4.6 Article

D-dimer and risk of thromboembolic and bleeding events in patients with atrial fibrillation - observations from the ARISTOTLE trial

期刊

JOURNAL OF THROMBOSIS AND HAEMOSTASIS
卷 12, 期 9, 页码 1401-1412

出版社

WILEY
DOI: 10.1111/jth.12638

关键词

apixaban; atrial fibrillation; D-dimer; risk assessment; warfarin

资金

  1. Medtronic. Inc.
  2. Baxter Healthcare Corporation
  3. Cardiovascular Research Foundation
  4. Merck Co. Inc.
  5. St Jude Medical
  6. Ortho-McNeil Janssen Scientific Affairs
  7. TEVA Pharmaceuticals
  8. Boston Scientific
  9. Bristol Myers Squibb
  10. Pfizer
  11. Daiichi
  12. Boehringer Ingelheim
  13. Janssen
  14. Glaxo SmithKline
  15. Sanofi-Aventis
  16. Takeda
  17. Medicine's Company
  18. Hoffmann-La Roche
  19. Lilly
  20. Ross Medical Corporation
  21. Salix Pharmaceuticals
  22. Astra Zeneca
  23. Medtronic Foundation
  24. Merck Co.
  25. Bayer
  26. Daiichi Sankyo
  27. Roche
  28. Bristol-Myers Squibb
  29. Ortho-McNeil-Janssen
  30. Abbott
  31. Athera Biotechnologies
  32. Regado Biosciences
  33. UCR

向作者/读者索取更多资源

BackgroundD-dimer is related to adverse outcomes in arterial and venous thromboembolic diseases. ObjectivesTo evaluate the predictive value of D-dimer level for stroke, other cardiovascular events, and bleeds, in patients with atrial fibrillation (AF) treated with oral anticoagulation with apixaban or warfarin; and to evaluate the relationship between the D-dimer levels at baseline and the treatment effect of apixaban vs. warfarin. MethodsIn the ARISTOTLE trial, 18201 patients with AF were randomized to apixaban or warfarin. D-dimer was analyzed in 14878 patients at randomization. The cohort was separated into two groups; not receiving vitaminK antagonist (VKA) treatment and receiving VKA treatment at randomization. ResultsHigher D-dimer levels were associated with increased frequencies of stroke or systemic embolism (hazard ratio [HR][Q4 vs. Q1]1.72, 95% confidence interval [CI]1.14-2.59, P=0.003), death (HR[Q4 vs. Q1]4.04, 95%CI3.06-5.33) and major bleeding (HR[Q4 vs. Q1]2.47, 95%CI1.77-3.45, P<0.0001) in the no-VKA group. Similar results were obtained in the on-VKA group. Adding D-dimer level to the CHADS(2) score improved the C-index from 0.646 to 0.655 for stroke or systemic embolism, and from 0.598 to 0.662 for death, in the no-VKA group. D-dimer level improved the HAS-BLED score for prediction of major bleeds, with an increase in the C-index from 0.610 to 0.641. There were no significant interactions between efficacy and safety of study treatment and D-dimer level. ConclusionIn anticoagulated patients with AF, the level of D-dimer is related to the risk of stroke, death, and bleeding, and adds to the predictive value of clinical risk scores. The benefits of apixaban were consistent, regardless of the baseline D-dimer level.

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