4.7 Article

Reduction in Ischemic Events With Ticagrelor in Diabetic Patients With Prior Myocardial Infarction in PEGASUS-TIMI 54

期刊

JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY
卷 67, 期 23, 页码 2732-2740

出版社

ELSEVIER SCIENCE INC
DOI: 10.1016/j.jacc.2016.03.529

关键词

acute coronary syndrome; dual antiplatelet therapy; myocardial infarction; platelets

资金

  1. AstraZeneca
  2. Amarin
  3. Bristol-Myers Squibb
  4. Eisai
  5. Ethicon
  6. Forest Laboratories
  7. Ischemix
  8. Medtronic
  9. Pfizer
  10. Roche
  11. Sanofi
  12. Medicines Company
  13. Merck
  14. Bayer
  15. Roche Diagnostics
  16. Eli Lilly
  17. Daiichi-Sankyo
  18. Abbott Vascular
  19. PLx Pharma
  20. GlaxoSmithKline
  21. Janssen Pharmaceuticals, Inc.
  22. Osprey Medical, Inc.
  23. Novartis
  24. CSL Behring
  25. Gilead
  26. Aspen
  27. Correvio
  28. PlaqueTec
  29. Thermo Fisher Scientific
  30. Brigham and Women's Hospital from AstraZeneca
  31. Brigham and Women's Hospital from Abbott Laboratories
  32. Amgen
  33. Critical Diagnostics
  34. Intarcia
  35. Poxel
  36. Takeda
  37. Alnylam
  38. CVS Caremark
  39. Servier
  40. Boehringer Ingelheim
  41. Lilly
  42. Janssen
  43. Regeneron

向作者/读者索取更多资源

BACKGROUND Patients with diabetes appear to be at elevated risk of atherothrombotic events. OBJECTIVES The purpose of this study was to determine the effect of antiplatelet therapy with ticagrelor on recurrent ischemic events in patients with diabetes and prior myocardial infarction (MI). METHODS We examined the subgroups of patients with diabetes (n = 6,806) and without diabetes (n = 14,355) from PEGASUS-TIMI 54 (Prevention of Cardiovascular Events in Patients With Prior Heart Attack Using Ticagrelor Compared to Placebo on a Background of Aspirin-Thrombolysis In Myocardial Infarction 54), in which 21,162 patients with a history of MI 1 to 3 years prior and with additional risk factors were randomized to ticagrelor (90 or 60 mg twice daily) or placebo. Patients were followed for a median of 33 months. The primary efficacy endpoint was major adverse cardiovascular events (MACE) (cardiovascular death, MI, stroke) and the primary safety endpoint was TIMI (Thrombolysis In Myocardial Infarction) major bleeding. RESULTS The relative risk reduction in MACE with ticagrelor was consistent for the pooled doses versus placebo in patients with diabetes (hazard ratio [HR]: 0.84; 95% confidence interval [CI]: 0.72 to 0.99; p = 0.035) and without diabetes (HR: 0.84; 95% CI: 0.74 to 0.96; p = 0.013; p interaction = 0.99). As patients with diabetes were at higher risk of MACE, the absolute risk reduction tended to be greater in patients with versus without diabetes (1.5% vs. 1.1%, with corresponding 3-year number needed to treat of 67 vs. 91). In patients with diabetes requiring pharmacological therapy (n = 5,960), the absolute risk reduction was 1.9% with a 3-year number needed to treat of 53. Additionally, in patients with diabetes, ticagrelor reduced cardiovascular death by 22% and coronary heart disease death by 34%. Similar to patients without diabetes, there was increased TIMI major bleeding in patients with diabetes (HR: 2.56; 95% CI: 1.52 to 4.33; p = 0.0004). CONCLUSIONS In patients with diabetes with prior MI, adding ticagrelor to aspirin significantly reduces the risk of recurrent ischemic events, including cardiovascular and coronary heart disease death. (C) 2016 by the American College of Cardiology Foundation.

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