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Treatment of Hepatitis C in Children: A Systematic Review
BACKGROUND: Current guidelines recommend children be treated for hepatitis C virus (HCV) using the same principles applied in adults. There are however few published studies which assess the efficacy and safety of HCV therapy in children. METHODOLOGY/PRINCIPAL FINDINGS: A systematic review of the li...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Public Library of Science
2010
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2903479/ https://www.ncbi.nlm.nih.gov/pubmed/20644626 http://dx.doi.org/10.1371/journal.pone.0011542 |
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author | Hu, Jia Doucette, Karen Hartling, Lisa Tjosvold, Lisa Robinson, Joan |
author_facet | Hu, Jia Doucette, Karen Hartling, Lisa Tjosvold, Lisa Robinson, Joan |
author_sort | Hu, Jia |
collection | PubMed |
description | BACKGROUND: Current guidelines recommend children be treated for hepatitis C virus (HCV) using the same principles applied in adults. There are however few published studies which assess the efficacy and safety of HCV therapy in children. METHODOLOGY/PRINCIPAL FINDINGS: A systematic review of the literature was completed for studies of any design that evaluated HCV therapy in children. The primary outcome was sustained virologic response (SVR), with sub-group analysis of response rates by genotype. There were 4 randomized controlled trials (RCTs) and 31 non-randomized studies, all involving interferon, pegylated interferon (PEG-IFN), or combinations of these drugs with ribavirin. The SVR rate could not be directly compared as the populations and interventions differed across studies. Genotype was not reported or differed substantially from study to study. The overall SVR rate for PEG-IFN and ribavirin ranged from 30 to 100% which is comparable to the rate in adults. Similar to adults, the SVR rates were significantly higher in children with genotype 2 or 3 compared to genotype 1. Adverse effects were primarily flu-like symptoms and neutropenia. There were insufficient data to assess the applicability of the week 12 stop rule (stopping therapy at week 12 if there is less than a 2 log drop in HCV RNA) or the efficacy of shortening therapy to 24 weeks in children with genotype 2 and 3. CONCLUSIONS/SIGNIFICANCE: Current guidelines for the treatment of HCV in children are based on limited data. Further research is needed to define the optimal therapy for HCV in children. |
format | Text |
id | pubmed-2903479 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-29034792010-07-19 Treatment of Hepatitis C in Children: A Systematic Review Hu, Jia Doucette, Karen Hartling, Lisa Tjosvold, Lisa Robinson, Joan PLoS One Research Article BACKGROUND: Current guidelines recommend children be treated for hepatitis C virus (HCV) using the same principles applied in adults. There are however few published studies which assess the efficacy and safety of HCV therapy in children. METHODOLOGY/PRINCIPAL FINDINGS: A systematic review of the literature was completed for studies of any design that evaluated HCV therapy in children. The primary outcome was sustained virologic response (SVR), with sub-group analysis of response rates by genotype. There were 4 randomized controlled trials (RCTs) and 31 non-randomized studies, all involving interferon, pegylated interferon (PEG-IFN), or combinations of these drugs with ribavirin. The SVR rate could not be directly compared as the populations and interventions differed across studies. Genotype was not reported or differed substantially from study to study. The overall SVR rate for PEG-IFN and ribavirin ranged from 30 to 100% which is comparable to the rate in adults. Similar to adults, the SVR rates were significantly higher in children with genotype 2 or 3 compared to genotype 1. Adverse effects were primarily flu-like symptoms and neutropenia. There were insufficient data to assess the applicability of the week 12 stop rule (stopping therapy at week 12 if there is less than a 2 log drop in HCV RNA) or the efficacy of shortening therapy to 24 weeks in children with genotype 2 and 3. CONCLUSIONS/SIGNIFICANCE: Current guidelines for the treatment of HCV in children are based on limited data. Further research is needed to define the optimal therapy for HCV in children. Public Library of Science 2010-07-13 /pmc/articles/PMC2903479/ /pubmed/20644626 http://dx.doi.org/10.1371/journal.pone.0011542 Text en Hu et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Hu, Jia Doucette, Karen Hartling, Lisa Tjosvold, Lisa Robinson, Joan Treatment of Hepatitis C in Children: A Systematic Review |
title | Treatment of Hepatitis C in Children: A Systematic Review |
title_full | Treatment of Hepatitis C in Children: A Systematic Review |
title_fullStr | Treatment of Hepatitis C in Children: A Systematic Review |
title_full_unstemmed | Treatment of Hepatitis C in Children: A Systematic Review |
title_short | Treatment of Hepatitis C in Children: A Systematic Review |
title_sort | treatment of hepatitis c in children: a systematic review |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2903479/ https://www.ncbi.nlm.nih.gov/pubmed/20644626 http://dx.doi.org/10.1371/journal.pone.0011542 |
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