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https://ahro.austin.org.au/austinjspui/handle/1/10412
Full metadata record
DC Field | Value | Language |
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dc.contributor.author | Berkovic, Samuel F | en |
dc.contributor.author | Knowlton, R C | en |
dc.contributor.author | Leroy, R F | en |
dc.contributor.author | Schiemann, J | en |
dc.contributor.author | Falter, U | en |
dc.date.accessioned | 2015-05-15T23:51:15Z | |
dc.date.available | 2015-05-15T23:51:15Z | |
dc.date.issued | 2007-07-11 | en |
dc.identifier.citation | Neurology 2007; 69(18): 1751-60 | en |
dc.identifier.govdoc | 17625106 | en |
dc.identifier.other | PUBMED | en |
dc.identifier.uri | https://ahro.austin.org.au/austinjspui/handle/1/10412 | en |
dc.description.abstract | To assess the efficacy and tolerability of adjunctive levetiracetam in patients with uncontrolled generalized tonic-clonic (GTC) seizures associated with idiopathic generalized epilepsies (IGE).This multicenter, randomized, double-blind, placebo-controlled, parallel-group study enrolled adults and children (4 to 65 years) with IGE experiencing >or=3 GTC seizures during the 8-week baseline period (4-week retrospective and 4-week prospective), despite receiving stable doses of one or two antiepileptic drugs (AEDs). Patients were randomized to levetiracetam (target dose 3,000 mg/day for adults; 60 mg/kg/day for children) or placebo and a 4-week titration period was followed by a 20-week evaluation period.Of 229 patients screened, 164 were randomized (levetiracetam, n = 80; placebo, n = 84). Levetiracetam produced a greater mean reduction in GTC seizure frequency per week over the treatment period (56.5%) than placebo (28.2%; p = 0.004). The percentage of patients who had >or=50% reduction of GTC seizure frequency per week (responders) during the treatment period was 72.2% for levetiracetam and 45.2% for placebo (p < 0.001; OR 3.28; 95% CI 1.68 to 6.38). During the first 2-week treatment 64.6% of patients on levetiracetam and 45.2% on placebo (p = 0.018) were classified as responders. During the evaluation period the percent of patients free of GTC seizures (34.2% vs 10.7%; p < 0.001) and all seizure types (24.1% vs 8.3%; p = 0.009) was greater for levetiracetam than placebo. Levetiracetam was well tolerated with 1.3% of patients discontinuing therapy due to adverse events vs 4.8% on placebo.Adjunctive levetiracetam is an effective and well-tolerated antiepileptic drug for treating generalized tonic-clonic seizures in patients with idiopathic generalized epilepsies. | en |
dc.language.iso | en | en |
dc.subject.other | Adolescent | en |
dc.subject.other | Adult | en |
dc.subject.other | Aged | en |
dc.subject.other | Anticonvulsants.therapeutic use | en |
dc.subject.other | Child | en |
dc.subject.other | Child, Preschool | en |
dc.subject.other | Double-Blind Method | en |
dc.subject.other | Epilepsy, Generalized.drug therapy | en |
dc.subject.other | Female | en |
dc.subject.other | Humans | en |
dc.subject.other | Male | en |
dc.subject.other | Middle Aged | en |
dc.subject.other | Piracetam.analogs & derivatives.therapeutic use | en |
dc.subject.other | Placebos | en |
dc.subject.other | Quality of Life | en |
dc.subject.other | Questionnaires | en |
dc.subject.other | Research Design | en |
dc.subject.other | Treatment Outcome | en |
dc.title | Placebo-controlled study of levetiracetam in idiopathic generalized epilepsy. | en |
dc.type | Journal Article | en |
dc.identifier.journaltitle | Neurology | en |
dc.identifier.affiliation | Epilepsy Research Center, Heidelberg Repatriation Hospital, Banksia Street, West Heidelberg, Victoria, Australia | en |
dc.identifier.doi | 10.1212/01.wnl.0000268699.34614.d3 | en |
dc.description.pages | 1751-60 | en |
dc.relation.url | https://pubmed.ncbi.nlm.nih.gov/17625106 | en |
dc.contributor.corpauthor | Levetiracetam N01057 Study Group | en |
dc.type.austin | Journal Article | en |
local.name.researcher | Berkovic, Samuel F | |
item.cerifentitytype | Publications | - |
item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
item.fulltext | No Fulltext | - |
item.openairetype | Journal Article | - |
item.grantfulltext | none | - |
item.languageiso639-1 | en | - |
crisitem.author.dept | Epilepsy Research Centre | - |
crisitem.author.dept | Neurology | - |
Appears in Collections: | Journal articles |
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