EFFICACY AND TOLERABILITY OF ANTIDEPRESSANTS IN PEDIATRIC ANXIETY DISORDERS: A SYSTEMATIC REVIEW AND META-ANALYSIS
Background Randomized controlled trials have demonstrated that antidepressants are efficacious in the treatment of anxiety disorders in youth. However, there are no recent, systematic analyses of the efficacy, safety, or tolerability of these medications in pediatric anxiety disorders. Methods A sys...
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Published in | Depression and anxiety Vol. 32; no. 3; pp. 149 - 157 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Blackwell Publishing Ltd
01.03.2015
John Wiley & Sons, Inc |
Subjects | |
Online Access | Get full text |
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Summary: | Background
Randomized controlled trials have demonstrated that antidepressants are efficacious in the treatment of anxiety disorders in youth. However, there are no recent, systematic analyses of the efficacy, safety, or tolerability of these medications in pediatric anxiety disorders.
Methods
A systematic review and meta‐analysis of prospective, randomized, parallel‐group, controlled trials of selective serotonin reuptake inhibitors (SSRIs) and selective serotonin–norepinephrine reuptake inhibitors (SSNRIs) in pediatric patients with non‐obsessive compulsive disorder (OCD) anxiety disorders was undertaken using a search of PubMed/Medline (1966–2014). The meta‐analysis utilized random‐effects models to evaluate change in the Pediatric Anxiety Rating Scale or similar anxiety scale, suicidality, and adverse events. Additionally, pharmacologic variables were explored with regard to effect size, although no correction for multiple comparisons was made with regard to these relationships.
Results
Nine trials involving 1,673 patients and six medications were included. All SSRI/SSNRIs evaluated demonstrated efficacy, and the meta‐analytic estimate of effect was of moderate magnitude (Cohen's d = 0.62, confidence interval [CI]: 0.34–0.89, P = .009) and there was evidence of modest heterogeneity (I2 = 0.29, P = .103). Activation trended toward being more likely with antidepressant treatment (OR: 1.86, CI: 0.98–3.53, P = .054), but no increased risk was observed for nausea/abdominal symptoms (P = .262), discontinuation as a result of an adverse event (P = .132), or suicidality (OR: 1.3, CI: 0.53–3.2, P = .514). Finally, the effect size correlated with the serotonergic specificity of the agent (R = .79, P = .021).
Conclusions
Data for nine SSRI/SSNRIs suggest superiority of antidepressants relative to placebo for the treatment of pediatric anxiety disorders with a moderate effect size. |
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Bibliography: | National Center for Advancing Translational Sciences ark:/67375/WNG-B3LHRF4R-F National Center for Research Resources Eli Lilly Shire National Institutes of Health (NIH) - No. 8 UL1 TR000077-04 Pfizer istex:74E38D8F12B7A27645697681A3616F67523B40A9 ArticleID:DA22329 Forest; Contract grant sponsor: Lundbeck National Institute of Mental Health - No. K23MH106037 National Institutes of Health - No. Grant 8 UL1 TR000077-04 Contract grant sponsor: National Center for Research Resources; Contract grant sponsor: National Center for Advancing Translational Sciences; Contract grant sponsor: National Institutes of Health (NIH); Contract grant number: Grant 8 UL1 TR000077‐04; Contract grant sponsor: Eli Lilly; Contract grant sponsor: Shire; Contract grant sponsor: Forest; Contract grant sponsor: Lundbeck; Contract grant sponsor: Pfizer. ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 ObjectType-Review-3 content type line 23 ObjectType-Undefined-4 |
ISSN: | 1091-4269 1520-6394 1520-6394 |
DOI: | 10.1002/da.22329 |