What is the coverage and dosage of cefepime for various infections?

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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

  1. 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
  2. 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.

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Antibiotic Therapy for Gram-Negative Sepsis

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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