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Updated: May 10, 2026

Experimental Human Pneumococcal Carriage
Published on: February 15, 2013
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
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.
Background And Objective:
Although effective in preventing pneumococcal disease, 13-valent pneumococcal conjugate vaccine (PCV13) is the most expensive vaccine on the routinely recommended pediatric schedule in the United States. We examined the cost-effectiveness of switching from 4 total doses to 3 total doses by removing the third dose in the primary series in the United States.
Methods:
We used a probabilistic model following a single birth cohort of 4.3 million to calculate societal cost savings and increased disease burden from removing the 6-month dose of PCV13. Based on modified estimates of 7-valent pneumococcal conjugate vaccine from randomized trials and observational studies, we assumed that vaccine effectiveness under the 2 schedules is identical for the first 6 months of life and largely similar after administration of the 12- to 15-month booster dose.
Results:
Removing the third dose of PCV13 would annually save $500 million (in 2011$) but would also result in an estimated 2.5 additional deaths among inpatients with pneumonia or invasive pneumococcal disease. Such dose removal would also result in 261,000 estimated otitis media and 12,000 estimated pneumonia cases annually. These additional illnesses could be prevented through modest increases in coverage. Overall, societal savings per additional life-year lost would be ∼$6 million. When nonfatal outcomes are also considered, savings would range from $143,000 to $4 million per additional quality adjusted life-year lost, depending on the assumptions used for otitis media.
Conclusions:
Sizable societal cost savings and a moderate pneumococcal disease increase could be expected from removing the PCV13 primary series' third dose.
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