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采用高效液相色谱-光电二极管阵列紫外检测法进行左乙拉西坦的治疗药物监测:难治性癫痫患者血浆浓度与临床反应相关性的初步观察

Therapeutic drug monitoring of levetiracetam by high-performance liquid chromatography with photodiode array ultraviolet detection: preliminary observations on correlation between plasma concentration and clinical response in patients with refractory epilepsy.

作者信息

Lancelin Frédérique, Franchon Emilie, Kraoul Linda, Garciau Isabelle, Brovedani Sophie, Tabaouti Khalid, Landré Elisabeth, Chassoux Francine, Paubel Pascal, Piketty Marie-Liesse

机构信息

Departments of Biology, Centre Hospitalier Sainte-Anne, Paris, France.

出版信息

Ther Drug Monit. 2007 Oct;29(5):576-83. doi: 10.1097/FTD.0b013e318157032d.

DOI:10.1097/FTD.0b013e318157032d
PMID:17898647
Abstract

Levetiracetam is a new antiepileptic drug prescribed for the treatment of patients with refractory partial seizures with or without secondary generalization as well as for the treatment of juvenile myoclonic epilepsy. A rapid and specific method by high-performance liquid chromatography diode array detection was developed to measure the concentration of levetiracetam in human plasma. The trough plasma concentrations measured in 69 epileptic patients treated with 500 to 3000 mg/d of levetiracetam ranged from 1.1 to 33.5 microg/mL. The mean (range) levetiracetam plasma concentrations in responders and nonresponders were 12.9 microg/mL (4.6-21 microg/mL) and 9.5 microg/mL (1.1-20.9 microg/mL), respectively. A wide variability in concentration-response relationships was observed in patients. Using a receiver operating characteristic curve, the threshold levetiracetam concentration for a therapeutic response was 11 microg/mL. The sensitivity and specificity for this threshold levetiracetam concentration were 73% and 71%, respectively. According to chi analysis, this finding was not significant probably because of the small number of patients and because of their refractory seizure type. Nevertheless, the levetiracetam plasma concentration could be used to help clinicians detect severe intoxication or to verify compliance by repeating the measurement in patients.

摘要

左乙拉西坦是一种新型抗癫痫药物,用于治疗伴有或不伴有继发性全身性发作的难治性部分性癫痫患者以及青少年肌阵挛性癫痫。建立了一种采用高效液相色谱二极管阵列检测的快速、特异方法,用于测定人血浆中左乙拉西坦的浓度。69例接受500至3000mg/d左乙拉西坦治疗的癫痫患者的谷浓度范围为1.1至33.5μg/mL。有反应者和无反应者的左乙拉西坦血浆平均(范围)浓度分别为12.9μg/mL(4.6 - 21μg/mL)和9.5μg/mL(1.1 - 20.9μg/mL)。在患者中观察到浓度 - 反应关系存在很大差异。使用受试者工作特征曲线,治疗反应的左乙拉西坦阈值浓度为11μg/mL。该左乙拉西坦阈值浓度的敏感性和特异性分别为73%和71%。根据卡方分析,这一发现可能不显著,原因可能是患者数量较少以及他们的癫痫发作类型为难治性。尽管如此,左乙拉西坦血浆浓度可用于帮助临床医生检测严重中毒情况或通过对患者重复测量来核实依从性。

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