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Levetiracetam: a review of its use in epilepsy.

机译:左乙拉西坦:综述其在癫痫中的用途。

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摘要

Levetiracetam (Keppra(R), E Keppra(R)) is an established second-generation antiepileptic drug (AED). Worldwide, levetiracetam is most commonly approved as adjunctive treatment of partial onset seizures with or without secondary generalization; other approved indications include monotherapy treatment of partial onset seizures with or without secondary generalization, and adjunctive treatment of myoclonic seizures associated with juvenile myoclonic epilepsy and primary generalized tonic-clonic (GTC) seizures associated with idiopathic generalized epilepsy. Levetiracetam has a novel structure and unique mechanisms of action. Unlike other AEDs, the mechanisms of action of levetiracetam appear to involve neuronal binding to synaptic vesicle protein 2A, inhibiting calcium release from intraneuronal stores, opposing the activity of negative modulators of GABA- and glycin-gated currents and inhibiting excessive synchronized activity between neurons. In addition, levetiracetam inhibits N-type calcium channels. Levetiracetam is associated with rapid and complete absorption, high oral bioavailability, minimal metabolism that consists of hydrolysis of the acetamide group, and primarily renal elimination. It lacks cytochrome P450 isoenzyme-inducing potential and is not associated with clinically significant pharmacokinetic interactions with other drugs, including other AEDs. The efficacy of oral immediate-release levetiracetam in controlling seizures has been established in numerous randomized, double-blind, controlled, multicentre trials in patients with epilepsy. Adjunctive levetiracetam reduced the frequency of seizures in paediatric and adult patients with refractory partial onset seizures to a significantly greater extent than placebo. Monotherapy with levetiracetam was noninferior to that with carbamazepine controlled release in controlling seizures in patients with newly diagnosed partial onset seizures. Levetiracetam also provided seizure control relative to placebo as adjunctive therapy in patients with idiopathic generalized epilepsy with myoclonic seizures or GTC seizures. In addition, patients receiving oral levetiracetam showed improvements in measures of health-related quality of life relative to those receiving placebo. Although treatment-emergent adverse events were commonly reported in the clinical trials of levetiracetam, the overall proportion of patients who experienced at least one treatment-emergent adverse event was broadly similar in the levetiracetam and placebo treatment groups, with most events being mild to moderate in severity. Levetiracetam is not associated with cognitive impairment or drug-induced weight gain, but has been associated with behavioural adverse effects in some patients.
机译:左乙拉西坦(Leepiracetam)是一种成熟的第二代抗癫痫药(AED)。在世界范围内,左乙拉西坦最普遍被批准为伴或不伴有继发性泛发的部分发作性癫痫的辅助治疗;其他批准的适应症包括有或没有继发性全身性发作的部分发作的单药治疗,以及与青少年性肌阵挛性癫痫和特发性全身性癫痫发作相关的肌阵挛性癫痫的辅助治疗。左乙拉西坦具有新颖的结构和独特的作用机制。不同于其他AED,左乙拉西坦的作用机制似乎涉及神经元与突触小泡蛋白2A的结合,抑制钙从神经元内存储释放,与GABA和甘氨酸门控电流的负调节剂的活性相反,并抑制神经元之间过度的同步活性。此外,左乙拉西坦还抑制N型钙通道。左乙拉西坦与快速和完全吸收,高口服生物利用度,由乙酰胺基团水解引起的新陈代谢最少以及主要消除肾脏有关。它缺乏诱导细胞色素P450同工酶的潜力,并且与与其他药物(包括其他AED)的临床上显着的药代动力学相互作用无关。口服速释左乙拉西坦在控制癫痫发作中的功效已在癫痫患者的众多随机,双盲,对照,多中心试验中得到证实。辅助性左乙拉西坦降低了难治性部分发作的小儿和成年患者的癫痫发作频率,其幅度明显大于安慰剂。在新诊断的部分发作的患者中,左乙拉西坦的单一疗法在控制癫痫发作方面不逊于卡马西平控释。对于患有肌阵挛性癫痫发作或GTC癫痫发作的特发性全身性癫痫患者,左乙拉西坦相对于安慰剂也可提供癫痫发作控制。此外,与接受安慰剂的患者相比,接受口服左乙拉西坦的患者在与健康相关的生活质量衡量上有所改善。尽管在左乙拉西坦的临床试验中普遍报告有治疗紧急不良事件,但在左乙拉西坦和安慰剂治疗组中经历至少一种治疗紧急不良事件的患者总体比例大致相同,大多数事件在轻度至中度严重性。左乙拉西坦与认知障碍或药物引起的体重增加无关,但与某些患者的行为不良影响有关。

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