Literature DB >> 7975572

Guidelines for treating epilepsy in the age of felbamate, vigabatrin, lamotrigine, and gabapentin.

K D Laxer1.   

Abstract

For the first time in 15 years, new antiepileptic medications are available for the treatment of patients with seizure disorders. These drugs have demonstrated efficacy in animal models of epilepsy and in controlled clinical trials. Felbamate was licensed in 1993 for use as adjunctive therapy or monotherapy in adults with partial or tonic-clonic seizures and as adjunctive therapy for children with the Lennox-Gastaut syndrome. Gabapentin was approved January 1994 as adjunctive therapy in patients 12 years or older with partial seizures, with or without secondary generalization. Lamotrigine is expected to be approved this year for the treatment of partial and tonic-clonic seizures in adults. Last, a new drug application has been filed for vigabatrin this year, with possible licensing next year. These four anticonvulsants present new options in the treatment of patients with refractory epilepsy and are not merely congeners of previously available treatments. They have unique clinical spectrums and are reported to be safer and better tolerated than conventional therapy. Trials to compare their use with that of conventional therapy have not been done, and their use in the initial treatment of patients with epilepsy is not completely clear.

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Year:  1994        PMID: 7975572      PMCID: PMC1011415     

Source DB:  PubMed          Journal:  West J Med        ISSN: 0093-0415


  27 in total

Review 1.  Myocardial beta-adrenoceptor function and regulation in heart failure: implications for therapy.

Authors:  D B Barnett
Journal:  Br J Clin Pharmacol       Date:  1989-05       Impact factor: 4.335

2.  The effects of carbamazepine on patients with psychomotor epilepsy: results of a double-blind study.

Authors:  E A Rodin; C S Rim; P M Rennick
Journal:  Epilepsia       Date:  1974-12       Impact factor: 5.864

3.  Effect of CGP 17/582, a selective beta-adrenoceptor antagonist, on the haemodynamic and hypokalaemic response to adrenaline.

Authors:  K F Whyte; P J De Vane; R Whitesmith; A Kelman; J L Reid
Journal:  Br J Clin Pharmacol       Date:  1989-05       Impact factor: 4.335

4.  Comparison of carbamazepine, phenobarbital, phenytoin, and primidone in partial and secondarily generalized tonic-clonic seizures.

Authors:  R H Mattson; J A Cramer; J F Collins; D B Smith; A V Delgado-Escueta; T R Browne; P D Williamson; D M Treiman; J O McNamara; C B McCutchen
Journal:  N Engl J Med       Date:  1985-07-18       Impact factor: 91.245

5.  Valproic acid hepatic fatalities. II. US experience since 1984.

Authors:  F E Dreifuss; D H Langer; K A Moline; J E Maxwell
Journal:  Neurology       Date:  1989-02       Impact factor: 9.910

6.  Effects of long-term vigabatrin on somatosensory-evoked potentials in epileptic patients.

Authors:  C Liegeois-Chauvel; P Marquis; D Gisselbrecht; R Pantieri; D Beaumont; P Chauvel
Journal:  Epilepsia       Date:  1989       Impact factor: 5.864

7.  Effect of felbamate on phenytoin and carbamazepine serum concentrations.

Authors:  N M Graves; G B Holmes; R H Fuerst; I E Leppik
Journal:  Epilepsia       Date:  1989 Mar-Apr       Impact factor: 5.864

8.  Pharmacological studies on lamotrigine, a novel potential antiepileptic drug: I. Anticonvulsant profile in mice and rats.

Authors:  A A Miller; P Wheatley; D A Sawyer; M G Baxter; B Roth
Journal:  Epilepsia       Date:  1986 Sep-Oct       Impact factor: 5.864

9.  Pharmacological studies on lamotrigine, a novel potential antiepileptic drug: II. Neurochemical studies on the mechanism of action.

Authors:  M J Leach; C M Marden; A A Miller
Journal:  Epilepsia       Date:  1986 Sep-Oct       Impact factor: 5.864

10.  Felbamate in the treatment of refractory partial-onset seizures.

Authors:  P K Jensen
Journal:  Epilepsia       Date:  1993       Impact factor: 5.864

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  1 in total

1.  Ligand binding studies, preliminary structure-activity relationship and detailed mechanistic characterization of 1-phenyl-6,6-dimethyl-1,3,5-triazine-2,4-diamine derivatives as inhibitors of Escherichia coli dihydrofolate reductase.

Authors:  Bharath Srinivasan; Sam Tonddast-Navaei; Jeffrey Skolnick
Journal:  Eur J Med Chem       Date:  2015-09-05       Impact factor: 6.514

  1 in total

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