Volume 29, Issue 12 pp. 1089-1098
ORIGINAL ARTICLE

MELD score < 18 rule out 28-day ACLF development among inpatients with hepatitis B-related previous compensated liver disease

Tingting Qi

Tingting Qi

Hepatology Unit, Department of Infectious Diseases, Nanfang Hospital, Southern Medical University, Guangzhou, China

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Congyan Zhu

Congyan Zhu

Hepatology Unit, Department of Infectious Diseases, Nanfang Hospital, Southern Medical University, Guangzhou, China

Hepatology Unit and Department of Infectious Disease, Zhuhai People's Hospital, Zhuhai, China

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Jiapeng Wang

Jiapeng Wang

Hepatology Unit, Department of Infectious Diseases, Nanfang Hospital, Southern Medical University, Guangzhou, China

Department of Infectious Diseases, Tianjin First Central Hospital, Tianjin, China

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Beiling Li

Beiling Li

Hepatology Unit, Department of Infectious Diseases, Nanfang Hospital, Southern Medical University, Guangzhou, China

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Zuxiong Huang

Zuxiong Huang

Department of Hepatology, Mengchao Hepatobiliary Hospital of Fujian Medical University, Fuzhou, China

Department of Hepatology, Affiliated Infectious Disease Hospital of Fujian Medical University, Fuzhou, China

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Zhibin Zhu

Zhibin Zhu

The Forth Department of Hepatology, The Third People's Hospital of Shenzhen, Affiliated with Guangdong Medical College, Shenzhen, China

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Minghan Tu

Minghan Tu

Department of Hepatology, The Ninth Hospital of Nanchang, Nanchang, China

Hepatology Unit, Zengcheng Branch, Nanfang Hospital, Southern Medical University, Guangzhou, China

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Guohong Deng

Guohong Deng

Department of Infectious Diseases, Southwest Hospital, Third Military Medical University (Army Medical University), Chongqing, China

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Xin Zheng

Xin Zheng

Department of Infectious Diseases, Institute of Infection and Immunology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China

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Yan Huang

Yan Huang

Department of Infectious Diseases, Hunan Key Laboratory of Viral Hepatitis, Xiangya Hospital, Central South University, Changsha, China

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Zhongji Meng

Zhongji Meng

Department of Infectious Diseases, Hubei Clinical Research Center for Precise Diagnosis and Treatment of Liver Cancer, Taihe Hospital, Hubei University of Medicine, Shiyan, Hubei, China

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Xianbo Wang

Xianbo Wang

Center of Integrative Medicine, Beijing Ditan Hospital, Capital Medical University, Beijing, China

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Zhiping Qian

Zhiping Qian

Department of Liver Intensive Care Unit, Shanghai Public Health Clinical Centre, Fudan University, Shanghai, China

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Hai Li

Hai Li

Department of Gastroenterology, Ren Ji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, China

Shanghai Institute of Digestive Disease, Key Laboratory of Gastroenterology and Hepatology, Chinese Ministry of Health (Shanghai Jiao Tong University), Shanghai, China

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Yanhang Gao

Yanhang Gao

Department of Hepatology, The First Hospital of Jilin University, Changchun, China

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Feng Liu

Feng Liu

Department of Infectious Diseases and Hepatology, The Second Hospital of Shandong University, Jinan, China

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Jia Shang

Jia Shang

Department of Infectious Diseases, Henan Provincial People's Hospital, Zhengzhou, China

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Yu Shi

Yu Shi

The State Key Laboratory for Diagnosis and Treatment of Infectious Diseases, The First Affiliated Hospital of School of Medicine, Zhejiang University, Hangzhou, China

Collaborative Innovation Center for Diagnosis and Treatment of Infectious Disease, Hangzhou, China

National Clinical Research Center of Infectious Disease, Hangzhou, China

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Xiaobo Lu

Xiaobo Lu

Infectious Disease Center, The First Affiliated Hospital of Xinjiang Medical University, Urumqi, China

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Shaoyang Wang

Shaoyang Wang

Department of Infectious Diseases, Fuzhou General Hospital of Nanjing Military Command, Fujian, China

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Hai Li

Corresponding Author

Hai Li

Department of Infectious Diseases, Affiliated Hospital of Logistics University of People's Armed Police Force, Tianjin, China

Correspondence

Jinjun Chen, Hepatology Unit, Department of Infectious Diseases, Nanfang Hospital, Southern Medical University, Guangzhou, China, Hepatology Unit, Zengcheng Branch, Nanfang Hospital, Southern Medical University, Guangzhou, China.

Email: [email protected]

Hai Li, Department of Gastroenterology, Ren Ji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, China.

Email: [email protected]

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Jinjun Chen

Corresponding Author

Jinjun Chen

Hepatology Unit, Department of Infectious Diseases, Nanfang Hospital, Southern Medical University, Guangzhou, China

Hepatology Unit, Zengcheng Branch, Nanfang Hospital, Southern Medical University, Guangzhou, China

Correspondence

Jinjun Chen, Hepatology Unit, Department of Infectious Diseases, Nanfang Hospital, Southern Medical University, Guangzhou, China, Hepatology Unit, Zengcheng Branch, Nanfang Hospital, Southern Medical University, Guangzhou, China.

Email: [email protected]

Hai Li, Department of Gastroenterology, Ren Ji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, China.

Email: [email protected]

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First published: 08 September 2022
Citations: 1

Tingting Qi, Congyan Zhu and Jiapeng Wang equally contributed and share first authorship.

Jinjun Chen and Hai Li equally contributed and share corresponding authorship.

Abstract

The acute-on-chronic liver failure (ACLF) development is highly dynamic. Currently, no satisfactory algorithm identifies patients with HBV at risk of this complication. The aim of the study was to characterize ACLF development in hospitalized HBV-related patients without previous decompensation and to test the performance of traditional prognostic models in ruling out ACLF development within 28 days on admission we conducted a cohort study. Two multi-center cohorts with hospitalized HBV-related previous compensated patients were analyzed. Performances of MELD, MELD-Na, CLIF-C AD, and CLIF-C ACLF-D in ruling out ACLF development within 28 days were compared and further validated by ROC analyses. In the derivation cohort (n = 892), there were 102 patients developed ACLF within 28 days, with profound systemic inflammatory levels and higher 28-day mortality rate (31.4% vs. 1.0%) than those without ACLF development. The MELD score (cut-off = 18) achieved acceptable missing rate (missed/total ACLF development) at 2.9%. In the validation cohort (n = 1656), the MELD score (<18) was able to rule out ACLF development within 28 days with missing rate at 3.0%. ACLF development within 28 days were both lower than 1% (0.6%, derivation cohort; 0.5%, validation cohort) in patients with MELD < 18. While in patients with MELD ≥ 18, 26.6% (99/372, derivation cohort) and 17.8% (130/732, validation cohort) developed into ACLF within 28 days, respectively. While MELD-Na score cut-off at 20 and CLIF-AD score cut-off at 42 did not have consistent performance in our two cohorts. MELD < 18 was able to safely rule out patients with ACLF development within 28 days in HBV-related patients without previous decompensation, which had a high 28-day mortality.

CONFLICT OF INTERESTS

The authors declare that they do not have anything to disclose regarding funding or conflict of interest with respect to this manuscript.

DATA AVAILABILITY STATEMENT

The data that support the findings of this study are available from the corresponding author upon reasonable request.

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