Division of Cardiology, Gangneung Asan Hospital, University of Ulsan College of Medicine, Gangneung, Republic of Korea.
Division of Cardiology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Republic of Korea.
EuroIntervention. 2024 Nov 4;20(21):e1355-e1362. doi: 10.4244/EIJ-D-24-00437.
Despite the use of conventional dual antiplatelet therapy (DAPT) after percutaneous coronary intervention (PCI), the risk of adverse events remains high among patients with increased thrombotic risk. Until recently, the optimal antiplatelet strategy to balance the ischaemic and bleeding risks in patients who are undergoing complex high-risk PCI has been unclear. The TAILored Versus COnventional AntithRombotic StratEgy IntenDed for Complex HIgh-Risk PCI (TAILORED-CHIP) trial is an investigator-initiated, multicentre, prospective randomised trial to evaluate the efficacy and safety of a time-dependent tailored antiplatelet therapy with an early (<6 months post-PCI) escalation (low-dose ticagrelor at 60 mg twice daily plus aspirin) and a late (>6 months post-PCI) de-escalation (clopidogrel monotherapy) in patients undergoing complex high-risk PCI as compared with standard DAPT (clopidogrel plus aspirin for 12 months). Eligible patients had to have at least one high-risk anatomical or procedural feature or clinical characteristic associated with an increased risk of ischaemic or thrombotic events. The primary endpoint was the net clinical outcome, a composite of death from any cause, myocardial infarction, stroke, stent thrombosis, urgent revascularisation, or clinically relevant bleeding (Bleeding Academic Research Consortium type 2, 3, or 5) at 12 months after randomisation. (ClinicalTrials.gov: NCT03465644).
尽管经皮冠状动脉介入治疗 (PCI) 后使用了常规双联抗血小板治疗 (DAPT),但高血栓风险患者的不良事件风险仍然很高。直到最近,在接受复杂高危 PCI 的患者中平衡缺血和出血风险的最佳抗血小板策略仍不清楚。旨在评估在接受复杂高危 PCI 的患者中进行时间依赖性个体化抗血小板治疗的疗效和安全性的 TAILored Versus COnventional AntithRombotic StratEgy IntenDed for Complex HIgh-Risk PCI(TAILORED-CHIP)试验是一项由研究者发起的、多中心、前瞻性随机试验,与标准 DAPT(PCI 后 6 个月内使用氯吡格雷 60mg 每日 2 次加阿司匹林;PCI 后 6 个月以上使用氯吡格雷单药治疗)相比,这种个体化抗血小板治疗采用早期(PCI 后 6 个月内)强化(低剂量替格瑞洛 60mg 每日 2 次加阿司匹林)和晚期(PCI 后 6 个月以上)减药(氯吡格雷单药治疗)策略。符合条件的患者必须至少有一个与缺血或血栓形成事件风险增加相关的高风险解剖或手术特征或临床特征。主要终点是在随机分组后 12 个月时的净临床结局,包括任何原因导致的死亡、心肌梗死、卒中和支架血栓形成、紧急血运重建或临床上相关的出血(BARC 类型 2、3 或 5)的复合终点。(ClinicalTrials.gov:NCT03465644)。