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Updated: May 14, 2026

Subcutaneous Infection of Methicillin Resistant Staphylococcus Aureus (MRSA)
Published on: February 9, 2011
Nasal carriage of Staphylococcus aureus in patients undergoing Mohs micrographic surgery is an important risk factor
Yee J Tai1, Kate L A Borchard, Todd H Gunson
1Oxford Day Surgery and Dermatology, Perth, Western Australia, Australia. yeejentai@yahoo.com
Background:
Surgical site infection (SSI) can be a problematic complication of Mohs micrographic surgery (MMS). Previous reports have cited nasal Staphylococcus aureus (S. aureus) carriage as a risk factor for SSI, but none thus far in dermatologic surgery.
Objective:
The aim was to determine the difference in infection rates between nasal carriers of S. aureus and non-carriers, and whether decolonisation with intranasal mupirocin ointment and chlorhexidine wash would reduce the infection rate in nasal carriers.
Methods:
In all, 738 patients presenting for MMS at the Oxford Day Surgery and Dermatology underwent a nasal swab to determine their S. aureus carriage status. S. aureus carriers were randomised for decolonisation with intranasal mupirocin ointment and chlorhexidine body wash. Non-carriers were untreated. All patients were followed up for SSI.
Results:
The rate of SSI was 11 per cent in untreated S. aureus carriers, 4 per cent in treated carriers, and 3 per cent in non-carriers. The difference in infection rate between carriers and non-carriers was significant (P < 0.001). The difference between treated and untreated carriers was also significant (P = 0.05).
Conclusion:
Nasal S. aureus carriage is an important risk factor for SSI in MMS, conferring an over threefold increase in SSI risk. A pre-operative nasal swab provides a simple and effective risk stratification tool. The use of a topical decolonisation regimen reduces the infection rate in carriers to a level approaching non-carriers without exposure to systemic antibiotics.
Insights
Nasal Staphylococcus aureus (S. aureus) carriage significantly increases surgical site infection (SSI) risk in Mohs surgery. Topical decolonization effectively reduces SSI rates in S. aureus carriers.
Area of Science:
- Dermatologic surgery
- Infectious disease epidemiology
- Surgical outcomes research
Background:
- Surgical site infection (SSI) is a significant complication following Mohs micrographic surgery (MMS).
- Nasal Staphylococcus aureus (S. aureus) carriage is a known risk factor for SSI, but its specific impact in dermatologic surgery requires further investigation.
- Understanding S. aureus carriage prevalence and its association with SSI is crucial for improving patient safety in MMS.
Purpose of the Study:
- To determine the difference in SSI rates between nasal S. aureus carriers and non-carriers undergoing MMS.
- To evaluate the efficacy of a decolonization regimen (intranasal mupirocin and chlorhexidine wash) in reducing SSI rates among S. aureus carriers.
- To assess the utility of pre-operative nasal swabs for risk stratification of SSI in MMS patients.
Main Methods:
- A prospective study involving 738 patients undergoing MMS at Oxford Day Surgery and Dermatology.
- Patients provided nasal swabs for S. aureus carriage status determination.
- S. aureus carriers were randomized to receive either a topical decolonization regimen or no treatment, while non-carriers remained untreated. All patients were monitored for SSI development.
Main Results:
- The SSI rate was 11% in untreated S. aureus carriers, 4% in treated carriers, and 3% in non-carriers.
- A significant difference in SSI rates was observed between S. aureus carriers and non-carriers (P < 0.001).
- The decolonization regimen significantly reduced SSI rates in carriers compared to untreated carriers (P = 0.05).
Conclusions:
- Nasal S. aureus carriage is a significant risk factor for SSI in Mohs micrographic surgery, increasing risk over threefold.
- Pre-operative nasal swabbing is a simple and effective tool for stratifying SSI risk in MMS patients.
- Topical decolonization effectively lowers SSI rates in carriers, approaching those of non-carriers without systemic antibiotic use.
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