Kubica Jacek, Adamski Piotr, Gajda Robert, Kubica Aldona, Ostrowska Małgorzata, Casu Gavino, Gorog Diana A, Gurbel Paul A, Hajdukiewicz Tomasz, Jaguszewski Miłosz, Jeong Young-Hoon, Kosobucka-Ozdoba Agata, Motovska Zuzana, Niezgoda Piotr, Piasecki Maciej, Podhajski Przemysław, Raggi Paolo, Rahimov Uzeyir, Siller-Matula Jolanta M, Skonieczny Grzegorz, Szarpak Łukasz, Szymański Paweł, Tantry Udaya, Navarese Eliano P
Department of Cardiology and Internal Medicine, Collegium Medicum, Nicolaus Copernicus University, Bydgoszcz, Poland.
Gajda-Med District Hospital in Pultusk, Poland.
Cardiol J. 2025;32(1):83-89. doi: 10.5603/cj.98323. Epub 2025 Jan 8.
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.
根据欧洲心脏病学会(ESC)指南,对于未使用过P2Y12抑制剂的急性冠状动脉综合征(ACS)患者,若接受经皮冠状动脉介入治疗(PCI),可考虑使用坎格雷洛。本综述的目的是总结关于坎格雷洛后使用P2Y12受体抑制剂进行最佳维持治疗的现有证据。从坎格雷洛转换为噻吩并吡啶类药物(而非替格瑞洛)可能会发生药物相互作用(DDI);因此,可在坎格雷洛输注前、输注期间或输注结束时的任何时间给予替格瑞洛负荷剂量(LD),而氯吡格雷或普拉格雷的负荷剂量应在坎格雷洛输注结束时给药,若为普拉格雷负荷剂量,则应在输注结束前30分钟内给药。在坎格雷洛输注结束时给予任何口服抗血小板药物也会导致血小板反应性短暂升高。这一时期的个体间变异性难以预测,因为它取决于许多与患者和治疗相关的因素。此外,实验研究表明,坎格雷洛可能在抑制血小板聚集之外还发挥心脏保护作用。考虑到现有数据,坎格雷洛在ACS患者中的潜在用途远远超出了目前的适应证。此外,我们认为,在坎格雷洛输注期间及输注后不久避免使用噻吩并吡啶类药物可能是谨慎的做法,直到有关于药物相互作用对临床结局影响的确切数据。另一方面,替格瑞洛似乎是接受坎格雷洛输注患者继续抑制P2Y12的最佳口服药物。