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Effect of COVID-19 on patients with compensated chronic liver diseases

BACKGROUND AND AIM: Cytokine storm has been reported in patients with coronavirus disease 2019 (COVID-19) due to severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) infection. We examine the incidence of acute on chronic liver failure (ACLF) in COVID-19 patients with pre-existing compensate...

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Autores principales: Ji, Dong, Zhang, Dawei, Yang, Tieniu, Mu, Jinsong, Zhao, Peng, Xu, Jing, Li, Chen, Cheng, Gregory, Wang, Yudong, Chen, Zhu, Qin, Enqiang, Lau, George
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer India 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7391917/
https://www.ncbi.nlm.nih.gov/pubmed/32734407
http://dx.doi.org/10.1007/s12072-020-10058-6
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author Ji, Dong
Zhang, Dawei
Yang, Tieniu
Mu, Jinsong
Zhao, Peng
Xu, Jing
Li, Chen
Cheng, Gregory
Wang, Yudong
Chen, Zhu
Qin, Enqiang
Lau, George
author_facet Ji, Dong
Zhang, Dawei
Yang, Tieniu
Mu, Jinsong
Zhao, Peng
Xu, Jing
Li, Chen
Cheng, Gregory
Wang, Yudong
Chen, Zhu
Qin, Enqiang
Lau, George
author_sort Ji, Dong
collection PubMed
description BACKGROUND AND AIM: Cytokine storm has been reported in patients with coronavirus disease 2019 (COVID-19) due to severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) infection. We examine the incidence of acute on chronic liver failure (ACLF) in COVID-19 patients with pre-existing compensated chronic liver disease (CLD). METHODS: From 20 Jan 2020 to 7 Feb 2020, we studied 140 consecutive COVID-19 patients admitted to either Fuyang Second People’s Hospital (FYSPH), Anhui or the Fifth Medical Center of Chinese PLA General Hospital (PLAGH) in Beijing, China. Pre-existing CLD includes those with liver cirrhosis assessed by APRI/FIB-4 score and /or ultrasound; NAFLD as identified by either ultrasound or hepatic steatosis index with significant liver fibrosis and chronic hepatitis B (CHB) or hepatitis C (CHC) infection. The diagnosis, grading of severity and clinical management of COVID-19 patients complied to the guideline and clinical protocol issued by the China National Health Commission. All patients had liver function test at least twice weekly till discharge with full recovery or death. RESULTS: In total, 3 had liver cirrhosis, 6 patients had CHB, 13 had NAFLD with significant liver fibrosis (one also had CHB). On admission, none had liver decompensation. COVID-19 disease progression was significantly less frequent in non-CLD patients (10/118 8.5%) than CLD patients (13/22 59.1%, p < 0.001). One patient with CLD had acute-on-chronic liver failure (ACLF). CONCLUSION: Disease progression is significantly higher in those COVID-19 patients with CLD as compared to those with no CLD. ACLF can also occur in patient with pre-existing compensated CLD who had severe COVID-19.
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spelling pubmed-73919172020-07-31 Effect of COVID-19 on patients with compensated chronic liver diseases Ji, Dong Zhang, Dawei Yang, Tieniu Mu, Jinsong Zhao, Peng Xu, Jing Li, Chen Cheng, Gregory Wang, Yudong Chen, Zhu Qin, Enqiang Lau, George Hepatol Int Original Article BACKGROUND AND AIM: Cytokine storm has been reported in patients with coronavirus disease 2019 (COVID-19) due to severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) infection. We examine the incidence of acute on chronic liver failure (ACLF) in COVID-19 patients with pre-existing compensated chronic liver disease (CLD). METHODS: From 20 Jan 2020 to 7 Feb 2020, we studied 140 consecutive COVID-19 patients admitted to either Fuyang Second People’s Hospital (FYSPH), Anhui or the Fifth Medical Center of Chinese PLA General Hospital (PLAGH) in Beijing, China. Pre-existing CLD includes those with liver cirrhosis assessed by APRI/FIB-4 score and /or ultrasound; NAFLD as identified by either ultrasound or hepatic steatosis index with significant liver fibrosis and chronic hepatitis B (CHB) or hepatitis C (CHC) infection. The diagnosis, grading of severity and clinical management of COVID-19 patients complied to the guideline and clinical protocol issued by the China National Health Commission. All patients had liver function test at least twice weekly till discharge with full recovery or death. RESULTS: In total, 3 had liver cirrhosis, 6 patients had CHB, 13 had NAFLD with significant liver fibrosis (one also had CHB). On admission, none had liver decompensation. COVID-19 disease progression was significantly less frequent in non-CLD patients (10/118 8.5%) than CLD patients (13/22 59.1%, p < 0.001). One patient with CLD had acute-on-chronic liver failure (ACLF). CONCLUSION: Disease progression is significantly higher in those COVID-19 patients with CLD as compared to those with no CLD. ACLF can also occur in patient with pre-existing compensated CLD who had severe COVID-19. Springer India 2020-07-30 /pmc/articles/PMC7391917/ /pubmed/32734407 http://dx.doi.org/10.1007/s12072-020-10058-6 Text en © Asian Pacific Association for the Study of the Liver 2020 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Original Article
Ji, Dong
Zhang, Dawei
Yang, Tieniu
Mu, Jinsong
Zhao, Peng
Xu, Jing
Li, Chen
Cheng, Gregory
Wang, Yudong
Chen, Zhu
Qin, Enqiang
Lau, George
Effect of COVID-19 on patients with compensated chronic liver diseases
title Effect of COVID-19 on patients with compensated chronic liver diseases
title_full Effect of COVID-19 on patients with compensated chronic liver diseases
title_fullStr Effect of COVID-19 on patients with compensated chronic liver diseases
title_full_unstemmed Effect of COVID-19 on patients with compensated chronic liver diseases
title_short Effect of COVID-19 on patients with compensated chronic liver diseases
title_sort effect of covid-19 on patients with compensated chronic liver diseases
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7391917/
https://www.ncbi.nlm.nih.gov/pubmed/32734407
http://dx.doi.org/10.1007/s12072-020-10058-6
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