Levetiracetam in tardive dyskinesia

Clin Neuropharmacol. 2006 Sep-Oct;29(5):265-8. doi: 10.1097/01.WNF.0000228807.49044.7D.

Abstract

Objectives: The aim of this study was to evaluate the effect of levetiracetam on tardive dyskinesia (TD), which is known to be a major limitation of chronic antipsychotic drug therapy, particularly with conventional antipsychotics.

Methods: Sixteen patients suffering from chronic psychosis with TD were enrolled consecutively. Levetiracetam was given in gradually increasing doses, starting with 125 twice a day until the best clinical benefit was achieved (mean dosage, 2,290 mg; range, 1,000-3,000 mg). Tardive dyskinesia was assessed using the Abnormal Involuntary Movement Scale at baseline and after 1 month and 3 months of treatment with levetiracetam.

Results: Compared with baseline, there was a significant improvement in the Abnormal Involuntary Movement Scale score after 1 month still present after 3 months (P < 0.001). All patients well tolerated levetiracetam, except one who dropped out of the trial after the first 2 weeks owing to excessive drowsiness.

Conclusions: The results of this open-label observational study suggest that levetiracetam is a well-tolerated drug and effectively controls TD.

Publication types

  • Clinical Trial
  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Aged, 80 and over
  • Anticonvulsants / therapeutic use*
  • Antipsychotic Agents / adverse effects
  • Dyskinesia, Drug-Induced / drug therapy*
  • Dyskinesia, Drug-Induced / etiology
  • Female
  • Humans
  • Levetiracetam
  • Male
  • Middle Aged
  • Piracetam / analogs & derivatives*
  • Piracetam / therapeutic use
  • Psychotic Disorders / drug therapy
  • Time Factors

Substances

  • Anticonvulsants
  • Antipsychotic Agents
  • Levetiracetam
  • Piracetam