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Acute on chronic liver failure: A South Australian experience
BACKGROUND AND AIM: Acute on chronic liver failure (ACLF) is a clinical syndrome described in patients with acute decompensation (AD) of cirrhosis, characterized by organ failures and high mortality. Intensive management, including liver transplantation (LT), has been shown to improve survival. To a...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wiley Publishing Asia Pty Ltd
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10615173/ https://www.ncbi.nlm.nih.gov/pubmed/37908287 http://dx.doi.org/10.1002/jgh3.12974 |
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author | Madigan, Shauna Tashkent, Yasmina Trehan, Sharad Muller, Kate Wigg, Alan Woodman, Richard Ramachandran, Jeyamani |
author_facet | Madigan, Shauna Tashkent, Yasmina Trehan, Sharad Muller, Kate Wigg, Alan Woodman, Richard Ramachandran, Jeyamani |
author_sort | Madigan, Shauna |
collection | PubMed |
description | BACKGROUND AND AIM: Acute on chronic liver failure (ACLF) is a clinical syndrome described in patients with acute decompensation (AD) of cirrhosis, characterized by organ failures and high mortality. Intensive management, including liver transplantation (LT), has been shown to improve survival. To address the limited Australian data on ACLF, we describe the prevalence, clinical profile, and outcome of ACLF in an Australian cohort of hospitalized patients. METHODS: A retrospective review of hepatology admissions in a tertiary hospital from 1 January 2017 to 31 December 2019 identified AD and ACLF cohorts, as defined by the European Association for Study of the Liver definition. Patient characteristics, clinical course, survival at 28‐ and 90‐day survival, and feasibility of LT were analyzed. RESULTS: Among the 192 admissions with AD, 74 admissions (39%) met ACLF criteria. A prior diagnosis of alcohol‐related cirrhosis was highly prevalent in both cohorts. Grade‐1 ACLF was the most frequent (60%), with renal failure being the commonest organ failure; 28‐day (23% vs 2%, P = <0.001) and 90‐day mortality (36% vs 16%, P = 0.002) were higher in ACLF than AD. Due to ongoing alcohol use disorder (AUD), only six patients underwent LT assessment during ACLF admission. CONCLUSION: ACLF was common in our cohort of cirrhosis with AD and was associated with high mortality. AUD despite prior cirrhosis diagnosis was a barrier to LT. Prioritization of ACLF patients for LT after addressing AUD and relaxation of the 6‐month abstinence rule may improve ACLF survival and should be addressed in prospective studies. |
format | Online Article Text |
id | pubmed-10615173 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Wiley Publishing Asia Pty Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-106151732023-10-31 Acute on chronic liver failure: A South Australian experience Madigan, Shauna Tashkent, Yasmina Trehan, Sharad Muller, Kate Wigg, Alan Woodman, Richard Ramachandran, Jeyamani JGH Open Original Articles BACKGROUND AND AIM: Acute on chronic liver failure (ACLF) is a clinical syndrome described in patients with acute decompensation (AD) of cirrhosis, characterized by organ failures and high mortality. Intensive management, including liver transplantation (LT), has been shown to improve survival. To address the limited Australian data on ACLF, we describe the prevalence, clinical profile, and outcome of ACLF in an Australian cohort of hospitalized patients. METHODS: A retrospective review of hepatology admissions in a tertiary hospital from 1 January 2017 to 31 December 2019 identified AD and ACLF cohorts, as defined by the European Association for Study of the Liver definition. Patient characteristics, clinical course, survival at 28‐ and 90‐day survival, and feasibility of LT were analyzed. RESULTS: Among the 192 admissions with AD, 74 admissions (39%) met ACLF criteria. A prior diagnosis of alcohol‐related cirrhosis was highly prevalent in both cohorts. Grade‐1 ACLF was the most frequent (60%), with renal failure being the commonest organ failure; 28‐day (23% vs 2%, P = <0.001) and 90‐day mortality (36% vs 16%, P = 0.002) were higher in ACLF than AD. Due to ongoing alcohol use disorder (AUD), only six patients underwent LT assessment during ACLF admission. CONCLUSION: ACLF was common in our cohort of cirrhosis with AD and was associated with high mortality. AUD despite prior cirrhosis diagnosis was a barrier to LT. Prioritization of ACLF patients for LT after addressing AUD and relaxation of the 6‐month abstinence rule may improve ACLF survival and should be addressed in prospective studies. Wiley Publishing Asia Pty Ltd 2023-10-03 /pmc/articles/PMC10615173/ /pubmed/37908287 http://dx.doi.org/10.1002/jgh3.12974 Text en © 2023 The Authors. JGH Open published by Journal of Gastroenterology and Hepatology Foundation and John Wiley & Sons Australia, Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Original Articles Madigan, Shauna Tashkent, Yasmina Trehan, Sharad Muller, Kate Wigg, Alan Woodman, Richard Ramachandran, Jeyamani Acute on chronic liver failure: A South Australian experience |
title | Acute on chronic liver failure: A South Australian experience |
title_full | Acute on chronic liver failure: A South Australian experience |
title_fullStr | Acute on chronic liver failure: A South Australian experience |
title_full_unstemmed | Acute on chronic liver failure: A South Australian experience |
title_short | Acute on chronic liver failure: A South Australian experience |
title_sort | acute on chronic liver failure: a south australian experience |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10615173/ https://www.ncbi.nlm.nih.gov/pubmed/37908287 http://dx.doi.org/10.1002/jgh3.12974 |
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