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dc.contributor.authorChaudhuri, Anamikaen_US
dc.date.accessioned2018-03-05T16:27:49Z
dc.date.issued2017
dc.identifier.urihttps://hdl.handle.net/2144/27368
dc.description.abstractProfiling medical sites is an important activity in both clinical research and practice. Many organizations provide public report cards comparing outcomes across hospitals. An analogous concept applied in multicenter clinical trials, such “report cards” guide sponsors to choose sites while designing a study, help identify areas of improvement for sites, and motivate sites to perform better. Sponsors include comparative performance of sites, a concept to perform risk-based monitoring and central statistical monitoring. In clinical research, report cards are powerful tools for relating site performance to treatment benefits. This study evaluates approaches to estimating the proportion of adverse events at the site-level in a multicenter clinical trial setting and also methods in detecting outlying sites. We address three topics. First we assess the performance of different models for obtaining estimates of adverse events rates utilizing Bayesian beta-binomial and binomial logit-normal models with MCMC estimation and fixed effects maximum likelihood estimation (MLE) methods. We - vary sample sizes, number of medical sites, overall adverse event rates, and intraclass correlation within sites. Second, we compare the performance of these methods in identifying outlier sites, contrasting MLE and Bayesian approaches. A fixed threshold method detects sites as outliers under a Bayesian approach, while in the fixed effects assumption, a 95% interval-based approach is applied. Third, we extend this approach in estimating multiple outcomes at the site level and detecting outlier sites. A standard bivariate normal MLE method is compared to a Bayesian bivariate binomial logit-normal MCMC. These are examined using simulation studies. Results show for single outcomes, Bayesian beta-binomial MCMC method perform well under certain parametric conditions for estimation and detecting outlier sites. For multiple outcomes with higher adverse event rate and larger difference between outliers and non-outliers, for detecting outlier sites, both methods – Bayesian MCMC and MLE work well, irrespective of the correlation between outcomes.en_US
dc.language.isoen_US
dc.subjectBiostatisticsen_US
dc.titleProfiling medical sites based on adverse events data for multi-center clinical trialsen_US
dc.typeThesis/Dissertationen_US
dc.date.updated2018-02-14T20:23:26Z
dc.description.embargo2020-02-14T00:00:00Z
etd.degree.nameDoctor of Philosophyen_US
etd.degree.leveldoctoralen_US
etd.degree.disciplineBiostatisticsen_US
etd.degree.grantorBoston Universityen_US


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