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Acute kidney injury is independently associated with death in patients with cirrhosis

BACKGROUND AND AIMS: Current creatine-based criteria for defining acute kidney injury (AKI) are validated in general hospitalised patients but their application to cirrhotics (who are younger and have reduced muscle mass) is less certain. We aimed to evaluate current definitions of AKI (acute kidney...

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Autores principales: Scott, Robert A, Austin, Andrew S, Kolhe, Nitin V, McIntyre, Chris W, Selby, Nicholas M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3955898/
https://www.ncbi.nlm.nih.gov/pubmed/24660054
http://dx.doi.org/10.1136/flgastro-2012-100291
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author Scott, Robert A
Austin, Andrew S
Kolhe, Nitin V
McIntyre, Chris W
Selby, Nicholas M
author_facet Scott, Robert A
Austin, Andrew S
Kolhe, Nitin V
McIntyre, Chris W
Selby, Nicholas M
author_sort Scott, Robert A
collection PubMed
description BACKGROUND AND AIMS: Current creatine-based criteria for defining acute kidney injury (AKI) are validated in general hospitalised patients but their application to cirrhotics (who are younger and have reduced muscle mass) is less certain. We aimed to evaluate current definitions of AKI (acute kidney injury network (AKIN) criteria) in a population of cirrhotic patients and correlate this with outcomes. METHODS: We prospectively identified patients with AKI and clinical, radiological or histological evidence of cirrhosis. We compared them with a control group with evidence of cirrhosis and no AKI. RESULTS: 162 cirrhotic patients were studied with a mean age of 56.8±14 years. They were predominantly male (65.4%) with alcoholic liver disease (78.4%). 110 patients had AKI: 44 stage 1, 32 stage 2 and 34 stage 3. They were well matched in age, sex and liver disease severity with 52 cirrhotics without AKI. AKI was associated with increased mortality (31.8% vs 3.8%, p<0.001). Mortality increased with each AKI stage; 3.8% in cirrhotics without AKI, 13.5% stage 1, 37.8% stage 2 and 43.2% stage 3 (p<0.001 for trend). Worsening liver disease (Child–Pugh class) correlated with increased mortality: 3.1% class A, 23.6% class B and 32.8% class C (p=0.006 for trend). AKI was associated with increased length of stay: median 6.0 days (IQR 4.0–8.75) versus 16.0 days (IQR 6.0–27.5), p<0.001. Multivariate analysis identified AKI and Child–Pugh classes B and C as independent factors associated with mortality. CONCLUSIONS: The utility of AKIN criteria is maintained in cirrhotic patients. Decompensated liver disease and AKI appear to be independent variables predicting death in cirrhotics.
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spelling pubmed-39558982014-03-20 Acute kidney injury is independently associated with death in patients with cirrhosis Scott, Robert A Austin, Andrew S Kolhe, Nitin V McIntyre, Chris W Selby, Nicholas M Frontline Gastroenterol Liver BACKGROUND AND AIMS: Current creatine-based criteria for defining acute kidney injury (AKI) are validated in general hospitalised patients but their application to cirrhotics (who are younger and have reduced muscle mass) is less certain. We aimed to evaluate current definitions of AKI (acute kidney injury network (AKIN) criteria) in a population of cirrhotic patients and correlate this with outcomes. METHODS: We prospectively identified patients with AKI and clinical, radiological or histological evidence of cirrhosis. We compared them with a control group with evidence of cirrhosis and no AKI. RESULTS: 162 cirrhotic patients were studied with a mean age of 56.8±14 years. They were predominantly male (65.4%) with alcoholic liver disease (78.4%). 110 patients had AKI: 44 stage 1, 32 stage 2 and 34 stage 3. They were well matched in age, sex and liver disease severity with 52 cirrhotics without AKI. AKI was associated with increased mortality (31.8% vs 3.8%, p<0.001). Mortality increased with each AKI stage; 3.8% in cirrhotics without AKI, 13.5% stage 1, 37.8% stage 2 and 43.2% stage 3 (p<0.001 for trend). Worsening liver disease (Child–Pugh class) correlated with increased mortality: 3.1% class A, 23.6% class B and 32.8% class C (p=0.006 for trend). AKI was associated with increased length of stay: median 6.0 days (IQR 4.0–8.75) versus 16.0 days (IQR 6.0–27.5), p<0.001. Multivariate analysis identified AKI and Child–Pugh classes B and C as independent factors associated with mortality. CONCLUSIONS: The utility of AKIN criteria is maintained in cirrhotic patients. Decompensated liver disease and AKI appear to be independent variables predicting death in cirrhotics. BMJ Publishing Group 2013-07 2013-04-18 /pmc/articles/PMC3955898/ /pubmed/24660054 http://dx.doi.org/10.1136/flgastro-2012-100291 Text en Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 3.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Liver
Scott, Robert A
Austin, Andrew S
Kolhe, Nitin V
McIntyre, Chris W
Selby, Nicholas M
Acute kidney injury is independently associated with death in patients with cirrhosis
title Acute kidney injury is independently associated with death in patients with cirrhosis
title_full Acute kidney injury is independently associated with death in patients with cirrhosis
title_fullStr Acute kidney injury is independently associated with death in patients with cirrhosis
title_full_unstemmed Acute kidney injury is independently associated with death in patients with cirrhosis
title_short Acute kidney injury is independently associated with death in patients with cirrhosis
title_sort acute kidney injury is independently associated with death in patients with cirrhosis
topic Liver
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3955898/
https://www.ncbi.nlm.nih.gov/pubmed/24660054
http://dx.doi.org/10.1136/flgastro-2012-100291
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