Abstract | OBJECTIVE: METHOD: Secondary analysis of a placebo-controlled study in ADHD patients (6-12 years old) treated with atomoxetine (target dose: 1.2 mg/kg per day). Cb- CPT/MT scores were analyzed using ANCOVA (last observation carried forward [LOCF]). RESULTS: The data (N = 125) suggested a more pronounced atomoxetine effect in the group with comorbid ODD/CD as measured by all cb- CPT/MT parameters except for "normalized variation of reaction time" (nVRT). CONCLUSION: The results showed that atomoxetine reduced ADHD severity as measured by cb- CPT and MT parameters regardless of whether comorbid ODD/CD was present. The treatment effect of atomoxetine on hyperactivity appears to be more pronounced in the subgroup of patients with comorbid ODD/CD than in the subgroup without this comorbidity.
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Authors | Peter M Wehmeier, Laura Kipp, Tobias Banaschewski, Ralf W Dittmann, Alexander Schacht |
Journal | Journal of attention disorders
(J Atten Disord)
Vol. 19
Issue 7
Pg. 591-602
(Jul 2015)
ISSN: 1557-1246 [Electronic] United States |
PMID | 22930789
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Copyright | © 2012 SAGE Publications. |
Chemical References |
- Adrenergic Uptake Inhibitors
- Propylamines
- Atomoxetine Hydrochloride
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Topics |
- Adolescent
- Adrenergic Uptake Inhibitors
(therapeutic use)
- Atomoxetine Hydrochloride
(therapeutic use)
- Attention Deficit Disorder with Hyperactivity
(diagnosis, drug therapy, epidemiology)
- Attention Deficit and Disruptive Behavior Disorders
(diagnosis, epidemiology)
- Comorbidity
- Conduct Disorder
(epidemiology)
- Double-Blind Method
- Female
- Humans
- Male
- Personality Assessment
- Propylamines
(therapeutic use)
- Quality of Life
(psychology)
- Reaction Time
(drug effects)
- Treatment Outcome
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