Management of Polymicrobial Wound Infection with MRSA and Pseudomonas aeruginosa
Switch from doxycycline to an antipseudomonal agent that also covers MRSA, or add an antipseudomonal agent to the current regimen, prioritizing treatment of the heavy Pseudomonas aeruginosa growth while maintaining MRSA coverage. 1
Immediate Antibiotic Adjustment Required
Doxycycline is inadequate for this infection. While doxycycline has activity against MRSA, it lacks reliable coverage for Pseudomonas aeruginosa, which is present in heavy growth and represents the dominant pathogen requiring targeted therapy. 1
Treatment Strategy Based on Infection Severity
For mild to moderate infections:
- Use a fluoroquinolone (ciprofloxacin or levofloxacin) as monotherapy if susceptibilities confirm activity against both organisms 1
- Ciprofloxacin provides antipseudomonal coverage while maintaining activity against many MRSA strains, though local resistance patterns must be considered 1
- If MRSA resistance to fluoroquinolones is documented, add trimethoprim-sulfamethoxazole or switch to combination therapy 2
For moderate to severe infections:
- Initiate parenteral therapy with piperacillin-tazobactam PLUS vancomycin or linezolid 1
- Alternative: cefepime or ceftazidime PLUS vancomycin 1
- Carbapenems (meropenem or imipenem) provide broad coverage but should be reserved for more severe cases 1
Critical Decision Point: Pseudomonas as Pathogen vs. Colonizer
The heavy growth of Pseudomonas aeruginosa strongly suggests pathogenic infection rather than colonization, particularly given the light MRSA growth. 1 However, the IDSA guidelines emphasize that Pseudomonas is frequently a colonizer in wounds. Consider these factors: 1
- Treat Pseudomonas if: Patient has failed prior non-pseudomonal therapy (as in this case with doxycycline), wound has been exposed to water/soaking, severe infection present, or warm climate setting 1
- Clinical response matters: If the patient had improved on doxycycline despite heavy Pseudomonas growth, continuation might be considered, but this scenario is unlikely given the need for contact 1
Addressing the MRSA Component
Light growth of MRSA requires coverage but may not be the primary driver of infection. 1 The IDSA guidelines note that patients sometimes improve despite therapy ineffective against isolated organisms when those organisms are colonizers rather than pathogens. 1
However, given the patient's prior treatment failure on doxycycline, both organisms should be covered definitively: 1
- Trimethoprim-sulfamethoxazole provides excellent MRSA coverage but NO Pseudomonas activity 2
- Vancomycin, linezolid, or daptomycin for parenteral MRSA coverage in severe infections 1, 2
- Fluoroquinolones may cover both if susceptibilities permit 1
Specific Antibiotic Recommendations
Oral regimen (mild infection, outpatient):
- Ciprofloxacin 500-750 mg twice daily (if susceptibilities confirm activity against both organisms) 1
- Consider adding trimethoprim-sulfamethoxazole 1-2 double-strength tablets twice daily if MRSA shows fluoroquinolone resistance 2
Parenteral regimen (moderate to severe infection):
- Piperacillin-tazobactam 4.5 g IV every 6 hours PLUS vancomycin 15-20 mg/kg IV every 8-12 hours 1
- Alternative: Cefepime 2 g IV every 8 hours PLUS vancomycin 1
- For severe infections or high-risk patients, consider combination antipseudomonal therapy (beta-lactam plus fluoroquinolone or aminoglycoside) 3, 4
Duration of Therapy
Treat for 1-2 weeks for mild infections and 2-3 weeks for moderate to severe infections, based on clinical response rather than complete wound healing. 1 Reassess at 48-72 hours to confirm clinical improvement. 1, 2
Essential Adjunctive Measures
Antibiotic therapy alone is insufficient—wound debridement and appropriate wound care are mandatory. 1
- Debride necrotic tissue and biofilm to enhance antibiotic penetration 1
- Maintain clean, dry dressings 2
- Consider topical antimicrobials (acetic acid for Pseudomonas) as adjunct after debridement 5
- Negative pressure wound therapy may reduce bacterial burden 1
Common Pitfalls to Avoid
Do not continue doxycycline monotherapy—it lacks adequate Pseudomonas coverage and the heavy growth indicates this organism requires targeted treatment. 1
Do not assume all isolated organisms require treatment—however, in this case with treatment failure and heavy Pseudomonas growth, both organisms warrant coverage. 1
Do not use empiric antipseudomonal therapy without considering susceptibilities—review the reported susceptibilities to guide definitive therapy. 1
Do not treat with antibiotics alone—inadequate debridement is a primary cause of treatment failure in wound infections. 1