论文标题

通过经常发生的事件进行层次生存数据的风险调整的发病率建模

Risk-Adjusted Incidence Modeling on Hierarchical Survival Data with Recurrent Events

论文作者

Jiang, Xiaotong, Stoudemire, William, Muhlebach, Marianne S., Kosorok, Michael R.

论文摘要

许多医疗保健计划一直需要及时解决预防和控制(IP&C)的问题。例如,即使使用现有建议的IP&C实践,也可以在医疗保健系统内的住院和门诊环境中在患有囊性纤维化(CF)的患者之间传播病原体,这些病原体通常与负临床结果负面。由于数据共享有限和延迟,CF程序需要一种可靠的方法来跟踪感染率。 CF注册表数据中有三个复杂的结构:由于患者和患者到患者的传播中的重复测量,反复感染,数据缺失和多级相关性。提出了一条逐步分析管道,以开发和验证一个经过风险调整的模型,以帮助医疗计划监控经常性事件的数量,同时考虑到丢失的数据以及右验证数据中重复测量的层次结构。我们扩展了对重要风险因素进行调整的混合效应Andersen-Gill模型(脆弱模型),并为预测的事件数量提供了置信区间,这些事件数量是从三个确定的来源估算的预测可变性的。估计置信区间的覆盖范围用于评估模型性能。模拟结果表明,我们方法的覆盖范围接近所需的置信度。为了证明其临床实用性,我们的管道使用美国注册表来监测两种关键CF病原体的感染率。结果表明,在CF示例中,更接近感兴趣的时间更接近感兴趣的时间。

There is a constant need for many healthcare programs to timely address problems with infection prevention and control (IP&C). For example, pathogens can be transmitted among patients with cystic fibrosis (CF) in both the inpatient and outpatient settings within the healthcare system even with the existing recommended IP&C practices, and these pathogens are often associated with negative clinical outcomes. Because of limited and delayed data sharing, CF programs need a reliable method to track infection rates. There are three complex structures in CF registry data: recurrent infections, missing data, and multilevel correlation due to repeated measures within a patient and patient-to-patient transmissions. A step-by-step analysis pipeline was proposed to develop and validate a risk-adjusted model to help healthcare programs monitor the number of recurrent events while taking into account missing data and the hierarchies of repeated measures in right-censored data. We extended the mixed-effect Andersen-Gill model (the frailty model), adjusted for important risk factors, and provided confidence intervals for the predicted number of events where the variability of the prediction was estimated from three identified sources. The coverage of the estimated confidence intervals was used to evaluate model performance. Simulation results indicated that the coverage of our method was close to the desired confidence level. To demonstrate its clinical practicality, our pipeline was applied to monitor the infection incidence rate of two key CF pathogens using a U.S. registry. Results showed that years closer to the time of interest were better at predicting future incidence rates in the CF example.

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