The population-attributable fraction for time-dependent exposures using dynamic prediction and landmarking

被引:5
|
作者
von Cube, Maja [1 ,2 ,3 ]
Schumacher, Martin [1 ,2 ,3 ]
Putter, Hein [4 ]
Timsit, Jean-Francois [5 ,6 ]
van de Velde, Cornelis [7 ]
Wolkewitz, Martin [1 ,2 ,3 ]
机构
[1] Univ Freiburg, Inst Med Biometry & Stat, Fac Med, Stefan Meier Str 26, D-79104 Freiburg, Germany
[2] Univ Freiburg, Med Ctr, Stefan Meier Str 26, D-79104 Freiburg, Germany
[3] Univ Freiburg, Freiburg Ctr Data Anal & Modeling, Freiburg, Germany
[4] Leiden Univ, Dept Med Stat & Bioinformat, Med Ctr, Leiden, Netherlands
[5] Univ Paris Diderot, INSERM, UMR 1137, IAME, Paris, France
[6] Hop Xavier Bichat, APHP Med & Infect Dis ICU, Paris, France
[7] Leiden Univ, Dept Surg, Med Ctr, Leiden, Netherlands
关键词
attributable risk; competing risks; dynamic prediction; landmarking; time-dependent exposure; PSEUDO-OBSERVATIONS; SURVIVAL; INFECTIONS; ESTIMATORS; MORTALITY; MODELS;
D O I
10.1002/bimj.201800252
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The public health impact of a harmful exposure can be quantified by the population-attributable fraction (PAF). The PAF describes the attributable risk due to an exposure and is often interpreted as the proportion of preventable cases if the exposure was extinct. Difficulties in the definition and interpretation of the PAF arise when the exposure of interest depends on time. Then, the definition of exposed and unexposed individuals is not straightforward. We propose dynamic prediction and landmarking to define and estimate a PAF in this data situation. Two estimands are discussed which are based on two hypothetical interventions that could prevent the exposure in different ways. Considering the first estimand, at each landmark the estimation problem is reduced to a time-independent setting. Then, estimation is simply performed by using a generalized-linear model accounting for the current exposure state and further (time-varying) covariates. The second estimand is based on counterfactual outcomes, estimation can be performed using pseudo-values or inverse-probability weights. The approach is explored in a simulation study and applied on two data examples. First, we study a large French database of intensive care unit patients to estimate the population-benefit of a pathogen-specific intervention that could prevent ventilator-associated pneumonia caused by the pathogen Pseudomonas aeruginosa. Moreover, we quantify the population-attributable burden of locoregional and distant recurrence in breast cancer patients.
引用
收藏
页码:583 / 597
页数:15
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