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Does a four-week delay in the introduction of medication alter the course of functional psychosis?

J Psychopharmacol. 1999;13(3):238-44. doi: 10.1177/026988119901300305.

Abstract

This study is an analysis of findings of a follow-up study of 105 patients with functional psychotic illness who had participated in a random and blind 4-week trial of pimozide, lithium, both and placebo. The intention was to examine the question of whether a 4-week delay in initiating antipsychotic treatment has a detrimental effect 2.5 years later. Detailed follow-up measures included need for care over the 2.5 years, treatments required, occupational decline, police contact, substance misuse, psychopathology and cognitive function. There was no evidence at all that those initially randomized to placebo had a poorer outcome in terms of any of these variables. It is concluded that a 4-week delay in initiating active treatment in patients with functional psychosis has no long-term adverse effects.

Publication types

  • Clinical Trial
  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Antimanic Agents / adverse effects
  • Antimanic Agents / therapeutic use
  • Antipsychotic Agents / administration & dosage*
  • Antipsychotic Agents / adverse effects
  • Antipsychotic Agents / therapeutic use*
  • Double-Blind Method
  • Employment
  • Female
  • Follow-Up Studies
  • Humans
  • Lithium / adverse effects
  • Lithium / therapeutic use
  • Male
  • Middle Aged
  • Pimozide / adverse effects
  • Pimozide / therapeutic use
  • Prognosis
  • Psychiatric Status Rating Scales
  • Psychotic Disorders / drug therapy*
  • Time Factors

Substances

  • Antimanic Agents
  • Antipsychotic Agents
  • Pimozide
  • Lithium