Meta-analysis of summary statistics versus individual participant-level data of trials with binary outcomes

dc.contributor.advisorChen, Ding-Geng (Din)
dc.contributor.emaillayla7.norman@gmail.comen_US
dc.contributor.postgraduateNorman, Layla
dc.date.accessioned2023-01-26T07:31:16Z
dc.date.available2023-01-26T07:31:16Z
dc.date.created2019-04-09
dc.date.issued2022
dc.descriptionDissertation (MSc (Advanced Data Analytics))--University of Pretoria, 2022.en_US
dc.description.abstractIn this essay we will consider the meta-analysis of summary statistics versus individual participant-level data of trials with binary outcomes. Numerous techniques will be considered to essentially determine, both theoretically as well as numerically, by the use of real data analysis, whether or not, in certain instances, analyzing individual participant data (IPD) from all investigations undoubtedly gains efficiency over combining summary statistics from each study in a binary setting. We will be considering both the one-step as well as two-step meta-analysis, with the focus being mainly on the standard fixed-effects model and partially on the random-effects model. An application of two different clinical studies will be considered. The first study is called the Cannon (Cannon et al., (2006)[13]) Cardiovascular Clinical Trials which consists of four clinical studies. The second study is called the Bacillus Calmette-Guerin Vaccine Study which consists of a total of 13 clinical studies. We observed that a meta-analysis of summary data is more similar to a meta-analysis of IPD data for the first study, but different for the second study. This is due to the fact that the number of studies are small in both studies. Therefore the asymptotic equivalence should be cautious when the sample size is small and the number of studies is small. In this case, the estimation of the between study variance will be very unstable which will lead to a different conclusion between a meta-analysis of summary statistics (SS) and a meta-analysis of individual participant-level (IPD) data.en_US
dc.description.availabilityUnrestricteden_US
dc.description.degreeMSc (Advanced Data Analytics)en_US
dc.description.departmentStatisticsen_US
dc.description.sponsorshipThis work is based upon research supported by the National Research Foundation, South Africa (South Africa DST-NRF-SAMRC SARChI Research Chair in Biostatistics to Professor Ding-Geng Chen, Grant number 114613). Opinions expressed and conclusions arrived at are those of the author and are not necessarily to be attributed to the NRF.en_US
dc.identifier.citation*en_US
dc.identifier.doi10.25403/UPresearchdata.21436074en_US
dc.identifier.otherS2023
dc.identifier.urihttps://repository.up.ac.za/handle/2263/88970
dc.language.isoenen_US
dc.publisherUniversity of Pretoria
dc.rights© 2022 University of Pretoria. All rights reserved. The copyright in this work vests in the University of Pretoria. No part of this work may be reproduced or transmitted in any form or by any means, without the prior written permission of the University of Pretoria.
dc.subjectMeta-analysisen_US
dc.subjectStatisticsen_US
dc.subjectBinary dataen_US
dc.subjectIndividual participant-level dataen_US
dc.subjectFixed-effectsen_US
dc.subjectRandom-effectsen_US
dc.subjectReal data analysisen_US
dc.subjectMedical sciencesen_US
dc.subjectBiostatisticsen_US
dc.subjectClinical trialsen_US
dc.subjectUCTDen_US
dc.titleMeta-analysis of summary statistics versus individual participant-level data of trials with binary outcomesen_US
dc.typeDissertationen_US

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