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Updated: Feb 8, 2026

Subcutaneous Infection of Methicillin Resistant Staphylococcus Aureus MRSA
Published on: February 9, 2011
Management of Pediatric Acute Hematogenous Osteomyelitis, Part II: A Focus on Methicillin-Resistant Staphylococcus
Kailynn J DeRonde1,2, Jennifer E Girotto1,2,3, David P Nicolau4,5
1Department of Pharmacy Practice, School of Pharmacy, University of Connecticut, Storrs, Connecticut.
Abstract:
Methicillin-resistant Staphylococcus aureus (MRSA) has become the most prevalent cause of acute hematogenous osteomyelitis (AHO) in pediatric patients. This increase in MRSA is due to the rise in community-acquired MRSA. Therefore, it is important that clinicians are aware of the various and upcoming therapies that cover this bacterium. A literature search of the Medline database was performed from creation through January 2018. Articles chosen for the review emphasize well-established MRSA treatment options for pediatric AHO, newer therapies on the horizon, and important pharmacokinetics and pharmacodynamic concepts for treatment. Traditional therapies, including vancomycin and clindamycin, remain effective for the treatment of pediatric AHO. When these agents cannot be used, evidence in AHO has been growing for daptomycin, linezolid, and ceftaroline. Further initial pediatric data with the long-acting lipoglycopeptides show promise and in the future may provide a role in AHO treatment in children.
Insights
Community-acquired Methicillin-resistant Staphylococcus aureus (MRSA) is the leading cause of pediatric osteomyelitis. Clinicians should be aware of established and emerging therapies, including vancomycin, clindamycin, daptomycin, and linezolid, for effective treatment.
Area of Science:
- Infectious Diseases
- Pediatric Orthopedics
- Pharmacology
Background:
- Methicillin-resistant Staphylococcus aureus (MRSA) is the predominant pathogen in pediatric acute hematogenous osteomyelitis (AHO).
- The increasing prevalence of community-acquired MRSA necessitates updated therapeutic strategies for pediatric AHO.
Purpose of the Study:
- To review established and emerging treatment options for pediatric AHO caused by MRSA.
- To highlight key pharmacokinetic and pharmacodynamic considerations for MRSA treatment in children.
Main Methods:
- A literature search of the Medline database was conducted from its inception through January 2018.
- Articles were selected based on their focus on well-established and novel MRSA therapies for pediatric AHO.
Main Results:
- Vancomycin and clindamycin remain effective traditional treatments for pediatric AHO.
- Daptomycin, linezolid, and ceftaroline show growing evidence for use when traditional agents are unsuitable.
- Long-acting lipoglycopeptides demonstrate promising initial pediatric data for future AHO treatment roles.
Conclusions:
- Clinicians require knowledge of current and novel MRSA therapies for pediatric AHO.
- A range of effective treatment options exist, with newer agents offering alternatives for complex cases.
- Emerging therapies like lipoglycopeptides may expand future treatment paradigms for pediatric osteomyelitis.
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