[en] BACKGROUND Whether successful catheter ablation for atrial fibrillation eliminates the need for long-term oral anticoagulant therapy is unknown. METHODS We conducted an international, open-label, randomized, blinded-outcome-assessment trial involving 1284 patients who had undergone successful catheter ablation for atrial fibrillation at least 1 year earlier and had a CHA 2 DS 2-VASc score (scores range from 0 to 9, with higher scores indicating a higher risk of stroke) of 1 or more (or ≥2 for women or for patients in whom vascular disease was a risk factor). Patients were randomly assigned to receive either aspirin (at a dose of 70 to 120 mg daily, depending on availability in the local jurisdiction) or rivaroxaban (at a dose of 15 mg) and followed for 3 years. Magnetic resonance imaging (MRI) of the head was performed after enrollment and at 3 years. The primary outcome was a composite of stroke, systemic embolism, or new covert embolic stroke (defined by ≥1 new infarct measuring ≥15 mm on MRI) at 3 years. RESULTS A total of 641 patients were assigned to the rivaroxaban group and 643 to the aspirin group. A primary-outcome event occurred in 5 patients (0.31 events per 100 patientyears) in the rivaroxaban group and in 9 patients (0.66 events per 100 patient-years) in the aspirin group (relative risk, 0.56; 95% confidence interval [CI], 0.19 to 1.65; absolute risk difference at 3 years, −0.6 percentage points; 95% CI, −1.8 to 0.5; P = 0.28). New cerebral infarcts measuring less than 15 mm occurred in 22 of 568 patients (3.9%) in the rivaroxaban group and in 26 of 590 patients (4.4%) in the aspirin group (relative risk, 0.89; 95% CI, 0.51 to 1.55). Fatal or major bleeding (the composite primary safety outcome) had occurred in 10 patients (1.6%) with rivaroxaban and in 4 patients (0.6%) with aspirin (hazard ratio, 2.51; 95% CI, 0.79 to 7.95) at 3 years. CONCLUSIONS Among patients who had had successful catheter ablation for atrial fibrillation at least 1 year earlier and had risk factors for stroke, treatment with rivaroxaban did not result in a significantly lower incidence of a composite of stroke, systemic embolism, or new covert embolic stroke than treatment with aspirin. (Funded by Bayer and others; OCEAN ClinicalTrials.gov number, NCT02168829.
Disciplines :
Cardiovascular & respiratory systems
Author, co-author :
Verma, Atul ; McGill University Health Centre, McGill University, Montreal
Birnie, David; University of Ottawa Heart Institute, Ottawa
Jiang, Chenyang; Sir Run Run Shaw Hospital, Zhejiang University School of Medicine, Zhejiang, China
Heidbüchel, Hein; University Hospital Antwerp, Antwerp, Belgium
Hindricks, Gerhard; Deutches Herzzentrum der Charité, Universitätsmedizin Berlin, member of Freie Universität Berlin and Humboldt Universität zu Berlin, Berlin
Healey, Jeff ; Hamilton Health Sciences, McMaster University, Hamilton, ON, Canada
Wang, Yunhe; Sir Run Run Shaw Hospital, Zhejiang University School of Medicine, Zhejiang, China
Dagres, Nikolaos; Deutches Herzzentrum der Charité, Universitätsmedizin Berlin, member of Freie Universität Berlin and Humboldt Universität zu Berlin, Berlin
Deyell, Marc; St. Paul’s Hospital, University of British Columbia, Vancouver, Canada
Sanders, Prashanthan; Centre for Heart Rhythm Disorders, Royal Adelaide Hospital, University of Adelaide, Adelaide, SA, Australia
Pathak, Rajeev; Canberra Heart Rhythm Centre, Canberra, ACT, Australia
Sharma, Mukul; Hamilton Health Sciences, McMaster University, Hamilton, ON, Canada
Ha, Andrew; University Health Network, University of Toronto, Toronto
Essebag, Vidal; McGill University Health Centre, McGill University, Montreal
Champagne, Jean; Institut Universitaire de Cardiologie et de Pneumologie de Quebéc, University of Laval, Quebec, QC, Canada
Hill, Michael ; Department of Clinical Neurosciences and Hotchkiss Brain Institute, Calgary Stroke Program, Cumming School of Medicine, University of Calgary, Calgary, AB, Canada
Smith, Eric; Department of Clinical Neurosciences and Hotchkiss Brain Institute, Calgary Stroke Program, Cumming School of Medicine, University of Calgary, Calgary, AB, Canada
Wells, George; University of Ottawa Heart Institute, Ottawa
Lancellotti, Patrizio ; Université de Liège - ULiège > Département des sciences cliniques > Cardiologie - Pathologie spéciale et réhabilitation
Bayer AG University of Ottawa CIHR - Canadian Institutes of Health Research
Funding text :
Supported by Bayer, Abbott, Biotronik, the Canadian Institutes
of Health Research, the University of Ottawa Heart
Institute Accelerate funding program, the Canadian Stroke Prevention
Intervention Network, the Brain-Heart Interconnectome
Canada First Research Excellence Fund, and the Rosenfeld Heart
Foundation.