Literature DB >> 22050371

Adjunctive levetiracetam in children, adolescents, and adults with primary generalized seizures: open-label, noncomparative, multicenter, long-term follow-up study.

Norman Delanty1, John Jones, Françoise Tonner.   

Abstract

PURPOSE: To evaluate the long-term efficacy and tolerability of adjunctive levetiracetam (LEV) in patients with uncontrolled idiopathic generalized epilepsy (IGE).
METHODS: This phase III, open-label, long-term, follow-up study (N167; NCT00150748) enrolled patients (4 to <65 years) with primary generalized seizures (tonic-clonic, myoclonic, absence). Patients received adjunctive LEV at individualized doses (1,000-4,000 mg/day; 20-80 mg/kg/day for children/adolescents weighing <50 kg). Efficacy results are reported for all seizure types [intention-to-treat (ITT) population, N = 217] and subpopulations with tonic-clonic (n = 152), myoclonic (n = 121), and/or absence (n = 70) seizures at baseline. KEY
FINDINGS: One hundred twenty-five (57.6%) of 217 patients were still receiving treatment at the end of the study. Mean (standard deviation, SD) LEV dose was 2,917.5 (562.9) mg/day. Median (Q1-Q3) exposure to LEV was 2.1 (1.5-2.8) years, and the maximum duration was 4.6 years. Most patients were taking one (124/217, 57.1%) or ≥2 (92/217, 42.4%) concomitant antiepileptic drugs (AEDs). Seizure freedom of ≥6 months (all seizure types; primary efficacy end point) was achieved by 122 (56.2%) of 217 patients, and 49 (22.6%) of 217 patients had complete seizure freedom. Seizure freedom of ≥6 months from tonic-clonic, myoclonic, and absence seizures was achieved by 95 (62.5%) of 152, 75 (62.0%) of 121, and 44 (62.9%) of 70 patients, respectively. Mean (SD) maximum seizure freedom duration was 371.7 (352.4) days. At least one treatment-emergent adverse event (TEAE) was reported by 165 (76%) of 217 patients; most TEAEs were mild/moderate in severity, with no indication of an increased incidence over time. Seventeen (7.8%) of 217 patients discontinued medication because of TEAEs. The most common psychiatric TEAEs were depression (16/217, 7.4%), insomnia (9/217, 4.1%), nervousness (8/217, 3.7%), and anxiety (7/217, 3.2%). SIGNIFICANCE: Adjunctive LEV (range 1,000-4,000 mg/day) demonstrated efficacy as a long-term treatment for primary generalized seizures in children, adolescents, and adults with IGE, and was well tolerated. Wiley Periodicals, Inc.
© 2011 International League Against Epilepsy.

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Year:  2011        PMID: 22050371     DOI: 10.1111/j.1528-1167.2011.03300.x

Source DB:  PubMed          Journal:  Epilepsia        ISSN: 0013-9580            Impact factor:   5.864


  10 in total

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2.  Levetiracetam-induced acute psychotic episode.

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Journal:  Innov Clin Neurosci       Date:  2012-10

Review 3.  Treatment and care of women with epilepsy before, during, and after pregnancy: a practical guide.

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Journal:  Ther Adv Neurol Disord       Date:  2022-06-11       Impact factor: 6.430

4.  Levetiracetam-induced acute psychosis in a child.

Authors:  Syed Ahmed Zaki; Saurabh Gupta
Journal:  Indian J Pharmacol       Date:  2014 May-Jun       Impact factor: 1.200

5.  Levetiracetam induced acute reversible psychosis in a patient with uncontrolled seizures.

Authors:  Nithin Kumar; H S Swaroop; Ananya Chakraborty; Suhas Chandran
Journal:  Indian J Pharmacol       Date:  2014 Sep-Oct       Impact factor: 1.200

6.  Phenytoin Augmentation of Levetiracetam Treatment: A Case of Forced Normalization With Emergence of Psychosis.

Authors:  Michael Esang; Vijaya Padma Kotapati; Saeed Ahmed
Journal:  Cureus       Date:  2018-04-05

7.  Adjunctive levetiracetam in the treatment of Chinese and Japanese adults with generalized tonic-clonic seizures: A double-blind, randomized, placebo-controlled trial.

Authors:  Liwen Wu; Kazuichi Yagi; Zhen Hong; Weiping Liao; Xuefeng Wang; Dong Zhou; Yushi Inoue; Yoko Ohtsuka; Mutsuo Sasagawa; Kiyohito Terada; Xinlu Du; Yoshihiro Muramoto; Tomonobu Sano
Journal:  Epilepsia Open       Date:  2018-09-29

8.  A pharmacogenomic assessment of psychiatric adverse drug reactions to levetiracetam.

Authors:  Ciarán Campbell; Mark McCormack; Sonn Patel; Caragh Stapleton; Dheeraj Bobbili; Roland Krause; Chantal Depondt; Graeme J Sills; Bobby P Koeleman; Pasquale Striano; Federico Zara; Josemir W Sander; Holger Lerche; Wolfram S Kunz; Kari Stefansson; Hreinn Stefansson; Colin P Doherty; Erin L Heinzen; Ingrid E Scheffer; David B Goldstein; Terence O'Brien; David Cotter; Samuel F Berkovic; Sanjay M Sisodiya; Norman Delanty; Gianpiero L Cavalleri
Journal:  Epilepsia       Date:  2022-04-01       Impact factor: 6.740

Review 9.  Clinical pharmacology and pharmacokinetics of levetiracetam.

Authors:  Chanin Wright; Jana Downing; Diana Mungall; Owais Khan; Amanda Williams; Ekokobe Fonkem; Darin Garrett; Jose Aceves; Batool Kirmani
Journal:  Front Neurol       Date:  2013-12-04       Impact factor: 4.003

10.  Clinical outcomes of intravenous levetiracetam treatment in patients with renal impairment.

Authors:  Anyamanee Lapmag; Sunee Lertsinudom; Aporanee Chaiyakam; Kittisak Sawanyawisuth; Somsak Tiamkao
Journal:  Neurol Int       Date:  2018-09-25
  10 in total

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