Progress in platelet blockers: the target is the P2Y12 receptor

J Cardiothorac Vasc Anesth. 2013 Jun;27(3):620-4. doi: 10.1053/j.jvca.2013.01.008.

Abstract

The considerable progress in P2Y12-platelet blockers has important perioperative implications due to a family of novel agents beyond clopidogrel. Although prasugrel is more potent than clopidogrel due to more efficient hepatic metabolism, it is limited clinically by its irreversibility and bleeding risks. Ticagrelor, as the first approved direct and reversible oral P2Y12 blocker, still is limited clinically by its novel side-effect profile. Intravenous reversible P2Y12 blockade is possible now with both cangrelor and elinogrel, although both agents are still in clinical development. Furthermore, elinogrel offers the possibility of both oral and parenteral P2Y12 blockade with a single agent. Future trials likely will continue to evaluate and compare the safety and efficacy of these agents in multiple clinical settings, including the perioperative period.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Adenosine / analogs & derivatives
  • Adenosine / pharmacology
  • Adenosine Monophosphate / analogs & derivatives
  • Adenosine Monophosphate / pharmacology
  • Humans
  • Perioperative Care
  • Piperazines / pharmacology
  • Platelet Aggregation Inhibitors / pharmacology*
  • Prasugrel Hydrochloride
  • Purinergic P2Y Receptor Antagonists / pharmacology*
  • Quinazolinones / pharmacology
  • Receptors, Purinergic P2Y12 / drug effects*
  • Sulfonamides / pharmacology
  • Thiophenes / pharmacology
  • Ticagrelor

Substances

  • Piperazines
  • Platelet Aggregation Inhibitors
  • Purinergic P2Y Receptor Antagonists
  • Quinazolinones
  • Receptors, Purinergic P2Y12
  • Sulfonamides
  • Thiophenes
  • Adenosine Monophosphate
  • cangrelor
  • elinogrel
  • Prasugrel Hydrochloride
  • Ticagrelor
  • Adenosine