Silva Rui, Almeida Anabela, Bicker Joana, Gonçalves Joana, Carona Andreia, Silva Ana, Santana Isabel, Sales Francisco, Falcão Amílcar, Fortuna Ana
Faculty of Pharmacy, University of Coimbra, Pólo das Ciências da Saúde, Azinhaga de Santa Comba, 3000-548 Coimbra, Portugal.
Coimbra Institute for Biomedical Imaging and Translational Research, University of Coimbra, 3000-548 Coimbra, Portugal.
Pharmaceutics. 2020 Oct 1;12(10):943. doi: 10.3390/pharmaceutics12100943.
Levetiracetam is a second-generation antiepileptic drug, widely used in the treatment of focal and generalized epilepsy due to its pharmacokinetic and safety profiles. Its pharmacokinetic monitoring is ascribed as useful to personalize its dosing regimen. The aim of the present study was to describe, for the first time, the pharmacokinetics of levetiracetam in Portuguese refractory epileptic patients. Therefore, a retrospective study was carried out on 65 Portuguese refractory epileptic patients (pharmacokinetic study: 48; validation study: 17) admitted to the Refractory Epilepsy Centre of the Centro Hospitalar e Universitário de Coimbra, Coimbra, Portugal. The pharmacokinetic parameters of levetiracetam were estimated by applying a one-compartment model with first-order absorption and elimination analysis. Male patients showed higher distribution volume (Vd/F) and oral clearance (CL/F) than female patients (median Vd/F: 52.40 L in males and 38.60 L in females, = 0.011; median CL/F: 4.71 L/h in males and 3.91 L/h in females, = 0.028). Higher values of Vd/F ( = 0.026) and CL/F ( = 0.003) were also found in overweight patients relative to normal weight and obese patients. Carbamazepine was the co-administered antiepileptic drug that mostly affected the pharmacokinetics of levetiracetam, increasing both Vd/F (61.30 L with carbamazepine and 39.10 L without carbamazepine, = 0.007) and CL/F (6.71 L/h with carbamazepine and 3.91 L/h without carbamazepine, < 0.001). The pharmacokinetics of levetiracetam was affected by gender, body mass index, and co-administration of carbamazepine. This study highlights the impact of several factors on the CL/ and Vd/F of levetiracetam when administered to refractory epileptic patients. The importance of its pharmacokinetic monitoring in clinical pharmacy stands out, thereby enabling the optimization of antiepileptic drug therapy.
左乙拉西坦是一种第二代抗癫痫药物,因其药代动力学特性和安全性,广泛用于治疗局灶性和全身性癫痫。其药代动力学监测有助于制定个性化给药方案。本研究的目的是首次描述左乙拉西坦在葡萄牙难治性癫痫患者中的药代动力学。因此,对葡萄牙科英布拉大学医院中心难治性癫痫中心收治的65例葡萄牙难治性癫痫患者进行了一项回顾性研究(药代动力学研究:48例;验证研究:17例)。采用具有一级吸收和消除分析的单室模型估算左乙拉西坦的药代动力学参数。男性患者的分布容积(Vd/F)和口服清除率(CL/F)高于女性患者(男性Vd/F中位数:52.40 L,女性为38.60 L,P = 0.011;男性CL/F中位数:4.71 L/h,女性为3.91 L/h,P = 0.028)。与正常体重和肥胖患者相比,超重患者的Vd/F(P = 0.026)和CL/F(P = 0.003)值也更高。卡马西平是联合使用的抗癫痫药物中对左乙拉西坦药代动力学影响最大的药物,它同时增加了Vd/F(卡马西平组为61.30 L,无卡马西平组为39.10 L,P = 0.007)和CL/F(卡马西平组为6.71 L/h,无卡马西平组为3.91 L/h,P < 0.001)。左乙拉西坦的药代动力学受性别、体重指数和卡马西平联合使用的影响。本研究强调了多种因素对难治性癫痫患者使用左乙拉西坦时CL/和Vd/F的影响。其药代动力学监测在临床药学中的重要性凸显出来,从而能够优化抗癫痫药物治疗。