the concentration of vapor (vapor pressure) in the chamber is constant. By adjusting the proportion of gas passing through the chamber, the concentration of agent delivered to the patient can be controlled accurately. This mechanism works well over a wide range of flow rates. The second type of vaporizer is designed for use with desflurane (Figure 7.16). Desflurane has a boiling point of 23.5°C, which is close to or below normal room temperature. This means that desflurane will vaporize very readily at temperatures normally found in operating rooms, which makes the use of a plenum-type vaporizer impossible; it would be extremely difficult to predict what the vapor pressure would be at any given time, and so the concentration of the agent taken by the air flowing through the plenum would vary greatly with slight temperature fluctuations, possibly even reaching lethal levels. To overcome this problem, desflurane vaporizers are heated by an electrical element and pressurized to about 200 kPa (double atmospheric pressure). The rate of Treatment Devices: Part Two FIGURE 7.16 221 Desflurane vaporizer. fresh gas flowing to the patient is measured by the system, and the amount of desflurane needed for a given concentration is calculated. The pressurized desflurane vapor is then injected in precise amounts into the fresh gas in order to meet the concentration requirements. ANESTHETIC GAS MONITORS During surgical procedures when general anesthesia is used, it is critical to maintain anesthetic agent delivery within certain limits. Agent vaporizers are engineered to deliver specified amounts of gas, but various factors from the vaporizer through blenders and the components that deliver gas to the patient can affect the final concentration. Additionally, some patients metabolize anesthetic agents more rapidly than others, and so might require extra amounts to be delivered to maintain adequate levels of consciousness. Anesthetic gas monitors (AGMs) allow users to have a quantitative measure of the concentration of common agents both inspired and expired by the patient. Most systems also measure oxygen, nitrous oxide, and carbon dioxide at the same time. 222 Introduction to Biomedical Engineering Technology Gas molecules of any substance will absorb various wavelengths of infrared light in patterns that are characteristic of that substance. By passing a broadband beam of infrared through a gas sample, measuring and analyzing the absorbance patterns, and comparing these to a table of patterns, the identity of the gas can be determined. Further, by looking at the amplitude of the absorbance values, a measure of concentration can be taken. Accuracy of these measurements is usually best when gases are within normally used levels. Information may be displayed on a built-in screen in both graphical and numeric forms, and/or it may be displayed on a secondary monitor. AGMs may be integrated into some anesthetic machines. ELECTROCONVULSIVE THERAPY MACHINES Mental illness has historically been difficult to treat, since there are often no obvious physical causes or physiological or anatomical changes. A variety of unusual treatments have been used, some seemingly in random attempts to find something that produced an improvement in the condition of the patient. It was discovered that some patients suffering from severe mental illness such as schizophrenia or depression responded positively to the application of electrical currents through their brains, delivered via electrodes on the head. Experimentation refined the technique to determine the optimum waveforms, amplitudes, delivery patterns, and treatment times in order to provide the maximum benefit with the minimum harmful side effects. Electrical signals passing through any part of the body cause currents to flow throughout the rest of the body, since tissues are conductive. This means that the high-voltage signals applied to the head to treat mental illness have the potential to cause severe muscle contractions in other parts of the body, in other words, a convulsion. This gave the technique its name, electroconvulsive therapy. When this technique was first used, the patient had to be physically restrained to prevent injuries to themselves or staff when their limbs moved harshly during treatment. Despite the restraints, injuries were common. Also, if the patient was conscious during the procedure, it was often found to be a traumatic experience, although the shock usually produced immediate unconsciousness. In current practice, the patient is first administered an agent to produce unconsciousness, and then a second agent that almost completely paralyzes their muscles. When this has taken effect, the ECT treatment proceeds. Muscle contractions, and their associated dangers, are largely avoided. ECT machines may include simple ECG and EEG monitors, or separate monitors may perform these functions (Figure 7.17). Some ECT units have a motionsensing device that can help determine if a shock has been delivered successfully; the patient’s muscles still have a small amount of ability to contract, and a twitch of one of the patient’s toes is a good indicator that the shock was delivered. Originally, ECT machines used AC almost directly from the mains supply, but modern units deliver pulsed stimuli at a constant current of up to 750 mA (set by the operator) for a period of 1–6 s (again, set by the operator). Since Treatment Devices: Part Two FIGURE 7.17 223 Electroconvulsive therapy machine. current is constant, the voltage is determined, via Ohm’s law, by the impedance of the patient, although maximum voltage is limited by circuitry, to perhaps 200 or 225 V. ECT was originally developed because it was thought that epilepsy and schizophrenia were opposite maladies, and that if convulsions similar to that or epilepsy could be induced in schizophrenic patients, the effects of their disorder might be reduced. This theory has long been abandoned, but controversy remains as to the exact mechanism of ECT. Generally, it is thought that the process acts either on the electrical function and blood flow in the brain, or on neurotransmitters in the brain, or on hormonal systems. In any case, it does seem to help certain patients who don’t respond to other forms of treatment. Side effects of ECT may include those commonly seen in response to the anaesthetizing and paralyzing agents: mental confusion, memory loss, and muscle aches. Some of these effects, particularly confusion and memory loss, may persist for long periods. DIGESTIVE SYSTEM The human machine needs both fuel and building materials in order to grow and function, and also a means of getting rid of the waste products of living. The digestive system provides these services (Figure 7.18). The human digestive system is made up of the mouth and throat, the stomach, the small and large intestines, the rectum and anus, and associated organs such as salivary glands, the pancreas, and the liver. Other than those involved in surgery, there are few devices used to support the digestive system. 224 Introduction to Biomedical Engineering Technology FIGURE 7.18 The human digestive system. FEEDING PUMPS Patients are often unable to take food by mouth. They may be suffering from surgical or accidental trauma to their mouth or throat, they may be unconsciousness or otherwise unable to swallow, or they may be on a ventilator, whose mechanism blocks swallowing. In such cases there are two means of providing the needed nutrition: intravenously, with a total parenteral nutrition program; or through the use of a tube that is passed into the stomach. Treatment Devices: Part Two 225 FIGURE 7.19 An enteral feeding pump. Liquids delivered to the patient through a feeding tube may be simply gravitydriven, but this doesn’t have accurate controls and may be blocked by stomach structures. A feeding pump provides control and sufficient pressure to ensure delivery (Figure 7.19). As with intravenous pumps, enteral feeding pumps have controls for setting flow rates and total volume to be delivered. Flow rates typically range from 1 to 300 mL/h, and volume limits from 1 to 9999 mL. Because feeding solutions have different characteristics than intravenous fluids, pump details are different in some aspects. • Feeding solutions are more viscous than IV fluids, so pump mechanisms must be robust and channels must be relatively large. Most feeding pumps use a rotary peristaltic mechanism, with a rubber section of tubing to fit into the pump head (Figure 7.20). • A few air bubbles entering the stomach will not cause any problems, so airin-line detectors are not needed. • Blockages are not as critical as with IV pumps, but alarms are needed to alert staff that flow has been interrupted. Typically, the delivery tubing set has a drip chamber which fits into a drip-sensing receptacle in the pump. Drips are counted and correlated to the set flow rate. If a discrepancy is found, an alarm sounds. Drops may have stopped because the fluid reservoir is empty, the line is kinked at some point, or the exit of the tubing in the stomach is occluded by tissue. Enteral feeding pumps normally have batteries to allow them to function when the patient is being transported from one area to another. 226 Introduction to Biomedical Engineering Technology FIGURE 7.20 Enteral feeding pump head. RENAL SYSTEM The renal system in humans consists of a pair of kidneys with associated blood supplies, ureters to drain urine from the kidneys, the bladder to store urine, and the urethra to empty the bladder (Figure 7.21). The kidneys perform a number of important functions in the body, with one of the most important being the removal of certain waste products by filtering them from the blood. Urea, a breakdown product of proteins, is the main waste to be removed; others include uric acid, creatinine, and other metabolic breakdown substances. The kidneys can also remove excess water and glucose as well as sodium, potassium, and other electrolytes (Figure 7.22). If the kidneys are not functioning adequately, waste products can build up in the body, and a variety of symptoms appear, including high blood pressure, weight loss, nausea, fatigue, muscle cramps, a yellowish-brown discoloration of the skin, and loss of mental acuity. If not treated, death can eventually result. HEMODIALYSIS Various means have been used throughout history to try to treat the symptoms of kidney failure, including hot baths, sweat lodges or steam baths, enemas, and bloodletting. There was some basis to these treatments, as some toxins can be excreted in Treatment Devices: Part Two 227 FIGURE 7.21 Urinary system. FIGURE 7.22 Kidneys. sweat, they can diffuse into an enema solution through the walls of the colon, and if some “bad” blood is removed, new “good” blood is generated to replace what was lost. There are limits to the amounts of toxins that can be removed by these methods, however, so more effective means were sought. 228 FIGURE 7.23 Introduction to Biomedical Engineering Technology Hemodialysis machine. As scientists learned more about such matters as diffusion and osmosis, and about blood chemistry, it became apparent that there might be ways of temporarily removing blood from the body of a kidney failure patient, removing much of the impurities, and returning the cleansed blood to the patient. This process would have to be repeated regularly. In some circumstances, the kidneys may regain their function, but most of the time, the only two alternatives to continued hemodialysis are kidney transplants and death. In 1945, Willem Kolff performed the first successful human hemodialysis treatment, in the Netherlands. The term hemodialysis comes from the roots “hemo,” referring to blood, “dia” meaning through, and lysis, meaning “a loosening.” Impurities are loosened from the blood by passing them through a membrane. A modern hemodialysis system consists of a water purification system, an access point to the patient’s blood stream, a number of different monitoring components for both patient and hardware, and the dialyzer itself (Figure 7.23). WATER PURIFICATION SYSTEM Since dialysis involves the use of large quantities of water, any impurities such as minerals or bacterial toxins can enter patient’s blood. Normally, the kidneys would remove much of these impurities, but of course, for dialysis patients, this is not an option. Therefore, the water used must be extremely pure. A very high-quality reverse osmosis system is generally used, with monitoring for specific contaminants such as chlorine and conductivity monitoring to detect the smallest amounts of any other ions. ACCESS POINT Hemodialysis is a long-term treatment method, and access to the patient’s blood stream must be safe and reliable. Repeated insertions of large-bore needles would soon exhaust the available sites, which would be the end of the road. Treatment Devices: Part Two FIGURE 7.24 229 Hemodialysis access port. Semi-permanent catheters (Figure 7.24) provide a simple, reliable access point, but are only suitable for relatively short-term applications, such as when recovery of kidney function is expected or a transplant is pending. Catheters, inserted into veins, may be “nontunneled” or “tunneled.” Nontunneled catheters are simply passed through the skin above the vein insertion site; this is only suitable for very short-term 230 Introduction to Biomedical Engineering Technology use because veins accessible for this purpose are too small to allow high flow rates. Tunneled catheters are passed through the skin at a somewhat convenient location, such as the chest wall, and are “tunneled” under the skin to a larger artery such as the internal jugular and then to the vena cava. Either catheter type access points are susceptible to infection and so are not suitable for long-term (more than about 10 days) use. The ideal method of accessing the blood system is through an arteriovenous (AV) fistula. A surgeon constructs this by joining a vein and an artery together, which allows a high rate of blood flow through the joint, since the capillary system is bypassed. Once this structure is healed, needles can be inserted in opposite directions, one to withdraw blood and the other to return it to the patient. AV fistulas are usually placed on the patient’s arm. Infections are much less common with fistulas than with catheters as the needles are only present for relatively short times, during all of which the sites are closely monitored. AV fistulas may reduce blood supply to the lower part of the limb in which they are used. A variation on the AV fistula uses an artificial material to connect (or graft) the artery and vein, which results in faster healing. They can also be installed in more locations that a fistula. However, such grafts are more prone to infection and the joint can become narrowed, restricting blood flow. MONITORING COMPONENTS As mentioned previously, water purity must be continuously monitored, and access points must be visually monitored for signs of infection or other tissue damage. Additionally, the patient must be carefully monitored. Since large amounts of fluids are being removed from and replaced in the patient’s body, balance is very important, so the patient is weighed precisely and continuously during treatment. Since fluids are retained in patients with kidney failure, staff must accurately estimate what the patient’s weight should be with normal fluid levels, which is the target weight. Blood pressure can fluctuate considerably with dialysis, and so this is monitored as well using a non-invasive blood pressure machine. Temperature and ECG are also monitored. DIALYZER Once blood is removed from the patient (Figure 7.25), it is pumped through the system using a peristaltic pump mechanism. This uses much larger tubing than either intravenous or feeding pumps. The peristaltic method allows pumping without having the pump mechanism come in contact with the blood, and also, especially with a large diameter, relatively slowly rotating pump head, mechanical disturbance of blood cells is minimized. Blood passes from the pump into a large number of fine parallel tubes made of semi-permeable material (Figure 7.26). The tubes are immersed in a bath of body temperature fluid (the dialysate), which contains isotonic levels of the chemicals that should stay in the blood, but hypotonic levels of the components that are to be removed. The dialysate is pumped in the Treatment Devices: Part Two FIGURE 7.25 Hemodialysis patient. FIGURE 7.26 Hemodialysis machine. 231 232 Introduction to Biomedical Engineering Technology opposite direction to the blood flowing in the tubules, and impurities diffuse from the blood into the dialysate. Since fluids have been retained by the patient as a result of their kidney failure, this excess must also be removed. This is accomplished by applying higher pressure to the blood than to the dialysate, causing water to move through the membrane from the blood into the dialysate. When treatment is concluded, the access connections are removed and the patient transferred to a recovery area, where vital signs, especially blood pressure and temperature, continue to be monitored until the patient is able to leave. PERITONEAL DIALYSIS For patients who cannot tolerate hemodialysis for any reason, or if their kidney failure is not complete, peritoneal dialysis offers an alternative. It is a much simpler process than hemodialysis, and the equipment is portable and simple enough to be used in patient’s homes or even while traveling. Peritoneal dialysis takes advantage of the fact that the abdominal cavity, or peritoneum, has a very large total surface area of well-vascularized membranes (Figure 7.27). By filling the peritoneum with a carefully formulated dialysate solution, urea and other waste products in the blood will diffuse across the peritoneal membranes and into the dialysate. The composition of the dialysate can also cause excess water to diffuse out of the blood stream if this is required. After a set period, the dialysate and waste products are drained from the abdomen; the process may be repeated depending on circumstances. Because large volumes of fluid are entering the body, they must be heated to near body temperature before infusion, or hypothermia can result. Only low pressures are required to move the fluid into the abdomen, so gravity feed is adequate; dialysate bags are simply hung a short distance above the patient. A catheter, which can be opened or closed, must be installed into the abdomen and left in place more or less permanently. This requires that the patient be diligent in keeping the site clean in order to avoid infection. A passage to the peritoneum means that infections can move beyond the surface, where they might be relatively minor, into the abdomen, where peritonitis can result. Peritonitis is much more difficult to treat and can be fatal. Peritoneal dialysis may be done in three somewhat different ways. Continuous cyclic peritoneal dialysis (CCPD) uses a relatively large volume of fluid per cycle and longer cycles, one cycle following the other immediately. The process is repeated perhaps once every 24 h and may be done at night while the patient is sleeping. A machine with a timer and valves controls the filling and draining cycles. Intermittent peritoneal dialysis (IPD) can use the same cycling device as CCPD, but set so that there is a time gap between one drain phase and the next fill phase. Continuous ambulatory peritoneal dialysis (CAPD) involves slower fluid exchanges with smaller volumes. Warmed fluid is instilled into the abdomen and then left there for 4 or 5 h. During this time, the patient can go about their daily activities. After the pre-set time (signaled by a timer, or simply when the patient sees that the time is up; no machines are required), the old dialysate is drained from the abdomen and a fresh Treatment Devices: Part Two 233 FIGURE 7.27 Peritoneal dialysis. batch is instilled again. Cycling goes on continuously. The timing of cycles is somewhat flexible and can be adapted to the patient’s lifestyle. Because of its simplicity and ease, CAPD is the most commonly used form of peritoneal dialysis. LITHOTRIPTORS The renal system is in the business of filtering waste products from the blood and concentrating them for removal from the body. Under some circumstances, related to diet, body chemistry, altered kidney function, or certain disease conditions, some of 234 Introduction to Biomedical Engineering Technology FIGURE 7.28 Kidney stones. the waste products can become so concentrated that they precipitate out of the urine. If this happens over a prolonged period, the precipitated material can bond together to form kidney stones, also called renal calculi (Figure 7.28). Kidney stones can form from a variety of chemicals. • About 80% of stones are formed from calcium oxalate, with most of the remainder forming from uric acid. • Some stones are formed by the action of bacteria in relation to ammonia, which forms crystalline stones called struvites. These stones can become very large, filling the renal pelvis and taking on a “stag horn” shape. These stones can be very difficult to remove and very harmful to the kidneys. They are most often seen in women who have frequent urinary tract infections. • Uric acid stones form due to an excess of, you guessed it, uric acid. Uric acid can also precipitate in joints, causing the painful condition known as gout. • A rare genetic condition can cause high levels of the amino acid cystine in the urine, which can result in stone formation. Treatment Devices: Part Two 235 FIGURE 7.29 Kidney stone fragments. FIGURE 7.30 Lithotripsy. Kidney stones can be removed from the body in three different ways: by passing them through the urinary system, which can be extremely painful, and, if the stone is too large, impossible; by surgery, which has its own set of dangers, especially involving the kidneys; or by breaking them into small pieces so they can pass with a minimum of discomfort (Figure 7.29). The process of breaking the stones into pieces is called lithotripsy, literally “stone crushing” (Figure 7.30). 236 FIGURE 7.31 Introduction to Biomedical Engineering Technology Extracorporeal shock wave lithotripsy machine. Some systems use a probe that is threaded up through the urinary tract until the tip comes in contact with the stone. The tip has an electrical terminal that produces a spark when triggered with a high-voltage pulse. The spark vaporizes a small amount of water, which in turn creates a sonic shock wave. Repeated over and over again, the sonic pulses can eventually break the stone apart. Fluoroscopic or ultrasonic imaging is used to locate the stone and guide the probe tip. It can be difficult to maintain contact with the stone, especially after it starts to break apart. ESWL takes advantage of the fact that sound waves can be made to focus in a very small volume (Figure 7.31). The sonic intensity at the focal point can be extremely high, and if it is located in the same space as the kidney stone, it can, with repeated applications, cause the stone to break apart. ESWL is performed by placing the patient in a water bath, or alternately by having bags of fluid contact the body at certain specific locations. In the latter case, coupling gel helps to ensure optimal transfer of sonic energy from the generator to the patient. This method is both more convenient and more common. Patients are sedated or sometimes anaesthetized, and usually connected to an ECG monitor. An imaging system is used to locate the stone, and targeting mechanisms Treatment Devices: Part Two 237 adjust the focal point of the sound generator so that it coincides with the position of the stone. Sonic pulses are initiated, and power levels increased to a set level. Eventually, the stone begins to break up, and treatment is continued until only small particles remain, usually in about an hour. The sound waves break up the stone by a combination of shear forces, where adjacent parts of the stone are trying to move in opposite directions due to the crest and trough of the sound wave being very close together, or from cavitation, where the low pressure in the trough of the sound wave is sufficient to produce a vacuum “bubble”; collapse of the bubble creates a mechanical shock. Sonic waves are generated by two methods. Immersed in water, a spark gap, somewhat like the spark plug of a car’s engine, carries a high-voltage pulse across its gap. This produces an explosive vaporization in the immediate area, which in turn produces a high-intensity sound wave in the fluid. More recently, ESWL systems use a large array of piezoelectric crystals. Again, a high-energy electrical pulse stimulates the crystals and causes them to produce a sound wave directly. With either method, the maximum intensity of the sound waves is at one focus of an ellipse, part of which is formed by the signal generating apparatus. The spark gap method uses a metal reflector to focus the waves on the stone. The piezoelectric crystals are arranged in an elliptical pattern that has its focal point at the stone. Laser lithotripsy is an effective alternative to ESWL in some instances, especially with larger stones. An endoscope is inserted into the urinary tract to the location of the stone, and then a fiber-optic light guide is introduced inside the endoscope until it contacts the stone. The small diameter of the light guide makes the procedure less invasive than spark-type systems, and the ability to accurately place the fiber tip against stones means that it is better for treating irregularly shaped stones and those that are embedded in kidney tissue than extracorporeal shock wave lithotripsy (ESWL). Laser pulses are sent through the light guide, and they gradually vaporize the stones. By vaporizing the stones, fewer particles remain after the treatment, which means fewer “seeds” are available for potential future stone formation, and also it is more comfortable for the patient afterward as they do not need to pass a number of sharp particles. Newer laser technologies promise more effective, faster stone ablation. SENSORY ORGANS Phacoemulsifiers Cataracts are a common cause of vision loss, especially in older patients. They form when the proteins that make up the lens of the eye change shape and orientation, reducing the clarity of the lens (Figure 7.32). Eventually, complete loss of vision can occur. Surgical techniques were developed in the eighteenth century that simply removed the clouded lens, which restored limited vision. Extremely thick eyeglasses provided some further improvement. 238 Introduction to Biomedical Engineering Technology FIGURE 7.32 Anatomy of the eye. During World War II, pilots sometimes suffered eye injuries when the plastic canopy of their plane was shattered. Doctors found that the shards of plastic were biologically inert, and not rejected by the eye. In 1949, one of these surgeons, Howard Ridley of Britain, had a lens fabricated from the same material as the airplane canopies and inserted it to a cataract patient’s eye after removing the clouded natural lens. Techniques and material evolved, and now only very small incisions are required to perform lens removal and replacement surgery. One of the main developments that allowed surgeons to use such small incisions was the phacoemulsifier (Figures 7.33 and 7.34). Removal of the old lens was always a limiting factor for the size of incision, since the lens is quite hard and inflexible. Phacoemulsifiers use ultrasound produced at the tip of a small probe to break up (emulsify) the lens, sometimes within its outer capsule, which usually remains clear in cataract patients. A plastic lens is then folded and inserted through the same incision as used for the probe. It is unfolded within the lens capsule, and small tabs on its rim help hold it in position. The incision in modern cataract/lens replacement surgery is so small that sutures are not required; this, combined with the small size, makes the healing process quite short (Figure 7.35). Patients are usually discharged within a few hours of the procedure. Surgery is performed with the aid of an operating microscope (Figure 7.36). Focusing and movement of the head of the scope (Figure 7.37) can be done using either hand controls or the footswitch shown at the bottom of the image. The phacoemulsifier system includes the components required to generate and control the ultrasound signal, as well as a means of removing the broken up pieces of lens. Intraocular pressure must be monitored and maintained throughout the procedure. A footswitch allows the surgeon to control most functions of the system, such as ultrasound power, suction, and irrigation, while keeping hands free for doing the actual surgery (Figure 7.38). Treatment Devices: Part Two 239 FIGURE 7.33 Phacoemulsifier system, with the phaco machine on the right, foot controls for the phaco at bottom, and the operating microscope used in conjunction with the machine on the left. OPHTHALMIC LASERS Ophthalmic lasers are much like the surgical lasers described in Chapter 8, but they have special design features that make them more suitable for ophthalmic procedures (Figure 7.39). The most common eye surgery using lasers is for vision correction. The cornea is part of the focusing system of the eye, and its shape helps determine where an image 240 Introduction to Biomedical Engineering Technology FIGURE 7.34 Phacoemulsifier machine display screen. FIGURE 7.35 An artificial lens is about to be inserted into a patient’s eye. is focused. If this focal point is not at the retina, vision is blurred and corrective lenses are needed to move the focal point to the retina, producing clear vision. Laser surgery can reshape the cornea sufficiently to correct focusing on its own, so that patients will no longer need glasses or contact lenses for clear vision. The patient’s vision is first measured carefully, and then the cornea is scanned to produce a three-dimensional model. This data can be analyzed to determine what adjustments must be made to the cornea to correct vision. The parameters are fed into a laser control system, which applies the laser beam in such a way as to produce the desired results. The most common methods of corneal vision correction are PRK and LASIK. Treatment Devices: Part Two 241 FIGURE 7.36 OPMI—operating microscope. PRK stands for photo-refractive keratectomy, in which a surgeon removes the outer layer of the cornea before the laser comes into play, which then vaporizes tiny parts of the cornea to adjust focusing. LASIK is laser-assisted in situ keratomileusis and is more invasive than PKR. The surgeon cuts a very small flap into the cornea, and then the laser is directed through the flap onto the underside of the cornea where it burns away enough tissue to produce corrected vision. A typical LASIK laser wavelength is 193 nm. Lasers are used in other ophthalmic procedures as well, such as retinal repair and to remove protein films on implanted lenses. 242 FIGURE 7.37 Introduction to Biomedical Engineering Technology Close up of the binocular head of the operating microscope. FIGURE 7.38 A surgeon performing cataract surgery via an operating microscope. Treatment Devices: Part Two 243 FIGURE 7.39 Ophthalmic laser. SUMMARY This chapter covered equipment relating to the nervous system. Anesthetic machine history and technology, types of anesthetic agents, and anesthetic machine features were described. Electroconvulsive therapy units were discussed. Enteral feeding pumps were covered. Relating to the renal system, kidney function was outlined, as well as hemodialysis: system features, theory, and methods of treatment. Peritoneal dialysis was described, plus the physics of lithotripter and a section about the treatment process. The sensory system focused on the eyes, with a discussion of cataracts and lens replacement using phacoemulsifiers, and the theory and applications of ophthalmic lasers. QUESTIONS 1. What are some of the disadvantages of ether as an anesthetic agent? 2. What must be done to allow anesthetic agents to be recirculated to the patient? 244 Introduction to Biomedical Engineering Technology 3. Why are heated humidifiers used during anesthesia? 4. How is gas concentration controlled in an isoflurane vaporizer? 5. Why is it important to monitor anesthetic gas concentrations? 6. Why are patients paralyzed during an ECT procedure? 7. What is the purpose of the drip chamber in an enteral feeding pump set-up? 8. Where does the urea excreted by the kidneys originate? 9. How is fluid balance monitored during hemodialysis? 10. Why are peristaltic-type pumps used for pumping blood in hemodialysis? 11. How does hemodialysis differentiate between substances that need to be removed from the patient’s blood and those that need to be retained? 12. Where does waste product removal from the blood take place in peritoneal dialysis? 13. What are some of the advantages of CAPD? 14. Why is coupling gel needed in ESWL? 15. What two forces can help to break up kidney stones in ESWL? 16. What are the advantages of laser lithotripsy? 17. How do phacoemulsifiers help to reduce recovery time for cataract surgery patients? 18. What are the main differences between PKR and LASIK? 8 Part Three Treatment Devices OBJECTIVES FOR THIS CHAPTER • To discuss the design, purpose, and function of treatment devices used in neonatology and in various applications involving skin, bones, and muscles. • Neonatology devices include bilirubin therapy units, infant incubators and resuscitators, and nitrous oxide (N2O) units for use during labor. • Other devices examined in this chapter include electrosurgery units, surgical lasers, cryosurgery units, operating microscopes, equipment sterilizers, and a range of physiotherapy machines. REPRODUCTION Bilirubin Therapy Systems Newborn babies often have an excess of bilirubin in their bodies. Bilirubin is a breakdown product of red blood cells that is normally excreted via the liver. If liver function isn’t up to normal capacity, the bilirubin can build up in tissues including the skin, giving it a yellowish color, a condition called jaundice. If bilirubin levels are too high, they can cause brain damage, so it is important to remove excess amounts as quickly as possible. Bilirubin in the skin can be broken down when exposed to certain wavelengths of light, with the greatest effect occurring at about 510 nM. The breakdown products can then be safely excreted in urine. Since light sources usually have a somewhat broad bandwidth, and since some photochemical breakdown of bilirubin occurs at wavelengths above and below 510 nM, lights with a bandwidth in the range of 360–520 nM are often used to treat hyperbilirubinemia in neonates. Light of the 510 nM optimal wavelength is green, but 360 nM is in the near-ultraviolet range, with violet and blue in between. The overall effect is that most treatment light appears to be blue (Figure 8.1). This light may be delivered by an overhead bank of special fluorescent tubes, either through the Plexiglas™ canopy of an infant incubator or directly through the air above a bassinette (Figures 8.2 and 8.3). With advances in LED technology, LED bili lights are available, being more reliable and consuming less power than fluorescents. With any bank of lights, as much of the infant’s skin must be exposed to the light as possible in order to maximize the therapeutic effect, but then environmental and body temperatures must be controlled and monitored carefully. Since incident radiation varies with the square of the distance from the source, since Plexiglas absorbs some light, and further since light output at the relevant wavelengths can vary with bulb age, light levels should be measured with an accurate, calibrated photometer that is sensitive to the relevant wavelengths (Figure 8.4). DOI: 10.1201/9781003140603-8 246 Introduction to Biomedical Engineering Technology FIGURE 8.1 An overhead bilirubin therapy light. FIGURE 8.2 Infant under bili light. Some systems reduce both the issue of light distance and the amount of exposed skin for the baby by using a blanket with embedded fiber-optic channels that are fed by a light source of the appropriate wavelength or LEDs. This type of system is also less bulky than the overhead lighting system. In all cases, as mentioned, measurement of light output using a calibrated photometer is very important. Since prolonged exposure of the eyes to light of these wavelengths can cause damage, infants must have a mask fitted to cover their eyes while undergoing light therapy. INFANT INCUBATORS Neonates, especially if of low birth weight and/or born prematurely, or if there are other medical conditions, may not have adequately developed thermoregulatory systems. In these cases, the infant is best kept in an environment with closely controlled Treatment Devices: Part Three FIGURE 8.3 A bilirubin therapy light over an infant incubator. FIGURE 8.4 Bili light photometer. 247 248 Introduction to Biomedical Engineering Technology temperature and humidity. Such infants may also have breathing difficulties, so an oxygen-enriched atmosphere may be beneficial. Infant incubators are designed to meet these needs (Figure 8.5). A number of design criteria must be met: • Temperature control must be precise and responsive. The temperature must be able to be set to an appropriate range of values, with alarms for over and under temperature. Since the incubator may have to be opened frequently for care purposes, exposing the interior to room temperature, the system must be able to return to the set temperature quickly. A heater element of adequate capacity is needed, along with an effective air circulation system. Most systems use double-walled construction to help insulate the interior. Airflow between inner and outer walls helps to maintain temperature and even out heat distribution. Temperature control may be done according to air temperature or infant skin temperature; control must be maintained should a sensor in use fail or become disconnected, which requires an independent, permanent temperature sensor located somewhere else in the system. • Access for routine care procedures must be easy, but still restrict heat and oxygen loss. Systems use multiple access hatches with gasket-sealed doors, FIGURE 8.5 An infant incubator. Note the bed surface inside is on a slant, an arrangement called the reverse Trendelenburg position, with the infant’s head higher than the rest of its body. This position makes it easier for the baby to breathe. Treatment Devices: Part Three 249 along with elasticized collars to fit around the arms of caregivers (Figures 8.6 and 8.7). There is usually a large side door to allow the infant to be moved in and out of the incubator as necessary. • Oxygen systems must provide sufficient flow to maintain maximum set levels when the incubator is closed and return to set levels in a short time after hatches or doors have been opened. Oxygen should be monitored continuously, with alarms for over and under measurements (Figure 8.8). Excess oxygen can cause problems with eye development in neonates, while too little oxygen may not be therapeutically adequate. Incubators are generally used in hospitals where line oxygen is available. • Humidity systems should be easy to use and effective, ideally with a humidity monitoring capability. FIGURE 8.6 Incubator with doors open. FIGURE 8.7 Baby care while in incubator. 250 Introduction to Biomedical Engineering Technology FIGURE 8.8 Incubator oxygen sensors from below. FIGURE 8.9 SpO2 probe on infant foot. • The infant must be easily visible at all times. Incubators use Plexiglas canopies for this purpose, with minimal obstructing hardware. • Since the interior of the incubator has many hard, flat, sound-reflecting surfaces and newborn ears are very sensitive, sounds inside the incubator should be kept to a minimum. This mainly relates to the air circulation system, which must use high-quality, quiet motors and well-designed fans that move air effectively but quietly. • Ideally, the body of the incubator should be able to be raised or lowered to accommodate different staff as they work with the infant. • Certain medical situations may require that the infant be placed in a headup or head-down position. This should be possible using external controls. • Air-tight access points should be available for SpO2 or ECG cables, ventilator hoses, or IV or feeding tubes (Figure 8.9). Treatment Devices: Part Three 251 FIGURE 8.10 Incubator display panel. • Since infant weight is an important parameter for monitoring growth as well as fluid balance, an integrated weigh scale is a valuable feature. • X-rays may need to be taken of the infant, so a tray for X-ray film cassettes under the bed means that the infant doesn’t have to be removed from the incubator. • A display system that shows values for current temperature (skin and/or air), set temperature, current and set humidity, and current and set oxygen levels is very useful. Such displays may also show graphs of the various parameters, as well as infant weights and other data, and alarm information (Figure 8.10). • An audible alarm to indicate loss of AC power is vital. • Built-in compartments for accessories and supplies are important. Transport incubators are specialized versions of infant incubators that are designed to fit into emergency vehicles (with smaller dimensions and collapsible undercarriage) and include oxygen tanks and powerful batteries to maintain functions while away from line power. INFANT RESUSCITATORS Immediately following birth, babies may need intensive treatment (Figure 8.11). Airways may need to be aspirated, oxygen administered, tests performed, and breathing augmented in an environment that provides quick heat and bright light. Infant resuscitators are devices that fulfill these requirements. Since they may need to be moved to other areas of the hospital (babies do not always choose to be born [Figure 8.12] in convenient locations), they usually have oxygen tanks on board, though they can run on line oxygen if it is available. Oxygen flowing through a venturi can produce suitable suction if wall suction is not available (Figure 8.13). Suction and oxygen must be readily available, and their controls easy to access. Because several people may be involved in the care of the neonate, access from three sides must be clear, with controls and support for heaters and lights on the fourth side (Figures 8.14 and 8.15). 252 FIGURE 8.11 Introduction to Biomedical Engineering Technology Pregnancy anatomy. FIGURE 8.12 Just born. Treatment Devices: Part Three FIGURE 8.13 Full view of resuscitator. FIGURE 8.14 Resuscitator controls + Apgar timer. 253 254 Introduction to Biomedical Engineering Technology FIGURE 8.15 Apgar timer. FIGURE 8.16 Resuscitator overhead arm with lights and heater elements. Since the working area is open, radiant heat is the best option, with overhead heating elements controlled by a skin sensor (Figure 8.16). This overhead heat and light fixture should be able to move aside to allow access for a C-arm X-ray machine, which also needs a film cassette chamber under the working surface of the resuscitator. Treatment Devices: Part Three 255 APGAR—a system used to evaluate the medical status of a newborn. It was introduced by Dr. Virginia Apgar in 1952 and consists of a set of observations made at 1 minute and 5 minutes after birth. Breathing effort, heart rate, muscle tone, reflexes, and skin color are each rated as 0, 1, or 2, and the scores added together. Scores of 7 to 10 are good; lower scores may indicate the need for intervention. The scores at 5 minutes should be as high or higher than those at 1 minute. An Apgar timer simply displays the time since birth and gives a tone when the 1 and 5 minute intervals are reached. N2O UNITS N2O has been found to be a safe, effective means of alleviating some of the pain of labor when delivered at the correct concentration. It is mixed about half and half with oxygen. The gases may be available from wall outlets or from portable tanks. The mechanism for delivering the mixture to the patient is usually nonelectrical, consisting of the necessary supply hoses and connectors, and a box containing regulators, a blender, overpressure alarms, possibly pressure gauges, and fittings to connect a patient line. The patient line carries the blended, pressure-reduced gas mixture to a demand valve, which only opens when the patient inhales. The demand valve fits on to a soft, snug-fitting mask that covers the patient’s nose and mouth (Figures 8.17 and 8.18). FIGURE 8.17 Nitrous oxide unit. 256 Introduction to Biomedical Engineering Technology FIGURE 8.18 Another view of nitrous unit. To prevent buildup of N2O in the area, a scavenging system may be in place that collects exhaled gases and draws them into the building air handling ducts where it dissipates to harmless levels. SKIN, BONE, MUSCLE, AND MISCELLANEOUS Electrosurgery Machines The art of surgery has been practiced for thousands of years, but bleeding was always a problem. Cutting into flesh in order to remove a body part or foreign object (including demons), or to repair some kind of damage, resulted in many small and large blood vessels being severed. Larger vessels could sometimes be tied off, but the smaller ones were impossible and the surgeon and patient just had to wait until the body’s natural clotting mechanism stemmed the flow, hopefully before the patient bled to death. Besides this rather inconvenient side effect, bleeding obscured the surgical site, making it hard for the surgeon to see what he was doing. Whether discovered accidentally or by experimentation, it was found, also long in the past, that high heat would sear, or cauterize, tissue and stop much of the bleeding Treatment Devices: Part Three 257 from a wound or incision. A red-hot iron did the job but was inconvenient and potentially extremely painful, as it was used long before the advent of anesthesia. A side benefit of cauterization by any means is that it kills most bacteria and viruses in the tissue being cauterized. When experimenters began working with electricity, one characteristic they noted was that electric current passing through an object generated heat. Eventually, it was found that this characteristic could be used to cauterize tissue, and if applied carefully, electricity could cut tissue as well. In 1920, William Bovie built the first practical electrosurgery generator. More models improved on his original, and his name was associated with the field for decades afterward—in fact, it’s not unusual to hear OR staff referring to electrosurgery units as “Bovies,” in the same way that photocopy machines are often called “xeroxes” (Figures 8.19 and 8.20). With experimentation, it was found that certain frequencies of electricity caused more nerve and muscle stimulation than others, and ESUs were designed to avoid these frequencies. Most units operate in the range from 100 KHz to 10 MHz. FIGURE 8.19 ESU front panel. FIGURE 8.20 An older electrosurgery unit. 258 Introduction to Biomedical Engineering Technology Applying electrical current to tissue results in the tissue being heated, but the specific features of the signal determine what happens to the tissue. As with any electrical circuit, there must be a complete pathway. In electrosurgery, the source of the current is called the active electrode, while the sink is called the return or grounding electrode. When a high-intensity, continuous sine wave signal is applied, the cells in the tissue rupture and any water rapidly boils away. This has the effect of cutting the tissue. However, the rapid drying of the material makes it less conductive, and so the current doesn’t spread very far from the point of application. The cut is thin and heating is minimal away from the cut point. Current is high enough in the cutting process that the active electrode doesn’t directly contact tissue; instead, sparks jump from the metal electrode to the tissue to carry out the action. If the same signal is cycled rapidly on and off, the cutting effect is reduced and heating occurs in a larger area. This has the effect of coagulating the tissue, that is, drying a wider path and stopping any bleeding. In some situations, it is useful to be able to dry out, or desiccate, larger areas. In this case, the duty cycle of the sine wave is further reduced, allowing greater current penetration to produce the desired result. Increased application of such signals will burn away the desiccated tissue, a process called fulguration. It is used to remove such structures as cancer tumors when simple excision is not possible, or to destroy sections of the vas deferens or fallopian tubes in sterilization procedures. Most ESUs have a “Blend” setting, which is intermediate between “Cut” and “Coagulate.” The settings used are often determined by individual surgeon preferences, though experience has shown that specific settings work best for some particular procedures. Staff members often attach notes to the ESUs with a list of settings and procedures. There are two general modes of operation for ESUs: monopolar and bipolar. MONOPOLAR ELECTROSURGERY In monopolar operation, surgical current is applied through an active electrode at the site. Active electrodes may be turned on and off using a footswitch, or they may have switches on the hand piece (Figures 8.21 and 8.22). Both types can select CUT or COAG. In an endoscopy procedure, such as a colonoscopy, an ESU electrode in the form of a wire snare may be used. The loop of the snare is pulled snug around the base of a polyp and current is applied, both severing the polyp and cauterizing the site (Figure 8.23). Once past the immediate area of application, current spreads out through the body, reducing current density enough that no significant heating occurs. The monopolar return electrode has a large surface area to keep current densities low (Figure 8.24). It is usually applied to an area of the body with a large, relatively smooth surface, such as the thigh or buttock. It is critical for the return electrode to maintain a large contact area to keep current density low enough that burns don’t develop at the electrode site. To this end, most ESU manufacturers have developed a system to measure contact quality. Treatment Devices: Part Three FIGURE 8.21 ESU pencil with hand switches. FIGURE 8.22 ESU pencil tip. FIGURE 8.23 ESU snare on colon polyp. 259 260 FIGURE 8.24 Introduction to Biomedical Engineering Technology Return electrode monitor pad. Valleylab™ uses an electrode with two sections. By applying a small voltage across the two sections and measuring the current flow, impedance is determined. If it is too low, indicating inadequate contact, an alarm will sound and operation of the ESU will be blocked. On the other hand, if the test current is too high, for example, if the two sections of the electrode have come away from the skin and contacted each other, or if some conductive material like blood has run between the sections, an alarm is also triggered, preventing machine operation. As in the story of Goldilocks, contact has to be “just right” in order for electrosurgery to proceed. ELECTROSURGERY UNIT INSPECTION AND PREVENTIVE MAINTENANCE Mike Cho looked at the note that Joe had left him, asking him to do an IPM service on one of the electrosurgery units from the OR. The unit was scheduled for work in their equipment control program and was sitting in the biomed lab (Figure 8.25). Mike started by calling up the IPM procedure on his tablet, then gathering the test equipment and other material required: the service manual for that model, the ESU analyzer, the electrical safety analyzer, and a set of active and return electrode cables. As he completed each step, he checked off the boxes on the form or filled in measured values. He would later transfer them to the control program. He first did a visual inspection of the device, looking over the chassis for signs of damage or spills, then checking the cart for the same, and rolling it back and forth to ensure the wheels were working properly. Foreign material sometimes got caught in the wheels or bearings making them balky, but this unit had smoothly functioning wheels. Treatment Devices: Part Three FIGURE 8.25 ESU. FIGURE 8.26 ESU disposables. 261 Next on the list was a check of the accessories that were with the unit, making sure that they were complete and in good condition, and that any items with an expiry date were still useable (Figure 8.26). The power cord was examined, checking for damage to the cord, condition of the AC plug, and adequacy of the strain relief where the cord entered the chassis. The ESU included two footswitches: one for monopolar operation and one for bipolar. Mike looked at the cables and connectors of the footswitches and operated the switch mechanisms to ensure they were working smoothly. Finished with the visual and external mechanical checks, Mike fired up the electrical safety analyzer and ran through the standard tests, including ground line impedance and 60 Hz leakage (Figure 8.27). 262 FIGURE 8.27 Introduction to Biomedical Engineering Technology Electrical safety analyzer. (Courtesy of Fluke Biomedical.) FIGURE 8.28 ESU analyzer. (Courtesy of Fluke Biomedical Everett, WA.) With the machine turned on, Mike checked the physical condition and operation of the various front panel controls and checked that the digital displays and indicator lights were all working. He did a quick test to ensure that the audible indicators and alarms were functioning, then connected the unit to the ESU analyzer. This model of ESU had a system to monitor the contact integrity of the return (or dispersive) electrodes, which is described in Chapter 9. The analyzer had a special function to test this monitoring system, activated as part of an automated test sequence (Figure 8.28). The unit passed, and Mike moved on to the RF power output portion of the test sequence. Treatment Devices: Part Three 263 The ESU could function in three different mode, CUT, COAG, or BLEND, and the ESU analyzer measured output at various levels for each of the three modes. These values were then compared to those specified in the service manual; all were within specifications. The final test involved measuring leakage current of the RF signals, at specific settings. Again, the unit passed, so Mike disconnected the various components, replaced the footswitches and accessories in their proper locations, and affixed a dated label to the unit indicating that it had passed inspection. He then entered the test information into a work order as part of the equipment control software system. Since he was going in the vicinity of the OR on another matter, he wheeled the unit back, letting the staff in the OR office know that it was back and in good operating order. BIPOLAR ELECTROSURGERY In some procedures, especially those performed laparoscopically (see Chapter 4), a return electrode arrangement as described above is not practical. In such circumstances, a bipolar arrangement is used, in which the source and sink of current are close to each other. This is usually in the form of forceps or pincers in which one jaw is a source and the other sink (Figures 8.29 and 8.30). FIGURE 8.29 ESU bipolar forceps. FIGURE 8.30 Bipolar forceps tip. 264 FIGURE 8.31 Introduction to Biomedical Engineering Technology Endoscopic view of an intestinal polyp. This makes a separate return electrode and associated wiring unnecessary, but is only useful for small structures such as fallopian tubes or intestinal polyps (Figure 8.31). When cutting tissues, ESUs can produce smoke which rises in a plume above the surgery site. This smoke can contain both toxic chemicals produced by the burning tissue, and also possibly virus particles should the patient be infected. The use of a smoke evacuator system is highly recommended in order to remove such smoke plumes from the area. SURGICAL LASERS Surgical lasers operate on the same end principle as electrosurgery machines, in that rapid heating of tissue can produce cutting and/or coagulation (Figure 8.32). Surgical lasers use their coherent beams of laser light to do the heating rather than an electrical current, which has advantages in certain situations. The laser beam can be very precisely focused to allow it to act on small structures without damaging adjacent tissues; it can be directed around corners and into very confined spaces; and it can be controlled in such a way that almost all of its power is focused at a specific, precise distance from the emitter. By using different materials and construction techniques, lasers can be produced that have different wavelengths. These various wavelengths are absorbed differentially by different tissues. Lasers are named according to the material used in the lasing tube. CARBON DIOXIDE LASERS Carbon dioxide (CO2) lasers have a wavelength of 10.6 μm (10,600 nm), which means that it is strongly absorbed by water. Since soft tissue in the body is composed mostly of water, the CO2 laser will cut them very effectively, but will only Treatment Devices: Part Three 265 FIGURE 8.32 Surgical laser. penetrate slightly. Cutting action extends to only about 0.1 mm into the tissue, while coagulation is only about 0.5 mm deep. With such characteristics, very precise procedures can be carried out. Because bone and teeth have much lower water contents than soft tissue, CO2 lasers are not used on them. Light at this wavelength doesn’t travel well through fiber-optic channels, and therefore CO2 lasers are mostly used on structures that are directly accessible, especially the skin. NEODYMIUM-DOPED YTTRIUM ALUMINUM GARNET LASERS Nd:YAG lasers operate at a wavelength of 1064 nm and beams are not absorbed preferentially by water. This means that cutting depth is up to 4 mm, much greater than the CO2 lasers. Coagulation effects are also deeper. Nd:YAG laser light will pass through fiber optics, so it can be used in endoscopic procedures. 266 Introduction to Biomedical Engineering Technology ARGON LASERS Argon lasers produce various wavelengths of light, with most of the power being concentrated at 488 and 514 nm. EXCIMER LASERS Excimer lasers use an inert gas such as argon or krypton combined with chlorine or fluorine to produce an ultraviolet laser beam. This beam can be very tightly focused and controlled, and its energy level means that tissue on which it is used vaporizes rather than burning. Excimer lasers are used to reshape the cornea of patients to correct their vision; by vaporizing specific areas, the cornea is deformed in such a way as to change the focus of the eye, reducing or eliminating the need for corrective lenses. LASER SAFETY Since surgical lasers emit high-powered beams of light energy, extreme care must be taken not to allow it to contact the wrong materials. Unlike ESU currents, laser light maintains its power over considerable distances through open air. Patients and staff must wear eye protection when lasers are in use, and doors must be closed and windows covered. A prominent sign must be posted outside the room warning others that lasers are in use. The retina can be seriously and almost instantaneously damaged by high-powered laser light. Flammable materials must be avoided in the area. Items such as surgical drapes must be dampened with water to prevent ignition should the laser beam comes in contact with them. Any other flammable objects that can’t be removed should be covered with damp cloth. Reflective surfaces should be avoided in the procedure room, since a stray beam could bounce off such a surface and enter the eye of a staff member whose perception is that they are safely looking away from the procedure. When cutting tissues, lasers can produce smoke, which rises in a plume above the surgery site. This smoke can contain both toxic chemicals produced by the burning tissue, and possibly virus particles should the patient be infected. The use of a smoke evacuator system is highly recommended in order to remove such smoke plumes from the area. SURGICAL ULTRASOUND High-intensity, high-frequency ultrasound waves can be focused in such a way as to heat tissue very rapidly, in much the same way as electrosurgery or surgical lasers, but without the need for return paths as in electrosurgery or the dangers of laser beams. Beams can be focused on tissues below the surface without damaging the overlying tissue, which has made the process especially suited for prostate treatment. Treatment Devices: Part Three 267 CRYOSURGERY UNITS As long as humans have been venturing outside in winter, it has been known that exposure to extreme cold can kill tissues. By using carefully controlled applications of super-cold objects to surface tissues such as warts, skin keratoses, and certain skin cancers, the tissue in question can be frozen and killed, with very little effect on the surrounding structures. After a few days, the “frostbitten” area will dry up and slough off, leaving almost no sign of it having been there. As caution is important in such applications, the first treatment may not get all of the offending tissue, so a follow-up may be required. The simplest cryosurgery technique uses a small piece of absorbent material on the end of a rod made of low heat conductivity material such as wood. The rod and material are dipped into a vacuum flask containing liquid nitrogen. The liquid nitrogen is absorbed by the material and stays in liquid form long enough for the rod to be removed from the flask. The soaked material is then applied to the target area. A few seconds of contact is usually sufficient to produce the desired result. Liquid nitrogen may not always be available or convenient, or may not last long enough for some procedures. Cryosurgery machines take advantage of the fact that gases cool rapidly when they expand. If a highly compressed gas is released from a cylinder and passed over or through a metal surface, the metal itself will cool rapidly. By repeating the gas release as necessary, the metal can be kept cold (Figures 8.33 and 8.34). Cryosurgery units use either CO2 or N2O to effect cooling of the metal probes used. Compressed CO2 is readily available and inexpensive, and is harmless when released into room air (unless it reaches very high concentrations), but it doesn’t reduce probe temperatures as effectively as N2O. N2O can be harmful at relatively low concentrations, especially with prolonged exposure, so a scavenging system must be used with N2O cryosurgery units in order to remove most of the exhaust gas from the area. FIGURE 8.33 Frosty cryosurgery probe. 268 FIGURE 8.34 Introduction to Biomedical Engineering Technology A cryosurgery unit. Probes come in various shapes and sizes for different applications. Most systems have two controls, one to pass the expanding N2O through the probe to cool it off, and the other to draw room air through the probe in order to warm it rapidly, as supercold probes can be dangerous if left out in the open after a cryosurgery procedure; they may inadvertently come in contract with the flesh of the patient or staff, causing damage, or they may freeze to other objects they come in contact with, which may cause an accident when moved. MICROSCOPES Human eyesight is limited in its ability to see very small objects. With the invention of lenses in about the eleventh century, these limitations were overcome, and by the sixteenth century, scientists were using simple microscopes to examine the previously invisible world of the very small. Single lens microscopes gave way to compound or multilens devices that offered much greater magnification with larger fields of view (Figure 8.35). These eventually led to the modern laboratory microscope, with its high power and binocular eyepieces (Figure 8.36). Lab scopes are outside the “scope” of this book; however, specialized microscopes are used in both direct diagnosis and in treatment situations. Operating microscopes mount a high-powered, high-quality binocular microscope on an articulating arm Treatment Devices: Part Three FIGURE 8.35 269 An old microscope. FIGURE 8.36 Modern microscope. that can be maneuvered in order to look at various structures during microsurgery (Figure 8.37). The arm may be placed on a mobile stand or fixed to a wall, floor, or ceiling mount. Controls for adjusting position, focus, and magnification are located on the head of the device, but usually they have servomotors attached that allow the controls to be operated using a special footswitch. Surgeons become adept at using the footswitch without looking at it, thus freeing their hands to perform surgical procedures (Figure 8.38). 270 FIGURE 8.37 Introduction to Biomedical Engineering Technology Overview of operating microscope. Operating microscopes (sometimes called OPMIs, though this is actually a model name for a specific device) are designed to provide the levels of magnification, field of view, and depth of focus that are required in microsurgery. Compared to a lab microscope, the magnification levels are considerably less, since it would be impossible to physically work on extremely small structures. Lab microscopes may magnify up to 1000× or more, while operating microscopes are usually limited to about 20×. Also, depth of focus is much greater for operating microscopes than for lab units, because the objective lens must be far enough away from the observing area to allow access for surgical instruments and the surgeon’s hands, and because structures being viewed are three dimensional. Some operating microscopes have two sets of binocular eyepieces (Figure 8.39) for instructional use, and they may also have a video camera integrated into the Treatment Devices: Part Three FIGURE 8.38 OPMI footswitch. FIGURE 8.39 OPMI binocular head. 271 272 Introduction to Biomedical Engineering Technology optics to allow viewing on a large video monitor, so that procedures can be recorded for later review. Illumination of the surgical field is critical, so high-intensity, color-correct light sources form part of the operating microscope system. Light is usually delivered to the site by fiber-optic cables. Systems may include various colored filters to help in imaging certain tissues or structures. STERILIZERS Although biomedical staff does not usually support hospital sterilizers, they will be discussed here briefly. Many types of medical equipment may come in contact with contaminated material, which means that they must be cleaned and sterilized before they can be used again. There are three general types of sterilizers: gas, heat, and liquid. GAS STERILIZERS Gas sterilizers use a poisonous gas such as ethylene oxide or chlorine dioxide. Instruments to be sterilized are placed in a chamber which is sealed and pumped full of gas. The interior is heated moderately (e.g., to about 55°C, to promote more rapid chemical action). Systems may have controls for temperature, humidity, gas concentration, and process time; certain parameters may have preset values for specific sterilization procedures. The gases in use must be safely evacuated from the chamber before opening to remove the instruments. Gas sterilizers are typically used for equipment that can’t tolerate high heat levels and/or liquid immersion. HEAT STERILIZERS For devices and parts that can tolerate high levels of heat, this method of sterilization offers faster processing than low-temperature gas sterilizers (Figure 8.40). Toxic gases and steam may be added to the chamber, though some systems may use dry heat only, especially for instruments such as scalpels whose edge may be degraded by contact with steam or corrosive chemicals. Steam sterilizers, or autoclaves, are pressurized so that they can be heated to about 120°C to increase sterilization effectiveness and reduce cycle times. Controls are otherwise similar to those of gas sterilizers. LIQUID STERILIZERS As their name implies, these units utilized toxic liquids to carry out sterilization. This is especially useful for instruments with small crevices or internal passageways that gas and heat may not reach effectively. These instruments must first be thoroughly cleaned physically before attempting sterilization. Treatment Devices: Part Three FIGURE 8.40 Steam sterilizer. FIGURE 8.41 Endoscope washer. 273 A specialized type of liquid sterilizer is used to clean endoscopes, since they have long internal passageways that can become contaminated with body fluids and possibly solids (Figure 8.41). Scopes are placed in the washer and connected to a fitting. The washer goes through a cycle, either pre-programmed or user-set. The scope is first flushed with water and then with a water–detergent combination, followed by another water flush. Then a sterilizing liquid such as glutaraldehyde is introduced into the scope and is left for a set time. Flushing with water and/or alcohol follows, and finally, air is blown through the scope to prepare it for its next use. 274 Introduction to Biomedical Engineering Technology PHYSIOTHERAPY EQUIPMENT Devices used in physiotherapy or rehabilitation departments may or may not be supported by biomed; some devices are strictly mechanical while others include varying levels of electronics. Generally, physiotherapy equipment is designed to maintain or improve range of motion, relieve pain, or promote healing; sometimes two or more of these goals may be attained through the use of one mode of therapy. CONTINUOUS PASSIVE MOTION Much range-of-motion work with patients is done by direct physical manipulation by the therapist, but machines can do some repetitive, simple actions (Figure 8.42). These continuous passive motion (CPM) devices simply flex and extend joints, especially knees, by gripping an extremity such as a foot and moving it back and forth. The rate and degree of motion can be set for each patient, and a timer may be used to set treatment duration. PAIN RELIEF A number of different techniques may be used for pain relief, many of which involve the use of heat. DIRECT HEAT Heat may be applied to a muscle group or joint by simple transfer, using a wax bath, moist hot packs, or whirlpool baths (Figures 8.43 and 8.44). Generally, controls on this type of equipment are limited to temperature adjustments and overtemperature alarms, and treatment timers. FIGURE 8.42 CPM device. Treatment Devices: Part Three FIGURE 8.43 Wax bath. FIGURE 8.44 Hot pack heater. 275 276 Introduction to Biomedical Engineering Technology INDUCED HEAT In the past, radio waves were used to deep-heat tissue with technology much like that found in a microwave oven. Possible negative effects were common with these shortwave diathermy machines, and they are rarely used today. Ultrasound can produce similar deep tissue heating much more safely. These units consist of ultrasound generators, various power heads to provide heating at different depths, and controls for power output and length of treatment (Figure 8.45). Ultrasound is produced in the power head with piezoelectric crystals. Some ultrasound therapy machines are combined with interferential therapy units (see below) (Figure 8.46). FIGURE 8.45 Therapeutic ultrasound machine. FIGURE 8.46 Combination ultrasound and interferential unit. Treatment Devices: Part Three 277 INTERFERENTIAL THERAPY These devices apply stimulating electrical currents to two pairs of electrodes, placed on the skin so that the currents cross each other diagonally. This sets up an interference pattern of muscle stimulation that has been found to be helpful in relieving some types of pain (Figure 8.47). These units may also use a suction cup system in conjunction with the electrical stimulation. Large cups (with electrodes built in) are placed over muscle groups, and suction is applied alternately to the cups, producing a massaging action (Figure 8.48). FIGURE 8.47 Interferential therapy unit. FIGURE 8.48 Interferential electrodes. 278 Introduction to Biomedical Engineering Technology FIGURE 8.49 Laser heat therapy unit. FIGURE 8.50 Laser therapy treatment. LASER THERAPY Certain wavelengths of laser light can penetrate surface tissues and produce deep heating (Figures 8.49 and 8.50). As with ultrasound therapy units, power levels and treatment times are controlled, and different applicators can determine the depth of heating. TRANSCUTANEOUS ELECTRICAL NERVE STIMULATORS It has been found that applying electrical signals of a specific amplitude, wave shape, and duration to particular locations on the body can result in the reduction of pain sensations in other areas, almost like the needles used in acupuncture. TENS units are small, battery-powered devices with controls for the parameters mentioned above Treatment Devices: Part Three 279 FIGURE 8.51 TENS device. (Figure 8.51). Stimulation signals are delivered by small electrodes often made of conductive rubber, which are placed on the designated skin locations. PROMOTION OF HEALING Ultraviolet Light Therapy Ultraviolet light has been found to help certain skin conditions such as psoriasis (Figure 8.52). By exposing as much skin as possible to UV rays, maximal benefit is achieved. Since UV rays can be harmful to the eyes, patients must wear a properly fitted, effective mask during treatment. Due to the physical construction of fluorescent bulbs, their UV output decreases with time. In order to ensure adequate therapeutic doses, UV output must be tested regularly with a calibrated meter using specific methods, such as having the bulbs on for a set period of time before measurement and placing the sensor in the same location each time. A timing circuit turns lights off after the specified treatment is completed. SEQUENTIAL COMPRESSION DEVICES After certain surgical procedures or with some medical conditions, lymphatic fluid does not return to the central venous system as quickly as it should. To aid in this process, devices were developed that use a large, compartmentalized cuff that is placed around the patient’s arm or leg (Figures 8.53 and 8.54). By inflating the compartments sequentially, the limb is compressed in a peristaltic fashion, with the wave 280 FIGURE 8.52 Introduction to Biomedical Engineering Technology Ultraviolet therapy booth. FIGURE 8.53 Sequential compression device. Treatment Devices: Part Three 281 FIGURE 8.54 Another SCD. FIGURE 8.55 Percussor. moving from the area further from the body to the area closest to the body. In this manner, lymphatic fluid is pushed up through the lymph ducts toward the heart. The control unit contains a pump, a valve system, and a distribution header, as well as a timing circuit. PERCUSSORS Lung congestion can sometimes be difficult for a patient to clear. Percussors aid in this by delivering a “thumping” motion to the chest wall, which helps to loosen mucus in the lungs (Figure 8.55). SUMMARY This chapter dealt with equipment for the care of neonates including bilirubin therapy systems, incubators, and resuscitators plus a section on N2O delivery units. Skin, bones, and miscellaneous were covered in the rest of the chapter, including electrosurgery unit history, theory and applications, surgical laser types, and cryosurgery. 282 Introduction to Biomedical Engineering Technology Microscopes and especially operating microscopes were discussed, with sterilizers and physiotherapy equipment rounding out the section. QUESTIONS 1. How is bilirubin broken down? 2. Why is it important to measure light output during bilirubin light therapy? 3. List some features of incubators that help maintain a suitable environment for neonates. 4. Why are electrosurgery units used? What are the benefits of using an electrosurgery unit? 5. What is the difference between monopolar electrosurgery and bipolar electrosurgery? 6. Why are lasers used for some surgeries? 7. What are some advantages and disadvantages of using liquid nitrogen for cryosurgery? 8. Why is the magnification of operating microscopes limited? 9. How do interferential therapy devices work? 10. How are sequential compression devices used to aid the lymphatic system? 9 HTMT Work OBJECTIVES FOR THIS CHAPTER • To examine some of the duties and responsibilities of HTM technologists and the range of their employment opportunities. • To discuss the importance of electrical safety and electrical safety testing. • To review other workplace safety considerations. • To outline some troubleshooting techniques. OVERVIEW HTM technologists (HTMTs or BMETs) can work in a wide variety of jobs. Many will be part of an in-hospital HTM department, large or small, but others will work for outside companies providing support to hospital equipment or doing repairs and calibrations off-site. Equipment vendors and manufacturers need skilled people to do bench repairs of equipment under warranty, to install new technology in hospitals, or to provide technical expertise to sales teams. Being part of the team researching, designing, and building new devices is an exciting and challenging option. The Armed Forces have hospital equipment that needs support and may provide their own training programs for biomed techs. Finally, there is a need for people with a talent for education, to teach biomeds in model-specific factory training courses, or in the many educational institutions that have HTM programs. This chapter will focus mainly on the work of biomeds in hospitals; the other areas of employment are almost too broad and varied to describe in any useful detail. ELECTRICAL SAFETY One of the original, primary functions of HTMTs in hospitals was to ensure that electrical devices that might come in contact with patients were not going to kill them. Electrical safety was big, partly because equipment design was not as closely regulated as it is now, and partly simply because it was an easy target. Almost anyone could design, build, and sell equipment to hospitals, and these devices might not have adequate grounding, they could be designed with very “leaky” components, or they could have potentially lethal output settings. The whole issue was exacerbated by a coincidental convergence of engineering and physiology. Power plant and grid designers throughout the world found that alternating current with a frequency of 50–60 Hz was effective for distributing electricity to customers. Medical researchers discovered that many functions of the human body, such as the vital beating of the heart, were mediated electrically. Experiments showed that outside electrical stimulation could disrupt the electrical signals in the heart, causing it to enter into a state of uncoordinated contractions. In this state, DOI: 10.1201/9781003140603-9 284 Introduction to Biomedical Engineering Technology called ventricular fibrillation, the heart no longer pumped blood, and death soon followed. Different frequencies of electricity were found to have differing effects, and testing showed that the most dangerous frequencies, those that were most likely to cause fibrillation, were from 50 to 60 Hz. Fate has conspired to make the most common form of electricity also the most dangerous. Hospital administrators were terrified of having patients electrocuted while in their facilities, and since testing for electrical safety was fairly simple, programs were put in place to rigorously check every electrical device as it entered the hospital and on a regular schedule thereafter. Hospital wiring, too, was subject to scheduled tests to ensure safety. Modern building codes and precise, well-designed manufacturing standards for medical equipment have made it so that it is very rare to find a new device that has inadequate grounding or excessive electrical leakage. Electrical safety is still a concern, however, since failures can occur in equipment, especially as it ages, and especially if it is subjected to harsh conditions. These failures can include those that can reduce grounding effectiveness or increase electrical leakage. When repairs or modifications have been made to equipment, testing should be performed to ensure that safety systems have not been compromised. There is a variety of medical device regulations and standards involving medical device safety, including electrical safety that are directly relevant to health technology management. They describe the construction and operation considerations that must be met to ensure device safety and efficacy, as well as testing methods that are to be followed in both manufacturing and ongoing preventive maintenance (PM). Some of the major regulations and standards are described in Chapter 13. The overall topic of health technology management is covered in Chapter 12. RATIONALE As described above, the common 50 or 60 Hz line power found in most areas of the world is the most dangerous in terms of causing fatal disruptions in cardiac rhythms. When line-powered electrical equipment is used with patients, there are two factors that must be present for harm to occur. • There must be a source of electrical current that can come in contact with the patient through an exposed surface. • There must be a pathway, or sink, for that current to flow through the patient to complete a circuit. • Current sources can result from a number of reasons. • Equipment may be built with components that have high intrinsic leakage, such as some transformers and capacitors. This leakage can find its way to patient contact surfaces. • Circuit design may bring current pathways or components together in such a way as to produce capacitive or inductive coupling to patient contact surfaces. • Components or conductors may connect with patient contact surfaces through improper design or through warping or breakage of structures. 285 HTMT Work Current pathways are mostly to various ground points, such as through the grounded chassis of another electrical device, through the grounded frame of a hospital bed, or through plumbing fixtures. If only one fault is present, no harm will result, but testing should catch single faults before there is a chance of the second fault occurring. TESTING METHODS Electrical safety testing of medical equipment must include measurement of grounding resistance, and of electrical leakage under various conditions, including power to the device being on or off, ground wiring being open or closed, and the hot and neutral supply wiring of the device being normal or reversed (Figure 9.1). FIGURE 9.1 Fluke ESA 620 electrical safety analyzer. (Courtesy of Fluke Biomedical.) FEATURES OF THE FLUKE BIOMEDICAL ESA620 ELECTRICAL SAFETY ANALYZER The ESA620 Electrical Safety Analyzer represents the next generation in portable, manual electrical-safety testers for the biomedical technician and clinical engineer that are performing tests on medical equipment. With selections of three test loads, protective earth test currents, and two insulation test voltages, this versatile product can be used worldwide to test to their standard of choice: IEC60601-1(partial), ANSI/AAMI ES60601, IEC62353, VDE 751, ANSI/AAMI ES1:1993, NFPA-99, AN/NZS 3551, and IEC61010. This multifaceted device performs all primary electrical safety tests, including mains voltage, protective earth resistance, insulation resistance, device current, earth, chassis, and patient leakages as well as several additional leakage 286 Introduction to Biomedical Engineering Technology tests to comply with EN62353. It comes with standard test leads for two-wire protective earth measurements, and with optional leads offers the time-saving four-wire technique. Additionally, the 20-A-device receptacle allows for testing of those devices that need it, so the technician is not limited to only test 15-A equipment (US only). New DSP technology offers better accuracy of leakage measurements throughout the ranges specified in the standards, and an intuitive interface guides the user through tests. The ESA620 features a large display to facilitate quick and clear indication of performed tests, criteria associated with test set up, device under test (DUT) receptacle conditions, and results. Equipped with 10 ECG posts, the ESA620 offers simulation of ECG and performance waveforms so both electrical safety and basic tests on patient monitors can be performed with a single connection. The unit is equipped with a standard USB interface for computer control and data transfer. When used with optional Ansur computer-based software plug-in, the ESA620 allows for standardization of test procedures, as well as result capturing, storage, and printing of reports. When combined with Ansur, the ESA620 becomes automated, capturing results and comparing them to standard limits, essentially enabling this manual unit the sophisticated performance of the high-end models at half the price. Key Features • • • • • • • • • • • • • • • • • • Compliance with multiple standards Three test loads Expanded leakage ranges through 10,000 µA AC-only, DC-only, and True RMS leakage readings 100% and 110% mains voltage for mains on applied part (lead isolation) test Five different insulation tests DSP filter technology 20 A equipment current More applied parts selections ECG and performance waveforms Improved user interface Easy-to-use applied parts (ECG) connections Insulation posts on applied parts connections Two- or (optional) four-wire ground wire resistance Large display with adjustable contrast Ergonomic design Optional Ansur plug-in software CE, C-Tick, and CSA for the United States and Canada certification Source: Fluke Biomedical. HTMT Work 287 If the device includes conductive components that normally come in contact with patients, such as ECG leads or defibrillator paddles, the leakage from these must be tested as well. Leakage between ECG leads can be dangerous, and so should be included in the testing process. Grounding and leakage testing can be done using appropriate bench test devices such as digital multimeters, but testing is made much more convenient using a specially designed electrical safety testing unit. Ground continuity is a simple measurement, though the test equipment must be able to measure low values of resistance. Typically, ground resistance is required to be less than 100 mΩ, so testing equipment must be accurate at these levels. (Note: the actual ground resistance limit may vary depending on national, local, or institutional standards.) Electrical leakage measurement is somewhat more complex. A sensitive meter could measure the total leakage current produced by a device by simply connecting it between the device and ground. Human beings have a characteristic impedance, however, and for measurements to be relevant, they must be made through a load that has an impedance approximately equivalent to that of the human body. Typical “patient loads” are a resistor–capacitor network that has been designed to simulate body impedance. Electrical safety testers, or analyzers, have been designed to streamline the testing process. They include circuitry to measure ground resistance both through the ground wire of the device being tested (sometimes referred to as the DUT) and through its chassis with the ground wire disconnected. A switch or an internal relay can open or close the ground connection. Ground resistance is usually measured using a double wire circuit that is designed to eliminate the resistance of test leads and contact points from the measurement. Safety analyzers also have a built-in patient load, which is used in conjunction with a micro-ammeter circuit to measure electrical leakage. Switches or relays can open or close ground, open or close the neutral supply line, or switch the hot and neutral supply lines. In order to facilitate measurements from ECG leads, testers have a set of contact posts that can accept a variety of common lead connectors, usually color coded and labelled. The power cord of the device being tested is plugged in to an outlet in the tester. Analyzers have a common display for the various parameters being measured and for set up and self-test information. Some extra features that analyzers may have include: • Circuitry to measure the current being drawn by the test device. • Measurement of line voltage. Some units can monitor line voltage over time to help detect line fluctuations, voltage spike, or other anomalies in supply that may affect instruments. • An internal clock, which is used in conjunction with test result printing. • A printer port, for test results. • A data communications port or wireless capability to connect to a computer, to allow test result transfer and computer control of test functions. 288 Introduction to Biomedical Engineering Technology • Automated routines for common testing situations. User-developed routines may be accommodated. • A bar code scanner or other input devices to identify the individual device being tested. This information would then form part of the test results and may be used to determine what type of tests are to be performed. Some systems work in conjunction with an equipment management software package to collect and organize test results and to schedule PM testing. Two large boxes—or rather, one large box and one huge box—were sitting in the middle of the floor when Joe arrived for work in the morning. Mike, who started early, swivelled in his workstation chair and waved a greeting. “The VSM arrived this morning, in case you didn’t notice.” “Thanks, Mike—I might have tripped over this stuff if you hadn’t warned me.” “No problem!” Joe hung up his jacket and logged on to the network, quickly checked for e-mail messages, then turned to the two boxes and retrieved the shipping paperwork and purchase order copy that were taped to the side of the smaller box. He grabbed a box cutter from his toolbox and sliced the boxes open. The smaller box had a packing slip inside, which he placed with the other papers. Opening the larger box, he pulled out another box from inside, and then retrieved a shiny metal tube. Underneath was a six-wheeled device set into a Styrofoam form. Joe pulled the six-wheeled unit from the Styrofoam and then opened the box that had been inside the first, large box. Inside this box were a wire basket and a plastic bag with a few items of hardware inside. He located a large hex-head bolt and washer, and then inserted the metal tube into a hole in the six-wheeled base. Flipping the assembly upside down, he threaded the bolt through a hole in the base and into the tube, tightening it with a socket wrench. Then he uprighted the stand and found the hardware to attach the basket to the middle section of the metal tube. He then turned his attention to the smaller of the original two boxes, referring to the packing slip and checking off the contents. The largest item was the vital signs monitor itself, but there was also an AC power cord, a battery, an SpO2 cable and sensor, a thermometer probe and several boxes of probe covers, an NIBP hose and one each of three different sizes of BP cuffs, a few rolls of recording paper, a quick-reference card, an operator’s manual, and a service manual CD. Joe affixed the monitor onto the stand and connected the various cables, then inserted the battery into its compartment, finally plugging in the AC cord. He noted that the AC power indicator and battery indicators both illuminated and that the monitor completed its power on self-test successfully. He knew it would take several hours of charging to ensure that the battery was fully charged, but he could complete some of the incoming inspection processes while it was charging (Figure 9.2). HTMT Work 289 FIGURE 9.2 Vital signs monitor on stand. Before beginning the tests, he noted the serial and model numbers of the unit, affixed an equipment control number sticker, and entered the information into the equipment database program. He unplugged the unit, rolled it closer to the test bench, and started the test device interface program on the laptop there. First test was electrical safety, so he plugged the AC cord into the safety analyzer and clipped the test cable to the ground pin on the back of the monitor. He selected the basic test routine on the laptop, which was connected to the safety analyzer through a serial cable, and started the tests. Relays clicked and the AC LED flickered on and off as the analyzer measured the line cord resistance, and the AC leakage current under several different conditions, including ground open and line/neutral reversal. The test results were logged automatically by the controlling laptop, and then sent over the network to the central server that held the equipment management database. Once the safety tests were completed with no warnings, Joe went on to the performance tests. First on that list was the SpO2, or pulse oximeter, tests. As with all the testing equipment, the SpO2 analyzer was connected and controlled through the laptop, with test results being fed to the equipment management database. The analyzer consisted of a box with an LCD display and a finger-like projection. Joe fitted the SpO2 sensor over the finger simulator, selected the specific manufacturer of the probe, and started the test process. The unit simulated various SpO2 percentages at several different perfusion levels as well as 290 FIGURE 9.3 Introduction to Biomedical Engineering Technology NIBP analyzer. (Courtesy of Fluke Biomedical.) producing motion artifacts to check the stability of the monitor. Joe entered the readings from the monitor when prompted by the test program. Next up, temperature tests. The temperature tester was one of the few test devices not integrated into the computerized system, being simply a calibrated, temperature-controlled well into which the probe was inserted. Two different temperatures could be selected, though it took several minutes to switch between the two due to thermal inertia. Joe placed a probe cover on the probe to ensure accurate measurements and inserted the probe. While he was waiting for the temperature reading, he connected the NIBP hose to the monitor and attached the normal adult cuff (Figure 9.3). By then the temperature reading was available, and he entered it manually into the testing program. He switched to the alternate temperature on the unit and went on to the NIBP tests while the temperature tested stabilized at the new setting. A T-fitting went between the cuff and the hose, with one arm of the T connecting to the NIBP analyzer. The cuff was wrapped around a plastic device that was a stand-in for a patient’s arm, and the test initiated. A pump internal to the analyzer inflated the cuff to a pre-set level and then pneumatic circuitry simulated the oscillometric variations of blood pulsing through a patient’s brachial artery while the pressure in the cuff is slowly bled off. Systolic and diastolic waveforms are simulated, and when cuff pressure drops a certain amount below diastolic, all pressure is released. The monitor calculates systolic, diastolic, and mean pressures as well as pulse rate, and Joe enters these values into HTMT Work 291 the program. The test is repeated at several different pressures, checking that high and low alarms are generated at appropriate pressure values. Once the NIBP tests are complete, the temperature tester has stabilized and Joe rechecks the temperature. Joe initiates a recording of measurements and visually checks the recorder for clarity and smooth operation. After the testing is complete, Joe closes the program and disconnects all the accessories. He then tidies the unit, coiling cords, and hoses carefully, then affixes a sticker indicating that the unit has been tested by biomed and is ready for use. He rolls the unit to the side and plugs it into AC so it can finish charging the battery overnight. In the morning, he will wheel it up to the ward where it will be used. OTHER SAFETY CONSIDERATIONS Electrical safety is only one aspect of overall safety in a hospital setting. FIRE SAFETY As in any building, fire safety is important. Staff members need to know fire alarm sounds and codes, fire extinguisher locations (Figure 9.4), fire response protocols, and fire escape routes. Hospital staff members may be assigned specific duties for patient evacuation in case of fire or other disaster. Typically, new employees are given fire safety training; this may be repeated on a scheduled basis. CHEMICAL SAFETY Biomed staff may come in contact with hazardous chemicals during the course of their work. They should be familiar with the variety of chemicals in their workplace, and with the hazards associated with each. Material safety data sheets (MSDSs) should be available in every area for each hazardous chemical found in that area; staff should know where the MSDS information is located (Figure 9.5) and be familiar with the characteristics of the chemicals. FIGURE 9.4 Fire extinguisher. 292 FIGURE 9.5 Introduction to Biomedical Engineering Technology MSDS sign. MSDS provides information about flammability, melting and boiling points, toxicity, health effects, first aid measures, chemical reactivity, requirements for protective gear, safe storage methods, spill or leak handling procedures, and proper disposal methods. MECHANICAL SAFETY BMETs may work with mechanical devices such as drills, grinders, and soldering irons. They should be familiar with the hazards associated with the devices they handle, and use proper protective equipment as necessary. Eye goggles or shields, gloves, masks, or ear protection may be required (Figure 9.6). FIGURE 9.6 Face shield and goggles. HTMT Work 293 INFECTION CONTROL Workers in any location can sometimes be exposed to infectious agents, but staff members in hospitals are especially at risk. Infection control manuals should be located in each department, and everyone should have infection control training and be familiar with the material in the infection control manual. Infection control is important to prevent illness in staff members but also to avoid transmission of illnesses to and between patients. Various means are used to help control infections. Face masks prevent many infectious agents from moving in or out of the respiratory system (Figure 9.7). The mask should fit snugly around the mouth and nose and be secured so that it will not fall off or slip down inadvertently. Frequent handwashing and the use of alcohol-based hand cleaners are important, especially before entering and when leaving a patient care area (Figure 9.8). Gloves should be used when there is a possibility of hand contact with infectious agents, patients, or sterile fields (Figure 9.9). Some equipment may have infectious material on outer or inner surfaces, in which case proper precautions must be followed. If at all possible, contaminated equipment should be sent to the hospital’s central processing area for cleaning and disinfection. Certain areas of the hospital will require special infection control techniques to be implemented by staff members before they enter the area. Such areas include isolation rooms where patients are known to have a contagious disease; special procedure areas, such as endoscopy rooms; maternity delivery rooms; operating rooms; and sterile material handling areas. Precautions may include the use of special foot coverings, head covers, and gowns, or staff may need to change in to “OR greens,” perform surgical handwashing (Figure 9.10), and wear head coverings, face masks, and surgical gloves. FIGURE 9.7 Surgical mask. 294 Introduction to Biomedical Engineering Technology FIGURE 9.8 Hand sanitizer station. FIGURE 9.9 Surgical glove. 295 HTMT Work FIGURE 9.10 Handwashing at an OR wash station. Some special areas may require even more stringent infection control methods. Staff should be familiar with the infection control requirements for the various areas of the hospital in which they may be working. If uncertain of the requirements for a particular area, nursing or other staff members will usually be willing to explain the procedures. Cleanup of biohazardous material spills should be performed by staff members trained in proper procedures and using appropriate materials and instruments. Generally, biomed techs should avoid such spills and call cleaning staff. SHARPS SAFETY The hospital environment contains many items that can cut or puncture skin, including hypodermic needles; scalpels; scissors; broken glass; and slivers of metal, wood, or plastic. These hazards should be handled in a safe manner, usually described in a policy and procedure or safety manual. All areas of the hospital should have “sharps” containers that are specially designed to safely contain sharp hazardous objects until they can be disposed of properly (Figure 9.11). Such containers should be clearly marked with warning and instruction labels. PERFORMANCE ASSURANCE For any device, the user wants it to function properly whenever it is used. When a device is used in the care of a patient, proper function is even more important and may be life critical. Effective performance assurance (PA) testing is the best means of ensuring that a given device will function as intended when it is called into use. (Note: The term “performance assurance” may be used interchangeably with or instead of “preventive maintenance,” though PA is usually more comprehensive.) Most manufacturers provide a recommended PA procedure, and while such procedures are very thorough, they often include steps that are not critical to end-user 296 Introduction to Biomedical Engineering Technology FIGURE 9.11 Sharps container. performance. To complete full manufacturer-recommended PA tests on a regular basis for all patient-care equipment would probably require that most biomed departments be quadrupled in size. However, the manufacturer’s guidelines can be used as a basis for a streamlined PA test procedure that still ensures proper performance. Some such procedures may be generic, for example, they may apply to all battery-powered defibrillator monitors, while others may be model-specific. Less critical equipment might only need a visual inspection and an electrical safety test. PA test procedures can be developed in-house if done carefully. If a biomedical engineer is on staff, they should be involved in the process of not arranging it entirely. PA procedures may be available through third-party sources as well. The developers of equipment control software such as Fluke Biomedical’s “Sentinel—Infinity” package or ECRI’s “Health Devices IPM System” may have PA procedures included, as well as the facility for developing user-specific procedures (see Chapter 13). It is important for both equipment management and legal purposes to keep clear, accurate, and accessible records of PA test results. If, for example, a patient is injured during a course of treatment, a lawsuit may result, in which case it may need to be shown that proper procedures were followed to ensure safe and adequate equipment operation, for any devices that were used with that patient. When performing PA tests, the technologist must have a good understanding of both the theory of operation of the DUT and also the way in which the device is used with patients and any relevant physiological or anatomical effects. This gives more meaning to the tests and also enables the technologist to better evaluate test results. There may be more than one PA test for a particular device; a shorter version to be repeated on a shorter schedule, and a longer version that is used for less frequent major tests or after significant repairs, or when the device is first received in the hospital. A separate “incoming inspection” procedure may be used, as well. 297 HTMT Work Joe Biomed sat at his workbench looking at two old Baxter 6201 infusion pumps (Figure 9.12). One had come down to the lab with a note saying “Won’t hold a charge,” while the other had been giving an error message that indicated the interface board needed to be replaced. Joe had performed both repairs the day before, a quick battery change for the first unit and a longer, more involved job of replacing one of the major circuit boards in the second pump. Because the battery change was a minor repair and the pump appeared to be in good condition, Joe ran it through a quick electrical safety test and then connected it to an IV pump tester (Figure 9.13). He purged the tester by allowing free flow of IV fluid through the test device, and then he threaded the IV tubing into the pump mechanism. Finally, he turned the pump on and programmed rate and volume-to-be-delivered settings into the pump. He first checked the flow rate of the pump as a few different flow rate settings, and then used the tester’s “occlusion test” function to check that the pump alarmed properly when the IV tubing was blocked. Finally, he started the pump at a medium flow rate and injected a measured bubble into the IV tubing above the pump and checked to see that an alarm sounded when the bubble entered the pump. Following this, Joe removed the tubing, put a sticker on the unit indicating when it was tested, and put it out for return to its home. With the second pump, a major repair had been completed, so a more thorough test was called for. Joe repeated the basic tests that he had performed on the first pump, and then pressed a combination of keys on the pump’s keypad to FIGURE 9.12 Baxter 6201 IV pump. 298 FIGURE 9.13 Biomedical.) Introduction to Biomedical Engineering Technology Fluke Biomedical IDA5 infusion pump analyzer. (Courtesy of Fluke enter a test mode. In this mode, internal circuitry measured the upstream and downstream occlusion sensors and the air-in-line sensor and displayed unitless values on the LCD displays of the pump. Consulting the service manual for the pump, Joe noted the readings were within specifications. He then placed a Baxter calibrated metal disk in the upstream occlusion sensor and noted the change in readings, again within spec (Figure 9.14). A repeat of this process with the downstream occlusion sensor was followed by a test in which an air-filled section of calibration was placed in the air-in-line sensor, then a water-filled section. Readings were noted for each step and compared to specified values. With all tests in order, Joe labeled the second pump and took both to the central pump storage area where they were cataloged and plugged in, ready for use. Returning to the lab, Joe entered the work he had just done in the department’s equipment control database (Figure 9.15) and went on to his next task. 299 HTMT Work FIGURE 9.14 Baxter 6201 pump showing pumping mechanism. FIGURE 9.15 Data entry—the end of a job. 300 Introduction to Biomedical Engineering Technology TROUBLESHOOTING TECHNIQUES Successful troubleshooting is the key to being able to diagnose problems and perform the right repair, returning the device in question to service as quickly as possible. Good troubleshooting requires an organized approach, knowledge of specific troubleshooting techniques, and thorough familiarity with both the theory of operation, the construction, and the proper use of the device in question. A calm and relaxed approach is always much more successful than a stressed-out panic method. Keep in mind that most problems are not as serious as they might first appear. Troubleshooting in general has moved away from component-level diagnosis to more board or assembly diagnosis. It may be more expedient and in the long run more economical to replace a board or assembly than to try to isolate and replace a single faulty component (Figure 9.16). Fewer and fewer discrete components are being used in circuit design, and replacement of individual ICs is often difficult or impossible. Multilayer circuit boards and surface mount technology require special tools for repair, if that is even deemed worthwhile at a factory depot. Manufacturer service information often doesn’t include component-level diagrams, descriptions, or parts lists, further adding to the difficulty of trying to go to the component level. Some circuitry may still lend itself to component-level troubleshooting and repair, however, so such skills should not be abandoned. Step zero may be to determine if the device is covered under any kind of warranty or service contract. If so, and the problem appears to be a real one, the problem is solved from your perspective. Ship it out and let the manufacturer fix it! Otherwise… The first step in troubleshooting is to gather as much information about the failure as possible. This includes asking whoever was using the device about the conditions that FIGURE 9.16 Troubleshooting a PC board. HTMT Work 301 were present when the failure occurred. Did the unit make any noises, was there a smell or smoke? Were any codes or trouble lights displayed? What accessories were being used with the equipment? If possible, get the accessories! Was there anything else unusual just before the failure occurred? What other equipment was being used at the time? This information is often impossible to obtain, as either users don’t recall or didn’t notice details, “Someone else was using the equipment and they are on night shift/ away on vacation/died.” Or nobody knows what happened or when. Equipment will often arrive for repair with a scrap of paper taped to it saying, “Broken.” Step two involves reviewing information about the device. It may be something you work with often and know the common problems almost automatically, or it may be a device you have never seen before. If a service manual is available, it can be consulted. Are there troubleshooting tables or flowcharts? Error code tables? Detailed and useful descriptions of the theory of operation? Sometimes the problem you are seeing is described in plain language in the manual, along with an outline of the steps needed to solve the problem. On the other hand, service manuals may provide very little useful information for troubleshooting. They may have tables that describe 100 other problems but not yours, or they may recommend solutions that don’t work. Service manuals are often written by someone who knows the equipment inside out but can’t put themselves in the place of someone unfamiliar with the device. Service manuals may not be available, too. They may have been lost, or the equipment vendor may not have supplied them. In this case, your own troubleshooting skills come in to play. Step three is to try to duplicate the problem. Some problems are intermittent, and just as your car never makes that funny noise when you take it to the garage, intermittent failures never seem to occur when you are testing a device in the lab. Try to recreate the conditions under which the failure occurred, insofar as these are known. Patience and a methodical approach help to reach this goal, and some techniques only come with experience. If and when the problem crops us again, note in as much detail the conditions preceding the failure, and any symptoms of the failure itself. You may find that the original user’s description was accurate, or it may be totally off base. In any case, repeating the failure in controlled conditions can provide vital clues as to the cause of the failure. It may not be possible to duplicate a problem. The device may be totally inoperative, or it may continue to run without apparent problems. In the latter case, you may have to decide whether or not to return the unit to service without doing anything further. Your judgment is called into play, but if you are unsure you might want to ask someone else or talk to factory service personnel. If the device is high risk, it may be prudent to arrange to have it returned to the manufacturer for testing and possible repair. If they can’t find a problem, it is then their responsibility of the device is returned to service and the causes problems. Sometimes a call to the manufacturer’s tech support department can sidestep the normal troubleshooting process as well as avoiding having to send equipment in for repair. Tech support staff (usually) have a great deal of experience with the equipment in question, as well as a wealth of resources that may not be available to you. 302 Introduction to Biomedical Engineering Technology FIGURE 9.17 Telephone consultation. “ProArrest tech support, can you give me your name and institution, please?” “My name is Joe Biomed, I’m with Hippocrates General Hospital in Cardiac, Ohio” “Hi, Joe—just give me a minute to pull up your file. OK, are you at 4635 Purkinje Avenue?” “That’s me.” “Your case number for this call is 24-DG610, that’s delta golf. What can I help you with today, Joe?” (Figure 9.17) “I have a ProArrest defib, model QRS45, that has a blank display.” “Do you have the serial number and option codes for that unit?” “Yeah, the serial number is QRS45–16556, options GT5, GT9, and GT14.” “OK, so that’s the model with the LCD display, am I correct?” “Yes.” “And are you getting power to the rest of the system?” “Yep, all the LEDs come on and the recorder gives a normal trace.” “Do you have the unit in front of you, Joe?” “Well, behind me actually, and it’s powered up.” “OK, I want you to look at the display screen from the side. See if you can get any reflected light on it.” “Just a sec. Ah, OK, I can see the graphics very faintly.” “All right, what I think is happening is the backlight is gone, and usually that’s caused by a fuse on the display board, F6.” “Does that fuse feed any other circuits?” “No, just the backlight. I’m not sure why they put that in there, I think maybe some engineer spilled coffee on his circuit sketch and the smudge ended up as a fuse on the final board. In any case, the fuse is a 1 amp fast-blow glass, one and a quarter inch, so once you get the case open, replacing it is a cinch.” “Yeah, getting the case open—I remember those 600 screws.” “Overkill, I agree. Engineers—can’t live with them, don’t have a job without them. Do you want me to hold while you check it out?” “No, that’s OK, I’ll call back if I run into any problems.” 303 HTMT Work “All right. My name is David, but all the notes from this call are on file, so just give the case number and anyone should be able to help. Can I do anything more to assist you today?” “No, that should do it, all those screws will keep me busy for a while. Thanks, David.” “No problem. Thank you for calling ProArrest tech support, you have yourself a nice day.” With an inoperative device or if its operation is very erratic, you may need to go on to the next step… after checking to be sure a good power cord is plugged in and any accessible fuses are intact. Oh, and that the power switch is turned on. In step four observe whether the case of the unit is smashed, which can be a good clue that it was involved in an accident (even if the end users deny this possibility), and further you may need to look for internal damage. Check the external of the device carefully for signs of damage, fluid entry, overheating, or tampering. Opening the case and looking for obvious signs is next, and an experienced nose can often diagnose a problem simply by smelling the inside of the box. A fried resistor has a distinctive odor. Components may be obviously burned or discolored from overheating, or circuit board traces may be vaporized. Physical shocks can cause heavy components like transformers to pull loose from their normal locations, and liquids entering the device can leave obvious signs of corrosion or shorting. Some devices may have internal fuses that can be checked for continuity (Figure 9.18). Replacing a burned out component may solve the problem, but often this is only a symptom of the underlying problem. Sometimes replacing the component and powering up the unit can give further clues, if the bad part wasn’t the actual problem. Service manuals may provide good troubleshooting guides that take you methodically through the system, checking various things such as voltages or waveforms at test points (Figure 9.19) or looking for specific responses from the device. In this case, the problem will usually become apparent eventually. FIGURE 9.18 Testing a circuit board. 304 Introduction to Biomedical Engineering Technology FIGURE 9.19 Fluke Biomedical 190M-4 Medical ScopeMeter. (Courtesy of Fluke Biomedical.) FIGURE 9.20 Component analyzer. If no useful troubleshooting information is available, you may have to work through the circuit on your own. If possible, identify the power input section and power supply. Check for voltages—they may be marked on circuit boards, or you may be able to make an educated guess as to what voltages should be at various points in the circuit. Check switches for continuity and also power supply transformer windings. If there appears to be no power coming from the power supply, it may need to be replaced. HTMT Work 305 Simple component faults can sometimes be diagnosed using a multimeter or component analyzer (Figure 9.20). A faulty component can be replaced if parts are available, but again this may only be a symptom of another problem. On the other hand, replacing a bad diode may be a miracle cure. If no individual component faults can be found, the next step may be called for. In step five check whether spare circuit boards or other assemblies are available for the device and if all other troubleshooting has failed to find the problem, you should try to replace boards/assemblies one at a time, beginning with the one you feel is most likely to be the source of the problem. A power supply board is a good place to start. If no spare boards are available, you may want to order them, but this is a judgment call. Unless you are sure that a particular board is causing the problem, you may just be extending the downtime of the equipment by such slow experimentation. Also, if circuit boards or assemblies are very expensive and the device itself is not, or if it is old and/or in poor condition otherwise, it may be more prudent to simply retire the device and tell the originating department that a new machine must be purchased (Step last!). The advice of a senior staff member or the head of the originating department may be in order; whoever holds the purse strings. In step six, if, after following all courses of action available to you the device is still not working, you may opt to send it to the manufacturer or approved repair facility. For large devices that are impractical to ship, an on-site service call would be required. Step six also means that you must hang your head in shame for the rest of the day and place a large red “F” (for failure) on the back of your lab coat. (Just kidding, of course—some problems are just not practically solvable in the lab.) ELECTROSTATIC DISCHARGE Semiconductor devices are vulnerable to damage by electrostatic discharge (ESD). This damage may or may not cause immediate failure; if not, it may be cumulative, resulting in failure at some point in the future. Failures caused by electrostatic shocks can be very expensive to repair and/or may result in extensive equipment downtime. Every precaution must be taken to prevent ESD damage. Newer semiconductors and circuit designs have increased the resistance of equipment to ESD damage, but precautions must still be observed. Components and circuit boards or assemblies that are vulnerable to ESD are shipped and stored in conductive plastic bags and/or with conductive foam sheets. These measures must be left in place until the part is about to be used. When working on any device that may be damaged by ESD, one should wear an effective grounding wrist strap. These straps are connected to ground through a high-value resistor, which bleeds static electricity harmlessly to ground (Figure 9.21). An antistatic desk mat is valuable as well; it will have a grounding connector like the wrist strap, with a resistor in line. Antistatic floor mats and grounded work-chairs can further ensure protection. 306 FIGURE 9.21 Introduction to Biomedical Engineering Technology Antistatic wrist strap in use. SUMMARY Safety, electrical and otherwise, was one focus of this chapter. Other topics covered were PA, troubleshooting techniques, and ESD. QUESTIONS 1. Explain how extraneous electrical currents can affect the heart. 2. What frequency range of electrical impulses is most likely to produce ventricular fibrillation if a person were to receive an electric shock? 3. What two factors must be present for harm to come to a patient from electrical devices? 4. What are some possible fault current sources? 5. What parameters are tested for with electrical safety testing? 6. Why is the design of the patient load in electrical safety testing important? 7. What kind of information is provided with MSDS? 8. What precautions must a hospital employee take before entering the OR? 9. What are the general steps in troubleshooting? 10. Why are grounding straps important when working on electronic devices? 11. How does a grounding strap or antistatic mat prevent ESD? 10 Testers and Tools OBJECTIVES FOR THIS CHAPTER • To review the variety and functions of test equipment and tools used in the course of BMET/HTM work. INTRODUCTION A wide variety of test equipment is used in supporting medical equipment, and it is critical that the test devices provide accurate measurements. To ensure accuracy, test equipment should be calibrated on a regular basis, typically once a year. Calibration should be done by qualified personnel using equipment whose own calibration can be traced to a reliable standard that is recognized by the regulating authorities in your area. Calibration records must be made and stored carefully. GENERAL TEST EQUIPMENT Much of the test equipment used in a biomed lab is the same as that used in any electronics repair shop, though it may tend to have somewhat higher specifications (Figures 10.1 and 10.2). DIGITAL MULTIMETERS An indispensable tool, a quality digital multimeter (DMM) performs a number of measurements (parameters will vary by model): • • • • • • AC and DC voltage and current Resistance Semiconductor junction state (working, open, or shorted) and polarity Continuity, indicated by a measured value and a tone Frequency Capacitance Some models select the proper measurement range automatically, while others must be switched manually. Measurements may be logged, high and low values recorded, and an interface to other devices may be included. A wide variety of attachments and special probes are available. These may allow the unit to measure temperature or humidity, high voltages, or current without direct contact. Some probes have very fine pincer tips that can connect to points on circuit boards without causing shorts (Figures 10.3 and 10.4). DOI: 10.1201/9781003140603-10 308 FIGURE 10.1 Introduction to Biomedical Engineering Technology Digital multimeter with high-voltage probe. FIGURE 10.2 Close up of DMM. OSCILLOSCOPES An oscilloscope is a device that can display a graph of voltage versus time. This is used to measure the signals found in electronic devices for troubleshooting or calibration. Oscilloscopes have a wide range of capabilities and may be specialized for particular applications such as television, radio, computer networking, or various industrial uses. Scopes commonly used CRT displays, but LCD displays are now almost universal. They can be cart mounted, rack mounted, or even hand-held. The latter may have some of the functions of a DMM included; these are referred to as “scopemeters” (Figure 10.5). Testers and Tools 309 FIGURE 10.3 DMM with noncontact current probe. FIGURE 10.4 A few other types of probes. FIGURE 10.5 Fluke Biomedical 190M Medical ScopeMeter® portable oscilloscope. (Courtesy of Fluke Biomedical, USA.) 310 Introduction to Biomedical Engineering Technology FEATURES OF THE FLUKE 190M MEDICAL SCOPEMETER • Fast and easy • Connect-and-view automated capture of complex waveforms: simplified connect-and-go for longer time-based measurements • Memory save and recall set-up • Waveform compare for quick and easy pass/fail • Single-button user interface very intuitive and easy to navigate • 3-in-1 multimeter, portable oscilloscope, and paperless recorder save you time and tools SIMPLIFIED DATA ANALYSIS 190M offers functions specifically designed to make data analysis easy. Waveform compare: 190M stores ideal waveforms for overlay against measured waveforms, giving you instant pass/fail indication. TrendplotTM paperless recorder: intermittent faults are common and can be the toughest to find and analyze. Fluke 190M handheld oscilloscopes can record any combination of voltages, amps, temperature, frequency, and phase for up to 16 days to pinpoint intermittent faults. 100-screen replay: with other scopes, it’s frustrating to see a one-time anomaly flash and miss it. The Fluke 190M portable oscilloscope solves the problem with a touch of the replay button. 190M Medical ScopeMeter® portable oscilloscope is used in medical applications. Fluke 190M ScopeMeter® portable digital handheld oscilloscope’s highresolution non-interlaced video provides the best image quality for detailed analysis of video information on any user-selected video line. Smart averaging gives the averaged waveform over successive acquisitions, reducing noise in the displayed waveform. Thanks to smart averaging, you can now also see an incidental curve of a different wave shape with no effect on the averaged curve. Thanks to smart averaging, the 190M digital handheld oscilloscope gives an immediate response when the signal makes large changes, for instance when probing around different test points, while retaining the benefits associated with averaging. mAs is a critical measurement in X-ray-based medical imaging, and having it incorporated in a multifunction tool allows for great efficiency. 190M can measure directly the amount of current flowing through the X-ray tube. Digital persistence mode is most beneficial when working on complex and modulated signals, and for displaying the envelopes of pulsed RF carriers, like those encountered in MRI systems. Independent referencing is critical for complex medical imaging systems, where timing and synchronization issues can cause multiple failures. Without Testers and Tools 311 this capability, the source of these types of failures might be impossible to detect—meaning more unnecessary down time, repairs, or board changes. 190M digital oscilloscope technology enables you to take multiple, independent measurements simultaneously to track down the root cause of your most complex troubleshooting challenges. Source: Fluke Biomedical. A valuable feature of oscilloscopes is the ability to store waveforms. This can make waveform comparisons easier, and it also allows the capture of transient events. Associated with storage functions is a delay feature that can help to visualize short duration events that occur over a longer period. Color displays can help to differentiate between various signals being analyzed (Figure 10.6). An automatic set-up feature is useful when examining a wide range of signal types. The scope detects the signal to which it is connected and analyzes it to determine frequency and amplitude, and uses this information to set time and voltage scales to provide the best possible waveform. Some scopes can further analyze waveforms and perform various measurements, giving numeric values to such parameters as frequency, peak amplitude, rise and fall times, positive and negative pulse widths, and more. Learning to use an oscilloscope effectively is very much a hands-on endeavor, since features and special applications are so varied. Some manufacturers provide tutorials, which may even be built into the scope, to aid in learning how to use the unit. A specialized type of oscilloscope can be very useful in troubleshooting electronic components. This unit can apply specific signals to semiconductors and FIGURE 10.6 An older oscilloscope with CRT display. 312 Introduction to Biomedical Engineering Technology FIGURE 10.7 Component tester. some other components, and displays a graph of the response. Certain patterns are indicative of the state of the component being tested. A wide variety of semiconductors, capacitors, resistors, and inductors can be evaluated this way (Figure 10.7). Units may have a feature that allows the rapid alteration of views of two sets of probes, which means that a questionable component can be compared to a known good one. OTHER TEST EQUIPMENT A number of other devices may be useful in a biomed lab. These include • Sound level meters—to provide a quantitative measure of sounds in various situations (Figure 10.8). • Thermometers—used to check medical thermometers or to help locate overheating components. These may be stand-alone devices or a special attachment for a DMM. • Tachometers—to measure the rotational speed of equipment such as centrifuges. Tachometers may operate by physical contact by an optical sensor. • Oxygen analyzers—to measure oxygen concentrations in devices such as infant incubators, oxygen concentrators, and ventilators (Figures 10.9 and 10.10). • Manometers—for pressure or vacuum measurement in ventilators, NIBP units, and suction machines. SPECIALIZED BIOMEDICAL TEST EQUIPMENT Many types of medical equipment have specific parameters that need to be tested when doing PA tests. Test equipment manufacturers have designed units that integrate various functions so they can perform the necessary test quickly and accurately. These special testers may have a printer port for making had copies of test results, or a serial port and/or wireless capability for connecting to a computer, smartphone, or tablet. This may be used to interface the device with an equipment control program. Testers and Tools FIGURE 10.8 Sound level (dB) meter. FIGURE 10.9 Oxygen analyzer. 313 314 Introduction to Biomedical Engineering Technology FIGURE 10.10 A maxtec maxO2 oxygen analyzer showing oxygen cell and connecting cable. (Courtesy of Fluke Biomedical.) As with all test equipment, these devices must be calibrated to a traceable standard on a regular schedule. (Note: Electrical Safety Analyzers were described in Chapter 9.) ESU ANALYZERS Electrosurgery machines put out high-powered electrical signals that must meet specific performance criteria for effective surgical function; ESU analyzers measure these criteria (Figures 10.11–10.13). They include • • • • Power output—units selectable Current Peak-to-peak voltage Crest factor, which is a unitless value equal to the peak amplitude divided by the RMS value of a signal; it is a measure of the “purity” of the waveform • RF leakage, a measure of safety since leakage can cause patient burns if it is high • Return electrode monitoring system upper and lower threshold values Since the impedance of tissue when undergoing ESU activity can vary greatly, ESU testers provide a number of different test load values to simulate changing loads. Power output and other parameters should stay within specified limits for the various loads. Testers and Tools 315 FIGURE 10.11 Fluke Biomedical Model QA-ES II ESU analyzer. (Courtesy of Fluke Biomedical.) FIGURE 10.12 An older ESU analyzer, Fluke 454A. FIGURE 10.13 Fluke RF-303 ESU analyzer. (Courtesy of Fluke Biomedical.) 316 Introduction to Biomedical Engineering Technology FEATURES OF THE FLUKE BIOMEDICAL QA-ES II ESU ANALYZER The QA-ES II is the easiest way to test all critical ESU functions and wirelessly download results to a PC. Its user-friendly interface guides you through test sequences, making it quick to collect all measurements, including vessel sealing, contact quality monitor (CQM), high-frequency (HF) leakage, and output power distribution (single or continuous mode). • Test all critical ESU functions with precise power, current, frequency, crest factor, and load resistance ranges. • Collect measurements in single and continuous mode. • Connect wirelessly via Bluetooth for easy record retrieval without interference or limitation by cables and wires. • Automatic power distribution measurement, including power, current, peak-to-peak voltage, and crest factor. • All-in-one tool: All hardware and software necessary to complete preventive maintenance and troubleshooting is built into the unit, eliminating the need to purchase or transport additional cables, leads, switch boxes, and RECM box. • User-friendly interface: Large buttons and LCD screen guide the user through test sequences. • Memory storage of up to 5000 test records, eliminating the need to download data after the completion of each preventive maintenance or troubleshooting session. • Complies to all global standards, including ANSI/AAMI and IEC. MODES OF OPERATION • Continuous operation: Continuous measurement of power, current, peak-to-peak voltage (closed load only), and crest factor. • Single operation: Single measurement after the set delay time of the ESU output of power, current, peak-to-peak voltage (closed load only), and crest factor. • Power distribution: Tests impedance-sensing circuitry in “power guarantee functions in new-generation ESU.” Applicable parameters—power, current, peak-to-peak voltage (closed load only), and crest factor—can easily be observed during the automatic, sequential output energy measurements. • RF leakage current: Provides connections and load configurations to measure HF leakage from both grounded and isolated equipment. • RECQM: Test the “return electrode” control quality monitoring using the QA-ES internal loads. Source: Fluke Biomedical. Testers and Tools 317 INFUSION DEVICE ANALYZERS Infusion pumps must deliver fluids at a set rate and also meet safety requirements. Infusion device analyzers measure flow rates and total volumes delivered so these values can be compared to pump settings (Figures 10.14 and 10.15). FIGURE 10.14 Biomedical.) FIGURE 10.15 Fluke Biomedical Model IDA 4 plus infusion device. (Courtesy of Fluke 318 Introduction to Biomedical Engineering Technology FEATURES OF THE FLUKE BIOMEDICAL IDA 5 INFUSION DEVICE ANALYZER Ensure infusion pumps are tested accurately and quickly with the IDA-5 infusion device analyzer. The IDA-5 infusion device tester is a multichannel infusion pump analyzer based on sophisticated measurement technology trusted by biomedical professionals around the world for over 20 years. Unlike other infusion device testers, the IDA-5 has built-in automation allowing users to create custom test templates for quick, standardized testing of intravenous pump devices with minimal user intervention. This automation bundle includes Ansur software for comprehensive testing. • Tests up to four infusion pumps at the same time. • Customizable test templates for quick and standardized infusion device testing. • Compatible with virtually any type of infusion device. • Real-time snapshots of flow and pressure for immediate issue recognition. • Instantaneous and average flow measurement of up to 1500 mL/h. • Occlusion pressure measurements to 45 psi. • Single-flow, dual-flow (piggyback), and PCA testing. • Auto-start mode enables unit to begin testing only when fluid is detected to maximize accuracy. • Ability to automatically end flow measurement based on user-defined time, volume, or both. • Convenient and easy data entry with plug-n-play, USB compatible, keyboard, or barcode scanner. • Compatible with a wide variety of off-the-shelf printers. • Built-in memory to save test results for printing or downloading to computer. • Optional Ansur automation software completely integrates medical device testing including electrical safety, visual inspection, and other performance parameters for total digital data management. • Tethers with other Ansur-automated test devices for harmonized workflow and reporting. • Global support network delivering prompt service and peace of mind to Fluke Biomedical customers worldwide. Source: Fluke Biomedical. Many pumps do not provide smooth fluid flow, especially at lower rates. The flow can be intermittent, with rates averaged over time. A pump analyzer must be able to measure such intermittent flows and accurately determine average flow rates. Occlusion alarms are an important part of pump function, and testers have facilities for measuring pressures that are developed when an occlusion occurs. Testers and Tools 319 PHYSIOLOGICAL SIMULATORS Testing and troubleshooting physiological monitors are much easier if realistic patient signals are available for connection to the monitor. Real patients can be hard to find, however, so simulators were developed to take their place (Figures 10.16 and 10.17). FIGURE 10.16 Biomedical.) Fluke Biomedical Model ProSim 8 Patient Simulator. (Courtesy of Fluke FIGURE 10.17 Fluke PS420 multiparameter simulator. (Courtesy of Fluke Biomedical.) 320 Introduction to Biomedical Engineering Technology FEATURES OF THE FLUKE BIOMEDICAL PROSIM 8 PATIENT SIMULATOR Designed to make comprehensive patient monitor testing fast and easy, ProSim 8 Vital Signs Simulator offers total patient monitor quality and safety testing from noninvasive blood pressure (NIBP) static pressure linearity and dynamic pressure repeatability tests, EC13 and ACLS ECG waveforms, to complete Nellcor and Nonin SpO2 low perfusion and Masimo Rainbow SET. Featuring specialized stay-connected ECG posts to ensure secure lead connections, ProSim 8 is the preferred tester for patient monitor quality assurance and safety professionals. The ProSim 8 tests ECG (including fetal ECG/IUP and arrhythmias), respiration, temperature, IBP/cardiac catheterization, cardiac output, NIBP, and SpO2 (including Masimo multiwavelength Rainbow SET) in a single 5-min PM testing tool. Wireless PC communication, customized presets, autosequences, barcode scanning, onboard memory, direct data capture, printing functions, and single-step adjustability maximizes testing productivity; a customized carry case doubles as a mobile work station. Multilanguage user interface available in English, Spanish, German, French, Japanese, Italian, and Chinese. • All-in-one patient simulator 80% smaller and 17 lb/7.7 k lighter than single-function simulator test tools. • 8-in-1 multifunction patient simulator is a combination of ECG simulator, fetal simulator, arrhythmia simulator, respiration simulator, temperature simulator, IBP simulator, cardiac output simulator, cardiac catheterization simulator, NIBP simulator, and SpO2 tester, and is the premier SpO2 simulator to test Rainbow multiwavelength waveforms. • Stay-connected ECG posts for easy/secure ECG snap and lead connections. • Custom SpO2r-curve for accurate testing of the latest and future oximetry technologies. • Static pressure linearity testing. • Repeatable NIBP simulation for dynamic pressure repeatability testing. • Physiologically synchronized pulses across all parameters. • Barcode scanning and direct data capture and printing functionality. • Onboard, customizable patient pre-sets and auto sequences for fast/ easy testing. • Multilanguage user interface offers the choice of language selection. • Integrated, easily replaceable long-life battery. • Optional PC interface software offers customizable procedures/ checklists and automated data capture/storage. • Wireless communication for remote PC control of test device, as well as data transfer and automated regulatory reporting. Source: Fluke Biomedical. Testers and Tools 321 FIGURE 10.18 Fluke PS320 fetal simulator plus MFH-1 mechanical fetal heart simulator. (Courtesy of Fluke Biomedical.) These units use microprocessor technology combined with digital-to-analog converters to generate accurate representations of many physiological signals. ECG is the most basic of these signals, but a modern simulator will produce not only normal QRS complexes at various rates and amplitudes, but also a range of different arrhythmia patterns, plus sine, square, and triangle waves. A set of color-coded posts allows various types of ECG electrode terminals to be connected to the simulator. Respiration signals can be included with ECG signals for monitors with such capability; rate, amplitude, and impedance can all be modified. Invasive pressure signals are another aspect of these simulators. Pressures include arterial blood pressure at various locations in the body, central venous pressure, and intracranial pressure. The rates for blood pressure waveforms are set by the ECG rate in use, and ECG arrhythmias will make for different pressure waveforms as well. Specialized simulators are available, for example, to simulate maternal and fetal parameters in one unit (Figure 10.18). NIBP ANALYZERS NIBP monitors determine blood pressure by inflating a cuff until blood flow is completely occluded, and then bleeding off pressure while noting when Korotkoff sounds start and end. To test for proper function, NIBP testers must be able to simulate the pulsatile pressure waveforms found in a real arm. An accurate manometer must be included, and the simulated pressure values displayed so they can be compared to the values determined by the monitor being tested (Figure 10.19). Since monitor accuracy may be different at different levels, the analyzer should be able to simulate a variety of blood pressure situations, including hypo- and hypertension and child or infant pressure patterns. 322 Introduction to Biomedical Engineering Technology FIGURE 10.19 Fluke Biomedical Model BP Pump 2 NIBP analyzer. (Courtesy of Fluke Biomedical.) FEATURES OF THE FLUKE BP PUMP 2 NIBP ANALYZER KEY FEATURES • Dynamic simulations for arm and wrist cuff monitors • Physiological waveform, internal pump for use in high- and low-pressure release verification, leak testing, and pressure sourcing • Preset mode for simulation of most patient conditions • User-definable systolic and diastolic values, along with heart rate and pulse volume and user-defined autosequences • Internal cuff volume for basic device testing • Respiratory artifacts, including spontaneous breathing and controlled ventilation • Arrhythmia simulations, including premature atrial contractions #1 and #2, atrial fibrillation, and PVCs • PC based Ansur test automation system to standardize testing protocol and documentation (optional) • High-accuracy pressure transducer (BP Pump 2M only) • Dynamic pressure repeatability within 2 mmHg at maximal pulse size independent of device under test BP Pump 2 tests for leaks, measures static pressure, generates pressure, and tests overpressure valves. For improved testing versatility, the analyzer’s recently upgraded waveform test suite includes additional physiological selections. BP Pump 2 comes in two models: the standard BP Pump 2L and the BP Pump 2M, which features a high-accuracy pressure transducer. BP Pump 2 also includes an optional five-lead synchronized ECG simulation to test monitors that monitor patient’s ECG. Source: Fluke Biomedical. Testers and Tools 323 NIBP monitors must meet specific standards for leak rates, and analyzers have facilities for inflating the NIBP system to specific pressures and then holding, measuring the drop in pressure (leak rate) over a given time, usually 1 min. If the NIBP system has a self-test or calibration mode, the analyzer should be able to apply set pressures so they can be compared to monitor values. This may be used to perform calibrations of the monitor if such a feature is available. VENTILATOR ANALYZERS Gas control is the primary function of medical ventilators. Gas pressure, flow curves, and frequency in both directions are handled in order to provide optimal respiratory support to the patient. Ventilators can respond to certain patient conditions, possibly modifying their behavior depending on feedback from the patient. In order to adequately test ventilator performance, an analyzer must be able to accurately measure gas flow and pressure and provide both numeric and graphic representations of these measurements so they can be compared to the expected performance of the ventilator (Figure 10.20). Range, accuracy, and response time of the analyzer must be sufficient to provide useful results. FIGURE 10.20 Fluke Biomedical Model VT PLUS HF gas-flow analyzer. (Courtesy of Fluke Biomedical.) 324 Introduction to Biomedical Engineering Technology FEATURES OF THE FLUKE VT PLUS HF GAS-FLOW ANALYZER The VT PLUS HF is Fluke Biomedical’s premier general-purpose gas-flow analyzer. In addition, special display modes and bidirectional flow make it perfect for fully and efficiently testing both conventional mechanical ventilators and HF ventilators. EC.6.20 now requires 100% completion of scheduled lifesupport device preventive maintenance every year, and VT PLUS HF can help meet those requirements. Multiple special-function tests make troubleshooting quick and efficient. VT PLUS HF has the capability to measure either high or low flow and pressure, replacing the need for gauges and flow meters. It measures 21 ventilator parameters and can display all of them on one screen. Results can be printed directly from the unit or from a PC with included Windowscompatible software. VT PLUS HF also has onboard graphing capability and shows the minimum, maximum, average, and absolute measurement for all parameters. Learning to use the VT PLUS HF is simple. Technicians control the unit using the VT PLUS HF user-friendly command system, or, if they’re familiar with the RT-200, they can switch to a special control mode that uses RT-200style commands. VT PLUS HF can be operated with a variety of precision test lungs to ensure that ventilators are tested to manufacturers’ specifications and clinical expectations with a fully NIST-traceable testing system. KEY FEATURES • Bidirectional flow, pressure, volume, and oxygen concentration, and pressure measurements • Low and high pressure, and flow measurement capability • Special HF mode—up to 900 BPM (15 Hz) • RS-232 and printer ports • Included Windows-compatible graphics software • All 21 ventilator parameters displayed at once on one screen • Operation by user-friendly VT PLUS HF command mode or special RT-200 command mode • Minimum, maximum, average, absolute, and graph for all parameters • Multiple special-function tests for efficient troubleshooting OPTIONAL FEATURES • Operation with a variety of precision test lungs available from Fluke Biomedical to complete a fully NIST-traceable ventilator testing system. Source: Fluke Biomedical. 325 Testers and Tools FIGURE 10.21 Fluke Biomedical Model ACCU LUNG precision test lung. (Courtesy of Fluke Biomedical.) The ability of the tester to simulate a patient may be useful; this involves the use of a model lung such as a rubber bag having similar characteristics to a real lung. Dedicated test lungs are also available (Figure 10.21). FEATURES OF THE FLUKE ACCU LUNG PRECISION TEST LUNG The ACCU LUNG Precision Test Lung is a lung simulator that presents a specific load comprised of user-selectable compliance and resistance for the purpose of evaluating ventilator performance according to clinical expectation and manufacturers’ specification. It is a portable unit that can be hung from a cart, the ventilator itself, or handheld, thus presenting a zero footprint. • • • • • Small, lightweight, and portable User-selectable compliance and resistance settings Calibrated accuracy for both resistance and compliance Complies with IEC standard for breathing-circuit connection Certified test lung for test system traceability to standards Source: Fluke Biomedical. INCUBATOR ANALYZERS Infant incubators provide an environment that causes minimal stress to babies so that they can recover from medical or surgical conditions more easily. In conflict 326 Introduction to Biomedical Engineering Technology FIGURE 10.22 Fluke Biomedical Model INCU™ II incubator/radiant warmer analyzer. (Courtesy of Fluke Biomedical.) with this goal is the need to give access to caregivers so they can provide care and treatment to the infant. Testing incubator performance focuses on the environmental factors, so an analyzer must be able to measure various parameters to ensure environmental integrity. Newborn infants often cannot adequately control their body temperature, so incubators must provide steady, even heat that can adjust rapidly to changing conditions such as opening and closing access doors. Temperature can vary throughout the interior of the incubator, so an analyzer should be able to monitor and verify temperature at multiple locations simultaneously (Figure 10.22). FEATURES OF THE FLUKE INCU™ II INCUBATOR/ RADIANT WARMER ANALYZER Infants cannot tell you what is wrong, which is why it is essential to regularly validate the performance and safety of incubators and radiant warmers. The Fluke Biomedical INCU II Incubator/Radiant Warmer Analyzer simplifies testing and verifying baby incubators, transport incubators, and radiant warmers are safe and conform to global IEC 60101-2-19 and IEC 60601-2-21 performance standards. Portable and intuitive-to-use, with a large easy-to-use LCD screen, the INCU II incubator tester operates as a stand-alone device, simultaneously testing and storing temperature, airflow, sound, humidity, and other common environmental and operational parameters. Along with standard tests, its onboard automation lets you create customized test groups. The INCU II incubator analyzer also simplifies test analysis and reporting. Not only are real-time results displayed, but pass/fail indicators make it quick to troubleshoot and pinpoint issues. An Excel add-in allows for detailed test analysis with visual graphs, and the option of creating one-off and standardized reports. Test results can be saved on the INCU II incubator analyzer or transferred to your computer. The 24 h battery allows for long-term testing, and the INCU II can store up to 48 h of test memory. 327 Testers and Tools • Enables simultaneous measurement of humidity, airflow, sound, and temperature from six different points. • Wireless functionality supports fast and convenient downloading of test results and data. • Simplifies set-up tests with color-coded temperature probes that match the color of input ports. • Displays pass/fail indicators and real-time test results on a large LCD screen. • Portable and compact design, weighs less than 9 lb. • Creates personalized test sequences for automatic test completion. • Able to choose from eight different language interfaces. • Complies with all global standards, including IEC 60601-2-19, IEC 60601-2-20, and IEC 60601-2-21. Source: Fluke Biomedical. Oxygen concentration, airflow rates, humidity, and sound levels are other important parameters that incubator testers should be able to analyze. SpO2 ANALYZERS Devices have been made that provide chambers in which a liquid or gel is located, the characteristics of which can be made to simulate that of oxygenated blood in a patient’s body part. Various pulse rates, oxygen levels, and perfusion levels can be simulated for testing SpO2 monitors (Figure 10.23). FIGURE 10.23 “ProSim SPOT Light SpO2 tester. (Courtesy of Fluke Biomedical.)(left) and Oxitest Plus 7 by DNI Nevada. (right)” 328 Introduction to Biomedical Engineering Technology FEATURES OF THE PROSIM SPOT LIGHT SpO2 TESTER PULSE OXIMETER ANALYZER Featuring an exclusive ergonomic design, the ProSim SPOT Light is the first comprehensive SpO2 functional tester to come in a handheld and easy-to-use device. SPOT Light is lightweight and flexible with three custom presets specially designed to make it the fastest and easiest-to-use pulse oximeter analysis device on the market today for SpO2 functional testing. A helpful LCD display and three simple buttons make it effortless to rapidly change parameters and view each signal output sent to the pulse oximeter at a glance. An interchangeable, long-life battery ensures uninterrupted all-day operation without need to connect to a power supply. SPOT Light sets up in seconds to send peripheral capillary oxygen saturation (SpO2), heart rate, perfusion, transmission, artifact noise, and eight different manufactures custom r-curves to a pulse oximeter or patient monitor. It is designed to take the abuse of everyday use, including the stresses of transportation, moving from room to room and device to device, and the occasional fall from the workbench. An increasing number of medical devices now have pulse oximetry built in. SPOT Light can be paired with other Fluke Biomedical test tools to make modern device testing task fast and easy. Need to check a defibrillator with pulse oximetry? SPOT Light with the Impulse 7000 Defibrillator Analyzer allows you to test any external defibrillator on the market today. Do you have a fleet of new patient monitors coming that require incoming inspection? Using SPOT Light with ProSim 4 Vital Signs Simulator allows you to easily accomplish this task in hours instead of days. • • • • • • • • • • Small, portable, and lightweight Large, easy to read LCD display Rechargeable battery lasts 10 h minimum Signal strength indicator SpO2 saturation: 80%, 85%, 90%, 95%, 97%, 98%, 99%, and 100% Heart rate: 30, 60, 80, 100, 120, 150, and 245 BPM Perfusion: 0.2%, 2%, and 10% Transmission: dark/thick, normal, and light/thin Artifacts: respiration and ambient light R-curves: Nonin, Masimo, Nellcor, Nihon Kohden, Mindray, GE, Philips, BCI ULTRASOUND ANALYZERS Both therapeutic and diagnostic ultrasound machines depend on having ultrasound power output within specifications. Ultrasound power meters convert sound energy into an electrical signal for measurement and display (Figure 10.24). Meters contain a reservoir of degassed water into which the ultrasound head is immersed; a detection transducer; and associated electronics. Sound levels can be measured as pulsed or continuous, and a serial port or wireless feature allows communication with a computer. Testers and Tools 329 FIGURE 10.24 Ultrasound Wattmeter. FIGURE 10.25 Fluke Biomedical Impulse 4000 defibrillator analyzer. (Courtesy of Fluke Biomedical.) DEFIBRILLATOR ANALYZERS Defibrillators are extremely critical life support/resuscitation devices and thus must be maintained in excellent working order at all times. This requires specialized equipment that can provide a load for discharging tests that is close to the human thorax in impedance and can absorb multiple discharges without overheating. The signals passing through this test load are analyzed to determine the energy delivered, and the unit must be able to analyze various common defib output waveforms, especially both monophasic and biphasic pulses. Defib testers display the calculated value and make the data available to computerized testing systems. Most analyzers include built-in ECG simulators to aid in testing the synchronized cardioversion function of defibrillators (Figure 10.25). 330 Introduction to Biomedical Engineering Technology FEATURES OF THE FLUKE BIOMEDICAL QED 6 DEFIBRILLATOR ANALYZER The QED 6 provides a scalable solution to accurately test defibrillators. Lightweight and portable, the QED 6 measures a wide range of defibrillator energy output parameters. A RS-232 serial port supports remote computer control and test documentation. KEY FEATURES • Defibrillator analyzer • Monophasic and biphasic DC energy measurement • Energy and cardioversion measurement • Peak voltage, peak current, and overshoot measurement • 2-Line × 24-character display • Bidirectional RS-232 port for computer control • Storage and playback of output waveform so results can be viewed in greater detail • Optional Ansur test automation software to standardize testing procedures, capture waveforms and test results, and print and document test results Source: Fluke Biomedical. PACEMAKER ANALYZERS Cardiac pacemakers, like defibrillators, must operate properly at all times. Voltage, current, frequency, and wave shape of the output signals must meet specific requirements, and testing these parameters is made easier by dedicated pacemaker analyzers (Figure 10.26). FIGURE 10.26 Biomedical.) Fluke Biomedical SigmaPace 1000 pacer analyzer. (Courtesy of Fluke 331 Testers and Tools FEATURES OF THE FLUKE BIOMEDICAL SIGMAPACE 1000 EXTERNAL PACEMAKER ANALYZER The SigmaPaceTM 1000 is a powerful handheld analyzer with a comprehensive range of test suites, measurement algorithms, and test loads—as specified by the external pacemaker manufacturers—to fulfill your testing requirements both quickly and efficiently. STANDARD FEATURES • Unique full-featured biomedical test product • Tests for both transcutaneous and transvenous external pacemakers • Full range of user-selectable measurement algorithms and test loads for external pacemakers • Dual-channel signal acquisition for capturing synchronous AV-sequential pulse data • Interactive pacemaker and ECG simulation with 5-lead output • Large 21-character × 8-line alphanumeric LCD readout • Exclusive readout “HOLD” function • Exclusive SigmaPaceTM 1000 test features: DC static/dynamic leakage, and current drain Source: Fluke Biomedical. SPECIALIZED CALIBRATION AND TESTING DEVICES Some manufacturers supply special test equipment to help field technologists to test and maintain their medical technologies. As an example, IVAC Corp. produces the Core Calibrator for use with IVAC tympanic thermometers (Figure 10.27). A cable connects the unit being tested to the calibrator, and the probe tip is inserted into a well containing a precisely controlled blackbody at 26°C. A measurement is triggered on the thermometer, and a value is displayed on the thermometer screen. The process is repeated with a second well at 38°C. If both of these values are within specifications, the unit can be returned to service. If one or both is out of range, then “calibration” is selected on the calibration unit. The probe is inserted into the 26°C well, and when the measure trigger is depressed, the unit is calibrated to exactly 26°C. Repeating at 38°C gives two reference points so that accurate calibration can be performed. Another example is the temperature probe simulator used for testing some older air-shields infant incubators (Figure 10.28). The device simply plugs into the incubator in place of the actual air and skin temperature probes. Internal resistors that simulate specific temperatures are selected by a rotary switch, which also has settings to simulate open or shorted probes. This allows a quick and accurate check of the temperature function of the incubator, as well as being used for calibration purposes. 332 Introduction to Biomedical Engineering Technology FIGURE 10.27 IVAC CoreChek thermometer test and calibration unit. FIGURE 10.28 Incubator temperature probe simulator. TOOLS Working with a wide range of medical devices means that a wide range of tools is required. These may be ordinary hand and power tools, or they may be specialized devices intended for use with just one specific model of equipment. Quality tools make a great difference in end use: they fit better, they last longer, they are harder and stronger, and they are less likely to damage hardware components. The extra initial price will be paid back many times over. GENERAL Hand tools include such things as screwdrivers, wrenches, hammers, pliers, cutters, and measuring devices (Figures 10.29 and 10.30). Testers and Tools 333 FIGURE 10.29 Pliers and cutters. FIGURE 10.30 Hammers. Screwdrivers come in a tremendous variety of types and sizes, and eventually, it seems you need just about everyone in the course of your work. Different manufacturers favor particular types of fasteners—one may use mostly slotted screws, while another uses only Philips and a third prefers Torx or Bristol splines or Allan-type screws (Figures 10.31 and 10.32). “Wrenches” includes everything from small open-end spanners to adjustable “Crescent” wrenches to metric and standard socket sets of every size (Figure 10.33). Some applications specify that fasteners be tightened to particular torque values, and this requires an accurate torque wrench handle. Pliers and cutters again come in a wide variety, and many different types will be needed in the lab. Quality once more is key, as cheap pliers can bend and lose their grip, while poor quality cutters simply mangle things instead of providing a clean, accurate cut. 334 Introduction to Biomedical Engineering Technology FIGURE 10.31 A variety of screwdriver tips. FIGURE 10.32 Specialized tips. FIGURE 10.33 Socket wrench set. Testers and Tools 335 FIGURE 10.34 IC removal tool + chip contact extender. FIGURE 10.35 Micrometer caliper. A very specialized form of grabber is used to remove integrated circuits from sockets (Figure 10.34). These can be further specialized for removing microprocessor and other similar chips. A good tape measure will be used often, for measuring cable runs or cabinet sizes, and a micrometer caliper (Figure 10.35) can be invaluable for ordering parts that don’t have part numbers. SPECIALIZED TOOLS AND COMPONENTS Certain pieces of equipment may utilize proprietary fittings that cannot be handled with off-the-shelf tools. In such cases, the manufacturer may supply or sell the special tools required, or a talented fabricator might be able to build them. This kind of unique hardware tends to make manufacturing more expensive and can be frustrating for service personnel, and so it seems not to be found as much as it once was. POWER TOOLS A few general power tools are essential in a biomed work area. These include power drills (Figure 10.36) and high-speed rotary tools, drill presses (Figure 10.37), and grinding wheels (Figure 10.38). When using any power tools, proper eye protection (Figure 10.39) is a must! 336 FIGURE 10.36 Introduction to Biomedical Engineering Technology Cordless drill. FIGURE 10.37 Drill press. Testers and Tools 337 FIGURE 10.38 Bench grinder. FIGURE 10.39 Face shield and safety goggles. SOLDERING Though component repair is becoming less and less common with medical equipment, it still may be necessary to unsolder and replace a resistor or diode occasionally. Soldering of wires and other connectors is also done often enough that a good soldering station is indispensable. A simple but quality soldering station consists of a power supply, a handle with replaceable soldering tip, a holder, and a sponge/wiping reservoir (Figure 10.40). Tip temperature is not adjustable but is set for the most common types of solder. 338 Introduction to Biomedical Engineering Technology FIGURE 10.40 Basic soldering station. FIGURE 10.41 High-end soldering station. More sophisticated stations include adjustable temperature, a wider variety of tips, a solder suction/blower module, and perhaps a smoke removal system (Figure 10.41). Solder comes in a variety of types and diameters. Most solder for electronic circuit repair has a rosin core that helps reduce oxidation on the parts to be soldered so that a better joint is produced. Common solder is a lead–tin alloy, but some materials don’t bond well with this type of solder. Specialty solders are available for particular applications, one of the more common being silver solder. Silver solder is still mostly lead and tin, but a portion of silver is added to modify its characteristics. Silver solder has a higher melting point than lead–tin solders (Figure 10.42). Removing components from a circuit board involves melting the solder that was used to install it originally, and then getting rid of the excess. This can be done with a vacuum system that forms part of the soldering station, or it can be done using a mechanical “solder sucker” (Figure 10.42). The process of soldering can produce considerable quantities of acrid smoke; prolonged exposure to such material is not recommended so high-use soldering systems Testers and Tools FIGURE 10.42 339 Different types of solder plus a solder sucker. need to have a smoke removal mechanism. This is just a vacuum device that pulls air and smoke from around the soldering tip and filters out the smoke particles. OTHER Many other materials are used in biomedical equipment support activities. Some of these include • Adhesives, such as silicone rubber glues and sealers, cyanoacrylate cements, epoxy cements (Figure 10.43), and thread locking compounds. Plexiglas can be almost impossible to repair with other adhesives, but wicking few drops of methylene dichloride into a joint will produce a strong bond. FIGURE 10.43 Epoxy mixer. 340 Introduction to Biomedical Engineering Technology FIGURE 10.44 Spray lubricant, the most valuable asset in your tool kit! (but beware of WD-40—it has its uses but can leave a sticky residue that may cause problems). FIGURE 10.45 Heat shrink tubing. • Lubricants include silicone greases, powdered graphite, specialty oils, and anti-seize compounds (Figure 10.44). • Solvents for cleaning equipment include various alcohols, special adhesive tape and label removers, and special formulations to remove the glaze and dirt from rubber surfaces. • Contact cleaners, which can remove dirt and oxidation from edge or pin connectors. • Heat shrink tubing, a special plastic tube material that reduces by one half or more in diameter but very little in length when heated; very useful for making tidy, long-lasting coverings for wires and other conductors (Figure 10.45). Testers and Tools FIGURE 10.46 Magnifier. FIGURE 10.47 Stereo microscope. 341 • Various magnifying devices or a stereo (dissecting) microscope can aid in examining circuit boards and other components in detail (Figures 10.46 and 10.47). SUMMARY This section was completely concerned with tools, from general and special testing units to hand and power tools. 342 Introduction to Biomedical Engineering Technology QUESTIONS 1. What basic parameters do digital multimeters measure? 2. What do oscilloscopes measure and how do they display the results? 3. List three other types of specialized test equipment and their function in a biomed lab. 4. List four parameters that an ESU analyzer might measure. 5. Why is it important that an infusion device analyzer be able to measure flow rates for both steady and intermittent fluid flows? 6. What are patient simulators used for? 7. How might a gas analyzer simulate a patient’s lungs when performing tests? 8. What parameters do incubator analyzers measure and why? 9. Why do high-end solders have a rosin core? 10. Why are smoke removal systems used with soldering stations? 11 Radiation and IT OBJECTIVES FOR THIS CHAPTER • To review the characteristics and range of electromagnetic radiation as it relates to medical technology. • To examine the role of computers in BMET/HTM work and the relationships between HTM and IT. • To discuss the various aspects. ELECTROMAGNETIC RADIATION Certain physical actions, such as heating, can result in a photon being emitted from a substance. Photons are elementary particles that are the basis of all electromagnetic phenomena, including light, radio waves, X-rays, and gamma rays. Photons have no mass and they travel at “the speed of light,” 300,000 km/s in a vacuum. One of the major characteristics of photons is their wavelength (or inversely, their frequency), as seen in the following list: Radiation Type Wavelength Gamma rays Hard X-rays Soft X-rays Extreme ultraviolet Near ultraviolet 1–10 pm 10–100 pm 100 pm–1 nm 1–10 nm 10 nm–380 nm Visible light Violet Blue Cyan Green Yellow Orange Red Near infrared Moderate infrared Far infrared Extremely high frequency radio (microwaves) Super high frequency (microwaves) Ultra high frequency Very high frequency High frequency Medium frequency Low frequency DOI: 10.1201/9781003140603-11 380–430 nm 430–500 nm 500–520 nm 520–565 nm 565–590 nm 590–625 nm 625–740 nm 740 nm–5 μm 5–12 μm 12–1 mm 1 mm–1 cm 1–10 cm 10 cm–1 m 1–10 m 10–100 m 100 m–1 km 1–10 km (Continued) 344 Introduction to Biomedical Engineering Technology Radiation Type Wavelength Very low frequency Voice frequency Extremely low frequency 10–100 km 100–1000 km 1000–10000 km Note: pm = picometers (10−12 m), nm = nanometers (10−9 m), and μm = micrometers (10−6 m). DIGITAL ELECTRONICS Almost all current medical electronic devices involve digital circuitry, and so a brief discussion of digital is in order. This is a very complex field, and many resources are available to provide further information. INTRODUCTION Natural signals are almost all analog, that is, if they are quantified, their measured values can be in any increment between the positive and negative extremes. A graph of signal versus time would be a smooth curve at any magnification level. Early electronic circuits dealt with signals in their analog forms, amplifying, filtering, or otherwise manipulating them but always with an infinite number of gradations between high and low. As technology advanced, it became apparent that some manipulations of electrical signals would be very difficult if only analog signals were used. Counting or assigning whole-number values to a measurement required that discrete levels be considered, and values between those discrete levels had to be changed either up or down to fit the numbers. If the number of steps is too few, important information about the signal can be lost. For any signal, however, there will be a point at which dividing a signal into many small, discrete levels will provide enough information about the signal for whatever purpose it is being analyzed. Conversely, if the number of steps is too great, there is a “waste” of information: the gradations between steps are smaller than is significant in analysis. DIGITAL SIGNALS Dividing analog signals into a number of discrete values is the basis of digital electronics. The term “digital” comes from “digit” or finger, meaning that values are represented as if you were using your fingers—in other words, whole numbers. In practice, almost all “digital” electronics use as a base only two whole numbers: zero and one. This two-state model lends itself to electronics in that circuit components can be turned on (representing a one) or off (representing a zero). No intermediate values needed, just on or off. In this way, perhaps devices should be called binary instead of digital, but the digital term is entrenched. Radiation and IT 345 BINARY NUMBERS Individual binary values are referred to as bits (Binary digits), and larger decimal numbers can be represented by binary bits using the base two counting system. This places a value on the position of a bit in a larger number, just as in base 10. A number in base 10 may be made up of several digits, each of which carries more or less weight depending on its position in the number. For example, in the base 10 number 3692, the digit 3 carries a weight of 1000, the 6 has a weight of 100, the 9 a weight of 10, and the 2 a weight of 1. This is shown in the way we would say such numbers: 3692. In this example, the three is the most significant digit, since it carries the most weight, while the two is the least significant digit. Base two numbers work the same way, except that only two digits (or bits) are involved, 0 and 1, and the position weight of each bit is a multiple of two. For example, in the binary number 11010011, the right-most 1 carries a weight of one, while the next 1 carries a weight of two, and so on until the left-most 1 carries a weight of 128 (two to the power of 7; the right-most bit is two to the power of 0). The decimal equivalent of 11010011 would be 1 × 128 + 1 × 64 + 0 × 32 + 1 × 16 + 0 × 8 + 0 × 4 + 1 × 2 + 1 × 1 = 211. By representing analog values as binary numbers, a great deal of manipulation becomes possible, as well as near-perfect data transmission, storage, and reproduction. ANALOG-TO-DIGITAL CONVERSION Converting analog signals to digital (binary) numbers requires that the end user decide how accurate the digital representation needs to be. This involves two factors: frequency and amplitude. With any analog signal, there are frequency and amplitude components. Frequency is a measure of how rapidly the signal changes with time, and amplitude measures the size of changes. To accurately represent frequency, an analog signal must be sampled often enough that important features of the signal are not missed. This feature is called sample rate. At a certain point, small changes in amplitude become insignificant in a given application. As long as a single binary bit value can represent the smallest significant change in amplitude, the signal can be represented with sufficient accuracy. Once this determination is made, it can be calculated how many bits are required to represent the largest analog value. For example, if the smallest significant component of a signal was 1 mV and the largest signal amplitude was 75 mV, 75 separate binary values must be available. A 7 bit number can have 128 possible values, from 0, represented by 0000000, to 127, represented by 1111111. So 7 bits would be more than adequate to accurately represent the analog signal. This feature is referred to as the resolution of the system. In practice, binary numbers are almost always grouped in powers of four—4, 8, 16, 32, 64, 128, … with groups of eight being a practical group—8 bits equaling 1 byte. Once the necessary sample rate and resolution are determined, the samples can be converted into digital values that are an adequate representation of the original signal. In practice, sample rates and resolution values are usually chosen to be larger than the minimum that has been determined. 346 Introduction to Biomedical Engineering Technology Analog signals are converted into digital data streams by devices called analogto-digital converters (A/D). There are a number of different techniques for performing the conversion, and details of circuits are not particularly relevant. Most A/D converters used in medical equipment are off-the-shelf packages. MICROPROCESSORS Integrated circuits were developed to manipulate digital information, and while some system designs use only relatively simple digital ICs, more and more use a special, complex type of IC called a microprocessor. These devices can take sets of digital information (data) and manipulate it in flexible ways controlled by a program, a series of commands that perform operations on the data. Microprocessor systems consist of four basic parts: input, storage, processor, and output. Of course, this encompasses a huge range, from tiny, cheap calculators in which almost everything is condensed into a single IC chip, to room-filling superpriced supercomputers. In a way, the whole of the Internet could be considered a planetary microprocessor system. COMPUTERS AND NETWORKS General-purpose computers based on microprocessors are used for a variety of purposes in the biomedical engineering technology field. Equipment management, work order processing, calibration and troubleshooting, parts ordering, research, report writing, and communication using e-mail are routine functions that computers can be used for to help staff members be more effective in their roles. Whether desktop, laptop, smartphone, or tablet, computers in hospitals are usually connected to an internal data network, which may be referred to as a LAN or intranet. This can allow communications with other hospital personnel, connection to various institution databases including patient care systems, and connection to the Internet. As cell phones get ever “smarter,” they can perform a valuable role in the information systems of the biomed program. More and more medical devices are using microprocessor systems much like general-purpose computers as the basis of their design. Packaging is modified to suit the application, and input and output devices are often special purpose designs, but the “guts” of the system are often standard components. Some manufacturers go a step further by using a quality off-the-shelf computer tower running a commercial operating system and adding their own software and proprietary input and output components to interface with their applications. This makes system design much easier and less expensive than designing everything from the ground up (often reinventing the wheel) and cuts development time and costs. Many systems use standard keyboards and mice, as well as commonly available (though usually high-end) display monitors and printers. Instead of designing and building a unique data communication system, again equipment manufacturers use standard serial ports, wireless methods, and networking systems for data communications. This makes it relatively simple for medical devices to connect to both in-hospital intranets and to the Internet. Radiation and IT 347 Data sharing, whether in-house or open to the world, allows distant specialists to examine patient records, including ECG patterns, lab reports, X-ray and MRI images, medication regimes, and vital sign records. They can then contact local medical personnel to consult regarding diagnoses and courses of treatment; this contact is more and more likely to be via computers and networks. Students can see real patient information and case histories and different institutions can share epidemiological data, while researchers may have access to vast amounts of data for their studies. Such connections must be used carefully, as medical systems often contain private patient medical and identity data. Robust security, regularly maintained, is vital. The responsibility for this security as well as other aspects of computer support may fall to biomed, or it may be taken over by the information management group, or there may be a division of labor. SUMMARY This chapter covered electromagnetic radiation, digital systems, and computers. QUESTIONS 1. How are hard X-rays and UHF radio signals related? How are they different? 2. What are the advantages of digital systems as compared to analog? 3. What two factors determine the accuracy of digital signals as compared to their analog counterparts? 4. What are the four basic parts of a microprocessor system? 5. Why might “off-the-shelf” computers be used as part of a medical system? 6. Why is data security especially important for medical networks? 12 Health Technology Management OBJECTIVES FOR THIS CHAPTER • To develop a better understanding of the factors involved in technology management. • To learn about some of the technology management software packages available. • To examine some details of a test automation application. INTRODUCTION Even a small hospital will have a considerable number and variety of patient care technology devices, and for them to be supported fully and effectively, a management system must be in place. GENERAL CONSIDERATIONS Technology management includes everything about medical equipment: planning, evaluation, acquisition, incoming testing, installation and commissioning, staff education, performance assurance (PA) testing, repairs, ongoing evaluation, life cycle cost analysis, utilization, vendor management, and decommissioning and retirement. Effective management can provide benefits such as obtaining the best value for money spent on equipment, maximizing uptime and minimizing risk, and optimal utilization of resources. Analyzing PA test results and repair data can provide insights regarding device or system replacement and future purchasing. Compliance with relevant regulations and standards is more easily assured with a complete management system, which can have practical, legal, and financial benefits. The HTM team consists of a manager (often a clinical engineer) and HTM technologists. The manager will set department policies, provide budget recommendations, supervise technical staff, arrange for training, set priorities for the department activities, and develop and administer the overall program. Technologists carry out the functions of the team. For the system to be effective, the team must truly function as a team. PLANNING Equipment planning involves having a clear understanding of the needs of both the patients who are being served by the hospital and the medical staff. Budget considerations are critical, as is a broad knowledge of both the theory of medical equipment function and its application. Awareness of the range of equipment available plus the DOI: 10.1201/9781003140603-12 350 Introduction to Biomedical Engineering Technology strengths and weaknesses of various manufacturers, vendors, and suppliers can help in making the best decisions regarding technology. Planning involves various processes: 1. Maintaining an accurate inventory of existing equipment 2. Evaluating requests for new equipment 3. Preparing and/or analyzing requests for proposals 4. Ensuring a fair bidding process 5. Processing quotes 6. Designing and performing comparative evaluations of competing equipment suppliers 7. Ensuring that all new pieces of equipment meets relevant standards (see Chapter 13) 8. PA and safety testing of all new equipment 9. Supervising and/or performing assembly/installation of new equipment 10. Supervising or tracking maintenance of equipment under contract to outside vendors 11. Performing remove/repair/replace evaluations following device failures 12. Following an effective preventive maintenance/PA program for all devices Various other departments may be involved in, or completely perform, some of the above processes. Internal politics are important and can cause delays or changes in the planning process; clear communication and diplomacy are critical! All parties must be educated (informed) regarding the clinical engineering implications of the specific planning processes. Parties potentially involved are as follows: 1. Biomedical/clinical engineering 2. Purchasing 3. Finance 4. Nursing 5. Physicians 6. Plant services 7. Sterilization department 8. Housekeeping 9. Primary equipment suppliers 10. Supporting outside contractors (building modifications, wiring, plumbing, HVAC requirements, etc.) TECHNOLOGY MANAGEMENT SOFTWARE Effective equipment management requires specialized software packages. Systems can be used to generate equipment inventories, track repair and maintenance costs, schedule PA testing, manage hazard and recall information, generate work orders, and track employee functions and performance. Some systems also handle parts inventories and Health Technology Management 351 outside vendor interfacing. Interconnecting with test equipment is increasingly common; such systems will interface with test equipment to generate work orders, identify equipment, control test procedures, and document and organize test results. ECRI Institute (formerly known as the Emergency Care Research Institute) developed one of the first equipment management software packages, which grew from a simple inventory database to one that included recording of PA results and schedules as well as a parts inventory and PA scheduling. There is now a wide variety of equipment management software systems available. Some of these include Biomed equipment management as part of a facilitywide program that also covers plant maintenance and non-technological nursing and housekeeping equipment, whereas others focus specifically on clinical systems. A few are able to interface with test equipment to integrate PA testing schedules and results with the overall management program. EQUIPMENT MANAGEMENT SYSTEMS Medixir (http://www.medixir.com/) • Focus on medical equipment • Connections to device suppliers • Accessible from different devices in any location • QR code function Meditrac (http://novosolutions.com/medical-tracking-software/) • Includes all hospital equipment, furniture, and devices, including biomedical • Used by various departments within the facility • Barcode function MSI Data (http://www.msidata.com/industries/healthcare-medical/) • Focus on external service provision companies • Service dispatch, service contracts, parts inventory, and asset tracking • Inspection management, including mobile inspection data acquisition Razorsync (http://www.razorsync.com/medical-service-software/) • Focus on outside service provision companies • Cell phone or office computer access • Maps clients and technicians Bluefolder (http://www.bluefolder.com/service-management-software/industries/medical -equipment-service-software.aspx) • External or internal service providers • Emphasis on regulations and standards • Web access • Customer portal allows clients to input requests and search for specific information • Integrated bookkeeping function • Integrated e-mail and calendar RAM Series4000 (http://www.realassetmgt.co.uk/market-sectors/medical-equipment -management-software.html) • Medical technology • Web based 352 Introduction to Biomedical Engineering Technology • Stock control and order requisitioning • UK specific TMS OnSite (http://www.frsoft.com/ProductsSolutions/TMSOnSite.aspx) • Modular to suit different users • Regulatory compliance monitoring • Internet access with any device • Multiple facility capability • ePartsFinder from PartsSource (http://www.partssource.com/) • Interfaces with Fluke Biomedical’s MedTester (see below) Maintenance Connection (http://www.maintenanceconnection.com/website/) • Mobile access capability • Work order management • Asset management • Preventive maintenance scheduling • Inventory tracking • Barcode function Hindsite (http://www.hindsitesoftware.com/medical-equipment-maintenance-software.cfm) • Focus on external service provision companies • Subset of a more general equipment management application • Mapping integration for scheduling at multiple sites • Billing tools included TEST AUTOMATION Ansur by Fluke Biomedical • Interfaces with most new Fluke Biomedical test devices, with separate plugins for each • Preset or customer-created test protocols • Step-by-step test guides • Test report generation • Automatic pass/fail assessment • Multiple devices can be tested simultaneously • Multiple preventive maintenance tests can be performed on a device in each individual procedure Text courtesy of Fluke Biomedical, USA. SUMMARY This chapter discussed the rationale and considerations of medical device management, and an outline of the equipment planning process. The chapter also examined various technology management software systems. 13 Regulations and Standards OBJECTIVES FOR THIS CHAPTER • To differentiate between regulations and standards, and to examine the purposes of each. • To provide an outline of some of the major regulations and standards organizations, with descriptions of some of their contents. • Links to the referenced standards and organizations can be found in the ancillary web page. INTRODUCTION Medical devices must be safe, effective, and reliable. In order to ensure that these devices being used with patients meet these criteria, there must be standards in place that define the parameters of each criterion, as well as regulations to enforce these standards. Regulations are generally legal requirements that must be met for a particular device to be sold and used. They may be international, national, or local. From a health technology management (HTM) perspective, regulations must be met by device manufacturers and vendors, and HTM personnel simply have to ensure that the device in question has a certification of compliance with the regulations. Regulations may refer to a specific set of standards that must be met before certification is granted. Standards are detailed descriptions of device construction and performance requirements. They may also encompass such things as the structure of quality management systems such as the ISO 9000 standards family. Adoption of some standards is voluntary; they may be adopted to give consumers an assurance of quality, or they may be required by specific bodies within a larger organization. Some standards bodies may only develop and present their standards, while others, such as Underwriters Laboratories (UL) or Canadian Standards Association (CSA), have the capability of testing devices to determine if they meet their standards. This allows manufacturers to submit products before they go on the market to DOI: 10.1201/9781003140603-13 354 Introduction to Biomedical Engineering Technology ensure compliance and also gives end users the means by which they can determine if a device not previously approved is able to meet specifications. International standards allow manufacturers in different countries to have access to wider markets and conversely allow end users (e.g., hospitals, clinics, and doctor’s offices) to have access to a wider range of products. Some international standards bodies, such as the International Electrotechnical Commission (IEC), were formed to coordinate standards among member countries, while others, such as the National Fire Protection Association (NFPA) in the United States, began as a country-specific organization but later gained international status as other countries adopted their standards. Certain bodies may present both regulations and standards. STANDARDS AND REGULATIONS ORGANIZATIONS* International Electrotechnical Commission http://www.iec.ch/ Millions of devices that contain electronics, and use or produce electricity, rely on IEC International Standards and Conformity Assessment Systems to perform, fit, and work safely together. Founded in 1906, the IEC is the world’s leading organization for the preparation and publication of international standards for all electrical, electronic, and related technologies. These are known collectively as electrotechnology. IEC provides a platform to companies, industries, and governments for meeting, discussing, and developing the international standards they require. All IEC International Standards are fully consensus based and represent the needs of key stakeholders of every nation participating in IEC work. Every member country, regardless of whether large or small, has one vote and a say in what goes into an IEC International Standard. The IEC is the world’s leading organization that prepares and publishes international standards for all electrical, electronic, and related technologies. Close to 20,000 experts from the industry, commerce, government, test and research labs, academia, and consumer groups participate in IEC standardization work. The IEC is one of three global sister organizations (IEC, ISO, and ITU) that develop international standards for the world. IEC 60601 https://webstore.iec.ch/publication/2612 Medical electrical equipment—Part 1: General requirements for basic safety and essential performance. IEC 60601-1:2005+A1:2012(E) contains requirements concerning basic safety and essential performance that are generally applicable to medical electrical equipment. * Descriptive excerpts are from respective websites. Regulations and Standards 355 IEC 62353 https://webstore.iec.ch/publication/6913 IEC 62353:2014 Medical electrical equipment—Recurrent test and test after repair of medical electrical equipment. IEC 62353:2014 applies to testing of medical electrical equipment and medical electrical systems, hereafter referred to as ME equipment and ME systems, or parts of such equipment or systems, which comply with IEC 60601-1:1988 (second edition) and its amendments and IEC 60601-1:2005 (third edition) and its amendments, before putting into service, during maintenance, inspection, servicing, and after repair or on occasion of recurrent tests to assess the safety of such ME equipment or ME systems or parts thereof. NATIONAL FIRE PROTECTION ASSOCIATION http://www.nfpa.org/ Founded in 1896, NFPA is a global, nonprofit organization devoted to eliminating death, injury, property, and economic loss due to fire, electrical, and related hazards. The association delivers information and knowledge through more than 300 consensus codes and standards, research, training, education, outreach, and advocacy, and by partnering with others who share an interest in furthering the NFPA mission. All NFPA codes and standards can be viewed online for free. NFPA’s membership totals more than 65,000 individuals around the world. http://catalog.nfpa.org/ NFPA-99-Health-Care-Facilities-Code-P1134.aspx?order_src=C900&gclid=CIDH sfqG6ckCFYqGfgod7qQKGg Building on its successful risk-based approach, the 2015 edition of NFPA 99: Health Care Facilities Code improves usability for better health-care safety. The 2015 edition NFPA 99: Health Care Facilities Code provides performance criteria for health-care facilities that builds on the risk-based approach introduced in the 2012 NFPA 99, where it is the risk posed to patients and staff, not the type of building, that defines safety guidelines. Provisions govern installation, inspection, testing, maintenance, performance, and safe practices for facilities, material, equipment, and appliances—including medical gas and vacuum systems formerly found in NFPA 99C. Major changes in the 2015 NFPA 99 make performance criteria more usable, enforceable, and adoptable: • Requirements correlate with the 2014 NFPA 70®: National Electrical Code®. • New provisions address using fuel cell systems for backup power, allowing the use of new technology while ensuring the same minimum level of safety. • Type 3 Essential Electrical System requirements have been removed from NFPA 99—deferring to other codes for required egress lighting. • Updated requirements for nurse call systems incorporate widely used terminology and align with the Facility Guidelines Institute. 356 Introduction to Biomedical Engineering Technology INTERNATIONAL ORGANIZATION FOR STANDARDIZATION http://www.iso.org/iso/home.html ABOUT ISO International Organization for Standardization (ISO) is an independent, nongovernmental international organization with a membership of 162 national standards bodies. Through its members, it brings together experts to share knowledge and develop voluntary, consensus-based, market-relevant international standards that support innovation and provide solutions to global challenges. Our central secretariat is based in Geneva. WHAT ARE STANDARDS? International standards make things work. They give world-class specifications for products, services, and systems, to ensure quality, safety, and efficiency. They are instrumental in facilitating international trade. ISO has published more than 20,500 international standards and related documents, covering almost every industry, from technology, to food safety, to agriculture, and health care. ISO International Standards impact everyone, everywhere. ISO 9000—QUALITY M ANAGEMENT http://www.iso.org/iso/home/standards/management-standards/iso_9000.htm The ISO 9000 family addresses various aspects of quality management and contains some of ISO’s best-known standards. The standards provide guidance and tools for companies and organizations who want to ensure that their products and services consistently meet customer’s requirements, and that quality is consistently improved. Standards in the ISO 9000 family include: • ISO 9001:2015—Sets out the requirements of a quality management system. • ISO 9000:2015—Covers the basic concepts and language. • ISO 9004:2009—Focuses on how to make a quality management system more efficient and effective. • ISO 19011:2011—Sets out guidance on internal and external audits of quality management systems. ISO 9001:2015 sets out the criteria for a quality management system and is the only standard in the family that can be certified to (although this is not a requirement). It can be used by any organization, large or small, regardless of its field of activity. In fact, there are over one million companies and organizations in over 170 countries certified to ISO 9001. This standard is based on a number of quality management principles, including a strong customer focus, the motivation and implication of top management, the process approach, and continual improvement. Regulations and Standards 357 ISO 31000—RISK M ANAGEMENT http://www.iso.org/iso/home/standards/iso31000.htm Risks affecting organizations can have consequences in terms of economic performance and professional reputation, as well as environmental, safety, and societal outcomes. Therefore, managing risk effectively helps organizations to perform well in an environment full of uncertainty. ISO 31000:2009, Risk management—Principles and guidelines, provides principles, framework, and a process for managing risk. It can be used by any organization regardless of its size, activity, or sector. Using ISO 31000 can help organizations increase the likelihood of achieving objectives, improve the identification of opportunities and threats, and effectively allocate and use resources for risk treatment. However, ISO 31000 cannot be used for certification purposes but does provide guidance for internal or external audit programs. Organizations using it can compare their risk management practices with an internationally recognized benchmark, providing sound principles for effective management and corporate governance. CSA http://www.csagroup.org/ ABOUT CSA GROUP Every day, the CSA Group works with businesses, organizations, and code authorities around the world to help create a safer, more sustainable world for people and for business. From testing and certifying your products today for safety and performance requirements, to developing leading-edge, consensus-based standards to support tomorrow’s technology, they develop solutions that strive to promote safety to the industry and society. Manufacturers, retailers, businesses, academia, consumers, and government organizations alike rely on CSA’s worldwide network to assist in their pursuit of innovative solutions for their evolving safety, reliability, and sustainability needs. Standards contribute to safer homes, workplaces, and public spaces. They address issues related to sustainability and the environment, and they encourage the adoption of new technologies and best practices that enhance trade and help make the industry more competitive in the global marketplace. Standards help advance today while anticipating tomorrow. Standards development is the foundation of the CSA Group. From our initial charter in 1919, we have grown to become the largest standards development organization (SDO) in Canada, with the widest subject area recognition. We also work with other SDOs around the world as a key contributor to international and harmonized standards activities. Our library of more than 3000 standards and codes addresses subjects that affect the interests of the industry, consumers, regulators, and the public at large. 358 Introduction to Biomedical Engineering Technology ELECTRO-MEDICAL EQUIPMENT The CSA Group tests and certifies your electro-medical equipment to applicable U.S., Canadian, and international standards to help you obtain the required approvals for your intended markets. With our network of offices and laboratories in North America, Europe, and Asia, our dedicated technical experts can serve you locally wherever you manufacture or sell your electro-medical devices. TESTING AND CERTIFICATION The CSA Group is your expert source for testing and certification for a wide variety of electro-medical devices, including: • • • • • • CT scanning equipment Defibrillators Electrocardiographs Incubators Monitoring equipment Ultrasound machines Their testing and certification programs extend to cover not only certification requirements but also applicable EMC testing to meet the requirements of the U.S. Federal Communications Commission (FCC), the European Union (EU), Industry Canada, and other regulatory bodies as well as battery certification. IEC 60601-1 third edition. They have the credentials to provide the approvals to help you sell your electro-medical devices around the world. In fact, they were the first North American organization accredited by ANSI to test to the requirements of the IEC 60601-1 third edition. Under the IECEE CB scheme, the CSA Group test reports can be used to secure approvals in many international markets. CSA STANDARDS CAN/CSA-C22.2 NO. 60601-1-1–02 (R2011)—Medical Electrical Equipment—Part 1-1: General Requirements for Safety—Collateral Standard: Safety Requirements for Medical Electrical Systems (Adapted CEI/IEC 60601-1-1:2000, second edition, 2000–12). This standard applies to the safety of MEDICAL ELECTRICAL SYSTEMS, as defined in 2.201. It describes the safety requirements necessary to provide protection for the PATIENT, the OPERATOR, and surroundings. CAN/CSA-C22.2 NO. 60601-1-6:11—Medical electrical equipment—Part 1–6: General requirements for basic safety and essential performance—Collateral standard: Usability (Adapted IEC 60601-1-6:2010, third edition, 2010–01). This is the third edition of CAN/CSA-C22.2 No. 60601-1-6, Medical electrical equipment—Part 1–6: General requirements for basic safety and essential performance—Collateral standard: Usability, which is an adoption without modification of the identically titled IEC (International Electrotechnical Commission) Standard Regulations and Standards 359 60601-1-6 (third edition, 2010–01). It supersedes the previous edition, published in 2008 as CAN/CSA-C22.2 No. 60601-1-6 (adapted IEC 60601-1-6:2006). It is one in a series of Standards issued by CSA under Part II of the Canadian Electrical Code. This International Standard specifies a PROCESS for a MANUFACTURER to analyze, specify, design, VERIFY, and VALIDATE USABILITY, as it relates to BASIC SAFETY and ESSENTIAL PERFORMANCE of MEDICAL ELECTRICAL EQUIPMENT, hereafter referred to as ME EQUIPMENT. This USABILITY ENGINEERING PROCESS assesses and mitigates RISKS caused by USABILITY problems associated with CORRECT USE and USE ERRORS, that is, NORMAL USE. It can be used to identify but does not assess or mitigate RISKS associated with ABNORMAL USE. If the USABILITY ENGINEERING PROCESS detailed in this collateral standard has been complied with and the acceptance criteria documented in the USABILITY VALIDATION plan have been met (see 5.9 of IEC 62366:2007), then the RESIDUAL RISKS, as defined in ISO 14971, associated with USABILITY of ME EQUIPMENT are presumed to be acceptable, unless there is OBJECTIVE EVIDENCE to the contrary (see 4.1.2 of IEC 62366:2007). UL AND ULC http://ul.com/ ABOUT UL UL is a global independent safety science company with more than a century of expertise innovating safety solutions from the public adoption of electricity to new breakthroughs in sustainability, renewable energy, and nanotechnology. Dedicated to promoting safe living and working environments, UL helps safeguard people, products, and places in important ways, facilitating trade and providing peace of mind. UL certifies, validates, tests, inspects, audits, advises, and educates. They provide the knowledge and expertise to help navigate growing complexities across the supply chain from compliance and regulatory issues to trade challenges and market access. ABOUT UNDERWRITERS LABORATORIES OF CANADA Underwriters Laboratories of Canada (ULC) is an independent product safety testing, certification, and inspection organization. They have tested products for public safety for 90 years, and they are accredited by the Standards Council of Canada (SCC). STANDARDS COUNCIL OF CANADA https://www.scc.ca/ ABOUT THE SCC The SCC has its mandate to promote efficient and effective standardization in Canada. 360 Introduction to Biomedical Engineering Technology ABOUT STANDARDIZATION Standardization is the development and application of standards publications that establish accepted practices, technical requirements, and terminologies for products, services, and systems. Standards help to ensure better, safer, and more efficient methods and products and are an essential element of technology, innovation, and trade. The Standards Council carries out a variety of functions intended to ensure the effective and coordinated operation of standardization in Canada. It also represents Canada’s interests on standards-related matters in foreign and international forums. FOOD AND DRUG ADMINISTRATION http://www.fda.gov/ Food and Drug Administration (FDA) is responsible for protecting the public health by assuring that foods (except for meat from livestock, poultry, and some egg products that are regulated by the U.S. Department of Agriculture) are safe, wholesome, sanitary, and properly labeled, ensuring that human and veterinary drugs, and vaccines and other biological products and medical devices intended for human use are safe and effective. PRODUCTS AND MEDICAL PROCEDURES Medical devices range from simple tongue depressors and bedpans to complex programmable pacemakers with microchip technology and laser surgical devices. In addition, medical devices include in vitro diagnostic products, such as general-purpose lab equipment, reagents, and test kits, which may include monoclonal antibody technology. Certain electronic radiation emitting products with medical application and claims meet the definition of medical device. Examples include diagnostic ultrasound products, X-ray machines, and medical lasers. MEDICAL DEVICE SAFETY FDA monitors reports of adverse events and other problems with medical devices and alerts health professionals and the public when needed to ensure proper use of devices and the health and safety of patients. HEALTH CANADA http://www.hc-sc.gc.ca/index-eng.php MEDICAL DEVICES The term medical devices, as defined in the Food and Drugs Act, covers a wide range of health or medical instruments used in the treatment, mitigation, diagnosis, or prevention of a disease or abnormal physical condition. Regulations and Standards 361 HEALTH CANADA’S ROLE Health Canada reviews medical devices to assess their safety, effectiveness, and quality before being authorized for sale in Canada. ASSOCIATION FOR THE ADVANCEMENT OF MEDICAL INSTRUMENTATION https://www.aami.org/home The Association for the Advancement of Medical Instrumentation (AAMI), founded in 1967, is a unique alliance of over 6000 members united by the common goal of increasing the understanding and beneficial use of medical instrumentation. AAMI is the primary source of consensus and timely information on medical instrumentation and technology. AAMI is the primary resource for the industry, professions, and government for national and international standards. AMERICAN NATIONAL STANDARDS INSTITUTE https://www.ansi.org/ American National Standards Institute (ANSI) facilitates the development of American National Standards (ANS) by accrediting the procedures of standards developing organizations (SDOs). These groups work cooperatively to develop voluntary national consensus standards. Accreditation by ANSI signifies that the procedures used by the standards body in connection with the development of ANS meet the institute’s essential requirements for openness, balance, consensus, and due process. INSTITUTE OF ELECTRICAL AND ELECTRONICS ENGINEERS http://www.ieee.org/portal/site Institute of Electrical and Electronics Engineers (IEEE) is the world’s largest professional association dedicated to advancing technological innovation and excellence for the benefit of humanity. IEEE and its members inspire a global community through its highly cited publications, conferences, technology standards, and professional and educational activities. IEEE QUICK FACTS IEEE has • Over 426,000 members in more than 160 countries, of whom over 50% are from outside the United States. • Over 117,000 student members. • 334 sections in 10 geographic regions worldwide. • 2116 chapters that unite local members with similar technical interests. 362 Introduction to Biomedical Engineering Technology • 2669 student branches at colleges and universities in 80 countries. • 922 student branch chapters of IEEE technical societies. • 440 affinity groups; IEEE affinity groups are nontechnical subunits of one or more sections or a council. The affinity group patent entities are the IEEE– USA Consultants’ Network, Young Professionals (YP), Women in Engineering (WIE), and Life Members (LM). IEEE • Has 39 societies and 7 technical councils representing a wide range of IEEE technical interests. • Has more than 3.5 million documents in the IEEE Xplore® Digital Library, with more than 8 million downloads each month. • Has more than 1671 standards and projects under development. • Publishes approximately 180 transactions, journals, and magazines. • Sponsors more than 1600 conferences in 91 countries while • Partnering with more than 1000 non-IEEE entities globally. • Attracting more than 480,000 conference attendees. • Publishing more than 1400 conference proceedings via IEEE Xplore. THERAPEUTIC GOODS ADMINISTRATION https://www.tga.gov.au/ As part of the Department of Health, the Therapeutic Goods Administration (TGA) safeguards and enhances the health of the Australian community through effective and timely regulation of therapeutic goods. The TGA is responsible for regulating the supply, import, export, manufacturing, and advertising of therapeutic goods. It regulates therapeutic goods through premarket assessment, postmarket monitoring and enforcement of standards, licensing of Australian manufacturers, and verifying overseas manufacturers’ compliance with the same standards as their Australian counterparts. BSI GROUP https://www.bsigroup.com/en-GB/standards/ BSI British Standards is the national standards body of the United Kingdom. The BSI Group • • • • • Develops private, national, and international standards. Certifies management systems and products. Provides testing and certification of products and services. Provides training and information on standards and international trade. Provides performance management and supply chain management software solutions. Regulations and Standards 363 SUMMARY This chapter examined the roles of regulations and standards in HTM and provided an outline of some of the major organizations involved. Links on ancillary website: 14 A Gallery of RealLife Problems The following are some examples of equipment problems encountered during the course of my work as a hospital biomedical equipment technician. Many issues are not amenable to images, but these might give the reader a feel for some of the things they could see in the workplace (Figures 14.1–14.23). FIGURE 14.1 This is the AC power cord of an infusion pump. Continual flexing of the cord eventually caused the insulation to split right at the end of the strain relief. While the insulation on the individual wires inside is still intact, this presents a potential shock hazard should further damage occur. The cord was replaced: a simple matter of undoing two restraining screws, removing the cord restraint, replacing the cord with a new one, and reinstalling the cord restraint. DOI: 10.1201/9781003140603-14 366 Introduction to Biomedical Engineering Technology FIGURE 14.2 Sometimes, electronic components fail explosively. This 8-pin IC from an infusion pump literally blew, resulting in complete failure of the pump. Though it is possible to replace surface mount components such as these, using specialized equipment, the repair can cause further damage, and there may have been other components damaged by the failure of the IC. For these reasons and in the interest of timely repair, the whole printed circuit board was replaced. FIGURE 14.3 When this feeding pump arrived in the hospital, it came to HTM for incoming inspection. One of the first tests revealed that the pump was not working at all. Further investigation showed that the screws in the AC plug that secure the conductors had not been tightened. If they had been making poor or intermittent contact, overheating and/or pump failure during use could have resulted. The factory maintenance checklist that came with the pump indicates that AC operation passed, illustrating the need for careful incoming inspections of equipment. Rather than going through all the paperwork and delays that would have been needed to return the unit, the wires were secured in the AC plug and the unit put into service, having passed all other incoming tests. A Gallery of Real-Life Problems 367 FIGURE 14.4 This is the inside of the heater chamber of an infant incubator. The fan on the right blows air through the chamber. The round heater element is normally covered by a finned metal radiator assembly, and the silvery rod next to it contains a temperature sensor, used to control the heat level. Linens and other material used in caring for infants in the incubator produce lint, and normally this is cleaned out of the unit when it is cleaned after each patient. However, in this case, some of the lint was missed, which could cause both reduced heating effectiveness and lint particles circulating within the patient compartment. The lint was removed from the chamber, and a note was sent to the cleaning department to remind them to check the heating chamber. FIGURE 14.5 Electrosurgery bipolar operation using forceps such as these can be used to cauterize small sections of tissue (such as blood vessels, polyps, or ducts) during laparoscopic procedures. The forceps have two conductive elements that pass through a metal tube, and these elements must be insulated from one another and from the tube. If the insulation breaks down, as in the picture, a short circuit results, which can cause inadvertent heating of nearby tissue, but more importantly, reduced or eliminated cautery effectiveness. Such instruments can be repaired at the factory but not in the field, so they must be sent in to an appropriate depot. 368 Introduction to Biomedical Engineering Technology FIGURE 14.6 Monopolar electrosurgery also depends on a complete circuit for operation. In this instance, the conductor of the return electrode cable was severed inside the insulation, either from over-stretching or from crushing, and a slight tug broke the insulation. In a pinch, the cable can be soldered together and the joint covered by heat-shrink tubing, but the cable should be replaced as soon as possible. FIGURE 14.7 The note on this infusion pump says, “Leaking oil, says ‘system failure’.” A number of problems are indicated: the system failure message is critical, and usually means that the main CPU board of the pump has to be replaced, though it can sometimes be caused by cable connectors not making adequate contact. Leaking oil is a problem of a different sort. Since there is no oil in these pumps, the leak must have been caused by some fluid being spilled on the pump, which means that proper care is not being exercised on the nursing floor. In addition, since the fluid is unknown, the pump needs to be sent for decontamination before it can be serviced. A Gallery of Real-Life Problems 369 FIGURE 14.8 These pictures are of two plastic shells for an infant incubator, turned upside down and showing the heating chamber. The open hole is a port that allows distilled water to enter the heating chamber via a metal nozzle, where it is vaporized and then blown throughout the interior of the incubator. The top image (a) is of a new shell, whereas the bottom one (b) has suffered extreme degradation of the plastic around the area where the nozzle was fitted. This allowed water to drip into the bottom section of the shell and eventually out onto the floor of the nursery. Biomed initially thought that a cleaning solvent may have been left in the chamber, eating away the plastic, but after communication with the incubator manufacturer, they indicated that simple moisture could cause this problem. The replacement shell was provided free of charge. 370 Introduction to Biomedical Engineering Technology FIGURE 14.9 This AC power cord from a laparoscopic surgery insufflator suffered from either excessive flexing or was run over by a heavy, wheeled device like a gurney. The physical damage resulted in one strand of one of the internal conductors breaking and being thrust through both the inner and outer insulation of the cord. It presents an electrical shock hazard as well as a physical puncture hazard. The damage to the conductors could also result in failure of the device during use. The cord was replaced and staff reminded to keep cords off the floor whenever possible and away from traffic paths. FIGURE 14.10 This is a fiber-optic channel used to carry laser pulses to target kidney stones, to break them up (lithotripsy). With normal wear and tear, or abuse, the fibers can develop internal cracks that, while not visible to the unaided eye, effectively block light transmission, making the fiber useless. Fibers must therefore be tested regularly to ensure patency. This can be done by passing an intense white light through the fiber, and looking carefully at the results. A break is indicated by light spilling from the break location, as in the illustration. A Gallery of Real-Life Problems 371 FIGURE 14.11 Immersion in liquids is generally not healthy for electronic components. This nerve stimulator was either dropped into some liquid (sometimes it is best not to ask what), or a liquid was spilled on the unit. In any case, a residue from the liquid was left on the leads of an IC, causing failure of the device. Owing to the relatively low cost of the device and the relatively high cost of replacement parts, the device was taken out of service. FIGURE 14.12 Nurses love tape! This is the patient end of a nitrous oxide unit, used in this case for administration of nitrous oxide as a pain reliever for pregnant patients during labor. A rubber facemask fits over the circular opening when in use with a patient. The tape was used when the corrugated plastic tubing (which removes exhaled nitrous oxide, in order to keep it from venting into the room) broke off. Tape can be useful for emergency, short-term repairs, but it will almost certainly fail in short order and is also a potential site for contamination as well as being aesthetically distressing. 372 Introduction to Biomedical Engineering Technology FIGURE 14.13 An intake filter from an oxygen concentrator. An object of some kind was drawn into the air intake of the unit with enough velocity to perforate the filter material, resulting in potential contamination of the delivered oxygen as well as improper pressures within the device. Normally, a foam filter prevents such occurrences, but in this case the primary filter was missing. FIGURE 14.14 This ophthalmoscope has a rechargeable battery in the handle, and a built-in charging circuit. The head of the unit unscrews to expose prongs that plug into any AC receptacle for charging the battery. Whoever sent the unit to Biomed with this note was unaware of this, pointing to the need for ongoing staff education in relevant areas. A Gallery of Real-Life Problems 373 FIGURE 14.15 Fragile components, regardless of their packing, can suffer damage in transit. This replacement central station monitor display screen arrived in Biomed like this, even though the box showed little outward damage. The screen was replaced by the manufacturer who presumably took the issue up with the shipping company, armed with our photos. FIGURE 14.16 Another example of damage to an AC power cord, apparently inflicted by a sharp instrument. 374 Introduction to Biomedical Engineering Technology FIGURE 14.17 Nurses and tape again. Normally power cords stay quite securely in place with friction, but this cord was loose and tape—lots of tape—provided a temporary, though unsightly, fix. Ideally, the unit would have been sent to Biomed for cord replacement as soon as the loose cord was noticed. FIGURE 14.18 And still more tape! Even though these vital signs monitors have a volume control, if one does not remember how to access it or is unaware of its existence, and alarms and other audible signals are just too loud… tape and a few gauze pads provide a muffler. Staff education required. A Gallery of Real-Life Problems 375 FIGURE 14.19 When sealed lead acid batteries are overcharged and/or improperly vented, gases and heat build-up inside the case and cause it to swell and warp. In extreme cases, the battery can explode from the pressure. Since they are usually inside a device, the damage caused is restricted to the inside of the device, likely causing immediate loss of function. The charging circuit of the unit may be faulty or the batteries may not be adequately designed for the environment. FIGURE 14.20 When IV pump doors are left open, they are vulnerable to damage by passing carts or other large objects. The door may even be broken off its hinges completely, making it so that, as the note so kindly points out, the door no longer works. Replacing a door on these pumps is somewhat fiddly mechanically, but also a tedious recalibration of pressure sensors is required, so Biomeds often go around the hospital closing pump doors whenever they see them. Another case for staff education, perhaps simply in the form of an e-mail to nursing supervisors asking them to remind staff to close pump doors when not in use. 376 Introduction to Biomedical Engineering Technology FIGURE 14.21 Some notes that accompany equipment are so helpful. FIGURE 14.22 The basic troubleshooting guide that is supplied (and hopefully kept) with every vital signs monitor indicates that when the NIBP pump keeps the pressure going up and down, there is probably a leak in the system, which is almost always caused by a hole in the cuff bladder. The cuff should then be replaced. However, it is easier just to send it to Biomed, even though the unit will then be out of service for hours if not days, as opposed to minutes if the cuff is replaced on the nursing floor. A Gallery of Real-Life Problems 377 FIGURE 14.23 Another helpful sign. (“Really, it’s broken? We thought it just came down here for a vacation!”) 15 Anatomy Color Insert These images are included in color to better illustrate relevant anatomical structures. They, and more, can be found at the ancillary web site (Figures 15.1–15.21). FIGURE 15.1 Digestive system. DOI: 10.1201/9781003140603-15 380 Introduction to Biomedical Engineering Technology FIGURE 15.2 Pancreas. Note that the pancreatic ducts and the bile duct (from the liver) both empty into the duodenum in the same vicinity. FIGURE 15.3 Cross section of the stomach. Food enters the stomach from the esophagus and empties into the duodenum. The cardiac and pyloric sphincters function to keep food in the stomach while that part of digestion takes place. Anatomy Color Insert 381 FIGURE 15.4 General anatomy of the liver and associated organs. FIGURE 15.5 The liver. Bile is collected from throughout the liver via the main hepatic duct and its smaller branches, and then either moved via the cystic duct and stored in the gall bladder until needed or passed directly into the duodenum via the common bile duct. 382 Introduction to Biomedical Engineering Technology FIGURE 15.6 The major arteries and veins of the human circulatory system. FIGURE 15.7 Schematic diagram of the circulatory system. Blood is pumped from the right atrium into the right ventricle, and from there to the lungs, where excess carbon dioxide is removed and fresh oxygen is acquired. Returning from the lungs, the blood passes through the left atrium and then the left ventricle to be distributed to the rest of the body, including the heart itself. Returning from the body, blood is now back at the right atrium. Anatomy Color Insert 383 FIGURE 15.8 Cross section of the heart. The structures within the ventricles are the chordae tendineae, which serve to keep the tricuspid and mitral valves from collapsing back into the heart during pumping contractions of the ventricles. FIGURE 15.9 The valves of the heart. The mitral valve is also known as the bicuspid valve; the aortic and pulmonary valves are sometimes referred to as the semilunar valves. 384 Introduction to Biomedical Engineering Technology FIGURE 15.10 Exterior views of the heart showing the coronary arteries, plus a schematic cross-sectional diagram of a coronary artery showing how arteriosclerosis can block the artery, reducing blood flow to the heart muscles: (a) anterior view and (b) posterior view. FIGURE 15.11 Schematic diagram showing placement of an internal cardiac pacemaker. Anatomy Color Insert FIGURE 15.12 385 The lungs. FIGURE 15.13 Schematic diagram of bronchioles and alveoli within the lungs. Blood flowing from the heart moves through smaller and smaller branches until it reaches the capillary nets that surround the alveoli. Oxygen is taken into the blood from inhaled air within the alveoli, and carbon dioxide is released from the blood into the alveoli; it is then expelled from the body during exhalation. 386 Introduction to Biomedical Engineering Technology FIGURE 15.14 The arrangement of the pancreas, kidneys, and adrenal glands within the abdomen. FIGURE 15.15 The kidneys and adrenal (or suprarenal) glands, including a cross section of one kidney. The adrenal glands produce a variety of endocrine hormones involved in metabolism. The kidneys filter impurities such as excess salt, urea, and ammonium and are also vitally involved in maintaining proper fluid balances within the body. Kidney stones or renal calculi are formed in the calyx, pelvis, ureters, or urinary bladder. Anatomy Color Insert 387 FIGURE 15.16 The urinary system. Urine is collected in the kidneys and drained via the ureters into the bladder, where it is held until it can be passed out of the body via the urethra. FIGURE 15.17 Anatomy of pregnancy. 388 Introduction to Biomedical Engineering Technology FIGURE 15.18 Anatomy of the brain. The pia mater, arachnoid, and dura mater are three membranes that surround and protect the brain within the skull. Cerebrospinal fluid circulates within the subarachnoid space and the ventricles of the brain, providing further cushioning. The main, folded part of the brain is the cerebrum and is mainly involved in perception and thought process. The lower reddish portion is the cerebrum, which coordinates balance and coordination. The brain stem, at the top of the spinal cord, controls basic functions such as breathing and heart rate. FIGURE 15.19 The ear. Sound is focused by the outer ear and carried inside by the auditory canal. It then causes vibration of the outer eardrum. These vibrations are amplified and modified by the ossicles (three bones called the incus, or anvil; the malleus, or hammer; and the stapes, or stirrup), and then transferred to the inner eardrum. The sound vibrations then pass into the cochlea where they are converted into nerve signals that correspond to different frequencies and amplitudes of sound. The semi-circular canals, though part of the inner ear structure, are involved in balance and spatial orientation rather than hearing. Anatomy Color Insert 389 FIGURE 15.20 The eye. Light passes through the cornea, which provides both structure to the eye and some initial focusing. The amount of light entering the inside of the eye is controlled by the iris, which contracts or expands in order to change the pupil opening. Further focusing is done by the lens, whose shape and therefore focal distance can be modified by the ciliary muscles. The focused light falls on the retina, where rod and cone cells convert the light into nerve signals corresponding to color and intensity. These signals are collected into the optic nerve and passed to the brain. The sclera, aqueous humor, and vitreous humor provide the physical structure of the eye. FIGURE 15.21 A surgeon prepares to insert an artificial intraocular lens into a patient’s eye, probably because the natural lens has been removed due to cataracts. Appendix A Normal Values In the course of working with various devices in medicine, you will come across measurements of different values and parameters. The below table is included to give perspective on some of the more common medical measurements. Normal values are the range of values found in healthy, normal individuals. Hematology—Red Blood Cells (Erythrocytes) RBC (male) RBC (female) RBC (child) 4.2–5.6 M/µL (million cells/µL) 3.8–5.1 M/µL 3.5–5.0 M/µL Hematology—White Blood Cells (Leukocytes) WBC (male) WBC (female) WBC (child) 3.8–11.0 K/mm3 (thousand cells/mm3) 3.8–11.0 K/mm3 5.0–10.0 K/mm3 Hemoglobin Hgb (male) Hgb (female) Hgb (child) Hgb (newborn) 14–18 g/dL 11–16 g/dL 10–14 g/dL 15–25 g/dL Hematocrit Hct (male) Hct (female) Hct (child) 39%–54% 34%–47% 30%–42% 392 Appendix A General Chemistry Bilirubin (total) BUN Calcium (total) Carbon dioxide Carbon monoxide 0.2–1.4 mg/dL 6–23 mg/dL 8–11 mg/dL 21–34 mEq/L (milliequivalents/L) symptoms at ≥10% saturation 96–112 mEq/L Chloride General Chemistry 0 mg%; Coma at ≥400–500 mg% 65–99 mg/dL 25–65 mg/dL 38–94 mg/dL 3.5–5.5 mEq/L 135–148 mEq/L 8–25 mg/dL Ethanol Glucose HDL (male) HDL (female) Potassium Sodium Urea nitrogen Lipid Panel (Adult) <200 mg/dL desirable 30–75 mg/dL <130 mg/dL desirable >40–170 mg/dL >35–135 mg/dL Cholesterol (total) Cholesterol (HDL) Cholesterol (LDL) Triglycerides (male) Triglycerides (female) Urine Specific gravity pH Na K Cl Osmolality Glucose 1.003–1.040 4.6–8.0 10–40 mEq/L <8 mEq/L <8 mEq/L 80–1300 mOsm/L ≥180 mg/dL Cerebrospinal Fluid Osmolality Pressure 290–298 mOsm/L 70–180 mm H2O 393 Appendix A Hemodynamic Parameters Cardiac index Cardiac output Stroke volume Systolic arterial pressure Diastolic arterial pressure Central venous pressure Ejection fraction Left atrial pressure 2.5–4.2 L/min/m2 4–8 L/min 60–100 mL/beat 90–140 mmHg 60–90 mmHg 2–6 mmHg 60%–75% 4–12 mmHg Hemodynamic Parameters Right atrial pressure Pulmonary artery (PA) systolic pressure PA diastolic pressure PA mean pressure PA wedge pressure PA end diastolic pressure Right ventricular end diastolic pressure 4–6 mmHg 15–30 mmHg 5–15 mmHg 10–20 mmHg 4–12 mmHg 8–10 mmHg 0–8 mmHg Neurological Values Intracranial pressure 5–15 mmHg Arterial Values pH PaCO2 HCO3 O2 saturation PaO2 7.35–7.45 35–45 mmHg 22–26 mEq/L 96%–100% 85–100 mmHg Venous Values pH PaCO2 HCO3 O2 saturation PaO2 7.31–7.41 41–51 mmHg 22–29 mEq/L 60%–85% 30–40 mmHg 394 Appendix A GLOSSARY FOR NORMAL VALUES bilirubin a by-product of the breakdown of red blood cells, it is normally destroyed by the liver. High levels can indicate liver problems. High concentrations of bilirubin in the body can cause the skin to turn yellow (jaundice). BUN blood urea nitrogen. cardiac index the amount of blood pumped by the heart per unit of time divided by body surface area, usually expressed in L/min/m2. cardiac output a measurement of blood flow through the heart, expressed in L/min. central venous pressure the blood pressure in the right atrium or veins near the heart, mainly the vena cava. cerebrospinal fluid a clear, colorless fluid containing small amounts of glucose and protein. Cerebrospinal fluid fills the ventricles of the brain, spaces between the brain and the cerebral membranes, and the central canal of the spinal cord. It acts as a shock absorber and carries some nutrients and materials involved in immune response. cholesterol a fatlike steroid alcohol found in animal fats and oils, in bile, blood, brain tissue, milk, yolk of egg, myelin sheaths of nerve fibers, the liver, kidneys, and adrenal glands. It is the main component of most gallstones and is involved in atherosclerosis (hardening of the arteries). diastolic arterial pressure the minimal pressure reached in arteries close to the heart (such as the ascending and descending aorta), corresponding to the maximal relaxation of the ventricles. ejection fraction a measure of the ability of the ventricles to contract. HCO3 bicarbonate A chemical produced in red blood cells, liberated through exchange with chloride. It may then be excreted by the kidneys. HDL high-density lipoprotein (good cholesterol). hematocrit (Hct) the relative volume of blood occupied by red blood cells. hemoglobin (Hgb) a molecule involved in carrying oxygen in the blood; an iron atom forms part of the molecule. intracranial pressure the pressure exerted by cerebrospinal fluid within the skull. O2 saturation a measure of the amount of oxygen carried by the blood compared to the maximum theoretically possible, expressed as a percentage. osmolality the concentration of osmotically active particles in solution expressed in terms of osmoles of solute per kilogram of solvent. PaCO2 partial pressure of carbon dioxide in the blood. PaO2 partial pressure of oxygen in the blood. pH a logarithmic measure of the activity of hydrogen ions in a solution, which also indicated relative acidity/alkalinity. pH 7 is neutral, pH 0 is extremely acidic, and pH 14 is extremely alkaline. pulmonary artery wedge pressure the pressure measured in the pulmonary artery when blood flow in the artery is occluded, usually by a small balloon on the tip of a catheter. This catheter also contains a pressure transducer. specific gravity the density of a liquid compared to water, pure water having a specific gravity of 1. Appendix A 395 stroke volume the amount of blood pumped out of one ventricle of the heart as the result of a single contraction. systolic arterial pressure the maximal pressure reached in arteries close to the heart (such as the ascending and descending aorta), corresponding to the maximal contraction of the ventricles. triglycerides glycerides in which the glycerol has three fatty acid molecules attached. They are the main constituent of vegetable oil and animal fats. Appendix B Image Credits All images are either by the author or in the public domain, except for the following: Note: Shutterstock images are copyright by the artists listed (as they are named on the Shutterstock web site, 2016). Used under license from http://Shutterstock.com. Some images have been modified by the author. Figure 1.1 Figure 1.2 Figure 1.3 Figure 1.4 Figure 1.5 Figure 1.7 Figure 1.8 Figure 1.11 Figure 1.12 Figure 1.17 Figure 1.18 Figure 1.19 Figure 1.25 Figure 1.26 Figure 1.27 Figure 1.28 Figure 1.29 Figure 2.1 Figure 2.2 Figure 2.3 Figure 2.4 Figure 2.5 Figure 2.8 Figure 2.12 Figure 2.13 Figure 2.22 Figure 2.28 Figure 3.1 Figure 3.2 Figure 3.3 Image by permission of Shutterstock, Artist Sokolenko Image by permission of Shutterstock, Artist s oleg Image by permission of Shutterstock, Artist ZIGROUP-CREATIONS Image by permission of Shutterstock, Artist Constantine Pankin Image by permission of Shutterstock, Artist bayualam Image by permission of Shutterstock, Artist Stockagogo, Craigbarhorst Image by permission of Shutterstock, Artist Vereshchagin Dmitry Image courtesy of Philips Canada Image courtesy of Philips Canada Figure 1–15 courtesy of Fluke Biomedical Image by permission of Shutterstock, Artist Iconic Bestiary Image by permission of Shutterstock, Artist snapgalleria Image by permission of Shutterstock, Artist file404 Image by permission of Shutterstock, Artist adike Image by permission of Shutterstock, Artist Alila Medical Media Image by permission of Shutterstock, Artist fi3 Image by permission of Shutterstock, Artist visceralimage Image by permission of Shutterstock, Artist Dean Drobot Image courtesy of Philips Canada Image courtesy of Philips Canada Image courtesy of Philips Canada Image courtesy of Philips Canada Image courtesy of Philips Canada Image by permission of Shutterstock, Artist canbedone Image by permission of Shutterstock, Artist snapgalleria Figure 2–15 Courtesy of Philips Medical Image by permission of Shutterstock, Artist santypan Image by permission of Shutterstock, Artist VIGE.CO Image by permission of Shutterstock, Artist cirkoglu Image by permission of Shutterstock, Artist microvector Image by permission of Shutterstock, Artist kurhan Image courtesy of Philips Canada (Continued) 398 Appendix B Figure 3.5 Figure 3.12 Figure 3.13 Figure 3.18 Figure 3.19 Figure 3.21 Figure 3.27 Figure 3.28 Figure 3.29 Figure 3.30 Figure 3.31 Figure 4.2 Figure 4.3 Figure 4.5 Figure 4.16 Figure 4.19 Figure 4.20 Figure 4.21 Figure 4.22 Figure 4.23 Figure 4.25 Figure 4.27 Figure 4.28 Figure 4.29 Figure 4.30 Figure 4.34 Figure 4.37 Figure 4.40 Figure 5.1 Figure 5.2 Figure 5.3 Figure 5.8 Figure 5.9 Figure 5.10 Figure 5.11 Figure 5.12 Figure 5.13 Image by permission of Shutterstock, Artist adike Figure 3.6 Courtesy of Philips Medical Figure 3.9 Courtesy of Masimo Figure 3.10 Courtesy of Philips Medical Image by permission of Shutterstock, Artist Ms. Abidika Image by permission of Shutterstock, Artist Blamb Image by permission of Shutterstock, Artist Sebastian Kaulitzki Image by permission of Shutterstock, Artist Alila Medical Media Image by permission of Shutterstock, Artist Lisa F. Young Figure 3.24 Courtesy of Philips Medical Image by permission of Shutterstock, Artist Iconic Bestiary Image by permission of Shutterstock, Artist ducu59us Image by permission of Shutterstock, Artist Alila Medical Media Image by permission of Shutterstock, Artist Steve Buckley Image by permission of Shutterstock, Artist Chaikom Figure 4.1 Courtesy of Medit Image by permission of Shutterstock, Artist Alila Medical Media Courtesy of Medit Image by permission of Shutterstock, Artist beerkoff Figure 4.10 Courtesy of Medit Image by permission of Shutterstock, Artist anekoho Image by permission of Shutterstock, Artist mmutlu Image by permission of Shutterstock, Artist Alila Medical Media Image by permission of Shutterstock, Artist Ruslan Kerimov Image by permission of Shutterstock, Artist Creations Image by permission of Shutterstock, Artist SandiMako Image by permission of Shutterstock, Artist Alila Medical Media Image courtesy of Philips Medical Image courtesy of Philips Canada Image courtesy of Philips Canada Image courtesy of Philips Canada Image courtesy of Philips Canada Image by permission of Shutterstock, Artist Suppakij1017 Image by permission of Shutterstock, Artist ellepigrafica Image by permission of Shutterstock, Artist Stokkete Image by permission of Shutterstock, Artist Viktor Gladkov Image by permission of Shutterstock, Artist dragos87 Figure 5.4 Courtesy of GE Medical Figure 5.5 Courtesy of Philips Medical Figure 5.6 Courtesy of GE Medical Figure 5.7 Courtesy of GE Medical Image by permission of Shutterstock, Artist Poznyakov Image by permission of Shutterstock, Artist Pavel L Photo and Video Image courtesy of Philips Medical Image courtesy of GE Medical Image Courtesy of GE Medical Image courtesy of GE Medical (Continued) 399 Appendix B Figure 5.14 Figure 5.15 Figure 5.16 Figure 5.18 Figure 5.21 Figure 5.24 Figure 5.25 Figure 6.6 Figure 6.11 Figure 6.12 Figure 6.14 Figure 6.15 Figure 6.16 Figure 6.31 Figure 6.37 Figure 6.38 Figure 7.1 Figure 7.2 Figure 7.16 Figure 7.18 Figure 7.21 Figure 7.22 Figure 7.23 Figure 7.24 Figure 7.25 Figure 7.26 Figure 7.28 Figure 7.29 Figure 7.30 Figure 7.32 Figure 7.35 Figure 8.2 Figure 8.9 Figure 8.11 Figure 8.12 Figure 8.23 Figure 8.27 Figure 8.28 Figure 8.35 Image by permission of Shutterstock, Artist Tyler Olson Image Courtesy of Philips Medical Image Courtesy of Philips Medical Image Courtesy of GE Medical Figure 5–20 Image courtesy of GE Medical Image by permission of Shutterstock, Artist Monkey Business Images Figure 5–22 Image courtesy of GE Medical Figure 5–23 Image courtesy of GE Medical Image by permission of Shutterstock, Artist Bork Image Courtesy of Philips Medical Figure 6.1 Image courtesy of Philips Medical Image by permission of Shutterstock, Artist SERGEI-T Figure 6.8 Image courtesy of Philips Medical Figure 6.9 Image courtesy of Philips Medical Figure 6.10 Image courtesy of Philips Medical Image by permission of Shutterstock, Artist hkann Image by permission of Shutterstock, Artist Swapan Photography Image by permission of Shutterstock, Artist tlorna Image by permission of Shutterstock, Artist Kent Weakley Image by permission of Shutterstock, Artist Adao Image courtesy of Philips Medical Image by permission of Shutterstock, Artist Blamb Image by permission of Shutterstock, Artist Zern Liew Image by permission of Shutterstock, Artist chromatos Image by permission of Shutterstock, Artist molecuul.be Figure 7.5 Courtesy of Philips Medical. Image by permission of Shutterstock, Artist stockshoppe Image by permission of Shutterstock, Artist Tefi Image by permission of Shutterstock, Artist Dario Lo Presti Image by permission of Shutterstock, Artist snapgalleria Image by permission of Shutterstock, Artist Tyler Olson Image by permission of Shutterstock, Artist Blamb Image by permission of Shutterstock, Artist Evan Lorne Image by permission of Shutterstock, Artist BlueRingMedia Image by permission of Shutterstock, Artist Designua Image by permission of Shutterstock, Artist Mr. High Sky Image by permission of Shutterstock, Artist kocakayaali Image by permission of Shutterstock, Artist Monkey Business Images Image by permission of Shutterstock, Artist Bork Image by permission of Shutterstock, Artist Oleksiy Rezin Image by permission of Shutterstock, Artist Anna Jurkovska Image by permission of Shutterstock, Artist Alila Medical Media Image by permission of Shutterstock, Artist Emin Kuliyev Image by permission of Shutterstock, Artist Sebastian Kaulitzki Image courtesy of Fluke Biomedical Image courtesy of Fluke Biomedical Image by permission of Shutterstock, Artist Oleg M (Continued) 400 Appendix B Figure 8.40 Figure 8.48 Figure 8.50 Figure 9.1 Figure 9.4 Figure 9.5 Figure 9.7 Figure 9.13 Figure 9.16 Figure 9.17 Figure 9.20 Figure 9.21 Figure 10.5 Figure 10.10 Figure 10.11 Figure 10.13 Figure 10.14 Figure 10.16 Figure 10.18 Figure 10.20 Figure 10.21 Figure 10.22 Figure 10.23 Figure 10.26 Figure 10.36 Figure 10.43 Figure 15.1 Figure 15.2 Figure 15.3 Figure 15.4 Figure 15.5 Figure 15.6 Figure 15.7 Figure 15.8 Figure 15.9 Figure 15.10 Figure 15.11 Figure 15.12 Figure 15.13 Figure 15.14 Figure 15.15 Figure 15.16 Figure 15.17 Figure 15.18 Figure 15.19 Figure 15.20 Figure 15.21 Image by permission of Shutterstock, Artist Pittawut Image by permission of Shutterstock, Artist Sergio Stankhnyk Image by permission of Shutterstock, Artist O. Bellin Image courtesy of Fluke Biomedical Figure 9.3 Courtesy of Fluke Niomedical Image by permission of Shutterstock, Artist Kostov Image by permission of Shutterstock, Artist STRINGER Image Image by permission of Shutterstock, Artist Neiron Photo Image courtesy of Fluke Biomedical Image by permission of Shutterstock, Artist Luis Bras Image by permission of Shutterstock, Artist schematic 146211257 Image by permission of Shutterstock, Artist Vertyr Image courtesy of Fluke Biomedical Image courtesy of Fluke Biomedical Image courtesy of Fluke Biomedical Image courtesy of Fluke Biomedical Image courtesy of Fluke Biomedical Image courtesy of Fluke Biomedical Image courtesy of Fluke Biomedical Image courtesy of Fluke Biomedical Image courtesy of Fluke Biomedical Image courtesy of Fluke Biomedical Image courtesy of Fluke Biomedical Image courtesy of Fluke Biomedical Image courtesy of Fluke Biomedical Image by permission of Shutterstock, Artist OlegSam Image by permission of Shutterstock, Artist Craig Wactor Image by permission of Shutterstock, Artist Oguz Aral Image by permission of Shutterstock, Artist hkann Image by permission of Shutterstock, Artist hkann Image by permission of Shutterstock, Artist mmutlu Image by permission of Shutterstock, Artist Lorelyn Medina Image by permission of Shutterstock, Artist Athanasia Nomikou Image by permission of Shutterstock, Artist hkann Image by permission of Shutterstock, Artist hkann Image by permission of Shutterstock, Artist hkann Image by permission of Shutterstock, Artist Blamb Image by permission of Shutterstock, Artist Alexonline Image by permission of Shutterstock, Artist Sebastian Kaulitzki Image by permission of Shutterstock, Artist Sebastian Kaulitzki Image by permission of Shutterstock, Artist Alexonline Image by permission of Shutterstock, Artist Oguz Aral Image by permission of Shutterstock, Artist Blamb Image by permission of Shutterstock, Artist mmutlu Image by permission of Shutterstock, Artist Blamb Image by permission of Shutterstock, Artist Oguz Aral Image by permission of Shutterstock, Artist mmutlu Image by permission of Shutterstock, Artist Bork Index A AAMI 195, 285, 316, 361 Abbott 89 abdomen 3–5, 23, 126, 128, 131, 145, 232, 386 abdominal 29, 109–110, 112, 131, 142, 212, 232 ability 7, 18, 43, 90, 103, 166, 222, 237, 268, 311, 318, 325, 394 ablation 11, 237 abnormal 11, 26, 59, 73–74, 100, 104, 113, 359, 360 abnormalities 63, 103–104, 174 abnormally 75 abrading 51 abrasive 51 absence 104 absorb 82, 153–154, 208, 222, 329 absorbance 82, 97, 222 absorbed 108, 119, 142, 155, 264–265, 267 absorbent 267 absorber 216, 394 absorbing 153, 214 absorbs 81, 97, 209, 214, 245 absorption 33, 84 AC 16, 37–39, 48, 53, 164–165, 176, 180, 222, 251, 261, 286, 288–289, 291, 307, 365–366, 370, 372–373 accelerated 142 accelerating 154 accelerators 154 accelerometer 178 acceptance 359 access iv, ix, xv, xx, 14, 118, 159, 195, 228–230, 232, 248, 250–251, 254, 270, 326, 347, 351–352, 354, 359, 374 accessible xv, 29, 63, 75, 135, 167, 170, 174–175, 180, 230, 265, 296, 303, 351 accessories 10, 15, 17–18, 39, 161, 174, 251, 261, 263, 291, 301 accidents 28, 167, 207, 268, 303 accidental 33, 224 accidentally 256 accommodate 68, 114, 116, 123, 165, 250 accommodated 288 accompanied 15 accreditation 361 accredited 358–359 accrediting 361 ACCU 325 accuracy 53, 76, 82, 84, 87, 118, 172, 187–188, 190–191, 193, 197, 202, 222, 286, 307, 318, 321–323, 325, 345, 347 accurate 20, 39, 44, 52, 61, 63, 68, 70, 75–76, 79, 81–82, 86–87, 97, 113, 116, 126, 138, 172, 187, 225, 245, 287, 290, 296, 301, 307, 320–321, 331, 333, 345, 350 acetylcholine 19, 102, 106 acetylcholinesterase 102 acid 4–5, 164, 176, 226, 234, 375, 395 acidic 394 acidity 394 acidosis 86 ACLS 320 acoustically 5 acquired 21, 382 acquisitions xix, 17, 195, 310, 331, 349, 351 acrid 338 acronyms 61, 134 act 88, 360 action 18–19, 21, 26, 48, 53, 102, 106, 184, 190, 202, 234, 258, 265, 272, 274, 277, 305, 343 activated 28, 31, 64, 136, 165, 206, 262 active 31, 46, 106, 132, 134, 258, 260, 394 activity 20, 32, 46, 57, 61, 103–104, 106, 134, 154, 166, 170, 178, 314, 356–357, 394 actuation 206 acuity 181, 226 acupuncture 278 acute xix adaptations 32 adapted 40, 172, 233, 358, 359 adapters 7 ADD 13 addresses 356–357 adept 2, 269 adequacy 206, 261 adequate 33, 43, 46, 58, 64, 69, 73–76, 79, 90, 98, 116, 119, 143, 159, 164, 174, 182, 191, 196, 198, 205, 213, 221, 232, 248–249, 279, 283, 296, 345, 368 adequately 226, 246, 323, 326, 375 adhere 89 adhesion 68 adhesives 18, 51, 84, 166, 176, 339, 340 adjacent 138, 237, 264 adjourned 196 adjust 82, 87, 99, 118, 189, 237, 241, 326 402 adjustability 320 adjustable 124, 182, 200, 286, 333, 337–338 adjusted 79, 84, 88, 123, 125, 131, 137, 189 adjusting 79, 220, 269 adjustments 115, 240, 274 administer 198, 349 administered 106, 125, 154, 160, 187, 190, 211, 213, 222, 251 administering 188 administration ix, xiii, 61, 89, 106, 167, 187, 193, 211, 360, 362, 371 adopted 7, 55, 165, 353–354 adoption 353, 357–359 adrenal 386, 394 adrenaline 19, 21 advanced 35, 177, 344 advancement xiii, 18, 196, 361 advances 69, 101, 157, 204, 217, 245, 357 advancing 211, 361 advantages 22, 34, 80–81, 140, 199, 209, 210, 212, 232, 236, 244, 264, 267, 282, 347 advent 5, 8, 157, 257 adventures xv adverse 360 advice 305 advises 359 advocacy 355 AEDs 166, 170, 175–176 affect 20, 33, 60, 79, 82, 102, 114, 138, 221, 287, 306, 357 affected 153 affecting 20, 82, 357 affinity 362 affixed 38, 263, 288–289 affixes 16, 39, 291 Africa 180 after xix, 4, 12, 15–16, 19, 23, 28, 67, 69, 76, 79, 88–89, 93–94, 119, 134, 136, 157, 162–165, 169, 172–173, 178, 195, 199, 203, 206–207, 214, 232, 236–238, 249, 255, 267, 268, 279, 291, 296, 303, 305, 316, 355, 367, 369 agent ix, 106, 165, 182, 188, 195, 196, 198, 211, 213, 217, 219–222, 223, 243, 293 agitated 11, 79 AGMs 221–222 agonists 102 agriculture 356, 360 Ah 302 AHTM 14 aid 25, 122, 123, 125, 134, 145, 172, 175, 238, 279, 281–282, 292, 311, 329, 341 aiding 20 ailments 1 Index air 28–29, 34, 77, 91, 93–95, 97, 99, 109, 112, 116, 119, 122, 137, 192, 198–201, 205, 207–208, 217, 219–220, 225, 245, 248, 250–251, 256, 266–268, 273, 298, 331, 339, 367, 372, 385 airflow 204, 209, 248, 326–327 airtight 165, 176 airway 28, 204, 207, 209, 219, 251 alarmed 297 alarms v, 15, 39, 43, 54, 59, 78, 79, 89, 119, 136, 171, 173–174, 185, 189, 198, 205, 209, 219, 225, 248–249, 255, 262, 274, 291, 297, 318, 374 alcohol 51, 71, 102, 135, 211, 273, 293, 340, 394 alert 202–203, 225, 360 alerted 43 algorithm 54, 84, 79, 82, 106, 135, 331 align 153, 355 aligned 153 alike 357 alkaline 394 alkalinity 394 alleviate 98, 119, 164, 205, 211 alleviated 184 alleviates 40 alleviating 217, 255 allocate 357 allocated 46 alloy 171, 338 Aloe 2 alpha 104 alphanumeric 172–173, 331 alter 34, 82, 184 alteration 312 altered 79, 90, 98, 233 altering 105 alternate 10, 39, 205, 290 alternately 236, 277 alternating 63, 165, 283 alternative 228, 232, 237 aluminum x, 265 alveoli 28, 385 ambient 34, 82, 328 ambulances 162 ambulatory vi, 49, 61, 68, 80, 232 amendments 355 America 46, 358 American xiii, 89, 175, 358, 361 amino 234 ammeter 287 ammonia 234 ammonium 386 amp 302 amphetamines 102 amplification 44, 49 Index amplified 5, 22, 51, 53, 58, 131–132, 388 amplifier v, 40, 43, 48, 51, 52, 103 AMPLIFIERS 51 amplify 51, 53, 143 amplifying 47, 53, 178, 344 amplitude 21–23, 50–51, 53, 75, 84, 104, 106, 107, 164–165, 172, 179–180, 222, 278, 311, 314, 321, 345, 388 amps 310 anaesthetized 236 anaesthetizing 223 anagement 356–357 analgesia ix, 193, 195 analgesic 193, 197 analog xii, 44, 51, 58, 65, 67, 69, 133, 201, 321, 344–345, 347 analogous 77 analogto 346 analysis vi, viii, 2, 20, 24–26, 42, 44, 54, 59–61, 68, 70, 73, 81, 86, 94–97, 105, 107, 167, 170, 172, 175, 178–179, 181, 196, 310, 326, 328, 344, 349 analyze 310–311, 327, 329, 359 analyzed 35, 51, 58, 61, 75, 77, 86, 87, 90, 97, 103–104, 169, 178, 240, 311, 329, 344 analyzer vi, xi, 15–16, 38–39, 61, 70, 87, 95, 99, 103, 108, 209, 260–263, 285, 287, 289–290, 298, 304–305, 313–315, 317–318, 321–324, 326, 329–331, 342 anatomical i, xv, xix, 18, 34, 222, 296, 379 anatomy i, v, xiii, 1, 35, 47, 108–109, 123, 161, 183, 211, 252, 379, 381, 383, 385, 387–389 ancillary i, xv, xx, 13, 18, 353, 363, 379 anesthetic 73, 79, 84, 98, 101, 103, 106, 188, 200, 209, 211–215, 217–219, 221–222, 243–244 anesthetists 182 anesthetized 198 aneurysms 74 angina 74 angioplasty 27 Anion 88 annihilated 155 annual 143, 195 anomalies 103, 287 anomaly 310 another xix, 3–5, 11, 16, 19, 27–28, 35, 37, 43, 45, 73, 84, 102, 138, 154, 167, 190, 196, 198, 204, 219, 225, 263, 273, 285, 288, 305, 321, 333, 367 ANS 361 ANSI 285, 316, 358, 361 Ansur xii, 286, 318, 322, 330, 352 answers 16 403 antagonists 102 antenna 44, 46, 71, 178 antepartum 128 anterior 384 anthropologist 1 antibody 360 antiseptic 1 Antistatic 305–306 anus 109–110, 223 anvil 388 anxiety 11 aorta 126, 128, 181, 394–395 aortic ix, 73, 126, 161, 181, 383 Apgar vii, 134, 253–255 aphasia 103 apnea 207 aprons 144 APRV 204 arachnoid 388 argon x, 266 array 117, 128, 165, 237 arrhythmia vi, 26, 32–33, 49, 54, 59, 60, 320–321 arterial 84, 321, 393–395 arteries vii, 27, 39, 70, 74, 77, 138, 148, 187, 230, 290, 382, 384, 394–395 arteriosclerosis 74, 384 arteriovenous 230 arthroscopic 109, 119 arthroscopy vii, 109, 121, 139 articulating 268 artifacts v, 39, 53–54, 290, 322, 328 artificial 27, 161, 180, 181, 198–199, 209, 214, 230, 240, 389 artificially 26 ascending 394–395 aspirated 251 assurance xi, 16, 295, 320, 349, 353 asystole 61 atherosclerosis 74, 394 atria 20–21, 23, 26, 61–62 atrial 23, 26, 61–62, 71, 162, 163, 166, 172, 210, 322, 393 atrioventricular 21, 26 atrium 20–21, 23, 179, 181, 382, 394 atropine 167, 169 AU xv, xx–1, 301, 353, 362 audio 173 auditory 388 audits 356, 359 Auel 1 auger 27 augmented 49, 56, 251 auscultation 76 auscultatory 46, 77–78, 80 autoclaves 272 404 autosequences 320, 322 AV 21, 23, 26, 230, 331 aVF 49, 56–57 aVL 49, 56 aVR 49, 56–57 axes 145 axial 149 axon 102 B backlight 302 badges 144 balance i, 29–30, 64, 86, 106, 132, 152, 230, 244, 251, 361, 388 Balke 68 balloon ix, 27, 161, 181, 394 bandwidth 58, 245 bar 82, 191, 288 barbiturates 102 barcode 318, 320, 351–352 barium 148 basic 359 bassinette 245 bath 34, 184, 186, 226, 230, 236, 274–275 bathing 4 battery 5, 17, 37–39, 43–44, 47, 53, 69, 80, 114, 122, 136, 148, 161, 164, 170–171, 178, 189, 196, 198, 201, 205–206, 210, 219, 278, 288, 291, 296–297, 320, 326, 328, 358, 372, 375 Baxter 297–299 BCI 328 BDU 202 Be 88 bell 5 bellows 95, 199–200, 216 belly 3–4 belt 3, 64 bench 18, 38, 84, 283, 287, 289, 337 benchmark 357 Bennett 201, 203 benzocaine 103 beta 104 bicarbonate 394 bicuspid 383 bidirectional 324, 330 bigelow 176 bigeminy 62 bile 380–381, 394 bilevel 205, 207 bili 245–247 bilirubin 245–247, 281–282, 392, 394 binary xii, 344–345 binds 28, 82 binocular 7, 9, 125, 242, 268, 270–271 biofeedback 105 Index biohazardous 295 biological 27, 142–143, 184, 360 biologically 171, 238 biomed i, xv, 15, 18, 195–196, 260, 274, 283, 291, 295–296, 307, 312, 335, 342, 346–347, 351, 369, 372–374, 376 biomedical i, iii, xi–xii, xv, xvii, xix, 2, 4, 6, 8, 10, 12–16, 18, 20, 22, 24, 26, 28, 30, 32, 34, 36, 38, 40, 42, 44, 46, 48, 50, 52, 54, 56, 58, 60, 62, 64, 66, 68, 70, 74, 76, 78, 80, 82, 84, 86, 88, 90, 92, 94, 96, 98–100, 102, 104, 106, 108, 110, 112, 114, 116, 118, 120, 122, 124, 126, 128, 130, 132, 134, 136, 138, 140, 142, 144, 146, 148, 150, 152, 154, 156, 158, 160, 162, 164, 166, 168, 170, 172, 174, 176, 178, 180, 182, 184, 186, 188, 190, 192, 194, 196, 198, 200, 202, 204, 206, 208, 210, 212, 214, 216, 218, 220, 222, 224, 226, 228, 230, 232, 234, 236, 238, 240, 242, 244, 246, 248, 250, 252, 254, 256, 258, 260, 262, 264, 266, 268, 270, 272, 274, 276, 278, 280, 282, 284–286, 288, 290, 292, 294, 296, 298, 300, 302, 304, 306, 308–312, 314–332, 334, 336, 338, 340, 342, 344, 346, 350, 352, 354, 356, 358, 360, 362, 366, 368, 370, 372, 374, 376, 380, 382, 384, 386, 388, 397, 399–400 biopsies 101, 120 BiPAP ix, 161, 207, 209 biphasic 165, 210, 329–330 bipolar x, 121, 258, 261, 263, 282, 367 birds 1 birth 134, 246, 251, 255 BIS vi, 106, 108 BiSpectral 103, 106 bits 58, 345 blackbody 331 bladder 30, 77, 109, 120, 187, 226, 376, 381, 386–387 blades 10, 122, 123 bled 39, 256, 290, 305 bleeding 10, 75, 256, 258, 321 blend 258, 263 blended 200, 255 blender 221, 255 blindness 30, 90, 98 block 41, 53, 63, 106, 114, 121–122, 133, 184, 198, 370, 384 blockage 25–26, 28, 75, 197, 225 blocked 19, 26–27, 76, 79, 141, 143, 199, 205, 225, 260, 297 blocking 28, 103, 187 blocks 28, 41, 71, 224 405 Index blood 1, v–vi, ix, 5–7, 20–21, 23, 25–30, 32, 34–35, 39–41, 44, 46, 59, 61, 63, 70–71, 73–82, 84, 86–93, 98, 107–108, 112, 119–120, 125, 138, 154, 161–164, 167, 171, 178, 181–187, 204, 209–210, 217, 223, 226–228, 230, 232–233, 244–245, 256, 260, 284, 290, 320–321, 327, 367, 382, 384–385, 394–395 bloodletting 226 bloodstream 27, 148, 187 bluefolder 351 Bluetooth 5, 69, 316 BME xv BMET i, xv, 12–13, 166, 174, 283, 292, 307, 343 BNP 88 board 15, 41, 196, 251, 297, 300, 302–303, 305, 311, 338, 341, 366, 368 boiling 212, 219–220, 292 boils 258 bolus 71, 193 bone vii, x, 1, 8, 31, 121, 138–139, 141, 245, 256, 265, 281, 388 boosted 53, 164, 178 boosts 187 bore 228 born 246, 251–252 bottle 3 Bovies 10, 257 BP 38, 47, 80–81, 288, 322 BPM 324, 328 bpm 26 brachial 39, 76–77, 290 bradycardia 60, 62, 63, 178 brain 9, 30, 32–34, 75, 97, 103–106, 123, 154, 156, 199, 223, 245, 388–389, 394 branch 21, 63, 362, 381, 385 breast 149 breath 29, 34, 93–94, 199–200, 205, 211 breathe 248 breathed 11, 94 breathing 3, 5, 81, 63, 91, 94–95, 98, 106, 135, 198–200, 205, 209, 214, 217, 248, 251, 255, 322, 325, 388 breaths 29, 97, 205 bridge 177, 181 brightness 196 Britain 162, 238 British xix, 362 broadband 222 broadcast 43 broken iv, 53, 101–102, 135, 238, 245, 282, 295, 301, 375, 377 bronchi 28, 100 bronchial xx, 101, 109, 212 bronchioles 28, 385 Bronchoscopes 101, 109 bronchoscopy vi, 73, 100 Bruce 49, 67–68 BSI xiii, 362 bsigroup 362 Buckley 398 buffers 30 bulb 113–114, 116, 122, 187, 245, 279 bullet 211 BUN 88, 392, 394 bundle 21, 26, 63, 318 burned 303 burning 10, 101, 264, 266 burns 17–18, 51, 143, 165, 241, 258, 314 button 44, 69, 87, 131, 136, 168–169, 193, 195, 310, 316, 328 bypass 219, 220 bypassed 27, 181, 230 bypassing 200, 208 byte 345 C CA 359–360 cabinet 46, 118, 184, 209, 335 Cable 129 cables xx, 38, 53, 67–68, 112, 117, 196, 250, 260–261, 272, 288–289, 314, 316, 331, 335, 368 cadmium 164 caesarian 212 calcareous 139 calcium 19–20, 29, 88, 234, 392 calculi 234, 386 calibrated 325 calibrated 39, 75, 88, 95, 99, 106, 138, 245–246, 279, 290, 298, 307, 314, 331 calibrations 46, 80, 82, 87, 88, 97–99, 185, 198, 201, 283, 298, 307–308, 323, 331–332, 346 calibrator 331 caliper 335 calyx 386 cam 191 camera vii, 7, 100–101, 109–110, 116–118, 140, 143, 270 cams 117 Canada xii–xiii, xv, xix, 12–13, 41, 50, 52, 54, 60, 89, 129–130, 133, 286, 357–361, 397–398 Canadian 176, 353, 358–359 canal 122, 137, 388, 394 cancer 120, 144, 149, 156, 258 cancerous 143 canister 214 cannula 75 canopies 238, 250 capability 35, 43–44, 171–172, 249, 287, 311–312, 321, 324, 352–353 406 capacitance 164, 307 capacitive 284 capacitor 164–165, 173, 284, 287, 312 capacity 30, 43, 59, 70, 94, 109, 182, 188, 205, 208, 245, 248 CAPD 232–233, 244 capillary 73, 86, 230, 328, 385 capnographs vi, 97, 107, 171, 173, 205 capsule 238 carbohydrates 27, 29 carbolic 4–5 carbon 20–21, 27–29, 34, 84, 86, 95, 97, 119, 140, 154, 157, 173, 181–182, 212, 214, 221, 264, 382, 385, 394 carboxyhemoglobin 84 cardiac 11, 14, 21, 24–27, 33–34, 41, 43, 47–49, 52, 55, 59–63, 67–71, 73–74, 84, 108, 148, 157, 162, 166, 170–171, 173, 175–179, 181, 198, 205, 212, 284, 320, 380, 384, 394 cardiologist 61, 162, 169 cardiology 176, 180 cardiopulmonary 163 cardiorespiratory 33 cardiotocographs 128 cardiovascular 162 cardioversion 26, 162, 172, 210, 329–330 carriers 310 cartilage 31, 86–87, 121, 139, 197 carts 171, 375 cassettes 143, 145, 190, 251, 254 CAT 40, 149 cataract 237, 238, 242, 243, 244, 389 catheter 27, 61, 70–71, 75, 181, 187–188, 198, 229, 230, 232, 394 catheterization 320 cauterization 10, 257 cauterize 10, 120, 256–257, 367 cauterized 257 cauterizing 112, 258 cautery 367 cava 181, 230, 394 cavitation 237 cavities 29, 119, 232 CB 358 CBET 13 CCC iv CCDs 143 CCl 212 CCPD 232 CCU 169 CD 38, 288 CE 286 CEI 358 Celite 88 Cell 351 Index cells 7, 18–19, 25, 27–28, 30, 81, 86, 90, 97, 99, 102, 143, 163, 182, 184, 230, 245, 258, 389, 391, 394 celsius 136 cements 339 central v, 15, 35, 38, 40–43, 45–46, 71, 86–87, 131, 159, 171, 193, 208, 279, 289, 293, 298, 321, 356, 373, 394 centrifugal 182 centrifuges 312 cephalic 179 cerebral 103, 394 cerebrospinal 388, 392, 394 cerebrum 388 certification xii, xv, 286, 353, 357–359, 362 certified 325, 356 certifies 358–359, 362 certifying 357 cessation 61, 163 CFM 352 CH 211 ch 354–355 chamber 20, 23, 27, 162, 184, 187, 190, 219–220, 225, 244, 254, 272, 367, 369 channel 44–46, 103, 109, 122, 140, 159, 185, 193, 219–220, 331, 370 charge 17, 143, 152, 155, 164–165, 171–176, 210, 297, 369 charged 38, 164, 288 charging 38–39, 164, 173–174, 176, 288, 291, 372, 375 chart 15, 42, 53, 68, 95, 131, 171–172, 210 charted 75 charting 35 chassis 44, 77, 173, 260–261, 285, 287 CHCl 211 check 1, 14, 16, 39, 43–44, 87, 174, 201–202, 261, 284, 290, 297, 301–302, 305, 312, 328, 331, 367 checked 11, 37, 260, 262, 288, 297, 303 checking 37, 39, 260–261, 288, 291, 303 checklist 320, 366 CHEM 88 chemical v, xi, 1, 18–19, 26, 29, 30, 34, 60, 86, 99, 102, 143, 184, 230, 234, 264, 266, 272, 291–292, 394 Chemistry vi, 86, 167, 184, 228, 233, 392 chest 24, 27, 29, 49, 55, 57, 74, 93, 97, 145, 161–162, 166, 168, 176, 179–180, 230, 281 child 1, 321, 391 childbirth 109 children xix, 33, 63 chip 101, 109, 117–118, 140, 335, 346 Index chloride 27, 51, 53, 88, 392, 394 chlorine 29, 228, 266, 272 chloro 212 chloroform 211 cholecystectomy 120 cholesterol 74, 392, 394 chordae 383 chromatos 399 chromosomes 143 CICU 14–17, 86 CIDH 355 ciliary 389 circuit 41, 51, 95, 98, 165, 173, 176, 178, 196, 201–202, 209, 214, 217, 258, 279, 281, 284, 287, 297, 300, 302–305, 307, 325, 338, 341, 344, 366–368, 372, 375 circuitry 11, 39, 44–45, 48, 51, 54, 84, 105, 133, 164–165, 170–171, 173–175, 181, 199, 223, 287, 290, 298, 300, 316, 344 circulate 181, 388 circulating 367 circulation v, 34, 70, 90, 209, 248, 250 circulatory 1, 32, 73, 98, 107, 161, 180, 382 Cl 88, 392 clarity 18, 39, 237, 291 classifications 26, 61 ClCH 212 Cleveland 11, 162 clinical i, xx, 35, 53, 70, 84, 101, 113, 162, 164, 174, 285, 324–325, 349–351 clinically 44, 52, 80, 172 clinician 76, 87, 106, 118, 123, 195 clinics 138, 171, 354 closure 79 clouded 237–238 cm 31, 79, 343 CO vi, 73, 86, 97–98, 110, 205, 216, 264–265, 267, 397 COAG 258, 263 coagulate 258 coagulating 53, 258 coagulation 10–11, 264–265 cocaine 102 cochlea 388 cognitive 75 coherent 264 coil 4, 49, 198 coiled 166 coiling 39, 291 coincides 237 cold 27, 33–34, 71, 267 collapse 198, 237 collapsed 3 collapsible 251 collapsing 383 collateral 10, 358, 359 407 college i, 13, 362 collides 142, 155 collimator 145, 148 collision 142 colon 109–110, 117, 227, 259 colonoscopes 109 colonoscopy 111, 258 coma 30, 86, 106, 392 comatose 4 communicate 88–89, 103, 178, 197 communication 32, 40, 43–44, 69, 159, 217, 320, 328, 346, 350, 369 compartment 38, 44, 136, 251, 279, 288, 367 compartmentalized 279 compatible 27, 318, 324 compensate 132 compensating 79 compensation 99 complex xix–xx, 12, 20, 23, 29, 54, 59, 86, 94–95, 106, 116, 125, 141, 152, 172, 198–199, 205, 207, 212, 287, 310–311, 321, 344, 346, 360 compliance 286, 325, 349, 352–354, 359, 362 compounds 27, 51, 143, 212, 268, 339–340 compress 149 compressed 6, 76, 131, 190–191, 199–200, 208, 267, 279 compresses 190 compressing 190 compression ix–x, 161, 183–184, 190–191, 280, 282 compressor 150, 199, 200–202, 206, 208 computer 7, 14, 16, 40–41, 44, 58, 61, 71, 82, 95, 145, 151, 205, 286–287, 308, 312, 318, 326, 328, 330, 346–347, 351 computerized 26, 39, 86, 94, 290, 329 computers i, 53, 70, 88–89, 157, 343, 346–347 computing 152 concentration 30, 41, 70–71, 82, 86, 97, 99, 105, 174, 205, 208–209, 217, 220–222, 244, 255, 267, 272, 312, 324, 327, 394 concentrators 161, 208–209, 312, 372 conditioner 34 conditioning 44, 62 conditions 20, 25–26, 33, 38, 73, 82, 86, 90, 104, 120, 122–123, 138, 141, 144, 172–174, 205, 207, 211, 233, 246, 279, 284–286, 289, 300–301, 322–323, 325–326 conducted 102 conducting 19 conduction 18–20, 25–26, 102 conductivity 51, 142, 228, 267 conductors 27, 120, 284, 340, 366, 368, 370 configurability 54 configuration 16, 42, 48, 196, 316 conformity 354 408 congestion 281 connectivity 46, 193, 197 connector 10, 40, 114, 116, 129, 171, 173, 186, 255, 261, 287, 305 connectors 10, 40, 116, 129, 255, 261, 287, 337, 340, 368 consciousness 104, 106, 221 console 110, 117 consumables 196 contact iv, 10, 22–23, 50, 53, 58, 69, 86, 97, 99, 136, 142, 165–166, 171, 176, 200, 230, 236, 240, 258, 260, 262, 266–268, 272, 283–284, 287, 291, 293, 307, 312, 316, 335, 347, 366, 368 contagious 293 contaminants 228 contaminated 53, 272–273, 293 contamination 84, 135, 209, 371–372 continual 356, 365 continue 14, 31, 33, 46, 62, 135, 162, 203–204, 206, 232, 301 continued 13, 26, 107, 181, 185, 204, 219, 228, 237, 343, 397–399 continues 5, 14, 169, 181 continuing 14 continuity 174, 287, 303–304, 307 continuous x, 47, 68, 81, 107, 119, 143, 176, 204, 207, 232, 316 continuously xix, 61, 164, 209, 230, 233, 249 contract 6, 20–21, 23, 25, 34, 52, 61–63, 180, 190, 196, 222, 268, 300, 350, 394 contracted 102 contracting 61, 162–163 contraction 20–21, 23, 26, 63, 106, 131–132, 162, 395 contracts 19, 29, 48, 351, 389 contrast 286 contribute 50, 357 controller vi ix, 63–65, 67, 187 controlling 11, 26, 30, 38, 64, 187, 289 controls 68, 114–115, 119, 173–174, 180, 195, 201, 214, 218, 225, 232, 238–239, 250–251, 253, 262, 268–269, 272, 274, 276, 278, 388 convergence 283 conversion 44, 58, 67, 133, 345, 346 convert 58, 89, 143, 165, 213, 328, 389 converted 28, 52, 58, 60, 345–346, 388 converters 58, 321, 346 converting 117, 345 converts 219 convulsions 34, 222, 223 convulsive 11 cooled 172, 186 coordinate 43, 354 coordinated 25, 47, 61–62, 157, 164, 360 Index coordinates 388 coordinating 11 coordination 21, 32, 182, 388 copper 142, 160 cord 16, 37–38, 40, 136, 166, 199, 207, 261, 287–289, 291, 303, 365, 370, 373–374, 388, 394 core 31–34, 135–136, 140, 331, 338, 342 cornea 239–241, 266, 389 corneal 240 corners 112, 264 coronary 384 correlation 78, 128, 131, 135 corresponding 54, 97, 104, 106, 128, 389, 394–395 corrosion 303 corrosive 272 counters 143 coupled 5, 143, 196 couplet 63 coupling 91, 126, 236, 244, 284 Covidien 203 CPAP ix, 161, 204–205, 207, 209 CPM 274 CPR 163, 166, 169, 175 CPU 15, 41, 368 CQM 316 cracked 101, 126 cracks 370 crash 15–16, 166–168, 171 creatinine 88, 226 credentials 358 crest 237, 314, 316 criteria 134, 248, 286, 314, 353, 355–356, 359 criterion 134, 353 critical 12, 21, 25, 28, 41, 43, 46, 50, 60–61, 68, 71, 80–81, 86–87, 97, 121, 137–138, 172, 174, 178, 187, 195–198, 203, 221, 225, 258, 272, 295–296, 307, 310, 316, 329, 349–350, 368 critically 134 Crookes 4 CRT 118, 171, 173, 308, 311 cryosurgery x, 245, 267–268, 281–282 crystalline 234 crystals 76, 91, 126, 128, 130, 157, 209, 237, 276 CSA xii, 286, 353, 357–359 csagroup 357 CSF 31 CT 27, 43, 61, 103, 141, 144, 149, 152, 155–156, 159–160, 358 cubital 76–77 cuff 38, 39, 46–47, 77–81, 279, 288, 290, 321–322, 376 cumulative 305 Index current i, xvii, 10–11, 15, 20, 34, 38, 51, 61, 82, 97, 116, 135, 142, 163, 165, 168–169, 178, 196, 202, 219, 222–223, 251, 257–258, 260, 263–264, 283–287, 289, 306–307, 309–310, 316, 330–331, 344 cushing 10 customized 320, 326 cut 8, 10, 64, 112, 154, 168, 257–258, 264, 295, 333 Cyan 343 cyanoacrylate 339 cycle 23, 26, 28, 73, 75, 79, 84, 91, 94, 184, 204, 232–233, 258, 272–273, 349 cycled 258 cyclic 73, 232 cycling 181, 232, 233 cyclopropane 200, 212 cyclotron 157 cystic 381 cystine 234 Cystoscope 109 D dampened 266 dangerous 71, 210, 217, 268, 284, 287 dangerously 78 dangers 135, 222, 235, 266 data iv, 14, 35, 40–43, 46, 60, 68, 70, 79–80, 90, 93, 95, 97, 131, 149, 151–152, 157, 159, 170, 172–173, 193, 210, 217, 240, 251, 286–287, 291, 299, 310, 316, 318, 320, 327, 329, 331, 345–347, 349, 351 databases 14, 16, 38–39, 159, 289, 298, 346, 351 dB 313 DC 53, 164–165, 286, 307, 330–331 DDT 102 decades 257 decays 144, 155, 177 deciliter 88 declines 32, 82 decommissioning 349 decontamination 368 default 16 defect 5 deferens 258 defib 161, 165, 168–169, 172–173, 175, 302, 329 defibrillate 161–162, 165 defibrillated 162 defibrillating 26, 166 defibrillations 26, 61, 162–163, 165, 166, 168–169, 172, 175, 177, 210 defibrillators v, viii, 11–12, 14–15, 17, 27, 34, 61, 79, 84, 161–162, 164–171, 166, 170–175, 177–180, 209, 210, 210, 287, 296, 329–330, 358 409 defibs 161, 164, 170–175, 178, 209 deflate 181, 184 deflation 184 deflection 94, 131 degassed 328 degraded 272 degrades 82 degree xx–1, 33, 54, 73, 81, 90, 106, 143, 164, 172, 193, 197, 274 delta 104, 302 demands 21, 165, 181, 255 dense 141, 143 densities v, 30–31, 34, 138, 164, 165, 258, 394 densitometers vii, 138 dental viii, 142, 144, 145 depleted 99 depolarization 19–20, 23 depolarized 102 depressors 360 derivatives 102 descending 181, 394–395 desensitized 19 desflurane 103, 212, 220–221 desiccate 258 desiccated 258 desiccation 217 detached 11, 28, 123 detectors vi–viii, 6, 90, 125–126, 128, 131, 141, 143, 145, 149, 151, 198, 225 DG 302 DI 141 diabetes 30, 87, 89 diabetic 87, 89, 123 diagnostic v–viii, 35, 37, 39, 41, 43, 45, 47, 49, 51, 53, 55, 57, 59, 61, 63, 65, 67, 69, 71, 73, 75, 77, 79, 81, 83, 85, 87, 89, 91, 93, 95, 97, 99, 101, 103, 105, 107, 109, 111, 113, 115, 117, 119, 121, 123, 125, 127, 129, 131, 133, 135, 137, 139, 141, 143, 145, 147, 149, 151, 153, 155, 157, 159 dialysate 230, 232 dialysis ix, 211, 228, 230, 232–233, 243–244 dialyzer ix, 228, 230 diaphragm 5, 29 diastole 49, 74, 84, 181 diastolic 39, 46, 73–74, 76–80, 290, 322, 393–394 diathermy 276 dichloride 339 dicrotic 73 differential 55 diffusion 228 difluoromethoxy 212 digestion 30, 380 digestive vii, ix, 1, 109, 139, 148, 211, 223–224, 379 digit 344–345 410 digital vi, xi–xii, 44, 46, 52, 54, 58, 59, 65, 67, 95, 119, 133, 143, 145, 157, 159, 201, 262, 287, 307, 308, 310–311, 318, 321, 342, 344–347, 362 digitally 42 digitize 69 digitized 54, 58, 60, 132 digitizer 103 digitizing 59, 71 digits 345 dilations 101, 123, 125 dilution 27 dioxide x, 20–21, 27–29, 34, 86, 95, 97, 119, 140, 173, 181–182, 214, 221, 264, 272, 305, 337, 382, 385, 392, 394 direct x, xx, 20, 35, 44–45, 75, 78, 82, 95, 112, 121, 136, 167, 198, 219, 268, 274, 307, 320 discharge viii, xi, 1, 43, 164, 165, 169, 172–174, 238, 305 discharged 164, 172, 238 discharging 174, 329 discoloration 226 discolored 303 disease 20, 25, 27–28, 30, 33, 63, 82, 90, 103, 154, 198, 233, 293, 360 disinfection 293 disorientation 32 dispersive 262 disposable 51, 84, 101, 113, 122, 136, 180, 261 dissecting 341 dissections 152 distal 101, 109, 111, 115, 117, 184, 191 distend 119 distension 112 dL 30, 88–90, 391–392 DMM 307–309, 312 DNA 29 documentation 86, 95, 322, 330 doesn 34, 80, 84, 93, 135, 225, 251, 258, 265, 267, 300 DOI iv, 1, 35, 73, 109, 141, 161, 211, 245, 283, 307, 343, 349, 353, 365, 379 donors 27, 181 dopamine 19 DOPED x, 265 Doppler vi, 6–7, 27, 34, 90–91, 108, 125–126 downstream 70–71, 197–198, 298 drift 44, 53, 138 drill 336 drip 187, 225, 244, 369 drones 11, 176 DSP 286 duodenum 48, 109, 380–381 dura 388 DUT 286–287, 296 Index DVT 183 dye 27, 61, 70–71, 82, 143, 148, 160 dynamic 58, 320, 331 dysfunction 70 E ear 5, 81, 84, 121–123, 135, 137, 292, 388 eardrum 388 ECGs vi, viii, 11, 22–27, 35, 38, 40, 42–44, 46–55, 57–63, 67–71, 80, 97, 103, 133, 168–175, 176, 177–179, 181, 217, 222, 230, 236, 250, 286–287, 320–322, 329, 331, 347 ECRI 296, 351 ECT 106, 211, 222–223, 244 edema 98 EEG vi, 73, 103–106, 108, 222 Einthoven 14, 49, 56, 71 ejection 393, 394 electrocardiogram 11, 49 electrocardiograph 35, 162, 358 electroconvulsive ix, 106, 222, 223, 243 electrode viii, 18, 22–25, 27, 48–53, 55–57, 68–69, 71, 86, 97, 99, 103, 105–106, 120, 165–166, 168, 171, 176, 179, 180, 210, 222, 258, 260, 263–264, 277, 279, 314, 316, 321, 368 electroencephalogram 103 electrogalvanic 99 electrolytes 20, 34, 53, 86, 164, 226 electrosurgery x, xx, 10, 53, 58, 106, 120, 121, 198, 245, 257–258, 260, 264, 266, 281–282, 314, 367, 368 electrotechnical xii, 354, 358 electrotechnology 354 embolism 28 EMC 358 EMG 52 emissions viii, 141, 155 EMR 153–155 emulsify 238 EN 286 en 362 endocardial 180 endocrine 386 endoscope vii, 109, 111–112, 113–115, 120, 140, 237, 273 endoscopic 100, 112–113, 264, 265 endoscopy 110, 113, 116–118, 120, 139–140, 159, 258, 293 endothermic 31 endotracheal 123–124, 166, 205 enhanced 87 enteral 225–226, 243, 244 enzyme 102 epidemiological 347 411 Index epidermis 52 epiglottis 100 epilepsy 103–104, 223 epinephrine 19, 21, 167–168 ER 16, 166, 168–169 ergonomic viii 174, 286, 328 ERs 35 erythrocytes 27, 391 ES 285, 315–316 ESA 285–286 ESD 305–306 esophagus 109, 380 EST 201–203 ESU xi 10, 17–18, 53, 106, 121, 257–263, 266, 314–316, 342 ESUs 10, 257–258, 264 ESWL 236–237, 244 ethanol 392 ether 4, 200, 212, 243 ethyl 212 ethylene 272 EU 358 Europe 358 European 358 evacuator 264, 266 Excel 326 Excimer x, 266 exhaled 94, 97, 173, 214, 256, 371 expiration 29, 204 expiratory 94, 201, 204–205 expired 29, 73, 204–205, 221 expiry 53, 261 exposure 50, 138, 142–145, 149, 151, 160, 246, 267, 338 extended 75, 174, 191, 201 extinguisher 291 extracorporeal 236, 237 eye 1, 11, 31, 121–125, 292, 237–240, 243, 246, 249, 266, 279, 292, 335, 370, 389 eyepieces 7, 112, 125, 268, 270 eyesight 268 F Facebook xv facts 361 Fahrenheit 136 fallopian 120, 258, 264 faults 18, 61, 285, 305, 310 FCC 358 FDA 360 female 186, 391–392 femur 1 fetal vii, 5, 6, 7, 34, 49, 84, 90, 125–126, 128–129, 131–132, 140, 157, 320–321 fetus 125, 127–128, 131, 157–158 FEV 94 Fi 46, 397 fibrillating 26, 61 fibrillation 11, 26, 61, 63, 71, 161–163, 166, 172, 210, 284, 306, 322 fibrin 28 fibrinogen 28 film 143, 145, 150, 159–160, 251, 254 filter 43, 48, 52, 53, 54, 123, 125, 201, 272, 286, 339, 372, 386 filtered 5, 22, 52–53, 200 filtering 28, 47, 54, 90, 226, 233, 344 Fisher xvii fistula 230 flatline 61 flexion 134 flowmeter 208 fluke xii, xvii, 15, 99, 262, 285–286, 290, 296, 298, 304, 309–311, 314–331, 352, 397, 399–400 fluoresce 143 fluorescent 245, 279 fluorine 157, 266 fluoroscopic 236 fluoroscopy 142, 143, 160 FMRI 154 footswitch 238, 258, 261, 263, 269, 271 forced 29, 93–94 forceps 263, 367 FPO 17, 31, 36–37, 41, 353, 363 Frank xvii, 49 Frankenstein 11 Fraser xix FRC 94, 108 Frederick 49 frequencies 44, 46, 91, 97, 104, 157, 257, 284, 307, 345, 388 frsoft 352 fulguration 258 functional 94, 154, 328 FVC 94, 108 G gallstones 394 galvanometer 48–49 gamma 343 gastroscope 109, 140 GE xvii, 146–147, 150–151, 155, 158, 328, 398–399 generators 177, 236–237, 276 glands 32, 34, 223, 386, 394 glaucoma 123 gloves 4, 292–293 Glu 88 glucometers vi, 31, 87, 89, 108 glucose 30, 87–90, 107, 226, 392, 394 glutaraldehyde 273 412 glycerides 395 glycerol 395 glycoprotein 28 gout 234 grabber 335 graft 230 graph 78, 82, 95, 308, 312, 324, 344 graphical 35, 60, 79, 90, 222 graphite 340 gray 31, 143, 160 grid 57, 172, 283 grimace 134 groin 27 grounding 16, 258, 283–285, 305–306 GUI 202 Gy 143 gynecologic 110 H Hall 136 halogen 113 halothane 212 handwashing 295 HBrClF 212 HCO 88, 393–394 Hct 88, 391, 394 HDL 392, 394 healthcare i, xvii, 13–14, 351 heart ix, 1, 3, 5–7, 11, 18, 20–27, 32, 34–35, 40–41, 47–49, 55, 57–59, 61, 63, 67–68, 70–71, 73–74, 79, 81, 89–90, 108, 110, 125–126, 128–129, 131–132, 134, 140, 161–166, 170, 174–182, 209, 255, 281, 283–284, 306, 321–322, 328, 382–385, 388, 394–395 heartbeats 5, 34, 108, 125, 128, 140, 181 HeartStart 175 heated 86, 119, 172, 184, 217, 220, 232, 244, 258, 272, 340 heater 248, 251, 254, 275, 367 hematocrit 87–88, 391, 394 hematology 391 hematoma 8 hemo 228 hemodialysis ix, 211, 226, 228, 231, 232, 243–244 hemodynamic 393 hemoglobin 81–82, 84, 87, 88, 108, 391, 394 heparin 182 hepatic 381 HF 316, 323–324 HFOV 205 Hgb 88, 391, 394 hierarchy 1 Hippocrates 14, 302 His 21, 48, 51, 167, 207 Holter 49, 68, 70–71 Index homeothermic 135 Hooke 7 hormones 20–21, 25, 386 HTM i, v, xii, xv 12–14, 18, 39, 283, 307, 343, 345, 347, 349, 353, 363, 366 HTMT xi, xv 13, 18, 174, 283, 285, 287, 289, 291, 293, 295, 297, 299, 301, 303, 305 humidifiers 161, 209, 217, 244 HVAC 350 hydride 164 hydrodynamic 90 hydrogen 153, 154, 394 hydroxide 99 hyperbilirubinemia 245 hypercapnia 86 hyperglycemia 30, 90 hypertension vi, 74, 79, 108, 123, 321 hyperthermia v 33, 34, 209 hypodermic 295 hypoglycemia 30, 89 hypotension vi, 75 hypothermia v 33–34, 182, 184, 217, 232 hypothermic 33 hypotonic 230 hypoxia 97 hysteresis 76 Hz 50, 53, 58, 104, 261, 283–284, 324 I IBP 320 IC 51, 94, 108, 335, 346, 366, 371 iCa 88 ICs 300, 346 ICU 196 IDA 298, 317–318 IEC xii, 285, 316, 325–327, 354–355, 358–359 IECEE 358 IEEE xiii, 361–362 IEEEUSA 362 imaging vii–viii, xx, 46, 61, 71, 101, 103, 118, 141, 145, 147, 149, 151–152, 154–155, 157, 159, 160, 236, 272, 310 impedance 46 impervious 50 implant 177 implantable viii, 170–171, 178–179, 181, 210 impulse 19, 162, 328–329 incandescent 114 incision 109–110, 120, 176, 238, 257 incisions 10, 110, 238 incoming 38, 288, 296, 328, 349, 366 INCU 326 incubators x, xi, 245, 246, 247–251, 281–282, 312, 326–327, 331, 342, 358, 367, 369 incus 388 indb i–400 413 Index induced 11, 33, 106, 172, 223, 276 infant vii, x, 1, 16, 82, 98, 133–134, 245–251, 312, 321, 325, 326, 331, 367, 369 infarction 59, 61, 70 inflate 184 inflated 39, 181, 184, 290 inflating 109, 279, 321, 323 inflation 181, 184 infrared 34, 45, 81, 97, 137–138, 222, 343 infuse 11 infused 184, 210 infusers ix, 187 infusion xi, 184, 187, 191, 198, 210, 232, 297–298, 317–318, 342, 365–366, 368 inhalation 5, 94, 219 inhibit 102 initiate 21, 87 inject 61, 217 injected 148, 168, 176, 221, 297 injecting 27 injection 143, 167, 169, 188 INOP 203 inoperative 136, 202, 301, 303 INR 88 inspection 15–16, 18, 37, 38, 176, 260, 263, 288, 296, 318, 328, 351, 355, 359, 366 inspiration xvii, 29, 199, 205, 207 inspiratory 29, 94, 200–201, 204–205, 207 instrumentation xiii, 18, 20, 361 insufflating 119 insufflation 100, 109–110, 112, 114–115, 119, 140 insufflator vii, 110, 119, 140, 370 insufflatory 119 insulin 30, 89, 188 intercostal 29 interfaces 38, 40, 43–45, 50–51, 63–64, 67, 70, 86, 89, 102, 105, 205, 286, 289, 297, 307, 310, 312, 316, 320, 346, 351 interference v 44, 48, 50, 52–53, 71, 84, 277, 316 interferential x, 276, 277, 282 internet 40, 70, 87, 159, 205, 346, 352 interpolation 79 interpretation 5, 68 intervals 49, 53, 67, 68–69, 79, 131, 135, 176, 188, 191, 195, 198, 255 intestinal 5, 90, 190, 264 intestine 109, 190, 223 intraaortic 181 intracranial 123, 321, 393, 394 intraocular 30, 238, 389 intravenous ix, 79, 167–168, 187–188, 225, 230, 318 intravenously 224 intubate 166, 168 intubating 123 intubation 215 invasive vi, 40, 70, 75, 77–78, 80, 90, 107–108, 110, 230, 237, 241, 321 inventory 350–351 ionic 18, 27 ionized 10, 88 ionizing 143 ions 19–20, 29–30, 51, 103, 164, 228, 394 IPD 232 IPM 260, 296 IR 138 iris 1, 121, 389 irrigation vii, 100, 109, 112, 114–116, 119, 139, 238 IRV 94, 205 ischemia 59, 61, 70 ISO xii, 353–354, 356–357, 359 isoflurane 103, 212, 219, 244 isolation vi, 58, 286, 293 isotonic 230 isotope 71, 155, 156, 157 IT xii, 343, 345, 347 IUP 320 IV ix, 14–15, 17, 161, 168, 187, 190–193, 195, 197–198, 209, 225, 250, 297, 375 IVAC 331–332 J jaundice 245, 394 jet 49 Joe xv 14–18, 37–39, 86, 195–196, 260, 288–291, 297–298, 302 Joule 143 joules 168 jugular 230 K keratectomy 241 keratomileusis 241 keratoses 267 kidneys 30, 74, 148, 226, 227, 228–230, 232–234, 236–237, 243–244, 370, 386–387, 394 knees 109, 139, 274 Korotkoff 5, 76–77, 321 kPa 220 krypton 266 KVA 198 kVp 142 L LA 23, 55–57 414 lab 14–18, 43, 81, 86, 167, 195, 260, 268, 270, 297–298, 301, 305, 307, 312, 333, 342, 347, 360 labor 245, 255, 347, 371 laboratory xx, 86, 87, 268 LAN 60, 71, 119, 346 laparoscope 109 laparoscopic 10, 110, 120–121, 367, 370 laparoscopically 120, 263 Laryngo vii, 121 laryngoscope vii, 122–124 larynx 100 lasers x, 11, 27, 42, 101, 211, 237, 239, 240–241, 243–244, 264–266, 278, 281, 282, 360, 370 LASIK 240–241, 244 lasing 264 Laudanum 3 LDL 392 leads v 4–5, 22–25, 42–43, 49, 51, 53, 55–57, 60, 68–69, 71, 74, 75, 78, 86, 90, 97, 102–103, 144, 164, 170, 171, 176, 179, 205, 209, 212, 286–287, 316, 320, 322, 331, 338, 371, 375 leaded 144 leakage 16, 38, 119, 261, 263, 284–287, 289, 314, 316, 331 Leeuwenhoek 7 lenses 7, 101, 111–112, 122–123, 125, 240–241, 243, 266, 268, 270, 389 leukocytes 391 lidocaine 167 lipid 392 lipoprotein 394 lithium 164, 176 lithotripsy 235–237, 244, 370 lithotripters ix, 211, 233, 243 liver 120, 223, 245, 380–381, 394 LL 23, 55–57 LoC iv loop 258 Lown 165 LRC 54, 165 lumen 119–120 lungs 1, 3, 5, 20–21, 27–30, 34, 81, 93–94, 97–98, 110, 161, 181, 198–200, 204, 205, 209, 281, 324–325, 342, 382, 385 lymph 281 lymphatic 184, 279, 281–282 lymphedema 183 lysis 228 M μSv 142 MA iv 142, 222, 310 macular 123 Index magnetic 65, 71, 97, 136, 152–154 maintenance viii, xix, 11, 31, 159, 161, 174, 199, 201, 260, 284, 295, 316, 324, 350–352, 355, 366 malleus 388 mammograms 142, 149, 150, 160 mammography viii, 149–151 management i, iii, xii, xvii, 1, 12–14, 38–39, 141, 284, 288–289, 296, 318, 346–347, 349–353, 356–357, 362 mandatory 205 manometers 5, 77, 312, 321 MAP 204 marijuana 102 marrow 31 Masimo xvii, 84, 320, 328, 398 maternity 293 maxtec 314 MB 88 ME xvii, xx, 3, 11, 37, 195, 288, 302–303, 355, 359 Medit xvii, 111, 116, 398 Meditrac 351 MedTester 352 mellitus 30 membranes 27, 30, 86, 102, 121–122, 135–137, 139, 181, 182, 228, 232 mEq 392–393 mercury 76, 135 mesh 28 metabolic 28, 33, 63, 156, 226 metabolism 32, 156, 386 metabolize 221 methemoglobin 82, 84 methylene 82, 339 mg 30, 88–90, 392 MHz 46, 257 microelectromechanical 178 micrometer 335 microscopes v, x, 7, 8–9, 238–239, 241–242, 245, 268–270, 272, 282, 341 microsurgery 159, 269–270 microwaves 155, 276, 343 milliamps 142, 179 milliequivalents 392 milligrams 88 millimeter 76 millimoles 88 minutes 4, 15, 39, 63, 87, 142, 175, 201, 255, 290, 376 mitral 383 mL 15, 29, 205, 225, 318, 393 mM 30 mmHg 76, 79, 184, 322, 393 mmol 30, 88–90 MMS 36 mobile 162, 269, 320, 351, 352 415 Index modified 73, 178, 321, 346, 388–389, 397 modules 36, 42, 44, 86, 89, 338 monitors vi–vii, 32, 35–41, 43, 46, 48, 68, 70, 76, 78, 80, 86–87, 95, 97, 106, 103, 118, 128–132, 140, 161–162, 171, 182, 204, 217, 221, 222, 236, 244, 260, 262, 272, 287–290, 316, 319–323, 326, 328, 373, 376 monitored 35, 41, 46, 65, 67, 73, 76, 81–82, 98, 161, 187, 197, 204, 230, 232, 238, 244–245, 249 monitoring v, ix, 15, 32, 35, 40, 43–46, 53, 58, 63, 68, 71, 73, 77, 84, 86–87, 131, 135, 140, 157, 167, 170–174, 193, 197, 199, 205, 228, 230, 249, 251, 262, 314, 316, 352, 358, 362 monophasic 165, 210, 330, 329 monopolar x, 258, 261, 282, 368 MRI 27, 43, 61, 103, 141, 152–156, 159–160, 310, 347 MSDS 291–292, 306 MSI 351 mSv 142, 143–144, 149 multimeters 287, 305, 307–308, 310, 342 multiparameter 35–37, 41, 206, 319 multiwavelength 320 mV 21–22, 76, 94, 204, 345 MVV 94 myelin 394 myocardial 59 myocardium 61, 181 mΩ 287 N Na 88, 392 NALYZERS 327 nanotubes 98 NBP vi, 46, 78, 80, 129 Nd 265 Neanderthal 1 nebulizers 209 necrosis 61 necrotized 59 Nellcor 203, 320, 328 NEODYMIUM 265 Neodymium x neonate(s) 82, 98, 134, 245, 246, 249, 251, 281–282 neonatology 245 network 13–14, 37–38, 70, 159, 287–289, 318, 346, 357–358, 362 networking i, 13–14, 308, 346 networks xii, 40, 45, 54, 157, 205, 346, 347 neurological 134, 393 neuromuscular 102, 106 neuron(s) 18, 19, 102 neurotransmitter(s) 19, 223 neutrons 152 newborn 245, 250, 255, 326, 391 NFPA 285, 354–355 NIBP xi, 38–39, 41, 44, 79, 171, 288, 290–291, 312, 320–323, 376 NiCad 164 NiCd 164 Nihon 328 NIST 324 nitrous 217, 221, 245, 255, 256, 371 NMRI 152 noise 44, 52, 67, 84, 91, 168–169, 301, 310, 328 noncardiac 25 noncontact 309 nonflammable 212 Nonin 320, 328 noninvasive vi, 41, 44, 63, 70–71, 76, 80, 107, 171, 199, 320 nonsynchronized 163 notch 73 nozzle 369 nuclear 152, 177–178 nursery 369 nurses 5, 15, 17–18, 169, 371, 374 nursing 15–16, 35, 41, 169, 195–196, 295, 351, 368, 375–376 nW 178 O OnSite 352 operating 138, 200, 213, 219–220, 238–239, 241–242, 245, 263, 268, 270, 272, 282, 293, 346 ophthalmic x, 211, 239, 241, 243 ophthalmoscope(s) vii, 121–125, 372 opium 211 OPMIs 241, 270, 271 optic(s) 101, 111–112, 116, 122–123,, 237, 246, 265, 272, 370, 389 optical 7, 40, 70, 100–101, 116, 118, 138, 205, 312 OR(s) 13–14, 17–18, 35, 214, 257, 260, 263, 293, 295, 306 oscillation(s) 78–79, 205 oscillometric 39, 77, 290 oscilloscope(s) xi, 175, 308–311, 342 osmolality 392, 394 osmoles 394 osmosis 228 osmotically 394 ossicles 388 osteoporosis 138 otoscope 122 oxalate 234 416 oximeter(s) 11, 16, 39, 63, 81–85, 173, 289, 328 oximetry 38, 41, 79, 81–82, 84, 95, 107–108, 171, 173, 320, 328 oxygenation 98, 181 oxyhemoglobin 81 P PA 17, 205, 295–296, 306, 312, 349–351, 393 pacemaker(s) viii–ix, xi, 11, 26–27, 34, 155, 161, 171, 173, 176–180, 209–210, 330–331, 360, 384 pacemaking 176 PaCO 393–394 PACs 62–63, 159–160 pad 18, 51, 176, 184, 260 paddle(s) viii, 161, 165–166, 168–169, 171, 173, 174, 176, 287 pads 165–166, 176, 374 pancreas 30, 223, 380, 386 pancreatic 380 pandemic 84 PaO 393–394 paralyzing 198, 214, 223 parenteral 224 patency 79, 370 PCA 161, 194–195, 197, 209–210, 318 pCO 88 PEEP 204–205 Percussor 281 performance 15–16, 18, 30, 39, 51, 76, 82, 126, 164, 174–176, 286, 289, 295–296, 314, 318, 323, 325–326, 349–350, 353–355, 357–359, 362 perfusion 39, 74–75, 81–82, 84, 86, 108, 181, 289, 320, 327–328 perfusionist 182 pericardium 110 Perinatal 140 periodic 46–47, 80–81, 201 peripheral 328 peristalsis 190 peristaltic ix, 182, 184, 190–192, 225, 230, 244, 279 Peristerakisxvii peritoneal ix, 211, 232–233, 243, 244 peritoneum 232 peritonitis 232 PET 43, 61, 103, 141, 155–157, 159–160 pH 30, 88, 392–394 phaco 239 phacoemulsifier x, 211, 237–240, 243–244 Philips xvii, 12, 17, 36–38, 41–42, 50, 52, 54, 60, 78, 129–130, 133, 142, 146, 149, 152–153, 162, 170–171, 175, 199, 214, 328, 333, 397–399 Index photochemical 245 photometer 245–247 photomultiplier 143 php 360 physics 81, 141, 152, 160, 243 physiological i, xix, 26, 29, 32, 34–36, 48, 52, 71, 73, 79, 84, 106, 198, 205–206, 217, 222, 296, 319, 321–322 physiotherapy 245, 274, 282 picking 48, 178, 209 piezo 76 piezoelectric 76, 91, 157, 237, 276 pincer(s) 120, 263, 307 PIP 204 piston 95, 190 PKR 241, 244 plasma 30, 173 Platelet 28 plenum 219–220 plethysmograph 46, 80, 84 pleura 110 pliers 332–333 plume 264, 266 plutonium 177 PMi–400 343–344 pneumatic(s) 39, 77, 201–202, 290 pneumography 97 pneumonia 5 pO 88 POC 86–87 polarity 307 polarization 7, 19–20, 24 Poliomyelitis 199 polyp(s) 112, 120, 258–259, 264, 367 polypropylene 182 POSITRON 155 potassium 19, 29, 87, 88, 99, 226, 392 potentiometer 65 precordial 61 pregnancy 109, 125, 252, 387 pregnant 371 premature 62–63, 71, 246, 322 prenatal 157 preset 204–205, 272 pressure vi, ix, 5, 8, 27, 30, 32, 34–35, 39–41, 44, 46, 63, 73–81, 84, 95, 107–108, 119, 123, 131, 171, 184, 187, 191, 198–200, 202, 204–210, 217, 219–220, 225–226, 230, 232, 237–238, 255, 290–291, 312, 318, 320–324, 372, 375–376, 392–395 PRK 240–241 ProArrest 302–303 probe(s) 16, 38–39, 91, 93, 120, 121, 135–138, 236, 238, 250, 267–268, 288–290, 307–309, 312, 327, 331–332 procaine 103 417 Index Proctoscope 110 programmable 195, 360 prongs 372 propofol 189 ProSim 319–320, 327–328 protocols 15, 46, 49, 67–68, 80, 291, 322, 352 protons 152 proximal 79, 101, 117, 184 psi 318 PSOL 202 psoriasis 279 PT 88 PTT 46, 80 pulmonary vi, 70, 91, 93–96, 98, 108, 383, 393, 394 pulsatile 84, 90, 321 pulse(s)/pulsing vi, 6, 11, 16, 26, 27, 34, 38–41, 46–47, 61, 63, 76, 79–85, 95, 106–108, 126, 134, 153–154, 163, 165, 166, 171, 173, 177, 178, 190, 210, 222, 236–237, 289–290, 310, 311, 320, 322, 327–329, 331, 370 pump(s) ix, 14–15, 17, 20, 27, 30, 39, 44, 47, 74, 79, 80, 89, 119, 161, 181–182, 184, 187–198, 209–221, 224–226, 230, 244, 281, 290, 297–299, 317–318, 322, 365–366, 368, 375–376 pumping 21, 26, 73, 77, 162, 173, 182, 191, 198, 230, 244, 299, 383 Puritan 201, 203 Purkinje 21, 302 PVCs 62–63, 322 pyloric 380 Q QA 315–316 QED 330 QR xv, xx, 13, 18, 351, 353 QRS 23, 49, 53, 59, 172, 302, 321 R RA 23, 55–57 rad 142–143, 160 radar 6 radial 76 radiant 254, 326 radiated 34 radiation xii, 34, 137, 142–144, 153–155, 160, 245, 343–345, 347, 360 radiologists 142 radionuclides 157 radiopaque 27, 143, 148, 160 ratio 94, 164, 204–205 RBBB 63 RBC 391 RC 54 recalibration 375 receptors 19 recirculated 214, 243 recorder(s) vi, vii, 39, 42–43, 49, 61, 62, 68–71, 75, 79, 86, 95, 100, 103, 105, 110, 118, 131, 171, 172, 205, 210, 291, 302, 310 Reeve 207 refractive 241 refractory 102 regulations xii, xv 349, 351, 353, 355, 357, 359, 361, 363 regulatory 320, 352, 358–359 relaxants 106 relay viii, 38, 117, 136, 165, 287, 289 rem 142, 160 renal ix, 30, 34, 74, 148, 211, 226, 233–234, 243, 386 repolarize 23 residual 94, 204, 359 resonance 71, 152 respiration v–vi, 28, 32, 34, 46, 81, 94–95, 97, 134, 173, 197, 212, 320, 321, 328 respiratory vi, ix, xx–1, 28–29, 35, 73, 91, 93–95, 100, 107–108, 161, 166, 198, 209, 293, 322, 323 respironics 199 resuscitator 16, 134, 253–254 resuscitators x, 134, 245, 251, 281 resynchronized 26 retina 98, 123, 240, 266, 389 retinal 11, 241 retinopathy 123 reusable 101, 113 RF 44, 46, 262–263, 310, 314–316 Rh 27 rhythm 11, 26, 60, 63, 161, 169 RIGID 111 rigid vii, 101, 108, 110–112, 131, 139–140 rim 191, 238 RL 23, 55–56 RMS 286, 314 RN iv RNA 29 Roentgen 5 Röntgen 141–142 RR 46 RSNA 195 RT 168, 324 Ruhmkorff 4 RV 94 S SA 21, 26 SaO 84 sarin 102 418 saturated 81, 209, 214 saturation 82, 84, 328, 392–394 scalpel 4, 10 scalpels 8, 10, 272, 295 scanners viii, 103, 141, 144, 149, 152, 155, 157, 160 scintillation 143, 155 scopemeter 304, 308–310 segment 54, 59–60, 71 self 201, 204 sensor(s) 38–39, 71, 82–85, 97–98, 101, 116–118, 131, 137, 138, 145, 173, 192, 198, 202, 248, 250, 254, 279, 288–289, 298, 312, 367, 375 sequential ix–x, 161, 183, 279, 280, 282, 316, 331 servomotors 269 SET 320 sevo 220 sevoflurane 103, 212, 219 shock(s) 5, 11, 26, 89, 165, 168, 170, 172, 211, 222, 236–237, 303, 305, 306, 365, 370, 394 shortwave 276 sidestream 98 Sievert 143, 160 Sigmoidoscope 110 simulator(s) xi, 39, 289, 319–321, 325, 328, 329, 331–332, 342 SIMV 205 sinoatrial 21, 26 sinus 60, 63, 161, 169 SLIT 124 slit vii, 123–126 smoke 264, 266, 301, 338–339, 342 snare(s) 120, 258–259 soldering 292, 337–339, 342 Sotera 46 SpCO 84 spectroscopy 98 spectrum 113, 141 SpHb 84 spin 152–154 spirometer(s) vi, 94–95, 108 SpMet 84 SpO xi, 38–41, 44, 46, 80, 84, 129, 217, 250, 288–289, 320, 327–328 SpOC 84 SPOT 327–328 ST 54, 59–60, 71 standardization 286, 354, 359–360 standards i, xii–xiii, 16, 40, 89, 284, 286–287, 316, 323, 325–327, 349–351, 353–363 STERILIZERS 272 stethoscopev 3, 5–6, 76, 125 stimulator(s) viix, 73, 103, 106–108, 278, 371 stress 49, 63, 65, 67–69, 71, 95, 105, 325 struvites 234 Index stylets 87, 89 subarachnoid 388 subclavian 179 subdural 8 subendocardial 21 suction vii, 100, 109, 112, 114–116, 119–120, 139, 167, 219, 238, 251, 277, 312, 338 superconducting 153 Superman 207 supramaximal 106 suprarenal 386 Supraventricular 63 surgery v, 3–4, 9, 17, 28, 34, 48, 90, 94, 106, 110, 162, 166, 181–184, 198, 209, 211, 214, 217, 223, 235, 238–240, 242, 244, 256, 264, 266, 370 surgical x, 4, 5, 8, 10–11, 35, 106, 109–110, 112, 119, 123, 181–182, 184, 187, 195, 211, 221, 224, 237, 239, 245, 256, 258, 264–266, 269–270, 272, 279, 281, 293–294, 314, 325, 360 Sv 142–144 SvO 84 SVT 63 synchronization 11, 26, 310 synchronized 26, 162, 172, 181, 205, 320, 322, 329 synchronous 331 syringe ix, 167, 168, 188–189, 197 systole 49, 84, 181 systolic 39, 46, 73–74, 76–80, 290, 322, 393, 395 T tachometer 65, 312 tachycardia 60, 63, 86 telemetry v, 43–46, 71, 84, 129 temperature v, 1, 16, 20, 31–35, 38–39, 46, 53, 71, 80–81, 97, 113–114, 119, 135–138, 140, 182, 184–185, 217, 219–220, 230, 232, 245, 248, 251, 267, 272, 274, 290–291, 307, 310, 320, 326–327, 331–332, 337–338, 367 tendineae 383 TENS 278–279 testers xi, 39, 202, 285, 287, 290–291, 297, 307, 309, 311, 312, 313, 314, 315, 316, 317, 318, 319, 320, 321, 323, 325–328, 329, 331, 333, 335, 337, 339, 341 TESTING 63, 174, 285, 331, 358 tetrafluoroethane 212 thermoelectric 177 thermometer(s) vii, 38, 135–138, 140, 288, 312, 331–332 thermopile 137 Theta 104 Thoracoscope 110 419 Index thoracoscopic 120 threechip 117 thrombosis 183 tidal 94, 204, 205 timer 88, 134, 136, 232, 253–255, 274 TOCO 129, 131–133 tocograph 131 tomography viii, 149, 155 torn 53, 139 tourniquet 184–185 tourniquets ix, 161, 184, 209 traceability 325 tracheostomy 199, 205, 206 transcutaneous vi, x, 86, 180, 278, 331 transducer(s) vi, 27, 75–76, 78, 80, 90–91, 95, 128, 130–131, 133, 140, 201, 322, 328, 394 transvenous 331 treadmill(s) 63–68 Trendelenburg 248 trepanation 8 trichloroethylene 212 tricuspid 383 trifluoro 212 trifluoroethane 212 trifluoromethyl 212 Trigeminy 63 triglycerides 392, 395 troubleshooting xi, 42, 44, 172, 175, 283, 300–301, 303–306, 308, 311, 316, 319, 324, 346, 376 tungsten 142 tunneled 229–230 tympanic vii, 121–122, 135–138, 140, 331 U UHF 347 UL xii, 353, 359 ULC xii, 359 Ultrasound vii, ix, 27, 90–91, 126, 157, 226, 276, 328–329, 358 ultrasound 27, 61, 71, 90–91, 125–126, 128, 130, 138, 140–141, 157–160, 198, 238, 266, 276, 278, 328, 360 Ultraviolet x, 279–280 Underwriters xii, 353, 359 unoxygenated 81 unsolder 337 unsynchronized 162 upstream 198, 298 urea 88, 226, 232, 244, 386, 392, 394 ureters 30, 226, 386–387 urethra 30, 109, 226, 387 urinary 109, 234–237, 386–387 USB 286, 318 utero 125, 127, 157 uterus 109, 120 UV 279 uvula 121–122 V Valley lab 260 vaporization 237 vaporize 209, 220, 237 vaporized 212, 303, 369 vaporizer(s) ix, 213, 219–221, 244 vascular 92–93 ventilate 203 ventilation 28, 34, 81, 94, 182, 198, 202–206, 214, 216, 322 ventilators ix, xi, 98, 106, 161, 198–207, 209, 210, 217, 224, 250, 312, 323–325 ventricles 20–21, 23, 26, 62–63, 162–163, 179, 383, 388, 394–395 ventricular ix, 21, 23, 26, 61, 63, 71, 161, 163, 172, 181, 210, 284, 306, 393 VFib 169 vital 5, 28, 30, 33, 35, 37–38, 40, 46–47, 73, 81, 86–87, 94–95, 126, 135, 167, 172, 174, 207, 217, 232, 251, 283, 288, 289, 301, 320, 328, 347, 374, 376 VSM 37, 288 W WA 262 WANs 40 warmer(s) ix, 161, 184, 186, 209, 326 Wattmeter 329 WBC 391 Wearable 69 website iv, xv, 352, 363 Welch 123 wireless 40, 46, 69, 170–171, 193, 197, 287, 312, 320, 327, 328, 346 workstation(s) 37, 159, 288 X xylocaine 103 Y YAG 265 Yttrium x, 265 Z zeolite 208–209 Zoll 162, 176 Taylor & Francis eBooks www.taylorfrancis.com A single destination for eBooks from Taylor & Francis with increased functionality and an improved user experience to meet the needs of our customers. 90,000+ eBooks of award-winning academic content in Humanities, Social Science, Science, Technology, Engineering, and Medical written by a global network of editors and authors. 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