Overview
- Staphylococcus aureus has innovative mechanisms to evade host defenses.
- Produces molecules that inhibit neutrophils and phagocytosis.
Methicillin Resistance
- History: Resistance was present by the 1950s.
- Methicillin is an old beta-lactam antibiotic.
- The term now applies to strains of Staphylococcus aureus resistant to all beta-lactams.
Acquisition of Resistance
- Intrinsic Resistance:
- Innate resistance of the cell wall to certain antibiotics.
- Acquired Resistance:
- Acquisition of the mecA gene:
- Encodes for penicillin-binding protein (PBP).
- Binds to beta-lactam antibiotics, reducing their effect on the cell wall.
- Formation of glycocalyx and biofilm when adherent to metalware:
- Increases resistance by over 100 times.
MRSA Carriage
- Nasal Carriage:
- Strains match those cultured from surgical site infections (SSI) in 85%.
- May spread to the bloodstream during intubation.
- Represents skin colonization.
- High-Risk Colonization Areas:
- Risks of Nasal Colonization with Staphylococcus aureus:
- Greatest independent risk factor for SSI.
- 9 times higher risk than uncolonized individuals.
- Fourfold increase in infection risk.
Screening
- Literature supports institution-wide screening, leading to a significant reduction in post-operative SSIs.
- Screening reduces transmission to elective patients undergoing arthroplasty.
- Routine Pre-Operative Screening:
- Swabs from nasal, groin, and axilla regions for Staphylococcus aureus.
- 20% of patients are Staphylococcus carriers.
- 5% are MRSA carriers.
Treatment
- Standard Treatment:
- Mupirocin nasal ointment and chlorhexidine washes for 5 days.
- Re-swab and repeat if still positive.
- Require 3 clear swabs at different times post-treatment prior to surgery.
- Success Rate:
- 90% eradication of nasal carriage.
Antibiotic Prophylaxis in Arthroplasty
- For MRSA-Treated Patients:
- Use of vancomycin is recommended.
- Routine Vancomycin Use:
- Not advised due to the risk of VRSA strain development.
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