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An open-label, rater-blinded, augmentation study of aripiprazole in treatment-resistant depression.

Publication ,  Journal Article
Patkar, AA; Peindl, K; Mago, R; Mannelli, P; Masand, PS
Published in: Prim Care Companion J Clin Psychiatry
2006

BACKGROUND: About 30% to 46% of patients with major depressive disorder (MDD) fail to fully respond to initial antidepressants. While treatment-resistant depression commonly refers to nonresponse or partial response to at least 2 adequate trials with antidepressants from different classes, due to variability in terminology, a staging system based on prior treatment response has been suggested. Aripiprazole is a novel atypical antipsychotic with partial agonism at dopamine D(2) and serotonin 5-HT(1A) receptors and antagonism at the 5-HT(2) receptors. The present study evaluated whether augmentation with aripiprazole would be beneficial and tolerable in patients with treatment-resistant MDD who had failed 1 or more trials of antidepressants. METHOD: In an open-label, rater-blinded study conducted from March 2003 through December 2003, 10 patients with DSM-IV MDD without psychotic features who had failed to respond to an adequate trial of at least 1 antidepressant were prescribed aripiprazole (10-30 mg/day) for 6 weeks. The dose of preexisting antidepressants remained unchanged. Treatment response was defined as a 50% or greater reduction in score on the Hamilton Rating Scale for Depression (HAM-D) from baseline to end of treatment. Secondary efficacy measures included scores on the Clinical Global Impressions-Improvement (CGI-I) and -Severity (CGI-S) scales. RESULTS: Eight of 10 patients had failed 2 or more antidepressant trials. The mean daily dose of aripiprazole was 13.21 mg. Intent-to-treat analysis showed that mean ± SD HAM-D scores reduced significantly from baseline (23.0 ± 8.1) to end of treatment (8.1 ± 6.0) (p < .001). There was a significant reduction in CGI-I (p < .05) and a trend toward decrease in CGI-S (p = .06) score. Seventy percent of the subjects were responders and 30% achieved remission. Common adverse effects were akathisia (20%), nausea (20%), and restlessness (20%). CONCLUSIONS: The study indicates the potential utility of aripiprazole as an augmenting agent in treatment-resistant depression, particularly in those who had failed 2 or more antidepressant trials. Adequately powered, randomized controlled trials are necessary to evaluate the role of aripiprazole in treatment-resistant depression.

Duke Scholars

Published In

Prim Care Companion J Clin Psychiatry

DOI

ISSN

1523-5998

Publication Date

2006

Volume

8

Issue

2

Start / End Page

82 / 87

Location

United States

Related Subject Headings

  • Psychiatry
  • 4203 Health services and systems
  • 3202 Clinical sciences
  • 1103 Clinical Sciences
 

Citation

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Patkar, A. A., Peindl, K., Mago, R., Mannelli, P., & Masand, P. S. (2006). An open-label, rater-blinded, augmentation study of aripiprazole in treatment-resistant depression. Prim Care Companion J Clin Psychiatry, 8(2), 82–87. https://doi.org/10.4088/pcc.v08n0205
Patkar, Ashwin A., Kathleen Peindl, Rajnish Mago, Paolo Mannelli, and Prakash S. Masand. “An open-label, rater-blinded, augmentation study of aripiprazole in treatment-resistant depression.Prim Care Companion J Clin Psychiatry 8, no. 2 (2006): 82–87. https://doi.org/10.4088/pcc.v08n0205.
Patkar AA, Peindl K, Mago R, Mannelli P, Masand PS. An open-label, rater-blinded, augmentation study of aripiprazole in treatment-resistant depression. Prim Care Companion J Clin Psychiatry. 2006;8(2):82–7.
Patkar, Ashwin A., et al. “An open-label, rater-blinded, augmentation study of aripiprazole in treatment-resistant depression.Prim Care Companion J Clin Psychiatry, vol. 8, no. 2, 2006, pp. 82–87. Pubmed, doi:10.4088/pcc.v08n0205.
Patkar AA, Peindl K, Mago R, Mannelli P, Masand PS. An open-label, rater-blinded, augmentation study of aripiprazole in treatment-resistant depression. Prim Care Companion J Clin Psychiatry. 2006;8(2):82–87.

Published In

Prim Care Companion J Clin Psychiatry

DOI

ISSN

1523-5998

Publication Date

2006

Volume

8

Issue

2

Start / End Page

82 / 87

Location

United States

Related Subject Headings

  • Psychiatry
  • 4203 Health services and systems
  • 3202 Clinical sciences
  • 1103 Clinical Sciences