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Using Marginal Structural Measurement-Error Models to Estimate the Long-term Effect of Antiretroviral Therapy on Incident AIDS or Death

机译:使用边缘结构测量误差模型估计抗逆转录病毒疗法对艾滋病或死亡的长期影响

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摘要

To estimate the net effect of imperfectly measured highly active antiretroviral therapy on incident acquired immunodeficiency syndrome or death, the authors combined inverse probability-of-treatment-and-censoring weighted estimation of a marginal structural Cox model with regression-calibration methods. Between 1995 and 2007, 950 human immunodeficiency virus–positive men and women were followed in 2 US cohort studies. During 4,054 person-years, 374 initiated highly active antiretroviral therapy, 211 developed acquired immunodeficiency syndrome or died, and 173 dropped out. Accounting for measured confounders and determinants of dropout, the weighted hazard ratio for acquired immunodeficiency syndrome or death comparing use of highly active antiretroviral therapy in the prior 2 years with no therapy was 0.36 (95% confidence limits: 0.21, 0.61). This association was relatively constant over follow-up (P = 0.19) and stronger than crude or adjusted hazard ratios of 0.75 and 0.95, respectively. Accounting for measurement error in reported exposure using external validation data on 331 men and women provided a hazard ratio of 0.17, with bias shifted from the hazard ratio to the estimate of precision as seen by the 2.5-fold wider confidence limits (95% confidence limits: 0.06, 0.43). Marginal structural measurement-error models can simultaneously account for 3 major sources of bias in epidemiologic research: validated exposure measurement error, measured selection bias, and measured time-fixed and time-varying confounding.
机译:为了评估不完全测量的高效抗逆转录病毒疗法对突发性获得性免疫缺陷综合症或死亡的净影响,作者将边缘结构Cox模型的逆治疗概率和删失加权估计与回归校准方法相结合。在1995年至2007年之间,美国进行了两项队列研究,追踪了950例人类免疫缺陷病毒阳性的男性和女性。在4,054人年中,有374例开始了积极的抗逆转录病毒治疗,有211例获得性免疫缺陷综合症或死亡,还有173例退出了研究。考虑到测得的混杂因素和辍学的决定因素,与过去两年未使用高效抗逆转录病毒疗法进行比较的后天免疫机能丧失综合症或死亡的加权危险比为0.36(95%的置信度极限:0.21、0.61)。这种联系在随访中相对稳定(P = 0.19),并且比粗略或调整后的危险比分别为0.75和0.95强。使用331名男性和女性的外部验证数据来计算报告的暴露中的测量误差,得出的危险比为0.17,偏差从危险比变为精确度估计值,这一范围由2.5倍的置信度上限(95%的置信度上限)看出:0.06,0.43)。边缘结构测量误差模型可以同时解释流行病学研究中三种主要的偏差来源:有效的暴露测量误差,测得的选择偏差以及测得的时间固定和时变混杂。

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