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Updated: May 7, 2026

Subcutaneous Infection of Methicillin Resistant Staphylococcus Aureus MRSA
Published on: February 9, 2011
Reliability of Methicillin-Resistant Staphylococcus aureus (MRSA) Nasal Swab Screening for Predicting MRSA Burn
Max L Silverstein1,2, Yvonne Karanas1,2, Clifford C Sheckter1,2
1Regional Burn Center, Santa Clara Valley Medical Center, San Jose, CA 95128, United States.
Abstract:
Infection is the primary cause of death among burn-injured patients, with soft tissue infection trailing only pneumonia as the most common source of sepsis. Methicillin-resistant Staphylococcus aureus (MRSA) has become endemic in burn units, resulting in the frequent initiation of empiric vancomycin therapy. Methicillin-resistant S aureus nasal swab screening rapidly identifies patients who are MRSA-colonized, informing contact precaution and decontamination protocols. We hypothesized that MRSA nasal swab results could also be used to reliably predict results of wound cultures obtained from infected burns. We performed a retrospective review of all 250 patients who underwent weekly nasal swab screening and developed a burn infection in our unit over a 36-month period. By comparing nasal screening results with bacterial cultures, we determined test performance metrics for MRSA nasal swabs: sensitivity 64.1%, specificity 96.2%, positive predictive value 75.8%, and negative predictive value 93.5%. Nasal swabs were slightly more sensitive for predicting community-acquired MRSA infections compared with hospital-acquired infections. In total, 30 patients (76.9%) presented with community-acquired MRSA infections; of those, 20 (66.7%) had tested positive for MRSA colonization on nasal screen. A total of 9 patients (23.1%) developed hospital-acquired MRSA infections; 5 (55.6%) had tested positive for MRSA on a preceding nasal swab. The NPV calculated here indicates that patients who test negative for MRSA colonization by recent nasal swab are highly unlikely to have a burn infection caused by MRSA. Burn centers should employ universal MRSA nasal screening and de-escalate MRSA antibiotic coverage when treating burn infections in patients with a negative nasal swab result.
Insights
Methicillin-resistant Staphylococcus aureus (MRSA) nasal swabs can predict burn wound culture results. A negative nasal swab strongly suggests a burn infection is not caused by MRSA, allowing for de-escalation of antibiotic therapy.
Area of Science:
- Infectious Diseases
- Burn Care
- Microbiology
Background:
- Infections are a leading cause of mortality in burn patients, with soft tissue infections being a significant source of sepsis.
- Methicillin-resistant Staphylococcus aureus (MRSA) is prevalent in burn units, often necessitating empiric vancomycin treatment.
- Nasal swab screening for MRSA colonization aids in infection control and decontamination strategies.
Purpose of the Study:
- To evaluate the utility of MRSA nasal swab screening in predicting MRSA presence in burn wound cultures.
- To determine the diagnostic accuracy of MRSA nasal swabs for infected burns.
Main Methods:
- Retrospective review of 250 burn patients undergoing weekly MRSA nasal swab screening and developing infections over 36 months.
- Comparison of nasal swab results with bacterial cultures from infected burn wounds.
- Calculation of test performance metrics: sensitivity, specificity, positive predictive value (PPV), and negative predictive value (NPV).
Main Results:
- MRSA nasal swabs demonstrated a sensitivity of 64.1%, specificity of 96.2%, PPV of 75.8%, and NPV of 93.5%.
- Nasal swabs were more sensitive in predicting community-acquired MRSA infections (66.7% positive) than hospital-acquired infections (55.6% positive).
- A negative nasal swab result indicates a low likelihood of MRSA-caused burn infections.
Conclusions:
- MRSA nasal swab screening is a valuable tool for predicting MRSA in burn wound infections.
- The high NPV supports de-escalating MRSA antibiotic coverage in patients with negative nasal swab results.
- Universal MRSA nasal screening should be implemented in burn centers to guide antimicrobial therapy decisions.
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