Related Experiment Video
Updated: Mar 13, 2026

Anesthesia and Intubation of Preadolescent Mouse Pups for Cardiothoracic Surgery
Published on: June 2, 2022
Maturation of oxycodone pharmacokinetics in neonates and infants: Oxycodone and its metabolites in plasma and urine
Merja Kokki1,2, Marja Heikkinen3, Pyry Välitalo4
1Department of Anaesthesia and Operative Services, Kuopio University Hospital, Kuopio, Finland.
Insights
Oxycodone elimination is slower in neonates than older infants, with higher variability. Careful dosing is crucial for neonates due to these pharmacokinetic differences.
Area of Science:
- Pharmacology
- Pediatric Medicine
- Drug Metabolism
Background:
- Oxycodone is commonly used for pain management in infants.
- Understanding its pharmacokinetics in this population is crucial for safe and effective dosing.
Purpose of the Study:
- To characterize the pharmacokinetics of oxycodone and its major metabolites in infants.
- To cover the age range from extremely preterm neonates to 2-year-old infants.
Main Methods:
- Seventy-nine infants received intravenous oxycodone (0.1 mg/kg).
- Plasma concentrations of oxycodone and metabolites were quantified.
- Pharmacokinetics were analyzed using noncompartmental analysis across six age groups.
Main Results:
- Oxycodone pharmacokinetics varied significantly with age, with higher variability in preterm neonates.
- Elimination half-life was longest in extremely preterm neonates (8.8 h) and shortest in 6-24 month olds (2.0 h).
- Noroxycodone was identified as the major metabolite in plasma and urine.
Conclusions:
- Oxycodone elimination is slower and more variable in neonates compared to older infants.
- These findings underscore the need for cautious dose titration in neonates.
- Age-dependent pharmacokinetic differences necessitate individualized dosing strategies.
Aims:
This study aimed to characterize the pharmacokinetics of oxycodone and its major metabolites in infants and covered the age range between extremely preterm neonates and 2-year-old infants.
Methods:
Seventy-nine infants (gestational age 23-42 weeks; postnatal age 0-650 days) received intravenous oxycodone hydrochloride trihydrate at a dose of 0.1 mg kg-1 during or after surgery. Three to seven blood samples were taken from each infant, and plasma concentrations of oxycodone, noroxycodone, oxymorphone, and noroxymorphone were quantified. The unconjugated forms of these compounds were determined in urine collected after up to 24 or 48 h from 25 infants. Pharmacokinetics was determined using noncompartmental analysis and reported for six clinically relevant age groups based on postmenstrual age.
Results:
Oxycodone pharmacokinetics changed markedly with patient age. Preterm neonates were found to have the highest pharmacokinetic variability out of the study population. In extremely preterm neonates (n = 6) median of elimination half-life was 8.8 h (range 6.8-12.5), in preterm (n = 11) 7.4 h (4.2-11.6), and in older neonates (n = 22) 4.1 h (2.4-5.8), all of which were significantly longer than that in infants aged 6-24 months (n = 12) 2.0 h (1.7-2.6). Median renal clearance was fairly constant in all age groups, whereas non-renal clearance markedly increased with age. Noroxycodone was the major metabolite in plasma and urine.
Conclusions:
Oxycodone elimination is slower and pharmacokinetic variability more pronounced in neonates when compared to older infants. These findings highlight the importance of careful dose titration for neonates.
More Related Videos
09:12Assessing Cellular Stress and Inflammation in Discrete Oxytocin-secreting Brain Nuclei in the Neonatal Rat Before and After First Colostrum Feeding
Published on: November 14, 2018
08:59An Intestine/Liver Microphysiological System for Drug Pharmacokinetic and Toxicological Assessment
Published on: December 3, 2020
Related Concept Videos
Pharmacokinetics in Pediatric Patients: Overview and Drug Absorption
Pharmacokinetics in Pediatric Patients: Drug Metabolism
Pharmacokinetics in Pediatric Patients: Drug Excretion
Pharmacokinetics in Pediatric Patients: Drug Distribution
Factors Affecting Drug Response: Overview
Drug Dosing: Infants and Children