Treatment of Stenotrophomonas maltophilia Infections
High-dose trimethoprim-sulfamethoxazole (TMP-SMX) at 15-20 mg/kg/day of the trimethoprim component is the first-line treatment for Stenotrophomonas maltophilia infections. 1
First-Line Treatment
- TMP-SMX (first choice):
- Dosing: 15-20 mg/kg/day of trimethoprim component
- Duration: 7-14 days, based on clinical response
- Administration: Can be given orally or intravenously depending on infection severity
- Evidence: Recommended by the American College of Clinical Pharmacy and supported by clinical outcomes 1
Alternative Options for TMP-SMX Intolerant or Resistant Cases
Minocycline:
Tigecycline:
Fluoroquinolones:
Combination Therapy for Severe Infections
The Infectious Diseases Society of America recommends considering combination therapy for severe S. maltophilia infections 1, 5. Potentially effective combinations include:
- TMP-SMX plus moxifloxacin (shows synergism against strains with low moxifloxacin MICs) 2
- Moxifloxacin plus minocycline 2
- Moxifloxacin plus tigecycline 2
Newer Treatment Options
For multidrug-resistant strains, newer options with promising clinical data include:
Antimicrobials with Poor Activity Against S. maltophilia
The following should be avoided as monotherapy:
- Ceftazidime (only 20% susceptibility) 2
- Polymyxin E/Colistin (22.5% susceptibility) 2
- Chloramphenicol (37.5% susceptibility) 2
Treatment Monitoring and Adjustment
- Evaluate clinical response daily
- If no improvement after 7 days, consider:
- Repeating microbiological studies
- Changing antimicrobial regimen
- Adding a second agent for synergistic effect 1
Important Considerations
- In vitro susceptibility may not always predict clinical efficacy for S. maltophilia infections 1
- Base antibiotic selection on local susceptibility patterns and specific isolate testing when available
- For immunocompromised patients, aggressive determination of infection etiology through aspiration/biopsy is recommended to guide therapy 1
The treatment of S. maltophilia infections remains challenging due to intrinsic multidrug resistance. While TMP-SMX remains the gold standard, minocycline and tigecycline offer effective alternatives with good clinical outcomes, particularly for TMP-SMX resistant strains.