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Empiric dosing strategies to predict lamotrigine concentrations during pregnancy

加药 药代动力学 医学 毒性 拉莫三嗪 人口 养生 怀孕 药理学 癫痫 麻醉 内科学 生物 遗传学 环境卫生 精神科
作者
Jessica M. Barry,Jacqueline A. French,Page B. Pennell,Ashwin Karanam,Cynthia L. Harden,Angela K. Birnbaum
出处
期刊:Pharmacotherapy [Wiley]
卷期号:43 (10): 998-1006 被引量:2
标识
DOI:10.1002/phar.2856
摘要

Abstract Introduction Maintaining seizure control with lamotrigine is complicated by altered pharmacokinetics and existence of subpopulations in whom clearance increases or remains constant during pregnancy. Objective Our objective was to characterize the potential for particular dosing scenarios to lead to increased seizure risk or toxicity. Methods Lamotrigine pharmacokinetic parameters obtained from our previous study were applied to a one‐compartment model structure with subpopulations (75:25%) exhibiting different clearance changes. A single‐patient simulation was conducted with typical pharmacokinetic parameter values from each subpopulation. Population‐level simulations ( N = 48,000) included six dosing scenarios and considered four preconception doses using the R package mrgsolve (Metrum Research Group). Thresholds for efficacy and toxicity were selected as drug concentration that are 65% lower than preconception concentrations and doubling of preconception concentrations, respectively. Results Individual simulation results demonstrated that without dose increases, concentrations fell below 0.65 at 6–8 weeks in the high clearance change (HC) subpopulation, depending on preconception clearance. While no simulated dosing regimen allowed all women in both subpopulations to maintain preconception concentrations, some regimens provided a more balanced risk profile than others. Predicted concentrations suggested potential increased seizure risk for 7%–100% of women in the HC group depending on preconception dose and subpopulation. Additionally, in 63% of dosing scenarios for women with low clearance change (LC), there was an increased risk of toxicity (34%–100% of women). Significance A substantial percentage of simulated individuals had concentrations low enough to potentially increase seizure risk or high enough to create toxicity. Early clearance changes indicate possible subpopulation categorization if therapeutic drug monitoring is conducted in the first trimester. An arbitrary “one‐size‐fits‐all” philosophy may not work well for lamotrigine dosing adjustments during pregnancy and reinforces the need for therapeutic drug monitoring until a patient is determined to be in the LC or HC group.
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