Causal Inference from Observational Studies with Clustered Interference

TL;DR

This paper develops new causal inference methods for observational studies with clustered interference, accounting for within-cluster treatment dependence, and demonstrates their application to cholera vaccination data.

Contribution

It introduces novel causal estimands that incorporate within-cluster treatment dependence and proposes inverse probability-weighted estimators for observational clustered interference studies.

Findings

Estimators have desirable large-sample properties.

Simulation shows good finite-sample performance.

Application to cholera data illustrates practical utility.

Abstract

Inferring causal effects from an observational study is challenging because participants are not randomized to treatment. Observational studies in infectious disease research present the additional challenge that one participant's treatment may affect another participant's outcome, i.e., there may be interference. In this paper recent approaches to defining causal effects in the presence of interference are considered, and new causal estimands designed specifically for use with observational studies are proposed. Previously defined estimands target counterfactual scenarios in which individuals independently select treatment with equal probability. However, in settings where there is interference between individuals within clusters, it may be unlikely that treatment selection is independent between individuals in the same cluster. The proposed causal estimands instead describe counterfactual scenarios in which the treatment selection correlation structure is the same as in the observed data distribution, allowing for within-cluster dependence in the individual treatment selections. These estimands may be more relevant for policy-makers or public health officials who desire to quantify the effect of increasing the proportion of treated individuals in a population. Inverse probability-weighted estimators for these estimands are proposed. The large-sample properties of the estimators are derived, and a simulation study demonstrating the finite-sample performance of the estimators is presented. The proposed methods are illustrated by analyzing data from a study of cholera vaccination in over 100,000 individuals in Bangladesh.