Department Of Laboratory Medicine CELLULAR PATHOLOGY AND MORTUARY USERGUIDE 2014 Document number: CEL EXDO 612 Author: P Williams Approved by:Dr M Perenyei WARNING: this is a controlled document Page:1 of 47 Date of Issue: Dec 2014 Revision: 12 Cellular Pathology Cellular Pathology Userguide 2014 CONTENTS Page HISTOLOGY Key Personnel and Laboratory Telephone Numbers 5 The Cellular Pathology Request Form (CELPTHY FRM-KPN-CEL-004) 6 Sample submission/Sample container 7 Histology Service 7 Routine Histopathology 8 Rapid Frozen section service 8 Rapid Processing and Urgent Histopathology 8 Skin Immunofluorescence 8 Lymph Node Analysis 8 MOHs Section 9 The Processing Of Foetuses, Retained Products And Placentas 10 Muscle Biopsies 11 Videoconferencing 12 Multidisciplinary Meetings 12 Digital Macro and Microphotography 12 CYTOLOGY Key Personnel and Laboratory Telephone Numbers 13 Sample submission/Sample container 14 The LBC Request Form (HMR101) 15 Labelling the Cytology sample 16 Liquid Based Cytology Samples 17 -18 Uncertainty of Measurement 19 Effusions 19 Urines 19 Respiratory Tract Specimens 19 Document number: CEL EXDO 612 Author: P Williams Approved by: Dr M Perenyei WARNING: this is a controlled document Page: 2 of 47 Date of Issue: May 2014 Revision: 12 Cellular Pathology Cellular Pathology Userguide 2014 Fine Needle Aspirations 20 Nipple Discharges 20 Aspirates of Breast Cysts 20 Cerebrospinal Fluids and Joint Aspirates 21 ANDROLOGY Key Personnel and Laboratory Telephone Numbers 22 Semen Analysis for Subfertility 23 Requesting a Semen Analysis 23 Producing the Semen Sample 24 The Semen Analysis Test 25 Results 26 Interpretation of Results 26 Repeat Tests 27 Post vasectomy semen analysis 27 Requesting a Post Vasectomy Analysis 27 Producing the Semen Sample 28 Post Vasectomy Analysis 29 Results 30 Clearance 30 Special Clearance 31 MORTUARY Key Personnel and Laboratory Telephone Numbers 32-34 General Information 34 Autopsies 34 Retained Products of Conception and Fetuses 35 Deaths 35 Death of a Patient 35-37 Document number: CEL EXDO 612 Author: P Williams Approved by: Dr M Perenyei WARNING: this is a controlled document Page: 3 of 47 Date of Issue: May 2014 Revision: 12 Cellular Pathology Cellular Pathology Userguide 2014 Medical Certificate of Cause of Death 37 Post Mortem Examinations 37 Coroners Cases 38 To Report a Death to the Coroner 39 Circumstances when a Death Must be Reported to the Coroner 39-42 Reporting Deaths Involving MRSA or other Infective Related Deaths 42 Reporting Obstetric/Neonate Deaths to the Coroner 42 Cremation Certificates 42 Bereaved Relatives 43 List of Referral Centres Document number: CEL EXDO 612 Author: P Williams Approved by: Dr M Perenyei 44-47 WARNING: this is a controlled document Page: 4 of 47 Date of Issue: May 2014 Revision: 12 Cellular Pathology Cellular Pathology Userguide 2014 INTRODUCTION The department of Cellular Pathology is centralised on a single site at the William Harvey hospital, Ashford. It provides diagnostic Histopathology and Cytopathology services. KEY PERSONNEL & LABORATORY NUMBERS Head of Service Dr Miklos Perenyei 01233 616183 (Ext: 723-6183) Head Biomedical Scientist Mr Paul Williams 01233 616129 (Ext: 723-6129) HISTOPATHOLOGY Subspecialties Dr Aminu Abdulkadir Dr Kareem Aboualfa Dr Salim Anjarwalla Dr Nipin Bagla Dr Nicola Chaston Dr Matthias Koslowski Dr Charles Lawson Dr Brigid Maguire Dr Miklos Perenyei Dr Doraline Phillips Dr Konstantinos Skendros Dr Susanna Szakacs Dr George Vittay Dr Cate Wight Consultants Lung, Gynae, Soft Tissue, Perinatal, Urology Gynae, Lung, Skin, Urology Upper and Lower GI, Lung,Cytology, Urology Lymphoreticular, Upper and Lower GI,Skin Upper & Lower GI, Liver, Head and Neck, Urology, Endocrine Urology, Gynae, Lower GI Lymphoreticular, Breast, Head and Neck, Soft Tissue, Upper GI Skin Endocrine, Breast, Upper & Lower GI, Cytology, Lymphoreticular Gynae, Breast,Cytology Liver, Upper and Lower GI, Skin, Urology Head and neck, Skin Upper and Lower GI, Breast, Cytology, Endocrine Gynae, Breast,Cytology Phone number 01233 616184 (Ext: 723-6184) 01233 618058 (Ext: 723-8058) 01233 618034 (Ext: 723-8034) 01233 616605 (Ext: 723-6605) 01233 616015 (Ext: 723-6015) 01233 618035 (Ext: 723-8035) 01233 616014(Ext: 723-6014) 01233 616794 (Ext: 723-6794) 01233 616183 (Ext: 723-6183) 01233 616604 (Ext: 723-6604) 01233 616187 (Ext: 723-6187) 01233 616792 (Ext: 723-6792) 01233 616793( Ext: 723-6793) 01233 618942 (Ext 723-8942) Chief Biomedical Scientist Mr Brian Murphy 01233 616253 (Ext: 723-6253) Results Enquiries 01233 616016 (Ext: 723-6016) MDM Co-ordinator 01233 616235 (Ext: 723-6235) Out of hours emergency services (including Bank holidays) are available via the hospital switchboard Laboratory Opening hours Document number: CEL EXDO 612 Author: P Williams Approved by: Dr M Perenyei 8.00am – 8.00pm Monday - Friday 9.00am – 5.00pm Saturday – Sunday WARNING: this is a controlled document Page: 5 of 47 Date of Issue: May 2014 Revision: 12 Cellular Pathology Cellular Pathology Userguide 2014 USE OF SERVICE All specimens must be accompanied by a histology request form CELPTHY FRM-KPN-CEL-004 which is LEGIBLE AND PROPERLY COMPLETED. Essential information includes:- NHS NUMBER FULL NAME DOB SURNAME FORENAME NHS / HOSP NO DOB HOSPITAL / WARD DATE / TIME SPECIMEN CONSULTANT/GP MANDATORY FIELDS * SIGNATURE / INITIALS ADDRESS GP/SURGERY SPECIMEN TYPES/SITES CLINICAL DETAILS HIGH RISK STICKER (IF APPLICABLE) INSTRUCTIONS FOR SAMPLE SUBMISSION Document number: CEL EXDO 612 Author: P Williams Approved by: Dr M Perenyei WARNING: this is a controlled document Page: 6 of 47 Date of Issue: May 2014 Revision: 12 Cellular Pathology Cellular Pathology Userguide 2014 LABELLING INSTRUCTIONS FOR SAMPLE CONTAINER Please note:- Accepted printed adhesive labels should never be placed on the container lid. SAMPLE TYPE Histology REQUIRED CONTAINER Labelled 10%formalin container showing appropriate hazard warning Sent to Histology ASAP in a dry labelled container Sent to Histology ASAP One sample in a labelled histology container One sample in Michels medium (cryotube to be placed in a clean 60ml sterile container) Histology - Frozen section Histology - Skin samples for immunofluorescence Histology MANDATORY Surname and at least one Forename NHS* Number Minimum mandatory criteria :- Date of Birth Two of these three patient identifiers Patient's Address (including Postcode) High Risk sticker (if applicable) - this must not cover patient details Site of sample Date/Time of collection The importance of handwritten labels on specimen containers should be emphasised. Clinics regularly dealing with multiple samples during a single procedure (i.e. endoscopy, colposcopy, and prostate biopsy clinics) may consider printed labels which must be created at the time and location of the procedure. Only data trace labels (or equivalent) are acceptable. Samples identified with both acceptable printed labels and legible handwritten container labels must be clearly dated, signed or initialled by the person who took the sample. Pre-printed labels such as addressograph labels are unacceptable. The department of Cellular Pathology will carry out site visits to clinics to audit and monitor adherence to this policy. This activity is required by CPA (Clinical Pathology Accreditation) and the aim is to standardise specimen labelling throughout the Trust minimising risk. *NHS number in some cases (e.g. A&E, new born, unregistered, oversees visitors) may not be available. In these cases hospital number/emergency number may be substituted. Some patients’ identity may be anonymous (e.g. GUM clinic, blind clinical trials): these patients will have a coded identifier, and will not have name, address nor NHS/hospital number. Please ensure that the tops of bottles etc. are securely fastened and not cross threaded to prevent leakage. High risk specimens should be clearly labelled double bagged and labelled Biohazard. Any samples failing to meet these acceptance criteria will result in delay and possibly the return of the sample to the requesting clinician for appropriate labeling. The range of services offered by the department are as follows: Document number: CEL EXDO 612 Author: P Williams Approved by: Dr M Perenyei WARNING: this is a controlled document Page: 7 of 47 Date of Issue: May 2014 Revision: 12 Cellular Pathology Cellular Pathology Userguide 2014 Routine diagnostic Histopathology Rapid Frozen sections Rapid processing for urgent histopathology Skin Immunofluorescence Lymph node analysis Mohs sections Muscle Biopsies The Processing Of Foetuses, Retained Products And Placentas Videoconferencing Multidisciplinary meetings Digital macro and microphotography Referral centres High Risk Specimens e.g. HIV, Hepatitis, TB, nv CJD including all specimens suspected of being high risk or from patients in a high risk category such as immuno compromised patients must be clearly labelled with a DANGER RISK OF INFECTION sticker. The nature of the risk MUST BE CLEARLY stated on the request form. The specimen MUST be sent to the laboratory double bagged. Routine Histopathology Specimens must be placed in an appropriate container with sufficient 10% Formalin to submerge the specimen. Certain specimens are best preserved with alternative fixatives e.g. Phaeochromocytoma, testicular biopsies. For information about alternative fixatives contact the laboratory. Turnaround time for reporting the result: Diagnostic biopsies 80% expected within 7 working days from collection date. All histology specimens 80% expected within 10 working days from collection date. Results are electronically available after authorisation by Pathologist. Cases for further opinion are always sent to a CPA accredited laboratory. Rapid Frozen section service This service offers an immediate diagnosis on specimens from patients who are under anaesthetic and must be booked at least 24 hours in advance with a Pathologist. When booking a frozen section with a Pathologist on extn 86016 it is essential to give all patient details and an indication of the expected time of arrival of the sample. Document number: CEL EXDO 612 Author: P Williams Approved by: Dr M Perenyei WARNING: this is a controlled document Page: 8 of 47 Date of Issue: May 2014 Revision: 12 Cellular Pathology Cellular Pathology Userguide 2014 The Cryostat is used to cut sections from fresh (unfixed) frozen tissue. Tissue debris collected in the cryochamber is potentially contaminated with pathogens from any hazard group (see ACDP guideline). There is a risk samples will be sent to the laboratory from patients known to be infected with hazard group 3 pathogens. These samples are not cut as frozen sections in this laboratory. Specimens must be sent immediately in a dry container with a properly completed request form. Please inform the laboratory when the specimen has been despatched. If at the time of surgery, it is decided not to proceed with the frozen section, please inform the laboratory. Urgent specimens including rapid access (other than frozen sections) A report can be issued on biopsies on the same day if the specimen is received before 11.30am. This service is by prior arrangement with the Subspecialist Pathologist on extn 86016. Skin Immunofluorescence Biopsies for immunofluorescence should be sent to the laboratory in Michels medium which can be obtained from Histology. Please inform the laboratory if such specimens are being sent on 01233 616016 ext: 86016 Samples must be received on the same working day. Lymph Node analysis Lymph nodes biopsy may be required to establish a diagnosis in cases of: Infection or Pyrexia of Unknown Origin (PUO) Unresolved lymphadenopathy Suspected lymphoma or haematological malignancy Metastatic disease In cases of suspected infection or PUO, a full serological work up should be instituted prior to biopsy. The sample should be divided and part sent fresh to the Microbiology department. (Typical sample size 0.5 cm³). The remainder of the node should be divided in half and placed in formalin. Document number: CEL EXDO 612 Author: P Williams Approved by: Dr M Perenyei WARNING: this is a controlled document Page: 9 of 47 Date of Issue: May 2014 Revision: 12 Cellular Pathology Cellular Pathology Userguide 2014 Appropriate serological work up should be completed before biopsy of unresolved lymphadenopathy typically to exclude EB virus (monospot), toxoplasma, viral screening and HIV if appropriate. A fresh sample may be sent if appropriate. In other cases especially suspected lymphoma or haematological malignancy the sample should be divided in half along the longest axis and placed in 10% formalin for histological analysis. Dividing the node allows for better fixation and cell preservation. Mohs Sections This service is provided by the laboratory in co-operation with the Consultant Dermatologist and should always be arranged at least one week in advance at KCH Dermatology unit between 0830 and 1700 hrs. Requirement for service beyond this time requires arrangement with Head BMS The Processing Of Foetuses, Retained Products And Placentas. The clinician / midwife should discuss with the Guys Hospital Regional Genetics Centre, the appropriate samples required from a foetus for cytogenetics investigation. The samples usually e.g. cord blood and skin must be taken by the clinician / midwife and dispatched to the regional genetics centre. The foetus can then be sent to the appropriate department as defined below according to gestation. In the case of suspected infection the clinician / midwife must take a swab of placenta and send promptly to microbiology. Depending on gestation age the foetus and placenta should promptly be sent via porter to the appropriate department as defined below. Terminations of pregnancy must be taken from the EAPU or Gynaecology Ward via porter directly to the hospital site mortuary. Foetus, retained products (suspect or clinical diagnosed products of conception labelled POC) and placentas not requiring post mortem or foetuses <16 weeks Send directly from the EPAU or gynae ward in an appropriate sized specimen container with sufficient 10% formalin to the histology department at the William Harvey Hospital via the pathology specimen reception at each site. It must be accompanied by a completed histology request form clearly stating whether an external examination of the foetus is required, and / or histopathological examination of the placenta. The form must clearly state: Patient’s Name NHS/Hospital Number Time event took place and Date Document number: CEL EXDO 612 Author: P Williams Approved by: Dr M Perenyei WARNING: this is a controlled document Page: 10 of 47 Date of Issue: May 2014 Revision: 12 Cellular Pathology Cellular Pathology Userguide 2014 Signature Of Doctor Ward Consultant Name Date of Specimen Clinical Details The Method and Date of Disposal The pot must also bear a completed label included patient’s name, DOB, hospital number, what the specimen is (labelled POC if retained products), the date the event took place. A certificate must accompany the specimen that includes: Name of Patient NHS/Hospital Number Time event took place and Date Signature of Nurse or Doctor certifying products of conception < 24 weeks gestation This certificate must accompany the specimen until final collection for disposal. If the specimen consists of retained products from a live birth it should be stated in the clinical details as ‘’post partum’’ and therefore does not require a certificate. Inform the porters who will transfer the specimen in a pot with formalin to pathology reception. Specimens from QEQM and KCH will be transported to the histopathology department at the William Harvey site in a secure transport container via the pathology specimen transport system. The laboratory staff will allocate a histology specimen number to the request form and specimen pot(s). A signed duplicated POC certificate should accompany products of conception. Please refer to: East Kent Hospitals NHS Trust Procedure For The Management Of Early And MidTerm Pregnancy Loss (Under 24 Weeks Gestation) Policy which is available on Sharepoint. Muscle Biopsies Protocol for sending to Neuropathology department, King’s College Hospital, London. Tel no: 9020 3299 1951 or 020 3299 1957 This protocol applies to both open and needle biopsies. The Neuropathology department at King’s College Hospital, London should be contacted to arrange mutually suitable times for the biopsy to be taken. Tel no: 9020 3299 1951 or 020 3299 1957 Document number: CEL EXDO 612 Author: P Williams Approved by: Dr M Perenyei WARNING: this is a controlled document Page: 11 of 47 Date of Issue: May 2014 Revision: 12 Cellular Pathology Cellular Pathology Userguide 2014 On removal from the patient, the muscle tissue should be placed in a dry specimen pot. A piece of dampened gauze should be placed in the pot also to create a humid atmosphere. This should not actually touch the tissue. (Open muscle biopsies may be stretched by applying sutures at either end and attaching them to dental wax, but this is not essential). The biopsy and relevant patient data should then be urgently dispatched to Neuropathology, King’s College Hospital, London with a request form noting of the time that the biopsy was taken. Neuropathology, King’s College Hospital, London should then be contacted to be told the estimated arrival time of the biopsy. Tel no: 9020 3299 1951 or 020 3299 1957 Videoconferencing This service provides microscope images from the Cellular Pathology Department at the WHH site to remote stations including Queen’s Centre for Clinical Studies, QEQM Hospital, Margate, Kent and Canterbury Hospital and also Oncology at Maidstone Hospital. Use of this equipment is arranged at least one week in advance with the multidisciplinary meetings secretary on ext: 84235 Multidisciplinary Meetings The list of patient cases to be discussed is compiled one week in advance by co ordination with Meeting Secretary on ext: 84235. Pathologist representation at every meeting is provided via videoconferencing or by a Pathologist attending in person. Late inclusion of patient cases is possible up to midday two working days prior to a forthcoming meeting by arrangement with the departments MDM coordinator on ext: 84235 Digital Macro and Microphotography of Surgical Specimens. This facility is available to clinicians for clinically important cases. This can be arranged through the multidisciplinary meeting, sub specialist Pathologist or stated on the Histology request form Document number: CEL EXDO 612 Author: P Williams Approved by: Dr M Perenyei WARNING: this is a controlled document Page: 12 of 47 Date of Issue: May 2014 Revision: 12 Cellular Pathology Cellular Pathology Userguide 2014 CYTOLOGY INTRODUCTION The department of Cellular Pathology is centralised on a single site at the William Harvey hospital, Ashford. It provides diagnostic Histopathology and Cytopathology services. KEY PERSONNEL & LABORATORY NUMBERS Head of Service Dr Miklos Perenyei Diagnostic Cytopathologists Dr George Vittay 01233 616183 (Ext: 723-6183) 01233 616793 (Ext: 723-6793) Dr Miklos Perenyei 01233 616183 (Ext: 723-6183) Dr Salim Anjarwalla 01233 618034 (Ext: 723-8034) Dr Doraline Philips 01233 616604 (Ext: 723-6604) Dr Cate Wight 01233 618942 (Ext: 723-8942 Head Of Gynaecological Cytology Dr Matthias Koslowski 01233 618035 (Ext: 723-8035) Chief Biomedical Scientist Mrs Shirley Moses 01233 616016 (Ext: 723-6016) Cytology Office For Results / Enquiries 01233 633331 (Ext: 723-8628 or 723-4233) Out of hours emergency services (including Bank holidays) are available via the hospital switchboard Laboratory Opening hours Document number: CEL EXDO 612 Author: P Williams Approved by: Dr M Perenyei 8.00am – 8.00pm 9.00am – 1.00pm WARNING: this is a controlled document Monday – Friday Saturday Page: 13 of 47 Date of Issue: May 2014 Revision: 12 Cellular Pathology Cellular Pathology Userguide 2014 GENERAL INFORMATION The following information although comprehensive may not cover all eventualities, and when any doubt exists as to the optimum way in which a sample should be collected and sent to the laboratory please telephone the laboratory for instructions BEFORE THE SPECIMEN IS OBTAINED. Fixative, special containers and transport boxes, if required are obtainable from the laboratory on request. INSTRUCTIONS FOR SAMPLE SUBMISSION SAMPLE TYPE Gynae cytology(Liquid based Cytology) Non gynae fluids Non gynae slides REQUIRED CONTAINER LBC container labelled prior to leaving the patient using the information confirmed during the positive patient identification process Labelled sterile container(25ml or 60ml) Slides labelled with patient Name, Date of Birth and site of specimen LABELLING INSTRUCTIONS FOR REQUEST FORM Non Gynae Cytology and Andrology. Complete the request form CELPTHY FRM-KPN-CEL-004 for The same acceptance criteria applies as in the Histology section. Please see page 5 Gynae Cytology. Complete the request form HMR101. In addition to the above the request form must state Smear Taker’s ST No and signature and also indicate Source of Smear, Reason for Smear, LMP, Last Smear Date, Previous History, Document number: CEL EXDO 612 Author: P Williams Approved by: Dr M Perenyei WARNING: this is a controlled document Page: 14 of 47 Date of Issue: May 2014 Revision: 12 Cellular Pathology Cellular Pathology Userguide 2014 FULL NAME, ADDRESS DOB NHS NUMBER NAME AND ADDRESS OF SENDER IF NOT GP PRACTICE NAME AND ADDRESS PLEASE COMPLETE BOXES 13-20. HIGH RISK STICKER MUST BE APPLIED (IF APPLICABLE) BOX 20 – ST NUMBER BOX 20 – ST NUMBER AND SIGNATURE MUST BE INCLUDED BOX 21 – 24 FOR LABORATORY USE ONLY BOXES 8 AND 9 - PLEASE USE THIS BOX FOR LOCAL CODES Document number: CEL EXDO 612 Author: P Williams Approved by:Dr M Perenyei WARNING: this is a controlled document Page:15 of 47 Date of Issue: May 2014 Revision: 12 Cellular Pathology Cellular Pathology Userguide 2014 LABELLING INSTRUCTIONS FOR SAMPLE CONTAINER Please note:- Accepted printed adhesive labels should never be placed on the container lid. LBC Samples and Non Gynae Cytology Fluids MANDATORY Surname and at least one Forename, NHS* Number Minimum mandatory criteria :- Date of Birth Two of these three patient identifiers Patient's Address (including Postcode) High Risk sticker (if applicable) - this must not cover patient details Sign/Initial Date/Time of collection Site of sample (Non Gynae Cytology Fluids) Criteria for Sample Acceptance – Non Gynae Slides Minimum mandatory criteria:- All patient identifiers Surname and at least one Forename, Date of Birth Site of Sample Criteria for Sample Acceptance – Non Gynae Slide Boxes MANDATORY Surname and at least one Forename, NHS* Number Minimum mandatory criteria :- Date of Birth Two of these three patient identifiers Patient's Address (including Postcode) High Risk sticker (if applicable) - this must not cover patient details The importance of handwritten labels on specimen containers should be emphasised. Clinics regularly dealing with multiple samples during a single procedure (i.e. endoscopy, colposcopy, and prostate biopsy clinics) may consider printed labels which must be created at the time and location of the procedure. Only data trace labels (or equivalent) are acceptable. Samples identified with both acceptable printed labels and legible handwritten container labels must be clearly dated, signed or initialled by the person who took the sample.Pre-printed labels such as addressograph labels are unacceptable. The department of Cellular Pathology will carry out site visits to clinics to audit and monitor adherence to this policy. This activity is required by CPA (Clinical Pathology Accreditation) and the aim is to standardise Document number: CEL EXDO 612 Author: P Williams Approved by:Dr M Perenyei specimen labelling throughout the WARNING: this is a controlled document Trust minimising Page:16 of 47 Date of Issue: Nov 2014 Revision: 12 risk. Cellular Pathology Cellular Pathology Userguide 2014 *NHS number in some cases (e.g. A&E, new born, unregistered, oversees visitors) may not be available. In these cases hospital number/emergency number may be substituted. Some patients’ identity may be anonymous (e.g. GUM clinic, blind clinical trials): these patients will have a coded identifier, and will not have name, address nor NHS/hospital number. Any samples failing to meet these acceptance criteria will result in delay and possibly the return of the sample to the requesting clinician for appropriate labeling. *NHS number in some cases (e.g. GUM, A&E, new born, unregistered, oversees visitors) may not be available. In these cases hospital number/emergency number/special code may be used. Please ensure that the tops of bottles etc. are securely fastened and not cross threaded to prevent leakage. High risk specimens should be clearly labelled double bagged and labelled Biohazard. Each specimen must be accompanied by the correct completed request form, CLEARLY LEGIBLE. For all gynae specimens the request form HMR101 must be used For all non gynae specimens the Kent and Medway Cellular Pathology request form must be used. In the case of cervical samples each request must include the full postal address of the woman and the full postal address of her GP. The smear takers number and signature must be included on the request form. Samples will be rejected by practitioners who do not hold a valid sample taker number Request form HMR101 must be used and all demographic, clinical and personal details must be completed on the form and include previous smear report if abnormal. The request form accompanying a High Risk specimen must show a biohazard sticker and the precise hazard must be clearly stated (e.g. Hepatitis B etc) Cervical Samples (LBC) Sample taking kits are available from the laboratory including request forms, vials of fixative, sample bags and sample taking devices (cervex brush). The brush should be rotated 5 times through 360º in the cervical os. Add the sample to the fixative by agitating the brush against the bottom of the vial 10 times. DO NOT detach the brush head into the vial. Secure the lid firmly. Ensure the vial is labelled with the patients details in ink. All samples must be accompanied by a fully completed cytology request form signed by the sample taker and indicating their sample taken number. Document number: CEL EXDO 612 Author: P Williams Approved by:Dr M Perenyei WARNING: this is a controlled document Page:17 of 47 Date of Issue: May 2014 Revision: 12 Cellular Pathology Cellular Pathology Userguide 2014 Indicate on the request form if the cervix was not visualised, also mention whether a vault or vaginal sample was taken. In some instances an endocervical brush may be used. It is important to state clearly if a specimen has been obtained using an endocervical brush rather than a cervical brush. For routine smears when both cervix and endocervical brushes are used the cervical brush sample should be taken first. Material from both devices should be placed in the same vial. Non- water based lubricants must not be used as they can lead to an inadequate sample report. Contact the laboratory for further details on the use of lubricants if required. Dispatch to laboratory without delay. The patient’s GP and/or sample taker are informed of the result by the laboratory. The patient is informed of the result by the Kent Primary Care Agency. 98% of results are available within 14 days. Human Papilloma Virus (HPV) Testing The aetiological role of Human Papilloma Virus (HPV) in the development of cervical cancer is well established. The NHSCSP has therefore introduced additional High Risk (HR) HPV testing on selected cervical cytology samples which has the benefit of fast tracking women at risk for treatment and also reduces unnecessary repeat tests. HPV Triage The HPV triage test is performed on routine cervical samples showing a low grade cytological abnormality. This includes borderline changes and mild dyskaryosis. A negative (not detected) HPV test allows a woman to return to normal recall whereas a positive (detected) HPV test initiates a referral to colposcopy. HPV Test of Cure The HPV Test of Cure (ToC) is performed on samples taken following large loop excision of the transformation zone (LLETZ) treatment for an abnormality. Negative samples and those showing low grade abnormalities (borderline changes and mild dyskaryosis) are tested. A negative (not detected) HPV test allows a woman to have a repeat test in 3 years before her return to normal recall. A positive (detected) HPV test returns the woman to colposcopy for further investigation. Histologically proven CGIN and women with invasive or micro invasive disease are excluded from the ToC protocol. Document number: CEL EXDO 612 Author: P Williams Approved by:Dr M Perenyei WARNING: this is a controlled document Page:18 of 47 Date of Issue: May 2014 Revision: 12 Cellular Pathology Cellular Pathology Userguide 2014 Uncertainty of measurement In cervical cytology the examination of the sample is used to indicate the presence or absence of disease. Where biological variation in samples occurs, this can lead to difficulties in interpreting results. Where there is genuine doubt as to whether cells changes are abnormal an equivocal report ‘Borderline changes’ is issued. This report will initiate either an HPV test on the original sample to aid patient management or a repeat test. Within the NHSCSP the sensitivity and specificity of the test is well understood and documented. All laboratories and screening individuals are monitored and expected to achieve sensitivities in excess of 90% for all abnormalities and more than 95 % for high grade abnormalities Diagnostic (Non-gynaecological) Samples Effusions Fluid should be sent to the laboratory in a labelled sterile container. DO NOT send the specimen in a catheter drain bag. Ideally 20ml of fluid should be collected particularly where malignancy is suspected so that immunohistochemistry, if necessary, can be performed. The specimen should be sent to the laboratory immediately. If collected at the weekend, the specimen should be kept in a refrigerator at 4ºC. Urines Voided urine should be sent from the second urine of the day, a catheter specimen or mid stream specimen is not satisfactory for cytological investigation. If the only specimen which can be obtained is a catheter, post cystoscopic or ileal conduit, it must be clearly stated on the request form. Urine must be collected into a labelled 25ml sterile container (not boric acid preservative) and sent to the laboratory immediately whilst fresh as cell morphology deteriorates rapidly in voided urine and specimens more than a few hours old maybe unsatisfactory for cytological assessment. Refrigerate if a delay in transportation is anticipated. Respiratory Tract Specimens Sputum: Early morning specimens should be sent fresh to the laboratory. Specimens should be collected on three consecutive days if carcinoma is suspected. Check the quantity is adequate Document number: CEL EXDO 612 Author: P Williams Approved by:Dr M Perenyei WARNING: this is a controlled document Page: 19 of 47 Date of Issue: May 2014 Revision: 12 Cellular Pathology Cellular Pathology Userguide 2014 and sputum is not contaminated with food, saliva, tobacco or toothpaste. A specimen after physiotherapy or postural drainage is very useful Bronchial Brush/Touch Preparation: Smears made from bronchial brushing/biopsies should be spread evenly and quickly on clean glass slides clearly labelled in pencil with the patient details shown in the table on page 13. The slides should be immediately air dried and placed into the slide transport box. Broncho alveolar lavages / induced sputum: These specimens should be taken into a labelled sterile containers and sent immediately to the laboratory (double bagged if known as a High Risk specimen). . Fine Needle Aspirates (FNA) Appropriate for palpable lumps in breast, thyroid, salivary gland and superficial lymph nodes, subcutaneous skin nodules and for imaging guided non palpable lesions. The sample must be spread onto clean slides that have been clearly labelled with the patient details shown on page 13. These labelled slides should be air dried, put into plastic slide mailer boxes and sent to the laboratory with completed accompanying request form. There are “one stop” breast and head and neck clinic sessions provided at Kent and Canterbury Hospital, Queen Elizabeth the Queen Mother Hospital (QEQM) and William Harvey Hospital (WHH) sites. Nipple Discharge The discharge should be smeared on to a slide clearly labelled with the patient details shown in the table on page 13, and air dried immediately. Aspirates of Breast Cysts The aspirate should be transferred to a labelled sterile container, or if less than 0.5 ml placed directly onto a glass slide labelled in pencil with the patient details shown in the table on page 13, then air dried. Fixative is not necessary. CSF Send as much of the specimen as can be spared to the Cytology and Microbiology laboratory, in a labelled sterile container. If there is unavoidable delay in sending a fresh specimen to the laboratory, it should be stored at 4º C. CSF investigations for Leukaemia should be suitably marked. Joint Aspirates Document number: CEL EXDO 612 Author: P Williams Approved by:Dr M Perenyei WARNING: this is a controlled document Page:20 of 47 Date of Issue: May 2014 Revision: 12 Cellular Pathology Cellular Pathology Userguide 2014 Joint aspirates requiring crystal identification should be collected into a clearly labelled sterile container. Results: Urgent samples: from sample receipt 24 hours (excluding weekends) Non urgent samples: from sample receipt 7 days (excluding weekends) Document number: CEL EXDO 615 Author: S Moses Approved by:P Williams WARNING: this is a controlled document Page:21 of 47 Date of Issue: Sept 2013 Revision:12 Cellular Pathology Cellular Pathology Userguide 2014 ANDROLOGY INTRODUCTION Andrology in East Kent and Maidstone is carried out in the Cytology Department of the William Harvey Hospital (WHH), Ashford and at Queen Elizabeth the Queen Mother Hospital (QEQM), Margate. KEY PERSONNEL & LABORATORY NUMBERS Clinical Lead Dr Matthias Koslowski 01233 618035 Chief Biomedical Scientist Mrs Shirley Moses 01233 616016 Results Enquiries 01233 633331 (Ext: 723-1857 or 723-4233) Availability of Service for Post Vasectomy Samples This service is available on any weekday Monday – Friday (excluding Bank Holidays) Samples can be taken to Pathology Reception at any of the following hospitals at the times indicated: William Harvey Hospital, Ashford 8.30 – 17.00 Queen Elizabeth the Queen Mother Hospital, Margate 8.45 - 15.45 Kent and Canterbury Hospital, Canterbury 8.30 - 16.00 Availability of Service for Subfertility Samples: Please note that patients with High Risk samples (Hepatitis, HIV) must go to the William Harvey Hospital for their semen analysis. Please ensure that the patient is aware that they can take samples to Pathology Reception at the following hospitals at specified times only (excluding Bank Holidays). Queen Elizabeth the Queen Mother Hospital – Wednesday 8.30am to 2pm by appointment Document number: CEL EXDO 615 Author: P Williams Approved byDr M Perenyei WARNING: this is a controlled document Page:22 of 47 Date of Issue: Sept 2013 Revision:12 Cellular Pathology Cellular Pathology Userguide 2014 SEMEN ANALYSIS FOR SUBFERTILITY Approximately 1 in 6 couples have difficulty conceiving and are referred for infertility investigations. The single most common cause of infertility is sperm dysfunction, which is apparent in approximately 30% of the men referred for analysis. A high quality Andrology service is therefore essential for correct management of the male patient. Staff in the East Kent Hospitals University Trust are fully trained scientists and are highly proficient in performing quality diagnostic semen analyses in line with current World Health Organisation and Association of Biomedical Andrologist guidelines. Currently we perform some 1200 semen analyses a year for infertility investigation. The laboratories conduct regular internal and external QC and participate in the National External Quality Assurance scheme for Andrology. REQUESTING A SEMEN ANALYSIS Please provide the patient with the following: Request form containing Patients full name, address with postcode, date of birth, partners name, NHS number (if known) clinical information and reason for request (infertility/ reversal of vasectomy). Please indicate requesting clinician’s name and location. Patients that are known to be an infection risk must have their forms clearly labelled. Please note that due to a change in facilities in the laboratory at Queen Elizabeth the Queen Mother Hospital samples from known High Risk (Hepatitis, HIV) patients can no longer be handled. These patients will need to go to the William Harvey Hospital for their semen analysis. Patients should be advised that they must bring the request form with them when delivering the specimen pot to the laboratory. Patient instruction sheet. Please ensure that the patient is aware of the different opening times for the following laboratories: Queen Elizabeth the Queen Mother Hospital – Wednesday 8.30am to 2pm An appointment must be booked for this test by ringing the blood test appointment line on 01843 23500 (It is essential to ask for a semen test). Appointments are available at 45 minute intervals. William Harvey Hospital - Monday and Wednesday 8.30am to 1pm - Friday 8.30am to 5pm. No appointments are needed at the William Harvey Hospital Document number: CEL EXDO 615 Author: P.Williams Approved by: Dr M. Perenyei WARNING: this is a controlled document Page:23 of 47 Date of Issue: Sept 2013 Revision:12 Cellular Pathology Cellular Pathology Userguide 2014 A wide mouthed 60ml specimen pot that has a CE mark (This is marked on the label by the manufacturer to indicate that it is fit for purpose). Please ensure that the patient is aware that they must label the pot in ink with their full name and date of birth as well as indicating the date and time of emission. Specimen bag. PRODUCING THE SEMEN SAMPLE PLEASE NOTE THAT FACILITIES ARE NOT AVAILABLE TO PRODUCE SEMEN SAMPLES AT HOSPITALS WITHIN THE EAST KENT HOSPITALS UNIVERSITY TRUST Prior to producing the sample the patient must have abstained from sexual intercourse/ masturbation for at least 2-3 days and no more than 7 days. He must be hygienic and wash his hands and genital area. Make sure that all soap is washed off as this will kill sperm. Check that the pot is free of cracks as leaking samples will be rejected. He must only use the pot supplied by his GP/Clinic as inappropriate pots will be rejected. The sample must be produced by masturbation directly into the clean plastic pot supplied by his doctor/consultant. It is important that the entire sample is collected in order that an accurate analysis can be carried out. The use of lubricants such as K-Y jelly must be avoided. Samples produced by the withdrawal method or into an ordinary condom are unsuitable for analysis. Ensure that the pot lid is tightly screwed up as if the pot leaks in transit it will not be analysed. Labelling the pot and completing the patients section of the request form. It is essential that the following information is written in ink on the label of the pot. Full name of patient (first name and surname). Date of birth Date of collection Time of collection Home postcode (as a patient identifier) Please add your initials at the bottom of the label to indicate that the information is correct. Document number: CEL EXDO 612 Author: P Williams Approved by:Dr M Perenyei WARNING: this is a controlled document Page: 24 of 47 Date of Issue: May 2014 Revision: 12 Cellular Pathology Cellular Pathology Userguide 2014 Fill in the patients section at the back of the instruction sheet to confirm that the complete sample has been collected and that the appropriate period of abstinence (sexual intercourse / masturbation) has been carried out. This section should be torn off and attached to the request form. What if the patient has problems collecting the sample? Be re-assured that when most men get over the initial embarrassment they usually manage to provide a specimen. However, for those who still can't, or have some religious or cultural objection, we can provide a non-spermicidal condom for specimen collection. If the patient needs to request one of these condoms please ask them to ring 01233 616016 and ask for Shirley Moses or Josephine Coglan Delivery of the Specimen Sperm are sensitive to temperature and the semen sample must therefore be protected from direct sunlight or extremes of cold. In order to keep the sample as close to body temperature as possible it is best to carry it close to the body, ideally in an inside pocket. The sample must reach the laboratory as soon as possible after production. Ideally this should be within 1 hour, but patients travelling greater distances are allowed up to 2 hours from the time of production. Rejection of Specimens for Infertility Investigation The laboratory will reject any specimen that is: Not produced into an appropriate container. Produced into an unlabelled container. Found to have leaked in transit. Delivered to any hospital other then the William Harvey Hospital or sent via the hospital or GP transport. Delivered at a time/day other than those specified. Received without a request form. THE SEMEN ANALYSIS TEST We examine the semen sample for a number of important factors according to the World Health Organisation Guidelines 2010. Document number: CEL EXDO 615 Author: P.williams Approved by: Dr M. Perenyei WARNING: this is a controlled document Page:25 of 47 Date of Issue: Sept 2013 Revision:12 Cellular Pathology Cellular Pathology Userguide 2014 Sperm Concentration Sperm count in millions per ml of semen. Normal samples have over 15 million per ml or 39 million for the whole ejaculate. Sperm Motility Sperm are graded according to their ability to swim. Sperm that swim in a progressive manner are graded as having rapid or sluggish motility. Normal samples should contain at least 32% progressive sperm and at least 40% motile sperm (progressive and non progressive) at 1 hour. Sperm Morphology The shape and size of the sperm are assessed on a stained preparation. The normal value in a fertile population is 4% or above. Vitality Test This test is included in results where the number of immotile sperm are greater than 60%. It is a staining technique that will identify if the immotile sperm are dead or just immotile and is reported as a percentage vitality. The normal value is 58% or above RESULTS A written report is sent back to the referring practitioner within 7 – 10 working days. If further copies are needed to forward onto other practices/ clinics please make a note on the original request form. Patients should be made aware that they cannot receive the result directly from the laboratory. If a report is required for a specific appointment date, this should be stated on the request form to allow the report to be fast tracked. INTERPRETATION Although there are strict guidelines for the measurement and quality control of semen variables they are not an absolute guide to a man’s fertility and no one parameter should ever be considered in isolation unless he has no sperm at all. Procedural errors are minimised by standardised methods of collection, analysis and reporting, therefore it is essential that the patient understands the instructions prior to production of the sample. Document number: CEL EXDO 612 Author: P Williams Approved by:Dr M Perenyei WARNING: this is a controlled document Page: 26 of 47 Date of Issue: May 2014 Revision: 12 Cellular Pathology Cellular Pathology Userguide 2014 The overall balance of the sample is much more indicative of fertility potential and should be considered alongside any investigations of the female partner. For example the term low sperm count is ambiguous and is often misinterpreted by the patient. His count may be rather low but an increased motility may be sufficiently high enough to compensate for any shortfall. The following table shows the distribution of values for semen parameters from men whose partners became pregnant within 12 months of discontinuing contraceptive use. WHO 2010 Parameter (units) 1941 1859 2.5 1.2 9 5 1.5 15 10 2.0 22 25 2.7 41 Centile 50 3.7 73 75 4.8 116 90 6.0 169 95 6.8 213 97.5 7.6 59 1859 23 39 69 142 255 422 647 802 928 1780 1778 1863 1851 428 28 1 19 3 53 32 1 22 4 58 39 2 25 5.5 64 47 3 31 9 72 55 5 39 15 79 62 9 46 24.5 84 69 15 54 36 88 72 18 59 44 91 75 22 65 48 92 N Semen volume (ml) 6 Sperm concentration (10 per ml) 6 Total sperm number (10 per ejaculate) Progressive motility (PR, %) Non-progressive motility (NP, %) Immotile spermatozoa (IM, %) Normal forms (%) Vitality (%) REPEAT TESTS If any of the factors tested are below the normal range it is advisable to repeat the semen analysis test. Abnormalities in the sample can occur for a number of reasons eg patient did not collect the whole sample. In addition illness, stress or medication can also affect sperm quality. Confirmation of a true sperm problem may require a second test. POST VASECTOMY SEMEN ANALYSIS Sperm tests to confirm the success (or otherwise) of a vasectomy operation are absolutely essential. Patients are required to produce a sample of seminal fluid at 18 WEEKS, 22 WEEKS and possibly an additional test at 28 WEEKS following vasectomy. REQUESTING A POST VASECTOMY SEMEN ANALYSIS Please provide the patient with the following: Request form containing Patients full name, address with postcode, date of birth, NHS number, reason for request and date of vasectomy. Please indicate requesting clinician’s name and location. (Patients that are known to be an infection risk must have their forms clearly labelled). Document number: CEL EXDO 615 Author: P.Williams Approved by: Dr M. Perenyei WARNING: this is a controlled document Page:27 of 47 Date of Issue: Sept 2013 Revision:12 Cellular Pathology Cellular Pathology Userguide 2014 Patients should be advised that they must bring the request form with them when delivering the specimen pot to the laboratory. The patient declaration section at the end of the instruction sheet must be completed to indicate whether the complete sample was collected. This must be attached to the request form Patient instruction sheet. This will give details of the times that samples can be delivered to the nearest hospital to the patient. Please ensure that the patient is aware that they must label the pot in ink with their full name, date of birth and home post code as well as indicating the date and time of emission. Please note that the service is available Monday to Friday (excluding Bank Holidays) Samples can either be brought directly to Pathology Reception at the William Harvey Hospital, Ashford between 8..45am and 5.00pm or taken to Pathology reception at the times specified for each of the other hospitals: Queen Elizabeth the Queen Mother Hospital, Margate 8.45am- 3.45pm Kent and Canterbury Hospital, Canterbury 8.30am- 4.00pm A wide mouthed 60ml specimen pot that has a CE mark (This is marked on the label by the manufacturer to indicate that it is fit for purpose) Specimen bag . PRODUCING THE SEMEN SAMPLE PLEASE NOTE THAT FACILITIES ARE NOT AVAILABLE TO PRODUCE SEMEN SAMPLES AT HOSPITALS WITHIN THE EAST KENT HOSPITALS TRUST He must be hygienic and wash his hands and genital area. Make sure that all soap is washed off as this will kill sperm. Check that the pot is free of cracks as leaking samples will be rejected. He must only use the pot supplied by his GP/Clinic as inappropriate pots will be rejected. The sample must be produced by masturbation directly into the clean plastic pot supplied by his doctor/consultant. It is important that the entire sample is collected in order that an accurate analysis can be carried out. The use of lubricants such as K-Y jelly must be Document number: CEL EXDO 612 Author: P Williams Approved by:Dr M Perenyei WARNING: this is a controlled document Page: 28 of 47 Date of Issue: May 2014 Revision: 12 Cellular Pathology Cellular Pathology Userguide 2014 avoided. Samples produced by the withdrawal method or into an ordinary condom are unsuitable for analysis. Ensure that the pot lid is tightly screwed up as if the pot leaks in transit it will not be analysed. Labelling the pot and completing the patients section of the request form. It is essential that the following information is written in ink on the label of the pot. Full name of patient (first name and surname). Date of birth Date of collection Time of collection Home postcode Please add your initials at the bottom of the label to indicate that the information is correct. Fill in the patients section at the back of the instruction sheet to confirm that the complete sample has been collected. This section should be torn off and attached to the request form. Delivery of the Specimen Sperm are sensitive to temperature and the semen sample must therefore be protected from direct sunlight or extremes of cold. In order to keep the sample as close to body temperature as possible it is best to carry it close to the body, ideally in an inside pocket. The sample must reach the laboratory as soon as possible after production. This should be on the day of production. Rejection of Specimens for Post Vasectomy Investigation The laboratory will reject any specimen that is: Not produced into an appropriate container. Produced into an unlabelled container. Found to have leaked in transit. Received without a request form. Produced earlier than 16 weeks after vasectomy. POST VASECTOMY ANALYSIS Document number: CEL EXDO 615 Author: P.Williams Approved by: Dr M.Perenyei WARNING: this is a controlled document Page:29 of 47 Date of Issue: Sept 2013 Revision:12 Cellular Pathology Cellular Pathology Userguide 2014 The semen sample is initially examined as a direct wet preparation and any spermatozoa present in a 10ul aliquot are counted and the result per ml of sample is calculated. Due to the delays between time of emission and examination there is no comment for non- motile sperm. There is no guarantee that nonmotile sperm were always non- motile and therefore a comment is only made if there are motile sperm present. If sperm are not seen in the original preparation a portion of the sample is centrifuged at high speed to produce a pellet and this provides a concentrate of the original sample. An aliquot of this concentrate is analysed for the presence of sperm and if any sperm are counted the result per ml of original sample can be calculated. Samples found to have very high counts and motile sperm will be analysed as infertility specimens. The test will be based on the numbers of spermatozoa. The presence of large number of spermatozoa may indicate a failed surgical procedure/ recanalisation. This is an infrequent event which will need to be confirmed by a sample delivered to the laboratory within 2 hours. The laboratory will advise the need for a repeat sample or re referral to the surgeon. RESULTS Reports will record the absence of sperm as:NO SPERMATOZOA SEEN IN A CENTRIFUGED DEPOSIT Reports will record the presence of sperm as:SPERM CONCENTRATION – ie Number of sperm per ml TOTAL COUNT – ie Number of sperm per ml x volume of semen Only sperm concentrations greater than 10,000 spermatozoa per ml are significant. CLEARANCE Will require either 2 samples with ‘No spermatozoa seen’ or 1 sample with ‘No spermatozoa seen’ and another with ‘Less than 10,000 spermatozoa per ml This will be adequate to confirm vasectomy. The laboratory will include in the report that no further samples are required. Document number: CEL EXDO 615 Author: P.Williams Approved by: Dr M. Perenyei WARNING: this is a controlled document Page:30 of 47 Date of Issue: Sept 2013 Revision:12 Cellular Pathology Cellular Pathology Userguide 2014 SPECIAL CLEARANCE Evidence based studies have shown that in a small minority of men non-motile spermatozoa persist after vasectomy. In such cases special clearance may be given if less than 10,000 spermatozoa per ml are seen in a sample examined at least 28 weeks after vasectomy. If all three samples (at 18, 22 and 28 weeks) show the presence of non motile sperm in concentrations of less than 10,000 spermatozoa per ml special clearance should be given to the patient by the doctor/ surgeon who performed the vasectomy. In these cases the report will read:– PERSISTENT RARE (< 10,000 spermatozoa/ml) SPERMATOZOA PRESENT. ADVISE SPECIAL CLEARANCE. NO FURTHER SPECIMENS REQUIRED. If you have any further queries or have any problems regarding the production and delivery of your semen sample please contact us on 01233 633331 (Ext: 88628 or 84233 Document number: CEL EXDO 612 Author: P Williams Approved by:Dr M Perenyei WARNING: this is a controlled document Page: 31 of 47 Date of Issue: May 2014 Revision: 12 Cellular Pathology Cellular Pathology Userguide 2014 MORTUARY INTRODUCTION The department of Cellular Pathology currently provides a hospital and public mortuary service on three East Kent hospital sites. These include Kent and Canterbury, Queen Elizabeth the Queen Mother, and William Harvey hospitals. KEY PERSONNEL & LABORATORY NUMBERS Lead Pathologist/ Designated Individual Dr Miklos Perenyei 01233 616183 (Ext: 723-6183) Deputy Lead Dr Nicola Chaston 01233 616793 (Ext: 723-6793) Lead Anatomical Pathology Technician Mr Adam Berry 01233 616606 (Ext: 723-6606) Lead Pathologist for perinatal Investigations Dr Aminu Abdulkadir 01233 616184 (Ext: 723-6184) Head Biomedical Scientist Mr Paul Williams 01233 616129 (Ext: 723-6129) Opening hours William Harvey Hospital 7.30 am – 4.00pm Monday-Friday Queen Elizabeth the Queen Mother Hospital 7.30 am – 4.00pm Monday-Friday Kent and Canterbury Hospital 8:00 am – 4.00pm Monday-Friday (Access outside these hours covered by portering services) Advice may also be obtained from the Consultant Histopathologists Contacting the On Call Mortuary Technicians out of normal working hours is done via the hospital switchboard. Viewings/ID’s by Police and/or Next of Kin will require prior arrangement with Mortuary staff or the On Call Technician. Document number: CEL EXDO 612 Author: P Williams Approved by:Dr M Perenyei WARNING: this is a controlled document Page:32 of 47 Date of Issue: May 2014 Revision: 12 Cellular Pathology Cellular Pathology Userguide 2014 Contacts Kent and Canterbury Hospital Relative Support Office 01227 766877 (Ext: 722-4112) Queen Elizabeth the Queen Mother Hospital Relative Support Office 01843 225544 (Ext: 725-3459) William Harvey Hospital Relative Support Office 01233 633331 (Ext: 723-8206) Senior Chaplain Rev. Christopher White 01843 225544 (Ext: 725-2578) 07717540972 Alternatively Coroner’s Office Ashford, Dover and Folkestone telephone: 01233 896242 Alternatively 07876356620 01233 896172 Alternatively 07879481594 01233 896171 Alternatively 07740185247 Canterbury and Margate telephone: 03000 410 603 Maidstone telephone: Document number: CEL EXDO 612 Author: P Williams Approved by:Dr M Perenyei 01622-820412 WARNING: this is a controlled document Page: 33 of 47 Date of Issue: May 2014 Revision: 12 Cellular Pathology Cellular Pathology Userguide 2014 General Information The three mortuaries each provide cold body storage. Autopsies are presently performed at Queen Elizabeth the Queen Mother Hospital and William Harvey Hospital mortuaries. Identification of deceased in the mortuary Identification of the deceased with the Notification of Death sheet must accompany the deceased. Patient identification labels should have been placed onto the deceased by the ward and must have at least two identification means i.e. full name, date of birth and ward or first line of address. Any property and valuables must be checked and recorded. A body that is known to be at risk of infection of a category 3 or 4 disease, must be treated with extra precaution. The body must be placed in a sealed body bag. Danger of Infection must be clearly marked on the outside of the bag Autopsies When an autopsy (Hospital Post Mortem) is requested for a patient dying in hospital, where there is no Coroner’s involvement, the documentation required is: a) A completed, signed informed consent form (available from the Bereavment office) b) The patient’s notes c) A concise summary of the case d) Medical Certificate of Cause of Death completed e) Completed cremation form where relevant These documents should then be taken to the Relative Support Office who will then make contact with the Mortuary & the Duty Pathologist to arrange a suitable time and day to carry out the autopsy. In certain circumstances deaths must be reported to the Coroner. Please refer to the guidelines issued by the Coroner, (Guidelines for Hospital Doctors on Reporting Deaths to Her Majesty’s Coroner). In these cases the Coroner will decide if an autopsy is required and make appropriate arrangements. Document number: CEL EXDO 612 Author: P Williams Approved by:Dr M Perenyei WARNING: this is a controlled document Page:34 of 47 Date of Issue: May 2014 Revision: 12 Cellular Pathology Cellular Pathology Userguide 2014 Telephone Numbers Kent and Canterbury Hospital Relative Support Office Ext 722-4006 Mortuary Ext 722-4352 Relative Support Office Ext 725-4452/725-3127/725-4233 Steve Burr Deputy Lead Anatomical Pathology Technician Ext 725-5079/725-3182 Relative Support Office Ext 723-8206 / 723-6887 Adam Berry Lead Anatomical Pathology Technician Ext 723-6606 Rev. Christopher White Trust Chaplain Ext 725-2578 Paul Williams Head Biomedical Scientist Ext 723-6129 Queen Elizabeth the Queen Mother Hospital William Harvey Hospital RETAINED PRODUCTS OF CONCEPTION AND FOETUSES All Retained products of conception, fetuses will be stored and disposed of in accordance with departmental Standard Operational Procedures. DEATHS Relative Support Office, see above for contact details. Death of a Patient A subject that is never very easy to deal with, even as you become more used to it. Continue to keep a healthy respect for the dead. Document number: CEL EXDO 612 Author: P Williams Approved by:Dr M Perenyei WARNING: this is a controlled document Page: 35 of 47 Date of Issue: May 2014 Revision: 12 Cellular Pathology Cellular Pathology Userguide 2014 Practical Points Confirm death. Talk to the relatives, should they request it. TRY NOT TO KEEP THE WARD WAITING Confirm: I. Pupils are fixed. II. Patient is un-responsive to a painful stimulant III. There are no palpable cardiac pulsations. IV. No heart or breath sounds, heard over one minute. Write all the information below in the notes: I. Date/Time. II. Circumstances. III. Declaration of Death. IV. Can certificate be issued? If so, what is the cause of death? V. Have the relatives been informed? If so, what were they told? VI. Sign the entry in the notes, clearly. Legal Certification of Death Can you issue a Medical Certificate of Cause of Death? Q: Were you in clinical attendance during the last illness and had you seen the patient during the 14 days prior to death. NB: See “24 hour rule”. Q: Do you know the Cause of Death (or think you do)? Q: Was death wholly due to NATURAL CAUSES with no unnatural event which has contributed to death? If the answer to ALL THREE of these questions is “yes”, then you MUST issue a certificate. Medical Certificate of Cause of Death are available through the Relative Support Office (or if death has occurred in ITU or A&E then certificates are available there) Once complete, the Relative Support Office (or ITU/A&E) liaises with the Next of Kin regarding the collection of the Medical Certificate of Cause of Death. Discuss any concerns with the Relative Support Officer or the Coroner. Document number: CEL EXDO 612 Author: P Williams Approved by:Dr M Perenyei WARNING: this is a controlled document Page:36 of 47 Date of Issue: May 2014 Revision: 12 Cellular Pathology Cellular Pathology Userguide 2014 Informing the GP When patients die the Relative Support Office are responsible for informing the GP. Please liaise with them on this. Medical Certificate of Cause of Death The Medical Certificate of Cause of Death will normally be completed by a member of the medical team, who has been attending the Deceased patient. This must be completed as soon as possible to avoid unnecessary delay and therefore distress to the relatives. If there is any doubt what to write on the Medical Certificate of Cause of Death or whether to report the case to the Coroner, the Consultant in charge must be consulted. If the case needs to be reported to the Coroner this must be done as soon as possible. Do not complete the Medical Certificate of Cause of Death in these circumstances unless the Coroner instructs otherwise. Once the ‘Cause of Death’ certificate has been handed to the relatives and registered it CANNOT BE CHANGED in relation to the stated cause of death Blank Medical Certificate of Cause of Death are kept by the Relative Support Office, also ITU & A&E. Medical Certificate of Cause of Death must be completed before 10 am on the morning following a death if the Doctor is working nights, any other time the Doctor will be contacted by the Relative Support Office to complete the paperwork. Post Mortem Examinations Coroner’s Post Mortems – once the case is accepted by the Coroner no further responsibility is devolved to the House Officer. Hospital requested Post Mortems – once it has been agreed that the Coroner is not involved, a Hospital Post Mortem may be requested. In this event the informed consent of the immediate Next of Kin is required. Before this is sought a Medical Certificate of Cause of Death must be completed. When consent has been obtained, a member of the medical team should fill in a Post Mortem request form and hand this, the consent form, and the full hospital notes to the Mortuary. Doctors are expected to attend the Post Mortem, and to contact the Consultant Pathologist to discuss the case beforehand. A Hospital Post Mortem examination must never be a substitute for, or a means of avoiding, one instructed by the Coroner, and Consultant Pathologists will refer any doubtful cases to the Coroner. Document number: CEL EXDO 612 Author: P Williams Approved by:Dr M Perenyei WARNING: this is a controlled document Page: 37 of 47 Date of Issue: May 2014 Revision: 12 Cellular Pathology Cellular Pathology Userguide 2014 Coroners Cases The duty of the Coroner is to investigate sudden or unexpected deaths in which the cause is uncertain. Deaths in the circumstances described below must be reported to the Coroner via the Coroner’s Office. The Coroner’s Officer’s can be contacted between 8:00am & 4:00pm Monday to Friday to obtain advice or report a death. Remember also to seek advice on difficult or urgent issues such as organ donation in respect of cases referred to the Coroner. In regards to tissue/organ donation, it’s usually the donation team that will contact the Coroner directly once they have been informed about a potential donor. To report a death to the Coroner Ring the number relevant to the site where the death occurred, Monday to Friday between 8:00am – 4:00pm, details of this number is available in the Relative Support office. If contact is made to the Coroner’s Officer’s and they are not available, follow the instructions on the answer phone. Ashford, Dover and Folkestone telephone: 03000 410804 Alternatively 07876356620 Alternatively 07879481594 Alternatively 07740185247 Canterbury and Margate telephone: 03000 410603 For Maidstone telephone: 01622 – 820412 Advice may also be obtained from the duty Consultant Pathologist. Write “Referred to the Coroner” on the patient’s notes to assist the Coroner’s Office and the Relative Support office. Document number: CEL EXDO 612 Author: P Williams Approved by:Dr M Perenyei WARNING: this is a controlled document Page:38 of 47 Date last reviewed : November 2014 Revision: 12 Cellular Pathology Cellular Pathology Userguide 2014 Circumstances when death must be reported to the Coroner If the Medical Officer in attendance on the patient is sure of the Cause of Death and it is natural they should complete a Medical Certificate of Cause of Death and need not report the case to the Coroner. If there is any doubt whatsoever regarding the Cause of Death, the case must be reported to Coroner. Deaths are reportable to the Coroner if they are sudden and unexpected, if the doctor is uncertain of the Cause of Death, and if it has been caused as a result of an accident or unusual circumstances or industrial disease (e.g. asbestos related) In no circumstances must relatives be offered the option of agreeing to allow a Hospital Post Mortem to be performed as an alternative to reporting the death to Coroner. Deaths in the following circumstances must be reported to the Coroner: ABORTION If the death is linked with an abortion ACCIDENTS If in any way it is thought that an accident may have contributed to the death. ALCOHOLISM Acute alcoholic poisoning ANAESTHETIC DEATHS Whether a patient dies during a procedure or afterwards, irrespective of the length of time involved after anaesthesia e.g. a cerebral anoxia case dying 6 months later. If you are in any doubt report the case to the Coroner. BLOOD TRANSFUSIONS Deaths thought to be due to a blood transfusion. COMPLAINTS If there is any suggestion that the relatives of the deceased are dissatisfied for any reason (this may be a valuable safeguard for the doctor in attendance). Document number: CEL EXDO 612 Author: P Williams Approved by:Dr M Perenyei WARNING: this is a controlled document Page: 39 of 47 Date of Issue: May 2014 Revision: 12 Cellular Pathology Cellular Pathology Userguide 2014 DELAY IN DIAGNOSIS If there is any possible delay in making a correct diagnosis, the death should be reported to the Coroner, e.g. meningitis DRUGS Deaths thought to be due to any drug, whether therapeutic or related to any form of abuse, including overdose, reaction, poisoning or addiction. Deaths related to solvent abuse FALLS & FRACTURES (Including pathological fractures) All deaths after a fall or a fracture which occurred in the last 3 months and all deaths where there have been older fractures or falls unless they were clearly unrelated to the cause of death HOSPITAL DEATHS If the doctor in attendance considers that there is any possibility for serious complaint about the treatment or otherwise of the Deceased, he should ensure the fact is mentioned in his report to the Coroner who will decide if the body should be removed to a place for a post mortem other than the hospital in which the patient died. If the death is related to a medical procedure or treatment, whether invasive or not. All deaths within 24 hours of (a) Admission (b) Any procedure (c) Anaesthetic (d) Discharge from hospital All alleged medical or nursing mishaps or if you have any reason to believe that such an allegation has been, or is likely to be made against any member of hospital staff. For example:- where death occurs before a diagnosis is established or where some event occurs which is unexpected and in which the doctor may think the death is not entirely natural, e.g. surgical complications post anaesthetic, anaesthetic complications, or a fall from a bed or trolley. Please Note: Deaths due to properly performed procedures are likely to be considered natural but are still reportable. Document number: CEL EXDO 612 Author: P Williams Approved by:Dr M Perenyei WARNING: this is a controlled document Page:40 of 47 Date of Issue: May 2014 Revision: 12 Cellular Pathology Cellular Pathology Userguide 2014 INDUSTRIAL DISEASES & DEATHS RELATED TO OCCUPATION Deaths associated with industrial exposure, e.g. asbestosis, or suspected mesotheliomas, pneumoconiosis, or any prescribed diseases or deaths which are thought to be due to any new unscheduled industrial substance must be reported to the Coroner. IN POLICE CUSTODY/VOLUNTARY ATTENDANCE AT A POLICE STATION If the death has occurred whilst in Police custody, prison or after recent contact with a Police station or prison. INVESTIGATORY PROCEDURES All deaths related to investigatory procedures, e.g. ECT, IVP, Biopsy, CV Lines, cardiac procedures, endoscopy, etc. MENTAL PATIENTS Deaths where the Deceased was detained under the Mental Health Act 1983. OPERATIONS If the death occurs within 14 days of an operation it must be reported to Her Majesty’s Coroner. If it is thought that the operation caused, accelerated, or in any way contributed to the death then it must be reported to the Coroner irrespective of when it took place. If the operation has been performed for an injury irrespective of how it was caused, please report the death to the Coroner. SERVICE & DISABILITY PENSIONERS Where the deceased was receiving any form of War Pension or Industrial Disability Pension, unless the death can be shown to be WHOLLY unconnected. STILLBIRTHS/INFANT DEATHS Where there is any doubt whether the child was born alive or obscure, neonate and infant deaths. Maternal deaths whilst pregnant or within 42 days of termination of pregnancy. VIOLENT OR UNNATURAL DEATHS If there is the slightest suspicion regarding the circumstances of the death, including violence or the possibility of an unnatural death, it must be reported to the Coroner, e.g., want, exposure, neglect/self Document number: CEL EXDO 612 Author: P Williams Approved by:Dr M Perenyei WARNING: this is a controlled document Page:41 of 47 Date of Issue: May 2014 Revision: 12 Cellular Pathology Cellular Pathology Userguide 2014 neglect, hypothermia, self injury or if the death could have occurred secondary to injuries from an accident that occurred a long time ago. Please Remember If the doctor in attendance requires assistance in knowing whether to report the death to the Coroner, please speak to the Coroner personally. Please have the notes with you when you call. The Coroner can, in many circumstances, support a Medical Certificate of Cause of Death with a Form A, (where the Coroner notifies the Registrar of Deaths that the case has been reported to him/her but it is unnecessary to perform a Post Mortem examination). This will overcome problems with Cremation and Registration of the Death. Reporting Deaths involving MRSA or other infection related deaths to the Coroner Deaths should be reported if all the following conditions are fulfilled:The infection, including MRSA, was contracted by the patient whilst in hospital; and The patient was subjected to a procedure whilst in hospital, whether a surgical intervention, the insertion of an IV line or a naso-gastric tube or any similar procedure and the infection occurred as a result; and The infection is a contributory factor in the cause of death. Reporting Obstetric/Neonate deaths to the Coroner The following deaths should be reported to the Coroner:All sudden unexpected maternal deaths associated with pregnancy. Deaths involving a non-viable foetus or a stillborn child are not reportable to the Coroner. However, if there is any doubt whether the fetus or child achieved an independent existence of its mother before death, no matter for how long, it must be reported to the Coroner. Further, if it is clear that the fetus or child has achieved independent status of its mother, and subsequently dies, it must be reported to the Coroner if the death appears to be violent or unnatural, or sudden and the Cause of Death is unknown or occurs within 24 hours of admission to hospital. Cremation Certificates When a deceased patient’s relatives request Cremation, the Relative Support Office will contact an appropriate member of the medical team. Complete the form and hand it back to the Relative Support Document number: CEL EXDO 612 Author: P Williams Approved by:Dr M Perenyei WARNING: this is a controlled document Page:42 of 47 Date of Issue: May 2014 Revision: 12 Cellular Pathology Cellular Pathology Userguide 2014 Office who will obtain a second signature. The Relative Support Office coordinates collection of the fee, and by custom this is shared between the two signatories. You are reminded that income from this source is liable to tax, and a record should therefore be kept of all fees received so that it may be declared to the Inland Revenue. Bereaved Relatives All medical staff are asked to communicate directly and sympathetically with the relatives of patients who die in hospital, especially when the death has been unexpected. Do not delay in completing Medical Certificate of Cause of Death. Also do not delay in reporting cases to the Coroner. A little consideration at this time often prevents long-standing grievance. Document number: CEL EXDO 612 Author: P Williams Approved by:Dr M Perenyei WARNING: this is a controlled document Page: 43 of 47 Date of Issue: May 2014 Revision: 12 Cellular Pathology Cellular Pathology Userguide 2014 List Of Referral Centres Histopathology Department Royal Marsden NHS Trust Fulham Road London SW3 6JJ Royal Victoria Hospital Department Of Pathology Grosvenor Road Belfast BT12 6BA Northern Ireland Pathology Western General Hospital Crewe Road Edinburgh EH4 2XU Department Of Histopathology UCLMS Rockefeller Building University Street London WC1E 6BJ Royal National Throat, Nose & Ear Hospital 330 Gray’s Inn Road London WC1X 8DA Department Of Cellular Pathology Medical School University Of Birmingham Edgbaston Birmingham B15 2TT South London Healthcare NHS Queen Elizabeth Hospital Stadium Road Woolwich London SE18 4QH Department Of Histopathology Frenchay Hospital Marlborough Street Bristol BS16 1LE Document number: CEL EXDO 612 Author: P Williams Approved by:Dr M Perenyei WARNING: this is a controlled document Page:44 of 47 Date of Issue: May 2014 Revision: 12 Cellular Pathology Cellular Pathology Userguide 2014 Leeds Teaching Hospitals Trust Department Of Histopathology 5th Floor Bexley Wind St James’s University Hospital Leeds LS9 7TF St John’s Institute Of Dermatology 3rd Floor, Southwark Wing Guy’s Hospital Great Maze Pond London SE1 9RT Histopathology Department Chase Farm Hospital The Ridgeway Enfield Middlesex EN2 8JL Liver Pathology King’s College Hospital Denmark Hill London EE5 9RS Institute Of Metabolic ScienceMetabolic Research Laboratories Universtiy Of Cambridge Box 289, Level 4 Cambridge CB2 0QQ Department Of Cellular Pathology Northwick Park Hospital Watford Road Harrow Middlesex HA1 3UJ Department Of Cellular Pathology Southmead Hospital Bristol BS10 5NB Histology Department Document number: CEL EXDO 612 Author: P Williams Approved by:Dr M Perenyei WARNING: this is a controlled document Page:45 of 47 Date of Issue: May 2014 Revision: 12 Cellular Pathology Cellular Pathology Userguide 2014 Macclesfield District General Hospital Victoria Road Macclesfield Cheshire SK10 4BL The Piccolo Laboratory Gi Cancer Translational Research Level 4 Wellcome-Brenner Building St James’s University Hospital Leeds Royal National Orthopaedic Hospital Histopathology Department Institute Of Orthopaedics Brockley Hill Stanmore Middlesex HA7 4LP Cellular Pathology Royal Hampshire County Hospital Romsey Road Winchester SO22 5DG St Thomas’s Hospital Westminster Bridge Road London SE1 7ET Stoke Mandeville Hospital Mandeville Road Aylesbury Buckinghamshire HP21 8AL Department of Histopathology St George’s Hospital Blackshaw Road London SW17 0QT The Great Western Hospital Marlborough Road Swindon SN3 6BB South West Thames Regional Genetics Service Medical Genetics Unit Document number: CEL EXDO 612 Author: P Williams Approved by:Dr M Perenyei WARNING: this is a controlled document Page:46 of 47 Date of Issue: May 2014 Revision: 12 Cellular Pathology Cellular Pathology Userguide 2014 St George’s Hospital Medical School Cranrner Terrace London, SW17 0RE Department Of Histopathology St Mary’s Hospital NHS Trust Praed Street London W2 1NY Division Of Haematological Oncology St. Bartholomew’s Hospital West Smithfield London EC1A 7BE Basildon University Hospital Nethermayne Basildon Essex SS16 5NL Department Of Histopathology Leeds General Infirmary Great George Street Leeds West Yorkshire LS1 3EX Department Of Histopathology Central Sheffield University Hospital NHS Trust Royal Hallamshire Hospital Glossop S10 2JF Document number: CEL EXDO 612 Author: P Williams Approved by:Dr M Perenyei WARNING: this is a controlled document Page: 47 of 47 Date of Issue: May 2014 Revision: 12