ADJUNCTIVE TREATMENT OF PARTIAL SEIZURES WITH TIAGABINE - A PLACEBO-CONTROLLED TRIAL

被引:94
作者
RICHENS, A
CHADWICK, DW
DUNCAN, JS
DAM, M
GRAM, L
MIKKELSEN, M
MORROW, J
MENGEL, H
SHU, V
MCKELVY, JF
PIERCE, MW
机构
[1] WALTON HOSP,LIVERPOOL L9 1AE,MERSEYSIDE,ENGLAND
[2] NATL HOSP NEUROL & NEUROSURG,LONDON WC1N 3BG,ENGLAND
[3] HVIDOVRE UNIV HOSP,COPENHAGEN,DENMARK
[4] ROYAL VICTORIA HOSP,BELFAST BT12 6BA,ANTRIM,NORTH IRELAND
[5] NOVO NORDISK AS,MALOV,DENMARK
[6] ABBOTT LABS,N CHICAGO,IL 60064
关键词
TIAGABINE; PARTIAL EPILEPSY; RESPONSE-DEPENDENT TRIAL;
D O I
10.1016/0920-1211(95)00006-V
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Tiagabine is a new antiepileptic drug which acts by a novel mechanism, inhibiting the reuptake of the inhibitory neurotransmitter gamma-aminobutyric acid (GABA) into neurones and glia. A double-blind, placebo-controlled, crossover trial was undertaken, based upon a response-dependent design. Ninety-four patients with complex partial seizures with or without secondary generalised tonic-clonic seizures were recruited into an open screening phase and tiagabine was added to their existing drug therapy in doses titrated to reduce seizure frequency by greater than or equal to 25% or to the limit of tolerance. Forty-six responders were subsequently randomised to a double-blind crossover trial in which tiagabine was compared with placebo. Forty-two patients completed the trial. A significant reduction in the frequency of complex partial and secondary generalised tonic clonic seizures was seen. Twenty-six percent had a reduction of greater than or equal to 50% in the frequency of their complex partial seizures, and of the 27 patients who also had secondary generalised tonic clonic seizures, 63% experienced a reduction of greater than or equal to 50%. No interactions with baseline antiepileptic drugs were detected and no serious adverse reactions occurred. The commonest adverse events were tiredness, dizziness and headache. We conclude that tiagabine has promising antiepileptic effects. Further trials are underway.
引用
收藏
页码:37 / 42
页数:6
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