Invasive pneumococcal disease caused by ceftriaxone-resistant Streptococcus pneumoniae in Taiwan

Hao-Yuan Lee1, Tsu-Lan Wu2, Lin-Hui Su3

  • 1Department of Nursing, Jen-Teh Junior College of Medicine, Nursing and Management, Miaoli, Taiwan; Molecular Infectious Disease Research Center, Chang Gung Memorial Hospital, Taoyuan, Taiwan; School of Medicine, College of Medicine, Fu Jen Catholic University, New Taipei, Taiwan.

Abstract

Insights

Invasive pneumococcal disease (IPD) mortality risk factors are complex. Ceftriaxone resistance in pneumococci, particularly from PCV7-excluded serotypes, is a significant concern, highlighting PCV13

Area of Science:

  • Medical Microbiology
  • Infectious Diseases
  • Vaccinology

Background:

  • Invasive pneumococcal disease (IPD) is a significant cause of mortality.
  • Risk factors contributing to IPD mortality remain incompletely understood.
  • Understanding serotype distribution and antimicrobial resistance is crucial for effective IPD management.

Purpose of the Study:

  • To investigate the risk factors associated with mortality in patients with invasive pneumococcal disease.
  • To analyze the serotype distribution and antimicrobial resistance patterns of IPD isolates.
  • To evaluate the potential impact of pneumococcal conjugate vaccines (PCVs) on IPD outcomes.

Main Methods:

  • A retrospective cohort study design was employed.
  • Clinical presentations and laboratory characteristics of 134 IPD patients from 2011-2013 were collected.
  • Serotype analysis and ceftriaxone resistance testing were performed on IPD isolates.

Main Results:

  • Half of the IPD isolates belonged to serotypes 19A, 6A, and 3, covered by PCV13 but not PCV7.
  • Ceftriaxone resistance was observed in 38% of isolates and was linked to inappropriate initial therapy and mortality.
  • Serotypes 6A, 15B, 19A, 19F, and 23F were associated with ceftriaxone resistance; PCV13 covered 94.1% of these resistant isolates, compared to 21.6% for PCV7.

Conclusions:

  • Increased ceftriaxone resistance in pneumococci, potentially driven by PCV7, is a concern.
  • The 13-valent pneumococcal conjugate vaccine (PCV13) is likely to provide protection against ceftriaxone-resistant strains in both children and the elderly.
  • Prompt administration of effective antibiotics like penicillin, fluoroquinolones, or vancomycin is essential for improving IPD patient outcomes.

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