Sharp Bounds for Treatment Effect Generalization under Outcome Distribution Shift

Fuente: arXiv
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Hauptverfasser: Asiaee, Amir, Pal, Samhita, Beck, Cole, Huling, Jared D.
Format: Preprint
Veröffentlicht: 2026
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author Asiaee, Amir
Pal, Samhita
Beck, Cole
Huling, Jared D.
author_facet Asiaee, Amir
Pal, Samhita
Beck, Cole
Huling, Jared D.
contents Generalizing treatment effects from a randomized trial to a target population requires the assumption that potential outcome distributions are invariant across populations after conditioning on observed covariates. This assumption fails when unmeasured effect modifiers are distributed differently between trial participants and the target population. We develop a sensitivity analysis framework that bounds how much conclusions can change when this transportability assumption is violated. Our approach constrains the likelihood ratio between target and trial outcome densities by a scalar parameter $Λ\geq 1$, with $Λ= 1$ recovering standard transportability. For each $Λ$, we derive sharp bounds on the target average treatment effect -- the tightest interval guaranteed to contain the true effect under all data-generating processes compatible with the observed data and the sensitivity model. We show that the optimal likelihood ratios have a simple threshold structure, leading to a closed-form greedy algorithm that requires only sorting trial outcomes and redistributing probability mass. The resulting estimator runs in $O(n \log n)$ time and is consistent under standard regularity conditions. Simulations demonstrate that our bounds achieve nominal coverage when the true outcome shift falls within the specified $Λ$, provide substantially tighter intervals than worst-case bounds, and remain informative across a range of realistic violations of transportability.
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spellingShingle Sharp Bounds for Treatment Effect Generalization under Outcome Distribution Shift
Asiaee, Amir
Pal, Samhita
Beck, Cole
Huling, Jared D.
Methodology
Generalizing treatment effects from a randomized trial to a target population requires the assumption that potential outcome distributions are invariant across populations after conditioning on observed covariates. This assumption fails when unmeasured effect modifiers are distributed differently between trial participants and the target population. We develop a sensitivity analysis framework that bounds how much conclusions can change when this transportability assumption is violated. Our approach constrains the likelihood ratio between target and trial outcome densities by a scalar parameter $Λ\geq 1$, with $Λ= 1$ recovering standard transportability. For each $Λ$, we derive sharp bounds on the target average treatment effect -- the tightest interval guaranteed to contain the true effect under all data-generating processes compatible with the observed data and the sensitivity model. We show that the optimal likelihood ratios have a simple threshold structure, leading to a closed-form greedy algorithm that requires only sorting trial outcomes and redistributing probability mass. The resulting estimator runs in $O(n \log n)$ time and is consistent under standard regularity conditions. Simulations demonstrate that our bounds achieve nominal coverage when the true outcome shift falls within the specified $Λ$, provide substantially tighter intervals than worst-case bounds, and remain informative across a range of realistic violations of transportability.
title Sharp Bounds for Treatment Effect Generalization under Outcome Distribution Shift
topic Methodology
url https://arxiv.org/abs/2602.09595