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Published on: July 9, 2014
Evaluation of Australia's varicella vaccination program for children and adolescents
Kirsten Ward1, Aditi Dey, Brynley Hull
1National Centre for Immunisation Research and Surveillance of Vaccine Preventable Diseases, The Children's Hospital at Westmead, Cnr Hawkesbury Road and Hainsworth Street, Westmead, New South Wales 2145, Australia.
Insights
Australia
Area of Science:
- Public Health
- Immunisation Programs
- Vaccinology
Background:
- The introduction of the monovalent varicella vaccine into Australia's National Immunisation Program (NIP) aimed to increase varicella (chickenpox) immunity in children and adolescents.
- Understanding the implementation process is crucial for optimising vaccine program delivery and uptake.
Purpose of the Study:
- To examine the implementation of the monovalent varicella vaccine program in Australia.
- To identify challenges and successes in program delivery for both childhood and adolescent catch-up doses.
Main Methods:
- Semi-structured interviews with key program implementers.
- Content analysis of interview themes.
- Analysis of childhood immunisation data from the Australian Childhood Immunisation Register (ACIR).
- Assessment of adolescent coverage via state/territory programs.
- Analysis of national seroprevalence data before and after program commencement.
Main Results:
- Key implementation challenges included parental reporting of prior infection, the introduction of a single vaccine dose at 18 months, and integrating the adolescent catch-up dose into school programs.
- Despite challenges, rapid childhood coverage reached 83% by 24 months, with 30-33% coverage for the adolescent catch-up dose.
- Seroprevalence data indicated high population immunity when combined with estimated natural immunity, though it under-estimated coverage in young children.
Conclusions:
- The varicella vaccination program successfully achieved high coverage in children and adolescents despite implementation hurdles.
- The exclusion criterion of reported natural infection warrants re-evaluation as the program matures and wild-type virus circulation declines.
- Development of sensitive laboratory assays is needed to accurately measure population-level vaccine-induced immunity.
Objective:
This paper examines how the monovalent varicella vaccine for children, with an adolescent catch-up dose, was introduced into Australia's National Immunisation Program (NIP), focusing on programme implementation.
Methods:
Semi-structured interviews were conducted with key informants involved in programme implementation. Key themes from interviews were identified through content analysis. Childhood coverage was assessed using data from the Australian Childhood Immunisation Register (ACIR) with adolescent coverage obtained from state/territory immunisation programmes. Seroprevalence data were analysed from national serosurveys conducted before and after programme commencement.
Results:
Implementation challenges for both parents and providers included: (a) parental report of previous infection as an exclusion criterion; (b) introducing a vaccine on its own at 18 months of age; and (c) adding the adolescent dose into existing school-based vaccination programmes with parental reported exclusion criteria. Despite these challenges, coverage rapidly reached 83% by 24 months of age and 30-33% for the adolescent catch-up dose. When considered in conjunction with estimated pre-vaccination natural immunity in both target groups (20% and 83%, respectively) coverage can be considered high. The serosurvey under-estimated coverage in 2-year-old children but was useful to assess trends in population immunity.
Conclusion:
The introduction of a single dose of monovalent varicella vaccine at 18 months of age and a school-based catch-up programme at 11-13 years of age successfully achieved high coverage, notwithstanding some challenges. Reported natural infection has been an exclusion criterion for vaccination, but as the programme matures and circulation of wild-type virus decreases, the need for this warrants consideration. There is a need for sensitive laboratory assays to measure vaccine-induced immunity at a population level.
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