Krasowski Matthew D
Department of Pathology, University of Iowa Hospitals and Clinics, 200 Hawkins Drive, RCP 6233, Iowa City, IA 52242.
Pharmaceuticals (Basel). 2010 Jun 11;3(6):1909-1935. doi: 10.3390/ph3061909.
In the past twenty years, 14 new antiepileptic drugs have been approved for use in the United States and/or Europe. These drugs are eslicarbazepine acetate, felbamate, gabapentin, lacosamide, lamotrigine, levetiracetam, oxcarbazepine, pregabalin, rufinamide, stiripentol, tiagabine, topiramate, vigabatrin and zonisamide. In general, the clinical utility of therapeutic drug monitoring has not been established in clinical trials for these new anticonvulsants, and clear guidelines for drug monitoring have yet to be defined. The antiepileptic drugs with the strongest justifications for drug monitoring are lamotrigine, oxcarbazepine, stiripentol, and zonisamide. Stiripentol and tiagabine are strongly protein bound and are candidates for free drug monitoring. Therapeutic drug monitoring has lower utility for gabapentin, pregabalin, and vigabatrin. Measurement of salivary drug concentrations has potential utility for therapeutic drug monitoring of lamotrigine, levetiracetam, and topiramate. Therapeutic drug monitoring of the new antiepileptic drugs will be discussed in managing patients with epilepsy.
在过去二十年中,有14种新型抗癫痫药物已获美国和/或欧洲批准使用。这些药物分别是醋酸艾司利卡西平、非氨酯、加巴喷丁、拉科酰胺、拉莫三嗪、左乙拉西坦、奥卡西平、普瑞巴林、卢非酰胺、司替戊醇、噻加宾、托吡酯、氨己烯酸和唑尼沙胺。总体而言,治疗药物监测在这些新型抗惊厥药物的临床试验中的临床实用性尚未确立,且尚未明确药物监测的指导原则。最有理由进行药物监测的抗癫痫药物是拉莫三嗪、奥卡西平、司替戊醇和唑尼沙胺。司替戊醇和噻加宾与蛋白质结合紧密,是游离药物监测的候选对象。治疗药物监测对加巴喷丁、普瑞巴林和氨己烯酸的实用性较低。唾液药物浓度测定对拉莫三嗪、左乙拉西坦和托吡酯的治疗药物监测具有潜在用途。将在癫痫患者的管理中讨论新型抗癫痫药物的治疗药物监测。