Duloxetine, 60 mg once daily, for major depressive disorder: A randomized double-blind placebo-controlled trial

被引:333
作者
Detke, MJ
Lu, YL
Goldstein, DJ
Hayes, JR
Demitrack, MA
机构
[1] Eli Lilly & Co, Lilly Res Labs, Indianapolis, IN 46285 USA
[2] Indiana Univ, Sch Med, Dept Psychiat, Indianapolis, IN 46202 USA
[3] McLean Hosp, Dept Psychiat, Belmont, MA USA
[4] Harvard Univ, Sch Med, Boston, MA USA
[5] Indiana Univ, Sch Med, Dept Pharmacol & Toxicol, Indianapolis, IN 46202 USA
关键词
D O I
10.4088/JCP.v63n0407
中图分类号
B849 [应用心理学];
学科分类号
040203 ;
摘要
Background: Despite treatment advances, major depressive disorder (MDD) is still a significant cause of morbidity and mortality, Current therapies frequently fall short of providing full remission. In addition. physical symptoms are commonly seen in MDD patients, increasing overall morbidity and health care utilization. Duloxetine hydrochloride, a dual reuptake inhibitor of serotonin and norepinephrine, was evaluated for efficacy and tolerability/safety in the treatment of MDD and associated physical symptoms. Method: In this multicenter, double-blind, parallel-group study, adult patients with DSM-IV MDD were randomly assigned to receive placebo (N = 122) or duloxetine (60 mg/day, N = 123) for 9 weeks. The primary efficacy measure was the 17-item Hamilton Rating Scale for Depression (HAM-D-17) total score. Painful physical symptoms were assessed using visual analog scales, and global illness and quality of life were evaluated using the Clinical Global Impressions-Severity scale, the Patient Global Impressions-Improvement scale, and the Quality of Life in Depression Scale. Safety and tolerability were determined by monitoring discontinuation rates, adverse events, vital signs. and laboratory results. Results: Duloxetine was significantly superior to placebo (p < .001) in reducing HAM-D-17 total scores, starting at week 2. The estimated probability of remission for duloxetine-treated patients (44%) was almost 3 times that of placebo patients (16%). Duloxetine significantly reduced painful physical symptoms in comparison with placebo. Discontinuation due to adverse events for duloxetine-treated patients (13.8%) compared favorably with the rates reported for SSRIs in other studies. Nausea, dry mouth, and somnolence were the most common adverse events', no significant incidence of hypertension was seen. Conclusion: Duloxetine, 60 mg/day, is a well-tolerated and effective treatment for MDD that reduces painful physical symptoms. These findings suggest that duloxetine may be a first-line treatment for patients with MDD and associated painful physical symptoms.
引用
收藏
页码:308 / 315
页数:8
相关论文
共 40 条
[1]  
American Psychiatric Association, 2000, Text revision (DSM-IV-TR), V4th, DOI [10.1176/dsm10.1176/appi.books.9780890420249.dsm-iv-tr, DOI 10.1176/DSM10.1176/APPI.BOOKS.9780890420249.DSM-IV-TR]
[2]  
Andersen B, 1990, J AFFECT DISORDERS, V18, P289
[3]  
ANDERSON IM, 1986, PSYCHOPHARMACOLOGY, V89, P131
[4]  
[Anonymous], 1990, ANN NY ACAD SCI
[5]   ENDOGENOUS PAIN CONTROL-SYSTEMS - BRAIN-STEM SPINAL PATHWAYS AND ENDORPHIN CIRCUITRY [J].
BASBAUM, AI ;
FIELDS, HL .
ANNUAL REVIEW OF NEUROSCIENCE, 1984, 7 :309-338
[6]  
CHALON S, 2000, 39 ANN M AM COLL NEU
[7]   A systematic review of the associations between dose regimens and medication compliance [J].
Claxton, AJ ;
Cramer, J ;
Pierce, C .
CLINICAL THERAPEUTICS, 2001, 23 (08) :1296-1310
[8]   Antidepressants and anticonvulsants for diabetic neuropathy and postherpetic neuralgia: A quantitative systematic review [J].
Collins, SL ;
Moore, RA ;
McQuay, HJ ;
Wiffen, P .
JOURNAL OF PAIN AND SYMPTOM MANAGEMENT, 2000, 20 (06) :449-458
[9]   The visual analog scale in the immediate postoperative period: Intrasubject variability and correlation with a numeric scale [J].
DeLoach, LJ ;
Higgins, MS ;
Caplan, AB ;
Stiff, JL .
ANESTHESIA AND ANALGESIA, 1998, 86 (01) :102-106
[10]  
DYMASTER FP, 2001, NEUROPSYCHOPHARMACOL, V25, P871