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Risk and protective factors of acute kidney injury in decompensated cirrhotic patients with ascites on tolvaptan

BACKGROUND AND AIM: Acute kidney injury (AKI) is a life‐threatening complication of liver cirrhosis. Here, we evaluated the risk factors and characteristics of AKI in cirrhosis. PATIENTS/METHODS: This was a single‐center retrospective study. A total of 199 Japanese patients with decompensated liver...

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Autores principales: Kogiso, Tomomi, Ogasawara, Yuri, Sagawa, Takaomi, Taniai, Makiko, Tokushige, Katsutoshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wiley Publishing Asia Pty Ltd 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8593781/
https://www.ncbi.nlm.nih.gov/pubmed/34816016
http://dx.doi.org/10.1002/jgh3.12672
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author Kogiso, Tomomi
Ogasawara, Yuri
Sagawa, Takaomi
Taniai, Makiko
Tokushige, Katsutoshi
author_facet Kogiso, Tomomi
Ogasawara, Yuri
Sagawa, Takaomi
Taniai, Makiko
Tokushige, Katsutoshi
author_sort Kogiso, Tomomi
collection PubMed
description BACKGROUND AND AIM: Acute kidney injury (AKI) is a life‐threatening complication of liver cirrhosis. Here, we evaluated the risk factors and characteristics of AKI in cirrhosis. PATIENTS/METHODS: This was a single‐center retrospective study. A total of 199 Japanese patients with decompensated liver cirrhosis (104 men, median age 61 years) were enrolled and received tolvaptan orally. Survival rates and new onset of AKI were monitored, and risk factors were evaluated. RESULTS: Forty‐six patients (23.1%) suffered an AKI complication and exhibited significantly poorer survival (P < 0.01). The rates of hepatic encephalopathy (P < 0.01) and chronic kidney disease (CKD; P = 0.02) were significantly increased in patients with AKI. The rate of proton pump inhibitor (PPI)/H2 blocker treatment (P = 0.04) was significantly lower, whereas that of ascites drainage was significantly higher in the AKI cases (P < 0.01). The AKI risk was significantly increased in patients with hepatic encephalopathy (HR 4.18, 95% CI 1.618–10.771). In contrast, the incidence of AKI was significantly lower in patients with a higher serum albumin level (HR 0.36, 95% CI 0.142–0.914, P = 0.03). Treatment with PPI/H2 blockers (HR 0.30, 95% CI 0.126–0.711, P < 0.01) or kanamycin/rifaximin (HR 0.26, 95% CI 0.075–0.929, P = 0.04) was significantly associated with a reduced risk of AKI development. CONCLUSIONS: AKI incidence was increased in patients with decreased liver function and was associated with poor survival. PPI/H2 blocker or kanamycin/rifaximin treatment may reduce the risk of AKI.
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spelling pubmed-85937812021-11-22 Risk and protective factors of acute kidney injury in decompensated cirrhotic patients with ascites on tolvaptan Kogiso, Tomomi Ogasawara, Yuri Sagawa, Takaomi Taniai, Makiko Tokushige, Katsutoshi JGH Open Original Articles BACKGROUND AND AIM: Acute kidney injury (AKI) is a life‐threatening complication of liver cirrhosis. Here, we evaluated the risk factors and characteristics of AKI in cirrhosis. PATIENTS/METHODS: This was a single‐center retrospective study. A total of 199 Japanese patients with decompensated liver cirrhosis (104 men, median age 61 years) were enrolled and received tolvaptan orally. Survival rates and new onset of AKI were monitored, and risk factors were evaluated. RESULTS: Forty‐six patients (23.1%) suffered an AKI complication and exhibited significantly poorer survival (P < 0.01). The rates of hepatic encephalopathy (P < 0.01) and chronic kidney disease (CKD; P = 0.02) were significantly increased in patients with AKI. The rate of proton pump inhibitor (PPI)/H2 blocker treatment (P = 0.04) was significantly lower, whereas that of ascites drainage was significantly higher in the AKI cases (P < 0.01). The AKI risk was significantly increased in patients with hepatic encephalopathy (HR 4.18, 95% CI 1.618–10.771). In contrast, the incidence of AKI was significantly lower in patients with a higher serum albumin level (HR 0.36, 95% CI 0.142–0.914, P = 0.03). Treatment with PPI/H2 blockers (HR 0.30, 95% CI 0.126–0.711, P < 0.01) or kanamycin/rifaximin (HR 0.26, 95% CI 0.075–0.929, P = 0.04) was significantly associated with a reduced risk of AKI development. CONCLUSIONS: AKI incidence was increased in patients with decreased liver function and was associated with poor survival. PPI/H2 blocker or kanamycin/rifaximin treatment may reduce the risk of AKI. Wiley Publishing Asia Pty Ltd 2021-11-01 /pmc/articles/PMC8593781/ /pubmed/34816016 http://dx.doi.org/10.1002/jgh3.12672 Text en © 2021 The Authors. JGH Open published by Journal of Gastroenterology and Hepatology Foundation and John Wiley & Sons Australia, Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Kogiso, Tomomi
Ogasawara, Yuri
Sagawa, Takaomi
Taniai, Makiko
Tokushige, Katsutoshi
Risk and protective factors of acute kidney injury in decompensated cirrhotic patients with ascites on tolvaptan
title Risk and protective factors of acute kidney injury in decompensated cirrhotic patients with ascites on tolvaptan
title_full Risk and protective factors of acute kidney injury in decompensated cirrhotic patients with ascites on tolvaptan
title_fullStr Risk and protective factors of acute kidney injury in decompensated cirrhotic patients with ascites on tolvaptan
title_full_unstemmed Risk and protective factors of acute kidney injury in decompensated cirrhotic patients with ascites on tolvaptan
title_short Risk and protective factors of acute kidney injury in decompensated cirrhotic patients with ascites on tolvaptan
title_sort risk and protective factors of acute kidney injury in decompensated cirrhotic patients with ascites on tolvaptan
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8593781/
https://www.ncbi.nlm.nih.gov/pubmed/34816016
http://dx.doi.org/10.1002/jgh3.12672
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