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Applications and Case Studies

Recurrent Events Analysis With Data Collected at Informative Clinical Visits in Electronic Health Records

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Pages 594-604 | Received 09 Jul 2018, Accepted 21 Jul 2020, Published online: 26 Aug 2020
 

Abstract

Although increasingly used as a data resource for assembling cohorts, electronic health records (EHRs) pose many analytic challenges. In particular, a patient’s health status influences when and what data are recorded, generating sampling bias in the collected data. In this article, we consider recurrent event analysis using EHR data. Conventional regression methods for event risk analysis usually require the values of covariates to be observed throughout the follow-up period. In EHR databases, time-dependent covariates are intermittently measured during clinical visits, and the timing of these visits is informative in the sense that it depends on the disease course. Simple methods, such as the last-observation-carried-forward approach, can lead to biased estimation. On the other hand, complex joint models require additional assumptions on the covariate process and cannot be easily extended to handle multiple longitudinal predictors. By incorporating sampling weights derived from estimating the observation time process, we develop a novel estimation procedure based on inverse-rate-weighting and kernel-smoothing for the semiparametric proportional rate model of recurrent events. The proposed methods do not require model specifications for the covariate processes and can easily handle multiple time-dependent covariates. Our methods are applied to a kidney transplant study for illustration. Supplementary materials for this article are available online.

Supplementary Materials

The supplementary materials contain simulation results using a different bandwidth, additional results of data analysis, and the proof of the large sample properties of the baseline mean function.

Additional information

Funding

This research was partially supported by NIH R01CA193888. The transplant study was supported in part by NIH K24AI085118. The first author’s research was partially supported by the Calderone Junior Faculty Prize from Columbia University Mailman School of Public Health.

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