Publication:
Comparison of the Long-Term Remission of Rituximab and Conventional Treatment for Acquired Thrombotic Thrombocytopenic Purpura: A Systematic Review and Meta-Analysis

dc.contributor.authorWeerapat Owattanapanichen_US
dc.contributor.authorChompunut Wongpraserten_US
dc.contributor.authorWannaphorn Rotchanapanyaen_US
dc.contributor.authorNatthida Owattanapanichen_US
dc.contributor.authorTheera Ruchutrakoolen_US
dc.contributor.otherFaculty of Medicine, Siriraj Hospital, Mahidol Universityen_US
dc.contributor.otherWattanosoth Hospitalen_US
dc.contributor.otherChiangrai Prachanukroh Hospitalen_US
dc.date.accessioned2020-01-27T10:12:11Z
dc.date.available2020-01-27T10:12:11Z
dc.date.issued2019-01-28en_US
dc.description.abstract© The Author(s) 2019. The current systematic review and meta-analysis aimed to summarize the results of all available studies to compare the efficacies of rituximab and conventional treatment for acquired thrombotic thrombocytopenic purpura (TTP). Three investigators independently searched studies in the MEDLINE and EMBASE databases published before December 11, 2018. To be included in the meta-analysis, studies needed to be randomized-controlled or cohort studies comparing the efficacies of rituximab and conventional therapy for TTP treatment. The effect estimates and 95% confidence intervals (CIs) from each study were collected, and Mantel-Haenszel methods were used to pool the data. A total of 570 patients from 9 eligible studies were included in the meta-analysis (280 patients in the rituximab arm and 290 in the conventional treatment arm). Patients receiving rituximab in an acute phase to induce disease remission had a significantly lower relapse rate than those given conventional treatment (odds ratio [OR]: 0.40, 95% CI: 0.19-0.85, P =.02, I 2 = 43%). Similarly, the relapse rate in the rituximab group for preemptive therapy to prevent clinical relapse was also significantly lower than in the control group (OR: 0.09, 95% CI: 0.04-0.24, P <.00001, I 2 = 11%). Furthermore, the conventional treatment group had a significantly higher mortality rate than the rituximab group during the follow-up (OR: 0.41, 95% CI: 0.18-0.91, P =.03, I 2 = 0%). Rituximab offered high efficacy for the prevention of relapses and lower mortality rate in cases of acquired TTP.en_US
dc.identifier.citationClinical and Applied Thrombosis/Hemostasis. Vol.25, (2019)en_US
dc.identifier.doi10.1177/1076029618825309en_US
dc.identifier.issn19382723en_US
dc.identifier.issn10760296en_US
dc.identifier.other2-s2.0-85061013425en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/51950
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85061013425&origin=inwarden_US
dc.subjectMedicineen_US
dc.titleComparison of the Long-Term Remission of Rituximab and Conventional Treatment for Acquired Thrombotic Thrombocytopenic Purpura: A Systematic Review and Meta-Analysisen_US
dc.typeReviewen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85061013425&origin=inwarden_US

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