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Updated: Jul 19, 2026

Subcutaneous Infection of Methicillin Resistant Staphylococcus Aureus (MRSA)
Published on: February 9, 2011
Evolving epidemiology of pediatric Staphylococcus aureus cutaneous infections in a Baltimore hospital
Aaron E Chen1, Mitchell Goldstein, Karen Carroll
1Department of Pediatrics, The Johns Hopkins University, Baltimore, MD, USA.
Insights
Community-associated methicillin-resistant Staphylococcus aureus (CA-MRSA) skin infections significantly increased in children during 2003. These infections often required drainage but were treatable with antibiotics like clindamycin and trimethoprim/sulfamethoxazole.
Area of Science:
- Infectious Diseases
- Pediatric Dermatology
- Microbiology
Background:
- Pediatric Staphylococcus aureus (SA) cutaneous infections are common.
- An increase in community-associated methicillin-resistant SA (CA-MRSA) was observed.
- Understanding the epidemiology and susceptibility of these infections is crucial.
Purpose of the Study:
- To analyze the epidemiology of pediatric SA cutaneous infections.
- To determine antibiotic susceptibility profiles of SA and MRSA isolates.
- To evaluate outcomes of CA-MRSA infections in children.
Main Methods:
- Retrospective review of pediatric SA skin and wound isolates from November 2002 to October 2003.
- Classification of isolates as health care-associated (HA) or community-associated (CA).
- Analysis of demographic, clinical data, and antibiotic susceptibility.
Main Results:
- 45% of 181 pediatric SA infections were MRSA, with 84% being CA-MRSA.
- CA-MRSA increased from 15% to 45% of SA infections within the study year.
- CA-MRSA showed high susceptibility to trimethoprim/sulfamethoxazole (98%) and clindamycin (94%).
- CA-MRSA infections frequently required drainage (70%) and were not associated with bacteremia.
Conclusions:
- CA-MRSA cutaneous infections rose significantly in urban pediatric populations in 2003.
- These infections were largely susceptible to clindamycin and trimethoprim/sulfamethoxazole.
- Management involves drainage, culture, and judicious use of antibiotics like clindamycin.
Objectives:
To examine the epidemiology, antibiotic susceptibility profiles, and outcomes in pediatric Staphylococcus aureus (SA) cutaneous infections at a time when community-associated (CA) methicillin-resistant SA (CA-MRSA) infections seemed to be increasing in our community.
Methods:
The hospital microbiology database was searched for unique skin and wound SA isolates among pediatric patients between November 2002 and October 2003. Demographic and clinical data were abstracted from medical records. Cases were classified as either health care-associated (HA) or CA.
Results:
Among 181 pediatric SA cutaneous infections, 81 (45%) were caused by MRSA. Most (84%) of these MRSA were CA. Between the first 6 months and second 6 months of the study period, CA-MRSA increased from 15% to 45% (P < 0.001) of all SA cutaneous infections. Ninety-eight percent and 94% of CA-MRSA were susceptible to trimethoprim/sulfamethoxazole and clindamycin (confirmed by D test), respectively. Hospitalization occurred for 25% of CA-MRSA and 75% of HA-MRSA (P = 0.004). Drainage procedures were performed for 70% of CA-MRSA. No cases of CA-MRSA skin infections were accompanied by bacteremia.
Conclusions:
The CA-MRSA cutaneous infections increased in children in our urban Baltimore hospital in 2003. These CA-MRSA were erythromycin resistant, clindamycin susceptible, and trimethoprim/sulfamethoxazole susceptible. The CA-MRSA cutaneous infections frequently required drainage and were not associated with bacteremia. Children with cutaneous MRSA infections were less likely to have traditional health care risk factors than children with cutaneous methicillin-sensitive SA infections--an inversion of past patterns of MRSA infections--but were equally likely to be hospitalized when other factors were considered. These CA-MRSA cutaneous infections can be managed with abscess drainage and culture, careful follow-up, and empirical clindamycin therapy when clinically indicated.
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