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Cited 7 time in webofscience Cited 7 time in scopus
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Impact of multi-vessel vasospastic angina on cardiovascular outcome

Authors
Han, Seung HwanLee, Kwan YongHer, Sung HoAhn, YoungkeunPark, Keun-HoKim, Dong-SooYang, Tae-HyunChoi, Dong-JuSuh, Jung-WonKwon, Hyuck MoonLee, Byoung KwonGwon, Hyeon-CheolRha, Seung-WoonJo, Sang-HoKo, Kwang-PilBaek, Sang Hong
Issue Date
Feb-2019
Publisher
ELSEVIER IRELAND LTD
Keywords
Coronary artery disease; Vasospasm; Multi-vessel; Prognosis
Citation
ATHEROSCLEROSIS, v.281, pp.107 - 113
Journal Title
ATHEROSCLEROSIS
Volume
281
Start Page
107
End Page
113
URI
https://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/1927
DOI
10.1016/j.atherosclerosis.2018.12.018
ISSN
0021-9150
Abstract
Background and aims: Since clinical characteristics and prognosis of patients with multi-vessel vasospastic angina (VSA) are not clear, we investigated the nature and prognosis of multi-vessel VSA in Koreans. Methods: Among 2960 patients enrolled in the VA-KOREA (Vasospastic Angina in Korea) registry, 104 definite multi-vessel VSA patients, 163 single vessel VSA patients and 737 non-VSA patients were identified using the intracoronary ergonovine provocation test. Results: Multi-vessel VSA and single vessel VSA groups showed similar baseline characteristics and medical treatment on discharge, but different from the non-VSA group. The primary composite endpoint (cardiac death, acute coronary syndrome, and symptomatic new onset arrhythmia) over a 36-month follow-up period was significantly higher in the multi-vessel VSA group than in the single vessel VSA and non-VSA groups (8.7% vs. 1.8% and 1.1%, each log-rank p < 0.05, respectively). The rate of death and acute coronary syndrome of the multi-vessel VSA group was higher than in the single vessel VSA and non-VSA groups (5.8% vs. 1.2% and 0.9%, each log-rank p < 0.05, respectively). In addition, multi-vessel VSA was an independent predictor of the primary composite endpoint at 36 months (HR 8.5, 95% CI [2.6-27.2], p < 0.0001). Conclusions: Patients with multi-vessel VSA had worse clinical outcomes than single vessel VSA and non-VSA groups, suggesting that the existence of multi-vessel VSA itself is highly prognostic.
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