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Immediate treatment for recent hepatitis C infection in people with high-risk behaviors: a systematic review and meta-analysis

Direct-acting antivirals (DAAs) are almost exclusively approved for the treatment of chronic HCV. This poses a significant barrier to the treatment of recently acquired HCV because of the limited access to DAAs. This review seeks to address this issue by synthesizing evidence of the benefits and har...

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Autores principales: Manoharan, Lakshmi, Latham, Ned H., Munari, Stephanie C., Traeger, Michael W., Menon, Vinay, Luhmann, Niklas, Baggaley, Rachel, Macdonald, Virginia, Verster, Annette, Siegfried, Nandi, Matthews, Gail V., Stoové, Mark, Hellard, Margaret E., Doyle, Joseph S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10027039/
https://www.ncbi.nlm.nih.gov/pubmed/36930865
http://dx.doi.org/10.1097/HC9.0000000000000082
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author Manoharan, Lakshmi
Latham, Ned H.
Munari, Stephanie C.
Traeger, Michael W.
Menon, Vinay
Luhmann, Niklas
Baggaley, Rachel
Macdonald, Virginia
Verster, Annette
Siegfried, Nandi
Matthews, Gail V.
Stoové, Mark
Hellard, Margaret E.
Doyle, Joseph S.
author_facet Manoharan, Lakshmi
Latham, Ned H.
Munari, Stephanie C.
Traeger, Michael W.
Menon, Vinay
Luhmann, Niklas
Baggaley, Rachel
Macdonald, Virginia
Verster, Annette
Siegfried, Nandi
Matthews, Gail V.
Stoové, Mark
Hellard, Margaret E.
Doyle, Joseph S.
author_sort Manoharan, Lakshmi
collection PubMed
description Direct-acting antivirals (DAAs) are almost exclusively approved for the treatment of chronic HCV. This poses a significant barrier to the treatment of recently acquired HCV because of the limited access to DAAs. This review seeks to address this issue by synthesizing evidence of the benefits and harms of immediate treatment after the detection of recently acquired HCV in people at higher risk of infection. APPROACH AND RESULTS: A systematic review and meta-analysis were conducted reporting on populations with recently acquired HCV at higher risk of infection. Studies were included if they assessed standard duration DAA treatment regimens and reported on the benefits and harms of immediate treatment (within one year of diagnosis). Outcomes included sustained virological response at 12 weeks post-treatment (SVR12), incidence, treatment initiation and adherence, overtreatment, engagement in care, and adverse events. Eight cohort studies, 3 open-label trials, and 1 case series study were included, reporting on 2085 participants with recently acquired HCV infection. No studies included a comparison group. Eight studies assessed DAA treatment in either men who have sex with men or men who have sex with men with HIV, 2 studies assessed treatment in people who inject drugs, and 2 among people living with HIV. Immediate treatment of HCV was associated with a pooled SVR12 of 95.9% (95% CI, 92.6%–99.3%). Three studies reported on hepatitis C incidence, where most participants were treated in the chronic phase of infection. A treatment completion rate of 100% was reported in 2 studies, and only 1 serious adverse event was described. CONCLUSIONS: High rates of cure were achieved with the treatment of recently acquired hepatitis C in people at higher risk of infection. Serious adverse events were rare, highlighting individual benefits consistent with the treatment of chronic hepatitis C. The impact of immediate treatment on HCV incidence requires further evaluation.
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spelling pubmed-100270392023-03-21 Immediate treatment for recent hepatitis C infection in people with high-risk behaviors: a systematic review and meta-analysis Manoharan, Lakshmi Latham, Ned H. Munari, Stephanie C. Traeger, Michael W. Menon, Vinay Luhmann, Niklas Baggaley, Rachel Macdonald, Virginia Verster, Annette Siegfried, Nandi Matthews, Gail V. Stoové, Mark Hellard, Margaret E. Doyle, Joseph S. Hepatol Commun Original Article Direct-acting antivirals (DAAs) are almost exclusively approved for the treatment of chronic HCV. This poses a significant barrier to the treatment of recently acquired HCV because of the limited access to DAAs. This review seeks to address this issue by synthesizing evidence of the benefits and harms of immediate treatment after the detection of recently acquired HCV in people at higher risk of infection. APPROACH AND RESULTS: A systematic review and meta-analysis were conducted reporting on populations with recently acquired HCV at higher risk of infection. Studies were included if they assessed standard duration DAA treatment regimens and reported on the benefits and harms of immediate treatment (within one year of diagnosis). Outcomes included sustained virological response at 12 weeks post-treatment (SVR12), incidence, treatment initiation and adherence, overtreatment, engagement in care, and adverse events. Eight cohort studies, 3 open-label trials, and 1 case series study were included, reporting on 2085 participants with recently acquired HCV infection. No studies included a comparison group. Eight studies assessed DAA treatment in either men who have sex with men or men who have sex with men with HIV, 2 studies assessed treatment in people who inject drugs, and 2 among people living with HIV. Immediate treatment of HCV was associated with a pooled SVR12 of 95.9% (95% CI, 92.6%–99.3%). Three studies reported on hepatitis C incidence, where most participants were treated in the chronic phase of infection. A treatment completion rate of 100% was reported in 2 studies, and only 1 serious adverse event was described. CONCLUSIONS: High rates of cure were achieved with the treatment of recently acquired hepatitis C in people at higher risk of infection. Serious adverse events were rare, highlighting individual benefits consistent with the treatment of chronic hepatitis C. The impact of immediate treatment on HCV incidence requires further evaluation. Lippincott Williams & Wilkins 2023-03-17 /pmc/articles/PMC10027039/ /pubmed/36930865 http://dx.doi.org/10.1097/HC9.0000000000000082 Text en Copyright © 2023 The Author(s). 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 Article
Manoharan, Lakshmi
Latham, Ned H.
Munari, Stephanie C.
Traeger, Michael W.
Menon, Vinay
Luhmann, Niklas
Baggaley, Rachel
Macdonald, Virginia
Verster, Annette
Siegfried, Nandi
Matthews, Gail V.
Stoové, Mark
Hellard, Margaret E.
Doyle, Joseph S.
Immediate treatment for recent hepatitis C infection in people with high-risk behaviors: a systematic review and meta-analysis
title Immediate treatment for recent hepatitis C infection in people with high-risk behaviors: a systematic review and meta-analysis
title_full Immediate treatment for recent hepatitis C infection in people with high-risk behaviors: a systematic review and meta-analysis
title_fullStr Immediate treatment for recent hepatitis C infection in people with high-risk behaviors: a systematic review and meta-analysis
title_full_unstemmed Immediate treatment for recent hepatitis C infection in people with high-risk behaviors: a systematic review and meta-analysis
title_short Immediate treatment for recent hepatitis C infection in people with high-risk behaviors: a systematic review and meta-analysis
title_sort immediate treatment for recent hepatitis c infection in people with high-risk behaviors: a systematic review and meta-analysis
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10027039/
https://www.ncbi.nlm.nih.gov/pubmed/36930865
http://dx.doi.org/10.1097/HC9.0000000000000082
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