4.7 Article

Outcomes After Cardioversion and Atrial Fibrillation Ablation in Patients Treated With Rivaroxaban and Warfarin in the ROCKET AF Trial

期刊

JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY
卷 61, 期 19, 页码 1998-2006

出版社

ELSEVIER SCIENCE INC
DOI: 10.1016/j.jacc.2013.02.025

关键词

atrial fibrillation; cardioversion; catheter ablation; stroke; rivaroxaban; warfarin

资金

  1. Johnson & Johnson Pharmaceutical Research and Development
  2. Bayer HealthCare AG
  3. Johnson Johnson
  4. Bayer
  5. Ortho McNeil Janssen
  6. Bayer HealthCare
  7. Eliot B. and Edith C. Shoolman fund of Massachusetts General Hospital
  8. Boehringer-Ingelheim
  9. Bristol-Myers Squibb
  10. Daiichi Sankyo
  11. Pfizer
  12. Sanofi
  13. Bristol Myers-Squibb
  14. AstraZeneca
  15. Eli Lilly
  16. GlaxoSmithKline
  17. Merck
  18. Momenta Pharmaceuticals
  19. Novartis
  20. Portola
  21. Pozen
  22. Regado Biotechnologies
  23. Sanofi-Aventis
  24. Medicines Company
  25. Ortho/McNeill
  26. Polymedix
  27. Lilly

向作者/读者索取更多资源

Objectives This study sought to investigate the outcomes following cardioversion or catheter ablation in patients with atrial fibrillation (AF) treated with warfarin or rivaroxaban. Background There are limited data on outcomes following cardioversion or catheter ablation in AF patients treated with factor Xa inhibitors. Methods We compared the incidence of electrical cardioversion (ECV), pharmacologic cardioversion (PCV), or AF ablation and subsequent outcomes in patients in a post hoc analysis of the ROCKET AF (Efficacy and Safety Study of Rivaroxaban With Warfarin for the Prevention of Stroke and Non-Central Nervous System Systemic Embolism in Patients With Non-Valvular Atrial Fibrillation) trial. Results Over a median follow-up of 2.1 years, 143 patients underwent ECV, 142 underwent PCV, and 79 underwent catheter ablation. The overall incidence of ECV, PCV, or AF ablation was 1.45 per 100 patient-years (n = 321; 1.44 [n = 161] in the warfarin arm, 1.46 [n = 160] in the rivaroxaban arm). The crude rates of stroke and death increased in the first 30 days after cardioversion or ablation. After adjustment for baseline differences, the long-term incidence of stroke or systemic embolism (hazard ratio [HR]: 1.38; 95% confidence interval [CI]: 0.61 to 3.11), cardiovascular death (HR: 1.57; 95% CI: 0.69 to 3.55), and death from all causes (HR: 1.75; 95% CI: 0.90 to 3.42) were not different before and after cardioversion or AF ablation. Hospitalization increased after cardioversion or AF ablation (HR: 2.01; 95% CI: 1.51 to 2.68), but there was no evidence of a differential effect by randomized treatment (p value for interaction = 0.58). The incidence of stroke or systemic embolism (1.88% vs. 1.86%) and death (1.88% vs. 3.73%) were similar in the rivaroxaban-treated and warfarin-treated groups. Conclusions Despite an increase in hospitalization, there were no differences in long-term stroke rates or survival following cardioversion or AF ablation. Outcomes were similar in patients treated with rivaroxaban or warfarin. (An Efficacy and Safety Study of Rivaroxaban With Warfarin for the Prevention of Stroke and Non-Central Nervous System Systemic Embolism in Patients With Non-Valvular Atrial Fibrillation [ROCKET AF]; NCT00403767) (C) 2013 by the American College of Cardiology Foundation

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