Vorapaxar

Antiplatelet drugs are the cornerstone of treatment for patients with acute coronary syndromes (ACS) undergoing percutaneous coronary intervention. Clopidogrel and aspirin improve long-term vascular clinical outcomes in these patients and have become a standard of care. However, many patients still...

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Main Authors: Gianluca Airoldi, Mauro Campanini
Format: Article
Language:English
Published: PAGEPress Publications 2013-04-01
Series:Italian Journal of Medicine
Subjects:
Online Access:http://www.italjmed.org/index.php/ijm/article/view/161
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spelling doaj-f613fa842711497b8bb2a5e297017a0c2020-11-25T03:55:53ZengPAGEPress PublicationsItalian Journal of Medicine1877-93441877-93522013-04-0172889510.4081/itjm.2013.88131VorapaxarGianluca Airoldi0Mauro Campanini1ASL NO, SC Medicina Generale, NovaraAOU Maggiore della Carità di Novara, SCDO Medicina Generale, NovaraAntiplatelet drugs are the cornerstone of treatment for patients with acute coronary syndromes (ACS) undergoing percutaneous coronary intervention. Clopidogrel and aspirin improve long-term vascular clinical outcomes in these patients and have become a standard of care. However, many patients still experience ischemic/thrombotic events, and it appears that insufficient response to both aspirin and clopidogrel contribute to this failure. Newer P2Y12 receptor blocker therapy resulted in only an approximately 2% reduction in absolute risk compared with clopidogrel. This indicates that residual ischemic events are mediated by other pathways that are unblocked by current dual antiplatelet therapy. Thrombin is the most potent platelet agonist (over 1000 times more than adenosine diphosphate on a molar basis). Thrombin-mediated platelet activation depends on proteaseactivated receptor (PAR) binding. PAR-1 is the main receptor for thrombin on human platelets; PAR-4 may contribute to platelet activation at much higher concentrations of thrombin. Inhibition of the PAR-1 may provide additional benefits over the standard dual antiplatelet therapy in attenuating ischemic event in patients with ACS. Vorapaxar is a new highly selective oral PAR-1 antagonist that inhibits thrombin-induced platelet activation. We review the pharmacokinetic, pharmacodynamic and clinical profile of vorapaxar. Although preliminary data indicated that vorapaxar may have the potential to improve ischemic outcomes without significantly increasing bleeding, more recent larger clinical trials seem to be less optimistic about both its effectiveness and safety. At this time, the role of vorapaxar in the settings of atherothrombotic disorders is not clear. Although it may be associated with less bleeding than P2Y12 receptor blockers, its antithrombotic effectiveness and side effects are major concerns.http://www.italjmed.org/index.php/ijm/article/view/161vorapaxar, ticagrelor, prasugrel, clopidogrel, aspirin, antiplatelet drug, acute coronary syndrome, percutaneous coronary intervention.
collection DOAJ
language English
format Article
sources DOAJ
author Gianluca Airoldi
Mauro Campanini
spellingShingle Gianluca Airoldi
Mauro Campanini
Vorapaxar
Italian Journal of Medicine
vorapaxar, ticagrelor, prasugrel, clopidogrel, aspirin, antiplatelet drug, acute coronary syndrome, percutaneous coronary intervention.
author_facet Gianluca Airoldi
Mauro Campanini
author_sort Gianluca Airoldi
title Vorapaxar
title_short Vorapaxar
title_full Vorapaxar
title_fullStr Vorapaxar
title_full_unstemmed Vorapaxar
title_sort vorapaxar
publisher PAGEPress Publications
series Italian Journal of Medicine
issn 1877-9344
1877-9352
publishDate 2013-04-01
description Antiplatelet drugs are the cornerstone of treatment for patients with acute coronary syndromes (ACS) undergoing percutaneous coronary intervention. Clopidogrel and aspirin improve long-term vascular clinical outcomes in these patients and have become a standard of care. However, many patients still experience ischemic/thrombotic events, and it appears that insufficient response to both aspirin and clopidogrel contribute to this failure. Newer P2Y12 receptor blocker therapy resulted in only an approximately 2% reduction in absolute risk compared with clopidogrel. This indicates that residual ischemic events are mediated by other pathways that are unblocked by current dual antiplatelet therapy. Thrombin is the most potent platelet agonist (over 1000 times more than adenosine diphosphate on a molar basis). Thrombin-mediated platelet activation depends on proteaseactivated receptor (PAR) binding. PAR-1 is the main receptor for thrombin on human platelets; PAR-4 may contribute to platelet activation at much higher concentrations of thrombin. Inhibition of the PAR-1 may provide additional benefits over the standard dual antiplatelet therapy in attenuating ischemic event in patients with ACS. Vorapaxar is a new highly selective oral PAR-1 antagonist that inhibits thrombin-induced platelet activation. We review the pharmacokinetic, pharmacodynamic and clinical profile of vorapaxar. Although preliminary data indicated that vorapaxar may have the potential to improve ischemic outcomes without significantly increasing bleeding, more recent larger clinical trials seem to be less optimistic about both its effectiveness and safety. At this time, the role of vorapaxar in the settings of atherothrombotic disorders is not clear. Although it may be associated with less bleeding than P2Y12 receptor blockers, its antithrombotic effectiveness and side effects are major concerns.
topic vorapaxar, ticagrelor, prasugrel, clopidogrel, aspirin, antiplatelet drug, acute coronary syndrome, percutaneous coronary intervention.
url http://www.italjmed.org/index.php/ijm/article/view/161
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