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Profound thrombocytopenia after primary exposure to eptifibatide

Eptifibatide is a glycoprotein IIb/IIIa receptor antagonist used to reduce the incidence of ischemic events in patients with acute coronary syndromes and those undergoing percutaneous coronary intervention. A minority of patients given eptifibatide develop acute, profound thrombocytopenia (<20,00...

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Detalles Bibliográficos
Autores principales: Norgard, Nicholas B, Badgley, Brian T
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3108691/
https://www.ncbi.nlm.nih.gov/pubmed/21701628
http://dx.doi.org/10.2147/DHPS.S13239
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author Norgard, Nicholas B
Badgley, Brian T
author_facet Norgard, Nicholas B
Badgley, Brian T
author_sort Norgard, Nicholas B
collection PubMed
description Eptifibatide is a glycoprotein IIb/IIIa receptor antagonist used to reduce the incidence of ischemic events in patients with acute coronary syndromes and those undergoing percutaneous coronary intervention. A minority of patients given eptifibatide develop acute, profound thrombocytopenia (<20,000 cells/mm(3)) within a few hours of receiving the drug. This case report discusses a patient who developed profound thrombocytopenia within hours of receiving eptifibatide for the first time. The Naranjo algorithm classified the likelihood that this patient’s thrombocytopenia was related to eptifibatide as probable. Profound thrombocytopenia is an uncommon but clinically important complication of eptifibatide. This case report emphasizes the importance of monitoring platelet counts routinely at baseline and within 2–6 hours of eptifibatide administration.
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spelling pubmed-31086912011-06-23 Profound thrombocytopenia after primary exposure to eptifibatide Norgard, Nicholas B Badgley, Brian T Drug Healthc Patient Saf Case Report Eptifibatide is a glycoprotein IIb/IIIa receptor antagonist used to reduce the incidence of ischemic events in patients with acute coronary syndromes and those undergoing percutaneous coronary intervention. A minority of patients given eptifibatide develop acute, profound thrombocytopenia (<20,000 cells/mm(3)) within a few hours of receiving the drug. This case report discusses a patient who developed profound thrombocytopenia within hours of receiving eptifibatide for the first time. The Naranjo algorithm classified the likelihood that this patient’s thrombocytopenia was related to eptifibatide as probable. Profound thrombocytopenia is an uncommon but clinically important complication of eptifibatide. This case report emphasizes the importance of monitoring platelet counts routinely at baseline and within 2–6 hours of eptifibatide administration. Dove Medical Press 2010-09-21 /pmc/articles/PMC3108691/ /pubmed/21701628 http://dx.doi.org/10.2147/DHPS.S13239 Text en © 2010 Norgard and Badgley, publisher and licensee Dove Medical Press Ltd. This is an Open Access article which permits unrestricted noncommercial use, provided the original work is properly cited.
spellingShingle Case Report
Norgard, Nicholas B
Badgley, Brian T
Profound thrombocytopenia after primary exposure to eptifibatide
title Profound thrombocytopenia after primary exposure to eptifibatide
title_full Profound thrombocytopenia after primary exposure to eptifibatide
title_fullStr Profound thrombocytopenia after primary exposure to eptifibatide
title_full_unstemmed Profound thrombocytopenia after primary exposure to eptifibatide
title_short Profound thrombocytopenia after primary exposure to eptifibatide
title_sort profound thrombocytopenia after primary exposure to eptifibatide
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3108691/
https://www.ncbi.nlm.nih.gov/pubmed/21701628
http://dx.doi.org/10.2147/DHPS.S13239
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