Aripiprazole as an adjunctive treatment for refractory unipolar depression
被引:27
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作者:
Hellerstein, David J.
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机构:
New York State Psychiat Inst & Hosp, New York, NY 10032 USA
Columbia Univ Coll Phys & Surg, New York, NY 10032 USANew York State Psychiat Inst & Hosp, New York, NY 10032 USA
Hellerstein, David J.
[1
,2
]
Batchelder, Sarai
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机构:
New York State Psychiat Inst & Hosp, New York, NY 10032 USANew York State Psychiat Inst & Hosp, New York, NY 10032 USA
Batchelder, Sarai
[1
]
Hyler, Steven
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机构:
New York State Psychiat Inst & Hosp, New York, NY 10032 USA
Columbia Univ Coll Phys & Surg, New York, NY 10032 USANew York State Psychiat Inst & Hosp, New York, NY 10032 USA
Hyler, Steven
[1
,2
]
Arnaout, Bachaar
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机构:New York State Psychiat Inst & Hosp, New York, NY 10032 USA
Arnaout, Bachaar
Corpuz, Virginia
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机构:New York State Psychiat Inst & Hosp, New York, NY 10032 USA
Corpuz, Virginia
Coram, Lisa
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机构:New York State Psychiat Inst & Hosp, New York, NY 10032 USA
Coram, Lisa
Weiss, Gony
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机构:New York State Psychiat Inst & Hosp, New York, NY 10032 USA
Weiss, Gony
机构:
[1] New York State Psychiat Inst & Hosp, New York, NY 10032 USA
[2] Columbia Univ Coll Phys & Surg, New York, NY 10032 USA
Introduction: Aripiprazole may be an effective adjunctive treatment in outpatients with unipolar depression that has been refractory to treatment with SSRI or SNRI medication. Methods: Fifteen subjects with a current DSM-IV diagnosis of MDD which had not responded to SSRI or SNRI treatment were enrolled in a 12 week open-label study of aripiprazole with a maximum dose of 30 mg/day. Patients' current episode averaged 10.4 +/- 16.6 years, with a range of 3 months to 54 years. Baseline severity averaged 30.1 +/- 7.1 on HDRS-24, and 19.7 +/- 8.4 on BDI. Patients had been treated with a mean dose of 79.2 +/- 28.2 mg/day of fluoxetine equivalents for an average of 1 year prior to starting the study. Five subjects were on SNRI medications and 10 on SSRIs. Results: Seven of 14 (50.0%) subjects were classified as treatment responders, as defined by at least 50% reduction in the HDRS-24 at week 12. Four subjects (28.6%) achieved remission, based on STAR*D criteria (HDRS-17 score <= 7). 26.7% (4/15) of subjects discontinued participation due to side effects. Two (40%) of 5 SNRI-treated subjects responded to aripiprazole augmentation. Conclusions: These findings support previous studies for the effectiveness of aripiprazole in augmenting SSRIs or SNRIs in treatment-resistant major depression. (C) 2007 Elsevier Inc. All rights reserved.
机构:
Nasr Psychiat Serv, Michigan City, IN USA
Indiana Univ, Dept Psychiat, Michigan City, IN USA
Univ Notre Dame, Dept Psychol, Notre Dame, IN 46556 USA
Mem Epworth Ctr, South Bend, IN 46617 USANasr Psychiat Serv, Michigan City, IN USA
Nasr, Suhayl
Wendt, Burdette
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机构:
Nasr Psychiat Serv, Michigan City, IN USANasr Psychiat Serv, Michigan City, IN USA
Wendt, Burdette
Popli, Anand
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机构:
Nasr Psychiat Serv, Michigan City, IN USA
Indiana Univ, Dept Psychiat, Michigan City, IN USANasr Psychiat Serv, Michigan City, IN USA
Popli, Anand
Crayton, John
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机构:
Nasr Psychiat Serv, Michigan City, IN USANasr Psychiat Serv, Michigan City, IN USA
机构:
Univ Calif Los Angeles, David Geffen Sch Med, Dept Psychiat & Biobehav Sci, Los Angeles, CA 90095 USAUniv Calif Los Angeles, David Geffen Sch Med, Dept Psychiat & Biobehav Sci, Los Angeles, CA 90095 USA
Schiffman, Jason E.
Gitlin, Michael J.
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机构:
Univ Calif Los Angeles, David Geffen Sch Med, Dept Psychiat & Biobehav Sci, Los Angeles, CA 90095 USAUniv Calif Los Angeles, David Geffen Sch Med, Dept Psychiat & Biobehav Sci, Los Angeles, CA 90095 USA