Community-Acquired Methicillin-Resistant Staphylococcus aureus Infections in Acutely Ill Children: A Retrospective

Saptharishi Lalgudi Ganesan1,2,3,4, Ankit Mehta4, Keshavmurthy Lakshmikantha4

  • 1Children's Hospital of Western Ontario, London Health Sciences Center, London, Canada.

Abstract

Insights

Community-acquired methicillin-resistant Staphylococcus aureus (CA-MRSA) is increasing in children. Admission variables cannot reliably distinguish CA-MRSA from methicillin-sensitive Staphylococcus aureus (MSSA) infections. Empiric broad-spectrum antibiotics may be needed for critically ill children.

Area of Science:

  • Pediatric Infectious Diseases
  • Clinical Microbiology
  • Epidemiology

Background:

  • Community-acquired methicillin-resistant Staphylococcus aureus (CA-MRSA) is a growing concern in pediatric populations.
  • Differentiating CA-MRSA from methicillin-sensitive Staphylococcus aureus (MSSA) infections in acutely ill children is clinically challenging.
  • Understanding the epidemiology and clinical features of Staphylococcal infections in hospitalized children is crucial for effective management.

Purpose of the Study:

  • To determine if initial clinical and laboratory findings can reliably differentiate CA-MRSA from MSSA infections in hospitalized children.
  • To describe the epidemiology, clinical presentation, and outcomes of pediatric Staphylococcal infections.
  • To identify predictors of CA-MRSA infection in this cohort.

Main Methods:

  • A retrospective case-control study comparing children with CA-MRSA and MSSA infections from June 2014 to June 2017.
  • Analysis of demographic, clinical, and laboratory variables at admission.
  • Multivariate logistic regression and Cox-proportional hazard analysis were used to identify predictors and compare survival.

Main Results:

  • The study included 73 children (35 CA-MRSA, 38 MSSA). CA-MRSA patients were younger (median 36 vs. 56 months).
  • Skin and soft tissue involvement rates were similar. CA-MRSA infections had a shorter median illness duration (6 vs. 8.5 days).
  • A total white blood cell count ≤8100 was 82% sensitive and 94% specific for MRSA sepsis. No admission variables predicted MRSA positivity on regression analysis. Mortality and ICU stay were similar.

Conclusions:

  • The incidence of CA-MRSA infections in hospitalized children appears to be rising.
  • No reliable clinical or laboratory markers at admission can differentiate CA-MRSA from MSSA infections in children.
  • Empiric broad-spectrum antibiotic coverage for both MSSA and MRSA is recommended for critically ill children with suspected Staphylococcal infections.