Global epidemiology of acute kidney injury in hospitalised patients with decompensated cirrhosis: the International Club of Ascites GLOBAL AKI prospective, multicentre, cohort study
- PMID: 40058397
- DOI: 10.1016/S2468-1253(25)00006-8
Global epidemiology of acute kidney injury in hospitalised patients with decompensated cirrhosis: the International Club of Ascites GLOBAL AKI prospective, multicentre, cohort study
Erratum in
-
Correction to Lancet Gastroenterol Hepatol 2025; 10: 418-30.Lancet Gastroenterol Hepatol. 2025 Jul;10(7):e9. doi: 10.1016/S2468-1253(25)00166-9. Lancet Gastroenterol Hepatol. 2025. PMID: 40482660 No abstract available.
Abstract
Background: Acute kidney injury (AKI) is a serious complication of cirrhosis. A systematic, global characterisation of AKI occurring in patients with cirrhosis is lacking. We therefore aimed to assess global differences in the characteristics, management, and outcomes of AKI in hospitalised patients with cirrhosis.
Methods: In this prospective, multicentre, cohort study, we enrolled adults (≥18 years) with decompensated cirrhosis who were hospitalised for a cirrhosis-related complication, with or without AKI, at 65 centres across five continents. We captured AKI prevalence, stage, phenotype, and details on AKI management and clinical course. Universal health coverage index and gross national income per capita were also collected. The primary outcome was 28-day mortality. Multivariable models including demographic and clinical variables, cirrhosis cause, cirrhosis severity, AKI severity, AKI management variables, universal health coverage, and gross national income were used to analyse independent associations with 28-day mortality. Secondary outcomes were AKI classification, progression, and resolution. This study is complete and registered with ClinicalTrials.gov (NCT05387811).
Findings: Between July 1, 2022, and May 31, 2023, we enrolled 3821 patients who were hospitalised for decompensated cirrhosis. Mean age was 57·7 years (SD 13·1), 2467 (64·6%) were men, and 1354 (35·4%) were women. Most patients were White (2128 [55·7%]). 1456 (38·1%, 95% CI 36·6-39·6) of 3821 patients had AKI (943 [64·8%] men and 513 [35·2%] women). Globally, patients presented with similar AKI stages, but patients from North America and Asia had the highest MELD-Na scores at presentation and the highest rates of peak AKI stage 3. Overall, hypovolaemic AKI was the most common phenotype (858 [58·9%] of 1456), followed by HRS-AKI (253 [17·4%]) and acute tubular necrosis (216 [14·8%]). The prevalences of hypovolaemic AKI and HRS-AKI were similar across regions, but acute tubular necrosis was more frequent in Asia (p<0·0001 across regions). Additionally, regional differences in the management of AKI (use of albumin, vasopressors, and diuretics) were found. 335 (28·6%) of 1171 patients with initial AKI stages 1 or 2 had progression to higher stages during hospitalisation. AKI resolved in 862 (59·2%) cases during hospitalisation. 333 (22·9%) patients with AKI had died by 28 days. Multivariable analyses showed that increased age, female sex, presence of ascites, presence of hepatic encephalopathy, increased white blood cell count, increased MELD-Na, hospital-acquired AKI, a lower universal health coverage index (<80), and not being in a high-income country were independently associated with an increased risk of 28-day mortality. Increased serum albumin was associated with a decreased risk of 28-day mortality.
Interpretation: This study found important regional differences in AKI severity, phenotype, management, and outcomes in patients with decompensated cirrhosis. Health-care coverage remains an important driver of survival in patients with cirrhosis and AKI.
Funding: European Association Study for the Study of the Liver and the Italian Society of Internal Medicine.
Copyright © 2025 Elsevier Ltd. All rights reserved, including those for text and data mining, AI training, and similar technologies.
Conflict of interest statement
Declaration of interests KRP received advisory board fees from Madrigal Pharmaceuticals. YJW received speaking fees from Gilead and AbbVie. NTP received research grants from OCELOT. DAS consulted for Mallinckrodt, BioVie, Evive, Resolution Therapeutics, PharmaIN, AstraZeneca, and Iota. MP received funding from the Ministry of Innovation and Technology of Hungary, and the National Research, Development and Innovation Fund. PC received speaking fees from Grifols, Octapharma, CSL Behring; research grants from Grifols and Octapharma; and advisory board fees from CSL Behring. CML received speakers honoraria and advisory board fees from AbbVie, Gilead, Falk, Eisai, Norgine, CSL Behring, Boston Scientific, AstraZeneca, Shionogi, Roche, and Sobi. VV received speaking fees from Orphalan; and advisory board fees from Ipsen. MaMe received speaker honoraria from Gore. AK has served as speaker for Novo Nordisk, Norgine, Siemens and Nordic Bioscience; and participated in advisory boards for Norgine, Siemens, Resalis Therapeutics, Boehringer Ingelheim, and Novo Nordisk, all outside the submitted work; has received research support from Norgine, Siemens, Nordic Bioscience, Astra, and Echosense; and is a board member and co-founder of Evido. TB received speaking fees, consulting fees or travel support from Abbvie, Gilead, SOBI, CSL Behring, Merck, Gore, and Advanz. ASA has received consulting fees from Mallinckrodt Pharmaceuticals, Ocelot Bio, Sequana Medical, Bioporto, and Motric Bio. FD received speaking fees from Biotest and Chiesi. PG received research funding from Gilead and Grifols; has consulted or attended advisory boards for Gilead, RallyBio, SeaBeLife, Merck, Sharp and Dohme, Ocelot Bio, CSL Behring, Roche Diagnostics International, Boehringer Ingelheim, and AstraZeneca; and has received speaking fees from Pfizer. PA received grant or research support from Grifols and CSL Behring; held a patent with Biovie; and served as consultant for Sequana Medical. SP served as consultant for Plasma Protein Therapeutics Association, Boehringer Ingelheim, and Resolution Therapeutics; and received speaking fees from Grifols, Ferring, and Medscape. All other authors declare no competing interests.
Comment in
-
Acute kidney injury in liver cirrhosis: a global challenge.Lancet Gastroenterol Hepatol. 2025 May;10(5):400-401. doi: 10.1016/S2468-1253(25)00044-5. Epub 2025 Mar 6. Lancet Gastroenterol Hepatol. 2025. PMID: 40058396 No abstract available.
Publication types
MeSH terms
Associated data
LinkOut - more resources
Full Text Sources
Medical
