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Early treatment with terlipressin in patients with hepatorenal syndrome yields improved clinical outcomes in North American studies
Hepatorenal syndrome type 1 (HRS-1) is a serious complication of advanced cirrhosis and a potentially reversible form of acute kidney injury that is associated with rapidly deteriorating kidney function. Liver transplantation remains the only curative treatment for decompensated cirrhosis. However,...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9827960/ https://www.ncbi.nlm.nih.gov/pubmed/36633470 http://dx.doi.org/10.1097/01.HC9.0000897228.91307.0c |
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author | Curry, Michael P. Vargas, Hugo E. Befeler, Alex S. Pyrsopoulos, Nikolaos T. Patwardhan, Vilas R. Jamil, Khurram |
author_facet | Curry, Michael P. Vargas, Hugo E. Befeler, Alex S. Pyrsopoulos, Nikolaos T. Patwardhan, Vilas R. Jamil, Khurram |
author_sort | Curry, Michael P. |
collection | PubMed |
description | Hepatorenal syndrome type 1 (HRS-1) is a serious complication of advanced cirrhosis and a potentially reversible form of acute kidney injury that is associated with rapidly deteriorating kidney function. Liver transplantation remains the only curative treatment for decompensated cirrhosis. However, terlipressin, a vasopressin analog, successfully reverses HRS-1, and may improve patient survival while awaiting liver transplantation. Patients with higher baseline serum creatinine have a reduced response to treatment with terlipressin. These post hoc analyses examined pooled data from 352 patients with HRS-1 treated with terlipressin in 3 North American-centric, Phase III, placebo-controlled clinical studies (i.e. OT-0401, REVERSE, and CONFIRM)—across 3 serum creatinine subgroups (i.e. <3, ≥3–<5, and ≥5 mg/dL)—to further delineate their correlation with HRS reversal, renal replacement therapy-free survival, and overall survival. Serum creatinine was significantly associated with HRS reversal in univariate and multivariate logistic regression analyses (P<0.001). The incidence of HRS reversal inversely correlated with serum creatinine subgroup (<3 mg/dL, 49.2%; ≥3–<5 mg/dL, 28.0%; ≥5 mg/dL, 9.1%). At Day 30 follow-up, renal replacement therapy-free survival was significantly higher for patients with HRS-1 in the lower serum creatinine subgroups than in the higher subgroup (<5 vs. >5 mg/dL; p=0.01). Terlipressin-treated patients with HRS-1, with a lower baseline serum creatinine level, had a higher overall survival (p<0.001) and higher transplant-free survival at Day 90 (p=0.04). Patients with HRS-1 and lower serum creatinine levels who were treated with terlipressin had higher HRS reversal and survival outcomes, highlighting the significant need to identify and treat patients with HRS-1 early when they often have lower serum creatinine levels, and likely a greater response to terlipressin. |
format | Online Article Text |
id | pubmed-9827960 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-98279602023-03-16 Early treatment with terlipressin in patients with hepatorenal syndrome yields improved clinical outcomes in North American studies Curry, Michael P. Vargas, Hugo E. Befeler, Alex S. Pyrsopoulos, Nikolaos T. Patwardhan, Vilas R. Jamil, Khurram Hepatol Commun Original Articles Hepatorenal syndrome type 1 (HRS-1) is a serious complication of advanced cirrhosis and a potentially reversible form of acute kidney injury that is associated with rapidly deteriorating kidney function. Liver transplantation remains the only curative treatment for decompensated cirrhosis. However, terlipressin, a vasopressin analog, successfully reverses HRS-1, and may improve patient survival while awaiting liver transplantation. Patients with higher baseline serum creatinine have a reduced response to treatment with terlipressin. These post hoc analyses examined pooled data from 352 patients with HRS-1 treated with terlipressin in 3 North American-centric, Phase III, placebo-controlled clinical studies (i.e. OT-0401, REVERSE, and CONFIRM)—across 3 serum creatinine subgroups (i.e. <3, ≥3–<5, and ≥5 mg/dL)—to further delineate their correlation with HRS reversal, renal replacement therapy-free survival, and overall survival. Serum creatinine was significantly associated with HRS reversal in univariate and multivariate logistic regression analyses (P<0.001). The incidence of HRS reversal inversely correlated with serum creatinine subgroup (<3 mg/dL, 49.2%; ≥3–<5 mg/dL, 28.0%; ≥5 mg/dL, 9.1%). At Day 30 follow-up, renal replacement therapy-free survival was significantly higher for patients with HRS-1 in the lower serum creatinine subgroups than in the higher subgroup (<5 vs. >5 mg/dL; p=0.01). Terlipressin-treated patients with HRS-1, with a lower baseline serum creatinine level, had a higher overall survival (p<0.001) and higher transplant-free survival at Day 90 (p=0.04). Patients with HRS-1 and lower serum creatinine levels who were treated with terlipressin had higher HRS reversal and survival outcomes, highlighting the significant need to identify and treat patients with HRS-1 early when they often have lower serum creatinine levels, and likely a greater response to terlipressin. Lippincott Williams & Wilkins 2023-01-03 /pmc/articles/PMC9827960/ /pubmed/36633470 http://dx.doi.org/10.1097/01.HC9.0000897228.91307.0c Text en Copyright © 2023 The Authors. Published by Wolters Kluwer Health, Inc. on behalf of the American Association for the Study of Liver Diseases. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) (CCBY-NC-ND), where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) |
spellingShingle | Original Articles Curry, Michael P. Vargas, Hugo E. Befeler, Alex S. Pyrsopoulos, Nikolaos T. Patwardhan, Vilas R. Jamil, Khurram Early treatment with terlipressin in patients with hepatorenal syndrome yields improved clinical outcomes in North American studies |
title | Early treatment with terlipressin in patients with hepatorenal syndrome yields improved clinical outcomes in North American studies |
title_full | Early treatment with terlipressin in patients with hepatorenal syndrome yields improved clinical outcomes in North American studies |
title_fullStr | Early treatment with terlipressin in patients with hepatorenal syndrome yields improved clinical outcomes in North American studies |
title_full_unstemmed | Early treatment with terlipressin in patients with hepatorenal syndrome yields improved clinical outcomes in North American studies |
title_short | Early treatment with terlipressin in patients with hepatorenal syndrome yields improved clinical outcomes in North American studies |
title_sort | early treatment with terlipressin in patients with hepatorenal syndrome yields improved clinical outcomes in north american studies |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9827960/ https://www.ncbi.nlm.nih.gov/pubmed/36633470 http://dx.doi.org/10.1097/01.HC9.0000897228.91307.0c |
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