4.6 Article

A bayesian analysis of mortality outcomes in multicentre clinical trials in critical care

Journal

BRITISH JOURNAL OF ANAESTHESIA
Volume 127, Issue 3, Pages 487-494

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.bja.2021.06.026

Keywords

Bayes theorem; critical care; healthcare; outcome assessment; randomised controlled trials; sample size; study power

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A small proportion of multicentre critical care trials report statistically significant differences in mortality outcomes, possibly due to lower-than-expected effect sizes and a low proportion of participants who could benefit from the interventions. Bayesian modelling suggests that researchers may overestimate the true population effect sizes for critical care interventions.
Background: Multicentre RCTs are widely used by critical care researchers to answer important clinical questions. However, few trials evaluating mortality outcomes report statistically significant results. We hypothesised that the low proportion of trials reporting statistically significant differences for mortality outcomes is plausibly explained by lower-than-expected effect sizes combined with a low proportion of participants who could realistically benefit from studied interventions. Methods: We reviewed multicentre trials in critical care published over a 10-yr period in the New England Journal of Medicine, the Journal of the American Medical Association, and the Lancet. To test our hypothesis, we analysed the results using a Bayesian model to investigate the relationship between the proportion of effective interventions and the proportion of statistically significant results for prior distributions of effect size and trial participant susceptibility. Results: Five of 54 trials (9.3%) reported a significant difference in mortality between the control and the intervention groups. The median expected and observed differences in absolute mortality were 8.0% and 2.0%, respectively. Our modelling shows that, across trials, a lower-than-expected effect size combined with a low proportion of potentially susceptible participants is consistent with the observed proportion of trials reporting significant differences even when most interventions are effective. Conclusions: When designing clinical trials, researchers most likely overestimate true population effect sizes for critical care interventions. Bayesian modelling demonstrates that that it is not necessarily the case that most studied interventions lack efficacy. In fact, it is plausible that many studied interventions have clinically important effects that are missed.

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