Moulias Athanasios, Papageorgiou Angeliki, Alexopoulos Dimitrios
Department of Cardiology, General University Hospital of Patras Patras, Greece.
Second Department of Cardiology, Attikon University Hospital, National and Kapodistrian University of Athens Medical School Athens, Greece.
US Cardiol. 2021 Aug 4;15:e14. doi: 10.15420/usc.2020.33. eCollection 2021.
Dual antiplatelet therapy (DAPT), comprising aspirin and a P2Y receptor inhibitor, is considered the cornerstone of treatment in patients who have undergone percutaneous coronary intervention (PCI). Patients with complex PCI (C-PCI) constitute a special PCI subpopulation, characterized by increased ischemic risk. Identifying the optimal DAPT strategy is often challenging and remains controversial in this setting. In an attempt to balance ischemic and bleeding risks in C-PCI patients receiving DAPT, treatment individualization regarding potency and duration has evolved as a feasible approach. Platelet function testing and genotyping have been evaluated in several trials with conflicting and mostly neutral results. The aim of this review is to critically appreciate the role of these tools for antiplatelet treatment tailoring specifically in C-PCI patients. Because existing evidence is limited, dedicated future studies are warranted to elucidate the utility of platelet function testing and genotyping in C-PCI.
双联抗血小板治疗(DAPT),由阿司匹林和一种P2Y受体抑制剂组成,被认为是接受经皮冠状动脉介入治疗(PCI)患者的治疗基石。复杂PCI(C-PCI)患者构成了一个特殊的PCI亚组,其特征是缺血风险增加。在这种情况下,确定最佳的DAPT策略往往具有挑战性,并且仍然存在争议。为了平衡接受DAPT的C-PCI患者的缺血和出血风险,关于效力和持续时间的治疗个体化已发展成为一种可行的方法。血小板功能检测和基因分型已在多项试验中进行了评估,结果相互矛盾且大多为中性。本综述的目的是批判性地评估这些工具在专门针对C-PCI患者进行抗血小板治疗调整中的作用。由于现有证据有限,未来需要进行专门的研究以阐明血小板功能检测和基因分型在C-PCI中的效用。