Antibiotics with Pseudomonas Coverage
The most effective antibiotics for pseudomonas coverage include antipseudomonal β-lactams (piperacillin-tazobactam, cefepime, ceftazidime, meropenem, imipenem), fluoroquinolones (ciprofloxacin, levofloxacin), aminoglycosides (amikacin, gentamicin, tobramycin), monobactams (aztreonam), and polymyxins (colistin). 1
Antipseudomonal Antibiotics by Class
β-lactams
Penicillins
Cephalosporins
Carbapenems
Fluoroquinolones
Aminoglycosides
Monobactams
- Aztreonam (1-2g IV q6-8h) 2
Polymyxins
Combination Therapy Recommendations
For severe Pseudomonas infections, combination therapy is often recommended:
First-line combination: Antipseudomonal β-lactam (cefepime, ceftazidime, or piperacillin-tazobactam) plus an aminoglycoside (amikacin preferred) 1
Alternative combinations:
Important Clinical Considerations
Resistance patterns: Local antibiograms should guide therapy as resistance patterns vary by institution 1
Site of infection: Dosing and duration may vary based on infection site:
De-escalation: Initial combination therapy for 3-5 days, then de-escalate to the most appropriate single agent once susceptibility results are available 1
Special populations:
Route of administration: Consider nebulized antibiotics (especially colistin, tobramycin) for respiratory infections in cystic fibrosis 2, 6
Caveats and Pitfalls
Aminoglycoside monotherapy should be avoided for Pseudomonas infections due to risk of resistance development 1, 5
For isolates with reduced susceptibility to piperacillin-tazobactam (MIC 32-64 mg/L), alternative agents should be considered 1
Monitoring renal function is essential when using aminoglycosides due to nephrotoxicity risk 1
Therapeutic drug monitoring for aminoglycosides is recommended to maintain optimal drug levels and minimize toxicity 1
Failure to adequately drain or debride infected sites (when applicable) is a common cause of treatment failure, regardless of antibiotic choice 1
By selecting appropriate anti-pseudomonal antibiotics and using combination therapy when indicated, clinicians can optimize treatment outcomes while minimizing the development of resistance.