Treatment Effect Risk: Bounds and Inference
Nathan Kallus

TL;DR
This paper develops methods to bound and infer the risk of negative treatment effects on subpopulations using covariates, addressing challenges in estimating individual treatment effect distributional risks.
Contribution
It introduces tight bounds on ITE-CVaR using covariate-conditional effects and proposes a debiasing estimation method that works with complex machine learning models.
Findings
Bounds reveal potential negative impacts on subpopulations.
Debiasing method provides reliable inference with complex models.
Application shows small benefits may entail significant risks.
Abstract
Since the average treatment effect (ATE) measures the change in social welfare, even if positive, there is a risk of negative effect on, say, some 10% of the population. Assessing such risk is difficult, however, because any one individual treatment effect (ITE) is never observed, so the 10% worst-affected cannot be identified, while distributional treatment effects only compare the first deciles within each treatment group, which does not correspond to any 10%-subpopulation. In this paper we consider how to nonetheless assess this important risk measure, formalized as the conditional value at risk (CVaR) of the ITE-distribution. We leverage the availability of pre-treatment covariates and characterize the tightest-possible upper and lower bounds on ITE-CVaR given by the covariate-conditional average treatment effect (CATE) function. We then proceed to study how to estimate these bounds…
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Taxonomy
TopicsAdvanced Causal Inference Techniques · Statistical Methods and Inference
