Adjunctive sleep medications and depression outcome in the treatment of serotonin-selective reuptake inhibitor resistant depression in adolescents study

Wael Shamseddeen, Gregory Clarke, Martin B. Keller, Karen Wagner, Boris Birmaher, Graham J. Emslie, Neal Ryan, Joan Rosenbaum Asarnow, Giovanna Porta, David A. Brent

Research output: Contribution to journalArticle

18 Citations (Scopus)

Abstract

Objective: In the Treatment of Resistant Depression in Adolescents, study participants who received medication for sleep had a lower response rate. This report sought to clarify this finding. Method: Depressed adolescents who had not responded to a previous adequate serotonin-selective reuptake inhibitor (SSRI) trial were randomly assigned to another SSRI, venlafaxine, another SSRI+cognitive behavior therapy (CBT), or venlafaxine+CBT. Augmentation with sleep medication was permitted as clinically indicated. Results: Youth who received trazodone were six times less likely to respond than those with no sleep medication (adjusted odds ratio [OR]=0.16, 95% confidence interval [CI]: 0.05-0.50, p=0.001) and were three times more likely to experience self-harm (OR=3.0, 95% CI: 1.1-7.9, p=0.03), even after adjusting for baseline differences associated with trazodone use. None (0/13) of those cotreated with trazodone and either paroxetine or fluoxetine responded. In contrast, those treated with other sleep medications had similar rates of response (60.0% vs. 50.4%, χ 2=0.85, p=0.36) and of self-harm events (OR=0.5, 95% CI: 0.1-2.6, p=0.53) as those who received no sleep medication. Conclusions: These findings should be interpreted cautiously because these sleep agents were not assigned randomly, but at clinician discretion. Nevertheless, they suggest that the use of trazodone for the management of sleep difficulties in adolescent depression should be re-evaluated and that future research on the management of sleep disturbance in adolescent depression is needed. The very low response rate of participants cotreated with trazodone and either fluoxetine or paroxetine could be due to inhibition of CYP 2D6 by these antidepressants.

Original languageEnglish (US)
Pages (from-to)29-36
Number of pages8
JournalJournal of Child and Adolescent Psychopharmacology
Volume22
Issue number1
DOIs
StatePublished - Feb 1 2012

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Serotonin Uptake Inhibitors
Trazodone
Sleep
Depression
Paroxetine
Fluoxetine
Odds Ratio
Cognitive Therapy
Confidence Intervals
Treatment-Resistant Depressive Disorder
Cytochrome P-450 CYP2D6
Antidepressive Agents

ASJC Scopus subject areas

  • Pharmacology (medical)
  • Pediatrics, Perinatology, and Child Health
  • Psychiatry and Mental health

Cite this

Adjunctive sleep medications and depression outcome in the treatment of serotonin-selective reuptake inhibitor resistant depression in adolescents study. / Shamseddeen, Wael; Clarke, Gregory; Keller, Martin B.; Wagner, Karen; Birmaher, Boris; Emslie, Graham J.; Ryan, Neal; Asarnow, Joan Rosenbaum; Porta, Giovanna; Brent, David A.

In: Journal of Child and Adolescent Psychopharmacology, Vol. 22, No. 1, 01.02.2012, p. 29-36.

Research output: Contribution to journalArticle

Shamseddeen, Wael ; Clarke, Gregory ; Keller, Martin B. ; Wagner, Karen ; Birmaher, Boris ; Emslie, Graham J. ; Ryan, Neal ; Asarnow, Joan Rosenbaum ; Porta, Giovanna ; Brent, David A. / Adjunctive sleep medications and depression outcome in the treatment of serotonin-selective reuptake inhibitor resistant depression in adolescents study. In: Journal of Child and Adolescent Psychopharmacology. 2012 ; Vol. 22, No. 1. pp. 29-36.
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abstract = "Objective: In the Treatment of Resistant Depression in Adolescents, study participants who received medication for sleep had a lower response rate. This report sought to clarify this finding. Method: Depressed adolescents who had not responded to a previous adequate serotonin-selective reuptake inhibitor (SSRI) trial were randomly assigned to another SSRI, venlafaxine, another SSRI+cognitive behavior therapy (CBT), or venlafaxine+CBT. Augmentation with sleep medication was permitted as clinically indicated. Results: Youth who received trazodone were six times less likely to respond than those with no sleep medication (adjusted odds ratio [OR]=0.16, 95{\%} confidence interval [CI]: 0.05-0.50, p=0.001) and were three times more likely to experience self-harm (OR=3.0, 95{\%} CI: 1.1-7.9, p=0.03), even after adjusting for baseline differences associated with trazodone use. None (0/13) of those cotreated with trazodone and either paroxetine or fluoxetine responded. In contrast, those treated with other sleep medications had similar rates of response (60.0{\%} vs. 50.4{\%}, χ 2=0.85, p=0.36) and of self-harm events (OR=0.5, 95{\%} CI: 0.1-2.6, p=0.53) as those who received no sleep medication. Conclusions: These findings should be interpreted cautiously because these sleep agents were not assigned randomly, but at clinician discretion. Nevertheless, they suggest that the use of trazodone for the management of sleep difficulties in adolescent depression should be re-evaluated and that future research on the management of sleep disturbance in adolescent depression is needed. The very low response rate of participants cotreated with trazodone and either fluoxetine or paroxetine could be due to inhibition of CYP 2D6 by these antidepressants.",
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