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Authors Hellenbart EL, Faulkenberg KD, Finks SW
Received 22 April 2017
Accepted for publication 19 June 2017
Published 23 August 2017 Volume 2017:13 Pages 325—342
DOI https://doi.org/10.2147/VHRM.S121661
Checked for plagiarism Yes
Review by Single-blind
Peer reviewers approved by Dr Colin Mak
Peer reviewer comments 5
Editor who approved publication: Prof. Dr. Daniel Duprez
Abstract: Direct oral anticoagulants (DOACs) are recognized by
evidence-based treatment guidelines as the first-line option for the treatment
of venous thromboembolism and prevention of stroke and systemic embolism in
nonvalvular atrial fibrillation. As use of these anticoagulants has become
favored over the past several years, reported bleeding-related adverse drug
events with these agents has increased. In randomized clinical trials, all
DOACs have a reduced risk for intracranial hemorrhage, while major and other
bleeding results have varied among the agents compared to vitamin K
antagonists. We have reviewed the bleeding incidence and severity from
randomized and real-world data in patients receiving DOACs in an effort to
provide the clinician with a critical review of bleeding and offer practical
considerations for avoiding adverse events with these anticoagulants.
Keywords: bleeding,
direct oral anticoagulants, dabigatran, rivaroxaban, apixaban, edoxaban,
post-market bleeding
摘要视频链接:Bleeding in patients
receiving DOACs