Essential Concepts in Clinical Research

2. Auflage 2018
ISBN: 978-0-7020-7394-6
Verlag: Elsevier Health Sciences

Buch, Englisch, 272 Seiten, Format (B × H): 177 mm x 225 mm, Gewicht: 404 g

This practical guide speaks to two audiences: those who read and those who conduct research. Clinicians are medical detectives by training. For each patient, they assemble clinical clues to establish causes of signs and symptoms. The task involves both clinical acumen and knowledge of medical research. This book helps guide clinicians through this detective work, by enabling them to make sense of research and to review medical literature critically. It will also be invaluable to researchers who conduct clinical research, particularly randomized controlled trials.

Building on previously published, peer-reviewed articles from The Lancet, this handbook is essential for busy clinicians and active researchers interested in research methods.
- Written by leaders in the field of clinical research who have published extensively with authorship of hundreds of articles in medical journals.

- The authorship includes one of the three authors of the CONSORT guidelines for the reporting of randomized controlled trials.

- The book presents the essential concepts to a wide array of topics including randomized control trials, descriptive studies, cohort studies, case-control studies, bias, and screening tests.

- The book utilises a readable and humorous prose style, lightening what can be a difficult area for clinical readers.

- Derived from decades of teaching clinical research in seminar settings the book will empower clinicians to make sense of, and critically appraise, current medical research and will enable researchers to enrich the quality of their work.

For this Second Edition, the authors have revised and updated the original 16 chapters and added six new chapters. For busy clinicians and active researchers interested in research methods, this book provides helpful tools to derive satisfaction - indeed, fun - from clinical science.

Autoren/Hrsg.

Schulz, Kenneth

Grimes, David A.

Fachgebiete

• Medizin | Veterinärmedizin Medizin | Public Health | Pharmazie | Zahnmedizin Medizin, Gesundheitswesen Medizinische Mathematik & Informatik
• Medizin | Veterinärmedizin Medizin | Public Health | Pharmazie | Zahnmedizin Medizin, Gesundheitswesen Epidemiologie, Medizinische Statistik
• Medizin | Veterinärmedizin Medizin | Public Health | Pharmazie | Zahnmedizin Medizin, Gesundheitswesen Biomedizin, Medizinische Forschung, Klinische Studien

Inhaltsverzeichnis

Introduction

1. An overview of clinical research: the lay of the land

Observational studies

2. Descriptive studies: what they can and cannot do

3. Bias and causal associations in observational research

4. Cohort studies: marching towards outcomes

5. Case-control studies: research in reverse

6. Finding controls for case-control studies: compared to what?

7. Limitations of observational epidemiology

Screening tests
8. Uses and abuses of screening tests

9. Refining clinical diagnosis with likelihood ratios

Randomized controlled trials
10. Boosting participant recruitment in trials

11. Sample size calculations in randomized trials: mandatory and mystical

12. Generation of allocation sequences in randomized trials: chance not choice

13. Generation of allocation sequences in non-double-blinded randomized trials: guarding against guessing

14. Allocation concealment in randomized trials: defending against deciphering

15. Exclusions and losses in randomized trials: sample size slippages

16. Blinding in randomized trials: hiding who got what

17. Implementing treatment blinding in randomized trials

18. Surrogate endpoints and composite outcomes: shortcuts to unknown destinations

19. Multiplicity in randomized trials I: endpoints and treatments

20. Multiplicity in randomized trials II: subgroup and interim analyses

21. Conducting randomized trials as part of a prospective meta-analysis

Publishing

22. Reporting studies in medical journals: CONSORT and other guidelines