What is the recommended dosing for cefepime in adults with normal and impaired renal function?

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Cefepime Dosing in Adults with Normal and Impaired Renal Function

The recommended dosing for cefepime in adults with normal renal function is 1-2g IV every 8-12 hours, with dose adjustments required for patients with renal impairment based on creatinine clearance. 1

Normal Renal Function (CrCl >60 mL/min)

Cefepime dosing varies based on the type and severity of infection:

  • Moderate to severe pneumonia: 1-2g IV every 8-12 hours for 10 days 1
  • Febrile neutropenia: 2g IV every 8 hours for 7 days or until resolution of neutropenia 1
  • Mild to moderate UTIs: 0.5-1g IV every 12 hours for 7-10 days 1
  • Severe UTIs: 2g IV every 12 hours for 10 days 1
  • Skin and skin structure infections: 2g IV every 12 hours for 10 days 1
  • Complicated intra-abdominal infections (with metronidazole): 2g IV every 8-12 hours for 7-10 days 1
  • Infective endocarditis: 2g IV every 8-12 hours 2

Renal Impairment Dosing Adjustments

Dosage adjustments are essential in patients with renal impairment to prevent drug accumulation and potential neurotoxicity 3, 4:

Creatinine Clearance (mL/min) 500mg dose 1g dose 2g dose 2g (q8h) dose
>60 q12h q12h q12h q8h
30-60 q24h q24h q24h q12h
11-29 q24h q24h q24h q24h
<11 q24h q24h q24h q24h

1

Special Populations

Hemodialysis patients:

  • Initial dose: 1g on day 1
  • Maintenance: 500mg every 24 hours (for most infections)
  • For febrile neutropenia: 1g every 24 hours
  • Administer after completion of hemodialysis on dialysis days 1

CAPD patients:

  • 500mg every 48 hours for standard doses
  • 1g every 48 hours for 1g doses
  • 2g every 48 hours for 2g doses 1

Monitoring Recommendations

  • Renal function: Monitor creatinine clearance regularly, especially in critically ill patients 3
  • Neurological symptoms: Watch for confusion, altered mental status, and muscle jerks, which may indicate cefepime-associated neurotoxicity, particularly in patients with severe renal impairment 3, 4
  • Therapeutic efficacy: Ensure appropriate dosing based on the suspected or confirmed pathogen's MIC 3

Important Clinical Considerations

  • Cefepime demonstrates linear pharmacokinetics with an elimination half-life of approximately 2-2.5 hours in patients with normal renal function 5
  • Approximately 80% of cefepime is excreted unchanged in the urine in patients with normal renal function 5
  • Cefepime is removed by hemodialysis (40-68% over 3 hours) and peritoneal dialysis (26% over 72 hours) 5
  • Plasma levels can vary significantly between individuals, with up to 40-fold differences in trough concentrations 3
  • Patients with severe renal dysfunction (CrCl <30 mL/min) receiving higher doses of cefepime may be at greater risk for neurotoxicity 4

Common Pitfalls to Avoid

  1. Failure to adjust doses in renal impairment: Even with dose adjustments, 10% of patients with renal impairment may still experience cefepime accumulation 3

  2. Missing signs of neurotoxicity: Confusion and muscle jerks may be misattributed to other causes in critically ill patients rather than recognized as cefepime toxicity 3, 4

  3. Inadequate dosing for resistant organisms: Standard dosing may be insufficient for pathogens with MICs ≥8 mg/L 3

  4. Overlooking drug administration timing in dialysis patients: Administer after hemodialysis to prevent premature removal of the drug 1

By following these evidence-based dosing recommendations and monitoring parameters, clinicians can optimize cefepime therapy while minimizing the risk of adverse effects in patients with both normal and impaired renal function.

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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