Literature DB >> 4061051

Long-term study of gamma-vinyl GABA in the treatment of epilepsy.

S A Pedersen, P Klosterskov, L Gram, M Dam.   

Abstract

The purpose of this study was to investigate the long-term efficacy and tolerability of gamma-vinyl GABA (GVG) in the treatment of epilepsy. 36 patients with severe therapy resistant epilepsies participated, the majority exhibiting complex partial seizures. The mean follow-up period was 9.3 months. GVG was administered as add-on therapy, to keep serum levels of concomitant treatment constant. The mean dose of GVG was 2.6 g's per day. Fifty-six per cent of the patients, including three patients with juvenile myoclonic epilepsy, experienced more than a 50% reduction in seizure frequency. No signs of tolerance development to the antiepileptic effect of GVG was demonstrated. Two patients were withdrawn from GVG treatment due to increased seizure frequency, and two due to side effects in the form of vomiting and nausea. Incidentally, the side effects observed were harmless and transient. Fifty per cent of the patients experienced no side effects at all. GVG seems to be a valuable antiepileptic compound. The results of this long-term study confirm observations from several short controlled trials.

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Year:  1985        PMID: 4061051     DOI: 10.1111/j.1600-0404.1985.tb00873.x

Source DB:  PubMed          Journal:  Acta Neurol Scand        ISSN: 0001-6314            Impact factor:   3.209


  16 in total

1.  Cognitive Activation of "Hyperexcitable Cortex" in JME: Can It Trigger Seizures?

Authors:  Gregory L Krauss
Journal:  Epilepsy Curr       Date:  2011-11       Impact factor: 7.500

Review 2.  Vigabatrin.

Authors:  E H Reynolds
Journal:  BMJ       Date:  1990-02-03

Review 3.  Vigabatrin. A review of its pharmacodynamic and pharmacokinetic properties, and therapeutic potential in epilepsy and disorders of motor control.

Authors:  S M Grant; R C Heel
Journal:  Drugs       Date:  1991-06       Impact factor: 9.546

Review 4.  A risk-benefit assessment of vigabatrin in the treatment of neurological disorders.

Authors:  J Srinivasan; A Richens
Journal:  Drug Saf       Date:  1994-05       Impact factor: 5.606

5.  A multicentre study of vigabatrin for drug-resistant epilepsy.

Authors:  T R Browne; R H Mattson; J K Penry; D B Smith; D M Treiman; B J Wilder; E Ben-Menachem; R M Miketta; K M Sherry; G K Szabo
Journal:  Br J Clin Pharmacol       Date:  1989       Impact factor: 4.335

Review 6.  Response to vigabatrin in relation to seizure type.

Authors:  R Michelucci; C A Tassinari
Journal:  Br J Clin Pharmacol       Date:  1989       Impact factor: 4.335

7.  The effect of vigabatrin on brain and platelet GABA-transaminase activities.

Authors:  J B Bolton; E Rimmer; J Williams; A Richens
Journal:  Br J Clin Pharmacol       Date:  1989       Impact factor: 4.335

8.  Effect of vigabatrin on sedation and cognitive function in patients with refractory epilepsy.

Authors:  R A Gillham; J Blacklaw; P J McKee; M J Brodie
Journal:  J Neurol Neurosurg Psychiatry       Date:  1993-12       Impact factor: 10.154

9.  Effects of vigabatrin on partial seizures and cognitive function.

Authors:  R A Grünewald; P J Thompson; R Corcoran; Z Corden; G D Jackson; J S Duncan
Journal:  J Neurol Neurosurg Psychiatry       Date:  1994-09       Impact factor: 10.154

Review 10.  Vigabatrin. Clinical pharmacokinetics.

Authors:  E Rey; G Pons; G Olive
Journal:  Clin Pharmacokinet       Date:  1992-10       Impact factor: 6.447

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