Fanella Martina, Morano Alessandra, Fattouch Jinane, Albini Mariarita, Basili Luca M, Casciato Sara, Manfredi Mario, Giallonardo Anna T, Di Bonaventura Carlo
Department of Neurology and Psychiatry, Neurology Unit, "Sapienza" University, Rome, Italy.
Clin Neuropharmacol. 2017 Nov/Dec;40(6):239-242. doi: 10.1097/WNF.0000000000000250.
Generic antiepileptic drugs represent a measure to maximize cost saving. Levetiracetam (LEV) is one of most commonly used and effective antiepileptic drugs. The objective of our work was to demonstrate the effectiveness and safety of overnight switch from monotherapy with Keppra (original drug) to epitiram (generic drug) at the same dose.
In our observational study, we consecutively enrolled 37 seizure-free patients with epilepsy who expressed the wish to switch to a generic drug for economic reasons. During the 6-month evaluation period, we assessed treatment efficacy, tolerability, compliance, and intersubject variability of LEV serum concentration. At each visit, clinical and neurological examination, scales, video-electroencephalogram, and blood sample analysis to evaluate LEV plasma level were performed.
A total of 36 of 37 enrolled patients switched from Keppra to epitiram, which was administered at the same dose in monotherapy. Three of 36 patients dropped out during follow-up for adverse events. The other 33 subjects had neither seizures nor adverse events. No significant differences in electroencephalogram features and scale scores were revealed; the intersubject variability of LEV serum concentration did not differ significantly at follow-up evaluation (P = 0.53). All the patients expressed good clinical personal impression and continued to take epitiram. The switchback rate was 8 %.
The switch from Keppra to epitiram was easy and safe in our population, and epitiram can be considered as effective and tolerable as Keppra. Only a slight, non-statistically significant variability in LEV serum concentration was documented after the switch from Keppra to epitiram. Larger epileptic populations should be studied to confirm these results.
通用型抗癫痫药物是实现成本节约最大化的一种措施。左乙拉西坦(LEV)是最常用且有效的抗癫痫药物之一。我们这项工作的目的是证明以相同剂量从开浦兰(原研药)单药治疗一夜之间转换为依匹西坦(通用型药物)的有效性和安全性。
在我们的观察性研究中,我们连续纳入了37例无癫痫发作的癫痫患者,这些患者出于经济原因希望转换为通用型药物。在6个月的评估期内,我们评估了左乙拉西坦的治疗效果、耐受性、依从性以及血清浓度的个体间变异性。每次就诊时,都进行临床和神经学检查、量表评估、视频脑电图检查以及用于评估左乙拉西坦血浆水平的血样分析。
37例纳入患者中有36例从开浦兰转换为依匹西坦,依匹西坦以相同剂量进行单药治疗。36例患者中有3例在随访期间因不良事件退出。其他33例受试者既无癫痫发作也无不良事件。脑电图特征和量表评分未显示出显著差异;随访评估时左乙拉西坦血清浓度的个体间变异性无显著差异(P = 0.53)。所有患者都表达了良好的临床个人感受,并继续服用依匹西坦。转回率为8%。
在我们的研究人群中,从开浦兰转换为依匹西坦既简便又安全,并且依匹西坦可被认为与开浦兰一样有效且耐受性良好。从开浦兰转换为依匹西坦后,仅记录到左乙拉西坦血清浓度有轻微的、无统计学意义的变异性。应研究更大规模的癫痫人群以证实这些结果。