A multicenter, placebo-controlled study of modafinil augmentation in partial responders to selective serotonin reuptake inhibitors with persistent fatigue and sleepiness

被引:139
作者
Fava, M
Thase, ME
DeBattista, C
机构
[1] Massachusetts Gen Hosp, Depress Clin & Res Program, Boston, MA 02114 USA
[2] Univ Pittsburgh, Med Ctr, Pittsburgh, PA USA
[3] Stanford Univ, Med Ctr, Stanford, CA 94305 USA
关键词
D O I
10.4088/JCP.v66n0112
中图分类号
B849 [应用心理学];
学科分类号
040203 [应用心理学];
摘要
Background: Up to one half of depressed patients have partial or no response to antidepressant monotherapy. This multicenter, placebo-controlled study evaluated the efficacy of modafinil augmentation in major depressive disorder (MDD) patients with fatigue and excessive sleepiness despite selective serotonin reuptake inhibitor (SSRI) monotherapy. Method: Patients (18-65 years) with a DSM-IV diagnosis of MDD and partial response to SSRI monotherapy (greater than or equal to 8 weeks) at a stable dose for greater than or equal to 4 weeks were eligible. Patients had screening/baseline 31-item Hamilton Rating Scale for Depression (HAM-D) scores of 14 to 26, Epworth Sleepiness Scale (ESS) scores greater than or equal to 10, and Fatigue Severity Scale (FSS) scores greater than or equal to 4. Patients were randomly assigned to augmentation therapy with modafinil 200 mg/day or placebo for 8 weeks. Assessments included the ESS. Clinical Global Impressions-Improvement scale (CGI-I). 31- and 17-item HAM-D, FSS, Brief Fatigue Inventory (BFI), and Montgomery-Asberg Depression Rating Scale (MADRS). Results: Of 311 enrolled patients who received 1 dose of study drug. 158 were randomly assigned to modafinil (70% women) and 153 to placebo (72% women); 85% of each treatment group completed the study. At final visit, modafinil significantly improved patients' overall clinical condition compared with placebo on the basis of CGI-I scores (p = .02), and there were trends toward greater mean reductions in ESS. 31- and 17-item HAM-D, and MADRS scores versus placebo. Modafinil significantly reduced BFI scores for worst fatigue at final visit (p < .05 vs. placebo). There were no significant differences between modafinil and placebo at final visit in FSS or BFI total scores. Adverse events significantly more common during modafinil compared with placebo treatment were nausea (9% vs. 2%; p = .01) and feeling jittery (4% vs. 1%; p = .03). Conclusion: These findings suggest that modafinil is a well-tolerated and potentially effective augmenting agent for SSRI partial responders with fatigue and sleepiness.
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页码:85 / 93
页数:9
相关论文
共 51 条
[1]
Meta-analytical studies on new antidepressants [J].
Anderson, IM .
BRITISH MEDICAL BULLETIN, 2001, 57 :161-178
[2]
[Anonymous], 2000, Stud. Dipterol
[3]
[Anonymous], 1976, ECDEU Assessment Manual for Psychopharmacology
[4]
Patients with severe depression may benefit from buspirone augmentation of selective serotonin reuptake inhibitors:: Results from a placebo-controlled, randomized, double-blind, placebo wash-in study [J].
Appelberg, BG ;
Syvälahti, EK ;
Koskinen, TE ;
Mehtonen, OP ;
Muhonen, TT ;
Naukkarinen, HH .
JOURNAL OF CLINICAL PSYCHIATRY, 2001, 62 (06) :448-452
[5]
DEPRESSIVE DISEASE - CLASSIFICATION AND CLINICAL CHARACTERISTICS [J].
BAKER, M ;
DORZAB, J ;
WINOKUR, G ;
CADORET, RJ .
COMPREHENSIVE PSYCHIATRY, 1971, 12 (04) :354-&
[6]
Adverse events and treatment discontinuations in clinical trials of fluoxetine in major depressive disorder: An updated meta-analysis [J].
Beasley, CM ;
Koke, SC ;
Nilsson, ME ;
Gonzales, JS .
CLINICAL THERAPEUTICS, 2000, 22 (11) :1319-+
[7]
Becker PM, 2000, NEUROLOGY, V54, P1166
[8]
Discontinuing or switching selective serotonin-reuptake inhibitors [J].
Bull, SA ;
Hunkeler, EM ;
Lee, JY ;
Rowland, CR ;
Williamson, TE ;
Schwab, JR ;
Hurt, SW .
ANNALS OF PHARMACOTHERAPY, 2002, 36 (04) :578-584
[9]
A double-blind, placebo-controlled study of antidepressant augmentation with mirtazapine [J].
Carpenter, LL ;
Yasmin, S ;
Price, LH .
BIOLOGICAL PSYCHIATRY, 2002, 51 (02) :183-188