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丙戊酸和拉莫三嗪治疗耐药性癫痫患儿:第一年之后。

Valproate and lamotrigine in pediatric patients with refractory epilepsy: after the first year.

机构信息

Laboratory of Clinical Neurophysiology, Institute of Psychiatry, University of São Paulo School of Medicine Hospital das Clínicas, São Paulo, Brazil.

出版信息

Pediatr Neurol. 2013 Jun;48(6):436-42. doi: 10.1016/j.pediatrneurol.2013.01.005.

Abstract

The combination of lamotrigine and valproate/divalproex sodium has been shown to be effective in the treatment of refractory epilepsy. This study aims to evaluate the pharmacologic properties of using this combination in a pediatric population refractory to antiepileptic drugs, with an extended follow-up. We studied a group of 51 patients, ranging from 4 to 16 years of age. Sixteen patients (31.4%) had generalized epilepsy and 35 (69.6%) had focal epilepsy. The combination was effective in 39 patients (76.5%) in the first year of follow-up and in 36 patients (70.6%) in the second year, with a reduction in drop attacks observed in 22 (88.5%). Adverse effects included rash, leading to discontinuation in four patients (7.8%). Slower introduction of lamotrigine minimizes adverse effects, thereby improving quality of life and adherence to treatment. In addition, therapeutic efficacy is maintained with lower doses of lamotrigine, even after the first year of treatment.

摘要

拉莫三嗪与丙戊酸钠/丙戊酸二钠联合应用已被证明对治疗耐药性癫痫有效。本研究旨在评估在对抗癫痫药物耐药的儿科人群中使用这种联合治疗的药效学特性,并进行了延长随访。我们研究了一组 51 名年龄在 4 至 16 岁的患者。16 名患者(31.4%)患有全面性癫痫,35 名患者(69.6%)患有局灶性癫痫。在随访的第一年,39 名患者(76.5%)和第二年的 36 名患者(70.6%)联合治疗有效,22 名患者(88.5%)的跌倒发作减少。不良反应包括皮疹,导致 4 名患者(7.8%)停药。拉莫三嗪的引入速度较慢可最大限度地减少不良反应,从而提高生活质量和治疗依从性。此外,即使在治疗的第一年之后,较低剂量的拉莫三嗪也能维持治疗效果。

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