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Optimal timing of revascularization for patients with non-ST segment elevation myocardial infarction and severe left ventricular dysfunctionopen access

Authors
Shin, YoonminLee, Seung HunLee, Sang HoonKim, Ji SungLim, Yong HwanAhn, Joon HoCho, Kyung HoonKim, Min ChulSim, Doo SunHong, Young JoonKim, Ju HanHwang, Jin-YongOh, Seok KyuSong, Pil SangPark, Yong HwanHur, Seung-HoYoon, Chang-HwanLee, Joo MyungSong, Young BinHahn, Joo-YongJeong, Myung HoAhn, Yongkeun
Issue Date
Aug-2024
Publisher
Lippincott Williams & Wilkins Ltd.
Keywords
acute myocardial infarction; echocardiography; left ventricular ejection fraction; percutaneous coronary intervention; prognosis
Citation
Medicine, v.103, no.35, pp e38483
Indexed
SCIE
SCOPUS
Journal Title
Medicine
Volume
103
Number
35
Start Page
e38483
URI
https://scholarworks.gnu.ac.kr/handle/sw.gnu/74003
DOI
10.1097/MD.0000000000038483
ISSN
0025-7974
1536-5964
Abstract
Optimal timing of revascularization for patients who presented with non-ST segment elevation myocardial infarction (NSTEMI) and severe left ventricular (LV) dysfunction is unclear. A total of 386 NSTEMI patients with severe LV dysfunction from the nationwide, multicenter, and prospective Korea Acute Myocardial Infarction Registry V (KAMIR-V) were enrolled. Severe LV dysfunction was defined as LV ejection fraction <= 35%. Patients with cardiogenic shock were excluded. Patients were stratified into two groups: PCI within 24 hours (early invasive group) and PCI over 24 hours (selective invasive group). Primary endpoint was major adverse cardiac and cerebrovascular events (MACCE) including all-cause death, non-fatal MI, repeat revascularization, and stroke at 12 months after index procedure. Early invasive group showed higher incidence of in-hospital death (9.4% vs 3.3%, P = .036) and cardiogenic shock (11.5% vs 4.6%, P = .030) after PCI. Early invasive group also showed higher maximum troponin I level during admission (27.7 +/- 44.8 ng/mL vs 14.9 +/- 24.6 ng/mL, P = .001), compared with the selective invasive group. Early invasive group had an increased risk of 12-month MACCE, compared with selective invasive group (25.6% vs 17.1%; adjusted HR = 2.10, 95% CI 1.17-3.77, P = .006). Among NSTEMI patients with severe LV dysfunction, the early invasive strategy did not improve the clinical outcomes. This data supports that an individualized approach may benefit high-risk NSTEMI patients rather than a routine invasive approach.
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