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Steady-state Pharmacokinetics of Phenytoin from Routinely Collected Patient Data

  • T. H. Grasela
  • , L. B. Sheiner
  • , B. Rambeck
  • , H. E. Boenigk
  • , A. Dunlop
  • , P. W. Mullen
  • , J. Wadsworth
  • , A. Richens
  • , T. Ishizaki
  • , K. Chiba
  • , H. Miura
  • , K. Minagawa
  • , P. G. Blain
  • , J. C. Mucklow
  • , C. T. Bacon
  • , M. Rawlins
  • University of California at San Francisco
  • Gesellschaft für Epilepsie-Forschung
  • University College London Hospitals NHS Foundation Trust
  • National Center for Global Health and Medicine
  • Kitasato University
  • Newcastle University

Research output: Contribution to journalArticlepeer-review

131 Scopus citations

Abstract

Previously reported routine Phenytoin clinical pharmacokinetic data from Japan, England, and Germany were analysed to estimate population pharmacokinetic parameters. There were 780 steady-state phenytoin concentrations and associated dosage rates (mg/day) from 322 patients. The patient group spanned paediatric and adult ages, mean age being 18.4 ± 17.3 (SD) years; 53% were males. The data were analysed using NONMEM, a computer programme designed for population pharmacokinetic analysis. Estimates of the influence of age, gender, data source, height and weight on the maximum elimination rate (Vm) and Michaelis-Menten constant (Km) were obtained. The Vm and Km of a 70kg adult male European were estimated to be 415 mg/day and 5.7 mg/L, respectively. Vm is not influenced by gender, age or data source. The parameters of a power function of height and weight were estimated to adjust Vm for body size. The best function adjusts Vm in proportion to weight to the 0.6 power; height contains no useful information. Km is not influenced by gender. The Km for patients less than 15 years old is 43% less than that of older patients. The Km of Japanese patients appears to be 23% less than that for European patients. Even after adjustments for age, etc., apparent Vm and Km vary unpredictably among individuals with a coefficient of variation between 10 to 20%, and approximately 50% respectively.

Original languageEnglish
Pages (from-to)355-364
Number of pages10
JournalClinical Pharmacokinetics
Volume8
Issue number4
DOIs
StatePublished - Aug 1983

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