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A clinico-epidemiological multicenter study of herpes zoster in immunocompetent and immunocompromised hospitalized children

PURPOSE: There are limited population-based data regarding herpes zoster in children. Thus we conducted a multi-institutional epidemiological analysis of herpes zoster in children and comparative analysis according to their immune status. MATERIALS AND METHODS: The study included 126 children under...

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Autores principales: Hwang, Ji Hyen, Kim, Ki Hwan, Han, Seung Beom, Kim, Hyun Hee, Kim, Jong-Hyun, Lee, Soo Young, Choi, Ui Yoon, Kang, Jin Han
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Vaccine Society 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6689498/
https://www.ncbi.nlm.nih.gov/pubmed/31406693
http://dx.doi.org/10.7774/cevr.2019.8.2.116
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author Hwang, Ji Hyen
Kim, Ki Hwan
Han, Seung Beom
Kim, Hyun Hee
Kim, Jong-Hyun
Lee, Soo Young
Choi, Ui Yoon
Kang, Jin Han
author_facet Hwang, Ji Hyen
Kim, Ki Hwan
Han, Seung Beom
Kim, Hyun Hee
Kim, Jong-Hyun
Lee, Soo Young
Choi, Ui Yoon
Kang, Jin Han
author_sort Hwang, Ji Hyen
collection PubMed
description PURPOSE: There are limited population-based data regarding herpes zoster in children. Thus we conducted a multi-institutional epidemiological analysis of herpes zoster in children and comparative analysis according to their immune status. MATERIALS AND METHODS: The study included 126 children under the age of 18 years who were hospitalized for herpes zoster at 8 hospitals in South Korea, between July 2009 and June 2015. The subjects were divided into 2 groups according to their immune status, and medical records were reviewed. RESULTS: There were 61 cases (48.4%) in the immunocompetent group and 65 cases (51.6%) in the immunocompromised group. Median age was older in immunocompromised group (11.4 vs. 8.6) (p<0.001). The mean duration of hospitalization was longer in immunocompromised group (11.0 vs. 6.6) (p<0.001). Patients were treated with oral or intravenous antiviral agents. A total of 12 in immunocompetent group were cured only by oral acyclovir. No treatment failure was found in both groups. Six immunocompromised patients had postherpetic neuralgia and 1 case was in immunocompetent group. In immunocompetent children, herpes zoster was likely caused by early varicella infection. There was no increase in progression of severity in both groups due to appropriate treatment. CONCLUSION: Early initiation of therapy is necessary for those in immunocompromised conditions. And inactivated herpes zoster vaccination may be considered in immunocompromised adolescents in the future.
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spelling pubmed-66894982019-08-12 A clinico-epidemiological multicenter study of herpes zoster in immunocompetent and immunocompromised hospitalized children Hwang, Ji Hyen Kim, Ki Hwan Han, Seung Beom Kim, Hyun Hee Kim, Jong-Hyun Lee, Soo Young Choi, Ui Yoon Kang, Jin Han Clin Exp Vaccine Res Original Article PURPOSE: There are limited population-based data regarding herpes zoster in children. Thus we conducted a multi-institutional epidemiological analysis of herpes zoster in children and comparative analysis according to their immune status. MATERIALS AND METHODS: The study included 126 children under the age of 18 years who were hospitalized for herpes zoster at 8 hospitals in South Korea, between July 2009 and June 2015. The subjects were divided into 2 groups according to their immune status, and medical records were reviewed. RESULTS: There were 61 cases (48.4%) in the immunocompetent group and 65 cases (51.6%) in the immunocompromised group. Median age was older in immunocompromised group (11.4 vs. 8.6) (p<0.001). The mean duration of hospitalization was longer in immunocompromised group (11.0 vs. 6.6) (p<0.001). Patients were treated with oral or intravenous antiviral agents. A total of 12 in immunocompetent group were cured only by oral acyclovir. No treatment failure was found in both groups. Six immunocompromised patients had postherpetic neuralgia and 1 case was in immunocompetent group. In immunocompetent children, herpes zoster was likely caused by early varicella infection. There was no increase in progression of severity in both groups due to appropriate treatment. CONCLUSION: Early initiation of therapy is necessary for those in immunocompromised conditions. And inactivated herpes zoster vaccination may be considered in immunocompromised adolescents in the future. The Korean Vaccine Society 2019-07 2019-07-31 /pmc/articles/PMC6689498/ /pubmed/31406693 http://dx.doi.org/10.7774/cevr.2019.8.2.116 Text en © Korean Vaccine Society. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Hwang, Ji Hyen
Kim, Ki Hwan
Han, Seung Beom
Kim, Hyun Hee
Kim, Jong-Hyun
Lee, Soo Young
Choi, Ui Yoon
Kang, Jin Han
A clinico-epidemiological multicenter study of herpes zoster in immunocompetent and immunocompromised hospitalized children
title A clinico-epidemiological multicenter study of herpes zoster in immunocompetent and immunocompromised hospitalized children
title_full A clinico-epidemiological multicenter study of herpes zoster in immunocompetent and immunocompromised hospitalized children
title_fullStr A clinico-epidemiological multicenter study of herpes zoster in immunocompetent and immunocompromised hospitalized children
title_full_unstemmed A clinico-epidemiological multicenter study of herpes zoster in immunocompetent and immunocompromised hospitalized children
title_short A clinico-epidemiological multicenter study of herpes zoster in immunocompetent and immunocompromised hospitalized children
title_sort clinico-epidemiological multicenter study of herpes zoster in immunocompetent and immunocompromised hospitalized children
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6689498/
https://www.ncbi.nlm.nih.gov/pubmed/31406693
http://dx.doi.org/10.7774/cevr.2019.8.2.116
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