P2Y12 inhibitor monotherapy in patients undergoing percutaneous coronary intervention

医学 P2Y12 经皮冠状动脉介入治疗 传统PCI 阿司匹林 氯吡格雷 药效学 抗血栓 指南 内科学 重症监护医学 心脏病学 心肌梗塞 药代动力学 病理
作者
Davide Capodanno,Usman Baber,Deepak L. Bhatt,Jean‐Philippe Collet,George Dangas,Francesco Franchi,C. Michael Gibson,Hyeon‐Cheol Gwon,Adnan Kastrati,Takeshi Kimura,Pedro A. Lemos,Renato D. Lópes,Roxana Mehran,Michelle L. O’Donoghue,Sunil V. Rao,Fabiana Rollini,Patrick Serruys,Philippe Gabríel Steg,Robert F. Storey,Marco Valgimigli
出处
期刊:Nature Reviews Cardiology [Nature Portfolio]
卷期号:19 (12): 829-844 被引量:57
标识
DOI:10.1038/s41569-022-00725-6
摘要

For 20 years, dual antiplatelet therapy (DAPT), consisting of the combination of aspirin and a platelet P2Y12 receptor inhibitor, has been the gold standard of antithrombotic pharmacology after percutaneous coronary intervention (PCI). In the past 5 years, several investigations have challenged this paradigm by testing the efficacy and safety of P2Y12 inhibitor monotherapy (that is, without aspirin) following a short course of DAPT. Collectively, these studies suggested a reduction in the risk of major bleeding and no significant increase in thrombotic or ischaemic events compared with guideline-recommended DAPT. Current recommendations are evolving to inform clinical practice on the ideal candidates for P2Y12 inhibitor monotherapy after PCI. Generalizing the results of studies of P2Y12 inhibitor monotherapy requires a thorough understanding of their design, populations, interventions, comparators and results. In this Review, we provide an up-to-date overview on the use of P2Y12 inhibitor monotherapy after PCI, including supporting pharmacodynamic and clinical evidence, practical recommendations and future directions.
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