Pharmacokinetics of intravenously and intramuscularly administered cefepime in infants and children

M D Reed1, T S Yamashita, C K Knupp

  • 1Center for Drug Research, Rainbow Babies and Childrens Hospital, Department of Pediatrics, School of Medicine, Case Western Reserve University School of Medicine, Cleveland, Ohio, USA.

Insights

This study on cefepime pharmacokinetics in infants and children found that a 50 mg/kg dose every 12 hours is effective for treating infections. Cefepime dosing can be simplified for patients two months and older.

Area of Science:

  • Pharmacology
  • Pediatric Infectious Diseases
  • Clinical Pharmacy

Background:

  • Cefepime is a broad-spectrum cephalosporin antibiotic used to treat various bacterial infections.
  • Understanding cefepime pharmacokinetics in pediatric populations is crucial for optimizing dosing regimens.
  • Previous studies have indicated variability in cefepime disposition based on age and renal function.

Purpose of the Study:

  • To characterize the pharmacokinetic properties of cefepime in infants and children.
  • To evaluate cefepime pharmacokinetics after single and multiple intravenous doses, and after intramuscular administration.
  • To determine an optimal cefepime dosing strategy for pediatric patients.

Main Methods:

  • 37 infants and children (2.1 months to 16.4 years) with normal renal function received cefepime 50 mg/kg intravenously every 8 hours.
  • Pharmacokinetics were assessed after the first dose (n=35) and at steady-state (n=31).
  • Eight subjects received an intramuscular dose to assess disposition and bioavailability.

Main Results:

  • Elimination half-life averaged 1.7 hours, steady-state volume of distribution was 0.35 L/kg, and total body clearance was 3.1 mL/min/kg.
  • Pharmacokinetics were similar between first-dose and steady-state evaluations, with slightly longer half-life and MRT in younger children (<6 months).
  • Intramuscular administration resulted in slightly prolonged half-life and MRT, with an average bioavailability of 82%.

Conclusions:

  • The pharmacokinetic data support a simplified cefepime dosing strategy for pediatric patients aged two months and older.
  • A cefepime dose of 50 mg/kg every 12 hours is recommended for treating infections caused by susceptible pathogens (MIC ≤ 8 mg/L).
  • This dosing regimen aims to ensure therapeutic efficacy while considering the pharmacokinetic profile in the pediatric population.

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