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本文引用的文献

1
Eptifibatide induced profound thrombocytopenia in a patient with pelvic malignancy: A case report.依替巴肽致一名盆腔恶性肿瘤患者严重血小板减少症:病例报告
Gynecol Oncol Case Rep. 2012 Mar 14;2(3):75-7. doi: 10.1016/j.gynor.2012.03.002. eCollection 2012.
2
Eptifibatide-Induced Thrombocytopenia--When Inhibitor Turns Killer.依替巴肽诱导的血小板减少症——当抑制剂变成杀手时。
Am J Ther. 2016 Jan-Feb;23(1):e298-9. doi: 10.1097/01.mjt.0000438283.01797.1a.
3
Established and new-generation antithrombotic drugs in patients with cirrhosis - possibilities and caveats.肝硬化患者的传统及新型抗血栓药物——可能性与注意事项。
J Hepatol. 2013 Aug;59(2):358-66. doi: 10.1016/j.jhep.2013.03.027. Epub 2013 Mar 30.
4
Eptifibatide-induced thrombocytopenia: with thrombosis and disseminated intravascular coagulation immediately after left main coronary artery percutaneous coronary angioplasty.依替巴肽诱导的血小板减少症:在左主干冠状动脉经皮冠状动脉介入治疗后立即出现血栓形成和弥散性血管内凝血。
Tex Heart Inst J. 2012;39(1):86-91.
5
Coronary artery stents and antiplatelet therapy in patients with cirrhosis.肝硬化患者的冠状动脉支架和抗血小板治疗。
J Clin Gastroenterol. 2012 Apr;46(4):339-44. doi: 10.1097/MCG.0b013e3182371258.
6
Profound thrombocytopenia after primary exposure to eptifibatide.初次接触依替巴肽后出现严重血小板减少症。
Drug Healthc Patient Saf. 2010;2:163-7. doi: 10.2147/DHPS.S13239. Epub 2010 Sep 21.
7
Acute profound thrombocytopenia following eptifibatide administration.依替巴肽给药后出现急性严重血小板减少症。
South Med J. 2010 Jun;103(6):596-7. doi: 10.1097/SMJ.0b013e3181de0cca.
8
Acute profound thrombocytopenia associated with readministration of eptifibatide: case report and review of the literature.依替巴肽再次给药相关的急性严重血小板减少症:病例报告及文献综述
Pharmacotherapy. 2009 Jul;29(7):867-74. doi: 10.1592/phco.29.7.867.
9
Acute profound thrombocytopenia with second exposure to eptifibatide associated with a strong antibody reaction.再次使用依替巴肽后出现急性严重血小板减少症,并伴有强烈的抗体反应。
Platelets. 2009 Feb;20(1):64-7. doi: 10.1080/09537100802592676.
10
Immune thrombocytopenia caused by glycoprotein IIb/IIIa inhibitors.糖蛋白IIb/IIIa抑制剂所致免疫性血小板减少症。
Chest. 2005 Feb;127(2 Suppl):53S-59S. doi: 10.1378/chest.127.2_suppl.53S.

依替巴肽与肝硬化:重新审视用于肝功能不全背景下急性冠脉综合征的糖蛋白IIb-IIIa抑制剂

Eptifibatide and Cirrhosis: Rethinking GPIIb-IIIa Inhibitors for Acute Coronary Syndrome in the Setting of Liver Dysfunction.

作者信息

Weinreich Michael, Mendoza Dexter, Pettei Thomas, Grayver Evelina

机构信息

Department of Medicine, North Shore Long Island Jewish Health System/Hofstra University School of Medicine, Manhasset, NY, USA.

Department of Cardiology, North Shore Long Island Jewish Health System/Hofstra University School of Medicine, Manhasset, NY, USA.

出版信息

Cardiol Res. 2014 Dec;5(6):191-194. doi: 10.14740/cr357w. Epub 2014 Dec 4.

DOI:10.14740/cr357w
PMID:28352453
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5358269/
Abstract

Glycoprotein IIb/IIIa (GPIIb/IIIa) inhibitors, such as eptifibatide, are routinely used in the setting of acute coronary syndrome (ACS) prior to or during percutaneous coronary intervention (PCI). While numerous studies have demonstrated improved clinical outcomes with eptifibatide use, adverse effects including thrombocytopenia have also been noted. For this reason, patients with baseline thrombocytopenia or liver disease should be cautiously evaluated prior to drug administration. Here we report a case of acute profound and prolonged eptifibatide-induced thrombocytopenia in a patient with cirrhotic liver dysfunction. We propose and discuss the need for a risk stratification tool to be established for identifying which patients with ACS in the setting of chronic liver disease receive GPIIb/IIIa inhibitors.

摘要

糖蛋白IIb/IIIa(GPIIb/IIIa)抑制剂,如依替巴肽,在经皮冠状动脉介入治疗(PCI)之前或期间常用于急性冠状动脉综合征(ACS)的治疗。虽然大量研究表明使用依替巴肽可改善临床结局,但也有包括血小板减少在内的不良反应的报道。因此,在给药前应谨慎评估基线血小板减少或患有肝病的患者。在此,我们报告1例肝硬化肝功能不全患者发生急性、严重且持续时间较长的依替巴肽诱导的血小板减少症的病例。我们提出并讨论了需要建立一种风险分层工具,以识别哪些慢性肝病背景下的ACS患者可接受GPIIb/IIIa抑制剂治疗。