A 32-Year Study of the Effect of Pneumococcal Vaccines on Invasive Streptococcus pneumoniae Disease

Ronald J Stanek1, Nancy B Norton2, Maurice A Mufson3

  • 1Department of Medicine, Marshall University Joan C. Edward School of Medicine, Huntington, West Virginia; Veterans Administration Medical Center, Huntington, West Virginia.

Abstract

Insights

Pneumococcal vaccines PCV7 and PCV13 significantly reduced invasive pneumococcal disease (IPD) in children. Adult IPD cases shifted to non-vaccine serotypes, with PPSV23 becoming dominant.

Area of Science:

  • Infectious Diseases
  • Vaccinology
  • Epidemiology

Background:

  • Streptococcus pneumoniae is a leading cause of community-acquired pneumonia and invasive pneumococcal infection (IPD).
  • IPD has high case fatality rates, particularly in adults.
  • Understanding serotype distribution and vaccine impact is crucial for public health.

Purpose of the Study:

  • To assess the long-term impact of pneumococcal conjugate vaccines (PCV7, PCV13) and polysaccharide vaccine (PPSV23) on serotype prevalence.
  • To evaluate changes in invasive pneumococcal infection (IPD) incidence and case fatality rates (CFR) in children and adults over 32 years.

Main Methods:

  • Retrospective study of invasive pneumococcal infection (IPD) cases from 1983-2014.
  • Serotyping of Streptococcus pneumoniae strains and penicillin susceptibility testing.
  • Abstraction of clinical data from hospital records.

Main Results:

  • Invasive pneumococcal infection (IPD) occurred in 193 children and 1,003 adults; adult CFR was 19.2%.
  • PCV7 introduction led to a decrease in PCV7 serotypes and IPD among children.
  • Following PCV13 introduction and continued PCV7 use, non-vaccine serotypes and PPSV23 serotypes became dominant.

Conclusions:

  • Widespread use of PCV7 and PCV13 has dramatically altered pneumococcal serotype epidemiology.
  • IPD in children has significantly declined, while serotype distribution has shifted in adults.
  • Emergence of non-vaccine serotypes necessitates ongoing surveillance and vaccine strategy evaluation.

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