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加巴喷丁作为难治性部分性癫痫的附加治疗:一项双盲、安慰剂对照、平行组研究。美国加巴喷丁研究组5号。

Gabapentin as add-on therapy in refractory partial epilepsy: a double-blind, placebo-controlled, parallel-group study. The US Gabapentin Study Group No. 5.

出版信息

Neurology. 1993 Nov;43(11):2292-8. doi: 10.1212/wnl.43.11.2292.

Abstract

Gabapentin, administered as add-on therapy, was safe and effective in this 12-week, multicenter, placebo-controlled, parallel-group study in 306 patients with refractory partial epilepsy. For patients in each gabapentin treatment group (600, 1,200, or 1,800 mg/d), the mean response ratio was significantly better than that of a placebo group. The percentage of patients achieving at least a 50% reduction in seizure frequency was 8% among placebo-treated patients and ranged from 18% to 26% for patients who received gabapentin. Adverse events were generally mild and transient and occurred at a slightly higher frequency among patients receiving gabapentin than among those receiving placebo. Gabapentin did not affect the serum concentrations of concurrent antiepileptic drugs and was not regularly associated with any deviations in clinical laboratory values. Gabapentin's low inherent toxicity and its lack of drug interactions make it an ideal candidate for use as add-on therapy in patients with refractory partial epilepsy.

摘要

在这项为期12周、多中心、安慰剂对照、平行组研究中,加用加巴喷丁对306例难治性部分性癫痫患者安全有效。在每个加巴喷丁治疗组(600、1200或1800mg/天)的患者中,平均缓解率显著优于安慰剂组。安慰剂治疗患者中癫痫发作频率至少降低50%的患者比例为8%,而接受加巴喷丁治疗的患者这一比例为18%至26%。不良事件一般为轻度且短暂,接受加巴喷丁治疗的患者中不良事件发生频率略高于接受安慰剂治疗的患者。加巴喷丁不影响同时服用的抗癫痫药物的血清浓度,也与临床实验室值的任何偏差无规律性关联。加巴喷丁固有的低毒性及其缺乏药物相互作用使其成为难治性部分性癫痫患者加用治疗的理想选择。

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