Toward Precision in Critical Care Research: Methods for Observational and Interventional Studies

Author:

Graham Linck Emma J.1ORCID,Goligher Ewan C.234,Semler Matthew W.56,Churpek Matthew M.17

Affiliation:

1. Department of Biostatistics and Medical Informatics, UW-Madison, Madison, WI.

2. Interdepartmental Division of Critical Care Medicine, Temerty Faculty of Medicine, University of Toronto, Toronto, ON, Canada.

3. Department of Physiology, University of Toronto, Toronto, ON, Canada.

4. Toronto General Hospital Research Institute, University Health Network, Toronto, ON, Canada.

5. Division of Allergy, Pulmonary, and Critical Care Medicine, Vanderbilt University Medical Center, Nashville, TN.

6. Vanderbilt Institute for Clinical and Translational Research, Vanderbilt University Medical Center, Nashville, TN.

7. Division of Pulmonary and Critical Care, Department of Medicine, University of Wisconsin-Madison, Madison, WI.

Abstract

Critical care trials evaluate the effect of interventions in patients with diverse personal histories and causes of illness, often under the umbrella of heterogeneous clinical syndromes, such as sepsis or acute respiratory distress syndrome. Given this variation, it is reasonable to expect that the effect of treatment on outcomes may differ for individuals with variable characteristics. However, in randomized controlled trials, efficacy is typically assessed by the average treatment effect (ATE), which quantifies the average effect of the intervention on the outcome in the study population. Importantly, the ATE may hide variations of the treatment’s effect on a clinical outcome across levels of patient characteristics, which may erroneously lead to the conclusion that an intervention does not work overall when it may in fact benefit certain patients. In this review, we describe methodological approaches for assessing heterogeneity of treatment effect (HTE), including expert-derived subgrouping, data-driven subgrouping, baseline risk modeling, treatment effect modeling, and individual treatment rule estimation. Next, we outline how insights from HTE analyses can be incorporated into the design of clinical trials. Finally, we propose a research agenda for advancing the field and bringing HTE approaches to the bedside.

Publisher

Ovid Technologies (Wolters Kluwer Health)

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