Recoverability and estimation of causal effects under typical multivariable missingness mechanisms

Author:

Zhang Jiaxin12ORCID,Dashti S. Ghazaleh12,Carlin John B.12ORCID,Lee Katherine J.12,Moreno‐Betancur Margarita12

Affiliation:

1. Clinical Epidemiology and Biostatistics Unit Department of Paediatrics University of Melbourne Parkville Australia

2. Clinical Epidemiology and Biostatistics Unit Murdoch Children's Research Institute Parkville Australia

Abstract

AbstractIn the context of missing data, the identifiability or “recoverability” of the average causal effect (ACE) depends not only on the usual causal assumptions but also on missingness assumptions that can be depicted by adding variable‐specific missingness indicators to causal diagrams, creating missingness directed acyclic graphs (m‐DAGs). Previous research described canonical m‐DAGs, representing typical multivariable missingness mechanisms in epidemiological studies, and examined mathematically the recoverability of the ACE in each case. However, this work assumed no effect modification and did not investigate methods for estimation across such scenarios. Here, we extend this research by determining the recoverability of the ACE in settings with effect modification and conducting a simulation study to evaluate the performance of widely used missing data methods when estimating the ACE using correctly specified g‐computation. Methods assessed were complete case analysis (CCA) and various implementations of multiple imputation (MI) with varying degrees of compatibility with the outcome model used in g‐computation. Simulations were based on an example from the Victorian Adolescent Health Cohort Study (VAHCS), where interest was in estimating the ACE of adolescent cannabis use on mental health in young adulthood. We found that the ACE is recoverable when no incomplete variable (exposure, outcome, or confounder) causes its own missingness, and nonrecoverable otherwise, in simplified versions of 10 canonical m‐DAGs that excluded unmeasured common causes of missingness indicators. Despite this nonrecoverability, simulations showed that MI approaches that are compatible with the outcome model in g‐computation may enable approximately unbiased estimation across all canonical m‐DAGs considered, except when the outcome causes its own missingness or causes the missingness of a variable that causes its own missingness. In the latter settings, researchers may need to consider sensitivity analysis methods incorporating external information (e.g., delta‐adjustment methods). The VAHCS case study illustrates the practical implications of these findings.

Funder

National Health and Medical Research Council

Statistical Society of Australia

Publisher

Wiley

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