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Staged versus immediate complete revascularization for non-culprit arteries in acute myocardial infarction: a post-hoc analysis of FRAME-AMIopen access

Authors
Lim, YongwhanJang, JaehyukLee, Seung HunAhn, Joon HoHong, Young JoonAhn, YoungkeunJeong, Myung HoKim, Chan JoonHahn, Joo-YongLee, Joo MyungPark, Keun HoChoo, Eun HoAhn, Sung GyunDoh, Joon-HyungLee, Sang YeubPark, Sang DonLee, Hyun-JongKang, Min GyuCho, Yun-KyeongNam, Chang WookBu, Sung HyunKim, Min Chul
Issue Date
Dec-2024
Publisher
Frontiers Media SA
Keywords
acute myocardial infarction; FRAME-AMI; immediate complete revascularization; multivessel disease; staged complete revascularization
Citation
Frontiers in Cardiovascular Medicine, v.11
Indexed
SCIE
SCOPUS
Journal Title
Frontiers in Cardiovascular Medicine
Volume
11
URI
https://scholarworks.gnu.ac.kr/handle/sw.gnu/75381
DOI
10.3389/fcvm.2024.1475483
ISSN
2297-055X
Abstract
Background and objectives: The optimal timing for complete revascularization (CR) in patients with acute myocardial infarction (AMI) and multivessel disease (MVD) remain uncertain. Methods: This post-hoc analysis of the FRAME-AMI trial included AMI patients with MVD (n = 549). They were classified into immediate (n = 329) and staged CR (n = 220) groups. All percutaneous coronary interventions were performed during inex hospitalization. The primary endpoint was a composite of all-cause death, acute myocardial infarction, and repeated revascularization. Secondary endpoints included each component of the primary endpoint. Additional comparisons for the outcomes in ST-segment elevation myocardial infarction (STEMI) and non-STEMI (NSTEMI) were also performed. Results: The incidence of the primary endpoint was not significantly different in any of the AMI patients [12.7% [immediate CR] vs. 17.4% [staged CR], p = 0.905, adjusted hazard ratio [HR] of staged CR = 0.81, 95% confidence interval = 0.43–1.53, p = 0.528]. Other secondary endpoints were also not significantly different. Analyses of STEMI and Neither the primary or secondary endpoints of NSTEMI patients were significantly different. Conclusions: In this post-hoc analysis of the FRAME-AMI trial, no significant difference in clinical outcomes was observed between the immediate and staged CR strategies for AMI with MVD and the subgroups, such as STEMI or NSTEMI. However, the results should be interpreted carefully because of the many limitations, including a limited sample size and a lack of statistical power. Trial Registration: FRAME-AMI clinicaltrials.gov, identifier (NCT02715518). 2024 Lim, Jang, Lee, Ahn, Hong, Ahn, Jeong, Kim, Hahn, Lee, Park, Choo, Ahn, Doh, Lee, Park, Lee, Kang, Cho, Nam, Bu and Kim.
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