Evidence map›Paper›PMID 42107856›Full record

ArticleClinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association2026

United States Experience With Terlipressin in Hepatorenal Syndrome: Response, Mortality, and Transplant Outcomes - Results From the HRS Harmony Consortium.

Kavish R Patidar, Giuseppe Cullaro, Eric S Orman, J Pedro Teixeira, Javier A Neyra, Jevon E Robinson, Aanchal Kapoor, Douglas A Simonetto, Stevan A Gonzalez, Sumeet K Asrani and 38 more

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Article in Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

48 authors.

Kavish R PatidarSherrie and Alan Conover Center for Liver Disease and Transplantation, J.C. Walter Jr Transplant Center, Houston Methodist Hospital, Houston, Texas.
Giuseppe CullaroCenter for Liver Disease and Transplantation, Columbia University Vagelos College of Physicians and Surgeons, New York, New York.
Eric S OrmanDivision of Gastroenterology and Hepatology, Indiana University School of Medicine, Indianapolis, Indiana.
J Pedro TeixeiraDivision of Nephrology, Department of Internal Medicine, University of New Mexico School of Medicine, Albuquerque, New Mexico.
Javier A NeyraDivision of Nephrology, Department of Medicine, University of Alabama at Birmingham, Birmingham, Alabama.
Jevon E RobinsonDivision of Nephrology, Department of Medicine, Massachusetts General Hospital, Boston, Massachusetts.
Aanchal KapoorDepartment of Critical Care, Integrated Hospital Institute, Cleveland Clinic, Cleveland, Ohio.
Douglas A SimonettoDivision of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota.
Stevan A GonzalezAnnette C. and Harold C. Simmons Transplant Institute, Baylor Scott & White All Saints Medical Center, Fort Worth, Texas; Burnett School of Medicine at TCU, Fort Worth, Texas.
Sumeet K AsraniAnnette C. and Harold C. Simmons Transplant Institute, Baylor Scott & White All Saints Medical Center, Fort Worth, Texas.
Hugo E VargasDivision of Gastroenterology and Hepatology, Mayo Clinic, Phoenix, Arizona.
Anjana RajanNorthwestern University, Chicago, Illinois.
Zachary FrickerDivision of Gastroenterology, Hepatology, and Nutrition, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts.
Ethan WeinbergDivision of Gastroenterology, University of Pennsylvania, Philadelphia, Pennsylvania.
Juan Carlos VelezDepartment of Nephrology, Ochsner Health, New Orleans, Louisiana; Ochsner Clinical School, The University of Queensland (Australia), New Orleans, Louisiana.
Justin M BelcherSection of Nephrology, Yale University School of Medicine, New Haven, Connecticut.
Hani WadeiMayo Clinic, Jacksonville, Florida.
Brett FortuneMontefiore Einstein Center for Transplantation, Bronx, New York.
R Todd FrederickDivision of Hepatology, Department of Advanced Organ Therapies and Transplantation, California Pacific Medical Center, San Francisco, California.
Omar MehkriDepartment of Critical Care, Integrated Hospital Institute, Cleveland Clinic, Cleveland, Ohio.
Bridget DolanDepartment of Critical Care, Integrated Hospital Institute, Cleveland Clinic, Cleveland, Ohio.
Caleigh PickettDepartment of Critical Care, Integrated Hospital Institute, Cleveland Clinic, Cleveland, Ohio.
Jeremy SkvarceDepartment of Internal Medicine, Primary Care Institute, Cleveland Clinic, Cleveland, Ohio.
Saloni SacharDepartment of Internal Medicine, Primary Care Institute, Cleveland Clinic, Cleveland, Ohio.
Christina LindenmeyerDepartment of Gastroenterology, Hepatology and Nutrition, Cleveland Clinic, Cleveland, Ohio.
Tianqi OuyangDivision of Nephrology, Department of Medicine, Massachusetts General Hospital, Boston, Massachusetts.
Nneka UfereDivision of Gastroenterology, Department of Medicine, Massachusetts General Hospital, Boston, Massachusetts.
Xing LiDivision of Gastroenterology, Department of Medicine, Massachusetts General Hospital, Boston, Massachusetts.
Lexie LopesDivision of Nephrology, Department of Medicine, Massachusetts General Hospital, Boston, Massachusetts.
Shelsea St HillienDivision of Nephrology, Department of Medicine, Massachusetts General Hospital, Boston, Massachusetts.
Sydney WhittakerDivision of Nephrology, Department of Medicine, Massachusetts General Hospital, Boston, Massachusetts.
Victoria KusztosDivision of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota.
Natalie VellutiniDivision of Gastroenterology and Hepatology, Indiana University School of Medicine, Indianapolis, Indiana.
Anand VissaUniversity of California San Francisco, San Francisco, California.
Olivia C WalkerAnnette C. and Harold C. Simmons Transplant Institute, Baylor Scott & White All Saints Medical Center, Fort Worth, Texas.
Connor FischbachAnnette C. and Harold C. Simmons Transplant Institute, Baylor Scott & White All Saints Medical Center, Fort Worth, Texas.
Justin BoikeNorthwestern University, Chicago, Illinois.
Madelyn SuboczTransplant Research Institute, Beth Israel Deaconess Medical Center, Boston, Massachusetts.
Sevda AghayevaDivision of Gastroenterology, University of Pennsylvania, Philadelphia, Pennsylvania.
Gavin SkipperDepartment of Research, Ochsner Medical Center, New Orleans, Louisiana; Louisiana State University Health School of Medicine, New Orleans, Louisiana.
Luis Madera MarinDivision of Nephrology, Department of Internal Medicine, University of New Mexico School of Medicine, Albuquerque, New Mexico.
Rohanit SinghSection of Nephrology, Yale University School of Medicine, New Haven, Connecticut.
Ibrahim AlhayaniMayo Clinic, Jacksonville, Florida.
George ZakourMayo Clinic, Jacksonville, Florida.
Walid HaddadMayo Clinic, Jacksonville, Florida.
Paola MejiaMontefiore Einstein Center for Transplantation, Bronx, New York.
Andrew S AllegrettiDivision of Nephrology, Department of Medicine, Massachusetts General Hospital, Boston, Massachusetts. Electronic address: aallegretti@mgh.harvard.edu.
HRS-HARMONY Research Collaboration

Funding

The Southeastern Acute Kidney Injury (SEAK) Alliance for the COPE-AKI ConsortiumU01DK129989 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Javier A. Neyra, Edward D Siew · 2021 to 2026
$4.7M
UAB-UCSD O'Brien Center for Acute Kidney Injury ResearchU54DK137307 · NIDDK · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI Javier A. Neyra · 2023 to 2026
$4.4M
Artificial Intelligence to Predict Outcomes in Patients with Acute Kidney Injury on Continuous Renal Replacement TherapyR01DK133539 · NIDDK · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI Girish Nitin Nadkarni, Javier A. Neyra · 2023 to 2026
$2.6M
The Relation of Soluble Klotho with Cardiovascular Disease, Chronic Kidney Disease Progression, and Blood Pressure in the Systolic Blood Pressure Intervention TrialR01DK128208 · NIDDK · TUFTS MEDICAL CENTER · PI DREW, DAVID ALAN, NEYRA, JAVIER A. · 2021 to 2025
$1.6M
Personalizing Therapies for Acute Kidney Injury in CirrhosisK23DK128567 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI Andrew S Allegretti · 2022 to 2026
$982k
Application of Novel Biomarkers of Renal Health in Cirrhosis Patients to Stratify Risk of Acute Kidney Injury Occurrence and ReversibilityK23DK131278 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Giuseppe Cullaro · 2022 to 2026
$812k
NIDDK NIH HHS K23 DK128567NIDDK NIH HHS K23 DK131278NIDDK NIH HHS L30 DK133959NIDDK NIH HHS R01 DK128208NIDDK NIH HHS R01 DK133539NIDDK NIH HHS U01 DK129989NIDDK NIH HHS U54 DK137307
6 · The paper itself

Abstract

BACKGROUND &

aimsTerlipressin became the first United States Food and Drug Administration-approved therapy for hepatorenal syndrome-acute kidney injury in 2022. We present its initial experience at 16 United States academic medical centers.

methodsConsecutive patients with hepatorenal syndrome-acute kidney injury treated with terlipressin were followed for 90 days. Patients met standard criteria (conforming to United States Food and Drug Administration labeling guidance) or extended criteria (presence of ≥1 United States Food and Drug Administration warning/limitation: acute-on-chronic liver failure grade 3, serum creatinine >5 mg/dL, or hypoxia at initiation). Primary outcomes were overall response (complete or partial response per guidelines) and hepatorenal syndrome reversal (terminal serum creatinine <1.5 mg/dL plus ≥0.3 mg/dL reduction). Fine and Gray models with liver transplant as a competing risk were used to assess 90-day mortality.

resultsA total of 243 patients were analyzed. 40.5% died and 27.2% received liver transplant by 90 days. Overall response occurred in 55.1% and hepatorenal syndrome reversal in 30.9%. Forty-nine percent met extended criteria, most commonly due to acute-on-chronic liver failure grade 3 (45%). Standard criteria was associated with higher overall response (62.9% vs 47.1%; P = .019) and fewer adverse events leading to terlipressin discontinuation (12.1% vs 22.7%; P = .044). In adjusted analysis, hepatorenal syndrome reversal was not associated with reduced mortality, but overall response was (subdistribution hazard ratio, 0.57; 95% confidence interval, 0.38-0.86; P = .01).

conclusionsThis United States multicenter study provides insights into real-world use of terlipressin for hepatorenal syndrome-acute kidney injury. Terlipressin was frequently used in patients with acute-on-chronic liver failure grade 3. Adherence to United States Food and Drug Administration labeling criteria was associated with superior efficacy and safety. The significant association between overall response and reduced mortality underscores its potential as a clinically relevant endpoint for future studies.

Indexed as

Acute Kidney InjuryAcute-on-Chronic Liver FailureCirrhosisLiver TransplantVasoconstrictor

Identifiers

PMID42107856
PMCPMC13191569

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