4.7 Article

Ticagrelor for Prevention of Ischemic Events After Myocardial Infarction in Patients With Peripheral Artery Disease

Journal

JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY
Volume 67, Issue 23, Pages 2719-2728

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.jacc.2016.03.524

Keywords

acute limb ischemia; major adverse cardiovascular events; major adverse limb events; peripheral arterial disease; ticagrelor

Funding

  1. AstraZeneca
  2. Merck
  3. Bayer
  4. Roche Diagnostics
  5. Amarin
  6. Bristol-Myers Squibb
  7. Eisai
  8. Ethicon
  9. Forest Laboratories
  10. Ischemix
  11. Medtronic
  12. Pfizer
  13. Roche
  14. Sanofi
  15. Medicines Company
  16. Aspen
  17. PlaqueTec
  18. Correvio
  19. Medscape
  20. Thermo Fisher Scientific
  21. Servier
  22. Janssen
  23. Maquet
  24. malpractice attorneys
  25. Bristol-Myers Squibb/Pfizer
  26. Boehringer Ingelheim
  27. Lilly
  28. Edwards Lifesciences
  29. Amgen
  30. GlaxoSmithKline
  31. Novartis
  32. Lilly/Daiichi-Sankyo
  33. DiscoveryHealth
  34. Daiichi-Sankyo
  35. Population Health Research Institute
  36. Brigham
  37. Women's Hospital from Abbott Laboratories
  38. Critical Diagnostics
  39. Gilead
  40. Intarcia
  41. Poxel
  42. Takeda

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BACKGROUND Peripheral artery disease (PAD) is associated with heightened ischemic and bleeding risk in patients with prior myocardial infarction (MI). OBJECTIVES This study evaluated the efficacy and safety of ticagrelor on major cardiovascular (CV) events and major adverse limb events in patients with PAD and a prior MI. METHODS 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) randomized 21,162 patients with prior MI (1 to 3 years) to ticagrelor 90 mg twice daily, ticagrelor 60 mg twice daily, or placebo, all on a background of low-dose aspirin. History of PAD was obtained at baseline. Occurrences of major adverse cardiovascular events (MACE) (defined as CV death, MI, or stroke) and major adverse limb events (MALE) (defined as acute limb ischemia or peripheral revascularization for ischemia) were recorded in follow-up. RESULTS A total of 1,143 patients (5%) had known PAD. In the placebo arm, those with PAD (n = 404) had higher rates of MACE at 3 years than those without (n = 6,663; 19.3% vs. 8.4%; p < 0.001), which persisted after adjusting for baseline differences (adjusted hazard ratio: 1.60; 95% confidence interval: 1.20 to 2.13; p = 0.0013), and higher rates of acute limb ischemia (1.0% vs. 0.1%) and peripheral revascularization procedures (9.15% vs. 0.46%). Whereas the relative risk reduction in MACE with ticagrelor was consistent, regardless of PAD, patients with PAD had a greater absolute risk reduction of 4.1% (number needed to treat: 25) due to their higher absolute risk. The absolute excess of TIMI major bleeding was 0.12% (number needed to harm: 834). The 60-mg dose had particularly favorable outcomes for CV and all-cause mortality. Ticagrelor (pooled doses) reduced the risk of MALE (hazard ratio: 0.65; 95% confidence interval: 0.44 to 0.95; p = 0.026). CONCLUSIONS Among stable patients with prior MI, those with concomitant PAD have heightened ischemic risk. In these patients, ticagrelor reduced MACE, with a large absolute risk reduction, and MALE. (Prevention of Cardiovascular Events in Patients With Prior Heart Attack Using Ticagrelor Compared to Placebo on a Background of Aspirin [PEGASUS-TIMI 54]; NCT01225562) (C) 2016 by the American College of Cardiology Foundation.

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