Martinussen T
Department of Biostatistics, University of Southern Denmark, J.B. Winslows Vej 9B, 5000 Odense C, Denmark.
Lifetime Data Anal. 2010 Jan;16(1):85-101. doi: 10.1007/s10985-009-9128-2. Epub 2009 Aug 22.
We consider the situation with a survival or more generally a counting process endpoint for which we wish to investigate the effect of an initial treatment. Besides the treatment indicator we also have information about a time-varying covariate that may be of importance for the survival endpoint. The treatment may possibly influence both the endpoint and the time-varying covariate, and the concern is whether or not one should correct for the effect of the dynamic covariate. Recently Fosen et al. (Biometrical J 48:381-398, 2006a) investigated this situation using the notion of dynamic path analysis and showed under the Aalen additive hazards model that the total effect of the treatment indicator can be decomposed as a sum of what they termed a direct and an indirect effect. In this paper, we give large sample properties of the estimator of the cumulative indirect effect that may be used to draw inferences. Small sample properties are investigated by Monte Carlo simulation and two applications are provided for illustration. We also consider the Cox model in the situation with recurrent events data and show that a similar decomposition of the total effect into a sum of direct and indirect effects holds under certain assumptions.
我们考虑一种情况,即生存或更一般地说计数过程终点,我们希望研究初始治疗的效果。除了治疗指标外,我们还拥有关于一个随时间变化的协变量的信息,该协变量可能对生存终点很重要。治疗可能会同时影响终点和随时间变化的协变量,问题在于是否应该校正动态协变量的影响。最近,福森等人(《生物统计学杂志》48:381 - 398,2006a)使用动态路径分析的概念研究了这种情况,并在阿伦加性风险模型下表明,治疗指标的总效应可以分解为他们所称的直接效应和间接效应之和。在本文中,我们给出了可用于进行推断的累积间接效应估计量的大样本性质。通过蒙特卡罗模拟研究了小样本性质,并提供了两个应用示例。我们还考虑了具有复发事件数据情况下的考克斯模型,并表明在某些假设下,总效应类似地分解为直接效应和间接效应之和成立。