G-computation and machine learning for estimating the causal effects of binary exposure statuses on binary outcomes

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作者
Florent Le Borgne
Arthur Chatton
Maxime Léger
Rémi Lenain
Yohann Foucher
机构
[1] Nantes University,INSERM UMR 1246
[2] Tours University, SPHERE
[3] IDBC-A2COM,Département D’Anesthésie Réanimation
[4] Centre Hospitalier Universitaire D’Angers,undefined
[5] Lille University Hospital,undefined
[6] Nantes University Hospital,undefined
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In clinical research, there is a growing interest in the use of propensity score-based methods to estimate causal effects. G-computation is an alternative because of its high statistical power. Machine learning is also increasingly used because of its possible robustness to model misspecification. In this paper, we aimed to propose an approach that combines machine learning and G-computation when both the outcome and the exposure status are binary and is able to deal with small samples. We evaluated the performances of several methods, including penalized logistic regressions, a neural network, a support vector machine, boosted classification and regression trees, and a super learner through simulations. We proposed six different scenarios characterised by various sample sizes, numbers of covariates and relationships between covariates, exposure statuses, and outcomes. We have also illustrated the application of these methods, in which they were used to estimate the efficacy of barbiturates prescribed during the first 24 h of an episode of intracranial hypertension. In the context of GC, for estimating the individual outcome probabilities in two counterfactual worlds, we reported that the super learner tended to outperform the other approaches in terms of both bias and variance, especially for small sample sizes. The support vector machine performed well, but its mean bias was slightly higher than that of the super learner. In the investigated scenarios, G-computation associated with the super learner was a performant method for drawing causal inferences, even from small sample sizes.
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