Comparison of Empiric Antibiotics for Acute Osteomyelitis in Children

Sarah McBride1, Cary Thurm2, Ramkiran Gouripeddi3

  • 1Boston Children's Hospital, Boston, Massachusetts; sarah.mcbride@childrens.harvard.edu.

Hospital Pediatrics
|April 8, 2018
PubMed
Abstract

Insights

Early antibiotics targeting methicillin-resistant Staphylococcus aureus (MRSA) in children with osteomyelitis increased repeat MRIs but did not affect readmission rates. Treatment for methicillin-sensitive Staphylococcus aureus (MSSA) showed better inflammatory marker normalization.

Area of Science:

  • Pediatric infectious diseases
  • Antibiotic stewardship
  • Osteomyelitis treatment

Background:

  • Broad-spectrum antibiotics are frequently used for empiric treatment of acute hematogenous osteomyelitis.
  • Targeting methicillin-resistant Staphylococcus aureus (MRSA) carries potential risks and uncertain benefits.

Purpose of the Study:

  • To compare clinical outcomes in pediatric osteomyelitis patients who received initial antibiotics targeting MRSA versus those who did not.

Main Methods:

  • Retrospective cohort study of 974 hospitalized children (ages 2-18).
  • Data sourced from the Pediatric Health Information System database and augmented with clinical data.
  • Comparison of hospital readmission, repeat MRI rates, and 72-hour inflammatory marker improvement between treatment groups.

Main Results:

  • Patients receiving initial MRSA coverage had higher rates of repeat MRI within 7 and 180 days compared to MSSA-only coverage (8.6% vs 4.1% and 12% vs 5.8%).
  • Hospital readmission rates at 90 and 180 days were similar between groups (approx. 9-11%).
  • MRSA coverage was associated with a lower rate of 72-hour white blood cell count normalization (4.2% vs 16.4%) compared to MSSA-only coverage.

Conclusions:

  • Early antibiotic treatment targeting MRSA in pediatric osteomyelitis is linked to increased repeat MRIs.
  • Hospital readmission rates were comparable regardless of initial MRSA-targeted antibiotic use.
  • Early MRSA-targeted therapy may not offer clinical advantages and could be associated with poorer inflammatory marker response.

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