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Interferon-free regimens in patients with hepatitis C infection and renal dysfunction or kidney transplantation

Treatment of patients with chronic kidney disease (CKD) and chronic hepatitis C (CHC) differs from that used in the general CHC population mostly when glomerular filtration rate (GFR) is below 30 mL/min, as sofosbuvir, the backbone of several current regimens, is officially contraindicated. Given th...

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Autores principales: Cholongitas, Evangelos, Pipili, Chrysoula, Papatheodoridis, George V
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5295158/
https://www.ncbi.nlm.nih.gov/pubmed/28217256
http://dx.doi.org/10.4254/wjh.v9.i4.180
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author Cholongitas, Evangelos
Pipili, Chrysoula
Papatheodoridis, George V
author_facet Cholongitas, Evangelos
Pipili, Chrysoula
Papatheodoridis, George V
author_sort Cholongitas, Evangelos
collection PubMed
description Treatment of patients with chronic kidney disease (CKD) and chronic hepatitis C (CHC) differs from that used in the general CHC population mostly when glomerular filtration rate (GFR) is below 30 mL/min, as sofosbuvir, the backbone of several current regimens, is officially contraindicated. Given that ribavirin free regimens are preferable in CKD, elbasvir/grazoprevir is offered in CHC patients with genotype 1 or 4 and ombitasvir/paritaprevir and dasabuvir in genotype 1b for 12 wk. Although regimens containing peginterferon with or without ribavirin are officially recommended for patients with CKD and genotype 2, 3, 5, 6, such regimens are rarely used because of their low efficacy and the poor safety and tolerance profile. In this setting, especially in the presence of advanced liver disease, sofosbuvir-based regimens are often used, despite sofosbuvir contraindication. It seems to have good overall safety with only 6% or 3.4% of CKD patients to discontinue therapy or develop serious adverse events without drug discontinuation. In addition, sustained virological response (SVR) rates with sofosbuvir based regimens in CKD patients appear to be comparable with SVR rates in patients with normal renal function. Treatment recommendations for kidney transplant recipients are the same with those for patients with CHC, taking into consideration potential drug-drug interactions and baseline GFR before treatment initiation. This review summarizes recent data on the current management of CHC in CKD patients highlighting their strengths and weaknesses and determining their usefulness in clinical practice.
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spelling pubmed-52951582017-02-18 Interferon-free regimens in patients with hepatitis C infection and renal dysfunction or kidney transplantation Cholongitas, Evangelos Pipili, Chrysoula Papatheodoridis, George V World J Hepatol Minireviews Treatment of patients with chronic kidney disease (CKD) and chronic hepatitis C (CHC) differs from that used in the general CHC population mostly when glomerular filtration rate (GFR) is below 30 mL/min, as sofosbuvir, the backbone of several current regimens, is officially contraindicated. Given that ribavirin free regimens are preferable in CKD, elbasvir/grazoprevir is offered in CHC patients with genotype 1 or 4 and ombitasvir/paritaprevir and dasabuvir in genotype 1b for 12 wk. Although regimens containing peginterferon with or without ribavirin are officially recommended for patients with CKD and genotype 2, 3, 5, 6, such regimens are rarely used because of their low efficacy and the poor safety and tolerance profile. In this setting, especially in the presence of advanced liver disease, sofosbuvir-based regimens are often used, despite sofosbuvir contraindication. It seems to have good overall safety with only 6% or 3.4% of CKD patients to discontinue therapy or develop serious adverse events without drug discontinuation. In addition, sustained virological response (SVR) rates with sofosbuvir based regimens in CKD patients appear to be comparable with SVR rates in patients with normal renal function. Treatment recommendations for kidney transplant recipients are the same with those for patients with CHC, taking into consideration potential drug-drug interactions and baseline GFR before treatment initiation. This review summarizes recent data on the current management of CHC in CKD patients highlighting their strengths and weaknesses and determining their usefulness in clinical practice. Baishideng Publishing Group Inc 2017-02-08 2017-02-08 /pmc/articles/PMC5295158/ /pubmed/28217256 http://dx.doi.org/10.4254/wjh.v9.i4.180 Text en ©The Author(s) 2017. Published by Baishideng Publishing Group Inc. All rights reserved. http://creativecommons.org/licenses/by-nc/4.0/ This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial.
spellingShingle Minireviews
Cholongitas, Evangelos
Pipili, Chrysoula
Papatheodoridis, George V
Interferon-free regimens in patients with hepatitis C infection and renal dysfunction or kidney transplantation
title Interferon-free regimens in patients with hepatitis C infection and renal dysfunction or kidney transplantation
title_full Interferon-free regimens in patients with hepatitis C infection and renal dysfunction or kidney transplantation
title_fullStr Interferon-free regimens in patients with hepatitis C infection and renal dysfunction or kidney transplantation
title_full_unstemmed Interferon-free regimens in patients with hepatitis C infection and renal dysfunction or kidney transplantation
title_short Interferon-free regimens in patients with hepatitis C infection and renal dysfunction or kidney transplantation
title_sort interferon-free regimens in patients with hepatitis c infection and renal dysfunction or kidney transplantation
topic Minireviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5295158/
https://www.ncbi.nlm.nih.gov/pubmed/28217256
http://dx.doi.org/10.4254/wjh.v9.i4.180
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