Cefepime Coverage and Dosage for Various Infections
Cefepime is a fourth-generation cephalosporin with broad-spectrum coverage that can be used at a dosage of 1-2g IV every 8-12 hours for most infections, with higher doses (2g every 8 hours) recommended for Pseudomonas aeruginosa infections.
Antimicrobial Spectrum
Cefepime has activity against:
Gram-positive organisms:
- Streptococcus pneumoniae (including penicillin-sensitive, -intermediate and -resistant strains)
- Staphylococcus aureus (methicillin-susceptible only)
Gram-negative organisms:
- Pseudomonas aeruginosa
- Enterobacteriaceae (including some ESBL-producing strains)
- Haemophilus influenzae
- HACEK group organisms
Key advantages:
- Stable against many common plasmid- and chromosome-mediated beta-lactamases
- Poor inducer of AmpC beta-lactamases
- Retains activity against some Enterobacteriaceae resistant to third-generation cephalosporins
Dosage Recommendations by Infection Type
Respiratory Tract Infections
- Moderate to severe pneumonia: 1-2g IV every 8-12 hours for 10 days 1
- For Pseudomonas aeruginosa pneumonia: 2g IV every 8 hours 1
- For carbapenem-resistant Pseudomonas aeruginosa: 2g IV every 8-12 hours 2
Urinary Tract Infections
- Mild to moderate uncomplicated/complicated UTI: 0.5-1g IV every 12 hours for 7-10 days 1
- Severe uncomplicated/complicated UTI: 2g IV every 12 hours for 10 days 1
Skin and Skin Structure Infections
- Moderate to severe uncomplicated infections: 2g IV every 12 hours for 10 days 1
Intra-abdominal Infections
- Complicated intra-abdominal infections: 2g IV every 8-12 hours for 7-10 days (in combination with metronidazole) 1
Febrile Neutropenia
- Empiric therapy: 2g IV every 8 hours until resolution of neutropenia 1
Endocarditis (HACEK organisms)
- Native and prosthetic valve endocarditis: Ceftriaxone is preferred, but cefepime can be substituted 2
Pediatric Dosing
- Children up to 40kg: 50 mg/kg/dose every 12 hours (every 8 hours for febrile neutropenia) 1
Special Considerations
Renal Dosage Adjustment
- Dosage adjustment required for patients with creatinine clearance ≤60 mL/min 1
Limitations and Warnings
ESBL-producing organisms:
- Inconsistent results against ESBL-producing Enterobacteriaceae
- Higher mortality observed with cefepime when MICs are in the susceptible dose-dependent range (≥8 μg/mL) 3
- Carbapenems preferred for confirmed ESBL infections
Multidrug-resistant organisms:
- For carbapenem-resistant organisms, combination therapy may be needed
- Not recommended as monotherapy for difficult-to-treat Pseudomonas aeruginosa (DTR-PA) 2
Administration
- Administer intravenously over approximately 30 minutes 1
- Duration of therapy depends on infection site and severity (typically 7-14 days)
Clinical Pearls
- Cefepime is particularly valuable for empiric therapy when Pseudomonas coverage is needed but carbapenem-sparing approaches are preferred
- For severe infections with suspected resistant pathogens, consider combination therapy initially until susceptibilities are known
- Local resistance patterns should guide empiric therapy decisions
- De-escalate to more targeted therapy once culture results are available
Cefepime remains a reliable option for many serious infections, but its use should be guided by local susceptibility patterns and patient-specific factors to optimize outcomes and minimize resistance development.