Risk and protective factors of acute kidney injury in decompensated cirrhotic patients with ascites on tolvaptan
Abstract 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...
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oai:doaj.org-article:ff3454c328a441bcb29330f82a08e43a2021-11-18T11:25:44ZRisk and protective factors of acute kidney injury in decompensated cirrhotic patients with ascites on tolvaptan2397-907010.1002/jgh3.12672https://doaj.org/article/ff3454c328a441bcb29330f82a08e43a2021-11-01T00:00:00Zhttps://doi.org/10.1002/jgh3.12672https://doaj.org/toc/2397-9070Abstract 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.Tomomi KogisoYuri OgasawaraTakaomi SagawaMakiko TaniaiKatsutoshi TokushigeWileyarticleacute kidney injurykanamycin/rifaximinliver cirrhosisproton pump inhibitor/H2 blockerstolvaptanDiseases of the digestive system. GastroenterologyRC799-869ENJGH Open, Vol 5, Iss 11, Pp 1298-1305 (2021) |
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acute kidney injury kanamycin/rifaximin liver cirrhosis proton pump inhibitor/H2 blockers tolvaptan Diseases of the digestive system. Gastroenterology RC799-869 |
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acute kidney injury kanamycin/rifaximin liver cirrhosis proton pump inhibitor/H2 blockers tolvaptan Diseases of the digestive system. Gastroenterology RC799-869 Tomomi Kogiso Yuri Ogasawara Takaomi Sagawa Makiko Taniai Katsutoshi Tokushige Risk and protective factors of acute kidney injury in decompensated cirrhotic patients with ascites on tolvaptan |
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Abstract 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. |
format |
article |
author |
Tomomi Kogiso Yuri Ogasawara Takaomi Sagawa Makiko Taniai Katsutoshi Tokushige |
author_facet |
Tomomi Kogiso Yuri Ogasawara Takaomi Sagawa Makiko Taniai Katsutoshi Tokushige |
author_sort |
Tomomi Kogiso |
title |
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_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_sort |
risk and protective factors of acute kidney injury in decompensated cirrhotic patients with ascites on tolvaptan |
publisher |
Wiley |
publishDate |
2021 |
url |
https://doaj.org/article/ff3454c328a441bcb29330f82a08e43a |
work_keys_str_mv |
AT tomomikogiso riskandprotectivefactorsofacutekidneyinjuryindecompensatedcirrhoticpatientswithascitesontolvaptan AT yuriogasawara riskandprotectivefactorsofacutekidneyinjuryindecompensatedcirrhoticpatientswithascitesontolvaptan AT takaomisagawa riskandprotectivefactorsofacutekidneyinjuryindecompensatedcirrhoticpatientswithascitesontolvaptan AT makikotaniai riskandprotectivefactorsofacutekidneyinjuryindecompensatedcirrhoticpatientswithascitesontolvaptan AT katsutoshitokushige riskandprotectivefactorsofacutekidneyinjuryindecompensatedcirrhoticpatientswithascitesontolvaptan |
_version_ |
1718420882620153856 |