Real-world Use of Terlipressin in Cirrhosis and Acute Kidney Injury: Frequent Use Beyond Hepatorenal Syndrome

Ann T Ma, Adrià Juanola, Kavish R Patidar, Anna Barone, Simone Incicco, Anand V Kulkarni, Nipun Verma, Christian M Lange, Qing Xie, Carlo Alessandria, Eira Cerda Reyes, Rakhi Maiwall, Jeong Han Kim, Sebastián Marciano, Alberto Queiroz Farias, Claudio Toledo, Silvia Nardelli, Julio D Vorobioff, Juan Pablo Roblero, Thierry ThévenotMaria Papp, Raoel Maan, Cristina Solé, Jacqueline Cordova-Gallardo, Douglas A Simonetto, Yasser Fouad, Lorenz Balcar, Sarah Raevens, Puria Nabilou, Paolo Caraceni, Manuela Merli, José Presa, Wim Laleman, Aleksander Krag, Tony Bruns, Gustavo Pereira, Angelo Z Mattos, Juan Pablo Arab, Brian Wentworth, Nadia Abdelaaty Abdelkader, Yu Jun Wong, Sung-Eun Kim, Olivier Roux, R Bart Takkenberg, Antonio Galante, Luciana Lofego Goncalves, Nikolaos T Pyrsopoulos, José Luis Pérez Hernández, Sumeet K Asrani, Aldo Torre, International Club of Ascites GLOBAL AKI team

Research output: Contribution to journalArticlepeer-review

Abstract

BACKGROUND & AIMS: Terlipressin is indicated to treat hepatorenal syndrome (HRS)-acute kidney injury (AKI) but is likely used outside this primary indication in clinical practice. We aimed to investigate real-world practice patterns on the use of terlipressin in AKI in cirrhosis.

METHODS: International prospective study including patients hospitalized for decompensated cirrhosis. This was a subgroup analysis of patients who received terlipressin to treat AKI. Primary outcome was AKI resolution. Secondary outcomes were respiratory failure and 28-day mortality.

RESULTS: Among 1456 patients with AKI, 243 (17%) received terlipressin. Terlipressin was predominantly administered as a continuous infusion (75%). The AKI phenotype was HRS-AKI in 50%, acute tubular necrosis (ATN) in 17%, hypovolemic in 25%, and other in 8%. AKI resolution occurred in 49% of the patients, and was lowest in ATN (29%), followed by HRS-AKI (51%) and hypovolemic (63%). ATN was independently associated with lack of AKI resolution (odds ratio, 2.77; 95% confidence interval, 1.24-6.54; P = .02). De novo respiratory failure occurred in 20% of patients. There were no significant differences in the amount of albumin received nor acute-on-chronic liver failure grade between those who did and did not develop respiratory failure. The presence of pneumonia independently predicted respiratory failure (odds ratio, 7.80; 95% confidence interval, 2.43-26.95; P < .001). Mortality rate at 28 days was 36%; ATN and hospital-acquired AKI independently predicted 28-day mortality.

CONCLUSIONS: Terlipressin is often used for treatment of AKI outside its primary indication of HRS-AKI. Compared with patients with HRS-AKI, response to terlipressin is significantly lower in patients with ATN, in whom the risks may outweigh the benefits. Respiratory failure is common but does not seem to be driven by the amount of albumin received nor acute-on-chronic liver failure grade.

Original languageEnglish (US)
JournalClinical Gastroenterology and Hepatology
DOIs
StateE-pub ahead of print - Sep 8 2025

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