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dc.contributor.authorLaura Fanningen_US
dc.contributor.authorIan C.K. Wongen_US
dc.contributor.authorXue Lien_US
dc.contributor.authorEsther W. Chanen_US
dc.contributor.authorPajaree Mongkhonen_US
dc.contributor.authorKenneth K.C. Manen_US
dc.contributor.authorLi Weien_US
dc.contributor.authorWai K. Leungen_US
dc.contributor.authorPeteris Darzinsen_US
dc.contributor.authorSimon Bellen_US
dc.contributor.authorJenni Ilomakien_US
dc.contributor.authorWallis C.Y. Lauen_US
dc.date.accessioned2020-10-14T08:45:50Z-
dc.date.available2020-10-14T08:45:50Z-
dc.date.issued2020-01-01en_US
dc.identifier.issn10991557en_US
dc.identifier.issn10538569en_US
dc.identifier.other2-s2.0-85090958669en_US
dc.identifier.other10.1002/pds.5130en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85090958669&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/70971-
dc.description.abstract© 2020 The Authors. Pharmacoepidemiology and Drug Safety published by John Wiley & Sons Ltd. Purpose: Comparative gastrointestinal bleeding (GIB) risk between rivaroxaban and low-dose aspirin is unknown in patients with atrial fibrillation (AF). This study investigated GIB risk with rivaroxaban vs aspirin among two separate AF cohorts in Hong Kong and the United Kingdom, using a common protocol approach. Methods: This was a population-based cohort study using separate data from the Clinical Data Analysis and Reporting System (CDARS) of the Hong Kong Hospital Authority (2010-2018) and The Health Improvement Network (THIN) database in the United Kingdom (2011-2017). Patients with AF newly prescribed aspirin or rivaroxaban were included. Cox proportional hazards regression was used to compare GIB risks for rivaroxaban vs aspirin, accounting for confounders using propensity score fine stratification approach. Results: In CDARS, 29 213 patients were included; n = 1052 (rivaroxaban), n = 28 161 (aspirin). Crude GIB event rates per 100 patient-years in CDARS were 3.0 (aspirin) and 2.6 (rivaroxaban). No difference in GIB risk was observed between rivaroxaban and aspirin overall (HR = 1.04, 95%CI = 0.76-1.42), and in dose-stratified analyses (HR = 1.21, 95%CI = 0.84-1.74 [20 mg/day]; HR = 0.80, 95%CI = 0.44-1.45 [≤15 mg/day]). In THIN, 11 549 patients were included, n = 3496 (rivaroxaban) and n = 8053 (aspirin). Crude GIB event rates were 1.3 (aspirin) and 2.4 (rivaroxaban) per 100 patient-years. No difference in GIB risk was observed between rivaroxaban and aspirin overall (HR = 1.40, 95%CI = 1.00-1.98) and low-dose rivaroxaban (≤15 mg/day) (HR = 1.00, 95%CI = 0.56-1.30), but increased GIB risk was observed for rivaroxaban 20 mg/day vs aspirin (HR = 1.57, 95%CI = 1.08-2.29). Conclusion: In patients with AF, GIB risk was comparable between aspirin and rivaroxaban ≤15 mg/day. GIB risk for rivaroxaban 20 mg/day vs aspirin remains uncertain and warrants further investigation.en_US
dc.subjectMedicineen_US
dc.titleGastrointestinal bleeding risk with rivaroxaban vs aspirin in atrial fibrillation: A multinational studyen_US
dc.typeJournalen_US
article.title.sourcetitlePharmacoepidemiology and Drug Safetyen_US
article.stream.affiliationsThe University of Hong Kong, Shenzhen Institute of Research and Innovationen_US
article.stream.affiliationsUniversity of Phayaoen_US
article.stream.affiliationsThe University of Hong Kong Li Ka Shing Faculty of Medicineen_US
article.stream.affiliationsUniversity College Londonen_US
article.stream.affiliationsMonash Universityen_US
article.stream.affiliationsThe University of Hong Kongen_US
article.stream.affiliationsChiang Mai Universityen_US
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