Conditional Permutation Tests and the Propensity Score in Observational Studies
观察性研究中的条件置换检验与倾向得分AI 解读 ↓
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In observational studies, the distribution of treatment assignments is unknown, and therefore randomization tests are not generally applicable. However, permutation tests that condition on sample information about the treatment assignment mechanism can be applicable in observational studies, provided treatment assignment is strongly ignorable. These tests use the conditional distribution of the treatment assignments given a sufficient statistic for the unknown parameter of the propensity score. Several tests that are commonly used in observational studies are particular instances of this general procedure. Moreover, conditional permutation tests and covariance adjustment are closely related, in the sense that the conditional permutation distribution of the covariance adjusted difference leads to the same inferences as the conditional permutation distribution of the unadjusted difference of sample means. A backtrack algorithm is developed to permit efficient calculation of the exact conditional significance level, and two approximations are discussed. A clinical study of treatments for lung cancer is used to illustrate the technique. Conditional permutation tests extend previous large sample results on the propensity score by providing a basis for exact tests and confidence intervals in small observational studies when treatment assignment is strongly ignorable.
Two frequent approaches for identifying structural VARs are external instruments, which carry economic content but are often weak, and non-Gaussianity of the shocks, which provides statistical identification but carries no economic meaning. We combine the two strategies in a single generalized method of moments framework. This hybrid approach point-identifies the target shocks while also identifying the non-target shocks up to sign and ordering. Under suitable rank…
克隆—删失—加权方法的形式化与一致性
Target trial emulation has become a standard framework for causal inference from observational data. Within this paradigm, the clone-censor-weight (CCW) methodology provides a practical way to deal with complex treatment and adherence definitions when treatment regimes are not distinguishable at baseline. Despite its increasing use, the statistical interpretation of CCW remains limited. In this work, we formalize the CCW methodology from a statistical viewpoint based on…
用匹配自适应随机化推断重新评估激素替代疗法对心脏病的影响
Matching is an appealing way to design observational studies because it mimics the data structure produced by stratified randomized trials, pairing treated individuals with similar controls. After matching, inference is often conducted using methods tailored for stratified randomized trials in which treatments are permuted within matched pairs. However, in observational studies, matched pairs are not predetermined before treatment; instead, they are constructed based on…
非精确匹配何时能在无需调整的情况下保证平衡与有效推断?
One-to-one matching without replacement is a classical approach to constructing comparable treated and control samples in the design of observational studies. It pairs each treated unit with a distinct control while minimizing a covariate distance objective. With continuous covariates, the matched pairs generally remain inexact, which contributes to bias in downstream analysis. Its key theoretical properties, such as the resulting imbalance between matched pairs and when it…
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…
以模型平均替代处理前趋势检验
We study difference-in-differences (DID) estimation of average treatment effects on the treated when the researcher is uncertain about which pre-treatment periods satisfy the parallel trends assumption. Roth (2022) shows that pre-trend testing can induce bias, complementing the statistical literature on post-selection inference. We propose the model averaged difference-in-differences (MADID) estimator, a weighted average of the candidate $2\times2$ DID estimators. The…