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Apples and Oranges? Interpretations of Risk Adjustment and Instrumental Variable Estimates of Intended Treatment Effects Using Observational Data

机译:苹果和橘子?使用观察数据解释风险调整和预期治疗效果的工具变量估计

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摘要

Instrumental variable (IV) and risk adjustment (RA) estimators, including propensity score adjustments, are both used to alleviate confounding problems in nonexperimental studies on treatment effects, but it is not clear how estimates based on these 2 approaches compare. Methodological considerations have shown that IV and RA estimators yield estimates of distinct types of causal treatment effects regardless of confounding problems. Many investigators have neglected these distinctions. In this paper, the authors use 3 schematic models to explain visually the relations between IV and RA estimates of intended treatment effects as demonstrated in the methodological studies. When treatment effects are homogeneous across a study population or when treatment effects are heterogeneous across the study population but treatment decisions are unrelated to the treatment effects, RA and IV estimates should be equivalent when the respective assumptions are met. In contrast, when treatment effects are heterogeneous and treatment decisions are related to the treatment effects, RA estimates of treatment effect can asymptotically differ from IV estimates, but both are correct even when the respective assumptions are met. Appropriate interpretations of IV or RA estimates can be facilitated by developing conceptual models related to treatment choice and treatment effect heterogeneity prior to analyses.
机译:工具变量(IV)和风险调整(RA)估计量(包括倾向评分调整量)均用于缓解治疗效果非实验研究中的混杂问题,但尚不清楚如何比较这两种方法的估计值。方法论上的考虑表明,IV和RA估计量可以得出因果治疗效果不同类型的估计值,而与混杂问题无关。许多调查员忽略了这些区别。在本文中,作者使用3个示意性模型从视觉上解释了预期治疗效果的IV和RA估计值之间的关系,如方法学研究所示。当研究人群中的治疗效果均一或当研究人群中的治疗效果不一,但治疗决策与治疗效果无关时,当满足各自的假设时,RA和IV估计值应相等。相反,当治疗效果不同且治疗决策与治疗效果相关时,RA的治疗效果估计值可能与IV估计值渐近地不同,但即使满足各自的假设,两者也是正确的。通过在分析之前建立与治疗选择和治疗效果异质性有关的概念模型,可以促进对IV或RA估计值的适当解释。

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  • 来源
    《American Journal of Epidemiology》 |2012年第1期|p.60-65|共6页
  • 作者单位

    Correspondence to Dr. Gang Fang, Division of Pharmaceutical Outcomes and Policy, Eshelman School of Pharmacy, 2202 Kerr Hall, University of North Carolina at Chapel Hill, Chapel Hill, NC27599-7573 (e-mail:;

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