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      Reversal of direct oral anticoagulants: Guidance from the Anticoagulation Forum

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          Most cited references45

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          Idarucizumab for Dabigatran Reversal - Full Cohort Analysis.

          Idarucizumab, a monoclonal antibody fragment, was developed to reverse the anticoagulant effect of dabigatran.
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            Full Study Report of Andexanet Alfa for Bleeding Associated with Factor Xa Inhibitors

            Andexanet alfa is a modified recombinant inactive form of human factor Xa developed for reversal of factor Xa inhibitors.
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              Is Open Access

              Uninterrupted rivaroxaban vs. uninterrupted vitamin K antagonists for catheter ablation in non-valvular atrial fibrillation

              Aims VENTURE-AF is the first prospective randomized trial of uninterrupted rivaroxaban and vitamin K antagonists (VKAs) in patients with non-valvular atrial fibrillation (NVAF) undergoing catheter ablation (CA). Methods and results Trial size was administratively set at 250, the protocol-specified target. Events were independently and blindly adjudicated. We randomly assigned 248 NVAF patients to uninterrupted rivaroxaban (20 mg once-daily) or to an uninterrupted VKA prior to CA and for 4 weeks afterwards. The primary endpoint was major bleeding events after CA. Secondary endpoints included thromboembolic events (composite of stroke, systemic embolism, myocardial infarction, and vascular death) and other bleeding or procedure-attributable events. Patients were 59.5 ± 10 years of age, 71% male, 74% paroxysmal AF, and had a CHA2DS2-VASc score of 1.6. The average total heparin dose used to manage activated clotting time (ACT) was slightly higher (13 871 vs. 10 964 units; P < 0.001) and the mean ACT level attained slightly lower (302 vs. 332 s; P < 0.001) in rivaroxaban and VKA arms, respectively. The incidence of major bleeding was low (0.4%; 1 major bleeding event). Similarly, thromboembolic events were low (0.8%; 1 ischemic stroke and 1 vascular death). All events occurred in the VKA arm and all after CA. The number of any adjudicated events (26 vs. 25), any bleeding events (21 vs. 18), and any other procedure-attributable events (5 vs. 5) were similar. Conclusion In patients undergoing CA for AF, the use of uninterrupted oral rivaroxaban was feasible and event rates were similar to those for uninterrupted VKA therapy. Name of the Trial Registry Clinicaltrials.gov trial registration number is NCT01729871.
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                Author and article information

                Journal
                American Journal of Hematology
                Am J Hematol
                Wiley
                0361-8609
                1096-8652
                April 16 2019
                June 2019
                April 16 2019
                June 2019
                : 94
                : 6
                : 697-709
                Affiliations
                [1 ]Department of Medicine and Department of Pathology and Laboratory MedicinePerelman School of Medicine, University of Pennsylvania Philadelphia Pennsylvania
                [2 ]Department of Pharmacy Practice and Administrative Sciences, University of New Mexico Health Sciences Center Albuquerque New Mexico
                [3 ]WellScriptEd Consulting, Inc. Clifton Park New York
                [4 ]Department of MedicineMcMaster University Hamilton Ontario Canada
                [5 ]Department of Medicine, Zucker School of Medicine at Hofstra/Northwell Hempstead New York
                [6 ]Department of PathologyMassachusetts General Hospital Boston Massachusetts
                [7 ]Department of Cardiology, Grady Memorial Hospital Atlanta Georgia
                [8 ]Division of Hospital MedicineHenry Ford Hospital Detroit Michigan
                Article
                10.1002/ajh.25475
                30916798
                26f964da-01d0-405e-abde-03d4c42672f6
                © 2019

                http://onlinelibrary.wiley.com/termsAndConditions#vor

                http://doi.wiley.com/10.1002/tdm_license_1.1

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