Pediatric Neurology
Volume 30, Issue 4 , Pages 254-256, April 2004

Levetiracetam in the treatment of Lennox-Gastaut syndrome

  • Emily C de los Reyes, MD

      Affiliations

    • University of Arkansas for Medical Sciences, Arkansas Children's Hospital, Little Rock, Arkansas, USA
    • Corresponding Author InformationCommunications should be addressed to:Dr. de los Reyes; Division of Neurology; Children's Hospital; 700 Children's Drive; Columbus, OH 43205, USA.
  • ,
  • Gregory B Sharp, MD

      Affiliations

    • University of Arkansas for Medical Sciences, Arkansas Children's Hospital, Little Rock, Arkansas, USA
  • ,
  • Jane P Williams, PhD

      Affiliations

    • University of Arkansas for Medical Sciences, Arkansas Children's Hospital, Little Rock, Arkansas, USA
  • ,
  • Sue E Hale, RN

      Affiliations

    • University of Arkansas for Medical Sciences, Arkansas Children's Hospital, Little Rock, Arkansas, USA

Received 3 June 2003; accepted 4 September 2003.

Abstract 

Lennox-Gastaut syndrome is an epileptic encephalopathy characterized by multiple seizure types, mental retardation, and a slow spike-and-wave pattern on electroencephalography. Medical intractability is common. We identified a case series of six patients diagnosed with Lennox-Gastaut syndrome in which levetiracetam was initiated as add-on therapy for the management of seizures. At follow-up, four patients experienced 100% reduction of their myoclonic seizures; two patients had greater than 50% reduction of their atonic seizures, and four patients experienced 100% reduction in their generalized tonic-clonic seizures. Tonic seizures were not responsive to treatment. The most common side effect was irritability; the most positive change involved alertness. In this small sample, levetiracetam appeared effective in reducing seizures in Lennox-Gastaut syndrome. This preliminary study is limited by its retrospective design and small number of patients, but positive findings warrant a larger scale, multicenter study.

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PII: S0887-8994(03)00472-7

doi:10.1016/j.pediatrneurol.2003.09.007

Pediatric Neurology
Volume 30, Issue 4 , Pages 254-256, April 2004