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Varicella paediatric hospitalisations in Belgium: a 1-year national survey

BACKGROUND: Varicella universal vaccination (UV) has been implemented in many countries for several years. Nevertheless, varicella UV remains debated in Europe and few data are available on the real burden of infection. We assessed the burden of varicella in Belgium through analysis of hospitalised...

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Autores principales: Blumental, Sophie, Sabbe, Martine, Lepage, Philippe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4717424/
https://www.ncbi.nlm.nih.gov/pubmed/26130380
http://dx.doi.org/10.1136/archdischild-2015-308283
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author Blumental, Sophie
Sabbe, Martine
Lepage, Philippe
author_facet Blumental, Sophie
Sabbe, Martine
Lepage, Philippe
author_sort Blumental, Sophie
collection PubMed
description BACKGROUND: Varicella universal vaccination (UV) has been implemented in many countries for several years. Nevertheless, varicella UV remains debated in Europe and few data are available on the real burden of infection. We assessed the burden of varicella in Belgium through analysis of hospitalised cases during a 1-year period. METHODS: Data on children admitted to hospital with varicella were collected through a national network from November 2011 to October 2012. Inclusion criteria were either acute varicella or related complications up to 3 weeks after the rash. RESULTS: Participation of 101 hospitals was obtained, covering 97.7% of the total paediatric beds in Belgium. 552 children were included with a median age of 2.1 years. Incidence of paediatric varicella hospitalisations reached 29.5/10(5) person-years, with the highest impact among those 0–4 years old (global incidence and odds of hospitalisation: 79/10(5) person-years and 1.6/100 varicella cases, respectively). Only 14% (79/552) of the cohort had an underlying chronic condition. 65% (357/552) of children had ≥1 complication justifying their admission, 49% were bacterial superinfections and 10% neurological disorders. Only a quarter of children (141/552) received acyclovir. Incidence of complicated hospitalised cases was 19/10(5) person-years. Paediatric intensive care unit admission and surgery were required in 4% and 3% of hospitalised cases, respectively. Mortality among Belgian paediatric population was 0.5/10(6) and fatality ratio 0.2% among our cohort. CONCLUSIONS: Varicella demonstrated a substantial burden of disease in Belgian children, especially among the youngest. Our thorough nationwide study, run in a country without varicella UV, offers data to support varicella UV in Belgium.
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spelling pubmed-47174242016-01-28 Varicella paediatric hospitalisations in Belgium: a 1-year national survey Blumental, Sophie Sabbe, Martine Lepage, Philippe Arch Dis Child Original Article BACKGROUND: Varicella universal vaccination (UV) has been implemented in many countries for several years. Nevertheless, varicella UV remains debated in Europe and few data are available on the real burden of infection. We assessed the burden of varicella in Belgium through analysis of hospitalised cases during a 1-year period. METHODS: Data on children admitted to hospital with varicella were collected through a national network from November 2011 to October 2012. Inclusion criteria were either acute varicella or related complications up to 3 weeks after the rash. RESULTS: Participation of 101 hospitals was obtained, covering 97.7% of the total paediatric beds in Belgium. 552 children were included with a median age of 2.1 years. Incidence of paediatric varicella hospitalisations reached 29.5/10(5) person-years, with the highest impact among those 0–4 years old (global incidence and odds of hospitalisation: 79/10(5) person-years and 1.6/100 varicella cases, respectively). Only 14% (79/552) of the cohort had an underlying chronic condition. 65% (357/552) of children had ≥1 complication justifying their admission, 49% were bacterial superinfections and 10% neurological disorders. Only a quarter of children (141/552) received acyclovir. Incidence of complicated hospitalised cases was 19/10(5) person-years. Paediatric intensive care unit admission and surgery were required in 4% and 3% of hospitalised cases, respectively. Mortality among Belgian paediatric population was 0.5/10(6) and fatality ratio 0.2% among our cohort. CONCLUSIONS: Varicella demonstrated a substantial burden of disease in Belgian children, especially among the youngest. Our thorough nationwide study, run in a country without varicella UV, offers data to support varicella UV in Belgium. BMJ Publishing Group 2016-01 2015-06-30 /pmc/articles/PMC4717424/ /pubmed/26130380 http://dx.doi.org/10.1136/archdischild-2015-308283 Text en Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing/ This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (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: http://creativecommons.org/licenses/by-nc/4.0/
spellingShingle Original Article
Blumental, Sophie
Sabbe, Martine
Lepage, Philippe
Varicella paediatric hospitalisations in Belgium: a 1-year national survey
title Varicella paediatric hospitalisations in Belgium: a 1-year national survey
title_full Varicella paediatric hospitalisations in Belgium: a 1-year national survey
title_fullStr Varicella paediatric hospitalisations in Belgium: a 1-year national survey
title_full_unstemmed Varicella paediatric hospitalisations in Belgium: a 1-year national survey
title_short Varicella paediatric hospitalisations in Belgium: a 1-year national survey
title_sort varicella paediatric hospitalisations in belgium: a 1-year national survey
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4717424/
https://www.ncbi.nlm.nih.gov/pubmed/26130380
http://dx.doi.org/10.1136/archdischild-2015-308283
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