ter Heine Rob, van Maarseveen Erik M, van der Westerlaken Monique M L, Braun Kees P J, Koudijs Suzanne M, Berg Maarten J Ten, Malingré Mirte M
Department of Clinical Pharmacy, Meander Medical Centre, Amersfoort, The Netherlands
Department of Clinical Pharmacy, University Medical Centre Utrecht, Utrecht, The Netherlands.
J Child Neurol. 2014 Jun;29(6):803-10. doi: 10.1177/0883073813486294. Epub 2013 May 13.
Dosing of phenytoin is difficult in children because of its variable pharmacokinetics and protein binding. Possible covariates for this protein binding have mostly been univariately investigated in small, and often adult, adult populations. We conducted a study to identify and quantify these covariates in children. We extracted data on serum phenytoin concentrations, albumin, triglycerides, urea, total bilirubin and creatinine concentrations and data on coadministration of valproic acid or carbamazepine in 186 children. Using nonlinear mixed effects modeling the effects of covariates on the unbound phenytoin fraction were investigated. Serum albumin, serum urea concentrations, and concomitant valproic acid use significantly influenced the unbound phenytoin fraction. For clinical practice, we recommend that unbound phenytoin concentrations are measured routinely. However, if this is impossible, we suggest to use our model to calculate the unbound concentration. In selected children, close treatment monitoring and dose reductions should be considered to prevent toxicity.
由于苯妥英钠的药代动力学和蛋白结合存在变异性,儿童的苯妥英钠给药较为困难。这种蛋白结合的可能协变量大多在小规模且通常为成人的人群中进行了单变量研究。我们开展了一项研究,以识别和量化儿童中的这些协变量。我们提取了186名儿童的血清苯妥英钠浓度、白蛋白、甘油三酯、尿素、总胆红素和肌酐浓度的数据,以及丙戊酸或卡马西平联合用药的数据。使用非线性混合效应模型研究了协变量对游离苯妥英分数的影响。血清白蛋白、血清尿素浓度以及丙戊酸的联合使用显著影响游离苯妥英分数。对于临床实践,我们建议常规测量游离苯妥英浓度。然而,如果无法做到这一点,我们建议使用我们的模型来计算游离浓度。对于特定儿童,应考虑密切的治疗监测和减少剂量以预防毒性。