首页> 外文期刊>Epilepsy research >Effect of levetiracetam on the pharmacokinetics of adjunctive antiepileptic drugs: a pooled analysis of data from randomized clinical trials.
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Effect of levetiracetam on the pharmacokinetics of adjunctive antiepileptic drugs: a pooled analysis of data from randomized clinical trials.

机译:左乙拉西坦对辅助抗癫痫药的药代动力学的影响:随机临床试验数据的汇总分析。

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The purpose of this study was to determine the influence of levetiracetam on the steady-state serum concentrations of other commonly used antiepileptic drugs (AEDs). Serum AED concentrations were measured at baseline and after adjunctive therapy with levetiracetam (1000-4000 mg/day) or placebo in four phase III trials in patients with refractory partial epilepsy receiving stable AED dosages. The data were pooled, and repeated measures covariance analysis was used to calculate the ratio (and 90% confidence intervals) of the geometric mean serum drug concentrations during adjunctive levetiracetam therapy relative to baseline. Levetiracetam did not increase or decrease mean steady-state serum concentrations of carbamazepine, phenytoin, valproic acid, lamotrigine, gabapentin, phenobarbital, or primidone. For each of these AEDs, the 90% confidence interval of the geometric mean drug concentrations ratio was included within the 80-125% bioequivalence range. Serum concentrations of these AEDs did not change over time after adjunctive levetiracetam therapy, irrespective of the dosage of levetiracetam used. For vigabatrin, there was no evidence for a significant change in serum drug concentration after the addition of levetiracetam, but the number of observations was too small for the limits of the confidence interval to fall within the 80-125% range. Thus, adjunctive therapy with levetiracetam does not influence the steady-state serum concentrations of concomitantly administered carbamazepine, phenytoin, valproic acid, lamotrigine, gabapentin, phenobarbital, or primidone. Consequently, no need for adjusting the dosages of these AEDs is anticipated when levetiracetam is added on or removed from a patient's therapeutic regimen.
机译:这项研究的目的是确定左乙拉西坦对其他常用抗癫痫药(AED)稳态血药浓度的影响。在接受稳定AED剂量的难治性部分性癫痫患者的四项III期临床试验中,在基线期和左乙拉西坦(1000-4000 mg /天)或安慰剂辅助治疗后测量血清AED浓度。汇总数据,并使用重复测量协方差分析来计算左乙拉西坦辅助治疗期间血清平均几何药物浓度相对于基线的比率(和90%置信区间)。左乙拉西坦不增加或减少卡马西平,苯妥英钠,丙戊酸,拉莫三嗪,加巴喷丁,苯巴比妥或普利米酮的稳态血药浓度。对于这些AED中的每一种,几何平均药物浓度比的90%置信区间包括在80-125%的生物等效性范围内。辅助左乙拉西坦治疗后,这些AED的血清浓度不会随时间变化,而与所用左乙拉西坦的剂量无关。对于vigabatrin,没有证据表明添加左乙拉西坦后血清药物浓度有显着变化,但观察次数太少,不足以使置信区间的限制落在80-125%的范围内。因此,左乙拉西坦的辅助治疗不会影响卡马西平,苯妥英钠,丙戊酸,拉莫三嗪,加巴喷丁,苯巴比妥或普立米酮的稳态血清浓度。因此,当将左乙拉西坦添加到患者的治疗方案上或从患者的治疗方案中去除时,预期不需要调节这些AED的剂量。

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