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External validation of the Melbourne ASSET score for pediatric cellulitis

Céline Thémelin1, Soha Rached Dastous1,2, Brandon Noyon3

  • 1Department of Pediatric Emergency Medicine, Centre Hospitalier Universitaire Sainte Justine, Université de Montréal, Montreal, QC, Canada.

CJEM
|July 23, 2026
PubMed

Insights

The Melbourne ASSET Score showed limited ability to predict intravenous antibiotic needs in pediatric cellulitis. It is best used for risk stratification, not as a strict rule for treatment.

Area of Science:

  • Pediatric Emergency Medicine
  • Infectious Diseases
  • Clinical Decision Support Tools

Background:

  • Cellulitis is a common pediatric emergency department (ED) presentation.
  • Accurate prediction of intravenous (IV) antibiotic therapy need is crucial for effective management.
  • The Melbourne ASSET Score was developed to aid this prediction.

Purpose of the Study:

  • To conduct the first external validation of the Melbourne ASSET Score.
  • To assess the score's accuracy in predicting IV antibiotic therapy for pediatric ED cellulitis.
  • To evaluate the score's performance in a Canadian tertiary pediatric ED setting.

Main Methods:

  • Prospective cohort study of children aged 6 months to 18 years with cellulitis.
  • Exclusion criteria included orbital cellulitis, immunocompromise, clinical toxicity, and inability to tolerate oral antibiotics.
  • Primary outcome: IV vs. oral antibiotic administration at 24 hours; secondary outcomes: interrater reliability and treatment failure.

Main Results:

  • The ASSET Score had limited discrimination (AUC 0.68) for predicting IV antibiotic use.
  • Sensitivity was 74% and specificity was 55% for IV antibiotic use.
  • Notably, 57% of children with scores ≥4 were successfully treated with oral antibiotics, and treatment failure was 12%.

Conclusions:

  • The Melbourne ASSET Score demonstrated limited discriminative performance for binary IV antibiotic decisions.
  • The score is influenced by successful high-dose oral antibiotic pathways.
  • It is best used as a risk-stratification tool alongside clinical judgment, not a strict mandate for IV therapy.
Abstract