Department of Clinical Neuroscience, Karolinska Institutet, Stockholm, Sweden.
Epilepsia. 2013 Mar;54(3):405-14. doi: 10.1111/epi.12109. Epub 2013 Jan 29.
Pregnancy is a state where pharmacokinetic changes are more pronounced and more rapid than during any other period of life. The consequences of such changes can be far reaching, not least in the management of epilepsy where the risks with uncontrolled seizures during pregnancy need to be balanced against potential teratogenic effects of antiepileptic drugs (AEDs). This article aims to review the literature on gestational effects on the pharmacokinetics of older and newer generation AEDs and discuss the implications for the treatment of epilepsy in women during pregnancy. Pregnancy can affect the pharmacokinetics of AEDs at any level from absorption, distribution, metabolism, to elimination. The effect varies depending on the type of AED. The most pronounced decline in serum concentrations is seen for AEDs that are eliminated by glucuronidation (UGT), in particular lamotrigine where the effect may be profound. Serum concentrations of AEDs that are cleared mainly through the kidneys, for example, levetiracetam, can also decline significantly. Some AEDs, such as carbamazepine seem to be affected only marginally by pregnancy. Data on pharmacokinetics during pregnancy are lacking completely for some of the newer generation AEDs: pregabalin, lacosamide, retigabine, and eslicarbazepine acetate. Where data are available, the effects of pregnancy on serum concentrations seem to vary considerably individually and are thus difficult to predict. Although large-scale systematic studies of the clinical relevance of the pharmacokinetic alterations are lacking, prospective and retrospective case series have reported an association between declining serum concentrations and deterioration in seizures control. The usefulness of routine monitoring of AED serum concentrations in pregnancy and of dose adjustments based on falling levels, are discussed in this review. We suggest that monitoring could be important, in particular when women have been titrated to the lowest effective AED dose and serum concentration before pregnancy, and when that individual optimal concentration can be used as reference.
妊娠是一个药物代谢动力学变化比生命中任何其他时期都更为明显和迅速的阶段。这些变化的后果可能是深远的,尤其是在癫痫的管理中,需要平衡妊娠期间不受控制的癫痫发作的风险与抗癫痫药物(AEDs)的潜在致畸作用。本文旨在综述关于妊娠对新一代和旧一代 AED 药代动力学的影响的文献,并讨论其对妊娠期间女性癫痫治疗的影响。妊娠可影响 AED 的药代动力学,从吸收、分布、代谢到消除,各个环节均可受到影响。其影响因 AED 类型而异。经葡萄糖醛酸化(UGT)消除的 AED(特别是拉莫三嗪)的血清浓度下降最为明显,其影响可能非常显著。主要通过肾脏清除的 AED(如左乙拉西坦)的血清浓度也可能显著下降。一些 AED(如卡马西平)似乎仅受妊娠轻微影响。一些新型 AED(如普瑞巴林、拉科酰胺、瑞替加滨和依佐加滨)在妊娠期间的药代动力学数据完全缺失。在有数据可用的情况下,妊娠对血清浓度的影响似乎因人而异,差异很大,因此难以预测。尽管缺乏关于药代动力学改变的临床相关性的大规模系统研究,但前瞻性和回顾性病例系列研究报告了血清浓度下降与癫痫控制恶化之间存在关联。本文讨论了在妊娠期间监测 AED 血清浓度和根据浓度下降调整剂量的有用性。我们建议,监测可能很重要,特别是在女性在妊娠前已经用最低有效 AED 剂量和血清浓度进行滴定,并且可以将该个体最佳浓度用作参考时。