Impact of the pneumococcal conjugate vaccine on pneumococcal parapneumonic empyema

Carrie L Byington1, Kent Korgenski, Judy Daly

  • 1Department of Pediatrics, University of Utah, Salt Lake City, USA. Carrie.Byington@hsc.utah.edu

Insights

Pediatric pneumococcal parapneumonic empyema (PPE) cases increased after PCV-7 vaccine introduction in Utah. Serotype 1 remains common, but other serotypes are emerging, highlighting the need for ongoing surveillance.

Area of Science:

  • Pediatric Infectious Diseases
  • Vaccinology
  • Epidemiology

Background:

  • Pediatric pneumococcal parapneumonic empyema (PPE) incidence has risen, with Utah reporting high rates attributed to Streptococcus pneumoniae serotype 1.
  • The introduction of the 7-valent pneumococcal conjugate vaccine (PCV-7) prompted an investigation into its impact on PPE trends.

Purpose of the Study:

  • To analyze temporal trends in pediatric PPE in Utah.
  • To compare PPE incidence and causative serotypes before and after PCV-7 vaccine availability.

Main Methods:

  • Retrospective cohort study using the Intermountain Health Care (IHC) data warehouse (March 1996-June 2005).
  • Inclusion criteria: children (<18 years) with empyema (ICD-9 code 510.9).
  • Serotyping of Streptococcus pneumoniae isolates from blood and pleural fluid; comparison of pre-PCV-7 (March 2000) and post-PCV-7 (January 2001) periods.

Main Results:

  • A significant increase in mean annual empyema cases was observed post-PCV-7 (71.5 vs. 38 cases/year).
  • PPE represented a higher proportion of invasive pneumococcal disease (IPD) post-PCV-7 (32% vs. 17.5%).
  • Serotype 1 remained prevalent, but serogroups 3 and 19A emerged as significant causes of PPE post-vaccination; vaccine-type serotypes were exclusively identified in immunized children.

Conclusions:

  • Pediatric PPE incidence and its proportion of IPD increased in the post-PCV-7 era in Utah.
  • PPE is associated with substantial morbidity and mortality in children.
  • While serotype 1 is still dominant, emerging serotypes 3 and 19A necessitate continued monitoring and potential vaccine strategy adjustments.
Abstract

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