Distribution of Streptococcus pneumoniae serotypes that cause parapneumonic empyema in Turkey

Mehmet Ceyhan1, Yasemin Ozsurekci, Nezahat Gürler

  • 1Department of Pediatric Infectious Diseases, Hacettepe University Faculty of Medicine, Ankara, Turkey.

Insights

Pediatric empyema in Turkey was primarily caused by Streptococcus pneumoniae serotypes not covered by the 7-valent pneumococcal conjugated vaccine (PCV-7). Continued surveillance is crucial for effective vaccine selection.

Area of Science:

  • Pediatric Infectious Diseases
  • Microbiology
  • Vaccinology

Background:

  • Streptococcus pneumoniae is a leading cause of complicated pneumonia, particularly empyema in children.
  • Despite the availability of pneumococcal vaccines, pediatric parapneumonic empyema remains a significant health concern.

Purpose of the Study:

  • To investigate the specific serotypes of Streptococcus pneumoniae responsible for empyema in unvaccinated children in Turkey.
  • To assess the potential coverage of existing pneumococcal vaccines against these identified serotypes.

Main Methods:

  • Analysis of pleural fluid samples from 156 children diagnosed with empyema across 13 hospitals in Turkey (2010-2012).
  • Detection of 14 Streptococcus pneumoniae serotypes/serogroups using a Bio-Plex multiplex antigen assay.
  • Evaluation of serotype coverage for PCV-7, PCV-10, and PCV-13 vaccines.

Main Results:

  • Streptococcus pneumoniae serotypes were identified in 33 of 156 cases; all children were unvaccinated.
  • Non-PCV-7 serotypes (1, 5, 3) were prevalent, accounting for a significant proportion of identified cases.
  • PCV-7 serotypes were detected in 16.3% of cases, while PCV-13 offered 60% potential coverage.

Conclusions:

  • Serotypes not included in the 7-valent pneumococcal conjugated vaccine are major contributors to pediatric empyema in the studied population.
  • Active surveillance for Streptococcus pneumoniae serotypes causing empyema is essential for optimizing pneumococcal vaccine strategies.
  • The findings underscore the need for updated vaccine formulations to address circulating, non-vaccine serotypes.

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