Eptifibatide-induced acute profound thrombocytopenia in a patient with left main artery plaque rupture complicated by cardiogenic shock and gastrointestinal bleeding

S. Nandal, W. van Gaal, F. Ponnuthurai
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引用次数: 0

Abstract

Eptifibatide inhibits platelet aggregation by reversibly binding to the platelet receptor glycoprotein (GP) IIb/IIIa of human platelets, thus preventing the binding of fibrinogen and adhesion proteins such as fibronectin, vitronectin, and von Willebrand factor to form cross bridges with adjacent platelets. There are two other GP IIb/IIIa inhibitors, namely abciximab and tirofiban, available for clinical use. Profound thrombocytopenia is an uncommon but clinically important complication of GP IIb/IIIa inhibitors. This case discusses a 64-year-old male patient who developed profound thrombocytopenia within 4 h of first administration of eptifibatide. This report adds a case of eptifibatide-induced thrombocytopenia complicated by gastrointestinal bleeding to the medical literature. It highlights the need for complex decision-making regarding cessation of antiplatelet therapy in patients with recent percutaneous coronary intervention and the lack of robust evidence for the benefit of GP IIb/IIIa inhibitors in the ticagrelor era when compared to clopidogrel and aspirin.
Eptifibatide诱导左大动脉斑块破裂并发心源性休克和胃肠道出血的急性严重血小板减少症
Eptifibatide通过与人血小板的血小板受体糖蛋白(GP) IIb/IIIa可逆结合,抑制血小板聚集,从而阻止纤维蛋白原与纤维连接蛋白、玻璃体连接蛋白、血管性血友病因子等黏附蛋白结合,与邻近血小板形成交叉桥。还有另外两种GP IIb/IIIa抑制剂,即阿昔单抗和替罗非班,可用于临床。重度血小板减少症是GP IIb/IIIa抑制剂不常见但临床上重要的并发症。本病例讨论了一位64岁男性患者,他在第一次服用依替巴肽后4小时内发生了严重的血小板减少症。本报告在医学文献中增加了一例依替巴肽诱导的血小板减少症合并胃肠道出血的病例。它强调了近期经皮冠状动脉介入治疗患者停止抗血小板治疗的复杂决策的必要性,以及与氯吡格雷和阿司匹林相比,在替格瑞洛时代GP IIb/IIIa抑制剂的益处缺乏强有力的证据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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