Doubly Robust Pointwise Confidence Intervals for a Monotonic Continuous Treatment Effect Curve
单调连续处理效应曲线的双重稳健逐点置信区间AI 解读 ↓
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单调连续处理效应曲线的双重稳健逐点置信区间AI 解读 ↓
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We study nonparametric inference for the causal dose–response curve when the treatment variable is continuous rather than discrete. We develop doubly robust confidence intervals for the continuous treatment effect curve (at a fixed point) under the assumption that it is monotonic, based on inverting a likelihood ratio-type test. Monotonicity of the treatment effect curve is often a very natural assumption, and this assumption removes the need to choose a smoothing or tuning parameter for the nonparametrically estimated curve. The likelihood ratio procedure is effective because it allows us to avoid estimating the curve’s unknown bias, which is challenging to do. Furthermore, we propose a version of our test or confidence interval that is adaptive to a range of the unknown curve’s flatness level. The test statistic is “doubly robust” in that a remainder term is the product of errors for the two so-called nuisance functions that naturally arise (outcome regression and generalized propensity score), which allows one nuisance to be estimated poorly if the other is estimated well. We present versions with and without cross fitting. We illustrate the new methods via simulations and a study of a dataset relating the effect of nurse staffing hours to hospital performance. Supplementary materials for this article are available online, including a standardized description of the materials available for reproducing the work.
We study difference-in-differences designs in which all units are initially untreated and later receive heterogeneous, strictly positive treatment doses. When quasi-untreated units receive doses close to zero, a difference-in-difference estimand using those units as the control group identifies a weighted average treatment effect per unit of treatment, under a parallel-trends assumption. We develop a nonparametric estimator and bias-corrected confidence intervals for this…
伪面板事件研究:可信应用的计量经济学基础
Event studies with panel data are widely used to estimate treatment effects. With repeated cross-sections, future treatment dates are unobserved for untreated individuals. Pseudo-panel event studies impute pre-treatment outcomes of the treated using matched untreated individuals. This paper establishes identification in such designs and characterizes bias when identification conditions fail. I show that the pseudo-panel regression is equivalent to weighted least squares with…
嵌套工具变量分析:转换者平均处理效应及可推广性
Instrumental variables (IVs) are widely used to estimate causal effects from non-randomized data. A canonical example is a randomized trial with noncompliance, in which the randomized treatment assignment serves as an IV for the non-ignorable treatment received. Under a monotonicity assumption, a valid IV nonparametrically identifies the average treatment effect among a latent complier subgroup, whose generalizability is often under debate. In many studies, there exist…
We study nonparametric inference for a continuous-treatment causal dose-response curve and its first derivative under unmeasured confounding, using treatment- and outcome-inducing proxies. We establish a proximal doubly robust pseudo-outcome whose conditional mean given treatment equals the dose-response curve whenever either bridge function is correctly specified. Their (smoothed) efficient influence function representations lead to cross-fitted local-polynomial estimators…
平均处理效应局部化:合成控制中的投影方法
Many real-world policies and business interventions require assessing short-term effects to inform timely decisions, even though most causal inference methods focus on long-term average treatment effects. In this article, we introduce average treatment effect localization (ATEL), which captures localized, short-term policy impacts in panel data settings with a single treated unit and provides early indicators of policy impact. To accommodate both time-varying and nonlinear…
利用辅助事件信息进行删失结局的因果推断
Clinical trials with survival endpoints lose information when participants are censored before death is observed. We develop target-preserving estimators that use posttreatment disease history, such as recurrence or progression, to recover information lost to censoring for marginal survival and restricted mean survival effects. The difficulty is that the intermediate event is downstream of treatment: naive adjustment can change the causal estimand, and the useful information…