Dynamic analysis of acute deterioration in chronic liver disease patients using modified quick sequential organ failure assessment
- Author:
Do Seon SONG
1
;
Hee Yeon KIM
;
Young Kul JUNG
;
Tae Hyung KIM
;
Hyung Joon YIM
;
Eileen L YOON
;
Ki Tae SUK
;
Jeong-ju YOO
;
Sang Gyune KIM
;
Moon Young KIM
;
Young CHANG
;
Soung Won JEONG
;
Jae Young JANG
;
Sung-Eun KIM
;
Jung-Hee KIM
;
Jung Gil PARK
;
Won KIM
;
Jin Mo YANG
;
Dong Joon KIM
;
Ashok Kumar CHOUDHURY
;
Vinod ARORA
;
Shiv Kumar SARIN
;
Author Information
- Publication Type:Original Article
- From:Clinical and Molecular Hepatology 2024;30(3):388-405
- CountryRepublic of Korea
- Language:EN
-
Abstract:
Background/Aims:Quick sequential organ failure assessment (qSOFA) is believed to identify patients at risk of poor outcomes in those with suspected infection. We aimed to evaluate the ability of modified qSOFA (m-qSOFA) to identify high-risk patients among those with acutely deteriorated chronic liver disease (CLD), especially those with acute-onchronic liver failure (ACLF).
Methods:We used data from both the Korean Acute-on-Chronic Liver Failure (KACLiF) and the Asian Pacific Association for the Study of the Liver ACLF Research Consortium (AARC) cohorts. qSOFA was modified by replacing the Glasgow Coma Scale with hepatic encephalopathy, and an m-qSOFA ≥2 was considered high.
Results:Patients with high m-qSOFA had a significantly lower 1-month transplant-free survival (TFS) in both cohorts and higher organ failure development in KACLiF than those with low m-qSOFA (Ps<0.05). Subgroup analysis by ACLF showed that patients with high m-qSOFA had lower TFS than those with low m-qSOFA. m-qSOFA was an independent prognostic factor (hazard ratios, HR=2.604, 95% confidence interval, CI 1.353–5.013, P=0.004 in KACLiF and HR=1.904, 95% CI 1.484– 2.442, P<0.001 in AARC). The patients with low m-qSOFA at baseline but high m-qSOFA on day 7 had a significantly lower 1-month TFS than those with high m-qSOFA at baseline but low m-qSOFA on day 7 (52.6% vs. 89.4%, P<0.001 in KACLiF and 26.9% vs. 61.5%, P<0.001 in AARC).
Conclusions:Baseline and dynamic changes in m-qSOFA may identify patients with a high risk of developing organ failure and short-term mortality among CLD patients with acute deterioration.
