Double-blind study of high-dose fluoxetine versus lithium or desipramine augmentation of fluoxetine in partial responders and nonresponders to fluoxetine

被引:105
作者
Fava, M [1 ]
Alpert, J [1 ]
Nierenberg, A [1 ]
Lagomasino, I [1 ]
Sonawalla, S [1 ]
Tedlow, J [1 ]
Worthington, J [1 ]
Baer, L [1 ]
Rosenbaum, JF [1 ]
机构
[1] Massachusetts Gen Hosp, Depress Clin & Res Program, Boston, MA 02114 USA
关键词
D O I
10.1097/00004714-200208000-00008
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
In a previous study, of 41 depressed patients who had not responded to fluoxetine 20 mg/day, 53% were treated with high-dose fluoxetine (40-60 mg/day) and responded (i.e., their 17-item Hamilton Rating Scale for Depression [HAM-D-17] score was <7) versus 29% and 25% of patients treated with fluoxetine plus lithium (300-600 mg/day) or fluoxetine plus desipramine (25-50 mg/day), respectively. We wanted to assess whether these findings could be replicated in a larger sample of depressed outpatients. We identified 101 outpatients with major depressive disorder (52 men and 49 women; mean age, 41.6 + 10.6 years) who were either partial responders (n = 49) or nonresponders (n = 52) to 8 weeks of treatment with fluoxetine 20 mg/day. These patients were randomized to 4 weeks of double-blind treatment with high-dose fluoxetine (40-60 mg/day), fluoxetine plus lithium (300-600 mg/day), or fluoxetine plus desipramine (25-50 mg/day). In the overall group of patients (N = 101), there was no significant difference in response rates across the three treatment groups (high-dose fluoxetine, 42.4%; fluoxetine plus desipramine, 29.4%; fluoxetine plus lithium, 23.5%). Dropout rates were also comparable, ranging from 9.1% (high-dose fluoxetine) to 14.7% (fluoxetine plus desipramine and fluoxetine plus lithium). There were also no significant differences in response rates across the three treatment groups among partial responders (high-dose fluoxetine, 50.0%; fluoxetine plus desipramine, 33.3%; fluoxetine plus lithium, 33.3%) and nonresponders (high-dose fluoxetine, 35.3%; fluoxetine plus desiprandne, 26.3%; fluoxetine plus lithium, 12.5%). At the end of the study, the mean lithium level was 0.37 + 0.15 mEq/L (n = 27; range, 0.1-0.8 mEq/L) among lithium-treated patients, and the mean desipramine level was 104.7 + 58.8 ng/ml, (n = 22; range, 25-257 ng/mL). There were no significant relationships between lithium or desipramine blood levels and degree of improvement (as measured by the change in HAM-D-17 score). We found no significant differences in efficacy among these three treatment strategies among patients who had failed to respond adequately to 8 weeks of treatment with fluoxetine 20 mg/day, although the high-fluoxetine group was associated with nonsignificantly higher response rates in both partial responders and nonresponders.
引用
收藏
页码:379 / 387
页数:9
相关论文
共 50 条
  • [1] Desipramine pharmacokinetics when coadministered with paroxetine or sertraline in extensive metabolizers
    Alderman, J
    Preskorn, SH
    Greenblatt, DJ
    Harrison, W
    Penenberg, D
    Allison, J
    Chung, M
    [J]. JOURNAL OF CLINICAL PSYCHOPHARMACOLOGY, 1997, 17 (04) : 284 - 291
  • [2] Amsterdam J D, 1997, Depress Anxiety, V5, P84, DOI 10.1002/(SICI)1520-6394(1997)5:2<84::AID-DA4>3.3.CO
  • [3] 2-N
  • [4] [Anonymous], 1976, DHEW PUB
  • [5] 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
    Appelberg, BG
    Syvälahti, EK
    Koskinen, TE
    Mehtonen, OP
    Muhonen, TT
    Naukkarinen, HH
    [J]. JOURNAL OF CLINICAL PSYCHIATRY, 2001, 62 (06) : 448 - 452
  • [6] Triiodothyronine augmentation in the treatment of refractory depression - A meta-analysis
    Aronson, R
    Offman, HJ
    Joffe, RT
    Naylor, CD
    [J]. ARCHIVES OF GENERAL PSYCHIATRY, 1996, 53 (09) : 842 - 848
  • [7] TRICYCLIC ANTIDEPRESSANT PLASMA-LEVELS AFTER AUGMENTATION WITH CITALOPRAM - A CASE-STUDY
    BAETTIG, D
    BONDOLFI, G
    MONTALDI, S
    AMEY, M
    BAUMANN, P
    [J]. EUROPEAN JOURNAL OF CLINICAL PHARMACOLOGY, 1993, 44 (04) : 403 - 405
  • [8] DEVELOPMENT OF BETA-ADRENERGIC-RECEPTOR SUBSENSITIVITY BY ANTIDEPRESSANTS
    BANERJEE, SP
    KUNG, LS
    RIGGI, SJ
    CHANDA, SK
    [J]. NATURE, 1977, 268 (5619) : 455 - 456
  • [9] RAPID DOWN REGULATION OF BETA-ADRENOCEPTORS BY CO-ADMINISTRATION OF DESIPRAMINE AND FLUOXETINE
    BARON, BM
    OGDEN, AM
    SIEGEL, BW
    STEGEMAN, J
    URSILLO, RC
    DUDLEY, MW
    [J]. EUROPEAN JOURNAL OF PHARMACOLOGY, 1988, 154 (02) : 125 - 134
  • [10] Lithium augmentation in treatment-resistant-depression:: Meta-analysis of placebo-controlled studies
    Bauer, M
    Döpfmer, S
    [J]. JOURNAL OF CLINICAL PSYCHOPHARMACOLOGY, 1999, 19 (05) : 427 - 434