Predicting the Onset of Hepatitis B Virus–Related Acute-on-Chronic Liver Failure

医学 内科学 胃肠病学 铁蛋白 肝移植 接收机工作特性 胆红素 肝病 慢性肝病 终末期肝病模型 丙氨酸转氨酶 肝功能 乙型肝炎病毒 移植 免疫学 病毒 肝硬化
作者
Jinjin Luo,Xi Liang,Jiaojiao Xin,Jiaqi Li,Peng Li,Qian Zhou,Shaorui Hao,Huafen Zhang,Yingyan Lu,Tianzhou Wu,Li Wang,Jiang Li,Li Tan,Keke Ren,Beibei Guo,Xingping Zhou,Jiaxian Chen,Lulu He,Hui Yang,Wen Hu,Shaoli You,Shaojie Xin,Jing Jiang,Dongyan Shi,Xin Chen,­Jun Li­
出处
期刊:Clinical Gastroenterology and Hepatology [Elsevier]
卷期号:21 (3): 681-693 被引量:14
标识
DOI:10.1016/j.cgh.2022.03.016
摘要

Acute-on-chronic liver failure (ACLF) is a life-threatening syndrome with rapid progression. This study aimed to develop and validate a prognostic score to predict the onset of ACLF in hepatitis B virus (HBV) etiology.The prospective clinical data of 1373 patients with acute deterioration of HBV-related chronic liver disease were used to identify clinical characteristics and develop a prognostic score for the onset of ACLF.Of the patients assessed using the Chinese Group on the Study of Severe Hepatitis B (COSSH)-ACLF criteria, 903 patients with non-ACLF at admission (1 received transplantation at 5 days) were stratified: 71 with progression to ACLF and 831 without progression to ACLF at 7 days. Four predictors (total bilirubin, international normalized ratio, alanine aminotransferase, and ferritin) were associated significantly with ACLF onset at 7 days. The COSSH-onset-ACLF score was constituted as follows: (0.101 × ln [alanine aminotransferase] + 0.819 × ln [total bilirubin] + 2.820 × ln [international normalized ratio] + 0.016 × ln [ferritin]). The C-indexes of the new score for 7-/14-/28-day onset (0.928/0.925/0.913) were significantly higher than those of 5 other scores (Chronic Liver Failure Consortium ACLF development score/Model for End-stage Liver Disease score/Model for End-stage Liver Disease sodium score/COSSH-ACLF score/Chronic liver failure Consortium ACLF score; all P < .001). The improvement in predictive errors, time-dependent receiver operating characteristic, probability density function evaluation, and calibration curves of the new score showed the highest predictive value for ACLF onset at 7/14/28 days. Risk stratification of the new score showed 2 strata with high and low risk (≥6.3/<6.3) of ACLF onset. The external validation group further confirmed the earlier results.A new prognostic score based on 4 predictors can accurately predict the 7-/14-/28-day onset of ACLF in patients with acute deterioration of HBV-related chronic liver disease and might be used to guide clinical management.
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