Abstract |
A group of 23 elderly outpatients with dysthymic disorder participated in a 13-week fluoxetine trial. Twelve responders received open continuation treatment and subsequently discontinued fluoxetine (mean: 32 weeks on medication). During the 24 weeks after discontinuation, 6 of the 12 patients relapsed. Clinical features, dose, and duration of fluoxetine treatment were not predictive of relapse. The 50% relapse rate in this small sample is lower than that reported in young adult dysthymic patients but is high enough to warrant clinical caution.
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Authors | D P Devanand, M K Kim, M S Nobler |
Journal | The American journal of geriatric psychiatry : official journal of the American Association for Geriatric Psychiatry
(Am J Geriatr Psychiatry)
Vol. 5
Issue 1
Pg. 83-7
( 1997)
ISSN: 1064-7481 [Print] England |
PMID | 9169249
(Publication Type: Clinical Trial, Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, P.H.S.)
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Chemical References |
- Antidepressive Agents, Second-Generation
- Fluoxetine
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Topics |
- Adult
- Aged
- Ambulatory Care
- Antidepressive Agents, Second-Generation
(administration & dosage, adverse effects)
- Dose-Response Relationship, Drug
- Dysthymic Disorder
(drug therapy, psychology)
- Female
- Fluoxetine
(administration & dosage, adverse effects)
- Humans
- Male
- Middle Aged
- Recurrence
- Risk Factors
- Single-Blind Method
- Substance Withdrawal Syndrome
(etiology)
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