Risk factors and prognostic impact of new decompensated events in hospitalized patients with decompensated cirrhosis

医学 肝病学 内科学 肝硬化 胃肠病学 重症监护医学
作者
Lan Yan,Yue Yu,Xiuding Zhang,Xianbin Xu,Yu Xia,Huilan Tu,Shaoheng Ye,Haoda Weng,Yu Shi,Jifang Sheng
出处
期刊:BMC Gastroenterology [BioMed Central]
卷期号:24 (1)
标识
DOI:10.1186/s12876-024-03494-3
摘要

Decompensated cirrhosis (DC) is prone to recurrent episodes of decompensation following the initial event. This study aimed to identify the risk factors for subsequent decompensation and assess their impact on the outcomes of patients hospitalized for DC. Patients with DC were divided into two groups based on the occurrence of new decompensated events during hospitalization. Logistic regression analysis was employed to identify risk factors for new decompensation. The Cox proportional hazards model was used to evaluate the relationship between new decompensation and short-term mortality risk in these patients. The study cohort consisted of 339 patients with DC, with a median age of 57 years. During hospitalization, 83 patients (24.5%) experienced new decompensated events, with bacterial infections (BIs) being the most common (n = 46, 13.6%). Multivariate analysis revealed that the Model for End-Stage Liver Disease (MELD) score at admission (OR = 1.06, 95% CI: 1.02–1.11, P = 0.005) was the sole risk factor for new decompensation during hospitalization. Patients who experienced new decompensation had significantly higher 28-day (28.9% vs. 7.0%, P < 0.001) and 90-day (33.7% vs. 15.2%, P < 0.001) transplant-free mortality compared to those who did not. After adjusting for white cell count, C-reactive protein, and MELD score, new decompensation during hospitalization was identified as an independent risk factor for 28-day and 90-day mortality (HR = 2.63, 95% CI: 1.42–4.87, P = 0.002 and HR = 1.73, 95% CI: 1.04–2.88, P = 0.033, respectively). Patients with high MELD scores are susceptible to new decompensation during hospitalization, and the occurrence of new decompensation adversely affects short-term mortality in patients with DC.
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