Estimating Longitudinal Causal Effects with Unobserved Noncompliance Using a Semi-Parametric G-computation Algorithm
Ross L Peterson, David M Vock, Joseph S Koopmeiners

TL;DR
This paper introduces a semi-parametric G-computation algorithm to estimate longitudinal causal effects in randomized trials with unobserved noncompliance and confounders, improving causal inference accuracy.
Contribution
It develops a novel G-computation estimator that handles unobserved compliance and confounder density misspecification using biomarker-based weights and predictive mean matching.
Findings
The proposed method performs well in simulations across various sample sizes.
It provides more accurate causal estimates in the nicotine trial.
Compared to existing estimators, it reduces bias caused by unobserved noncompliance.
Abstract
Participant noncompliance, in which participants do not follow their assigned treatment protocol, often obscures the causal relationship between treatment and treatment effect in randomized trials. In the longitudinal setting, the G-computation algorithm can adjust for confounding to estimate causal effects. Typically, G-computation assumes that both 1) compliance is observed; and 2) the densities of the confounders can be correctly specified. We aim to develop a G-computation estimator in the setting where both assumptions are violated. For 1), in place of unobserved compliance, we substitute in probability weights derived from modeling a biomarker associated with compliance. For 2), we fit semiparametric models using predictive mean matching. Specifically, we parametrically specify only the conditional mean of the confounders, and then use predictive mean matching to randomly generate…
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Taxonomy
TopicsAdvanced Causal Inference Techniques · Statistical Methods in Clinical Trials · Statistical Methods and Inference
