Combination of Antidepressant Medications From Treatment Initiation for Major Depressive Disorder: A Double-Blind Randomized Study

被引:210
作者
Blier, Pierre [1 ]
Ward, Herbert E.
Tremblay, Philippe
Laberge, Louise
Hebert, Chantal
Bergeron, Richard
机构
[1] Univ Ottawa, Univ Ottawa Inst Mental Hlth Res, Ottawa, ON K1Z 7K4, Canada
关键词
ANTAGONIST MIRTAZAPINE; REMISSION; NOREPINEPHRINE; AUGMENTATION; CITALOPRAM; ADHERENCE; SEROTONIN; RECOVERY; EFFICACY; FAILURE;
D O I
10.1176/appi.ajp.2009.09020186
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Objective: Various classes of antidepressant medications generally induce remission of major depressive disorder in only about one-third of patients. In a previous study using mirtazapine or paroxetine alone or in combination from treatment initiation, the rate of patients who remitted within a 6-week period was twice that of patients using either drug alone. In this double-blind study, the authors sought to produce evidence for the superiority of different combinations of antidepressant drugs from treatment initiation. Method: Patients (N=105) meeting DSM-IV criteria for major depressive disorder were randomly assigned to receive, from treatment initiation, either fluoxetine monotherapy (20 mg/day) or mirtazapine (30 mg/day) in combination with fluoxetine (20 mg/day), venlafaxine (225 mg/day titrated in 14 days), or bupropion (150 mg/day) for 6 weeks. The primary outcome measure was the Hamilton Depression Rating Scale (HAM-D) score. Results: The overall dropout rate was 15%, without notable differences among the four groups. Compared with fluoxetine monotherapy, all three combination groups had significantly greater improvements on the HAM-D. Remission rates (defined as a HAM-D score of 7 or less) were 25% for fluoxetine, 52% for mirtazapine plus fluoxetine, 58% for mirtazapine plus venlafaxine, and 46% for mirtazapine plus bupropion. Among patients who had a marked response, double-blind discontinuation of one agent produced a relapse in about 40% of cases. Conclusions: The combination treatments were as well tolerated as fluoxetine monotherapy and more clinically effective. The study results, which add to a growing body of evidence, suggest that use of antidepressant combinations from treatment initiation may double the likelihood of remission compared with use of a single medication.
引用
收藏
页码:281 / 288
页数:8
相关论文
共 35 条
[1]  
ALDOSARY F, 2007, AM COLL NEUR 46 ANN, P254
[2]  
[Anonymous], 2000, COCHRANE DB SYST REV
[3]  
[Anonymous], 2000, DIAGN STAT MAN MENT, DOI DOI 10.1176/APPI.BOOKS.9780890425787
[4]   Effects of the co-administration of mirtazapine and paroxetine on serotonergic neurotransmission in the rat brain [J].
Besson, A ;
Haddjeri, N ;
Blier, P ;
de Montigny, C .
EUROPEAN NEUROPSYCHOPHARMACOLOGY, 2000, 10 (03) :177-188
[5]  
BLIER P, 2006, AM PSYCHIAT PUBLISHI, P509
[6]   Mirtazapine and paroxetine in major depression: A comparison of monotherapy versus their combination from treatment initiation [J].
Blier, Pierre ;
Gobbi, Gabriella ;
Turcotte, Julie E. ;
de Montigny, Claude ;
Boucher, Nathalie ;
Hebert, Chantal ;
Debonnel, Guy .
EUROPEAN NEUROPSYCHOPHARMACOLOGY, 2009, 19 (07) :457-465
[7]   The Montgomery Asberg and the Hamilton ratings of depression: A comparison of measures [J].
Carmody, Thomas J. ;
Rush, A. John ;
Bernstein, Ira ;
Warden, Diane ;
Brannan, Stephen ;
Burnham, Daniel ;
Woo, Ada ;
Trivedi, Madhukar H. .
EUROPEAN NEUROPSYCHOPHARMACOLOGY, 2006, 16 (08) :601-611
[8]   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
[9]   Differential physiological effects of a low dose and high doses of venlafaxine in major depression [J].
Debonnel, Guy ;
Saint-Andre, Elise ;
Hebert, Chantal ;
de Montigny, Claude ;
Lavoie, Normand ;
Blier, Pierre .
INTERNATIONAL JOURNAL OF NEUROPSYCHOPHARMACOLOGY, 2007, 10 (01) :51-61
[10]   Modification of norepinephrine and serotonin, but not dopamine, neuron firing by sustained bupropion treatment [J].
Dong, J ;
Blier, P .
PSYCHOPHARMACOLOGY, 2001, 155 (01) :52-57