Bekaert Maarten, Vansteelandt Stijn, Mertens Karl
Department of Applied Mathematics and Computer Science, Ghent University, Ghent, Belgium.
Lifetime Data Anal. 2010 Jan;16(1):45-70. doi: 10.1007/s10985-009-9130-8. Epub 2009 Oct 10.
Despite decades of research in the medical literature, assessment of the attributable mortality due to nosocomial infections in the intensive care unit (ICU) remains controversial, with different studies describing effect estimates ranging from being neutral to extremely risk increasing. Interpretation of study results is further hindered by inappropriate adjustment (a) for censoring of the survival time by discharge from the ICU, and (b) for time-dependent confounders on the causal path from infection to mortality. In previous work (Vansteelandt et al. Biostatistics 10:46-59), we have accommodated this through inverse probability of treatment and censoring weighting. Because censoring due to discharge from the ICU is so intimately connected with a patient's health condition, the ensuing inverse weighting analyses suffer from influential weights and rely heavily on the assumption that one has measured all common risk factors of ICU discharge and mortality. In this paper, we consider ICU discharge as a competing risk in the sense that we aim to infer the risk of 'ICU mortality' over time that would be observed if nosocomial infections could be prevented for the entire study population. For this purpose we develop marginal structural subdistribution hazard models with accompanying estimation methods. In contrast to subdistribution hazard models with time-varying covariates, the proposed approach (a) can accommodate high-dimensional confounders, (b) avoids regression adjustment for post-infection measurements and thereby so-called collider-stratification bias, and (c) results in a well-defined model for the cumulative incidence function. The methods are used to quantify the causal effect of nosocomial pneumonia on ICU mortality using data from the National Surveillance Study of Nosocomial Infections in ICU's (Belgium).
尽管医学文献中已有数十年的研究,但对重症监护病房(ICU)医院感染所致归因死亡率的评估仍存在争议,不同研究描述的效应估计范围从无影响到极高的风险增加。研究结果的解读还受到以下因素的进一步阻碍:(a)因从ICU出院而对生存时间进行删失的不恰当调整,以及(b)对从感染到死亡的因果路径上随时间变化的混杂因素的不恰当调整。在之前的工作中(Vansteelandt等人,《生物统计学》10:46 - 59),我们通过治疗和删失加权的逆概率来解决这个问题。由于因从ICU出院导致的删失与患者的健康状况密切相关,随后的逆加权分析存在有影响的权重,并且严重依赖于已测量了ICU出院和死亡的所有常见风险因素这一假设。在本文中,我们将ICU出院视为一种竞争风险,即我们旨在推断如果能在整个研究人群中预防医院感染,随时间推移所观察到的“ICU死亡率”风险。为此,我们开发了边际结构子分布风险模型及相应的估计方法。与具有随时间变化协变量的子分布风险模型不同,所提出的方法(a)能够处理高维混杂因素,(b)避免对感染后测量值进行回归调整,从而避免所谓的对撞分层偏差,并且(c)得到一个定义明确的累积发病率函数模型。我们使用来自比利时ICU医院感染国家监测研究的数据,运用这些方法来量化医院获得性肺炎对ICU死亡率的因果效应。