Please use this identifier to cite or link to this item: https://dora.health.qld.gov.au/qldresearchjspui/handle/1/4572
Title: Severe and Complicated Varicella and Associated Genotypes 10 Years After Introduction of a One-Dose Varicella Vaccine Program
Authors: Investigators, Paeds
Kynaston, Anne 
Marshall, Helen S.
Clarke, Michelle
Heath, Christine
Quinn, Helen
Richmond, Peter C.
Crawford, Nigel
Elliott, Elizabeth
Toi, Cheryl
Booy, Robert
Macartney, Kristine
Investigators, The Paeds
Issue Date: 2019
Source: 219, (3), 2019, p. 391-399
Pages: 391-399
Journal: Journal of Infectious Diseases
Abstract: Background: This national, sentinel prospective study aimed to identify children with severe hospitalized varicella, despite availability of universal 1-dose vaccination since 2005, and determine associations between virus genotypes and disease severity.Methods: Children with varicella or zoster from 5 Paediatric Active Enhanced Disease Surveillance hospitals were enrolled. Lesions were swabbed for genotyping. Associations with disease severity were analyzed using multiple regression.Results: From 2007 to 2015, 327 children with confirmed varicella (n = 238) or zoster (n = 89) were enrolled. Two hundred three (62%) were immunocompetent children; including 5 of 8 children who required intensive care unit management. Eighteen percent (36 of 203) of immunocompetent children had been previously vaccinated. Vaccinated children aged >18 months were less likely to have severe disease (9%; 5 of 56) than unvaccinated children (21%; 21 of 100; P = .05). Three of 126 children who had virus genotyping (2 immunocompromised) had varicella (n = 2) or zoster (n = 2) due to the Oka/vaccine strain. European origin clades predominated and were independently associated with more severe disease (odds ratio = 3.2; 95% confidence interval, 1.1- 9.5; P = .04).Conclusions: Severe hospitalized varicella still occurs with a 1-dose varicella program, although predominantly in unvaccinated children. Most 1-dose vaccine recipients were protected against severe disease. Viral genotyping in complex hospitalized cases is important to assist in monitoring disease due to Oka-vaccine strain.research. Journal Subset: Biomedical; Editorial Board Reviewed; Peer Reviewed; USA. NLM UID: 0413675.PMID: NLM30184182.
DOI: 10.1093/infdis/jiy518
Resources: https://search.ebscohost.com/login.aspx?direct=true&AuthType=ip,athens&db=ccm&AN=134122846&site=ehost-live
Keywords: Multicenter Studies;Child, Preschool;HerpesvirusesImmunization Programs;Severity of Illness Indices;Chickenpox -- Immunology;Chickenpox -- Prevention and Control;Genotype;Chickenpox Vaccine -- Administration and Dosage;Prospective Studies;Herpes Zoster -- Epidemiology;Australia;Child, Hospitalized;Human;Herpes Zoster -- Immunology;Immunocompromised Host;Herpes Zoster -- Prevention and Control;Male;Chickenpox Vaccine -- Immunology;Chickenpox;Chickenpox -- Epidemiology;Infant;Female;Immunization;Child;Validation Studies;Comparative Studies;Evaluation Research
Type: Article
Appears in Sites:Children's Health Queensland Publications

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