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Updated: Sep 21, 2026

Subcutaneous Infection of Methicillin Resistant Staphylococcus Aureus (MRSA)
Published on: February 9, 2011
Infection characteristics and treatment of Staphylococcus aureus bacteraemia at a tertiary children's hospital
Alasdair P S Munro1,2, Christopher C Blyth3,4,5,6, Anita J Campbell3,4,6
1Department of Infectious Diseases, Perth Children's Hospital, Hospital Ave, Nedlands, WA, 6009, Australia. a.munro@doctors.org.uk.
Insights
This pilot study classified pediatric Staphylococcus aureus bacteremia (SAB) into simple and complex cases. Complex pediatric SAB cases showed increased C-reactive protein, longer hospital stays, and longer antibiotic treatment durations.
Area of Science:
- Pediatric Infectious Diseases
- Clinical Microbiology
- Epidemiology
Background:
- Staphylococcus aureus bacteraemia (SAB) presents significant morbidity and mortality in children.
- Limited pediatric clinical trial data and poorly understood epidemiology hinder effective management.
- A pilot study was conducted to characterize SAB and validate a severity classification.
Purpose of the Study:
- To characterize the epidemiology of pediatric Staphylococcus aureus bacteraemia (SAB).
- To validate a simple versus complex classification for SAB severity.
- To identify risk factors and markers associated with SAB severity in children.
Main Methods:
- Prospective identification of SAB patients at a children's hospital from May 2011 to December 2013.
- Retrospective data collection from clinical and laboratory records.
- Classification of cases as simple (peripheral focus) or complex (multi-site, deep tissue, sepsis) based on predefined criteria.
Main Results:
- 49 pediatric SAB cases were identified; 61% were simple and 39% were complex.
- No deaths or relapses occurred. Methicillin-resistant S. aureus (MRSA) accounted for 10% of isolates, none healthcare-associated.
- Complex infections were associated with higher C-reactive protein (CRP), longer length of stay, and longer antibiotic duration (p < 0.001). Pre-existing malignancy was a risk factor for complex infection (p=0.02).
Conclusions:
- This study provides the first categorization of pediatric SAB into simple and complex types for clinical guidance.
- A spectrum of disease severity exists in pediatric SAB, with complex cases exhibiting worse outcomes.
- Distinct simple and complex pediatric SAB cohorts are identified, potentially serving as targets for future clinical trials.
Background:
Staphylococcus aureus bacteraemia (SAB) causes considerable morbidity and mortality in children. Despite this, its epidemiology and risk factors are poorly understood, with minimal paediatric clinical trial data available to guide clinicians in management. We conducted a pilot study to characterise SAB and validate a severity classification for use in future clinical trials.
Methods:
Patients with SAB were prospectively identified at Princess Margaret Hospital for Children (Perth, Western Australia) from May 2011 to December 2013. Retrospective data were collected from clinical and laboratory records. Cases were classified based on a priori defined criteria as simple (single or contiguous, peripheral site focus) or complex (multi-site, deep tissue, no focus or sepsis) and tested against risk factors and markers of severity of infection.
Results:
There were 49 cases of SAB (median age 7.7 years), with classification as simple (n = 30, 61%) and complex (n = 19, 39%) respectively. There were no deaths or relapses in our cohort. Only 10% of isolates were methicillin resistant S. aureus (MRSA), and none of these were healthcare-associated. Age, gender, Indigenous status, MRSA and healthcare-associated infections were not predictive of complex infection. Pre-existing malignancy was a risk factor for complex infection (p = 0.02). Complex infections were associated with a higher median maximum C reactive protein (216 mg/L vs 50 mg/L, p = < 0.001), longer median length of stay (42 vs 10 days, p = < 0.001) and longer duration of antibiotic therapy (43 vs 34 days, p = 0.03).
Discussion:
This is the first attempt to categorise paediatric SAB as simple versus complex, to guide clinicians in decision making.
Conclusions:
There is a wide spectrum of disease severity in paediatric SAB, with maximum CRP, length of stay, and duration of therapy greater in those with complex disease. Distinct cohorts with simple and complex courses which may be a target for future clinical trials have been described.
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