Efficacy and safety of fluoxetine in treating bipolar II major depressive episode

被引:118
作者
Amsterdam, JD
Garcia-España, F
Fawcett, J
Quitkin, FM
Reimherr, FW
Rosenbaum, JF
Schweizer, E
Beasley, C
机构
[1] Univ Penn, Med Ctr, Philadelphia, PA 19104 USA
[2] Rush Presbyterian St Lukes Med Ctr, Chicago, IL USA
[3] New York State Psychiat Inst, New York, NY USA
[4] Univ Utah, Sch Med, Salt Lake City, UT USA
[5] Massachusetts Gen Hosp, Boston, MA 02114 USA
[6] Lilly Res Labs, Indianapolis, IN USA
关键词
D O I
10.1097/00004714-199812000-00003
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
As many as 45% of patients with major depressive episode also meet DSM-TV criteria for bipolar II (BP II) disorder. Although some clinicians advocate using a mood stabilizer in treating BP II depression, antidepressant monotherapy has been less well studied in this disorder. As part of a prospective, placebo-controlled, relapse-prevention study in 839 patients, the efficacy and safety of short- and long-term fluoxetine treatment in patients with BP II major depression compared with patients with unipolar (UP) major depression was retrospectively examined. Eighty-nine BP II patients (mean age, 41 +/- 11 years) were compared with 89 age- and gender-matched UP patients and with 661 unmatched UP patients (mean age, 39 +/- 11 years). All received short-term fluoxetine therapy at 20 mg daily for up to 12 weeks. Complete remission was defined as a final Hamilton Rating Scale for Depression score less than or equal to 7 by meek 9 that was then maintained for 3 additional weeks. Remitted patients were then randomly assigned to receive double-blind treatment with one of the following: (1) fluoxetine 20 mg daily for 52 weeks; (2) fluoxetine for 38 weeks, then placebo for 14 weeks; (3) fluoxetine for 14 weeks, then placebo for 38 weeks; or (4) placebo for 52 weeks. Antidepressant efficacy mas similar in BP and UP patients during short-term therapy. Discontinuation for lack of efficacy was lower in BP II (5%) than in UP (12%) patients (p = not significant [NS]), whereas dropouts for adverse events mere similar in BP II(11%) and UP (9%) patients. During longterm relapse-prevention therapy, relapse rates mere similar in BP II and UP patients (p = NS) During short-term fluoxetine therapy, three BP II (3.8%) versus no matched UP (p = NS) and 0.3% unmatched UP (p = 0.01) patients had a "manic switch." During long-term fluoxetine therapy, one (2%) BP II and three (1%) unmatched UP patients (one taking placebo) had a manic switch (p = NS). In conclusion, fluoxetine may be a safe and effective antidepressant monotherapy for the shortterm treatment of BP II depression with a relatively low manic switch rate. Fluoxetine may also be effective in relapse-prevention therapy in patients with BP II disorder.
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页码:435 / 440
页数:6
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