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2223. Effect of Direct-Acting Antivirals in Hemodialysis Patients with HCV: Real-Life Data

BACKGROUND: Hepatitis C virus (HCV) infection is widespread in hemodialysis patients worldwide. Studies of the effectiveness of new generation DAAs in the treatment of HCV infection in hemodialysis patients are limited.We investigated the effectiveness of DAAs in hemodialysis patients with HCV infec...

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Autores principales: Aydin, Nurten Nur, Aksoy, Firdevs, Yavuz, Ilknur, Iskender, Serap, Yildirim, Arzu Altunçekic, Yildiz, Ilknur Esen, Koksal, Iftihar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6252828/
http://dx.doi.org/10.1093/ofid/ofy210.1876
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author Aydin, Nurten Nur
Aksoy, Firdevs
Yavuz, Ilknur
Iskender, Serap
Yildirim, Arzu Altunçekic
Yildiz, Ilknur Esen
Koksal, Iftihar
author_facet Aydin, Nurten Nur
Aksoy, Firdevs
Yavuz, Ilknur
Iskender, Serap
Yildirim, Arzu Altunçekic
Yildiz, Ilknur Esen
Koksal, Iftihar
author_sort Aydin, Nurten Nur
collection PubMed
description BACKGROUND: Hepatitis C virus (HCV) infection is widespread in hemodialysis patients worldwide. Studies of the effectiveness of new generation DAAs in the treatment of HCV infection in hemodialysis patients are limited.We investigated the effectiveness of DAAs in hemodialysis patients with HCV infection. METHODS: Twenty-three HCV-positive treatment naïve or experienced (IFN/pegIFN±RBV) hemodialysis patients were enrolled.Three patients were excluded for not attending follow-ups regularly, and the data for 20 patients were included. Patients’ demographic, virological, and genotypic characteristics, liver fibrosis status, DAAs started, and sustained virological responses at the 12th week (SVR12) were recorded. DAA regimens based on the treatments patients were using and potential drug interactions.Patients completing treatment were followed for 12 weeks for SVR. RESULTS: The mean age of the patients was 57.8 (±10.5). Ninety percent were men; 55% were treatment-experienced and 45% were treatment naïve. Ninety percent were noncirrhotic and 10% had compensated cirrhosis. Of the treatment-experienced patients, 45.5% were nonresponder and 54.5% were relapsed (Table 1). Eighteen patients with Genotype 1b were treated with paritepravir-ritonavir-ombitasvir-dasabuvir(ProD) for 12 weeks, one patient with Genotype 4 received ProD+ribavirin for 12 weeks, and one patient with Genotype 2 received sofosbuvir+ribavirin for 24 weeks. HCVRNA was negative on the 4th week in 85% of patients, and was negative in all patients on the 12th week, apart from the patient receiving the sofosbuvir+ribavirinregimen. At the end of treatment, HCVRNA was negative in all patients, and the SVR12 rate was 100%. Patients’ treatment responses were independent of previous treatments, liver fibrosis status, and hemodialysis duration. No marked side effects or complications were observed, apart from sleeplessness in one patient (Table 1). CONCLUSION: Our study data confirm that new generation DAAs in hemodialysis patients provide high SVR and are well tolerated, as in patients other than those with chronic kidney disease. Achieving cure in hemodialysis patients is important in terms of preventing cross-contamination and of global elimination of HCV. [Image: see text] DISCLOSURES: All authors: No reported disclosures.
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spelling pubmed-62528282018-11-28 2223. Effect of Direct-Acting Antivirals in Hemodialysis Patients with HCV: Real-Life Data Aydin, Nurten Nur Aksoy, Firdevs Yavuz, Ilknur Iskender, Serap Yildirim, Arzu Altunçekic Yildiz, Ilknur Esen Koksal, Iftihar Open Forum Infect Dis Abstracts BACKGROUND: Hepatitis C virus (HCV) infection is widespread in hemodialysis patients worldwide. Studies of the effectiveness of new generation DAAs in the treatment of HCV infection in hemodialysis patients are limited.We investigated the effectiveness of DAAs in hemodialysis patients with HCV infection. METHODS: Twenty-three HCV-positive treatment naïve or experienced (IFN/pegIFN±RBV) hemodialysis patients were enrolled.Three patients were excluded for not attending follow-ups regularly, and the data for 20 patients were included. Patients’ demographic, virological, and genotypic characteristics, liver fibrosis status, DAAs started, and sustained virological responses at the 12th week (SVR12) were recorded. DAA regimens based on the treatments patients were using and potential drug interactions.Patients completing treatment were followed for 12 weeks for SVR. RESULTS: The mean age of the patients was 57.8 (±10.5). Ninety percent were men; 55% were treatment-experienced and 45% were treatment naïve. Ninety percent were noncirrhotic and 10% had compensated cirrhosis. Of the treatment-experienced patients, 45.5% were nonresponder and 54.5% were relapsed (Table 1). Eighteen patients with Genotype 1b were treated with paritepravir-ritonavir-ombitasvir-dasabuvir(ProD) for 12 weeks, one patient with Genotype 4 received ProD+ribavirin for 12 weeks, and one patient with Genotype 2 received sofosbuvir+ribavirin for 24 weeks. HCVRNA was negative on the 4th week in 85% of patients, and was negative in all patients on the 12th week, apart from the patient receiving the sofosbuvir+ribavirinregimen. At the end of treatment, HCVRNA was negative in all patients, and the SVR12 rate was 100%. Patients’ treatment responses were independent of previous treatments, liver fibrosis status, and hemodialysis duration. No marked side effects or complications were observed, apart from sleeplessness in one patient (Table 1). CONCLUSION: Our study data confirm that new generation DAAs in hemodialysis patients provide high SVR and are well tolerated, as in patients other than those with chronic kidney disease. Achieving cure in hemodialysis patients is important in terms of preventing cross-contamination and of global elimination of HCV. [Image: see text] DISCLOSURES: All authors: No reported disclosures. Oxford University Press 2018-11-26 /pmc/articles/PMC6252828/ http://dx.doi.org/10.1093/ofid/ofy210.1876 Text en © The Author(s) 2018. Published by Oxford University Press on behalf of Infectious Diseases Society of America. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Abstracts
Aydin, Nurten Nur
Aksoy, Firdevs
Yavuz, Ilknur
Iskender, Serap
Yildirim, Arzu Altunçekic
Yildiz, Ilknur Esen
Koksal, Iftihar
2223. Effect of Direct-Acting Antivirals in Hemodialysis Patients with HCV: Real-Life Data
title 2223. Effect of Direct-Acting Antivirals in Hemodialysis Patients with HCV: Real-Life Data
title_full 2223. Effect of Direct-Acting Antivirals in Hemodialysis Patients with HCV: Real-Life Data
title_fullStr 2223. Effect of Direct-Acting Antivirals in Hemodialysis Patients with HCV: Real-Life Data
title_full_unstemmed 2223. Effect of Direct-Acting Antivirals in Hemodialysis Patients with HCV: Real-Life Data
title_short 2223. Effect of Direct-Acting Antivirals in Hemodialysis Patients with HCV: Real-Life Data
title_sort 2223. effect of direct-acting antivirals in hemodialysis patients with hcv: real-life data
topic Abstracts
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6252828/
http://dx.doi.org/10.1093/ofid/ofy210.1876
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