Outcomes in children treated for perineal group A beta-hemolytic streptococcal dermatitis

Dan Olson1, M Bruce Edmonson

  • 1Division of General Pediatrics and Adolescent Medicine, Department of Pediatrics, University of Wisconsin School of Medicine and Public Health, Madison, WI, USA.

Insights

Perineal streptococcal dermatitis (PSD) treated with penicillin or amoxicillin shows a high recurrence rate in children. Further trials are needed to confirm if beta-lactamase resistant agents reduce this risk.

Area of Science:

  • Pediatric infectious diseases
  • Dermatology
  • Pharmacology

Background:

  • Perineal streptococcal dermatitis (PSD) is a common infection in children.
  • Recurrence of PSD can occur, impacting treatment effectiveness.
  • The choice of initial antimicrobial therapy may influence recurrence rates.

Purpose of the Study:

  • To evaluate the relationship between initial antimicrobial treatment and recurrence of perineal streptococcal dermatitis in children.
  • To determine if specific antibiotic classes are associated with higher rates of PSD recurrence.

Main Methods:

  • Retrospective audit of laboratory logs and medical records for culture-confirmed PSD cases in children (2006-2008).
  • Estimation of recurrence rates (defined as repeat diagnosis within 6 months).
  • Meta-analysis combining current data with 8 previous studies on PSD recurrence.

Main Results:

  • Of 81 children with incident PSD, 26 (32.1%) experienced recurrence, with most within 6 weeks.
  • Recurrence rates were higher following penicillin or amoxicillin (38.1%) compared to beta-lactamase resistant agents (27.8%).
  • Meta-analysis confirmed a pooled recurrence rate of 37.4% for penicillin/amoxicillin versus a lower rate for resistant agents (OR: 2.39).

Conclusions:

  • Initial treatment of PSD with penicillin or amoxicillin is linked to a high risk of recurrence.
  • The benefit of using beta-lactamase resistant agents to reduce PSD recurrence requires further investigation.
  • A clinical trial is recommended to definitively assess the efficacy of beta-lactamase resistant agents in preventing PSD recurrence.
Abstract

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