Multicenter Population Pharmacokinetics of Fentanyl in Neonatal Surgical Patients Using Dried Blood Spot Specimen Collection Demonstrates Maturation of Elimination Clearance

Author:

Rzasa Lynn Rachael S.1,Henthorn Thomas K.12,Zuk Jeannie1,Hammer Gregory B.3,Drover David R.3,Levy Richard J.4,Maxwell Lynne G.5,Sadhasivam Senthilkumar6,Suresh Santhanam7,Galinkin Jeffrey L.8

Affiliation:

1. Department of Anesthesiology, University of Colorado School of Medicine, Aurora, Colorado

2. Department of Pharmaceutical Sciences, Skaggs School of Pharmacy and Pharmaceutical Sciences, University of Colorado, Aurora, Colorado

3. Department of Anesthesiology, Perioperative and Pain Medicine, Stanford University School of Medicine, Palo Alto, California

4. Department of Anesthesiology, Columbia University Medical Center, New York, New York

5. Department of Anesthesiology and Critical Care Medicine, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, Pennsylvania

6. Department of Anesthesiology and Perioperative Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania

7. Department of Anesthesiology, Northwestern University Feinberg School of Medicine, Chicago, Illinois

8. US Anesthesia Partners of Colorado, Greenwood Village, Colorado.

Abstract

BACKGROUND: Fentanyl is widely used for analgesia and sedation in neonates, but pharmacokinetic (PK) analysis in this population has been limited by the relatively large sample volumes required for plasma-based assays. METHODS: In this multicenter observational study of fentanyl kinetics in neonates up to 42 weeks of postmenstrual age (PMA) who received fentanyl boluses and continuous infusions, dried blood spots were used for small-volume sampling. A population PK analysis was used to describe fentanyl disposition in term and preterm neonates. Covariates for the model parameters, including body weight, PMA, birth status (preterm or term), and presence of congenital cardiac disease, were assessed in a stepwise manner. RESULTS: Clearance was estimated to be greater than adult clearance of fentanyl and varied with weight. Covariate selection did not yield a significant relationship for age as a continuous or dichotomous variable (term or preterm, the latter defined as birth with PMA of <37 weeks) and clearance. CONCLUSIONS: A supra-allometric effect on clearance was determined during covariate analyses (exponential scaling factor for body weight >0.75), as has been described in population PK models that account for maturation of intrinsic clearance (here, predominantly hepatic microsomal activity) in addition to scaling for weight, both of which impact clearance in this age group.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Reference38 articles.

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