4.7 Article

Bridging Antiplatelet Therapy With Cangrelor in Patients Undergoing Cardiac Surgery A Randomized Controlled Trial

Journal

JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION
Volume 307, Issue 3, Pages 265-274

Publisher

AMER MEDICAL ASSOC
DOI: 10.1001/jama.2011.2002

Keywords

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Funding

  1. Bristol-Myers Squibb-sanofi-aventis
  2. Eli Lilly Co-Daiichi Sankyo
  3. Medicines Company
  4. Portola
  5. Novartis
  6. Medicure
  7. Accumetrics
  8. Arena Pharmaceuticals
  9. AstraZeneca
  10. Abbott Vascular
  11. GlaxoSmithKline
  12. Boston Scientific
  13. Otsuka
  14. Schering-Plough
  15. Johnson Johnson
  16. Eisai
  17. sanofi-aventis
  18. Quest Diagnostics
  19. Medtronic
  20. Cordis-Johnson Johnson
  21. Bayer Healthcare
  22. Bristol-Myers Squibb
  23. CardioMems
  24. Corindus
  25. Eli Lilly
  26. Foxhollow
  27. Genentech
  28. Regado Biosciences
  29. Stereotaxis
  30. IIT CSL Behring
  31. CSL Behring
  32. Bayer
  33. Boehringer Ingelheim
  34. Cardiovascular Research Foundation
  35. Cleveland Clinic Research Foundation
  36. Daiichi-Sankyo
  37. Duke Institute
  38. Europa
  39. Lead-Up
  40. Institut de Cardiologie de Montreal
  41. Menarini
  42. Nanosheres
  43. Pfizer
  44. TIMI Study Group
  45. Abbott Vascular AstraZeneca
  46. BMS
  47. Cordis
  48. Eli Lilly Federation Francaise de Cardiologie
  49. Fondation de France
  50. Guerbet Medical
  51. INSERM
  52. ITC Edison
  53. Servier
  54. Societe Francaise de Cardiologie
  55. Stago
  56. Guerbet Medical INSERM
  57. ITC Edison Medronic
  58. National Institutes of Health-National Center for Research Resources [UL1 RR025774]
  59. Eli Lilly-Daiichi Sankyo

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Context Thienopyridines are among the most widely prescribed medications, but their use can be complicated by the unanticipated need for surgery. Despite increased risk of thrombosis, guidelines recommend discontinuing thienopyridines 5 to 7 days prior to surgery to minimize bleeding. Objective To evaluate the use of cangrelor, an intravenous, reversible P2Y(12) platelet inhibitor for bridging thienopyridine-treated patients to coronary artery bypass grafting (CABG) surgery. Design, Setting, and Patients Prospective, randomized, double-blind, placebo-controlled, multicenter trial, involving 210 patients with an acute coronary syndrome (ACS) or treated with a coronary stent and receiving a thienopyridine awaiting CABG surgery to receive either cangrelor or placebo after an initial open-label, dose-finding phase (n=11) conducted between January 2009 and April 2011. Interventions Thienopyridines were stopped and patients were administered cangrelor or placebo for at least 48 hours, which was discontinued 1 to 6 hours before CABG surgery. Main Outcome Measures The primary efficacy end point was platelet reactivity (measured in P2Y(12) reaction units [PRUs]), assessed daily. The main safety end point was excessive CABG surgery-related bleeding. Results The dose of cangrelor determined in 10 patients in the open-label stage was 0.75 mu g/kg per minute. In the randomized phase, a greater proportion of patients treated with cangrelor had low levels of platelet reactivity throughout the entire treatment period compared with placebo (primary end point, PRU <240; 98.8% (83 of 84) vs 19.0% (16 of 84); relative risk [RR], 5.2 [95% CI, 3.3-8.1] P<.001). Excessive CABG surgery-related bleeding occurred in 11.8% (12 of 102) vs 10.4% (10 of 96) in the cangrelor and placebo groups, respectively (RR, 1.1 [95% CI, 0.5-2.5] P=.763). There were no significant differences in major bleeding prior to CABG surgery, although minor bleeding episodes were numerically higher with cangrelor. Conclusions Among patients who discontinue thienopyridine therapy prior to cardiac surgery, the use of cangrelor compared with placebo resulted in a higher rate of maintenance of platelet inhibition.

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