跳到正文
← 返回论文列表与筛选
阅读说明

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。

本页为预印本版本;arXiv 收录、作者填写的期刊信息以及作者既有发表经历,都不单独证明本篇已接收。作者发表记录按 OpenAlex 身份与完整姓名、本站覆盖期刊 ISSN 及正式卷期核对,只展示已核实例,档案仍可能误合并。

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。

关注作者按书目中的完整姓名匹配,同名和姓名变体需人工辨别。相关论文先按共享细分方向和具体方法排列,再参考通用方法与发表日期。

分类依据与纠错

AI 根据所提供的论文材料归类:摘要明确研究时变混杂下持续干预的因果效应,并提出 g 计算估计方法。

反馈分类问题

Novel g-computation algorithms for time-varying actions with recurrent and semi-competing events

时变行动下处理复发事件与半竞争事件的新型 g 计算算法

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
Lucas M. Neuroth
Jessie K Edwards
Chantel L. Martin
Paul N Zivich

时变行动下处理复发事件与半竞争事件的新型 g 计算算法

研究问题
在长期随访中,死亡会阻止非终末事件发生,干预与混杂因素又随时间变化,如何评估持续干预的因果影响?
方法与思路
作者提出两种处理时变行动与半竞争事件的 g 计算算法,通过蒙特卡洛模拟及吸烟预防与高血压的队列应用评估表现。
材料陈述的贡献
摘要称,两种估计量在所设模拟中偏差较小、区间覆盖适当;应用估计提示持续预防吸烟可小幅降低中年高血压患病率和死亡风险。
阅读关注点
应核对两种算法的目标参数、死亡与复发事件的处理方式、时变混杂的识别要求,以及模拟比较和置信区间的构造。
阅读边界
这是 arXiv 预印本,同行评审及期刊接收未核实。摘要未说明完整识别条件、算法细节或效应数值,模拟优势不能直接推广。

原文摘要

Background: A core aspect of epidemiology is determining the impacts of potential public health interventions over time. With long follow-up periods, epidemiologists may need to consider semi-competing events, in which a terminal event, like death, precludes a non-terminal event, like hypertension. Time-varying confounding poses an additional challenge when studying time-varying interventions or actions. Existing methods do not simultaneously address semi- competing events and time-varying confounding. Methods: We propose two novel g-computation algorithms for causal effects with semi- competing events and time-varying actions. To explore performance of our novel g-computation estimators, we conducted a Monte Carlo simulation study. We then applied our estimator to investigate how cigarette smoking prevention throughout young and middle adulthood might impact prevalent hypertension using data from Waves III (aged 18-26 years) - VI (aged 39-51 years) of the National Longitudinal Study of Adolescent to Adult Health. Results: Our simulations show that the novel g-computation estimators had little bias and appropriate confidence interval coverage. They outperformed existing alternative estimators across sample sizes. In the illustrative application, the novel estimator identified a small reduction in prevalence of hypertension and risk of death in midlife had all cigarette smoking been prevented across follow-up compared to the observed smoking patterns. Conclusion: As long-running cohorts progress in age, death within the study sample will become an increasing concern for studies of aging-related outcomes, life course analyses, and investigations into chronic disease development. Our novel g-computation estimators provide a simultaneous solution.

笔记与分组