Related Experiment Video
Updated: Jul 11, 2026

Transcutaneous Microcirculatory Imaging in Preterm Neonates
Published on: December 31, 2015
Vancomycin pharmacokinetics in preterm infants
Jose Kleber Kobol Machado1, Rubens Feferbaum, Celia Etsuco Kobayashi
1University of Sao Paulo, Medical School, Sao Paulo, SP, Brazil.
Insights
Vancomycin trough plasma concentration in preterm infants is influenced by pharmacokinetic factors. These factors, including volume of distribution and half-life, vary with postconceptional and postnatal age.
Area of Science:
- Pharmacology
- Neonatal Medicine
- Clinical Pharmacokinetics
Background:
- Vancomycin is crucial for treating infections in preterm infants.
- Understanding vancomycin pharmacokinetics is essential for optimizing therapeutic efficacy and minimizing toxicity in this vulnerable population.
- Postconceptional age (PCA) and postnatal age (PNA) significantly impact drug disposition in neonates.
Purpose of the Study:
- To evaluate the kinetic disposition of vancomycin in preterm infants.
- To determine the relationship between apparent volume of distribution, biological half-life, total body clearance, and vancomycin trough plasma concentration.
- To assess the influence of PCA and PNA on these pharmacokinetic parameters.
Main Methods:
- A study involving 25 preterm infants divided into two groups based on PCA and PNA.
- Analysis of pharmacokinetic parameters including apparent volume of distribution, biological half-life, and total body clearance.
- Multiple linear regression analysis to correlate pharmacokinetic parameters with vancomycin trough plasma concentration.
Main Results:
- Apparent volume of distribution was significantly higher in the younger PCA group (group 1) compared to the older PCA group (group 2).
- A strong linear correlation was observed between vancomycin trough plasma concentration and apparent volume of distribution/biological half-life in group 1 (r=0.85).
- A strong linear correlation was observed between vancomycin trough plasma concentration and total body clearance in group 2 (r=0.91).
Conclusions:
- Vancomycin trough plasma concentration is dependent on pharmacokinetic parameters.
- The relationship between pharmacokinetic parameters and vancomycin trough concentration varies with PCA and PNA in preterm infants.
- These findings highlight the importance of age-specific pharmacokinetic monitoring for vancomycin therapy in preterm neonates.
Objective:
[corrected] The objective of the present study was to evaluate the kinetic disposition of vancomycin in preterm infants with emphasis on the apparent volume of distribution, biological half-life, and total body clearance as well as whether their variations cause significant modification of the trough plasma concentration of the drug, depending on the postconceptional age (PCA) and the postnatal age (PNA).
Material And Method:
Twenty-five selected patients were distributed into 2 groups which differed significantly in terms of mean PCA (31.2-32.3 weeks in group 1, n = 13; 33.5-34.1 weeks in group 2, n = 12: CI95%, P < .001) and PNA (group 1, 12.0-18.5 days; group 2, 18.0-34.0 days, CI95%, P < .05). The parents were informed and signed a written consent for participation of the infants in the protocol that had been previously approved by the Ethics Committee of the hospital.
Results:
Apparent volume of distribution was significantly increased in group 1 compared with patients of group 2 (0.85 vs. 0.56 L/kg, respectively; P = .01,). Additionally multiple linear regression revealed a good linear correlation (r = 0.85) of trough plasma concentration of vancomycin with the apparent volume of distribution and also with the biological half-life in patients of group 1, while a good correlation (r = 0.91) was obtained for the trough plasma concentration with total body clearance in infants of group 2. The influence of these kinetic parameters on the trough concentration of vancomycin in preterm infants seems to vary according to PCA and PNA.
Conclusion:
In conclusion, the trough plasma concentration of vancomycin depends on the pharmacokinetics, and multiple linear correlation indicates that it varies according to the postconceptional and postnatal age of preterm infants.
Related Concept Videos
Pharmacokinetics in Pediatric Patients: Drug Excretion
Pharmacokinetics in Pediatric Patients: Drug Metabolism
Pharmacokinetics in Pediatric Patients: Overview and Drug Absorption
Pharmacokinetics in Pediatric Patients: Drug Distribution
Drug Dosing: Infants and Children
Estimation of k and VD of Aminoglycosides
