A double-blind, placebo-controlled trial of tiagabine given three-times daily as add-on therapy for refractory partial seizures

被引:69
作者
Kälviäinen, R [1 ]
Brodie, MJ
Duncan, J
Chadwick, D
Edwards, D
Lyby, K
机构
[1] Kuopio Univ Hosp, Dept Neurol, SF-70210 Kuopio, Finland
[2] Univ Glasgow, Western Infirm, Dept Med & Therapeut, Epilepsy Unit, Glasgow G11 6NT, Lanark, Scotland
[3] Chalfont Ctr Epilepsy, Chalfont St Peter, Bucks, England
[4] Univ Liverpool, Dept Neurol Sci, Walton Ctr Neurol & Neurosurg, Liverpool L69 3BX, Merseyside, England
[5] Novo Nordisk AS, DK-2880 Bagsvaerd, Denmark
关键词
antiepileptic drugs; add-on therapy; partial seizures; tiagabine;
D O I
10.1016/S0920-1211(97)00082-X
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
In a multicentre, double-blind, parallel-group, placebo-controlled trial, a three-times daily regimen of tiagabine was evaluated as add-on therapy in 154 adult patients with refractory partial seizures. A total of 77 patients were randomised to treatment in each arm. Tiagabine HCl was titrated from an initial dose of 12-30 mg/day over 4 weeks. During the 12-week fixed-dose period, there was a significant reduction in the median 4-weekly seizure rate for all partial seizures and simple partial seizures (P < 0.05 in each case). Furthermore, the proportion of patients with a reduction of 50% or more in all partial seizures was higher in the tiagabine group than in the placebo group (14 versus 6%), though the difference did not achieve statistical significance. The difference with respect to simple partial seizures was significant (21 versus 6%, P < 0.01). The percentage of patients achieving an increase of at least 50% in the proportion of days free of all partial seizures was significantly greater in the tiagabine group compared to placebo (14 versus 4%, P < 0.01). Tiagabine did not appear to influence the plasma concentrations of other concomitant antiepileptic drugs and was generally well tolerated, with most drug-related adverse events being mild or moderate in severity. The most common adverse events were dizziness, asthenia, headache and somnolence. Adverse event incidence was similar between tiagabine and placebo groups, except for dizziness which was more common with tiagabine (29 versus 10%, P < 0.01). Tiagabine had no significant effects on laboratory tests or vital signs. The present study shows that tiagabine, at a dose of 10 mg administered three-times daily, which is at the lower end of the usual recommended dose range (30-50 mg/day, tiagabine base), is generally well tolerated and demonstrates efficacy for the treatment of refractory partial seizures. (C) 1998 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:31 / 40
页数:10
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