Clindamycin treatment of methicillin-resistant Staphylococcus aureus infections in children

Arthur L Frank1, John F Marcinak, P Daisy Mangat

  • 1Department of Pediatrics, College of Medicine, University of Illinois at Chicago, USA.

Abstract

Insights

Erythromycin-resistant MRSA in children can develop clindamycin resistance during treatment. Microbiological testing is crucial for safe clindamycin use in these pediatric infections.

Area of Science:

  • Pediatric Infectious Diseases
  • Antimicrobial Resistance
  • Clinical Microbiology

Background:

  • Emergence of Methicillin-resistant Staphylococcus aureus (MRSA) with limited antibiotic resistance patterns.
  • Potential for clindamycin resistance development during therapy for erythromycin-resistant MRSA due to linked resistance mechanisms.

Purpose of the Study:

  • To analyze clindamycin-susceptible MRSA isolates from children.
  • To investigate the prevalence of erythromycin resistance and associated linked resistance mechanisms.
  • To assess the risk of clindamycin resistance development during treatment.

Main Methods:

  • Analysis of pediatric MRSA isolates (1987-2000) and clinical data.
  • Determination of antibiotic susceptibilities.
  • Pulsed field gel electrophoresis (PFGE) for strain typing.
  • D test to detect inducible clindamycin resistance (erythromycin-resistant isolates).

Main Results:

  • 38% of clindamycin-susceptible MRSA isolates from children were erythromycin-resistant.
  • Erythromycin-resistant isolates were more common in infants and less frequently community-acquired.
  • The D test identified inducible clindamycin resistance in most erythromycin-resistant isolates.
  • One case of clindamycin resistance development and clinical relapse occurred during therapy.

Conclusions:

  • Erythromycin resistance is a significant finding in pediatric MRSA.
  • Clindamycin resistance can emerge during treatment, necessitating careful monitoring.
  • Clindamycin can be a viable option if laboratories notify clinicians of resistance risks and the clinical context is appropriate.

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