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Cited 10 time in webofscience Cited 10 time in scopus
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Differential clinical features and long-term prognosis of acute aortic syndrome according to disease entity

Authors
Ahn, Jung-MinKim, HoyunKwon, OsungOm, Sang Yong)Heo, RanLee, SahminKim, Dae-HeeKim, Ho JinKim, Joon BumJung, Sung HoChoo, Suk JungSong, Jong-MinKang, Duk-HyunChung, Cheol HyunLee, Jae WonSong, Jae-Kwan
Issue Date
Aug-2019
Publisher
OXFORD UNIV PRESS
Keywords
Acute aortic syndrome; Aortic dissection; Aortic intramural haematoma; Outcome
Citation
EUROPEAN HEART JOURNAL, v.40, no.32, pp.2727 - 2736
Indexed
SCIE
SCOPUS
Journal Title
EUROPEAN HEART JOURNAL
Volume
40
Number
32
Start Page
2727
End Page
2736
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/3273
DOI
10.1093/eurheartj/ehz153
ISSN
0195-668X
Abstract
Aims To evaluate the acute and long-term prognosis of acute aortic syndrome (AAS) according to the disease entity [intramural haematoma (IMH) vs. aortic dissection (AD)] and the anatomical location (type A vs. B). Methods and results A total of 1012 patients [672 with AD and 340 with IMH (33.6%)] were enrolled between 1993 and 2015. Compared with AD patients, IMH patients were older and had higher frequency of female sex and distal aorta involvement. The overall crude in-hospital mortality of AAS was 8.6%; type A AD [15.0%; adjusted hazard ratio (aHR) 30.4; 95% confidence interval (CI) 8.62-107.3; P ˂ 0.001], type A IMH (8.0%; aHR 4.85; 95% CI 1.29-18.2; P = 0.019), type B AD (5.0%; aHR 3.51; 95% CI 1.00-12.4; P = 0.051), and type B IMH [1.5%; aHR 1.00 (reference)]. During a median follow-up duration of 8.5 years (interquartile range: 4.0-13.5 years), AD (aHR 2.78; 95% CI 1.87-4.14; P ˂ 0.001) and type A (aHR 2.28; 95% CI 1.45-3.58; P ˂ 0.001) was associated with a higher risk of aortic death. After 90 days, a risk of aortic death was no longer associated with anatomical location (aHR 0.74; 95% CI 0.40-1.36; P = 0.33), but remained associated with disease entity (aHR 1.83; 95% CI 1.10-3.04; P = 0.02). Conclusion The clinical features, response to treatment strategy, and outcomes of IMH patients were distinct from those of AD patients. Both early and late survival was better for IMH than for AD. In addition to the anatomical location of AAS, the disease entity is an independent factor associated with both acute and long-term mortality in patients with AAS. Further investigation is necessary to confirm the prognostic implication of disease entity in different patient populations.
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