Prospective validation of the EASL management algorithm for acute kidney injury in cirrhosis

dc.contributor.author
Ma, Ann T.
dc.contributor.author
Solé, Cristina
dc.contributor.author
Juanola, Adrià
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Escudé, Laia
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Napoleone, Laura
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Avitabile, Emma
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Pérez-Guasch, Martina
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Carol, Marta
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Pompili, Enrico
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Gratacós Ginès, Jordi
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Soria, Anna
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Rubio, Ana Belén
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Cervera Carbonell, Marta
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Moreta, Maria José
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Morales Ruiz, Manuel
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Solà, Elsa
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Poch, Esteban
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Fabrellas i Padrès, Núria
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Graupera, Isabel
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Pose Méndez, Elisa
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Ginès i Gibert, Pere
dc.date.accessioned
2026-04-14T09:34:20Z
dc.date.available
2026-04-14T09:34:20Z
dc.date.issued
2026-04-13T17:14:40Z
dc.date.issued
2026-04-13T17:14:40Z
dc.date.issued
2024-09
dc.date.issued
2026-04-13T17:14:40Z
dc.identifier
0168-8278
dc.identifier
https://hdl.handle.net/2445/228874
dc.identifier
747550
dc.identifier
38479614
dc.identifier.uri
https://hdl.handle.net/2445/228874
dc.description.abstract
Background & Aims The management of acute kidney injury (AKI) in cirrhosis is challenging. The EASL guidelines proposed an algorithm for the management of AKI, but this has never been validated. We aimed to prospectively evaluate this algorithm in clinical practice. Methods We performed a prospective cohort study in consecutive hospitalized patients with cirrhosis and AKI. The EASL management algorithm includes identification/treatment of precipitating factors, 2-day albumin infusion in patients with AKI ≥stage 1B, and treatment with terlipressin in patients with hepatorenal syndrome (HRS-AKI). The primary outcome was treatment response, which included both full and partial response. Secondary outcomes were survival and adverse events associated with terlipressin therapy. Results A total of 202 AKI episodes in 139 patients were included. Overall treatment response was 80%, while renal replacement therapy was required in only 8%. Response to albumin infusion was achieved in one-third of episodes. Of patients not responding to albumin, most (74%) did not meet the diagnostic criteria of HRS-AKI, with acute tubular necrosis (ATN) being the most common phenotype. The response rate in patients not meeting the criteria for HRS-AKI was 70%. Only 30 patients met the diagnostic criteria for HRS-AKI, and their response rate to terlipressin was 61%. Median time from AKI diagnosis to terlipressin initiation was only 2.5 days. While uNGAL (urinary neutrophil gelatinase-associated lipocalin) could differentiate ATN from other phenotypes (AUROC 0.78), it did not predict response to therapy in HRS-AKI. Ninety-day transplant-free survival was negatively associated with MELD-Na, ATN and HRS-AKI as well as uNGAL. Three patients treated with terlipressin developed pulmonary edema. Conclusions The application of the EASL AKI algorithm is associated with very good response rates and does not significantly delay initiation of terlipressin therapy. Impact and implications The occurrence of acute kidney injury (AKI) in patients with cirrhosis is associated with poor short-term mortality. Improving its rapid identification and prompt management was the focus of the recently proposed EASL AKI algorithm. This is the first prospective study demonstrating that high AKI response rates are achieved with the use of this algorithm, which includes identification of AKI, treatment of precipitating factors, a 2-day albumin challenge in patients with AKI ≥1B, and supportive therapy in patients with persistent AKI not meeting HRS-AKI criteria or terlipressin with albumin in those with HRS-AKI. These findings support the use of this algorithm in clinical practice.
dc.format
11 p.
dc.format
application/pdf
dc.language
eng
dc.publisher
Elsevier
dc.relation
Reproducció del document publicat a: https://doi.org/10.1016/j.jhep.2024.03.006
dc.relation
Journal of Hepatology, 2024, vol. 81, num.3, p. 441-450
dc.relation
https://doi.org/10.1016/j.jhep.2024.03.006
dc.rights
cc-by-nc-nd (c) Ma, Ann T. et al., 2024
dc.rights
http://creativecommons.org/licenses/by-nc-nd/4.0/
dc.rights
info:eu-repo/semantics/openAccess
dc.subject
Malalties del ronyó
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Cirrosi hepàtica
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Marcadors bioquímics
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Insuficiència renal aguda
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Kidney diseases
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Hepatic cirrhosis
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Biochemical markers
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Acute renal failure
dc.title
Prospective validation of the EASL management algorithm for acute kidney injury in cirrhosis
dc.type
info:eu-repo/semantics/article
dc.type
info:eu-repo/semantics/publishedVersion


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