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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。

引用量采用 OpenAlex 单条关联记录,不合计多个记录;关联记录可能包含正式发表版本,不等于此版本单独引用。缺失不视为零,引用指标不代表论文质量。

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分类依据与纠错

AI 根据所提供的论文材料归类:摘要目标是诊断 AUC 与缺失确诊校正,未研究因果效应,双重稳健术语本身不足以归入因果推断。

反馈分类问题

正在核对关联版本…

代码、数据与补充材料

正在核对对应版本的资源…

关注这篇论文的作者
Andrea Rotnitzky
David Faraggi

存在确诊选择偏差时 ROC 曲线下面积的双重稳健估计

研究问题
患者是否接受确诊取决于诊断结果和其他特征时,如何校正仅使用确诊患者估计诊断 AUC 所产生的偏差?
方法与思路
作者结合疾病模型与确诊选择模型,调整已测协变量和诊断结果,并对假定的残余选择关联进行敏感性分析。
材料陈述的贡献
摘要称双重稳健 AUC 估计在疾病模型或选择模型至少一个正确时具有一致性与渐近正态性,标志物可采用任意尺度。
阅读关注点
应核对残余选择偏差参数的定义、识别条件、双重稳健结论适用的敏感性设定,以及连续变量的建模要求。
阅读边界
仅据版本未注明的 OpenAlex 索引摘要;残余偏差设定与识别条件未详述,双重稳健不等于任意选择偏差均可消除。

原文摘要

The area under the receiver operating characteristic curve (AUC) is a popular summary measure of the efficacy of a medical diagnostic test to discriminate between healthy and diseased subjects. A frequently encountered problem in studies that evaluate a new diagnostic test is that not all patients undergo disease verification because the verification test is expensive, invasive, or both. Furthermore, the decision to send patients to verification often depends on the new test and on other predictors of true disease status. In such cases, usual estimators of the AUC based on verified patients only are biased. In this article we develop estimators of the AUC of markers measured on any scale that adjust for selection to verification. These estimators adjust for measured patient covariates and diagnostic test results and also for an assumed degree of residual selection bias. They can then be used in a sensitivity analysis to examine how the AUC estimates change when different plausible degrees of residual association are assumed. As with other missing-data problems, due to the curse of dimensionality, a model for disease or a model for selection is needed to obtain well-behaved estimators of the AUC when the marker and/or the measured covariates are continuous. We describe a doubly robust estimator that has the attractive feature of being consistent and asymptotically normal if either the disease or the selection model (but not necessarily both) is correct.

笔记与分组
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