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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.

医学 降级 传统PCI 内科学 随机对照试验 心脏病学 肿瘤科 心肌梗塞
作者
Hanbit Park,Do‐Yoon Kang,So-Min Lim,Sung-Cheol Yun,Kyong Hwa 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,Sang‐Hyun Kim,Cheol Hyun Lee,Young Keun Ahn,J H Oh,JAESEOK BAE,Chul Soo Park,Jae Woong 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
出处
期刊:PubMed 卷期号:20 (21): e1355-e1362
标识
DOI:10.4244/eij-d-24-00437
摘要

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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