Anesthesia In Children With Congenital Heart Disease For Non-cardiac Surgery Dr. Fady Adib Lecturer Of Anesthesia Ain-Shams University Oct. 2012 The question facing anesthetists are: 1 . Should the patient be referred to specialist cardiologist before surgery? 2 . Should surgery be performed in a center specializing in congenital cardiology? 3 . How should anesthesia be conducted safely in the presence of congenital heart disease? INTRODUCTION The Incidence of CHD is about 1% of the newborn infants - Surgery: - Noncardiac conditions ( inguinal hernia, circumcision, or tonsillectomy). - Associated noncardiac congenital anomalies (orthopedic or genitourinary). - Due to advances in diagnosis, medical, critical and surgical care for CHD - Therefore, it is common for patients with CHD to present for non-cardiac surgery, and even in patient with corrected CHD significant residual problems (arrhythmias, ventricular dysfunction, shunts, valvular stenosis, and PH) may be exist. Anatomical & Physiological Differences CVS: Anatomical Differences - Myocardium is less compliant: Cardiac Output is H.R. dependent. - It can’t withstand a volume load. - Decreased sympathetic innervation: catecholamine stores Autonomic Development - Beta receptors develop with age - alpha receptors less developed So V.C response to volume loss is decreased - Parasympathetic response supervens - Net result: - Volume load heart failure - Volume loss decrease vasoconstriction - Hypotension CLASSIFICATION OF CHD I- Acyanotic congenital heart disease: 1- ASD 2- VSD 3- PDA II- Cyanotic congenital heart disease: 1- Tetralogy of Fallot, with severe right ventricular outflow obstruction 2- TGA 3- Pulmonary atresia or severe stenosis 4- Tricuspid atresia with pulmonary stenosis 5- Truncus Arteriosus Pathophysiological classification of congenital heart disease - Shunt lesions - Mixing lesions - Obstructive lesions - Regurgitation lesions Shunt lesions Intracadriac Extracardiac: e.g. ASD, VSD e.g. PDA - Direction & magnitude: depends on size of shunt orifice pressure on both sides of the shunt - Lt.-to-Rt. Shunt ( e.g. VSD,PDA) - Rt.-to-Lt. Shunt (e.g. Fallot 4) OVERLOAD VOLUME OVERLOAD PRESSURE ..Shunt lesions.. (continued) Lt-to-Rt shunt e.g. ASD, VSD - Volume overload on pulmonary circulation - Increased cardiac work of Rt. Ventricle - Excessive pulmonary blood flow=++ PVR Rt-to-Lt shunt e.g. F4 - ↓ Pulmonary blood flow= hypoxemia - Pressure overload of the Rt. ventricle Mixing lesions (large orifice) - e.g. TGA, Univentricular heart - Direction & Magnitude: Depend on PRESSURE on both sides of the lesion - Usually CYANOTIC - With VOLUME & PRESSURE overload Obstructive lesions - e.g. Aortic stenosis, Coarctation of Aorta - Pressure overload ventricular hypertrophy impaired coronary perfusion systemic hypotension Regurgitation lesions (uncommon) - Volume overload dilatation ventricular Once full details of the anatomy, surgical history and current pathophysiology are obtained patient can be divided into the following categories: 1 . Congenital heart disease, yet to be surgically treated. 2 . Surgically corrected, symptom free with no new development. 3 . Surgically corrected, symptomatic heart diseases 4 . Surgically palliated. Symptoms stable with no new development 5 . Surgically palliated with severe symptoms or no new development Types of Cardiac Surgery Biventricular Univentricular Usually Palliative e.g. Shunts, Banding •Problems encountered: Usually complete repair ( Corrective ) Debubbling & Antibiotic coverage, As the lesion is still persistent e.g. VSD - Corrective surgery: Correct anatomy - Palliative surgery: The aim is to increase or decrease pulmonary blood flow Corrective Surgery Corrected ASD VSD PDA: Near normal patient. Only needs antibiotic prophylaxis. Repaired TOF: Residual defects: VSD, outflow tract obstruction, pulmonary regurge, ,Heart block Corrected coarcitation usually require long .term treatment of hypertension Palliative surgery Decrease PBF: Pulmonary artery banding (VSD) Increase PBF: In Pulmonary atresia BT shunt: Subclavian artery to .Pulmonary artery Gllen: SVC to Pulmonary artery Fontan after Gllen IVC to Pulmonary artery Physiology of different types of circulation - Normal or ‘series’ circulation. - - Parallel or ‘balanced’ circulation. - Single-ventricle circulation - - Risk classification increased risk of mortality and morbidity. - factors associated with a high risk of perioperative complications, - {disease complexity, } Most Important - {physiological status,} - type of surgery, young age, and Hospital Stay . Complexity of heart disease - single-ventricle physiology - balanced circulation physiology - cardiomyopathy - aortic stenosis Physiological status Physiological status can be divided into four major risk factors: - Cardiac failure - Pulmonary hypertension - Arrhythmias - Cyanosis ANESTHETIC MANAGEMENT - Perioperative management requires a team approach - CHD is polymorphic and may clinically manifest across a broad clinical spectrum - The plane of Anesthetic Management includes the following: A - Preoperative Management B - Intraoperative Management C - Postoperative Management Preoperative Anesthetic Considerations 1- Complete history and physical examin. 2- Review all investigations 3- Hydration should be maintained 4- All cardiac medication except possibly digitalis ,ACE and diuretics should be continued until surgery 5- Premedication should be give particularly to patients at risk for right to left shunt 6- Antibiotic prophylaxis against endocarditis must be given Preoperative Anesthetic Management: A- History B- physical examination C- Investigations D- Premedications E- Fasting Guidelines HISTORY & PHYSICAL EXAMINATION - Assess functional status - daily activities - exercise tolerance - ↓ cardiac reserve - cyanosis - respiratory distress during feeding - Cyanosis - Dyspnea - Fainting attack - Fatigue - Palpitations - chest pain - Syncope - Abdominal fullness - Leg swelling - Medications - Vital signs - Airway abnormality - Associated extracardiac congenital anomalies - Tachypnea, dyspnea, cyanosis - Squatting - Clubbing of digits - Heart murmur (s) - CHF: - Jugular venous distention. - Hepatomegally - Ascitis - Peripheral edema MRI Laboratory Evaluation 12 Lead ECG INVESTIGATIONS chest X – Ray Echocardiography Cardiac Catheterization Regarding investigations of CHD patients for non-cardiac surgery: A- Chest X – Ray has no rule B- Cardiac Catheterization is the first choice for diagnosis of CHD C- Echocardiography non invasive method for diagnosis of CHD D- MRI cannot give us idea about pulmonary veins IM Premedication for CHD patients presenting for non-cardiac suergery: A- Cooperative or unable to take orally B- Ketamine 1mg/kg C- Midazolam 5 mg/kg D -Glycopyrrolate or Atropine 0.02 mg/kg Procedural antibiotic prophylaxis is required in patients with A- Aortic valve replacement B- Mitral valve prolapse with regurge C- Previous history of infective endocarditis D- Ostium secundum ASD AHA guidelines for bacterial endocarditis Prophylaxis in patients with cardiac conditions Endocarditis prophylaxis recommended Endocarditis prophylaxis not recommended High-risk category - Complex cyanotic congenital heart disease : Transposition of the great vessels Tetralogy of Fallot - Surgically created systemic-to-pulmonary shuntsor conduits - Prosthetic, Bioprosthetic, Homograft valves - Previous bacterial endocarditis Negligible-risk category - Physiologic, or functional heart murmurs Moderate-risk category - Other congenital cardiac anomalies - Acquired valvular dysfunction - Hypertrophic cardiomyopathies - Mitral valve prolapse with valvar- Regurg - Surgical repair without residua beyond 6 months : ASD, PDA,VSD - Cardiac pacemaker or - implanted defibrillator - Isolated secundum atrial septal defect - Mitral valve prolapse without reg. - Previous coronary artery bypass surgery - Previous rheumatic heart disease without valvular dysfunction AHA guidelines for antibiotic prophylaxis: dental, oral, Respiratory tract and esophageal procedures Standard prophylaxis Amoxicillin 1 h before procedure -Children: 50 mg/kg p.o. -.Adults: 2.0 g p.o Unable to take oral medications Ampicillin within 30 min before procedure - Children: 50 mg/ kg i.m. or i.v. -.Adults: 2.0 g i.m. or i.v Allergic to penicillin Clindamycin 1 h before procedure Children: 20 mg/kg p.o. Adults: 600 mg p.o. OR Azithromycin or clarithromycin 1 h before procedure -Children: 15 mg/kg p.o. - .Adults: 500 mg p.o Unable to take oral medications AND allergic to penicillin Clindamycin within 30 min before procedur -Children: 20 mg/ kg i.v - .-Adult: 600 mg i.v. AHA guidelines for antibiotic prophylaxis: genitourinary and gastrointestinal procedures High risk patients - within 30 min before procedure - Children: Ampicillin 50 mg/ kg .and gentaicin 1.5 mg/kg i.m or i.v - Adults: Ampicillin 2.0 g and gentamicin 1.5 mg/kg i.m or i.v High risk patients Allergic to penicillin - Complete infusion 30 min before procedure - Children: Vancomycin 20 mg/kg i.v over 1-2 hr gentamicin 1.5 mg/kg i.m or i.v -Adults: Vancomycin 1g/kg i.v over 1-2 hr gentamicin 1.5 mg/kg i.m or i.v Moderate risk patients - Ampicillin within 30 min before procedure - Children: 50 mg/ kg i.m. or .iv - Adults: 2.0 g i.m or i.v Moderate risk patients AND allergic to penicillin - Complete infusion 30 min before procedure - Children: Vancomycin 20 mg/kg i.v over 1-2 hr -Adults: Vancomycin 1g/kg i.v over 1-2 hr Anesthetic Management A - Preoperative Management B - Intraoperative Management : 1- Monitoring 2- Choice of anesthetic agent 3- Maintenance of anesthesia 4- Emergence from anesthesia Anesthetic Management Preoperative Assessment - Associated congenital anomalies (difficult airway) - Chest: signs of H.F.& chest infection…postpone - Liver: ●enlarged in Rt. Sided failure ●shrunken in Lt. sided failure, diuretics, ↓feeding - Cyanotic spells - Acute hypertensive pulmonary crisis Anesthetic Management Investigations - Hematocrit:….thromboembolism - Electrolytes:…..arrhythmias..(should be corrected) - Blood gases:…cyanotic may be acidotic - Echocardiography: satisfactory in simple cases - Catheterization: - Coagulation profile: cyanotic patients usually suffer from coagulopathies. Premedication - - - Oral Premedication: - Midazolam 0.25 -1.0 mg/kg - Ketamine 2 - 4 mg/kg - Atropine 0.02 mg/kg IV Premedication: - Midazolam 0.02 - 0.05 mg/kg titrated in small increments - Ketamine 1-2 mg/kg IM Premedication: - Uncooperative or unable to take orally - Ketamine 5 – 10 mg/kg - Midazolam 0.2 mg/kg - Glycopyrrolate or Atropine 0.02 mg/kg Fasting Guidelines Anesthetic Management Premedication - Fasting: clear sugar fluid allowed till 4 hours - ↓ 6 months: No premedication - 6-9 months: optional e.g. to avoid spell or crisis - ↑9 months: -atraumatic (oral midazolam) -IM: ketamine 2mg/kg add Atropine 0.02mg/kg Anesthetic Management O.R. preparation - Temperature control: mattress & O.R. temp. - Anesthetic machine: with O2, Air, N2O - Infusion set…… free of air bubbles - Drugs: Atropine, Bicarb., Epinephrine, Phenylephrine - Inotropic infusion should be premixed before induction in high risk patient (e.g.Dobutamine) Anesthetic Management Monitoring & Lines - ECG - Pulse Oximetry: inaccurate in deep hypothermia - Invasive B.P.: Lt. Radial, Rt. Radial, Femoral art. - CV. Cannulation: Rt. & Lt. IJV, Femoral vein - Temperature: central & peripheral - Urine output: - Capnography: - Blood gases & electrolytes. Monitoring Non-invasive - Clinical observation - ECG - NIBP - Pulse oximetry - Precordial stethoscope - Continuous airway manometry - Multiple site temperature measurement Invasive - Volumetric urine collection - Art. catheterization - CVP - PAC - TEE Inraoperative management The goals of Intraoperative management - Prophylaxis against Subacute bacterial endocarditis. - Prophylaxis against Air bubble embolism. - Hemodynamic management. PVR SVR Contractility Air bubble precautions - Check and remove all air bubbles from IV tubing, injection ports, and stopcocks - Connect the IV tubing to the venous cannula while there is a free flowing IV fluid and blood. - Before IV injection into the cannula, small amount if fluid is injected into the hub of the cannula. Air bubble precautions Aspiration before injection to clear any air. Hold the syringe upright to keep the bubbles away. Do not inject the last milliliters from the syringe. Do not leave the central line open to air. N2O is better avoided. Hemodynamic management Left to right shunts: ( pulmonary blood flow) - The aim is to prevent: in SVR in PVR contractility Avoid vasodilators high FiO2 hypocapnea and alkalosis Right to left shunts: ( pulmonary blood flow) - The aim is to prevent: in SVR in PVR contractility Avoid Sympathetic stimulation low FiO2 hypercapnea .acidosis Avoid N2O Anesthetic Management Induction - Aim: to preserve SVR & PVR - Method: ● Inhalational: Sevoflurane ● I.V.: ketamine 2 mg/kg + fentanyl 2-3μg/kg+ Pancuronium 0.1 mg/kg - Antibiotic Prophylaxis: - Intubation: Oral/ Nasal (postoperative) - Corticosteroids: decrease systemic inflammatory response The effect of shunt on the speed of induction of anesthesia: - In patients with a right-to-left shunt: Inhalation induction is prolonged . Intravenous induction is more rapid. - In patients with left-to-right shunting, the speed of inhalation or intravenous induction is not changed . Factors Affecting PVR Factors Increasing: - PEEP - High airway pressure Atelectasis,hypoxia ,hypercarbia - Acidosis - Catecholamine -High hematocrite Factors Decreasing: - No PEEP - Low airway pressure - High FiO2, hypocarbia - Alkalosis - Vasodilators - Low hematocrite - Nitric oxide Anesthetic Management Maintenance - Patient with Poor Myocardium: - Narcotic based....Extubation not advisable - Patient with Good Myocardium: - Inhalational (isoflurane, sevoflurane) - Most Stressful Situations: - Skin incision - Sternotomy - Major vessels cannulation (Aorta, SVC,IVC) Choice of anesthetic Regimen Development of anesthetic regimen is based on various factors such as presence and direction of shunts , arrhythmia , pulmonary HF, circulation, and lowering or maintenance of PVR ● Choice of Anesthetic Agent Intravenous anesthetics • Volatile anesthetics Muscle relaxants Ketamine : No change in PVR in children when airway maintained & ventilation supported Sympathomimetic effects help maintain HR, SVR, MAP and contractility Greater hemodynamic stability in hypovolemic patients Copious secretions (laryngospasm) • Etomidate : Induction dose of 0.3mg/kg no change in mean pulmonary artery pressure and PVR, pulmonary blood flow, PHT or myocardial function • Propofol : decrease in SBP and SVR, and increase in SBF in all patients, whereas HR ,PAP, PBF remained unchanged • OPIOD: Excellent induction agents in very sick children No cardiodepressant effects if bradycardia avoided Fentanyl 15-25 µg/kg IV , Sufentanil 5-20 µg/kg IV • Barbiturates : Not recommended in patients with severe cardiac reserve Choice of Anesthetic Agent (Cont.) - Desflurane Pungent , PAP and PVR, Less myocardial depression than Halothane HR , SVR - Halothane PBF not affecting PVR, Depresses myocardial function, alters sinus node function, sensitizes myocardium to catecholamines - Isoflurane Pungent, PAP not affecting PVR, Less myocardial depression than Vasodilatation leads to SVR → MAP , HR which can lead to CI - Sevoflurane Less myocardial depression than Halothane, more in PAP compared with isoflurane, No HR, Mild SVR, Can produce diastolic dysfunction - Nitrous oxide At 50% concentration does not affect PVR and PAP in children Avoid in children with limited pulmonary blood flow, PHT or myocardial function Neuromuscular Blocking Drugs Depolarizing - Succinylcholine in pediatric controversial is - If used should be with atropine, to avoid associated bradycardia or sinus arrest - also if used with potent narcotic atropine should be used avoid severe to bradycardia in children with CR Nondepolarizing - Atracuruim and vecronium: have few cardiovascular side effects in children when given in recommended doses. - Pancuronuim if given slowly doesn't produce HR or BP changes. if given as bolus doses it can produce tachycardia , ↑BP (through sympathomimetic effect ) -Cisatracuruim and Rocuroinuim: safe Anestheia of Fallot patient: - The aim is to prevent intraoperative cyanotic spells. - Avoid prolonged fasting - Heavy sedative premedication. - Intravenous induction. - Ketamine, Fentanyl, Pancronium, Halothane. - Adequate intravascular volume. - Avoid systemic vasodilatation. - Adequate anesthetic depth to avoid sympathetic stimulation. Management of intra operative cyanotic spells in Fallot patient - Direct abdominal or aortic compression - IV vasoconstricror as ephedrine, phenylephrine, or dopamine - IV fluid. - Deep level of anesthesia. - Beta adrenergic blockers as osmolol or propranolol REGIONAL ANESTHESIA &ANALGESIA • Considerations : - Coarctation of aorta considerations - Childern with chronic cyanosis risk of coagulation abnormality - VD : which can: 1- be hazardous in patients with significant AS or left-sided obstructive lesions 2- Cause oxyhemoglobin saturation in R-L shunts Postoperative Anesthetic Management - Supplemental O2 and maintain patent airway. - In patients with single ventricle titrate SaO2 to 85%. Higher oxygen sat. can PVR PBF SBF Pain catech. which can affect VR and shunt direction Pain infundibular spasm in TOF RVOT obstruction cyanosis, hypoxia, syncope, seizures, acidosis and death Anticipate conduction disturbances in septal defects Remember Management of - Acute hypertensive pulmonary crisis: - Ventilatory manipulation: reduce PVR (PaO2, PaCO2, PH, Lung volumes) - Drugs: Milrinone, Isopril, PgE2 Remember Management of - Intraoperative Cyanotic Spells -Increase S.V.R.: by direct aortic compression ± vasopressor (phenylephrine, ephedrine…..) -Reduce infundibular obstruction by ß-Blockers (esmolol, propranolol…), OR Halothane -Deepen the level of anesthesia. -Adequate hydration (ample fluid and decrease viscosity) SUMMARY - Familiarity with the CHD pathophysiology, adequate preoperative preparation, choice of monitors, induction, maintenance , emergence from anesthesia, and plans for the postoperative period to avoid major problems in anesthetic management - A wide variety of anesthetic regimens is used for patients with congenital heart disease (CHD) undergoing cardiac or non-cardiac surgery, or other diagnostic or therapeutic procedures. The goal of all of these regimens is to produce anesthesia or adequate sedation, while preserving systemic cardiac output and oxygen delivery