Patient compliance to a new enteric-coated weekly formulation of fluoxetine during continuation treatment of major depressive disorder

J Clin Psychiatry. 2000 Dec;61(12):928-32. doi: 10.4088/jcp.v61n1207.

Abstract

Background: A new formulation of enteric-coated fluoxetine given once weekly could be a useful option for the long-term treatment of depression, but compliance to once-weekly fluoxetine treatment has not been assessed.

Method: Patients were adults from the United Kingdom who had responded to fluoxetine treatment for a current episode of depression (DSM-IV criteria). In the baseline assessment phase, all patients (N = 117) were continued on 20 mg of open-label fluoxetine once daily for 4 weeks. In the follow-up phase, patients (N = 109) were randomly assigned to once-weekly or once-daily fluoxetine for 3 months. Patient compliance was monitored by electronic devices during both phases of the study.

Results: Compliance to once-weekly fluoxetine treatment was higher than compliance to once-daily fluoxetine (85.9% vs. 79.4%, respectively).

Conclusion: Once-weekly fluoxetine treatment allows for new flexibility for both the clinician and the patient, and this study alleviates the concern that patients will forget weekly doses.

Publication types

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

MeSH terms

  • Adult
  • Depressive Disorder / diagnosis
  • Depressive Disorder / drug therapy*
  • Depressive Disorder / psychology
  • Drug Administration Schedule
  • Drug Packaging / instrumentation
  • Female
  • Fluoxetine / administration & dosage*
  • Fluoxetine / therapeutic use
  • Humans
  • Male
  • Middle Aged
  • Patient Compliance
  • Psychiatric Status Rating Scales / statistics & numerical data
  • Secondary Prevention
  • Tablets, Enteric-Coated
  • Treatment Outcome

Substances

  • Tablets, Enteric-Coated
  • Fluoxetine