Statistical Inference with Data-Dependent Treatment Allocation Rules
数据依赖型治疗分配规则下的统计推断AI 解读 ↓
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数据依赖型治疗分配规则下的统计推断AI 解读 ↓
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In comparing two treatments with dichotomous responses, the randomized play-the-winner rule (Wei and Durham 1978) tends to assign more study subjects to the better treatment. For ethical reasons, this property is desirable for studies on human subjects. The randomized play-the-winner rule, which is a modification of Zelen's play-the-winner rule (Zelen 1969), is not deterministic and is less vulnerable to experimental bias than other adaptive designs. Recently, this design has been used in a trial to evaluate extracorporeal membrane oxygenation (ECMO) for treating newborns with respiratory failures at the University of Michigan. In this article, exact conditional, exact unconditional, and approximate confidence intervals for the treatment difference are studied from a frequentist point of view with the randomized play-the-winner rule. For small and moderate-sized trials, the exact unconditional procedures perform much better than the conditional ones because of the adaptive nature of the designs. Furthermore, we find that the design used for the trial should not be ignored in the analysis. The large-sample unconditional confidence intervals based on likelihood ratio statistics are not very sensitive to the design and perform well for moderate-sized trials. On the other hand, the intervals derived from the maximum likelihood estimates behave poorly under the adaptive design. All of the procedures are illustrated with the Michigan ECMO data.
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Online multifactorial experiments requires early stopping for practically negligible effects while controlling false stopping under continuous monitoring and retaining precise treatment-effect estimation. We develop a design-driven framework that chooses allocation and the evidence rule jointly, treating allocation as evidence collection and testing and estimation as complementary uses of the same evidence. For multifactor experiments with nuisance block effects and…
小样本多协变量随机对照试验中的G计算
In contemporary randomized controlled trials (RCTs), the number of patients is often small relative to the number of baseline covariates collected. In such settings, maximum likelihood estimators of conditional treatment effects in generalized linear models, along with their standard errors, may exhibit substantial bias. This study examines whether similar bias arises in G-computation estimators of marginal treatment effects, which are known for their robustness to model…
广义线性模型中多层模型与固定效应方法的比较
We extend prior work comparing linear multilevel models (MLM) and fixed effect (FE) models to the generalized linear model (GLM) setting, where the coefficient on a treatment variable is of primary interest. This leads to three insights. (i) First, as in the linear setting, MLM can be thought of as a regularized form of FE (RegFE). This explains why group-level confounding can greatly bias MLM's treatment coefficient estimates. However, unlike the linear setting, there is…
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Exploiting the equality restrictions that nested Markov models encode requires their tangent-space geometry. For strictly positive finite-state models on arbitrary acyclic directed mixed graphs (ADMGs), we differentiate the recursive-head chart and prove that the range of its score map is the full tangent space. Intrinsic-set coordinate blocks form an algebraic direct sum, blocks of distinct districts are orthogonal, and the resulting Gram projection needs neither…
靶向深度生存对比:神经网络下处理特定生存收益的有效推断
Neural survival models are increasingly asked to support counterfactual claims---how much a treatment would change survival in a population---rather than only prognostic risk scores. Answering such questions from observational data requires valid inference for treatment-specific survival contrasts under confounding and covariate-dependent censoring, targets for which standard deep survival estimators are biased and provide no honest uncertainty. We propose Targeted Deep…
诊断测试与人工智能医疗器械的因果评估:效应修饰与信息增强决策
Diagnostic medical tests and devices provide useful information for evaluating the potential benefits and risks of therapeutic treatments. However, unlike treatments, their impact on health outcomes is generally indirect because measuring diagnostic information typically does not itself affect patient outcomes, which complicates evaluation of their effectiveness. In this work, we develop a causal inference approach for evaluating diagnostic tests by distinguishing…