Cost-effectiveness of using 2 vs 3 primary doses of 13-valent pneumococcal conjugate vaccine

Charles Stoecker1, Lee M Hampton, Ruth Link-Gelles

  • 1National Center for Immunization and Respiratory Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia 30329, USA. cfstoecker@tulane.edu

Pediatrics
|July 4, 2013
PubMed

Insights

Reducing the 13-valent pneumococcal conjugate vaccine (PCV13) to three doses could save $500 million annually in the US. However, this change may lead to more deaths and illnesses from pneumococcal disease.

Area of Science:

  • Public Health
  • Vaccinology
  • Health Economics

Background:

  • 13-valent pneumococcal conjugate vaccine (PCV13) is crucial for preventing pneumococcal disease but is the most expensive vaccine on the US pediatric schedule.
  • The current pediatric schedule includes four doses of PCV13.

Purpose of the Study:

  • To evaluate the cost-effectiveness of reducing the PCV13 primary series from four to three doses by removing the 6-month dose.
  • To assess the potential societal cost savings and changes in disease burden associated with this dose reduction.

Main Methods:

  • A probabilistic model was used to simulate a birth cohort of 4.3 million individuals.
  • The model compared two PCV13 schedules: the current four-dose schedule and a proposed three-dose schedule (removing the 6-month dose).
  • Assumptions on vaccine effectiveness were based on existing data for pneumococcal conjugate vaccines.

Main Results:

  • Removing the third PCV13 dose could result in annual societal cost savings of approximately $500 million (in 2011 dollars).
  • This reduction may lead to an estimated 2.5 additional deaths from pneumonia or invasive pneumococcal disease annually.
  • An increase in cases of otitis media (261,000) and pneumonia (12,000) is also projected, though these could be mitigated by increased vaccine coverage.

Conclusions:

  • Reducing the PCV13 primary series to three doses offers substantial societal cost savings.
  • A moderate increase in pneumococcal disease burden is a potential consequence of this dose reduction.
  • The trade-off between cost savings and increased disease burden warrants careful consideration.
Abstract

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