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How to request a test: A clinician's guide to the interpretation and evaluation of medical tests PDF

129 Pages·2023·8.866 MB·English
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How to Request a Test How to Request a Test A Clinician’s Guide to the Interpretation and Evaluation of Medical Tests Tom Boyles Honorary Associate Professor, London School of Hygiene and Tropical Medicine, London, United Kingdom Researcher, Clinical HIV Research Unit, University of the Witwatersrand, Johannesburg, South Africa Great Clarendon Street, Oxford, OX2 6DP, United Kingdom Oxford University Press is a department of the University of Oxford. It furthers the University’s objective of excellence in research, scholarship, and education by publishing worldwide. Oxford is a registered trade mark of Oxford University Press in the UK and in certain other countries © Oxford University Press 2023 The moral rights of the author have been asserted First Edition published in 2023 Impression: 1 All rights reserved. No part of this publication may be reproduced, stored in a retrieval system, or transmitted, in any form or by any means, without the prior permission in writing of Oxford University Press, or as expressly permitted by law, by licence or under terms agreed with the appropriate reprographics rights organization. Enquiries concerning reproduction outside the scope of the above should be sent to the Rights Department, Oxford University Press, at the address above You must not circulate this work in any other form and you must impose this same condition on any acquirer Published in the United States of America by Oxford University Press 198 Madison Avenue, New York, NY 10016, United States of America British Library Cataloguing in Publication Data Data available Library of Congress Control Number: 2022943242 ISBN 978– 0– 19– 286661– 5 DOI: 10.1093/ med/ 9780192866615.001.0001 Printed and bound by CPI Group (UK) Ltd, Croydon, CR0 4YY Oxford University Press makes no representation, express or implied, that the drug dosages in this book are correct. Readers must therefore always check the product information and clinical procedures with the most up-t o- date published product information and data sheets provided by the manufacturers and the most recent codes of conduct and safety regulations. The authors and the publishers do not accept responsibility or legal liability for any errors in the text or for the misuse or misapplication of material in this work. Except where otherwise stated, drug dosages and recommendations are for the non-p regnant adult who is not breast-f eeding Links to third party websites are provided by Oxford in good faith and for information only. Oxford disclaims any responsibility for the materials contained in any third party website referenced in this work. For Robert Graham Boyles, 1935–2022. Preface I didn’t write this book because I am an expert on the topic, I wrote it because after more than two decades of thinking and reading about the subject, I finally feel that I can convey my knowledge in the way I would like to have learned it from the begin- ning. In short, it is a book I wish was in my coat pocket as a medical student and junior doctor. Testing is ubiquitous in medicine and the task of requesting tests often falls to the most junior members of the team, despite being vitally important and extremely costly. In many settings, requesting tests is a simple matter of filling out a form, ticking any number of boxes, and leaving the rest to phlebotomists, radiographers, and la- boratory staff. While this has freed up junior doctors’ time, it can lead to a laissez- faire attitude to testing. As an intern, it was important to have a range of test results written in the notes as a post- intake ward round approached. Woe betide anyone who did not have a troponin result for a patient with chest pain or an amylase for a patient with abdominal pain. However, I quickly realized that experienced clinicians barely looked at some of my tests, particularly on follow- up rounds when I thought a new and pristine set of re- sults was a core part of my job. They saw no value in my multiple C- reactive protein tests to check that a patient was recovering from pneumonia, for example, instead being happy with a brief history, examination, and inspection of the vitals chart. At the time this puzzled me and I began reading about the application of medical tests and particularly Bayes’ theorem. Gradually I built up an understanding of why and when we do tests and, importantly, when not to do them. Now I have gained a degree of experience, particularly within my specialty of infec- tious diseases, I see the errors I made being repeated. Typically, it is an over- reliance on tests or an overestimation of their value. Often, when doctors are unsure of the diagnosis, they request a broad range of tests in the hope that some abnormal result will lead them in the right direction. While there are some tests that are indicated for almost all patients, such as a full blood count for a patient admitted under medi- cine or surgery, there should be no such thing as ‘routine bloods’. As a consultant, I am frequently presented with pages of blood test results that I have very little if any interest in reading. To make matters worse, sometimes the single key test I really want is not there. Sometimes I am asked to review a patient simply because a test result is ‘abnormal’ rather than because there is a specified clinical problem: ‘We measured the beta- D- glucan [a component of the cell wall of some fungi] and it’s high, please tell us which fungus the patient has’ is a typical question to infectious diseases. The oncologist might similarly be faced with ‘We requested a panel of tumour markers and one is elevated, come and treat this patient’s cancer’. These are typical examples viii of performing tests without thinking through the problem in advance, and without having a full understanding of the strengths and weaknesses of the tests at hand. The appropriate steps in evaluating and applying a new medicine is usually taught well in medical schools and most medical students and junior doctors could tell you about the four phases of clinical trials and that regulatory approval typically occurs after phase III trials confirm efficacy and safety. The same cannot be said for the evalu- ation of tests; this is partly because even experts disagree on the framework for test evaluation, but also because it is perceived as having less value. After reading this book, my hope is that medical students and junior doctors will have a greater appre- ciation of how to use tests efficiently and effectively. The quantity of tests they request is likely to decrease, which will save time and money, while the quality will increase, improving patient care. Acknowledgements This book would not have been possible without the love and support of my family. I would like to thank my partner, Lynne, and our two wonderful children, Maya and Kai, for putting up with me while I wrote it. The staff at Oxford University Press have been helpful and supportive throughout, particular thanks go to Nicola Wilson for all the effort she has put in. A number of people kindly reviewed earlier drafts and gave constructive feedback, I’d like to thank Druin Burch, Joe Wilson, Evie Rothwell, and Hywel Jones. The latter introduced me to Bayes’ theorem on a ward round circa 1998, when I was a medical student— thank you for setting me on this path.

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