Time course of lamotrigine de-induction: impact of step-wise withdrawal of carbamazepine or phenytoin

被引:27
作者
Anderson, GD
Gidal, BE
Messenheimer, JA
Gilliam, FG
机构
[1] Univ Wisconsin, Sch Pharm, Madison, WI 53706 USA
[2] Univ Wisconsin, Dept Neurol, Madison, WI 53706 USA
[3] Univ Washington, Dept Pharm, Seattle, WA 98195 USA
[4] GlaxoSmithKline, Res Triangle Pk, NC USA
[5] Univ Washington, Dept Neurol, St Lois, MO USA
关键词
lamotrigine; carbamazepine; phenytoin; de-induction; pharmacokinetics; drug interactions;
D O I
10.1016/S0920-1211(02)00033-5
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective: The objective of the present analysis is to examine lamotrigine (LTG) pharmacokinetics both during polytherapy with enzyme inducing antiepileptic drugs and to evaluate the time course of de-induction following the step-wise withdrawal of enzyme inducers. Background: LTG pharmacokinetics can be significantly influenced by concomitant AEDs, and the addition of enzyme inducers can markedly increase LTG clearance. thereby reducing serum concentrations. A clinically relevant question is how will LTG clearance and resulting plasma concentrations be altered during concomitant enzyme inducer withdrawal; conversion process. Design/Method: As part of a previously published, active-control, LTG monotherapy trial. dose and plasma concentration data for LTG. carbamazepine (CBZ) or phenytoin (PHT) were obtained. Following the attainment of a LTG target dose of 500 mg/day, CZB or PHT were withdrawn in weekly 20%,, decrements. Following inducer withdrawal, LTG was then continued as monotherapy for an additional 12 weeks. Plasma concentrations and daily doses of LTG, CBZ, or PHT were obtained at regularly scheduled study visits during inducer withdrawal and during LTG monotherapy. Pharmacokinetic analysis of the plasma concentration data was done to determine the time-course and effect or inducer plasma concentration on LTG oral clearance (Cl.), where LTG Cl. was estimated as the dose/concentration ratio. Results: Of the 156 patients enrolled in this trial. 76 were assigned to LTG arm. 43 completed the withdrawal to monotherapy phase with 28 successfully completing the study. In a subset analysis of completers. LTG Cl. determined prior to withdrawal of the inducers was significantly greater in patients (n = 28) on LTG + PHT (160%, increase) than in those (n = 48) receiving LTG + CBZ (62%, increase): 1.77 +/- 0,77 vs. 1.06 +/- 0.41 ml/min/kg, respectively, p = 0.017. The significant reduction in LTG Cl. occurred only when CBZ plasma concentrations reached approximately 2 mug/ml or PHT plasma concentrations reached zero. Conclusions: Mean LTG plasma concentrations will approximately double following the withdrawal PHT, however increases of only 60% may occur following the withdrawal of CBZ. Importantly, these data suggest that LTG concentrations would not be expected to increase until the concomitant inducer is almost completely removed. (C) 2002 Published by Elsevier Science B.V.
引用
收藏
页码:211 / 217
页数:7
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