Treatment of Burkholderia cepacia Bacteremia
For patients with Burkholderia cepacia bacteremia, initiate combination antimicrobial therapy with trimethoprim-sulfamethoxazole (TMP-SMX) as first-line when susceptible, or ceftazidime, meropenem, or ceftazidime-avibactam based on susceptibility testing, and remove any indwelling catheters immediately to reduce treatment failure and improve survival. 1, 2
Antimicrobial Selection Strategy
First-line therapy:
- TMP-SMX remains the preferred agent when the organism demonstrates susceptibility 1
- For severe infections or when TMP-SMX cannot be used (allergy, resistance, intolerance), select alternatives based on susceptibility testing 1, 3
Alternative agents with proven efficacy:
- Ceftazidime is the most effective antimicrobial in vitro and clinically, with cure rates of 73.7% in case reports and favorable outcomes in 68.4-100% of cohort studies 2, 3, 4
- Meropenem shows clinical efficacy despite intrinsic resistance patterns, with 66.7-71.4% favorable outcomes 1, 3, 4
- Piperacillin (or other penicillins) demonstrates 75% improvement rates when used appropriately 3
- Minocycline inhibits 38% of strains and represents another viable option 4, 5
Combination therapy is typically required for severe infections rather than monotherapy, though synergy studies show limited additive benefit (only 1-15% of strains demonstrate synergy with various combinations) 4
Source Control
Catheter removal is critical for catheter-related bloodstream infections - this intervention reduces treatment failure rates and improves survival outcomes 1
Susceptibility Testing Requirements
- Broth microdilution, agar dilution, or Etest should be used rather than disc diffusion, which is poorly reproducible for B. cepacia complex 5
- Susceptibility testing is essential because resistance patterns vary significantly, with the organism showing intrinsic resistance to carboxypenicillins, polymyxins, and often aminoglycosides 5
- Most isolates demonstrate susceptibility to ceftazidime, carbapenems, and TMP-SMX in descending order of frequency 6
Special Populations
Cystic fibrosis patients:
- Avoid chronic macrolide therapy (azithromycin) in patients with documented B. cepacia, as this is an exclusion criterion in major CF antibiotic trials 7
- Inhaled tobramycin should not be used for maintenance therapy in B. cepacia colonized patients 1
- Use separate nebulizer equipment for B. cepacia versus Pseudomonas aeruginosa to prevent cross-contamination 1
Immunocompromised patients:
- These patients have higher mortality risk, particularly with respiratory failure, unknown infection source, ICU admission, or shock 2
- The overall mortality rate is 28.6%, with 44.4% of deaths directly attributable to B. cepacia bacteremia 2
Infection Control Measures
Implement strict contact precautions:
- Gown and gloves for all patient encounters 7, 1
- Cohort B. cepacia-infected patients in designated areas 7, 1
- Communicate B. cepacia status when transferring patients to other healthcare facilities 7, 1
- Perform environmental screening and intensive cleaning of surfaces in contact with colonized patients 1
Treatment Duration and Monitoring
- Mean time to positive blood culture is 45 days after admission, indicating these are typically healthcare-associated infections 2
- Baseline and interval testing for drug toxicity is essential when using aminoglycosides, carbapenems, or other potentially toxic agents 1
- Most patients respond to appropriate antibiotic therapy, though 5 patients in one series died despite receiving appropriate treatment 2
Clinical Pitfalls
Common errors to avoid:
- Do not rely on disc diffusion for susceptibility testing - it lacks reproducibility 5
- Do not assume carbapenem resistance based on intrinsic mechanisms alone - meropenem shows paradoxical clinical efficacy 1
- Do not delay catheter removal in catheter-related infections 1
- Do not use inhaled aminoglycosides for B. cepacia in CF patients 1
Hospital-acquired infections predominate (59.1% of cases), with bacteremia being the most common presentation (38.6%), followed by skin/soft tissue infections (36.4%) 6