4.7 Article

Efficacy of apixaban when compared with warfarin in relation to renal function in patients with atrial fibrillation: insights from the ARISTOTLE trial

Journal

EUROPEAN HEART JOURNAL
Volume 33, Issue 22, Pages 2821-2830

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/eurheartj/ehs274

Keywords

Atrial fibrillation; Anticoagulation; Stroke prevention; Bleeding; Apixaban

Funding

  1. Bristol-Myers Squibb
  2. Pfizer
  3. BMS
  4. Sanofi-aventis
  5. Cardiome
  6. BI
  7. Johnson Johnson
  8. St Jude Medical
  9. Boehringer Ingelheim
  10. Merck/Schering-Plough
  11. Regado Biosciences
  12. AstraZeneca
  13. Ortho-McNeil-Janssen Pharmaceuticals
  14. PolyMedix
  15. Bayer
  16. DaiichiSankyo
  17. Bristol-Myers Squibb/Pfizer
  18. Astellas
  19. GlaxoSmithKline
  20. Medtronic foundation
  21. Merck
  22. Medicine's Company
  23. Lilly
  24. Hoffman-La Roche
  25. Novartis
  26. Otsuka
  27. Schering-Plough
  28. Medtronic

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Atrial fibrillation (AF) is common among patients with impaired renal function. Apixaban, a novel oral anticoagulant with partial renal excretion, was compared with warfarin and reduced the rate stroke, death and bleeding in the ARISTOTLE trial. We evaluated these outcomes in relation to renal function. Baseline glomerular filtration rate (GFR) was estimated using the CockcroftGault and Chronic Kidney Disease Epidemiology Collaboration (CKD-EPI) equations as well as cystatin C measurements. According to baseline CockcroftGault, there were 7518 patients (42) with an estimated GFR (eGFR) of 80 mL/min, 7587 (42) between 50 and 80 mL/min, and 3017 (15) with an eGFR of 50 mL/min. The rate of cardiovascular events and bleeding was higher at impaired renal function (80 mL/min). Apixaban was more effective than warfarin in preventing stroke or systemic embolism and reducing mortality irrespective of renal function. These results were consistent, regardless of methods for GFR estimation. Apixaban was associated with less major bleeding events across all ranges of eGFRs. The relative risk reduction in major bleeding was greater in patients with an eGFR of 50 mL/min using CockcroftGault {hazard ratio (HR) 0.50 [95 confidence interval (CI) 0.380.66], interaction P 0.005} or CKD-EPI equations [HR 0.48 (95 CI 0.370.64), interaction P 0.003]. In patients with AF, renal impairment was associated with increased risk of cardiovascular events and bleeding. When compared with warfarin, apixaban treatment reduced the rate of stroke, death, and major bleeding, regardless of renal function. Patients with impaired renal function seemed to have the greatest reduction in major bleeding with apixaban.

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