(p < for group 1 or 2 vs. group 3)

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Luigi Oltrona Visconti Divisione di Cardiologia IRCCS Fondazione Policlinico S. Matteo Pavia Sindromi coronariche acute nei pazienti con fibrillazione.
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(p < 0.001 for group 1 or 2 vs. group 3) PIONEER AF-PCI Trial design: Patients with AF and PCI randomized to: Group 1: Rivaroxaban 15 mg daily plus P2Y12 inhibitor for 12 months (n = 709). Group 2: Rivaroxaban 2.5 mg twice daily plus DAPT for 1-12 months (n = 709). Group 3: warfarin plus DAPT for 1-12 months (n = 706). Results (p < 0.001 for group 1 or 2 vs. group 3) Clinically significant bleeding: 16.8% in group 1 vs. 18.0% in group 2 vs. 26.7% in group 3 (HR 0.59, p < 0.001 for group 1 vs. 3); (HR 0.63, p < 0.001 for group 2 vs. 3) Stent thrombosis: 0.8% in group 1 vs. 0.9% in group 2 vs. 0.7% in group 3 (HR 1.20, p = 0.79 for group 1 vs. 3; HR 1.44, p = 0.57 for group 2 vs. 3) 26.7 % 18.0 16.8 Conclusions Among patients with nonvalvular AF who underwent PCI, a rivaroxaban-based strategy was associated with a lower frequency of clinically significant bleeding compared with a warfarin/DAPT strategy Stent thrombosis appeared to be similar between the three groups Rivaroxaban 15 mg daily, P2Y12 for 12 months Rivaroxaban 2.5 mg daily, DAPT for 1-12 months Warfarin, DAPT for 1-12 months Gibson CM, et al. N Engl J Med 2016;375:2423-34