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Rifaximin Reduces Risk of All-Cause Hospitalization in Cirrhotic Liver Transplant Candidates with Hepatic Encephalopathy

In cirrhotic patients listed for liver transplantation (LT) with a history of hepatic encephalopathy (HE), rifaximin reduces the number of hospitalizations, but whether it influences the time to first hospitalization is unknown. Aims: to evaluate the time-dependent impact of rifaximin on the risk of...

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Autores principales: Parisse, Simona, Lai, Quirino, Martini, Francesca, Martini, Alice, Ferri, Flaminia, Mischitelli, Monica, Melandro, Fabio, Mennini, Gianluca, Rossi, Massimo, Alvaro, Domenico, Ginanni Corradini, Stefano
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10647372/
https://www.ncbi.nlm.nih.gov/pubmed/37959336
http://dx.doi.org/10.3390/jcm12216871
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author Parisse, Simona
Lai, Quirino
Martini, Francesca
Martini, Alice
Ferri, Flaminia
Mischitelli, Monica
Melandro, Fabio
Mennini, Gianluca
Rossi, Massimo
Alvaro, Domenico
Ginanni Corradini, Stefano
author_facet Parisse, Simona
Lai, Quirino
Martini, Francesca
Martini, Alice
Ferri, Flaminia
Mischitelli, Monica
Melandro, Fabio
Mennini, Gianluca
Rossi, Massimo
Alvaro, Domenico
Ginanni Corradini, Stefano
author_sort Parisse, Simona
collection PubMed
description In cirrhotic patients listed for liver transplantation (LT) with a history of hepatic encephalopathy (HE), rifaximin reduces the number of hospitalizations, but whether it influences the time to first hospitalization is unknown. Aims: to evaluate the time-dependent impact of rifaximin on the risk of all-cause hospitalization and dropout in patients on the LT waiting list. Methods: Consecutive patients listed for LT were retrospectively enrolled. After balancing populations with and without rifaximin treatment using the inverse probability therapy weighting analysis, Fine–Gray multivariable competing risk analyses were run to explore risk factors for the first episode of hospitalization and dropout. Results: When comparing 92 patients taking rifaximin to the untreated group of 152, rifaximin treatment was not associated with any of the study outcomes. In the subset of patients with a history of HE at waitlist entry (N = 81 rifaximin-treated and N = 39 untreated), rifaximin intake was independently associated with a lower risk of hospitalization for all causes (SHR 0.638; 95.0% CI 0.418–0.973; p = 0.037) and for HE (SHR 0.379; 95.0% CI 0.207–0.693; p = 0.002). Conclusions: cirrhotic LT candidates with a prior history of HE rifaximin treatment are associated with a lower risk of time-dependent all-cause hospitalization, likely due to its unique effect on gut microbiome composition/function.
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spelling pubmed-106473722023-10-31 Rifaximin Reduces Risk of All-Cause Hospitalization in Cirrhotic Liver Transplant Candidates with Hepatic Encephalopathy Parisse, Simona Lai, Quirino Martini, Francesca Martini, Alice Ferri, Flaminia Mischitelli, Monica Melandro, Fabio Mennini, Gianluca Rossi, Massimo Alvaro, Domenico Ginanni Corradini, Stefano J Clin Med Article In cirrhotic patients listed for liver transplantation (LT) with a history of hepatic encephalopathy (HE), rifaximin reduces the number of hospitalizations, but whether it influences the time to first hospitalization is unknown. Aims: to evaluate the time-dependent impact of rifaximin on the risk of all-cause hospitalization and dropout in patients on the LT waiting list. Methods: Consecutive patients listed for LT were retrospectively enrolled. After balancing populations with and without rifaximin treatment using the inverse probability therapy weighting analysis, Fine–Gray multivariable competing risk analyses were run to explore risk factors for the first episode of hospitalization and dropout. Results: When comparing 92 patients taking rifaximin to the untreated group of 152, rifaximin treatment was not associated with any of the study outcomes. In the subset of patients with a history of HE at waitlist entry (N = 81 rifaximin-treated and N = 39 untreated), rifaximin intake was independently associated with a lower risk of hospitalization for all causes (SHR 0.638; 95.0% CI 0.418–0.973; p = 0.037) and for HE (SHR 0.379; 95.0% CI 0.207–0.693; p = 0.002). Conclusions: cirrhotic LT candidates with a prior history of HE rifaximin treatment are associated with a lower risk of time-dependent all-cause hospitalization, likely due to its unique effect on gut microbiome composition/function. MDPI 2023-10-31 /pmc/articles/PMC10647372/ /pubmed/37959336 http://dx.doi.org/10.3390/jcm12216871 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Parisse, Simona
Lai, Quirino
Martini, Francesca
Martini, Alice
Ferri, Flaminia
Mischitelli, Monica
Melandro, Fabio
Mennini, Gianluca
Rossi, Massimo
Alvaro, Domenico
Ginanni Corradini, Stefano
Rifaximin Reduces Risk of All-Cause Hospitalization in Cirrhotic Liver Transplant Candidates with Hepatic Encephalopathy
title Rifaximin Reduces Risk of All-Cause Hospitalization in Cirrhotic Liver Transplant Candidates with Hepatic Encephalopathy
title_full Rifaximin Reduces Risk of All-Cause Hospitalization in Cirrhotic Liver Transplant Candidates with Hepatic Encephalopathy
title_fullStr Rifaximin Reduces Risk of All-Cause Hospitalization in Cirrhotic Liver Transplant Candidates with Hepatic Encephalopathy
title_full_unstemmed Rifaximin Reduces Risk of All-Cause Hospitalization in Cirrhotic Liver Transplant Candidates with Hepatic Encephalopathy
title_short Rifaximin Reduces Risk of All-Cause Hospitalization in Cirrhotic Liver Transplant Candidates with Hepatic Encephalopathy
title_sort rifaximin reduces risk of all-cause hospitalization in cirrhotic liver transplant candidates with hepatic encephalopathy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10647372/
https://www.ncbi.nlm.nih.gov/pubmed/37959336
http://dx.doi.org/10.3390/jcm12216871
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