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Association between polyvascular disease and clinical outcomes in patients with cardiogenic shock: Results from the RESCUE registry

Authors
 Jang, Woo Jin  ;  Park, Ik Hyun  ;  Yang, Jeong Hoon  ;  Chun, Woo Jung  ;  Oh, Ju Hyeon  ;  Park, Yong Hwan  ;  Ko, Young Guk  ;  Yu, Cheol Woong  ;  Kim, Hyun-Joong  ;  Kim, Bum Sung  ;  Lee, Hyun Jong  ;  Jeong, Jin-Ok  ;  Gwon, Hyeon-Cheol 
Citation
 International Journal of Cardiology, Vol.339 : 70-74, 2021-09 
Journal Title
INTERNATIONAL JOURNAL OF CARDIOLOGY
ISSN
 0167-5273 
Issue Date
2021-09
Keywords
Polyvascular disease ; Cardiogenic shock ; Prognosis
Abstract
Background: Clinical implications of systemic atherosclerosis in patients with cardiogenic shock (CS) remain unclear. This study investigated the association between polyvascular disease (PVD) and clinical outcome in CS patients. Methods: A total of 1247 CS patients was enrolled from the RESCUE registry, a multicenter, observational cohort between January 2014 and December 2018. They were divided into two groups according to presence of PVD, defined as >2 coexistence of coronary artery disease, peripheral arterial disease, or cerebrovascular disease. Primary outcome was all-cause death during 12 months of follow-up. Results: 136 (10.9%) patients were diagnosed with PVD. The risk of 12-month all-cause death was significantly higher in the PVD group than in the non-PVD group (54.4% versus 40.4%, adjusted hazard ratio [HR] 1.31, 95% confidence interval [CI] 1.02-1.69, p = 0.034). There was a significant interaction between PVD and vasoactive inotropic score (VIS) (p for interaction = 0.014). Among the 945 patients with VIS <84, PVD was associated with a higher risk of 12-month all-cause death (unadjusted HR 1.77, 95% CI 1.30-2.41, p = 0.030); among the 302 patients with VIS >84, the incidence of 12-month all-cause death was similar between the PVD and non-PVD groups (unadjusted HR 1.03, 95% CI 0.68-1.56, p = 0.301). Conclusions: Presence of PVD was associated with 12-month all-cause mortality in patients with CS, especially for less severe forms of CS patients with VIS <84. Clinical trials.gov number: NCT02985008
DOI
10.1016/j.ijcard.2021.07.008
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers
Yonsei Authors
Ko, Young Guk(고영국) ORCID logo https://orcid.org/0000-0001-7748-5788
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/190501
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