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Updated: Feb 21, 2026

Subcutaneous Infection of Methicillin Resistant Staphylococcus Aureus MRSA
Published on: February 9, 2011
Impact of Systemic Antibiotics on Staphylococcus aureus Colonization and Recurrent Skin Infection
Patrick G Hogan1, Marcela Rodriguez2, Allison M Spenner2
1Department of Pediatrics, Washington University School of Medicine, St Louis, Missouri.
Insights
Systemic antibiotics for Staphylococcus aureus skin infections reduce colonization and prevent recurrence. Clindamycin showed greater efficacy than trimethoprim-sulfamethoxazole in preventing recurrent infections.
Area of Science:
- Infectious Diseases
- Microbiology
- Dermatology
Background:
- Staphylococcus aureus colonization increases the risk of skin and soft tissue infections (SSTI).
- Effective management of S. aureus SSTI is crucial to prevent recurrent infections and reduce bacterial colonization.
Purpose of the Study:
- To investigate the impact of systemic antibiotics, alongside incision and drainage, on S. aureus colonization and recurrent SSTI.
- To compare the effectiveness of different antibiotic regimens in managing S. aureus SSTI.
Main Methods:
- Prospective evaluation of 383 children with S. aureus SSTI requiring incision and drainage.
- Baseline and follow-up (within 3 months) S. aureus colonization screening.
- Ascertainment of recurrent SSTI incidence for up to 1 year.
Main Results:
- Guideline-recommended antibiotics reduced S. aureus colonization (aHR, 0.49) and recurrent SSTI (aHR, 0.57).
- Persistent colonization was linked to a higher risk of recurrent infection (aHR, 2.37).
- Clindamycin was more effective than trimethoprim-sulfamethoxazole in eradicating colonization and preventing recurrence.
Conclusions:
- Systemic antibiotics are integral to managing acute SSTI, reducing S. aureus colonization and subsequent infections.
- The differential efficacy of clindamycin versus trimethoprim-sulfamethoxazole warrants further investigation.
Background:
Staphylococcus aureus colonization poses risk for subsequent skin and soft tissue infection (SSTI). We hypothesized that including systemic antibiotics in the management of S. aureus SSTI, in conjunction with incision and drainage, would reduce S. aureus colonization and incidence of recurrent infection.
Methods:
We prospectively evaluated 383 children with S. aureus SSTI requiring incision and drainage and S. aureus colonization in the anterior nares, axillae, or inguinal folds at baseline screening. Systemic antibiotic prescribing at the point of care was recorded. Repeat colonization sampling was performed within 3 months (median, 38 days; interquartile range, 22-50 days) in 357 participants. Incidence of recurrent infection was ascertained for up to 1 year.
Results:
Participants prescribed guideline-recommended empiric antibiotics for purulent SSTI were less likely to remain colonized at follow-up sampling (adjusted hazard ratio [aHR], 0.49; 95% confidence interval [CI], .30-.79) and less likely to have recurrent SSTI (aHR, 0.57; 95% CI, .34-.94) than those not receiving guideline-recommended empiric antibiotics for their SSTI. Additionally, participants remaining colonized at repeat sampling were more likely to report a recurrent infection over 12 months (aHR, 2.37; 95% CI, 1.69-3.31). Clindamycin was more effective than trimethoprim-sulfamethoxazole (TMP-SMX) in eradicating S. aureus colonization (44% vs 57% remained colonized, P = .03) and preventing recurrent SSTI (31% vs 47% experienced recurrence, P = .008).
Conclusions:
Systemic antibiotics, as part of acute SSTI management, impact S. aureus colonization, contributing to a decreased incidence of recurrent SSTI. The mechanism by which clindamycin differentially affects colonization and recurrent SSTI compared to TMP-SMX warrants further study.
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