Clinical experience with topiramate dosing and serum levels in children 12 years or under with epilepsy

J Child Neurol. 2001 Nov;16(11):806-8. doi: 10.1177/08830738010160110501.

Abstract

Only a limited topiramate dosing range (5-9 mg/kg/day) is approved by the U.S. Food and Drug Administration (FDA). We reviewed our topiramate dosing (mg/kg/d) and corresponding serum levels (microg/mL) (n = 77) in 41 children who were treated to clinical response or tolerability. The patients were divided into older (6-12 years [n = 21]) and younger (< or = 5 years [n = 20]) groups. Topiramate was given as monotherapy (n = 9), with an enzyme-inducing antiepileptic drug (n = 16) (phebarbital, phenytoin, or carbamazepine), or as polytherapy (n =17) (another antiepileptic drug). In the older children, there was a good dosage to serum level correspondence. However, younger children on topiramate monotherapy or cotherapy with an enzyme-inducing antiepileptic drug had relatively lower serum levels, but the serum level was increased if they were on polytherapy without an enzyme-inducing drug. This study supports a wider dosing range (7-22 mg/kg/day) of topiramate and dosage escalation beyond the approved range. Serum levels are useful in guiding topiramate dosing, especially in young children.

Publication types

  • Clinical Trial

MeSH terms

  • Anticonvulsants / administration & dosage*
  • Anticonvulsants / blood
  • Anticonvulsants / therapeutic use
  • Child
  • Drug Monitoring
  • Epilepsy / drug therapy*
  • Female
  • Fructose / administration & dosage*
  • Fructose / analogs & derivatives*
  • Fructose / blood
  • Fructose / therapeutic use
  • Humans
  • Infant
  • Male
  • Topiramate

Substances

  • Anticonvulsants
  • Topiramate
  • Fructose