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dc.creatorSagris D., Leventis I., Georgiopoulos G., Korompoki E., Makaritsis K., Vemmos K., Milionis H., Lip G.Y.H., Ntaios G.en
dc.date.accessioned2023-01-31T09:52:40Z
dc.date.available2023-01-31T09:52:40Z
dc.date.issued2020
dc.identifier10.1016/j.ejim.2020.05.001
dc.identifier.issn09536205
dc.identifier.urihttp://hdl.handle.net/11615/78661
dc.description.abstractBackground: A considerable proportion of patients with atrial fibrillation (AF) are still treated with aspirin despite current guidelines due to presumed favorable safety. Aim: We performed a systematic review and meta-analysis of bleeding outcomes in randomized controlled trials (RCTs) comparing direct oral anticoagulants (DOACs) at doses approved for AF vs. aspirin. Methods: We searched PubMed and Scopus for phase-III RCTs of DOACs at AF-approved doses vs. aspirin. Outcomes assessed were major-, intracranial-, gastrointestinal-, clinically-relevant-non-major- and fatal bleeding. We performed two subgroup analyses: one per patient population i.e. those at high risk of arterial or venous thromboembolism, and one per DOAC. We also performed a meta-regression to assess the association with patient age. Results: In 4 eligible trials (20,440 patients) comparing DOACs vs. aspirin, the ORs were: 1.52 (95%CI: 0.91–2.53) for major bleeding in patients at high risk of arterial thromboembolism and 1.55 (95%CI:0.99-2.45, relative-risk-increase:55%, absolute-risk-increase:0.6%, number-needed-to-harm:170) in the overall analysis; 1.39 (95%CI:0.62–3.14) for intracranial bleeding in patients at high risk of arterial thromboembolism which was similar for the overall analysis; 1.27 (95%CI: 0.84–1.92) for gastrointestinal bleeding in patients at high risk of arterial thromboembolism and 1.26 (95%CI:0.86-1.85) in the overall analysis. Patient age was not a predictor of the magnitude of ORs for all bleeding outcomes. Conclusion: The present meta-analysis does not support the use of aspirin over DOACs in AF. Accordingly, the level of evidence of the related recommendations should be upgraded, which in turn may reduce further the proportion of AF patients treated with antiplatelets. © 2020 European Federation of Internal Medicineen
dc.language.isoenen
dc.sourceEuropean Journal of Internal Medicineen
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85084382678&doi=10.1016%2fj.ejim.2020.05.001&partnerID=40&md5=d41717e8d02ba6e67baa765e787326c5
dc.subjectacetylsalicylic aciden
dc.subjectanticoagulant agenten
dc.subjectapixabanen
dc.subjectdabigatranen
dc.subjectrivaroxabanen
dc.subjectacetylsalicylic aciden
dc.subjectanticoagulant agenten
dc.subjectarterial thromboembolismen
dc.subjectArticleen
dc.subjectatrial fibrillationen
dc.subjectbleedingen
dc.subjectbrain hemorrhageen
dc.subjectfollow upen
dc.subjectgastrointestinal hemorrhageen
dc.subjecthigh risk patienten
dc.subjecthumanen
dc.subjectmeta analysisen
dc.subjectoutcome assessmenten
dc.subjectsystematic reviewen
dc.subjectvenous thromboembolismen
dc.subjectatrial fibrillationen
dc.subjectcerebrovascular accidenten
dc.subjectoral drug administrationen
dc.subjectvenous thromboembolismen
dc.subjectAdministration, Oralen
dc.subjectAnticoagulantsen
dc.subjectAspirinen
dc.subjectAtrial Fibrillationen
dc.subjectHumansen
dc.subjectStrokeen
dc.subjectVenous Thromboembolismen
dc.subjectElsevier B.V.en
dc.titleBleeding risk comparison between direct oral anticoagulants at doses approved for atrial fibrillation and aspirin: systematic review, meta-analysis and meta-regressionen
dc.typejournalArticleen


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