Pregabalin for the management of partial epilepsy

Philippe Ryvlin1, Emilio Perucca2, Sylvain Rheims11Service de Neurologie et d’Epileptologie, Hôpital Neurologique, Hospices Civils de Lyon, Université Lyon 1, INSERM U821 and CTRSIDÉE, Lyon, France; 2Clinical Trial Centre, Institute of Neurol...

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Autores principales: Philippe Ryvlin, Emilio Perucca, Sylvain Rheims
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Publicado: Dove Medical Press 2008
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spelling oai:doaj.org-article:9ccf453834e9493c9bcfa7db6de0d76d2021-12-02T02:43:14ZPregabalin for the management of partial epilepsy1176-63281178-2021https://doaj.org/article/9ccf453834e9493c9bcfa7db6de0d76d2008-11-01T00:00:00Zhttp://www.dovepress.com/pregabalin-for-the-management-of-partial-epilepsy-a2634https://doaj.org/toc/1176-6328https://doaj.org/toc/1178-2021Philippe Ryvlin1, Emilio Perucca2, Sylvain Rheims11Service de Neurologie et d’Epileptologie, Hôpital Neurologique, Hospices Civils de Lyon, Université Lyon 1, INSERM U821 and CTRSIDÉE, Lyon, France; 2Clinical Trial Centre, Institute of Neurology IRCCS C Mondino Foundation, and Clinical Pharmacology Unit, Department of Internal Medicine and Therapeutics, University of Pavia, Pavia, ItalyAbstract: Pregabalin is one of the latest antiepileptic drugs introduced for the treatment of partial epilepsy. Its efficacy and safety as adjunctive therapy in refractory partial epilepsy have been established in four double-blind placebo-controlled trials (n = 1396) and 4 long-term open-label studies (n = 1480). In 3 fixed-dose trials, the proportion of patients with a ≥50% reduction in seizure frequency across the effective dose-range (150–600 mg/day) ranged between 14% and 51%, with a clear dose-response relationship. Suppression of seizure activity could be demonstrated as early as day 2. The most frequently reported CNS-related adverse events included dizziness, somnolence, ataxia and fatigue, were usually mild or moderate, and tended to be dose related. In long-term studies, weight gain was reported as an adverse event by 24% of patients. When pregabalin dose was individualized to according to response within the 150 to 600 mg/day dose range, tolerability was considerably improved compared with use of a high-dose, fixed-dose regimen (600 mg/day) without titration. In long-term studies up to 4 years, no evidence of loss efficacy was identified. During the last year on pregabalin, 3.7% of patients were seizure-free. Pregabalin appears to be a useful addition to the therapeutic armamentariun for the management of refractory partial epilepsy.Keywords: pregabalin, antiepileptic drugs, adjunctive therapy, partial seizures, efficacy, tolerability, clinical trials Philippe RyvlinEmilio PeruccaSylvain RheimsDove Medical PressarticleNeurosciences. Biological psychiatry. NeuropsychiatryRC321-571Neurology. Diseases of the nervous systemRC346-429ENNeuropsychiatric Disease and Treatment, Vol 2008, Iss Issue 6, Pp 1211-1224 (2008)
institution DOAJ
collection DOAJ
language EN
topic Neurosciences. Biological psychiatry. Neuropsychiatry
RC321-571
Neurology. Diseases of the nervous system
RC346-429
spellingShingle Neurosciences. Biological psychiatry. Neuropsychiatry
RC321-571
Neurology. Diseases of the nervous system
RC346-429
Philippe Ryvlin
Emilio Perucca
Sylvain Rheims
Pregabalin for the management of partial epilepsy
description Philippe Ryvlin1, Emilio Perucca2, Sylvain Rheims11Service de Neurologie et d’Epileptologie, Hôpital Neurologique, Hospices Civils de Lyon, Université Lyon 1, INSERM U821 and CTRSIDÉE, Lyon, France; 2Clinical Trial Centre, Institute of Neurology IRCCS C Mondino Foundation, and Clinical Pharmacology Unit, Department of Internal Medicine and Therapeutics, University of Pavia, Pavia, ItalyAbstract: Pregabalin is one of the latest antiepileptic drugs introduced for the treatment of partial epilepsy. Its efficacy and safety as adjunctive therapy in refractory partial epilepsy have been established in four double-blind placebo-controlled trials (n = 1396) and 4 long-term open-label studies (n = 1480). In 3 fixed-dose trials, the proportion of patients with a ≥50% reduction in seizure frequency across the effective dose-range (150–600 mg/day) ranged between 14% and 51%, with a clear dose-response relationship. Suppression of seizure activity could be demonstrated as early as day 2. The most frequently reported CNS-related adverse events included dizziness, somnolence, ataxia and fatigue, were usually mild or moderate, and tended to be dose related. In long-term studies, weight gain was reported as an adverse event by 24% of patients. When pregabalin dose was individualized to according to response within the 150 to 600 mg/day dose range, tolerability was considerably improved compared with use of a high-dose, fixed-dose regimen (600 mg/day) without titration. In long-term studies up to 4 years, no evidence of loss efficacy was identified. During the last year on pregabalin, 3.7% of patients were seizure-free. Pregabalin appears to be a useful addition to the therapeutic armamentariun for the management of refractory partial epilepsy.Keywords: pregabalin, antiepileptic drugs, adjunctive therapy, partial seizures, efficacy, tolerability, clinical trials
format article
author Philippe Ryvlin
Emilio Perucca
Sylvain Rheims
author_facet Philippe Ryvlin
Emilio Perucca
Sylvain Rheims
author_sort Philippe Ryvlin
title Pregabalin for the management of partial epilepsy
title_short Pregabalin for the management of partial epilepsy
title_full Pregabalin for the management of partial epilepsy
title_fullStr Pregabalin for the management of partial epilepsy
title_full_unstemmed Pregabalin for the management of partial epilepsy
title_sort pregabalin for the management of partial epilepsy
publisher Dove Medical Press
publishDate 2008
url https://doaj.org/article/9ccf453834e9493c9bcfa7db6de0d76d
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AT emilioperucca pregabalinforthemanagementofpartialepilepsy
AT sylvainrheims pregabalinforthemanagementofpartialepilepsy
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