急性冠脉综合征患者在康格瑞洛后使用P2Y12受体抑制剂进行维持治疗。ELECTRA-SIRIO 2调查人员的观点。

Jacek Kubica, Piotr Adamski, Robert Gajda, Aldona Kubica, Małgorzata Ostrowska, Gavino Casu, Diana A Gorog, Paul A Gurbel, Tomasz Hajdukiewicz, Miłosz Jaguszewski, Young-Hoon Jeong, Agata Kosobucka-Ozdoba, Zuzana Motovska, Piotr Niezgoda, Maciej Piasecki, Przemysław Podhajski, Paolo Raggi, Uzeyir Rahimov, Jolanta M Siller-Matula, Grzegorz Skonieczny, Łukasz Szarpak, Paweł Szymański, Udaya Tantry, Eliano P Navarese
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引用次数: 0

摘要

根据ESC指南,可考虑在P2Y12-inhibitor-naïve急性冠状动脉综合征(ACS)患者接受经皮冠状动脉介入治疗(PCI)。本综述的目的是总结现有的证据,在康格瑞洛之后使用P2Y12受体抑制剂进行最佳维持治疗。从替格瑞洛过渡到噻吩吡啶,但不是替格瑞洛,可能与药物-药物相互作用(DDI)有关;因此,替格瑞洛的负荷剂量(LD)可以在康格雷洛输注前、输注期间或输注结束时的任何时间给予,而氯吡格雷或普拉格雷的负荷剂量应在康格雷洛输注结束时给予,如果普拉格雷有负荷剂量,则应在输注结束前30分钟内给予。在输注康格瑞洛结束时给予任何口服抗血小板药物也会导致短暂的血小板反应性增加。这一时期的个体间变异性很难预测,因为它取决于与患者和治疗相关的许多因素。此外,实验研究表明,康奈洛可能发挥心脏保护作用,而不是阻断血小板聚集。考虑到现有的数据,canrelor在ACS患者中的潜在应用远远超出了目前的适应症。此外,我们认为,在获得关于DDI对临床结果影响的确凿数据之前,在输注康格洛期间和输注后不久避免使用噻吩吡啶可能是谨慎的。另一方面,替格瑞洛似乎是接受康格洛输注的患者继续抑制P2Y12的最佳口服药物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Maintenance therapy with a P2Y12 receptor inhibitor after cangrelor in patients with acute coronary syndrome. The ELECTRA-SIRIO 2 investigators' viewpoint.

According to the ESC guidelines, cangrelor may be considered in P2Y12-inhibitor-naïve acute coronary syndrome (ACS) patients undergoing percutaneous coronary intervention (PCI). The aim of this review is to summarize available evidence on the optimal maintenance therapy with P2Y12 receptor inhibitor after cangrelor. Transitioning from cangrelor to a thienopyridine, but not ticagrelor, can be associated with a drug-drug interaction (DDI); therefore, a ticagrelor loading dose (LD) can be given any time before, during, or at the end of a cangrelor infusion, while a LD of clopidogrel or prasugrel should be administered at the time the infusion of cangrelor ends or within 30 minutes before the end of infusion in the case of a LD of prasugrel. Administration of any oral antiplatelet agent at the end of a cangrelor infusion will also result in a transient period of increased platelet reactivity. The inter-individual variability of this period is difficult to predict because it depends on many factors related to the patient and the treatment. In addition, experimental studies indicate that cangrelor may exert a cardioprotective effect beyond the blockade of platelet aggregation. Considering the available data, the potential use of cangrelor in ACS patients goes well beyond the current indications. Furthermore, we believe that it might be prudent to avoid use of thienopyridines during and soon after a cangrelor infusion until conclusive data on the effect of the DDI on the clinical outcome are available. On the other hand, ticagrelor seems to be an optimal oral agent for continuation of P2Y12 inhibition in patients receiving cangrelor infusion.

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