Weinreich Michael, Mendoza Dexter, Pettei Thomas, Grayver Evelina
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.
Cardiol Res. 2014 Dec;5(6):191-194. doi: 10.14740/cr357w. Epub 2014 Dec 4.
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.
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。