4.4 Article

Effects of Ranolazine in Patients With Chronic Angina in Patients With and Without Percutaneous Coronary Intervention for Acute Coronary Syndrome: Observations From the MERLIN-TIMI 36 Trial

Journal

CLINICAL CARDIOLOGY
Volume 38, Issue 8, Pages 469-475

Publisher

WILEY
DOI: 10.1002/clc.22425

Keywords

-

Funding

  1. Boehringer Ingelheim
  2. TIMI Study Group
  3. Brigham and Women's Hospital from AstraZeneca
  4. Bristol-Myers Squibb
  5. Daiichi-Sankyo
  6. GlaxoSmithKline
  7. Johnson and Johnson
  8. Bayer Healthcare
  9. Gilead
  10. Eisai
  11. Merck
  12. Brigham and Women's Hospital from Accumetrics
  13. Amgen
  14. AstraZeneca
  15. Beckman Coulter
  16. CV Therapeutics
  17. Daiichi Sankyo Co Ltd
  18. Eli Lilly and Co
  19. Integrated Therapeutics
  20. Merck and Co
  21. Nanosphere
  22. Novartis Pharmaceuticals
  23. Nuvelo
  24. Ortho-Clinical Diagnostics
  25. Pfizer
  26. Roche Diagnostics
  27. Sanofi-Aventis
  28. Sanofi-Synthelabo
  29. Siemens Medical Solutions
  30. Singulex
  31. Abbott Laboratories
  32. Daiichi Sankyo
  33. diaDexus
  34. Instrumentation Laboratory
  35. Konica Minolta
  36. Novartis
  37. TIMI Study
  38. Arena
  39. Boston Clinical Research Institute
  40. Covance
  41. Elsevier Practice Update Cardiology
  42. Forest Pharmaceuticals
  43. GE Healthcare
  44. Lexicon
  45. St. Jude's Medical
  46. University of Calgary

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BackgroundRanolazine, a piperazine derivative with anti-ischemic effects, reduces the frequency of angina and improves exercise performance in patients with chronic angina. The effects of ranolazine in patients with established ischemic heart disease and chronic angina undergoing percutaneous coronary intervention (PCI) for acute coronary syndromes (ACS) is not well described. We hypothesized that ranolazine would reduce ischemic events, regardless of revascularization. MethodsWe examined the 1-year incidence of recurrent cardiovascular (CV) events in the subgroup of patients with prior chronic angina (n=3565) enrolled in the randomized, double-blind, placebo-controlled Metabolic Efficiency with Ranolazine for Less Ischemia in Non-ST-Elevation ACS (MERLIN)-Thrombolysis In Myocardial Infarction (TIMI) 36 trial who did or did not have a PCI within 30 days of the index event. ResultsRanolazine reduced the risk of recurrent ischemia following admission regardless of whether patients had (hazard ratio [HR], 0.69; 95% confidence interval [CI] 0.51-0.92] or did not have PCI (HR, 0.81; 95% CI, 0.66-0.99; P interaction=0.39). CV death, myocardial infarction, and recurrent ischemia were similarly lower with ranolazine in the PCI group (HR, 0.71; 95% CI, 0.55-0.91) vs the non-PCI group (HR, 0.91; 95% CI, 0.78-1.06; P interaction=0.10), with a nominally significant decrease in CV death (HR, 0.39; 95% CI, 0.16-0.93) in the PCI group vs no difference in the non-PCI group (HR, 1.19; 95% CI, 0.89-1.59; P interaction=0.02). ConclusionsIn patients with chronic angina, ranolazine reduced recurrent ischemic events, regardless of whether patients did or did not receive PCI within 30 days of a non-ST-segment ACS.

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