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Mupirocin-based nasal decolonization to prevent Staphylococcus aureus surgical site infections: A meta-analysis of
Xin Zhou1, Ezra Valido2, Jörg Krebs3
1SCI Population Biobanking and Translational Research, Swiss Paraplegic Research, Nottwil, Switzerland; Graduate School for Cellular and Biomedical Sciences, University of Bern, Switzerland.
Objectives:
To determine whether mupirocin-based decolonization, compared with placebo, no treatment, or alternative agents, reduces Staphylococcus aureus-related surgical site infection (SA-SSI), nasal S. aureus colonization, and overall SSIs incidence in elective surgery.
Methods:
We searched EMBASE, Medline (Ovid), PubMed, CENTRAL, and Google Scholar to May 15, 2024, for randomized controlled trials (RCTs). Risk ratios (RRs) were pooled using a random-effects model with the restricted maximum likelihood estimator with the Hartung-Knapp adjustment. Prespecified subgroup analyses evaluated application strategy, surgical type, and chlorhexidine gluconate (CHG) co-administration.
Results:
Seventeen RCTs (15,533 participants) were included. In trials with no-treatment or placebo controls, mupirocin-based decolonization reduced SA-SSI (RR 0.67, 95% confidence interval (CI) 0.49-0.91) and nasal colonization (RR 0.22, 95% CI 0.18-0.26). Effects were larger with targeted use in confirmed carriers and when combined with CHG. No reduction was observed for overall SSIs, except in orthopedic surgery (RR 0.80, 95% CI 0.65-0.99). Head-to-head data vs active alternatives were sparse and did not show a consistent advantage for mupirocin.
Conclusion:
Targeted preoperative mupirocin, especially when combined with CHG, reduces SA-SSI in elective surgery. The lack of significant impact on overall SSIs is interpreted as a reflection of polymicrobial etiologies in surgical infections. Given the emerging risk of mupirocin resistance, further adequately powered head-to-head trials with standardized outcomes and integrated resistance surveillance are warranted.
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