Stenotrophomonas maltophilia: An Opportunistic Multidrug-Resistant Pathogen
Stenotrophomonas maltophilia is a gram-negative, non-fermenting bacillus that has emerged as an important opportunistic nosocomial pathogen, particularly in immunocompromised patients, characterized by intrinsic multidrug resistance and causing infections with significant morbidity and mortality. 1
Microbiology and Epidemiology
- Originally classified as Pseudomonas maltophilia, later Xanthomonas maltophilia, before receiving its current classification
- Ubiquitous organism found in water sources, soil, and plants
- Increasingly recognized in healthcare settings, particularly on medical devices and equipment 2
- Intrinsically resistant to many antibiotics due to:
- Low outer membrane permeability
- Multidrug-resistance efflux systems
- Two chromosomally encoded β-lactamases
- Intrinsic resistance to carbapenems due to metallo-β-lactamase 1
Clinical Presentations
S. maltophilia can cause various infections, most commonly:
- Respiratory tract infections: Particularly pneumonia in ventilated patients
- Bloodstream infections: Often associated with indwelling catheters
- Skin and soft tissue infections (SSTIs):
- Can present as cellulitis, abscesses, or ecthyma gangrenosum
- Ecthyma gangrenosum appears as painless erythematous papules that rapidly become painful and necrotic within 24 hours 3
- Urinary tract infections: Often associated with urinary catheters
Risk Factors
- Immunocompromised status: Particularly neutropenia 3
- Prolonged hospitalization
- Prior broad-spectrum antibiotic therapy
- Mechanical ventilation
- Indwelling medical devices: Catheters, endoscopes, ventilators 2
- Hematologic malignancies
Diagnosis
- Culture and identification from clinical specimens
- Molecular methods for rapid identification
- Antimicrobial susceptibility testing is essential but challenging due to:
- Molecular heterogeneity among strains
- Uneven distribution of resistance determinants
- Lack of standardized breakpoints for many antibiotics 4
Treatment
First-Line Therapy:
- High-dose trimethoprim-sulfamethoxazole (TMP-SMX): 15-20 mg/kg/day of the trimethoprim component for 7-14 days 1
Alternative Options (when TMP-SMX cannot be used):
- Minocycline: Comparable efficacy to TMP-SMX, particularly useful in patients with acute kidney injury 1
- Fluoroquinolones: Based on susceptibility testing
- Tigecycline: Shows favorable in vitro activity against S. maltophilia 1
For Severe Infections:
- Consider combination therapy for severe infections 1
- Duration of treatment for most bacterial SSTIs should be 7-14 days 3
Infection Control Measures
Based on ESCMID guidelines for managing multidrug-resistant gram-negative bacteria 3:
Hand hygiene: Strong recommendation with moderate evidence
- Implement hand hygiene education programs
- Use alcohol-based hand rub before and after patient contact
- Soap and water when hands are visibly soiled
Contact precautions: Conditional recommendation with moderate evidence
- Gloves and gowns for all colonized patient encounters
- Prompt removal after care followed by hand hygiene
- Regular audit of adherence
Environmental cleaning: Conditional recommendation with moderate evidence
- Monitor cleaning performance
- Review disinfectant agents and methods
- Consider environmental sampling from surfaces in contact with colonized patients
Education: Conditional recommendation with moderate evidence
- Ensure healthcare workers understand the epidemiological importance of S. maltophilia
- Regular multidisciplinary meetings to implement interventions
Special Considerations
- In neutropenic patients, S. maltophilia can cause ecthyma gangrenosum, a cutaneous vasculitis that may be rapidly progressive 3
- Surgical intervention is recommended for drainage of soft tissue abscesses after marrow recovery 3
- Colony-stimulating factor therapy or granulocyte transfusions are not routinely recommended for neutropenic patients with S. maltophilia infections 3
Prognosis
- Infections can be associated with significant mortality, particularly in immunocompromised hosts
- Early appropriate antimicrobial therapy is crucial for improved outcomes
- Regular monitoring of clinical response is essential, with consideration of alternative therapy if no improvement after 7 days 1