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Published on: November 27, 2019
Etiology and Prognostic Criteria for Liver Failure in Southeast China: A Multicenter Retrospective Cohort Study
Chunyan Lyu1,2, Jun Han3, Naling Kang4
1Clinical Medical Research Center, The Fifth People's Hospital of Wuxi, Wuxi, China.
Insights
Hepatitis B virus (HBV) infection is a leading cause of liver failure (LF), with lower survival rates and distinct clinical indicators for nonsurvivors. Antithrombin III (AT III) shows promise as a prognostic criterion for specific HBV-related liver failure subclasses.
Area of Science:
- Hepatology and Gastroenterology
- Clinical Prognostics
- Epidemiology of Liver Disease
Background:
- Prognosis in liver failure (LF) is influenced by etiology and clinical indicators.
- Understanding these indicators is crucial for developing predictive outcome measures.
- This study analyzes basic clinical indicators in various LF subclasses.
Purpose of the Study:
- To identify clinical indicators for predicting outcomes in liver failure patients.
- To analyze prognostic criteria across different etiologies and LF subclasses.
- To evaluate the role of specific biomarkers like Antithrombin III (AT III) in prognosis.
Main Methods:
- Multi-center data collection across Southeast China, including ALF, SLF, ACLF, SALF, and CLF subclasses.
- Multivariate logistic regression analysis to identify indicators of nonsurvivors.
- Receiver operating characteristic (ROC) curve analysis and cutoff value determination for prognostic criteria.
Main Results:
- Hepatitis B virus (HBV) infection is the primary etiology (64.52%) of liver failure.
- Subacute-on-chronic liver failure (SALF) and chronic liver failure (CLF) are predominant subclasses.
- HBV-related liver failure (HBV-LF) shows decreased incidence but lower survival rates compared to non-HBV-LF.
- Infection and cirrhosis are leading causes of death; nonsurvivors exhibit higher age, total bilirubin, and shorter hospitalization.
- Proposed prognostic criteria include PT-INR and AT III for specific LF subclasses (HBV-SALF, non-HBV-SLF, non-HBV-ACLF, HBV-ALF).
Conclusions:
- The incidence of HBV-related liver failure is declining annually.
- Antithrombin III (AT III) demonstrates significant discriminative ability as an independent prognostic criterion for HBV-ALF outcomes.
Abstract:
Background: The prognosis of patients with liver failure (LF) depends significantly on the etiology and clinical indicators. This analysis of these basic indicators can help provide a basis for the study of predictive outcome indicators. Methods: We collected the data from multiple centers in Southeast China, including subclasses of acute liver failure (ALF), subacute liver failure (SLF), acute-on-chronic liver failure (ACLF), subacute-on-chronic liver failure (SALF), and chronic liver failure (CLF). Multivariate logistic regression analysis was used to screen for clinical indicators of nonsurvivors. We analyzed receiver operating characteristic (ROC) curves and cutoff values to assess the prognostic criteria. Results: Hepatitis B virus (HBV) infection is the leading etiology of patients with LF (64.52% (411/637)). SALF (41.36%) and CLF (32.30%) are the main subclasses of the hepatitis B virus-related liver failure (HBV-LF) group and the non-HBV-related LF group in Southeast China, respectively. Between 2018 and 2020, the incidence of HBV-LF decreased significantly, ranging from 72.36% to 59.74%, and the spontaneous survival rates of patients with HBV-LF were substantially lower than those of non-HBV-LF patients (36.43%~44.93% vs. 58.97%~63.64%). Infection and cirrhosis were the leading causes of death in both groups. The age and total bilirubin value of the nonsurvivors with HBV-LF were significantly higher, and the number of days of hospitalization was significantly shorter than that of the survivors. The ages of the nonsurvivors in the non-HBV-LF group were significantly higher than those of the survivors. The prothrombin time-international normalized ratio (PT-INR) is 2.05, 1.92, or 2.11, and antithrombin III (AT III) is 24.50%, which are proposed as prognostic criteria for the HBV-SALF (hepatitis B virus-related subacute-on-chronic liver failure), non-HBV-SLF (non-hepatitis B virus-related subacute liver failure), non-HBV-ACLF (non-hepatitis B virus-related acute-on-chronic liver failure), and HBV-ALF (hepatitis B virus-related acute liver failure) subclasses, respectively. Conclusions: The incidence of HBV-LF is decreasing annually. AT III, as an independent prognostic criterion, has excellent discriminative ability for the outcomes of the HBV-ALF subclass.
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