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首页> 外文期刊>The annals of pharmacotherapy >Rufinamide: a new antiepileptic medication for the treatment of seizures associated with lennox-gastaut syndrome.
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Rufinamide: a new antiepileptic medication for the treatment of seizures associated with lennox-gastaut syndrome.

机译:Rufinamide:一种新的抗癫痫药,用于治疗与lennox-gastaut综合征相关的癫痫发作。

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摘要

OBJECTIVE: To review the pharmacology, pharmacokinetics, efficacy, and safety of rufinamide in the treatment of epileptic seizures and describe its potential place in therapy. DATA SOURCES: MEDLINE (1966-January 2010) and PubMed (1966-January 2010) literature searches were conducted to identify primary literature investigating rufinamide. References from selected publications discussing rufinamide, as well as the package insert, were reviewed. STUDY SELECTION AND DATA EXTRACTION: Published controlled trials describing the efficacy and safety of rufinamide were given preference. Available abstracts were also reviewed. Four published trials were identified and included and a retrospective review of the clinical use of rufinamide was also analyzed. The remainder of the information described is from 4 abstracts. DATA SYNTHESIS: Rufinamide is a new antiepileptic agent that differs structurally from other antiepileptic drugs and is approved as adjunctive therapy for Lennox-Gastaut syndrome (LGS). It presumably provides its antiseizure activity by prolonging sodium channel inactivity, stabilizing cell membranes. It is absorbed and metabolized extensively, then excreted renally as an inactive metabolite. Clinical trials show that adjunctive rufinamide is effective at reducing seizure frequency in patients with LGS and refractory partial seizures. Rufinamide showed no effect on cognitive function in patients with refractory partial seizures. Short-term adverse event rates were similar to those of placebo. Safety data from long-term studies show that rufinamide is well tolerated, causing headache, dizziness, and fatigue at rates of >10%. Rufinamide has few clinically relevant drug interactions, although it does increase phenytoin serum concentrations, while valproate increases rufinamide serum concentrations. CONCLUSIONS: Data show that rufinamide is safe and effective as an adjunctive agent for LGS and may be used to treat partial seizures. The benefits of rufinamide include its pharmacokinetics, limited drug interactions, and lack of effect on cognitive function, but its use is limited by the rarity of LGS and the lack of comparative data with other antiepileptic agents.
机译:目的:探讨芦丁酰胺治疗癫痫发作的药理学,药代动力学,疗效和安全性,并描述其在治疗中的潜在地位。数据来源:进行了MEDLINE(1966年-2010年1月)和PubMed(1966年-2010年1月)文献检索,以鉴定研究芦丁酰胺的主要文献。审查了有关rufinamide的精选出版物的参考文献以及包装说明书。研究的选择和数据提取:优先选择描述鲁芬酰胺的疗效和安全性的已发表对照试验。还审查了可用的摘要。确定并纳入了四项已发表的试验,并对芦丁酰胺的临床使用进行了回顾性回顾。所描述的其余信息来自4个摘要。数据合成:Rufinamide是一种新型抗癫痫药,其结构与其他抗癫痫药不同,已被批准作为Lennox-Gastaut综合征(LGS)的辅助疗法。据推测,它可以通过延长钠通道的无活性,稳定细胞膜来提供抗癫痫活性。它被广泛吸收和代谢,然后作为非活性代谢物经肾脏排泄。临床试验表明,rufinamide辅助剂可有效降低LGS和难治性部分性癫痫发作的发作频率。鲁芬酰胺对难治性部分性癫痫患者的认知功能无影响。短期不良事件发生率与安慰剂相似。长期研究的安全性数据表明,rufinamide耐受性良好,可导致头痛,头晕和疲劳,发生率> 10%。鲁芬酰胺几乎没有与临床相关的药物相互作用,尽管它确实会增加苯妥英钠的血清浓度,而丙戊酸盐会提高鲁芬酰胺的血清浓度。结论:数据表明,芦丁酰胺作为LGS的辅助剂是安全有效的,可用于治疗部分性癫痫。 rufinamide的优势包括其药代动力学,有限的药物相互作用以及对认知功能的影响,但其使用受到LGS稀少和缺乏与其他抗癫痫药比较数据的限制。

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