<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Clement DY</submitter><funding>NIGMS NIH HHS</funding><pagination>451-67</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC2697342</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>10(3)</volume><pubmed_abstract>This paper deals with the analysis of recurrent event data subject to censored observation. Using a suitable adaptation of generalized estimating equations for longitudinal data, we propose a straightforward methodology for estimating the parameters indexing the conditional means and variances of the process interevent (i.e. gap) times. The proposed methodology permits the use of both time-fixed and time-varying covariates, as well as transformations of the gap times, creating a flexible and useful class of methods for analyzing gap-time data. Censoring is dealt with by imposing a parametric assumption on the censored gap times, and extensive simulation results demonstrate the relative robustness of parameter estimates even when this parametric assumption is incorrect. A suitable large-sample theory is developed. Finally, we use our methods to analyze data from a randomized trial of asthma prevention in young children.</pubmed_abstract><journal>Biostatistics (Oxford, England)</journal><pubmed_title>Conditional GEE for recurrent event gap times.</pubmed_title><pmcid>PMC2697342</pmcid><funding_grant_id>R01 GM056182</funding_grant_id><pubmed_authors>Clement DY</pubmed_authors><pubmed_authors>Strawderman RL</pubmed_authors></additional><is_claimable>false</is_claimable><name>Conditional GEE for recurrent event gap times.</name><description>This paper deals with the analysis of recurrent event data subject to censored observation. Using a suitable adaptation of generalized estimating equations for longitudinal data, we propose a straightforward methodology for estimating the parameters indexing the conditional means and variances of the process interevent (i.e. gap) times. The proposed methodology permits the use of both time-fixed and time-varying covariates, as well as transformations of the gap times, creating a flexible and useful class of methods for analyzing gap-time data. Censoring is dealt with by imposing a parametric assumption on the censored gap times, and extensive simulation results demonstrate the relative robustness of parameter estimates even when this parametric assumption is incorrect. A suitable large-sample theory is developed. Finally, we use our methods to analyze data from a randomized trial of asthma prevention in young children.</description><dates><release>2009-01-01T00:00:00Z</release><publication>2009 Jul</publication><modification>2025-04-26T00:29:03.609Z</modification><creation>2019-03-27T00:22:59Z</creation></dates><accession>S-EPMC2697342</accession><cross_references><pubmed>19297655</pubmed><doi>10.1093/biostatistics/kxp004</doi></cross_references></HashMap>