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首页> 外文期刊>Angiology: the Journal of Vascular Diseases >Profound thrombocytopenia associated with tirofiban-case report and review of literature.
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Profound thrombocytopenia associated with tirofiban-case report and review of literature.

机译:与替罗非班病例报告和文献复习相关的严重血小板减少症。

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摘要

Platelet glycoprotein (GP)IIb/IIIa inhibitors prevent fibrinogen binding and platelet aggregation. Inhibition of platelet activity at the injured coronary plaque is a target for novel therapeutic strategies. They decrease ischemic complications associated with non-ST-segment elevation acute coronary syndromes and percutaneous coronary intervention. Thrombocytopenia is a serious complication well described with the use of the prototype GP IIb/IIIa inhibitor abciximab. Its association with other agents of this class has been underemphasized. It is important to monitor platelet counts closely after initiation of GP IIb/IIIa inhibitor therapy, not only for abciximab, but also for small molecule inhibitors such as eptifibatide and tirofiban. Monitoring of platelet counts at 2 to 6 hours and 24 hours will detect most cases of acute thrombocytopenia. Adverse events may be prevented by prompt discontinuation of GP IIb/IIIa inhibitor therapy. The authors present a case of profound thrombocytopenia after the administration of tirofiban in the treatment of a patient with an acute coronary syndrome.
机译:血小板糖蛋白(GP)IIb / IIIa抑制剂可防止纤维蛋白原结合和血小板聚集。抑制冠状动脉斑块处的血小板活性是新治疗策略的目标。它们减少了与非ST段抬高的急性冠状动脉综合征和经皮冠状动脉介入治疗相关的缺血性并发症。血小板减少症是使用原型GP IIb / IIIa抑制剂abciximab所描述的严重并发症。它与此类其他代理的关联已被过分强调。在启动GP IIb / IIIa抑制剂治疗后,密切监视血小板计数非常重要,这不仅对于abciximab,而且对于小分子抑制剂(如埃替非巴肽和替罗非班)也是如此。在2至6小时和24小时监测血小板计数将发现大多数急性血小板减少症。迅速停止GP IIb / IIIa抑制剂治疗可预防不良事件。作者介绍了在服用替罗非班治疗急性冠状动脉综合征患者后发生严重血小板减少的情况。

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