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Hepatitis A virus infections and outbreaks in asylum seekers arriving to Germany, September 2015 to March 2016

From September 2015 to March 2016, hepatitis A notifications in Germany increased by 45% to 699 cases compared to 482 cases in the same period of the previous year. Children aged five to nine years were predominantly affected (22% of all cases in this period). We hypothesized that this increase coul...

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Autores principales: Michaelis, Kai, Wenzel, Jürgen J, Stark, Klaus, Faber, Mirko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5457677/
https://www.ncbi.nlm.nih.gov/pubmed/28442750
http://dx.doi.org/10.1038/emi.2017.11
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author Michaelis, Kai
Wenzel, Jürgen J
Stark, Klaus
Faber, Mirko
author_facet Michaelis, Kai
Wenzel, Jürgen J
Stark, Klaus
Faber, Mirko
author_sort Michaelis, Kai
collection PubMed
description From September 2015 to March 2016, hepatitis A notifications in Germany increased by 45% to 699 cases compared to 482 cases in the same period of the previous year. Children aged five to nine years were predominantly affected (22% of all cases in this period). We hypothesized that this increase could be explained by the marked influx of asylum seekers in this time period. We analysed national surveillance data and estimated the number of imported and autochthonous hepatitis A cases in asylum seekers. We also investigated molecular signatures of hepatitis A viruses sampled from asylum seekers to identify chains of transmission. We found that 40% (278 cases) of all 699 hepatitis A cases notified between September 2015 and March 2016 in Germany concerned asylum seekers. Most infections were acquired abroad, but at least 24% accounted for autochthonous infections. Among asylum seekers, children aged five to nine years were overrepresented with 97 of 278 (35%) notified cases. The analysed hepatitis A virus sequences were primarily subgenotype IB strains and clustered with previously isolated samples from the Middle East, Turkey, Pakistan and East Africa. Except one transmission from an asymptomatic child to a nursery nurse working in a mass accommodation, we are not aware of infection chains involving asylum seekers and German residents. We conclude that asylum-seeking children and adolescents are susceptible to hepatitis A virus infections, particularly children aged five to nine years. Measures to prevent secondary infections in asylum seekers such as extended hygiene measures and post-exposure prophylaxis seem advisable.
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spelling pubmed-54576772017-06-07 Hepatitis A virus infections and outbreaks in asylum seekers arriving to Germany, September 2015 to March 2016 Michaelis, Kai Wenzel, Jürgen J Stark, Klaus Faber, Mirko Emerg Microbes Infect Original Article From September 2015 to March 2016, hepatitis A notifications in Germany increased by 45% to 699 cases compared to 482 cases in the same period of the previous year. Children aged five to nine years were predominantly affected (22% of all cases in this period). We hypothesized that this increase could be explained by the marked influx of asylum seekers in this time period. We analysed national surveillance data and estimated the number of imported and autochthonous hepatitis A cases in asylum seekers. We also investigated molecular signatures of hepatitis A viruses sampled from asylum seekers to identify chains of transmission. We found that 40% (278 cases) of all 699 hepatitis A cases notified between September 2015 and March 2016 in Germany concerned asylum seekers. Most infections were acquired abroad, but at least 24% accounted for autochthonous infections. Among asylum seekers, children aged five to nine years were overrepresented with 97 of 278 (35%) notified cases. The analysed hepatitis A virus sequences were primarily subgenotype IB strains and clustered with previously isolated samples from the Middle East, Turkey, Pakistan and East Africa. Except one transmission from an asymptomatic child to a nursery nurse working in a mass accommodation, we are not aware of infection chains involving asylum seekers and German residents. We conclude that asylum-seeking children and adolescents are susceptible to hepatitis A virus infections, particularly children aged five to nine years. Measures to prevent secondary infections in asylum seekers such as extended hygiene measures and post-exposure prophylaxis seem advisable. Nature Publishing Group 2017-04 2017-04-26 /pmc/articles/PMC5457677/ /pubmed/28442750 http://dx.doi.org/10.1038/emi.2017.11 Text en Copyright © 2017 The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Original Article
Michaelis, Kai
Wenzel, Jürgen J
Stark, Klaus
Faber, Mirko
Hepatitis A virus infections and outbreaks in asylum seekers arriving to Germany, September 2015 to March 2016
title Hepatitis A virus infections and outbreaks in asylum seekers arriving to Germany, September 2015 to March 2016
title_full Hepatitis A virus infections and outbreaks in asylum seekers arriving to Germany, September 2015 to March 2016
title_fullStr Hepatitis A virus infections and outbreaks in asylum seekers arriving to Germany, September 2015 to March 2016
title_full_unstemmed Hepatitis A virus infections and outbreaks in asylum seekers arriving to Germany, September 2015 to March 2016
title_short Hepatitis A virus infections and outbreaks in asylum seekers arriving to Germany, September 2015 to March 2016
title_sort hepatitis a virus infections and outbreaks in asylum seekers arriving to germany, september 2015 to march 2016
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5457677/
https://www.ncbi.nlm.nih.gov/pubmed/28442750
http://dx.doi.org/10.1038/emi.2017.11
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