Managing penicillin resistant pneumococcal meningitis: an international id-iri study

Hakan Erdem1, Elif Dogan2, Handan Ankarali3

  • 1Department of Infectious Diseases & Clinical Microbiology, Health Sciences University, Gülhane School of Medicine, Ankara, Türkiye. hakanerdem1969@yahoo.com.

Insights

Penicillin-resistant pneumococcal meningitis (PRPM) is a severe infection with high mortality and sequelae rates. Early indicators like ICU admission and mechanical ventilation predict worse outcomes, while moxifloxacin shows promising susceptibility.

Area of Science:

  • Infectious Diseases
  • Clinical Microbiology
  • Epidemiology

Background:

  • Penicillin-resistant pneumococcal meningitis (PRPM) presents significant clinical challenges and high fatality rates.
  • Understanding the clinical features, outcomes, and antimicrobial resistance patterns is crucial for effective management.

Purpose of the Study:

  • To evaluate clinical characteristics, outcomes, and predictors of mortality and sequelae in PRPM patients.
  • To assess antimicrobial efficacy and drug susceptibility patterns in a global cohort.

Main Methods:

  • A multicentre, international retrospective study involving 138 PRPM patients from 33 centers in 11 countries (2019-2024).
  • Univariate and multivariate analyses were employed to identify outcome predictors.
  • Antibiotic susceptibility testing was performed on bacterial isolates.

Main Results:

  • Overall, 60.1% of patients were cured, 19.6% died, and 20.3% survived with sequelae.
  • Mortality was associated with ICU admission, mechanical ventilation, and vasopressor use.
  • Moxifloxacin demonstrated high susceptibility (97.9%), while ceftriaxone (55.9%) and meropenem (59%) showed lower rates.

Conclusions:

  • PRPM remains a life-threatening infection, with nearly two-fifths experiencing mortality or sequelae.
  • Severe illness markers and recurrent meningitis are linked to adverse outcomes.
  • Corticosteroid therapy may offer a protective effect, and moxifloxacin shows potential for treating PRPM despite resistance challenges.

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