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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

Authors
Park, HanbitKang, Do-YoonAhn, Jung-MinYun, Sung-CheolPark, Kyoung-HaKang, Se-HunSuh, JonBae, Jang-WhanPark, SangwooCho, Jang HyunSuh, Jung-WonLee, Bong-KiRha, Seung-WoonWon, HoyounJang, Jae-SikKim, Moo HyunLee, Cheol HyunAhn, Young KeunOh, Jun-HyokBae, Jae-SeokPark, Chul SooChoi, JaewoongLee, Jin-BaeLee, Se-WhanHur, Sung-HoKwon, OsungPark, Seung-JungPark, Duk-Woo
Issue Date
Nov-2024
Publisher
Europa Ed
Keywords
adjunctive pharmacotherapy; bleeding; clinical trials; drug-eluting stent; stent thrombosis
Citation
EuroIntervention, v.20, no.21, pp e1355 - e1362
Indexed
SCIE
SCOPUS
Journal Title
EuroIntervention
Volume
20
Number
21
Start Page
e1355
End Page
e1362
URI
https://scholarworks.gnu.ac.kr/handle/sw.gnu/74755
DOI
10.4244/EIJ-D-24-00437
ISSN
1774-024X
1969-6213
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).
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