García-Albéniz Xabier, Hsu John, Hernán Miguel A
Department of Epidemiology, Harvard T.H. Chan School of Public Health, 677 Huntington Ave, Boston, MA, 02115, USA.
Mongan Institute, Massachusetts General Hospital, Boston, MA, USA.
Eur J Epidemiol. 2017 Jun;32(6):495-500. doi: 10.1007/s10654-017-0287-2. Epub 2017 Jul 26.
Observational analyses for causal inference often rely on real world data collected for purposes other than research. A frequent goal of these observational analyses is to use the data to emulate a hypothetical randomized experiment, i.e., the target trial, that mimics the design features of a true experiment, including a clear definition of time zero with synchronization of treatment assignment and determination of eligibility. We review a recent observational analysis that explicitly emulated a target trial of screening colonoscopy using insurance claims from U.S. Medicare. We then compare this explicit emulation with alternative, simpler observational analyses that do not synchronize treatment assignment and eligibility determination at time zero and/or do not allow for repeated eligibility. This empirical comparison suggests that lack of an explicit emulation of the target trial leads to biased estimates, and shows that allowing for repeated eligibility increases the statistical efficiency of the estimates.
用于因果推断的观察性分析通常依赖于为非研究目的收集的真实世界数据。这些观察性分析的一个常见目标是利用这些数据来模拟一个假设的随机试验,即目标试验,该试验模仿真实试验的设计特征,包括明确界定时间零点,使治疗分配同步,并确定入选资格。我们回顾了最近一项观察性分析,该分析使用美国医疗保险的保险理赔数据明确模拟了结肠镜筛查的目标试验。然后,我们将这种明确的模拟与其他更简单的观察性分析进行比较,这些分析在时间零点不同步治疗分配和入选资格确定,和/或不允许重复入选资格。这种实证比较表明,缺乏对目标试验的明确模拟会导致估计偏差,并表明允许重复入选资格会提高估计的统计效率。