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Varicella vaccine effectiveness over 10 years in Australia; moderate protection from 1-dose program
Helen E Quinn1, Heather F Gidding2, Helen S Marshall3
1National Centre for Immunisation Research and Surveillance of Vaccine Preventable Diseases (NCIRS), Children's Hospital at Westmead, Cnr Hawkesbury Road and Hainsworth Street, Westmead, NSW 2145, Australia; Discipline of Child and Adolescent Health, University of Sydney, Sydney, Australia.
Insights
Australia's single-dose varicella vaccination program shows moderate effectiveness in preventing hospitalizations. A second vaccine dose may further reduce varicella disease burden and transmission.
Area of Science:
- Immunology
- Vaccinology
- Public Health
Background:
- Australia implemented a single-dose infant varicella vaccination program.
- The program's impact on preventing hospitalised varicella disease required assessment.
Purpose of the Study:
- To evaluate the effectiveness of a single-dose varicella vaccine in preventing hospitalised disease.
- To compare two distinct methods for estimating vaccine effectiveness.
Main Methods:
- Utilized a case-control study design with clinically confirmed varicella cases.
- Age-matched controls were sourced from the Australian Immunisation Register.
- Employed conditional logistic regression models to estimate vaccine effectiveness (VE).
Main Results:
- Identified 78 hospitalised varicella cases between January 2008 and December 2015.
- Estimated single-dose varicella vaccine effectiveness against hospitalisation was 64.7% (95% CI: 43.3-78.0%).
- Excluding immunocompromised children did not significantly alter VE estimates.
Conclusions:
- The single-dose varicella vaccination program has influenced varicella disease burden in Australia.
- Moderate effectiveness suggests potential benefits from a two-dose vaccination schedule to minimize breakthrough infections and transmission.
Objectives:
To examine the impact of Australia's single dose infant varicella vaccination program, we assessed single dose varicella vaccine effectiveness (VE) in preventing hospitalised disease using two methods.
Methods:
Clinically confirmed varicella cases from the Paediatric Active Enhanced Disease Surveillance (PAEDS) sentinel network were age-matched to 20 controls obtained from the Australian Immunisation Register. Conditional logistic regression models were used to estimate VE and compared with estimates obtained using our second approach.
Results:
There were 78 hospitalised varicella cases during the post vaccine introduction period from January 2008 to December 2015, who were eligible for funded varicella vaccination. Median age at onset was 4.5 years and more than half (59%) were vaccinated. The majority of children received one vaccine brand (Varilrix, GSK). The estimated case-control VE for one dose of vaccine against hospitalised varicella was 64.7% (95% CI: 43.3-78.0%); estimates using the screening method were not significantly different. Exclusion of children who were immunocompromised did not significantly alter VE estimates.
Conclusions:
Although Australia's program has impacted on the burden of varicella disease, single dose VE against varicella hospitalisation is only moderate. Greater reductions in varicella disease could potentially be achieved by incorporation of a second vaccine dose into the program to minimise breakthrough disease and interrupt virus circulation.
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