复杂高风险 PCI 患者抗血小板治疗的时间调节(早期升级和晚期降级):TAILORED-CHIP 试验的原理和设计。

IF 7.6 1区 医学 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS
Hanbit Park, Do-Yoon Kang, Jung-Min Ahn, Sung-Cheol Yun, Kyoung-Ha Park, Se-Hun Kang, Jon Suh, Jang-Whan Bae, Sangwoo Park, Jang Hyun Cho, Jung-Won Suh, Bong-Ki Lee, Seung-Woon Rha, Hoyoun Won, Jae-Sik Jang, Moo Hyun Kim, Cheol Hyun Lee, Young Keun Ahn, Jun-Hyok Oh, Jae-Seok Bae, Chul Soo Park, Jaewoong Choi, Jin-Bae Lee, Se-Whan Lee, Sung-Ho Hur, Osung Kwon, Seung-Jung Park, Duk-Woo Park, On Behalf Of The Tailored-Chip Trial Investigators
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引用次数: 0

摘要

尽管经皮冠状动脉介入治疗(PCI)后使用了传统的双联抗血小板疗法(DAPT),但血栓风险增加的患者发生不良事件的风险仍然很高。直到最近,在接受复杂的高风险 PCI 治疗的患者中,平衡缺血和出血风险的最佳抗血小板策略仍不明确。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、该试验是一项由研究者发起的多中心前瞻性随机试验,旨在评估在接受复杂高风险 PCI 治疗的患者中,与标准 DAPT(氯吡格雷加阿司匹林治疗 12 个月)相比,采用早期(PCI 术后 6 个月)降级(氯吡格雷单药治疗)的时间依赖性定制抗血小板疗法的疗效和安全性。符合条件的患者必须至少具有一种与缺血或血栓事件风险增加相关的高风险解剖或手术特征或临床特征。主要终点是随机分组后12个月的净临床结果,即任何原因导致的死亡、心肌梗死、中风、支架血栓、紧急血管重建或临床相关出血(出血学术研究联盟2、3或5型)的综合结果。(ClinicalTrials.gov:NCT03465644)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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.

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).

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来源期刊
Eurointervention
Eurointervention CARDIAC & CARDIOVASCULAR SYSTEMS-
CiteScore
10.30
自引率
4.80%
发文量
380
审稿时长
3-8 weeks
期刊介绍: EuroIntervention Journal is an international, English language, peer-reviewed journal whose aim is to create a community of high quality research and education in the field of percutaneous and surgical cardiovascular interventions.
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