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The progression of hepatorenal syndrome–acute kidney injury in acute alcohol-associated hepatitis: renal outcomes after liver transplant
BACKGROUND: Hepatorenal syndrome–acute kidney injury (HRS-AKI) is a complication of advanced liver disease in patients with ascites and circulatory dysfunction. Little data remain on the relationship between HRS-AKI outcomes and different etiologies of liver disease post-liver transplant (LT). OBJEC...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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SAGE Publications
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10392193/ https://www.ncbi.nlm.nih.gov/pubmed/37533707 http://dx.doi.org/10.1177/17562848231188813 |
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author | Colletta, Alessandro Cooper, Katherine M. Devuni, Deepika |
author_facet | Colletta, Alessandro Cooper, Katherine M. Devuni, Deepika |
author_sort | Colletta, Alessandro |
collection | PubMed |
description | BACKGROUND: Hepatorenal syndrome–acute kidney injury (HRS-AKI) is a complication of advanced liver disease in patients with ascites and circulatory dysfunction. Little data remain on the relationship between HRS-AKI outcomes and different etiologies of liver disease post-liver transplant (LT). OBJECTIVES: The primary aim was to evaluate the effect of HRS-AKI on renal outcomes in patients with acute alcohol-associated hepatitis (AAH) compared to chronic liver disease (CLD) after LT. The secondary aim was to evaluate the impact of acuity and chronicity of alcohol-associated liver disease in patients with HRS-AKI post-LT renal outcomes. DESIGN: A retrospective observational study of patients undergoing urgent inpatient liver transplant evaluation (LTE) for cirrhosis and AAH at single academic LT center between October 2017 and July 2021 was conducted. METHODS: Patients with HRS-AKI were selected based on indication for LTE: acute AAH(HRS) or CLD(HRS). CLD(HRS) was categorized by disease etiology: cirrhosis due to alcohol (A-CLD(HRS)) versus cirrhosis from other causes (O-CLD(HRS)). CLD patients without HRS-AKI were labeled CLD(no HRS). RESULTS: A total of 210 subjects underwent LTE; 25% were evaluated for AAH and 75% were evaluated for CLD. Hepatorenal syndrome was more common in subjects evaluated for AAH (37/47) than CLD (104/163) (78.7 versus 63.8%, p = 0.04). For the primary outcome, AAH(HRS) subjects required ⩾30 days post-LT renal replacement therapy (RRT) more often than subjects with CLD(HRS) (p = 0.02) and CLD(no HRS) (p < 0.01). There was no significant difference in other forms of long-term renal outcomes including kidney transplant referral and kidney transplant among cohorts. In subgroup analysis, 30-days post-LT RRT was more common in AAH(HRS) than in A-CLD(HRS) (p = 0.08). Logistic regression showed that AAH(HRS) conferred a 20× and 3.3× odds of requiring ⩾30 days post-LT RRT compared to CLD(no HRS) and CLD(HRS), respectively. Postoperative complications were similar across cohorts, but had a significant effect on 30-day renal outcome post-LT. CONCLUSIONS: Patients with AAH were more likely to develop HRS and require RRT pre- and post-LT at our center. The etiology of hepatic decompensation and postoperative complications affect renal recovery post-LT. The systemic inflammation of AAH in addition to conditions favoring renal hypoperfusion may contribute to the unfavorable outcomes of HRS-AKI after LT in this patient population. |
format | Online Article Text |
id | pubmed-10392193 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-103921932023-08-02 The progression of hepatorenal syndrome–acute kidney injury in acute alcohol-associated hepatitis: renal outcomes after liver transplant Colletta, Alessandro Cooper, Katherine M. Devuni, Deepika Therap Adv Gastroenterol Original Research BACKGROUND: Hepatorenal syndrome–acute kidney injury (HRS-AKI) is a complication of advanced liver disease in patients with ascites and circulatory dysfunction. Little data remain on the relationship between HRS-AKI outcomes and different etiologies of liver disease post-liver transplant (LT). OBJECTIVES: The primary aim was to evaluate the effect of HRS-AKI on renal outcomes in patients with acute alcohol-associated hepatitis (AAH) compared to chronic liver disease (CLD) after LT. The secondary aim was to evaluate the impact of acuity and chronicity of alcohol-associated liver disease in patients with HRS-AKI post-LT renal outcomes. DESIGN: A retrospective observational study of patients undergoing urgent inpatient liver transplant evaluation (LTE) for cirrhosis and AAH at single academic LT center between October 2017 and July 2021 was conducted. METHODS: Patients with HRS-AKI were selected based on indication for LTE: acute AAH(HRS) or CLD(HRS). CLD(HRS) was categorized by disease etiology: cirrhosis due to alcohol (A-CLD(HRS)) versus cirrhosis from other causes (O-CLD(HRS)). CLD patients without HRS-AKI were labeled CLD(no HRS). RESULTS: A total of 210 subjects underwent LTE; 25% were evaluated for AAH and 75% were evaluated for CLD. Hepatorenal syndrome was more common in subjects evaluated for AAH (37/47) than CLD (104/163) (78.7 versus 63.8%, p = 0.04). For the primary outcome, AAH(HRS) subjects required ⩾30 days post-LT renal replacement therapy (RRT) more often than subjects with CLD(HRS) (p = 0.02) and CLD(no HRS) (p < 0.01). There was no significant difference in other forms of long-term renal outcomes including kidney transplant referral and kidney transplant among cohorts. In subgroup analysis, 30-days post-LT RRT was more common in AAH(HRS) than in A-CLD(HRS) (p = 0.08). Logistic regression showed that AAH(HRS) conferred a 20× and 3.3× odds of requiring ⩾30 days post-LT RRT compared to CLD(no HRS) and CLD(HRS), respectively. Postoperative complications were similar across cohorts, but had a significant effect on 30-day renal outcome post-LT. CONCLUSIONS: Patients with AAH were more likely to develop HRS and require RRT pre- and post-LT at our center. The etiology of hepatic decompensation and postoperative complications affect renal recovery post-LT. The systemic inflammation of AAH in addition to conditions favoring renal hypoperfusion may contribute to the unfavorable outcomes of HRS-AKI after LT in this patient population. SAGE Publications 2023-07-31 /pmc/articles/PMC10392193/ /pubmed/37533707 http://dx.doi.org/10.1177/17562848231188813 Text en © The Author(s), 2023 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Original Research Colletta, Alessandro Cooper, Katherine M. Devuni, Deepika The progression of hepatorenal syndrome–acute kidney injury in acute alcohol-associated hepatitis: renal outcomes after liver transplant |
title | The progression of hepatorenal syndrome–acute kidney injury in acute alcohol-associated hepatitis: renal outcomes after liver transplant |
title_full | The progression of hepatorenal syndrome–acute kidney injury in acute alcohol-associated hepatitis: renal outcomes after liver transplant |
title_fullStr | The progression of hepatorenal syndrome–acute kidney injury in acute alcohol-associated hepatitis: renal outcomes after liver transplant |
title_full_unstemmed | The progression of hepatorenal syndrome–acute kidney injury in acute alcohol-associated hepatitis: renal outcomes after liver transplant |
title_short | The progression of hepatorenal syndrome–acute kidney injury in acute alcohol-associated hepatitis: renal outcomes after liver transplant |
title_sort | progression of hepatorenal syndrome–acute kidney injury in acute alcohol-associated hepatitis: renal outcomes after liver transplant |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10392193/ https://www.ncbi.nlm.nih.gov/pubmed/37533707 http://dx.doi.org/10.1177/17562848231188813 |
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