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Author Notes:

lpeng@emory.edu

The authors would like to thank the Cystic Fibrosis Foundation for the use of CF Foundation Patient Registry data to conduct this study.

Additionally, we would like to thank the patients, care providers and clinic coordinators at CF Centers throughout the United States for their contributions to the CF Foundation Patient Registry.

Subjects:

Research Funding:

This work is partially supported by National Institutes of Health Grants R01HL113548 and R01DK072126.

Keywords:

  • Science & Technology
  • Life Sciences & Biomedicine
  • Physical Sciences
  • Biology
  • Mathematical & Computational Biology
  • Statistics & Probability
  • Life Sciences & Biomedicine - Other Topics
  • Mathematics
  • Accelerated recurrence time model
  • Missing at random
  • Multivariate recurrent event data
  • Nadaraya-Watson kernel estimator
  • COMPETING RISKS DATA
  • QUANTILE REGRESSION
  • RATES MODEL
  • CATEGORY

Generalized accelerated recurrence time model for multivariate recurrent event data with missing event type

Tools:

Journal Title:

Biometrics

Volume:

Volume 74, Number 3

Publisher:

, Pages 954-965

Type of Work:

Article | Post-print: After Peer Review

Abstract:

Recurrent events data are frequently encountered in biomedical follow-up studies. The generalized accelerated recurrence time (GART) model (Sun et al., 2016), which formulates covariate effects on the time scale of the mean function of recurrent events (i.e., time to expected frequency), has arisen as a useful secondary analysis tool to provide meaningful physical interpretations. In this article, we investigate the GART model in a multivariate recurrent events setting, where subjects may experience multiple types of recurrent events and some event types may be missing. We propose methods for the GART model that utilize the inverse probability weighting technique or the estimating equation projection strategy to handle event types that are missing at random. The new methods do not require imposing any parametric model for the missing mechanism, and thus are robust; moreover, they enjoy easy and stable implementation. We establish the uniform consistency and weak convergence of the resulting estimators and develop appropriate inferential procedures. Extensive simulation studies and an application to a dataset from Cystic Fibrosis Foundation Patient Registry (CFFPR) illustrate the validity and practical utility of the proposed methods.

Copyright information:

© 2018, The International Biometric Society

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