Htoo Phyo T, Edwards Jessie K, Gokhale Mugdha, Pate Virginia, Buse John B, Jonsson-Funk Michele, Stürmer Til
Division of Pharmacoepidemiology and Pharmacoeconomics, Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, United States.
Department of Epidemiology, Gillings School of Global Public Health, University of North Carolina at Chapel Hill, Chapel Hill, NC, United States.
Am J Epidemiol. 2025 Jun 3;194(6):1544-1555. doi: 10.1093/aje/kwae329.
One obstacle to adopting instrumental variable (IV) methods in pharmacoepidemiology is their reliance on strong, unverifiable assumptions. We can falsify IV assumptions by leveraging the causal structure, which can strengthen or refute their plausibility and increase the validity of effect estimates. We illustrate a systematic approach to evaluate calendar-time IV assumptions in estimating the known effect of thiazolidinediones on hospitalized heart failure. Using cohort entry time before and after September 2010, when the US Food and Drug Administration issued a safety communication, as a proposed IV, we estimated IV and propensity score-weighted 2-year risk differences (RDs) using Medicare data (2008-2014). We (1) performed inequality tests, (2) identified the negative control IV/outcome using causal assumptions, (3) estimated RDs after narrowing the calendar time range and excluding patients likely associated with unmeasured confounding, (4) derived bounds for RDs, and (5) estimated the proportion of compliers and their characteristics. The findings revealed that IV assumptions were violated and RDs were extreme, but the assumptions became more plausible upon narrowing the calendar time range and restricting the cohort by excluding prevalent heart failure (the strongest measured predictor of outcome). Systematically evaluating IV assumptions could help detect bias in IV estimators and increase their validity. This article is part of a Special Collection on Pharmacoepidemiology.
在药物流行病学中采用工具变量(IV)方法的一个障碍是它们依赖于强大的、无法验证的假设。我们可以通过利用因果结构来证伪IV假设,这可以增强或反驳其合理性,并提高效应估计的有效性。我们阐述了一种系统方法,用于在估计噻唑烷二酮类药物对住院心力衰竭的已知效应时评估日历时间IV假设。使用2010年9月美国食品药品监督管理局发布安全通报前后的队列进入时间作为拟议的IV,我们使用医疗保险数据(2008 - 2014年)估计了IV和倾向评分加权的2年风险差异(RDs)。我们(1)进行了不等式检验,(2)使用因果假设确定了阴性对照IV/结局,(3)在缩小日历时间范围并排除可能与未测量混杂因素相关的患者后估计RDs,(4)得出RDs的界限,以及(5)估计依从者的比例及其特征。研究结果表明IV假设被违反且RDs很极端,但在缩小日历时间范围并通过排除现患心力衰竭(结局最强的测量预测因素)来限制队列后,这些假设变得更合理。系统地评估IV假设有助于检测IV估计器中的偏差并提高其有效性。本文是药物流行病学特刊的一部分。