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首页> 外文期刊>BioDrugs: Clinical immunotherapeutics, biopharmaceuticals, and gene therapy >Spotlight on eptifibatide in patients with acute coronary syndromes and/or undergoing percutaneous coronary intervention.
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Spotlight on eptifibatide in patients with acute coronary syndromes and/or undergoing percutaneous coronary intervention.

机译:聚焦于急性肺动脉综合征和/或经皮冠状动脉介入治疗患者中的依替巴肽。

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摘要

Eptifibatide (Integrilin) is a highly specific, reversible, intravenously administered glycoprotein IIb/IIIa receptor antagonist that acts at the final common step of the platelet aggregation pathway. Data from large clinical trials indicate that intravenous eptifibatide as adjunctive therapy to standard care is effective in patients with non-ST-segment elevation (NSTE) acute coronary syndromes (ACS) and/or undergoing percutaneous coronary intervention (PCI). In the ESPRIT (Enhanced Suppression of the Platelet glycoprotein IIb/IIIa Receptor with Integrilin Therapy) trial in patients undergoing PCI with stenting, eptifibatide, compared with placebo, achieved significant reductions in death and ischemic complications and was better than a strategy of reserving treatment for the bailout situation. In the large PURSUIT (Platelet IIb/IIIa in Unstable angina: Receptor Suppression Using Integrilin Therapy) trial in patients with NSTE ACS, eptifibatide was associated with a significant reduction in the incidence of death or myocardial infarction (MI) compared with placebo. Eptifibatide is well tolerated in these trials. Ongoing trials are currently investigating the efficacy and tolerability of regimens that include this agent in other indications, including ST-segment elevation MI.
机译:依替巴肽(Integrilin)是一种高度特异性的,可逆的,静脉内施用的糖蛋白IIb / IIIa受体拮抗剂,在血小板聚集途径的最终共同步骤中起作用。大型临床试验的数据表明,静脉注射依替巴肽作为标准护理的辅助治疗对非ST段抬高(NSTE)急性冠状动脉综合征(ACS)和/或接受经皮冠状动脉介入治疗(PCI)的患者有效。在ESPRIT(使用Integrilin治疗增强血小板糖蛋白IIb / IIIa受体抑制)试验中,在接受PCI支架置入术的患者中,与安慰剂相比,依替非巴肽显着减少了死亡和缺血性并发症,并且优于保留治疗策略救援情况。在NSTE ACS患者的大型PURSUIT(不稳定型心绞痛中的血小板IIb / IIIa:使用Integrilin治疗抑制受体)试验中,与安慰剂相比,依替非巴肽显着降低了死亡或心肌梗塞(MI)的发生率。在这些试验中,埃替非巴肽具有良好的耐受性。目前正在进行的试验正在研究在其他适应症(包括ST段抬高MI)中包括该药的治疗方案的疗效和耐受性。

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