Case Study
Fluoxetine Treatment of Children and Adolescents with Tourette's and Obsessive Compulsive Disorders: Preliminary Clinical Experience

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Abstract.

Fluoxetine hydrochloride is the first selective serotonin uptake inhibitor introduced commercially in the United States. This report describes preliminary clinical experience with fluoxetine in 10 children and adolescents, aged 8 to 15 years, with primary obsessive compulsive disorder (OCD) or Tourette's syndrome (TS) plus OCD. In general, fluoxetine, which was administered from 4 to 20 weeks at a dosage of 10 or 40 mg per day, was well tolerated. Adverse effects included behavioral agitation/activation in four patients and mild gastrointestinal symptoms in two patients. No abnormalities were noted in the seven children who had follow-up EKGs. Five of the 10 patients (50%) were considered responders; their obsessive-compulsive symptoms decreased substantially during treatment with fluoxetine. Responder rates were similar in the primary OCD (two of four, 50%) and TS + OCD (three of six, 50%) groups. In conclusion, short-term fluoxetine administration appears to be safe in children and adolescents. Placebo-controlled trials are needed to further assess the efficacy of fluoxetine.

Key Words:

fluoxetine
psychopharmacology
obsessive compulsive disorder
Tourette's syndrome

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This research was supported in part by the following USPHS grants: Clinical Research Center Grant MH-30929 from the National Institute of Mental Health, Research Resources Grant RR-00125 from the National Institutes of Health, and Grant HD-03008 from the National Institute of Child Health and Human Development. Support was also received from the Leon Lowenstein Foundation.

The authors thank the staff and trainees of the Children's Psychiatric Inpatient Service, Yale-New Haven Hospital for skilled clinical care. The authors also thank Drs. Donald J. Cohen and James F. Leckman for their comments and support.