Treatment of Staphylococcus hominis Infections
For methicillin-susceptible S. hominis infections, nafcillin or other penicillinase-resistant penicillins are the antibiotics of choice, while methicillin-resistant strains require vancomycin as first-line therapy. 1, 2
Initial Assessment and Empiric Therapy
Determine Methicillin Susceptibility Status
- Culture and susceptibility testing must be performed immediately to guide definitive therapy, as over 74% of S. hominis strains are methicillin-resistant (harboring mecA gene) 3
- Empiric therapy should include vancomycin 30-60 mg/kg/day IV divided every 6-12 hours until susceptibility results are available 4
- If local epidemiology suggests high rates of methicillin resistance, start with vancomycin rather than beta-lactams 5
Definitive Treatment Based on Susceptibility
For Methicillin-Susceptible S. hominis (MSSA)
- Nafcillin 2g IV every 4 hours is the treatment of choice for serious infections 1, 2
- Alternative penicillinase-resistant penicillins (oxacillin, flucloxacillin) are equally effective 6, 7
- First-generation cephalosporins (cefazolin) can be used for less severe infections 6
- For penicillin-allergic patients: Use vancomycin or clindamycin (only if local resistance <10%) 8, 6
For Methicillin-Resistant S. hominis (MRSA)
- Vancomycin 30-60 mg/kg/day IV divided every 6-12 hours remains first-line therapy 4, 6
- Target vancomycin trough levels of 15-20 mcg/mL for serious infections 8, 4
- Alternative agents for vancomycin-intolerant patients:
- Critical caveat: Over 80% of S. hominis strains demonstrate multidrug resistance, with some resistant to 7+ antibiotics 3
Treatment Duration by Infection Type
Uncomplicated Skin and Soft Tissue Infections
- 5-10 days of therapy for localized infections 8
- Minor superficial infections may respond to topical mupirocin 2% three times daily 9
Complicated or Hospitalized Infections
- 7-14 days depending on clinical response 8
- For cellulitis with prosthetic material (surgical clips, hardware): Consider adding NSAIDs to hasten resolution after appropriate antibiotic coverage 10
Bacteremia
- Minimum 2 weeks for uncomplicated bacteremia 8
- 4-6 weeks for complicated bacteremia or when source control is incomplete 8
Endocarditis
- Initial therapy: 10 weeks of nafcillin (if susceptible) or vancomycin 2
- Surgical intervention (valve replacement) may be required for definitive cure, especially with recurrent bacteremia 2
- Monitor for embolic complications (splenic/renal infarcts, discitis) 2
Implant-Related Infections
- With implant retention: 12 weeks total antibiotic therapy 5
- After implant removal: 6 weeks is sufficient 5
- Limit IV therapy to 1-2 weeks, then transition to oral agents once clinically stable 5
Special Considerations for Biofilm Infections
When Prosthetic Material is Present
- Rifampicin 600 mg daily (or 300-450 mg twice daily) should be added after thorough debridement and when wounds are dry 5, 4
- Rifampicin must always be combined with a companion antibiotic to prevent resistance 5
- Fluoroquinolones are preferred companions for staphylococcal biofilm infections, but only after debridement 5
- Alternative companions include cotrimoxazole, minocycline, or fusidic acid (less studied) 5
Source Control is Mandatory
- Surgical drainage of abscesses and purulent collections is essential 8
- Debride necrotic tissue in complicated infections 8
- Remove or replace infected prosthetic material when feasible 2, 10
Monitoring and Follow-Up
Early Assessment
- Monitor clinical response within 48-72 hours of initiating therapy 8, 9
- Adjust antibiotics based on culture and susceptibility results as soon as available 5, 8
- For vancomycin, check trough levels targeting 15-20 mcg/mL 8, 4
Long-Term Follow-Up
- Minimum 12 months follow-up after cessation of therapy for implant-related infections 5
- Monitor inflammatory markers (ESR, CRP) to guide treatment duration 4
Critical Pitfalls to Avoid
- Never use nafcillin or other beta-lactams for methicillin-resistant strains - discontinue immediately if resistance is confirmed 1
- Do not use rifampicin or fluoroquinolones as monotherapy - rapid resistance emergence occurs 5
- Avoid starting rifampicin before adequate debridement - risk of superinfection with resistant organisms 5
- Do not assume blood culture contamination - S. hominis can cause true bacteremia and endocarditis, especially with prosthetic material present 2, 10
- All S. hominis strains remain vancomycin-susceptible, though some show reduced sensitivity (heterogeneous resistance) 3