Treatment of neuroleptic induced akathisia with the 5-HT2 antagonist ritanserin

Psychopharmacol Bull. 1990;26(3):373-6.

Abstract

Akathisia is a frequent and distressing side effect of antipsychotic medication. Little is known about its pathophysiology. Treatment trials of serotonin antagonists in Parkinson's disease and neuroleptic-induced Parkinsonism have been disappointing, with the possible exception of akathisia which has been reported to respond favorably to ritanserin. We report first results of a single-blind trial of ritanserin in the treatment of neuroleptic-induced akathisia. Ten patients received a mean dose of 13.5 mg/day (SD +/- 5.8) ritanserin for 2 to 4 days. Treatment response was assessed by the Hillside Akathisia Scale (HAS). HAS baseline ratings were 16.4 (+/- 6). After 3 days of treatment, these values dropped to 7.4 (+/- 5.2). This amelioration was statistically significant (p = .0069 matched-pairs signed rank test). Two patients did not respond. These results, although preliminary in nature, are encouraging and warrant further studies.

Publication types

  • Clinical Trial

MeSH terms

  • Administration, Oral
  • Adult
  • Akathisia, Drug-Induced*
  • Antipsychotic Agents / adverse effects*
  • Female
  • Humans
  • Male
  • Piperidines / administration & dosage
  • Piperidines / therapeutic use*
  • Psychomotor Agitation / drug therapy
  • Ritanserin
  • Serotonin Antagonists / administration & dosage
  • Serotonin Antagonists / therapeutic use*

Substances

  • Antipsychotic Agents
  • Piperidines
  • Serotonin Antagonists
  • Ritanserin