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Published on: February 9, 2011
Clinical Outcomes of Oral Antibiotic Switch in Children with Staphylococcus aureus Bacteremia
Salih Demirhan1,2, Brenda I Anosike1,2
1Albert Einstein College of Medicine, Bronx, New York.
Insights
Pediatric Staphylococcus aureus bacteremia (SAB) is manageable with oral antibiotics. Switching to oral therapy in selected children with SAB was not linked to poor outcomes, suggesting a safe and effective treatment option.
Area of Science:
- Pediatrics
- Infectious Diseases
- Clinical Microbiology
Background:
- Staphylococcus aureus bacteremia (SAB) is a significant pediatric infection.
- Effective management strategies, including oral antibiotic transitions, are crucial for improving outcomes.
Purpose of the Study:
- To assess the etiology, management, and outcomes of pediatric SAB.
- To specifically evaluate the safety and efficacy of transitioning to oral antibiotic therapy in children with SAB.
Main Methods:
- Retrospective cohort study of children (≤19 years) with SAB over a 5-year period.
- Analysis of clinical data, including sources of infection, antibiotic treatment, and patient outcomes.
- Defined poor clinical outcome as SAB recurrence or all-cause mortality within 30 days.
Main Results:
- 88 SAB episodes in 76 patients were analyzed.
- Central lines and osteoarticular infections were common SAB sources.
- 45.5% of patients successfully transitioned to oral antibiotics, with no reported poor clinical outcomes in this group.
Conclusions:
- Pediatric SAB has low 30-day mortality and recurrence rates.
- Transitioning selected pediatric patients with SAB to oral antibiotics is a safe and effective strategy.
- Findings support the use of oral switch therapy in pediatric SAB management, aligning with adult literature.
Abstract:
Staphylococcus aureus is one of the leading causes of bacteremia in children. In this study, we aimed to evaluate our center's experience on the etiology, management, and outcomes of pediatric Staphylococcus aureus bacteremia (SAB) with particular focus on transitioning to oral antibiotic therapy. This retrospective cohort study included children aged ≤ 19 years diagnosed with SAB over a 5-year period. The main outcome was poor clinical outcome related to SAB defined as (1) recurrence of SAB within 30 days after discontinuation of SAB treatment and (2) any-cause mortality within 30 days after detection of SAB. Over a 5-year period, 88 SAB episodes of 76 unique patients were included. The most common source of SAB attributed to central line (n = 34), followed by osteoarticular (n = 24), infections. All patients received at least one day of intravenous (IV) antibiotics and treatment was switched to an oral agent in 45.5% of SAB episodes. Sources of SAB in the oral switch group were osteoarticular (n = 21), skin and soft tissue (n = 7), central line (n = 3), thrombophlebitis (n = 2), head and neck infection (n = 1), and unknown (n = 6). 30-day mortality and SAB recurrence within 30 days after initial treatment completion occurred in 3 and 5 SAB episodes, respectively. None of the patients in oral switch group had poor clinical outcomes. Our study results indicate that 30-day any-cause mortality and SAB-related mortality is low in children. Similar to growing adult literature, oral switch in SAB treatment was not associated with poor SAB outcomes in selected patients.
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