Cited by 21Attention Deficit Hyperactivity DisorderPharmaceutical studies and practicesDevelopmental and Educational Neuropsychology

Atomoxetine Treatment in Adolescents with Attention-Deficit/Hyperactivity Disorder

Wietecha, Linda A., Williams, David W., Herbert, Michael, Melmed, Raun D., Greenbaum, Michael, Schuh, Kory·2009·Journal of Child and Adolescent Psychopharmacology

Abstract

INTRODUCTION: This study compared two atomoxetine titration dosing schedules and two atomoxetine maintenance doses for treating adolescent attention-deficit/hyperactivity disorder (ADHD) inattention and hyperactivity/impulsivity. METHODS: Adolescents (N = 267) were randomized to a slow or fast titration schedule. Patients who responded continued on a 40-week maintenance treatment, randomized to either 0.8 or 1.4 mg/kg/day. RESULTS: During the acute period, significant benefit was demonstrated with both titration schedules on the ADHD Rating Scale total score. Although patients in both groups maintained benefit relative to week 0, statistically significant loss of benefit was found for patients maintained on 0.8 mg/kg/day but not on 1.4 mg/kg/day. A similar pattern was observed on the Clinical Global Impressions-ADHD-Severity scores and Life Participation Scale for ADHD-Child Version scores. Mean grades for most subjects improved for patients in both maintenance treatment groups although most improvements were not statistically significant. CONCLUSIONS: In adolescents with ADHD, treatment benefit at 8 weeks was better maintained long-term with 1.4 mg/kg/day than with 0.8 mg/kg/day. Improvement in adaptive functioning and age-appropriate developmental function was also demonstrated. Atomoxetine 0.8 and 1.4 mg/kg/day were equally well tolerated. CLINICAL TRIALS REGISTRY: Maintenance of benefit with atomoxetine hydrochloride in adolescents with ADHD, NCT00191035.

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Crossref · 10.1089/cap.2008.074

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  • In adolescents, higher doses of atomoxetine have been associated with greater long-term efficacy.

    “In adolescents, doses in the higher ranges have been associated with greater long-term efficacy [85].”

    From Advances in understanding and treating ADHD (2011) · cites this paper as [85]

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Authors
Wietecha, L. A., Williams, D. W., Herbert, M., Melmed, R. D., Greenbaum, M., & Schuh, K.
Affiliations
  • Eli Lilly (United States) (US)
  • Utah Personnel Development Center, Salt Lake City, UT.
  • Melmed Center, Scottsdale, AZ.
  • Reprogenetics (US)
Corresponding author
Wietecha, Linda A.
Venue
Journal of Child and Adolescent Psychopharmacology
Published
2009-12
Volume
19
Issue
6
Pages
719-730
ISSN
  • 1044-5463 (ISSN-L)
  • 1557-8992
OpenAlex
W2086807967
Cited by
21
References
19
Citations by year
2019: 1 · 2017: 2 · 2016: 3 · 2015: 3 · 2014: 3 · 2013: 1 · 2012: 2
FWCI
1.65
Type
journal article
Language
en
Open access
closed
Locations
  • Journal of Child and Adolescent Psychopharmacology (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Health Sciences › Medicine › Psychiatry and Mental health › Attention Deficit Hyperactivity Disorder
  • Health Sciences › Medicine › Pediatrics, Perinatology and Child Health › Pharmaceutical studies and practices
  • Social Sciences › Psychology › Neuropsychology and Physiological Psychology › Developmental and Educational Neuropsychology
Keywords
atomoxetine, attention deficit hyperactivity disorder, adolescents, dose titration, maintenance dose, inattention, hyperactivity/impulsivity, treatment response maintenance, adaptive behavior, drug tolerability
MeSH terms
Atomoxetine Hydrochloride, Adaptation, Psychological, Adolescent, Adolescent Behavior, Attention Deficit Disorder with Hyperactivity, Dose-Response Relationship, Drug, Drug Administration Schedule, Educational Status, Female, Humans, Male, Propylamines, Psychiatric Status Rating Scales, Severity of Illness Index, Treatment Outcome, Adrenergic Uptake Inhibitors

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