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Published in: Trials 1/2016

Open Access 01-12-2016 | Research

The ethics of future trials: qualitative analysis of physicians’ decision making

Authors: Fiona Webster, Charles Weijer, Laura Todd, Jeremy M. Grimshaw, Andrea P. Marshall, Deborah Cook, Graeme MacLennan, Brian H. Cuthbertson, Jill J. Francis, for the SuDDICU international group

Published in: Trials | Issue 1/2016

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Abstract

Background

The decision to conduct a randomized controlled trial (RCT) in a field raises ethical as well as scientific issues. From the clinical equipoise literature, future trials are justifiable if there is ”honest, professional disagreement in the community of expert practitioners as to the preferred treatment”. Empirical data are sparse about how clinicians apply the principles of equipoise to the justification of future RCTs. For example, selective decontamination of the digestive tract (SDD) is not widely used in critical care practice despite the strength of the evidence base and therefore provides a unique opportunity to learn how clinicians think about the ethics of further RCTs in critical care.

Methods

In an international interview study of views of healthcare professionals about SDD, we undertook a secondary analysis of qualitative data collected using a Theoretical Domains Framework of clinical behaviour. We adopted a general descriptive approach to explore how physicians determined whether another RCT of SDD is ethical. Following a constant comparison approach, three investigators reviewed 54 purposively chosen transcripts from three international regions. We interpreted the data using thematic analysis.

Results

We grouped participants’ responses into four inter-related themes: 1) cultural norms about evidence and practice within healthcare; 2) personal views about what evidence is current or applicable; 3) the interpersonal and relational nature of professional decision making locally; and 4) an a priori commitment to future trials. The analysis also identified several unresolved tensions regarding when a future RCT should be pursued. These tensions focused on a clash between potential benefits to current individual patients and potential future harms to patients more broadly.

Conclusions

Our study suggests that ethical decision making about future RCTs in the field of SDD does not rely strongly on appeals to evidence, even when the quality of the evidence is reasonably high. Rather, “extra-evidential” reasons, including social, professional, and relational factors, seem to influence opinions regarding the ethics of future trials. Further work is required to see if these conclusions are applicable to other clinical topics and settings.
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Metadata
Title
The ethics of future trials: qualitative analysis of physicians’ decision making
Authors
Fiona Webster
Charles Weijer
Laura Todd
Jeremy M. Grimshaw
Andrea P. Marshall
Deborah Cook
Graeme MacLennan
Brian H. Cuthbertson
Jill J. Francis
for the SuDDICU international group
Publication date
01-12-2016
Publisher
BioMed Central
Published in
Trials / Issue 1/2016
Electronic ISSN: 1745-6215
DOI
https://doi.org/10.1186/s13063-015-1137-8

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