An open-label, prospective study of levetiracetam in children and adolescents with Tourette syndrome

Eur J Paediatr Neurol. 2009 Nov;13(6):541-5. doi: 10.1016/j.ejpn.2008.12.006. Epub 2009 Feb 10.

Abstract

Objectives: To evaluate the usefulness of levetiracetam (LEV) for the treatment of tics in patients with Tourette syndrome (TS) by means of a prospective, open-label, 12-week study.

Material and methods: Twenty-nine patients with TS who received LEV to control their tics were admitted to the study. The authors recorded the following variables: initial status (Yale Global Tic Severity Scale - YGTSS - and the scale of Modified Clinical Global Impression -MCGI), the clinical status at 3 months using the same scales, and clinical/medical impression of improvement.

Results: The mean age of the patients studied was 12 years; 25 males (86%) and 4 females (14%). Participants received 800-2000 mg/day of LEV. Of the 29 patients, 21 children (72%) improved according to YGTSS and MCGI scores. Mean YGTSS Total Tic Score at baseline and after treatment with LEV were 67 and 44, respectively. The statistical analysis confirmed a significant improvement with a p-value of <0.001 on the YGTSS and MCGI. In 3 cases, treatment was suspended due to adverse effects.

Conclusions: Treatment with LEV can constitute a treatment option for tics in patients with TS. Double-blind trials of longer duration are needed in larger samples in order to establish both the benefit, as well as what patients are eligible for treatment.

Publication types

  • Clinical Trial

MeSH terms

  • Adolescent
  • Child
  • Dose-Response Relationship, Drug
  • Female
  • Humans
  • Levetiracetam
  • Male
  • Nootropic Agents / therapeutic use*
  • Piracetam / analogs & derivatives*
  • Piracetam / therapeutic use
  • Prospective Studies
  • Psychiatric Status Rating Scales
  • Severity of Illness Index
  • Tourette Syndrome / drug therapy*
  • Treatment Outcome

Substances

  • Nootropic Agents
  • Levetiracetam
  • Piracetam