Pediatric parapneumonic effusion before and after national pneumococcal vaccination programs in Taiwan

Jun Yi Sim1, Luan-Yin Chang2, Tu-Hsuan Chang3

  • 1Department of Pediatrics, Taipei Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation, 289 Jianguo Road, Xindian District, New Taipei City, 23142, Taiwan.

Insights

Pneumococcal conjugate vaccines (PCVs) significantly reduced pneumococcal empyema in children. Continuous surveillance is crucial for monitoring other pathogens like Mycoplasma pneumoniae.

Area of Science:

  • Pediatric Infectious Diseases
  • Vaccinology
  • Respiratory Medicine

Background:

  • Limited data exists on the impact of pneumococcal conjugate vaccines (PCVs) on pediatric parapneumonic effusion.
  • This study investigates changes in pediatric parapneumonic effusion cases and causes before and after PCV13 introduction.

Purpose of the Study:

  • To evaluate the effectiveness of national PCV13 vaccination programs on pediatric parapneumonic effusion.
  • To identify changes in the etiology of pediatric parapneumonic effusion post-PCV13 implementation.

Main Methods:

  • Retrospective analysis of medical records of children (0-18 years) admitted with lobar pneumonia and parapneumonic effusion (2008-2017).
  • Inclusion of patients with effusion analyses, examining blood, pleural fluid, and respiratory specimens.
  • Comparison of data before and after the national PCV13 vaccination program in Taiwan.

Main Results:

  • A pathogen was identified in 85% of 202 children with lobar pneumonia and parapneumonic effusion.
  • Pneumococcal empyema decreased by 72% in 2- to 5-year-olds post-PCV13 immunization.
  • Mycoplasma pneumoniae emerged as the second most common cause, with distinct clinical characteristics compared to pneumococcal infections.

Conclusions:

  • National PCV13 immunization programs demonstrated significant effectiveness against pneumococcal empyema in children, sustained over 4 years.
  • Ongoing surveillance is essential to track the emergence of non-PCV serotypes and other pathogens like M. pneumoniae.
Abstract

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