Clonidine clearance matures rapidly during the early postnatal period: A population pharmacokinetic analysis in newborns with neonatal abstinence syndrome

Hong Guang Xie, Ying Jun Cao, Estelle B. Gauda, Alexander G. Agthe, Craig W. Hendrix, Howard Lee

Research output: Contribution to journalArticle

Abstract

The population pharmacokinetic (PK) profile of oral clonidine was characterized in newborns with neonatal abstinence syndrome, and significant covariates affecting its PK parameters were identified. Plasma clonidine concentration data were obtained from a clinical trial in which 36 newborns, aged 1 to 25 days (postnatal age, PNA) and weighing 2.1 to 3.9 kg, were enrolled to take multiple oral doses of clonidine. The population PK model of clonidine was developed by NONMEM, and significant covariates were identified, followed by nonparametric bootstraps (2000 replicates) and simulation experiments. A 1-compartment open linear PK model was chosen to describe plasma concentrations of clonidine, and body weight and PNA were significant covariates for apparent clearance (CL/F) as follows: CL/F (L/h) = 15.2 × [body weight (kg)/70]0.75 × [PNA (day)0.441/(4.060.441 + PNA (day)0.441)]. Furthermore, CL/F of clonidine increased rapidly with PNA during the first month of life after body weight was adjusted. Any optimal dosage regimen for clonidine in term neonates should be based on infant's age and body weight, and 1.5 μg/kg every 4 hours is proposed starting the second week of life based on the simulation results.

Original languageEnglish (US)
Pages (from-to)502-511
Number of pages10
JournalJournal of clinical pharmacology
Volume51
Issue number4
DOIs
StatePublished - Apr 1 2011

Keywords

  • Clonidine
  • Modeling
  • Neonatal abstinence syndrome
  • Neonate
  • Pediatrics
  • Population pharmacokinetics
  • Renal clearance

ASJC Scopus subject areas

  • Pharmacology
  • Pharmacology (medical)

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