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.

Vaccine
|January 8, 2013
PubMed

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.
Abstract

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