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Transfusion-transmitted hepatitis E: What we know so far?
Hepatitis E virus (HEV) is a major cause of viral hepatitis globally. There is growing concern about transfusion-transmitted HEV (TT-HEV) as an emerging global health problem. HEV can potentially result in chronic infection in immunocompromised patients, leading to a higher risk of liver cirrhosis a...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Baishideng Publishing Group Inc
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8793017/ https://www.ncbi.nlm.nih.gov/pubmed/35125819 http://dx.doi.org/10.3748/wjg.v28.i1.47 |
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author | Cheung, Carmen Ka Man Wong, Sunny Hei Law, Alvin Wing Hin Law, Man Fai |
author_facet | Cheung, Carmen Ka Man Wong, Sunny Hei Law, Alvin Wing Hin Law, Man Fai |
author_sort | Cheung, Carmen Ka Man |
collection | PubMed |
description | Hepatitis E virus (HEV) is a major cause of viral hepatitis globally. There is growing concern about transfusion-transmitted HEV (TT-HEV) as an emerging global health problem. HEV can potentially result in chronic infection in immunocompromised patients, leading to a higher risk of liver cirrhosis and even death. Between 0.0013% and 0.281% of asymptomatic blood donors around the world have HEV viremia, and 0.27% to 60.5% have anti-HEV immunoglobulin G. HEV is infectious even at very low blood concentrations of the virus. Immunosuppressed patients who develop persistent hepatitis E infection should have their immunosuppressant regimen reduced; ribavirin may be considered as treatment. Pegylated interferon can be considered in those who are refractory or intolerant to ribavirin. Sofosbuvir, a nucleotide analog, showed modest antiviral activity in some clinical studies but sustained viral response was not achieved. Therefore, rescue treatment remains an unmet need. The need for HEV screening of all blood donations remains controversial. Universal screening has been adopted in some countries after consideration of risk and resource availability. Various pathogen reduction methods have also been proposed to reduce the risk of TT-HEV. Future studies are needed to define the incidence of transmission through transfusion, their clinical features, outcomes and prognosis. |
format | Online Article Text |
id | pubmed-8793017 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Baishideng Publishing Group Inc |
record_format | MEDLINE/PubMed |
spelling | pubmed-87930172022-02-03 Transfusion-transmitted hepatitis E: What we know so far? Cheung, Carmen Ka Man Wong, Sunny Hei Law, Alvin Wing Hin Law, Man Fai World J Gastroenterol Review Hepatitis E virus (HEV) is a major cause of viral hepatitis globally. There is growing concern about transfusion-transmitted HEV (TT-HEV) as an emerging global health problem. HEV can potentially result in chronic infection in immunocompromised patients, leading to a higher risk of liver cirrhosis and even death. Between 0.0013% and 0.281% of asymptomatic blood donors around the world have HEV viremia, and 0.27% to 60.5% have anti-HEV immunoglobulin G. HEV is infectious even at very low blood concentrations of the virus. Immunosuppressed patients who develop persistent hepatitis E infection should have their immunosuppressant regimen reduced; ribavirin may be considered as treatment. Pegylated interferon can be considered in those who are refractory or intolerant to ribavirin. Sofosbuvir, a nucleotide analog, showed modest antiviral activity in some clinical studies but sustained viral response was not achieved. Therefore, rescue treatment remains an unmet need. The need for HEV screening of all blood donations remains controversial. Universal screening has been adopted in some countries after consideration of risk and resource availability. Various pathogen reduction methods have also been proposed to reduce the risk of TT-HEV. Future studies are needed to define the incidence of transmission through transfusion, their clinical features, outcomes and prognosis. Baishideng Publishing Group Inc 2022-01-07 2022-01-07 /pmc/articles/PMC8793017/ /pubmed/35125819 http://dx.doi.org/10.3748/wjg.v28.i1.47 Text en ©The Author(s) 2022. Published by Baishideng Publishing Group Inc. All rights reserved. https://creativecommons.org/licenses/by-nc/4.0/This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (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. See: https://creativecommons.org/Licenses/by-nc/4.0/ |
spellingShingle | Review Cheung, Carmen Ka Man Wong, Sunny Hei Law, Alvin Wing Hin Law, Man Fai Transfusion-transmitted hepatitis E: What we know so far? |
title | Transfusion-transmitted hepatitis E: What we know so far? |
title_full | Transfusion-transmitted hepatitis E: What we know so far? |
title_fullStr | Transfusion-transmitted hepatitis E: What we know so far? |
title_full_unstemmed | Transfusion-transmitted hepatitis E: What we know so far? |
title_short | Transfusion-transmitted hepatitis E: What we know so far? |
title_sort | transfusion-transmitted hepatitis e: what we know so far? |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8793017/ https://www.ncbi.nlm.nih.gov/pubmed/35125819 http://dx.doi.org/10.3748/wjg.v28.i1.47 |
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