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Role of precipitants in transition of acute decompensation to acute-on-chronic liver failure in patients with HBV-related cirrhosis

BACKGROUND & AIMS: Pre-acute-on-chronic liver failure (ACLF) is a distinct intermediate stage between acute decompensation (AD) and ACLF. However, identifying patients with pre-ACLF and predicting progression from AD to ACLF is difficult. This study aimed to identify pre-ACLF within 28 days, and...

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Detalles Bibliográficos
Autores principales: Wang, Tongyu, Tan, Wenting, Wang, Xianbo, Zheng, Xin, Huang, Yan, Li, Beiling, Meng, Zhongji, Gao, Yanhang, Qian, Zhiping, Liu, Feng, Lu, Xiaobo, Yan, Huadong, Zheng, Yubao, Zhang, Weituo, Yin, Shan, Gu, Wenyi, Zhang, Yan, Dong, Fuchen, Wei, Jianyi, Deng, Guohong, Xiang, Xiaomei, Zhou, Yi, Hou, Yixin, Zhang, Qun, Xiong, Shue, Liu, Jing, Long, Liyuan, Chen, Ruochan, Chen, Jinjun, Jiang, Xiuhua, Luo, Sen, Chen, Yuanyuan, Jiang, Chang, Zhao, Jinming, Ji, Liujuan, Mei, Xue, Li, Jing, Li, Tao, Zheng, Rongjiong, Zhou, Xinyi, Ren, Haotang, Shi, Yu, Li, Hai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9424579/
https://www.ncbi.nlm.nih.gov/pubmed/36052222
http://dx.doi.org/10.1016/j.jhepr.2022.100529
Descripción
Sumario:BACKGROUND & AIMS: Pre-acute-on-chronic liver failure (ACLF) is a distinct intermediate stage between acute decompensation (AD) and ACLF. However, identifying patients with pre-ACLF and predicting progression from AD to ACLF is difficult. This study aimed to identify pre-ACLF within 28 days, and to develop and validate a prediction model for ACLF in patients with HBV-related decompensated cirrhosis. METHODS: In total, 1,736 patients with HBV-related cirrhosis and AD were enrolled from 2 large-scale, multicenter, prospective cohorts. ACLF occurrence within 28 days, readmission, and 3-month and 1-year outcomes were collected. RESULTS: Among 970 patients with AD without ACLF in the derivation cohort, the 94 (9.6%) patients with pre-ACLF had the highest 3-month and 1-year LT-free mortality (61.6% and 70.9%, respectively), which was comparable to those with ACLF at enrollment (57.1% and 67.1%); the 251 (25.9%) patients with unstable decompensated cirrhosis had mortality rates of 22.4% and 32.1%, respectively; while the 507 (57.9%) patients with stable decompensated cirrhosis had the best outcomes (1-year mortality rate of 2.6%). Through Cox proportional hazard regression, specific precipitants, including hepatitis B flare with HBV reactivation, spontaneous hepatitis B flare with high viral load, superimposed infection on HBV, and bacterial infection, were identified to be significantly associated with ACLF occurrence in the derivation cohort. A model that incorporated precipitants, indicators of systemic inflammation and organ injuries reached a high C-index of 0.90 and 0.86 in derivation and validation cohorts, respectively. The optimal cut-off value (0.22) differentiated high-risk and low-risk patients, with a negative predictive value of 0.95. CONCLUSIONS: Three distinct clinical courses of patients with AD are validated in the HBV-etiology population. The precipitants significantly impact on AD-ACLF transition. A model developed by the precipitant–systemic inflammation–organ injury framework could be a useful tool for predicting ACLF occurrence. CLINICAL TRIAL NUMBER: NCT02457637 and NCT03641872. LAY SUMMARY: It was previously shown that patients with decompensated cirrhosis could be stratified into 3 groups based on their short-term clinical prognoses. Herein, we showed that this stratification applies to patients who develop cirrhosis as a result of hepatitis B virus infection. We also developed a precipitant-based model (i.e. a model that incorporated information about the exact cause of decompensation) that could predict the likelihood of these patients developing a very severe liver disease called acute-on-chronic liver failure (or ACLF).