Generalized difference-in-differences
广义双重差分AI 解读 ↓
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We propose a new method for estimating causal effects in longitudinal/panel data settings that we call generalized difference-in-differences. Our approach unifies two alternative approaches in these settings: ignorability estimators (e.g., synthetic controls) and difference-in-differences (DiD) estimators. We propose a new identifying assumption -- a stable bias assumption -- which generalizes the conditional parallel trends assumption in DiD, leading to the proposed generalized DiD framework. This change gives generalized DiD estimators the flexibility of ignorability estimators while maintaining the robustness to unobserved confounding of DiD. We also show how ignorability and DiD estimators are special cases of generalized DiD. We then propose influence-function based estimators of the observed data functional, allowing the use of double/debiased machine learning for estimation. We also show how generalized DiD easily extends to include clustered treatment assignment and staggered adoption settings, and we discuss how the framework can facilitate estimation of other treatment effects beyond the average treatment effect on the treated. Finally, we provide simulations which show that generalized DiD outperforms ignorability and DiD estimators when their identifying assumptions are not met, while being competitive with these special cases when their identifying assumptions are met.
含不良控制变量的双重差分
This paper considers difference-in-differences identification strategies when the parallel trends assumption holds after conditioning on covariates that may themselves be affected by the treatment (often referred to as "bad controls"). We show that common approaches such as simply dropping bad controls are often ill-advised and develop two alternative approaches that allow bad controls to function as genuine controls despite being affected by treatment. First, we derive…
用于交错实施的固定效应因果森林及其医保扩张应用
Difference-in-differences with staggered adoption identifies group-time average treatment effects ATT(g,t) by comparing each cohort to units not yet treated, which avoids the "forbidden comparisons" that bias two-way fixed-effects estimators when effects are heterogeneous. This paper studies the covariate-conditional version of that object, tau_{g,t}(x), and estimates it with a fixed-effects causal forest. Within each (g,t) comparison block, the outcome and treatment are…
无混杂与共同趋势的联合检验
ABSTRACT We introduce an overidentification test of two alternative assumptions to identify the average treatment effect on the treated in a two‐period panel data setting: unconfoundedness and common trends. Under unconfoundedness, treatment assignment and post‐treatment outcomes are independent, conditional on control variables and pre‐treatment outcomes, which motivates including the pre‐treatment outcomes in the set of controls. Under common trends, the trend and the…
双重稳健的工具变量双重差分
We study estimation of the local average treatment effect on the treated ($LATT$) in instrumented difference-in-differences (IDiD) designs with covariates and staggered instrument exposure. We derive the efficient influence function (EIF) of the target parameter in both panel and repeated cross-sections settings, allowing for two classes of control groups: never-exposed and not-yet-exposed. Building on the EIF, we construct doubly robust estimands and corresponding…
使用双重机器学习的双重差分中介分析
We propose a difference-in-differences (DiD) framework with mediation for possibly multivalued discrete or continuous treatments and mediators, aimed at identifying the direct effect of the treatment on the outcome (net of effects operating through the mediator), the indirect effect via the mediator, and the joint effects of treatment and mediator, consistent with the framework of dynamic treatment effects. Identification relies on a conditional parallel trends assumption…
高维实验与观察性研究中的效应同质性及混杂检验
We propose a framework for testing the homogeneity of conditional average treatment effects (CATEs) across multiple experimental and observational studies. Our approach leverages multiple randomized trials to assess whether treatment effects vary with unobserved heterogeneity that differs across trials: if CATEs are homogeneous, this indicates the absence of interactions between treatment and unobservables in the mean effect. Comparing CATEs between experimental and…