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Treatment for chronic hepatitis E virus infection: A systematic review and meta‐analysis
Hepatitis E virus infection can cause chronic hepatitis in immunocompromised patients with significant chance of progressive fibrosis and possibly cirrhosis. The aim of this systematic review was to summarize the efficacy and safety of the various treatment options for chronic hepatitis E. We perfor...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7898834/ https://www.ncbi.nlm.nih.gov/pubmed/33301609 http://dx.doi.org/10.1111/jvh.13456 |
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author | Gorris, Myrte van der Lecq, Bernice M. van Erpecum, Karel J. de Bruijne, Joep |
author_facet | Gorris, Myrte van der Lecq, Bernice M. van Erpecum, Karel J. de Bruijne, Joep |
author_sort | Gorris, Myrte |
collection | PubMed |
description | Hepatitis E virus infection can cause chronic hepatitis in immunocompromised patients with significant chance of progressive fibrosis and possibly cirrhosis. The aim of this systematic review was to summarize the efficacy and safety of the various treatment options for chronic hepatitis E. We performed a systematic literature search. The primary outcome measure was a sustained virological response (SVR). Secondary end points were rapid virological response (RVR), relapse rates, side effects and adverse events. Forty‐four articles were included with a total of 582 patients. Reduction of immunosuppressive medication induced viral clearance in 55/174 (32%) of the patients. Meta‐analysis of 395 patients showed a pooled SVR rate of 78% (95‐CI 72%–84%) after ribavirin treatment. Twenty‐five per cent of the patients obtained a RVR, whereas a relapse occurred in 18% of the patients. Anaemia during treatment led to dose reduction, use of erythropoietin and/or blood transfusion in 37% of the patients. A second treatment attempt with ribavirin led to a SVR in 39/51 (76%) of the patients. Pegylated interferon‐alpha was administered to 13 patients and SVR was obtained in 85%. Two patients (15%) suffered from acute transplant rejection during treatment with interferon. In conclusion, reduction of immunosuppressive medication and treatment with ribavirin is safe, generally well tolerated and induced viral clearance in 32% and 78% of patients, respectively. Therefore, ribavirin should be considered as first treatment step for chronic hepatitis E. Treatment with pegylated interferon‐alpha increases the risk of transplant rejection and should therefore be administered with great caution. |
format | Online Article Text |
id | pubmed-7898834 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-78988342021-03-03 Treatment for chronic hepatitis E virus infection: A systematic review and meta‐analysis Gorris, Myrte van der Lecq, Bernice M. van Erpecum, Karel J. de Bruijne, Joep J Viral Hepat Meta–Analysis Hepatitis E virus infection can cause chronic hepatitis in immunocompromised patients with significant chance of progressive fibrosis and possibly cirrhosis. The aim of this systematic review was to summarize the efficacy and safety of the various treatment options for chronic hepatitis E. We performed a systematic literature search. The primary outcome measure was a sustained virological response (SVR). Secondary end points were rapid virological response (RVR), relapse rates, side effects and adverse events. Forty‐four articles were included with a total of 582 patients. Reduction of immunosuppressive medication induced viral clearance in 55/174 (32%) of the patients. Meta‐analysis of 395 patients showed a pooled SVR rate of 78% (95‐CI 72%–84%) after ribavirin treatment. Twenty‐five per cent of the patients obtained a RVR, whereas a relapse occurred in 18% of the patients. Anaemia during treatment led to dose reduction, use of erythropoietin and/or blood transfusion in 37% of the patients. A second treatment attempt with ribavirin led to a SVR in 39/51 (76%) of the patients. Pegylated interferon‐alpha was administered to 13 patients and SVR was obtained in 85%. Two patients (15%) suffered from acute transplant rejection during treatment with interferon. In conclusion, reduction of immunosuppressive medication and treatment with ribavirin is safe, generally well tolerated and induced viral clearance in 32% and 78% of patients, respectively. Therefore, ribavirin should be considered as first treatment step for chronic hepatitis E. Treatment with pegylated interferon‐alpha increases the risk of transplant rejection and should therefore be administered with great caution. John Wiley and Sons Inc. 2020-12-20 2021-03 /pmc/articles/PMC7898834/ /pubmed/33301609 http://dx.doi.org/10.1111/jvh.13456 Text en © 2020 The Authors. Journal of Viral Hepatitis published by John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Meta–Analysis Gorris, Myrte van der Lecq, Bernice M. van Erpecum, Karel J. de Bruijne, Joep Treatment for chronic hepatitis E virus infection: A systematic review and meta‐analysis |
title | Treatment for chronic hepatitis E virus infection: A systematic review and meta‐analysis |
title_full | Treatment for chronic hepatitis E virus infection: A systematic review and meta‐analysis |
title_fullStr | Treatment for chronic hepatitis E virus infection: A systematic review and meta‐analysis |
title_full_unstemmed | Treatment for chronic hepatitis E virus infection: A systematic review and meta‐analysis |
title_short | Treatment for chronic hepatitis E virus infection: A systematic review and meta‐analysis |
title_sort | treatment for chronic hepatitis e virus infection: a systematic review and meta‐analysis |
topic | Meta–Analysis |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7898834/ https://www.ncbi.nlm.nih.gov/pubmed/33301609 http://dx.doi.org/10.1111/jvh.13456 |
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