GUANFACINE TREATMENT OF COMORBID ATTENTION-DEFICIT HYPERACTIVITY DISORDER AND TOURETTES-SYNDROME - PRELIMINARY CLINICAL-EXPERIENCE

Citation
Pb. Chappell et al., GUANFACINE TREATMENT OF COMORBID ATTENTION-DEFICIT HYPERACTIVITY DISORDER AND TOURETTES-SYNDROME - PRELIMINARY CLINICAL-EXPERIENCE, Journal of the American Academy of Child and Adolescent Psychiatry, 34(9), 1995, pp. 1140-1146
Citations number
37
Categorie Soggetti
Psychiatry
ISSN journal
08908567
Volume
34
Issue
9
Year of publication
1995
Pages
1140 - 1146
Database
ISI
SICI code
0890-8567(1995)34:9<1140:GTOCAH>2.0.ZU;2-M
Abstract
Objective: Many children with Tourette's syndrome (TS) are handicapped more by difficulties with inattention, impulsivity, and hyperactivity than by their ties. However, stimulant medications used to treat atte ntion-deficit hyperactivity disorder (ADHD) can exacerbate ties. Guanf acine is an alpha(2)-adrenergic agonist that may have beneficial effec ts on attention, without the hypotensive or sedative effects of clonid ine, which is often used as an alternative to stimulants. Method:, An open-label study of guanfacine was performed in 10 children with TS+AD HD, aged 8 to 16 years. The duration of follow-up was 4 to 20 weeks, a nd the majority of subjects were treated with 1.5 mg/day. Ratings of t ic severity and ADHD symptoms were obtained using the Yale Global Tic Severity Scale (YGTSS), the Tic Symptom Self Report (TSSR), and the Co nners Parent Rating Scale. In addition, blind Continuous Performance T ests (CPTs) were performed at baseline and at two follow-up intervals in eight subjects. Results: Guanfacine was associated with significant decreases in both commission errors (p <.02) and omission errors (p < .01) on the CPT. In addition, guanfacine caused a significant decrease in severity of motor (p <.02) and phonic (p <.02) ties as measured by the TSSR and the YGTSS, respectively. The most common side effects we re transient sedation and headaches. Conclusion: Guanfacine may provid e a safe alternative therapy for children with ADHD in the presence of ties. Future double-blind, controlled trials should be undertaken.