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Center-specific causal inference with multicenter trials: reinterpreting trial evidence in the context of each participating center

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arxiv 2104.05905 v2 pith:WOQE6TS5 submitted 2021-04-13 stat.ME

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keywords treatmentcenter-specificwhenassociationscenterseffectstrialcenter
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In multicenter randomized trials, when effect modifiers have a different distribution across centers, comparisons between treatment groups that average over centers may not apply to any of the populations underlying the individual centers. Here, we describe methods for reinterpreting the evidence produced by a multicenter trial in the context of the population underlying each center. We describe how to identify center-specific effects under identifiability conditions that are largely supported by the study design and when associations between center membership and the outcome may be present, given baseline covariates and treatment ("center-outcome associations"). We then consider an additional condition of no center-outcome associations given baseline covariates and treatment. We show that this condition can be assessed using the trial data; when it holds, center-specific treatment effects can be estimated using analyses that completely pool information across centers. We propose methods for estimating center-specific average treatment effects, when center-outcome associations may be present and when they are absent, and describe approaches for assessing whether center-specific treatment effects are homogeneous. We evaluate the performance of the methods in a simulation study and illustrate their implementation using data from the Hepatitis C Antiviral Long-Term Treatment Against Cirrhosis trial.

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Cited by 1 Pith paper

Reviewed papers in the Pith corpus that reference this work. Sorted by Pith novelty score. Full citation record

  1. Causal Perspectives on Network Meta-Analysis

    stat.ME 2026-07 conditional novelty 6.0 of 10

    Causal identification for aggregate-data pairwise and network meta-analysis yields arm-level estimators that target explicit populations without needing the treatment network or transitivity.

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