4.4 Article

Impact of Switching From a Vitamin K Antagonist to Rivaroxaban on Satisfaction With Anticoagulation Therapy: The XANTUS-ACTS Substudy

期刊

CLINICAL CARDIOLOGY
卷 39, 期 10, 页码 565-569

出版社

WILEY
DOI: 10.1002/clc.22565

关键词

-

资金

  1. Bayer HealthCare Pharmaceuticals
  2. Bayer Pharma AG
  3. Janssen Scientific Affairs
  4. Boehringer Ingelheim Pharmaceuticals Inc.
  5. Daiichi Sankyo Company
  6. Portola Pharmaceuticals
  7. Janssen Research & Development, LLC
  8. 3M Medica
  9. MEDA Pharma
  10. AstraZeneca
  11. Bayer HealthCare
  12. Biosense Webster
  13. Boehringer Ingelheim
  14. Daiichi Sankyo
  15. German Cardiac Society
  16. Medtronic
  17. Merck
  18. MSD
  19. Otsuka Pharma
  20. Pfizer/Bristol-Myers Squibb
  21. Sanofi
  22. Servier
  23. Siemens
  24. Takeda
  25. British Heart Foundation [FS/13/43/30324] Funding Source: researchfish

向作者/读者索取更多资源

Background: The efficacy, safety, and ease of use of rivaroxaban may reduce anticoagulation-treatment burden and improve nonvalvular atrial fibrillation (NVAF) patient satisfaction compared with vitamin K antagonists (VKAs). Hypothesis: Transitioning from a VKA to rivaroxaban improves treatment satisfaction in routine practice. Methods: Xarelto for Prevention of Stroke in Patients With Atrial Fibrillation (XANTUS) is a prospective, noninterventional study in patients with NVAF prescribed rivaroxaban for prevention of stroke in routine practice. Patients receiving a VKA 4 weeks prior to the initial XANTUS study visit and switched to rivaroxaban were asked to complete the Anti-Clot Treatment Scale (ACTS). Changes from the initial visit to the first follow-up visit at similar to 3 months (corresponding to a comparison of rivaroxaban vs prior VKA) for ACTS burden and benefit scores were calculated using and reported as least squared mean differences (LSMDs) with 95% confidence intervals (CIs). Results: The study included 1291 NVAF patients with prior VKA treatment. The mean baseline ACTS burden and benefit scores were 50.51+/-8.42 and 10.30+/-2.70, respectively. After similar to 3 months of rivaroxaban treatment, LSMDs were 4.38 points (95% CI: 2.53-6.22, P < 0.0001) for the burden and 1.01 points (95% CI: 0.27-1.75, P = 0.0075) for the benefit score. Fifty-four percent and 48% of patients reported experiencing at least a minimally important clinical difference in burden and benefit scores, respectively. Conclusions: Within this XANTUS cohort, switching from a VKA to rivaroxaban yielded statistically and clinically significant improvements in ACT burden and benefit scores.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.4
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据