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Propensity Score Matching in Randomized Clinical Trials

dc.contributor.authorXu, Zhenzhenen_US
dc.contributor.authorKalbfleisch, John D.en_US
dc.date.accessioned2011-01-13T19:40:34Z
dc.date.available2011-01-13T19:40:34Z
dc.date.issued2010-09en_US
dc.identifier.citationXu, Zhenzhen; Kalbfleisch, John D.; (2010). "Propensity Score Matching in Randomized Clinical Trials." Biometrics 66(3): 813-823. <http://hdl.handle.net/2027.42/78638>en_US
dc.identifier.issn0006-341Xen_US
dc.identifier.issn1541-0420en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/78638
dc.description.abstractCluster randomization trials with relatively few clusters have been widely used in recent years for evaluation of health-care strategies. On average, randomized treatment assignment achieves balance in both known and unknown confounding factors between treatment groups, however, in practice investigators can only introduce a small amount of stratification and cannot balance on all the important variables simultaneously. The limitation arises especially when there are many confounding variables in small studies. Such is the case in the  INSTINCT  trial designed to investigate the effectiveness of an education program in enhancing the tPA use in stroke patients. In this article, we introduce a new randomization design, the balance match weighted (BMW) design, which applies the optimal matching with constraints technique to a prospective randomized design and aims to minimize the mean squared error (MSE) of the treatment effect estimator. A simulation study shows that, under various confounding scenarios, the BMW design can yield substantial reductions in the MSE for the treatment effect estimator compared to a completely randomized or matched-pair design. The BMW design is also compared with a model-based approach adjusting for the estimated propensity score and Robins-Mark-Newey E-estimation procedure in terms of efficiency and robustness of the treatment effect estimator. These investigations suggest that the BMW design is more robust and usually, although not always, more efficient than either of the approaches. The design is also seen to be robust against heterogeneous error. We illustrate these methods in proposing a design for the  INSTINCT  trial.en_US
dc.format.extent214529 bytes
dc.format.extent3106 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.publisherBlackwell Publishing Incen_US
dc.subject.otherClustered Randomized Trialen_US
dc.subject.otherExperimental Designen_US
dc.subject.otherOptimal Full Matchingen_US
dc.subject.otherPropensity Score Matchingen_US
dc.subject.otherRandomization Studyen_US
dc.titlePropensity Score Matching in Randomized Clinical Trialsen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelMathematicsen_US
dc.subject.hlbtoplevelScienceen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Biostatistics, University of Michigan, Ann Arbor, Michighan 48109, U.S.A.en_US
dc.identifier.pmid19995353en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/78638/1/j.1541-0420.2009.01364.x.pdf
dc.identifier.doi10.1111/j.1541-0420.2009.01364.xen_US
dc.identifier.sourceBiometricsen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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