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本页整理公开书目信息,不生成学术质量评分。AI 解读根据题名及所注明的摘要或原文片段生成,未完成全文核验,可能有误;具体假设、证明与结论请核对原文。摘要保留来源文本,未经模型改写。

DOI 首次登记不等于接收或发表日期。部分更正、评论等条目没有独立摘要;缺少可靠材料时保留待补状态。

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分类依据与纠错

AI 根据所提供的论文材料归类:摘要明确研究观察研究及不依从随机试验中的暴露因果效应。

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代码、数据与补充材料

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关注这篇论文的作者
S. Vansteelandt
E. Goetghebeur

使用广义结构均值模型进行因果推断

研究问题
研究暴露未完全受控、试验存在不依从或自选治疗转换时,如何估计非线性平均暴露效应,尤其处理二元结局带来的模型限制。
方法与思路
作者提出半参数两阶段模型,以结构模型对比实际结局和潜在无暴露结局的均值,再引入关联型干扰模型识别参数并构造估计方程。
材料陈述的贡献
摘要称,模型下可获得一致、渐近正态且有效的估计,并讨论误设稳健性;进一步发展双逻辑结构均值模型用于不依从试验。
阅读关注点
应核对因果参数的目标人群、识别所需条件和两阶段模型的作用,特别区分一般误设分析与仅在无暴露效应时构造的稳健估计。
阅读边界
仅据所给 Crossref 摘要,不推断其他版本变化。摘要未列出完整识别条件;无暴露效应下的稳健性不能推广为普遍双重稳健。

原文摘要

Summary We estimate cause–effect relationships in empirical research where exposures are not completely controlled, as in observational studies or with patient non-compliance and self-selected treatment switches in randomized clinical trials. Additive and multiplicative structural mean models have proved useful for this but suffer from the classical limitations of linear and log-linear models when accommodating binary data. We propose the generalized structural mean model to overcome these limitations. This is a semiparametric two-stage model which extends the structural mean model to handle non-linear average exposure effects. The first-stage structural model describes the causal effect of received exposure by contrasting the means of observed and potential exposure-free outcomes in exposed subsets of the population. For identification of the structural parameters, a second stage ‘nuisance’ model is introduced. This takes the form of a classical association model for expected outcomes given observed exposure. Under the model, we derive estimating equations which yield consistent, asymptotically normal and efficient estimators of the structural effects. We examine their robustness to model misspecification and construct robust estimators in the absence of any exposure effect. The double-logistic structural mean model is developed in more detail to estimate the effect of observed exposure on the success of treatment in a randomized controlled blood pressure reduction trial with self-selected non-compliance.

笔记与分组