Related Experiment Video
Updated: Jul 29, 2026

Preterm EEG: A Multimodal Neurophysiological Protocol
Published on: February 18, 2012
Pharmacokinetics of ceftazidime in premature, newborn and young infants
Insights
Ceftazidime serum concentrations were higher in younger infants. Dosing for infants under 2 months and 2-12 months appears appropriate, but monitoring is advised for neonates.
Area of Science:
- Pharmacology
- Pediatric Medicine
- Infectious Diseases
Background:
- Ceftazidime is a broad-spectrum cephalosporin antibiotic.
- It exhibits high activity against Pseudomonas aeruginosa.
- Understanding its pharmacokinetics in infants is crucial for effective treatment.
Purpose of the Study:
- To determine the pharmacokinetics of ceftazidime in preterm, full-term, and young infants.
- To evaluate the safety and appropriateness of current dosing regimens.
- To establish optimal therapeutic concentrations in pediatric populations.
Main Methods:
- Pharmacokinetic study involving 50 infants.
- Intravenous bolus dose of 30 mg/kg ceftazidime administered.
- Serum concentrations were measured and analyzed.
Main Results:
- Higher serum ceftazidime concentrations observed in younger infants (preterm and full-term).
- Blood levels in infants over 2 months were comparable to adult levels.
- No adverse effects were reported during the study.
Conclusions:
- Current ceftazidime dosing schedules (25-50 mg/kg/d for <2 months, 50-100 mg/kg/d for 2-12 months) seem appropriate.
- Monitoring trough levels in neonates is recommended until further data is available.
- Ceftazidime demonstrates a favorable pharmacokinetic profile in infants.
Abstract:
The pharmacokinetics of ceftazidime, a new injectable broad-spectrum cephalosporin with high anti-pseudomonal activity, were studied in 50 preterm, full-term and young infants after an intravenous bolus dose of 30 mg/kg. The serum concentrations of ceftazidime were higher in the younger babies, both premature and full-term. In infants over 2 months of age blood levels were similar to those of adult volunteer subjects. No untoward effects were encountered. Considering the in vitro activity of ceftazidime against a wide spectrum of pathogenic bacteria, the present dose schedules, 25-50 mg/kg/d for babies less than 2 months of age and 50-100 mg/kg/d for those 2-12 months of age, appear to be appropriate. Until more experience is gained with ceftazidime in neonates, monitoring of trough levels to ensure adequate blood concentrations would be ideal.
More Related Videos
06:14Optimized LC-MS/MS Method for the High-throughput Analysis of Clinical Samples of Ivacaftor, Its Major Metabolites, and Lumacaftor in Biological Fluids of Cystic Fibrosis Patients
Published on: October 15, 2017
11:15Quadruple-Checkerboard: A Modification of the Three-Dimensional Checkerboard for Studying Drug Combinations
Published on: July 24, 2021
Related Concept Videos
Pharmaceutical Alternatives: Stability-Related Therapeutic Nonequivalence
Drug Dosing: Infants and Children
Pharmacokinetics in Pediatric Patients: Overview and Drug Absorption
Pharmacokinetics in Pediatric Patients: Drug Distribution
Pharmacokinetics in Pediatric Patients: Drug Metabolism
Pharmacokinetics in Pediatric Patients: Drug Excretion