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Updated: Sep 3, 2026

Subcutaneous Infection of Methicillin Resistant Staphylococcus Aureus (MRSA)
Published on: February 9, 2011
Treatment of community-acquired methicillin-resistant Staphylococcus aureus in children
John F Marcinak1, Arthur L Frank
1Department of Pediatrics, University of Chicago, Chicago, Illinois, USA.
Purpose Of Review:
The concept of methicillin-resistant Staphylococcus aureus (MRSA) associated with broad resistance, nosocomial acquisition, and known risk factors has recently been expanded. A new type of MRSA that is resistant to fewer antibiotics has emerged in pediatric practice since the mid-1990s. These isolates are community acquired and have been reported from diverse geographic regions. Awareness of these organisms is important for appropriate treatment of S. aureus infections in children.
Recent Findings:
Community-acquired MRSA (CA-MRSA) isolates are similar in many respects to community-acquired methicillin-susceptible S. aureus (CA-MSSA). There are usually no differences in risk factors between children with CA-MRSA infections and those with CA-MSSA infections or their household contacts. In one study, however, multivariate analysis showed that age greater than 1 year and health care contact in the preceding month were significant risk factors for CA-MRSA. Skin and soft tissue infections are the most common manifestations, although serious invasive infections and death may occur. Pneumonia has been reported more often in children with CA-MRSA than in those with CA-MSSA. Clindamycin is an effective therapy for CA-MRSA, but there is a risk for development of clindamycin resistance during treatment of a CA-MRSA that is clindamycin susceptible and inducibly erythromycin resistant. Trimethoprim-sulfamethoxazole is likely to be effective, and linezolid is a new option for treatment.
Summary:
The appearance of CA-MRSA has important implications for therapy of infections caused by S. aureus in children. Three specific issues are the development of resistance during clindamycin therapy, insufficient data on the use of trimethoprim-sulfamethoxazole in serious CA-MRSA infections, and the appropriate role for newer antibiotics such as linezolid.
Insights
A new strain of community-acquired methicillin-resistant Staphylococcus aureus (CA-MRSA) is emerging in children, differing from traditional hospital-acquired strains. Awareness and appropriate antibiotic selection are crucial for treating these pediatric S. aureus infections.
Area of Science:
- Pediatric Infectious Diseases
- Antimicrobial Resistance
- Staphylococcus aureus Infections
Background:
- Methicillin-resistant Staphylococcus aureus (MRSA) is a significant pathogen, traditionally associated with healthcare settings.
- A distinct form of MRSA, termed community-acquired MRSA (CA-MRSA), has emerged in pediatric populations since the mid-1990s.
- CA-MRSA isolates exhibit reduced antibiotic resistance compared to traditional MRSA strains.
Purpose of the Study:
- To review the evolving landscape of MRSA in pediatric practice.
- To highlight the characteristics and implications of community-acquired MRSA (CA-MRSA) in children.
- To inform appropriate treatment strategies for S. aureus infections in pediatric patients.
Main Methods:
- Review of recent literature on CA-MRSA in pediatric populations.
- Analysis of clinical manifestations, risk factors, and treatment outcomes.
- Comparison of CA-MRSA with community-acquired methicillin-susceptible S. aureus (CA-MSSA).
Main Results:
- CA-MRSA infections in children are often indistinguishable from CA-MSSA infections regarding risk factors.
- Skin and soft tissue infections are most common, but invasive disease, including pneumonia, can occur.
- Clindamycin resistance can develop during treatment; trimethoprim-sulfamethoxazole and linezolid are alternative therapeutic options.
Conclusions:
- The emergence of CA-MRSA necessitates updated therapeutic approaches for pediatric S. aureus infections.
- Key considerations include the potential for clindamycin resistance, limited data on trimethoprim-sulfamethoxazole for severe infections, and the role of newer agents like linezolid.
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