Safety and efficacy of continuous terlipressin infusion in HRS-AKI in a transplant population.


Journal

Liver transplantation : official publication of the American Association for the Study of Liver Diseases and the International Liver Transplantation Society
ISSN: 1527-6473
Titre abrégé: Liver Transpl
Pays: United States
ID NLM: 100909185

Informations de publication

Date de publication:
22 May 2024
Historique:
received: 02 12 2023
accepted: 06 05 2024
medline: 21 5 2024
pubmed: 21 5 2024
entrez: 21 5 2024
Statut: aheadofprint

Résumé

Hepatorenal syndrome-acute kidney injury (HRS-AKI) is associated with significant morbidity and mortality. While liver transplantation is the definitive treatment, continuous terlipressin infusion for HRS-AKI may provide benefit and as such was assessed in a population comprised of liver transplant (LT) candidates. Fifty hospitalized, LT-eligible patients with HRS-AKI received a single bolus followed by continuous terlipressin infusion. ACLF grade 3, serum creatinine (SCr)>5.0 mg/dL, or MELD≥35 were exclusions. Fifty hospitalized patients who received midodrine and octreotide (M&O) or norepinephrine (NorEpi) for HRS-AKI served as a historical comparator cohort. Complete response (CR) was defined as ≥30% decrease in SCr with EOT SCr≤1.5, partial response (PR) as ≥30% decrease in SCr with EOT SCr>1.5, and non-response (NR) as <30% decrease in SCr. CR rate was significantly higher in the terlipressin cohort compared to the historical cohort (64% vs. 16%, p<0.001). Survival, while numerically higher in those who received terlipressin, was statistically similar (D30: 94% vs. 82%, p=0.12; D90: 78% vs. 68%, p=0.37). Renal replacement therapy (RRT) was more common among terlipressin NR than CR and PR (70% vs. 3% vs. 13%, p<0.001). EOT MELD and SCr were significantly lower within terlipressin cohort (MELD: 19 vs. 25, SCr: 1.4 vs. 2.1 mg/dL, p<0.001). Sixteen of 40 terlipressin-treated patients received LT-alone (terlipressin CR in 10/16). One patient on terlipressin had hypoxic respiratory failure that responded to diuretics; one possibly had drug-related rash. With continuous terlipressin infusion, a CR rate of 64% was observed with a favorable safety profile. Terlipressin use was associated with lower EOT MELD and SCr than the historical M&O/NorEpi cohort; LT-alone was accomplished in a high proportion of complete terlipressin responders.

Sections du résumé

BACKGROUND AND AIMS OBJECTIVE
Hepatorenal syndrome-acute kidney injury (HRS-AKI) is associated with significant morbidity and mortality. While liver transplantation is the definitive treatment, continuous terlipressin infusion for HRS-AKI may provide benefit and as such was assessed in a population comprised of liver transplant (LT) candidates.
METHODS AND RESULTS RESULTS
Fifty hospitalized, LT-eligible patients with HRS-AKI received a single bolus followed by continuous terlipressin infusion. ACLF grade 3, serum creatinine (SCr)>5.0 mg/dL, or MELD≥35 were exclusions. Fifty hospitalized patients who received midodrine and octreotide (M&O) or norepinephrine (NorEpi) for HRS-AKI served as a historical comparator cohort. Complete response (CR) was defined as ≥30% decrease in SCr with EOT SCr≤1.5, partial response (PR) as ≥30% decrease in SCr with EOT SCr>1.5, and non-response (NR) as <30% decrease in SCr. CR rate was significantly higher in the terlipressin cohort compared to the historical cohort (64% vs. 16%, p<0.001). Survival, while numerically higher in those who received terlipressin, was statistically similar (D30: 94% vs. 82%, p=0.12; D90: 78% vs. 68%, p=0.37). Renal replacement therapy (RRT) was more common among terlipressin NR than CR and PR (70% vs. 3% vs. 13%, p<0.001). EOT MELD and SCr were significantly lower within terlipressin cohort (MELD: 19 vs. 25, SCr: 1.4 vs. 2.1 mg/dL, p<0.001). Sixteen of 40 terlipressin-treated patients received LT-alone (terlipressin CR in 10/16). One patient on terlipressin had hypoxic respiratory failure that responded to diuretics; one possibly had drug-related rash.
CONCLUSIONS CONCLUSIONS
With continuous terlipressin infusion, a CR rate of 64% was observed with a favorable safety profile. Terlipressin use was associated with lower EOT MELD and SCr than the historical M&O/NorEpi cohort; LT-alone was accomplished in a high proportion of complete terlipressin responders.

Identifiants

pubmed: 38771635
doi: 10.1097/LVT.0000000000000399
pii: 01445473-990000000-00385
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2024 The Author(s). Published by Wolters Kluwer Health, Inc.

Auteurs

K Rajender Reddy (KR)

Division of Gastroenterology and Hepatology, University of Pennsylvania Perelman School of Medicine.

Ethan M Weinberg (EM)

Division of Gastroenterology and Hepatology, University of Pennsylvania Perelman School of Medicine.

Stevan A Gonzalez (SA)

Division of Hepatology, Simmons Transplant Institute, Baylor Scott & White All Saints Medical Center.

Manhal J Izzy (MJ)

Department of Gastroenterology, Hepatology, and Nutrition, Vanderbilt University Medical Center.

Douglas A Simonetto (DA)

Division of Gastroenterology and Hepatology, Mayo Clinic.

R Todd Frederick (RT)

Hepatology and Liver Transplantation, California Pacific Medical Center.

Raymond A Rubin (RA)

Department of Transplantation, Piedmont Transplant Institute, Piedmont Healthcare.

Zachary Fricker (Z)

Division of Gastroenterology, Hepatology, and Nutrition, Beth Israel Deaconess Medical Center, Harvard Medical School.

Jade Ikahihifo-Bender (J)

Division of Gastroenterology and Hepatology, University of Pennsylvania Perelman School of Medicine.

Maggie Harte (M)

Division of Gastroenterology and Hepatology, University of Pennsylvania Perelman School of Medicine.

Sandra Garcia (S)

Division of Hepatology, Simmons Transplant Institute, Baylor Scott & White All Saints Medical Center.

Kathryn Campbell (K)

Department of Gastroenterology, Hepatology, and Nutrition, Vanderbilt University Medical Center.

Amy Olofson (A)

Division of Gastroenterology and Hepatology, Mayo Clinic.

Ryan F Razavi (RF)

Hepatology and Liver Transplantation, California Pacific Medical Center.

Janelle M James (JM)

Department of Transplantation, Piedmont Transplant Institute, Piedmont Healthcare.

Het Patel (H)

Division of Gastroenterology, Hepatology, and Nutrition, Beth Israel Deaconess Medical Center, Harvard Medical School.

Grace Kim-Lee (G)

Division of Gastroenterology and Hepatology, University of Pennsylvania Perelman School of Medicine.

Sherry Witkiewicz (S)

International HealthCare, LLC.

William Tobin (W)

International HealthCare, LLC.

Khurram Jamil (K)

Formerly at Mallinckrodt Pharmaceuticals, Scientific Affairs.

Classifications MeSH