Faculty of Medicine, University of Southampton.
University Hospital Southampton NHS FT.
Future Cardiol. 2024;20(9):499-515. doi: 10.1080/14796678.2024.2384217. Epub 2024 Aug 2.
Cardiovascular disease is the leading cause of death worldwide. Dual antiplatelet therapy (DAPT), with aspirin plus a P2Y12 inhibitor, is currently recommended as a default for patients after acute coronary syndrome (ACS) and following percutaneous coronary intervention (PCI). However, controversies arise over the role of aspirin, the optimal duration of DAPT after drug-eluting stent (DES) implantation, the choice of P2Y12 inhibitor and the variability in individual responses to antiplatelet agents. Recent data indicate that monotherapy with a P2Y12 inhibitor may have adequate anti-ischemic effects with lower bleeding risk. Additionally, discrepancies in DAPT duration recommendations and the optimal P2Y12 inhibitor, provides more uncertainty. We ask the question "does one size really fits all?" or should a more personalized strategy should be implemented.
心血管疾病是全球范围内的主要死亡原因。双联抗血小板治疗(DAPT),即阿司匹林加 P2Y12 抑制剂,目前被推荐为急性冠脉综合征(ACS)和经皮冠状动脉介入治疗(PCI)后患者的默认治疗方法。然而,关于阿司匹林的作用、药物洗脱支架(DES)植入后 DAPT 的最佳持续时间、P2Y12 抑制剂的选择以及个体对抗血小板药物反应的变异性等问题仍存在争议。最近的数据表明,P2Y12 抑制剂单药治疗可能具有足够的抗缺血作用,且出血风险较低。此外,DAPT 持续时间推荐和最佳 P2Y12 抑制剂的差异也增加了不确定性。我们不禁要问:“一刀切真的合适吗?”或者是否应该实施更个性化的策略。