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复杂高危 PCI 患者抗血小板治疗的时间调制(早期强化和晚期下调):TAILORED-CHIP 试验的原理和设计。

Temporal modulation (early escalation and late de-escalation) of antiplatelet therapy in patients undergoing complex high-risk PCI: rationale and design of the TAILORED-CHIP trial.

机构信息

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.

出版信息

EuroIntervention. 2024 Nov 4;20(21):e1355-e1362. doi: 10.4244/EIJ-D-24-00437.

DOI:10.4244/EIJ-D-24-00437
PMID:39492701
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11522859/
Abstract

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).

摘要

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)。

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本文引用的文献

1
Ticagrelor vs Clopidogrel for Complex Percutaneous Coronary Intervention in Chronic Coronary Syndrome.替格瑞洛与氯吡格雷用于慢性冠状动脉综合征患者复杂经皮冠状动脉介入治疗。
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Quantifying Treatment Effects in Trials with Multiple Event-Time Outcomes.在具有多个事件时间结局的试验中量化治疗效果
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Defining Strategies of Modulation of Antiplatelet Therapy in Patients With Coronary Artery Disease: A Consensus Document from the Academic Research Consortium.定义冠心病患者抗血小板治疗的调节策略:来自学术研究联盟的共识文件。
Circulation. 2023 Jun 20;147(25):1933-1944. doi: 10.1161/CIRCULATIONAHA.123.064473. Epub 2023 Jun 19.
4
P2Y Inhibitor Monotherapy or Dual Antiplatelet Therapy After Complex Percutaneous Coronary Interventions.复杂经皮冠状动脉介入治疗后 P2Y 抑制剂单药治疗或双联抗血小板治疗。
J Am Coll Cardiol. 2023 Feb 14;81(6):537-552. doi: 10.1016/j.jacc.2022.11.041.
5
Timing, Selection, Modulation, and Duration of P2Y Inhibitors for Patients With Acute Coronary Syndromes Undergoing PCI.接受经皮冠状动脉介入治疗的急性冠状动脉综合征患者使用P2Y抑制剂的时机、选择、调整及持续时间
JACC Cardiovasc Interv. 2023 Jan 9;16(1):1-18. doi: 10.1016/j.jcin.2022.10.023.
6
Ticagrelor vs Prasugrel in a Contemporary Real-World Cohort Undergoing Percutaneous Coronary Intervention.替格瑞洛与普拉格雷在接受经皮冠状动脉介入治疗的当代真实世界队列中的比较。
JACC Cardiovasc Interv. 2022 Nov 28;15(22):2270-2280. doi: 10.1016/j.jcin.2022.09.021.
7
Unguided de-escalation from ticagrelor to clopidogrel in stabilised patients with acute myocardial infarction undergoing percutaneous coronary intervention (TALOS-AMI): an investigator-initiated, open-label, multicentre, non-inferiority, randomised trial.替格瑞洛未指导降级为氯吡格雷在稳定的急性心肌梗死行经皮冠状动脉介入治疗患者(TALOS-AMI):一项研究者发起的、开放标签、多中心、非劣效性、随机试验。
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8
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Lancet. 2021 Jun 26;397(10293):2487-2496. doi: 10.1016/S0140-6736(21)01063-1. Epub 2021 May 16.
9
Management of Antithrombotic Therapy after Acute Coronary Syndromes.急性冠状动脉综合征后抗栓治疗的管理
N Engl J Med. 2021 Feb 4;384(5):452-460. doi: 10.1056/NEJMra1607714.
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Lancet. 2020 Nov 28;396(10264):1737-1744. doi: 10.1016/S0140-6736(20)32236-4. Epub 2020 Nov 14.