An open study of tiagabine in partial epilepsy

被引:16
作者
Arroyo, S
Salas-Puig, J
机构
[1] Hosp Clin Barcelona, Unidad Epilepsia, Serv Neurol, E-08036 Barcelona, Spain
[2] Univ Barcelona, Inst Invest Biomed August Pi I Sunyer, IDIBAPS, E-08036 Barcelona, Spain
[3] Univ Asturias, Cent Hosp, Serv Neurol, Oviedo, Asturias, Spain
关键词
antiepileptic drugs; epilepsy; partial seizures; tiagabine;
D O I
10.33588/rn.3211.2001090
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective. To make an open assessment of the efficacy and tolerance of tiagabine in a population of patients with drug-resistant partial seizures. Patients and methods. We did an open multicentric study, in Spain, in which patients with partial epilepsy treated with one or more drugs were also given tiagabine. The main objective of the study was to determine the initial dose and titration of the drug and secondly to evaluate its efficacy and safety. We recorded data on the etiology of the seizures, their frequency and type and the occurrence of adverse effects. The study took place over a period of one year during which there were five appointments for consultation (after six weeks, three months, six months, nine months and one year). Results. We initially included 1,010 patients of which 941 fulfilled the selection criteria. The average age was 32.2 years. The aetiology was symptomatic in 45%. 61.7% of the patients had had previous treatment with three or more antiepileptic drugs. The doses were changed at a rate of 5 mg/day per week The average dose of tiagabine reached during the maintenance phase was 34 mg/day. 9.9% of the patients who were followed-up for one year (426) had no seizures after the second consultation (when the maintenance dose of tiagabine was reached). 35% of those who came to their final consultation appointment had had no seizures in the previous three months. 81.7% of the patients followed-up for a year had an overall reduction in the number of seizures of over 50% between the first and last consultations. An over 50% reduction in seizures was seen in both those of 12-25 years and the 26-65 years old (75% and 73.1% respectively) whilst 86.7% of the patients aged over 65 years also had this degree of improvement. 48.5% of the patients had some type of adverse effect during the study. Somnolence was the commonest side-effect (28.2% of the patients),followed by dizziness (21.5%). In most cases the adverse effects were transient or mild (tolerable) During the study 104 patients had their treatment with tiagabine stopped (11.1%) or intolerance and 113 patients (12%)because it was ineffective. No patient had non-convulsive status epilepticus. Conclusion. Tiagabine is an effective, well-tolerated drug when used as additional treatment in patients with partial epilepsy.
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页码:1041 / 1046
页数:6
相关论文
共 20 条
[1]   Tiagabine - A review of its pharmacodynamic and pharmacokinetic properties and therapeutic potential in the management of epilepsy [J].
Adkins, JC ;
Noble, S .
DRUGS, 1998, 55 (03) :437-460
[2]   International experience with tiagabine add-on therapy [J].
BenMenachem, E .
EPILEPSIA, 1995, 36 :S14-S21
[3]   Antiepileptic drugs, clinical trials, and the marketplace [J].
Brodie, MJ .
LANCET, 1996, 347 (9004) :777-779
[4]  
Dalby NO, 1997, NEUROSCI LETT, V229, P135
[5]   Cognitive and quality of life effects of differing dosages of tiagabine in epilepsy [J].
Dodrill, CB ;
Arnett, JL ;
Sommerville, KW ;
Shu, V .
NEUROLOGY, 1997, 48 (04) :1025-1031
[6]   Nonconvulsive status epilepticus in two patients receiving tiagabine treatment [J].
Eckardt, KM ;
Steinhoff, BJ .
EPILEPSIA, 1998, 39 (06) :671-674
[7]   Utility of the lethargic (lh/lh) mouse model of absence seizures in predicting the effects of lamotrigine, vigabatrin, tiagabine, gabapentin, and topiramate against human absence seizures [J].
Hosford, DA ;
Wang, Y .
EPILEPSIA, 1997, 38 (04) :408-414
[8]   A double-blind, placebo-controlled trial of tiagabine given three-times daily as add-on therapy for refractory partial seizures [J].
Kälviäinen, R ;
Brodie, MJ ;
Duncan, J ;
Chadwick, D ;
Edwards, D ;
Lyby, K .
EPILEPSY RESEARCH, 1998, 30 (01) :31-40
[9]   Safety of tiagabine: summary of 53 trials [J].
Leppik, IE ;
Gram, L ;
Deaton, R ;
Sommerville, KW .
EPILEPSY RESEARCH, 1999, 33 (2-3) :235-246
[10]  
LEPPIK IE, 1995, EPILIPSIA, V36, P10