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拉莫三嗪。其药理学特性及在癫痫治疗中的临床疗效综述。

Lamotrigine. A review of its pharmacological properties and clinical efficacy in epilepsy.

作者信息

Goa K L, Ross S R, Chrisp P

机构信息

Adis International Limited, Auckland, New Zealand.

出版信息

Drugs. 1993 Jul;46(1):152-76. doi: 10.2165/00003495-199346010-00009.

Abstract

Lamotrigine is an antiepileptic drug which is believed to suppress seizures by inhibiting the release of excitatory neurotransmitters. Efficacy has been demonstrated for lamotrigine as add-on therapy to existing regimens in patients with resistant partial seizures. Total seizure frequency was reduced by 17 to 59% compared with placebo, and 13 to 67% of patients experienced reductions of > or = 50% in seizure frequency. Secondarily generalised tonic-clonic seizures respond well to lamotrigine, and there is preliminary evidence of improvement in patients with primary generalised seizures, Lennox-Gastaut syndrome and in children with multiple seizure types. Seizure control has been maintained in patients who have continued to receive lamotrigine as monotherapy after discontinuation of other medications. Results of one trial suggest similar efficacy for lamotrigine monotherapy as for carbamazepine, but confirmation of its use in this setting awaits more extensive controlled comparisons with established agents. Adverse events associated with lamotrigine as add-on therapy are typical of antiepileptic drugs, namely dizziness, ataxia and other CNS-related symptoms. Rash, which has occurred in 10% of patients in placebo-controlled trials, may be severe and its appearance has led to discontinuation of therapy in 1% of patients. Lamotrigine appears well tolerated in the longer term, but this facet of its profile requires further monitoring. Influences of valproic acid and enzyme-inducing anti-epileptics on lamotrigine eliminate necessitate dosage modification of lamotrigine. Conversely, lamotrigine has little apparent influence on the pharmacokinetics of other agents, although it may increase plasma concentrations of the active metabolite of carbamazepine during concomitant administration. Thus, lamotrigine permits improved seizure control in some patients with refractory partial seizures, and may prove to be especially effective in secondarily generalised tonic-clonic seizures. As is usual at this stage in a drug's development, several aspects of the profile of lamotrigine are incompletely defined, notably its efficacy in other seizure types, in children, as monotherapy, and its longer term tolerability. Nonetheless, lamotrigine presently offers a worthwhile alternative for the physician confronted with the challenge of treating patients with intractable partial seizures with or without secondarily generalised seizures, and shows potential for broader applications in other areas of epilepsy management.

摘要

拉莫三嗪是一种抗癫痫药物,据信它通过抑制兴奋性神经递质的释放来抑制癫痫发作。对于难治性部分性癫痫患者,拉莫三嗪作为现有治疗方案的附加疗法已证明有效。与安慰剂相比,总癫痫发作频率降低了17%至59%,13%至67%的患者癫痫发作频率降低了≥50%。继发性全身性强直阵挛性癫痫对拉莫三嗪反应良好,并且有初步证据表明原发性全身性癫痫、Lennox-Gastaut综合征患者以及患有多种癫痫发作类型的儿童的病情有所改善。在停用其他药物后继续接受拉莫三嗪单药治疗的患者中,癫痫发作得到了控制。一项试验结果表明,拉莫三嗪单药治疗的疗效与卡马西平相似,但在这种情况下其使用的确认有待与已确立的药物进行更广泛的对照比较。作为附加疗法,与拉莫三嗪相关的不良事件是抗癫痫药物的典型事件,即头晕、共济失调和其他中枢神经系统相关症状。皮疹在安慰剂对照试验中的发生率为10%,可能很严重,1%的患者因皮疹出现而停药。从长期来看,拉莫三嗪似乎耐受性良好,但其这方面的情况需要进一步监测。丙戊酸和酶诱导性抗癫痫药物对拉莫三嗪消除的影响需要调整拉莫三嗪的剂量。相反,拉莫三嗪对其他药物的药代动力学几乎没有明显影响,尽管在联合给药期间它可能会增加卡马西平活性代谢物的血浆浓度。因此,拉莫三嗪可使一些难治性部分性癫痫患者的癫痫发作得到更好的控制,并且可能在继发性全身性强直阵挛性癫痫中特别有效。正如药物研发现阶段常见的情况一样,拉莫三嗪的几个方面尚未完全明确,特别是其在其他癫痫发作类型、儿童、作为单药治疗时的疗效以及其长期耐受性。尽管如此,对于面临治疗伴有或不伴有继发性全身性癫痫的难治性部分性癫痫患者挑战的医生来说,拉莫三嗪目前提供了一个有价值的选择,并且在癫痫管理的其他领域显示出更广泛应用的潜力。

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