Antibiotics Effective Against Pseudomonas aeruginosa
The most effective antibiotics for treating Pseudomonas aeruginosa infections include antipseudomonal β-lactams (piperacillin-tazobactam, ceftazidime, cefepime, meropenem), aminoglycosides (tobramycin, amikacin), and fluoroquinolones (ciprofloxacin), with combination therapy recommended for severe infections to reduce resistance development. 1, 2
First-Line Antipseudomonal Antibiotics
Intravenous Options
- Piperacillin-tazobactam: 3.375g every 6 hours (standard infections) or 4.5g every 6 hours (nosocomial pneumonia) 3
- Ceftazidime: 150-250 mg/kg/day divided in 3-4 doses (maximum 12g daily) 2
- Cefepime: 100-150 mg/kg/day divided in 2-3 doses (maximum 6g daily) 2
- Meropenem: 60-120 mg/kg/day divided in 3 doses (maximum 6g daily) 2
- Imipenem: 50-100 mg/kg/day divided in 3-4 doses (maximum 4g daily) 2, 4
Oral Options
- Ciprofloxacin: 750mg twice daily (high-dose regimen for Pseudomonas infections) 1
Inhaled Options (for respiratory infections)
Combination Therapy Recommendations
For Severe Infections
For Nosocomial Pneumonia with Pseudomonas Risk
- Antipseudomonal cephalosporin or acylureidopenicillin/β-lactamase inhibitor or carbapenem PLUS ciprofloxacin OR macrolide plus aminoglycoside 2
Special Considerations
Resistance Patterns
- Regular monitoring of susceptibility patterns is essential, particularly with long-term therapy 1
- Carbapenems (meropenem preferred) should be reserved for resistant strains to prevent further resistance development 7
- Colistin can be used for multidrug-resistant strains when other options fail 1, 2
Dosing Considerations
- Higher doses are often needed for Pseudomonas infections compared to other gram-negative infections 2
- Extended or continuous infusions of β-lactams may improve efficacy against Pseudomonas 8
- Aminoglycosides require therapeutic drug monitoring to optimize efficacy and minimize toxicity 2
Treatment Duration
- Standard duration: 7-14 days depending on infection site and severity 1, 2
- Longer courses may be needed for immunocompromised hosts 1
Common Pitfalls and Caveats
- Underestimating resistance potential with monotherapy in severe infections 1
- Not considering local resistance patterns when selecting empiric therapy 1
- Inadequate dosing leading to treatment failure and resistance development 1
- Carbapenems show higher rates of subsequent resistance emergence compared to ceftazidime or piperacillin-tazobactam 7
- Combination of β-lactam plus aminoglycoside shows faster killing and less regrowth compared to β-lactam plus fluoroquinolone combinations 6
Treatment Algorithm for Pseudomonas Infections
Mild-moderate infections:
Severe infections or immunocompromised hosts:
Multidrug-resistant strains:
Respiratory infections in cystic fibrosis:
- Consider inhaled antibiotics (tobramycin or colistin) in addition to systemic therapy 2