Six-Week Open-Label Reboxetine Treatment in Children and Adolescents With Attention-Deficit/Hyperactivity Disorder

This open-label study assessed the effectiveness of reboxetine, a selective norepinephrine reuptake inhibitor, in children and adolescents with attention-deficit/hyperactivity disorder (ADHD) resistant to a previous methylphenidate trial. Thirty-one child and adolescent outpatients, aged 8 to 18 (me...

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Veröffentlicht in:Journal of the American Academy of Child and Adolescent Psychiatry 2005-05, Vol.44 (5), p.428-433
Hauptverfasser: Ratner, Sharon, Laor, Nathaniel, Bronstein, Yifat, Weizman, Abraham, Toren, Paz
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container_end_page 433
container_issue 5
container_start_page 428
container_title Journal of the American Academy of Child and Adolescent Psychiatry
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creator Ratner, Sharon
Laor, Nathaniel
Bronstein, Yifat
Weizman, Abraham
Toren, Paz
description This open-label study assessed the effectiveness of reboxetine, a selective norepinephrine reuptake inhibitor, in children and adolescents with attention-deficit/hyperactivity disorder (ADHD) resistant to a previous methylphenidate trial. Thirty-one child and adolescent outpatients, aged 8 to 18 (mean age, 11.7; SD = 2.87) years, diagnosed with ADHD were enrolled in a 6-week open-label study. Assessments included rater-administered scales (DSM-IV ADHD Scale; Clinical Global Impressions Scale), parent-administered scales (the Abbreviated Conners Rating Scale), and self-administered-scales for the evaluation of depressive (Children's Depression Inventory) and anxiety (the Revised Children's Manifest Anxiety Scale) symptoms. Reboxetine was initiated and maintained at a dose of 4 mg/day. A significant decrease in ADHD symptoms, on all scales measured, was noted. Adverse effects were relatively mild and transient. The most common adverse effects were drowsiness/sedation and gastrointestinal complaints. The results of the current open-label study suggest the effectiveness of reboxetine in the treatment of ADHD in methylphenidate-resistant children and adolescents. Double-blind, placebo-, and active comparator-controlled studies are indicated to rigorously test the efficacy of reboxetine in ADHD.
doi_str_mv 10.1097/01.chi.0000155327.30017.8c
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subjects Adolescent
Adolescents
Adrenergic Uptake Inhibitors - administration & dosage
Adrenergic Uptake Inhibitors - adverse effects
Adrenergic Uptake Inhibitors - therapeutic use
Adult and adolescent clinical studies
Anxiety
anxiety symptoms
Attention Deficit and Disruptive Behavior Disorders - epidemiology
Attention Deficit Disorder with Hyperactivity - diagnosis
Attention Deficit Disorder with Hyperactivity - drug therapy
Attention Deficit Disorder with Hyperactivity - epidemiology
Attention Deficit Disorders
Attention deficit hyperactivity disorder
Biological and medical sciences
Child
Clinical trials
Depression
Depression (Psychology)
depressive symptoms
Diagnostic and Statistical Manual of Mental Disorders
Double-Blind Method
Drug therapy
Effectiveness studies
Female
Humans
Hyperactivity
Inhibitor drugs
Male
Manifest Anxiety Scale
Medical sciences
Mental depression
Mood disorders
Morpholines - administration & dosage
Morpholines - adverse effects
Morpholines - therapeutic use
Neuropharmacology
Pediatrics
Pharmacology. Drug treatments
Program Effectiveness
Psychiatry
Psychoanaleptics: cns stimulant, antidepressant agent, nootropic agent, mood stabilizer..., (alzheimer disease)
Psychology. Psychoanalysis. Psychiatry
Psychopathology. Psychiatry
Psychopharmacology
Rating Scales
reboxetine
title Six-Week Open-Label Reboxetine Treatment in Children and Adolescents With Attention-Deficit/Hyperactivity Disorder
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