Continuation treatment of major depressive disorder: is there a case for duloxetine?

被引:0
作者
Norman, Trevor R. [1 ]
Olver, James S. [1 ]
机构
[1] Univ Melbourne, Austin Hosp, Dept Psychiat, Heidelberg, Vic 3084, Australia
关键词
major depression; duloxetine; continuation treatment; placebo studies; relapse prevention; clinical trials;
D O I
暂无
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Duloxetine is a serotonin-noradrenaline reuptake inhibitor with established efficacy for the short-term treatment of major depressive disorder. Efficacy in continuation treatment (greater than six months of continuous treatment) has been established from both open and placebo-controlled relapse prevention and comparative studies. Seven published studies were available for review and showed that in both younger and older populations (aged more than 65 years) the acute efficacy of duloxetine was maintained for up to one year. Response to treatment was based on accepted criteria for remission of depression and in continuation studies remission rates were greater than 70%. Comparative studies showed that duloxetine was superior to placebo and comparable to paroxetine and escitalopram in relapse prevention. Importantly a study of duloxetine in patients prone to relapse of major depressive disorder showed that the medication was more effective than placebo in this difficult to treat population. Side effects of duloxetine during continuation treatment were predictable on the basis of the known pharmacology of the drug. In particular there were no significant life-threatening events which emerged with continued use of the medication. On the other hand vigilance is required since the data base on which to judge very rare events is limited by the relatively low exposure to the drug. Duloxetine has established both efficacy and safety for continuation treatment but its place as a first-line treatment of relapse prevention requires further experience. In particular further comparative studies against established agents would be useful in deciding the place of duloxetine in therapy.
引用
收藏
页码:19 / 31
页数:13
相关论文
共 58 条
[31]   Metabolism, excretion, and pharmacokinetics of duloxetine in healthy human subjects [J].
Lantz, RJ ;
Gillespie, TA ;
Rash, TJ ;
Kuo, F ;
Skinner, M ;
Kuan, HY ;
Knadler, MP .
DRUG METABOLISM AND DISPOSITION, 2003, 31 (09) :1142-1150
[32]   The effect of anxiety disorder comorbidity on treatment resistant bipolar disorders [J].
Lee, John H. ;
Dunner, David L. .
DEPRESSION AND ANXIETY, 2008, 25 (02) :91-97
[33]   Drug therapy - The medical management of depression [J].
Mann, JJ .
NEW ENGLAND JOURNAL OF MEDICINE, 2005, 353 (17) :1819-1834
[34]   PAROXETINE IS BETTER THAN PLACEBO IN RELAPSE PREVENTION AND THE PROPHYLAXIS OF RECURRENT DEPRESSION [J].
MONTGOMERY, SA ;
DUNBAR, G .
INTERNATIONAL CLINICAL PSYCHOPHARMACOLOGY, 1993, 8 (03) :189-195
[35]  
MONTGOMERY SA, 1988, BRIT J PSYCHIAT, V153, P69
[36]  
Mueller TI, 1999, AM J PSYCHIAT, V156, P1000
[37]   RESIDUAL SYMPTOMS AFTER PARTIAL REMISSION - AN IMPORTANT OUTCOME IN DEPRESSION [J].
PAYKEL, ES ;
RAMANA, R ;
COOPER, Z ;
HAYHURST, H ;
KERR, J ;
BAROCKA, A .
PSYCHOLOGICAL MEDICINE, 1995, 25 (06) :1171-1180
[38]   Duloxetine in the Prevention of Depressive Recurrences: A Randomized, Double-Blind, Placebo-Controlled Trial [J].
Perahia, David G. S. ;
Maina, Giuseppe ;
Thase, Michael E. ;
Spann, Melissa E. ;
Wang, Fujun ;
Walker, Daniel J. ;
Detke, Michael J. .
JOURNAL OF CLINICAL PSYCHIATRY, 2009, 70 (05) :706-716
[39]   Duloxetine in the prevention of relapse of major depressive disorder - Double-blind placebo-controlled study [J].
Perahia, DG ;
Gilaberte, I ;
Wang, FJ ;
Wiltse, CG ;
Huckins, SA ;
Clemens, JW ;
Montgomery, SA ;
Montejo, AL ;
Detke, MJ .
BRITISH JOURNAL OF PSYCHIATRY, 2006, 188 :346-353
[40]  
PRIEN RF, 1984, ARCH GEN PSYCHIAT, V41, P1096