4.8 Article

International Expert Consensus on Switching Platelet P2Y12 Receptor-Inhibiting Therapies

Journal

CIRCULATION
Volume 136, Issue 20, Pages 1955-+

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1161/CIRCULATIONAHA.117.031164

Keywords

drug interactions; hemorrhage; pharmacodynamics; platelet aggregation inhibitors; P2Y(12) receptor inhibitors; thrombosis

Funding

  1. Amgen
  2. Aralez
  3. AstraZeneca
  4. Bayer
  5. Biosensors
  6. Chiesi
  7. Daiichi-Sankyo
  8. Eli Lilly
  9. Janssen
  10. Merck
  11. PLx Pharma
  12. Pfizer
  13. Sanofi
  14. Medicines Company
  15. CeloNova
  16. St. Jude Medical
  17. CSL Behring
  18. Eisai
  19. Eli-Lilly
  20. Gilead
  21. Matsutani Chemical Industry Co
  22. Novartis
  23. Osprey Medical
  24. Renal Guard Solutions
  25. Scott R. MacKenzie Foundation
  26. National Institutes of Health/National Center for Advancing Translational Sciences [UL1 TR000064]
  27. National Institutes of Health/NHGRI [U01 HG007269]
  28. DSI/Lilly
  29. Roche Diagnostics
  30. Bayer AG
  31. MSD Pharma
  32. Amarin
  33. Bristol-Myers Squibb
  34. Ethicon
  35. Forest Laboratories
  36. Ironwood
  37. Ischemix
  38. Lilly
  39. Medtronic
  40. Roche
  41. Sanofi Aventis
  42. Boston
  43. Abbott
  44. Boston Scientific
  45. Biotronik
  46. Sanofi-Aventis
  47. Terumo
  48. Abbott Vascular
  49. Aspen
  50. Boehringer-Ingelheim
  51. Daiichi Sankyo
  52. Pharmevo
  53. Menarini
  54. Haemonetics
  55. DCRI
  56. Medicure
  57. National Institutes of Health
  58. Medimmune
  59. Coramed
  60. Boehringer
  61. UptoDate
  62. Boehringer Ingelheim
  63. BMS
  64. Lilly/Daiichi Sankyo
  65. Covidien
  66. Janssen (J+J)
  67. Actelion
  68. Beth Israel Deaconess Medical
  69. Brigham Women's Hospital
  70. Cardiovascular Research Foundation
  71. CCC
  72. Celladon
  73. CME Resources
  74. Europa
  75. Elsevier
  76. Federation Francaise de Cardiologie
  77. ICAN
  78. INSERM
  79. Lead-Up
  80. MSD
  81. Servier
  82. Janssen Pharmaceuticals
  83. Bayer Vital
  84. Astra Zeneca Canada
  85. PlaqueTec
  86. Avacta
  87. Bristol Myers Squibb/Pfizer
  88. ThermoFisher Scientific
  89. Berlin Chemie
  90. Boehringer Ingelheim KG
  91. Bristol Myers Squibb
  92. Terumo Medical
  93. Cordis
  94. Biotronik AG
  95. Medtronic Vascular
  96. Med Alliance
  97. Volcano Philips
  98. Gilead Sciences
  99. Regeneron
  100. TIMI Study Group
  101. WebMD

Ask authors/readers for more resources

Dual antiplatelet therapy with aspirin and a P2Y(12) inhibitor is the treatment of choice for the prevention of atherothrombotic events in patients with acute coronary syndromes and for those undergoing percutaneous coronary interventions. The availability of different oral P2Y(12) inhibitors (clopidogrel, prasugrel, ticagrelor) has enabled physicians to contemplate switching among therapies because of specific clinical scenarios. The recent introduction of an intravenous P2Y(12) inhibitor (cangrelor) further adds to the multitude of modalities and settings in which switching therapies may occur. In clinical practice, it is not uncommon to switch P2Y(12) inhibitor, and switching may be attributed to a variety of factors. However, concerns about the safety of switching between these agents have emerged. Practice guidelines have not fully elaborated on how to switch therapies, leaving clinicians with limited guidance on when and how to switch therapies when needed. This prompted the development of this expert consensus document by key leaders from North America and Europe with expertise in basic, translational, and clinical sciences in the field of antiplatelet therapy. This expert consensus provides an overview of the pharmacology of P2Y(12) inhibitors, different modalities and definitions of switching, and available literature and recommendations for switching between P2Y(12) inhibitors.

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