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Timing of Hepatitis C Virus Treatment in Liver Transplant Candidates in the Era of Direct-acting Antiviral Agents

Chronic hepatitis C virus (HCV) infection remains the leading indication for liver transplantation (LT) in the United States. While most patients with chronic HCV infection remain asymptomatic, up to one-third develop progressive liver disease resulting in cirrhosis. LT is often the only curative tr...

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Autores principales: Cholankeril, George, Joseph-Talreja, Mairin, Perumpail, Brandon J., Liu, Andy, Yoo, Eric R., Ahmed, Aijaz, Goel, Aparna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: XIA & HE Publishing Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5719193/
https://www.ncbi.nlm.nih.gov/pubmed/29226102
http://dx.doi.org/10.14218/JCTH.2017.00007
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author Cholankeril, George
Joseph-Talreja, Mairin
Perumpail, Brandon J.
Liu, Andy
Yoo, Eric R.
Ahmed, Aijaz
Goel, Aparna
author_facet Cholankeril, George
Joseph-Talreja, Mairin
Perumpail, Brandon J.
Liu, Andy
Yoo, Eric R.
Ahmed, Aijaz
Goel, Aparna
author_sort Cholankeril, George
collection PubMed
description Chronic hepatitis C virus (HCV) infection remains the leading indication for liver transplantation (LT) in the United States. While most patients with chronic HCV infection remain asymptomatic, up to one-third develop progressive liver disease resulting in cirrhosis. LT is often the only curative treatment once significant hepatic decompensation develops. However, antiviral therapy for HCV infection has advanced markedly in the past 5 years with the discovery and approval of direct-acting antiviral agents. These new regimens are well tolerated, of short duration and highly effective, unlike the traditional treatment with pegylated-interferon and ribavirin. As achieving sustained virological response becomes increasingly attainable for a majority of HCV-infected patients, concerns have been raised regarding the optimal timing of treatment for HCV infection in the setting of end-stage liver disease and during the peri-transplant period. On one hand, HCV treatment may improve hepatic function and negate the need for LT in some, which is crucial given the scarcity of donor organs and mortality on the waiting list in certain regions. On the other hand, HCV treatment may result in lowering the priority for LT without improving quality of life, thereby delaying potentially curative LT surgery. This review evaluates the evidence supporting the use of direct-acting antiviral agents in the period before and following LT.
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spelling pubmed-57191932017-12-08 Timing of Hepatitis C Virus Treatment in Liver Transplant Candidates in the Era of Direct-acting Antiviral Agents Cholankeril, George Joseph-Talreja, Mairin Perumpail, Brandon J. Liu, Andy Yoo, Eric R. Ahmed, Aijaz Goel, Aparna J Clin Transl Hepatol Review Article Chronic hepatitis C virus (HCV) infection remains the leading indication for liver transplantation (LT) in the United States. While most patients with chronic HCV infection remain asymptomatic, up to one-third develop progressive liver disease resulting in cirrhosis. LT is often the only curative treatment once significant hepatic decompensation develops. However, antiviral therapy for HCV infection has advanced markedly in the past 5 years with the discovery and approval of direct-acting antiviral agents. These new regimens are well tolerated, of short duration and highly effective, unlike the traditional treatment with pegylated-interferon and ribavirin. As achieving sustained virological response becomes increasingly attainable for a majority of HCV-infected patients, concerns have been raised regarding the optimal timing of treatment for HCV infection in the setting of end-stage liver disease and during the peri-transplant period. On one hand, HCV treatment may improve hepatic function and negate the need for LT in some, which is crucial given the scarcity of donor organs and mortality on the waiting list in certain regions. On the other hand, HCV treatment may result in lowering the priority for LT without improving quality of life, thereby delaying potentially curative LT surgery. This review evaluates the evidence supporting the use of direct-acting antiviral agents in the period before and following LT. XIA & HE Publishing Inc. 2017-09-14 2017-12-28 /pmc/articles/PMC5719193/ /pubmed/29226102 http://dx.doi.org/10.14218/JCTH.2017.00007 Text en © 2017 Authors. http://creativecommons.org/licenses/by-nc/4.0/ This article has been published under the terms of Creative Commons Attribution-NonCommercial 4.0 International (CC BY-NC 4.0), which permits noncommercial unrestricted use, distribution, and reproduction in any medium, provided that the following statement is provided. “This article has been published in Journal of Clinical and Translational Hepatology at DOI: 10.14218/JCTH.2017.00007 and can also be viewed on the Journal’s website at http://www.jcthnet.com”.
spellingShingle Review Article
Cholankeril, George
Joseph-Talreja, Mairin
Perumpail, Brandon J.
Liu, Andy
Yoo, Eric R.
Ahmed, Aijaz
Goel, Aparna
Timing of Hepatitis C Virus Treatment in Liver Transplant Candidates in the Era of Direct-acting Antiviral Agents
title Timing of Hepatitis C Virus Treatment in Liver Transplant Candidates in the Era of Direct-acting Antiviral Agents
title_full Timing of Hepatitis C Virus Treatment in Liver Transplant Candidates in the Era of Direct-acting Antiviral Agents
title_fullStr Timing of Hepatitis C Virus Treatment in Liver Transplant Candidates in the Era of Direct-acting Antiviral Agents
title_full_unstemmed Timing of Hepatitis C Virus Treatment in Liver Transplant Candidates in the Era of Direct-acting Antiviral Agents
title_short Timing of Hepatitis C Virus Treatment in Liver Transplant Candidates in the Era of Direct-acting Antiviral Agents
title_sort timing of hepatitis c virus treatment in liver transplant candidates in the era of direct-acting antiviral agents
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5719193/
https://www.ncbi.nlm.nih.gov/pubmed/29226102
http://dx.doi.org/10.14218/JCTH.2017.00007
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