Early Improvement in the First 2 Weeks as a Predictor of Treatment Outcome in Patients With Major Depressive Disorder: A Meta-Analysis Including 6562 Patients

被引:305
作者
Szegedi, Armin [1 ]
Jansen, Wim T.
van Willigenburg, Arjen P. P. [1 ]
van der Meulen, Egbert
Stassen, Hans H. [2 ]
Thase, Michael E. [3 ,4 ,5 ]
机构
[1] Organon, Roseland, NJ USA
[2] Psychiat Univ Hosp, Zurich, Switzerland
[3] Univ Penn, Sch Med, Philadelphia, PA 19104 USA
[4] Philadelphia Vet Affairs Med Ctr, Philadelphia, PA USA
[5] Univ Pittsburgh, Med Ctr, Pittsburgh, PA 15260 USA
关键词
STAR-ASTERISK-D; ANTIDEPRESSANT ACTION; TREATMENT RESPONSE; DRUG RESPONSE; DELAYED-ONSET; FLUOXETINE; GUIDELINES; PAROXETINE; SERTRALINE; TITRATION;
D O I
10.4088/JCP.07m03780
中图分类号
B849 [应用心理学];
学科分类号
040203 [应用心理学];
摘要
Objective: New evidence indicates that treatment response can be predicted with high sensitivity after 2 weeks of treatment. Here, we assess whether early improvement with antidepressant treatment predicts treatment outcome in patients with major depressive disorder (MDD). Data Sources: Forty-one clinical trials comparing mirtazapine with active comparators or placebo in inpatients and outpatients (all-treated population, N = 6907; intent-to-treat population, N = 6562) with MDD (DSM-III-R or DSM-IV Criteria) were examined for early improvement (>= 20% score reduction from baseline on the 17-item Hamilton Rating Scale for Depression [HAM-D-17] within 2 weeks of treatment) and its relationship to treatment outcome. Study Selection: Data were obtained from a systematic search of single- or double-blind clinical trials (clinical trials database, Organon, a part of Schering-Plough Corporation, Oss, The Netherlands). All included trials (a total of 41) employed antidepressant treatment for more than 4 weeks and a maximum of 8 weeks. The studies ranged from March 1982 to December 2003. Trials were excluded if there were no HAM-D-17 ratings available, no diagnosis of MDD, or if the study was not blinded. Trials were also excluded if HAM-D-17 assessments were not available at week 2, week 4. and at least once beyond week 4. Data Synthesis: Early improvement predicted stable response and stable remission with high sensitivity (>= 81% and >= 87%, respectively). Studies utilizing rapid titration vs. slow titration of mirtazapine demonstrated improved sensitivity for stable responders (98%, [95% CI = 93% to 100%] vs. 91% [95% CI = 89% to 93%]) and stable remitters (100%, [95% CI = 92% to 100%] vs. 93% [95% CI = 91% to 95%]). Negative predictive values for stable responders and stable remitters were much higher (range = 82%-100%) than positive predictive values (range = 19%-60%). Conclusions: These results indicate that early improvement with antidepressant medication can predict subsequent treatment outcome with high sensitivity in patients with major depressive disorder. The high negative predictive values indicate little chance of stable response or stable remission in the absence of improvement within 2 weeks. A lack of improvement during the first 2 weeks of therapy may indicate that changes in depression management should be considered earlier than conventionally thought.
引用
收藏
页码:344 / 353
页数:10
相关论文
共 34 条
[1]
Evidence-based guidelines for treating depressive disorders with antidepressants: a revision of the 1993 British Association for Psychopharmacology guidelines [J].
Anderson, IM ;
Nutt, DJ ;
Deakin, JFW .
JOURNAL OF PSYCHOPHARMACOLOGY, 2000, 14 (01) :3-20
[2]
[Anonymous], 2000, Am J Psychiatry, V157, P1
[3]
Bauer Michael, 2002, World J Biol Psychiatry, V3, P5, DOI 10.3109/15622970209150599
[4]
Dose escalation vs. Continued doses of paroxetine and maprotiline: A prospective study in depressed out-patients with inadequate treatment response [J].
Benkert, O ;
Szegedi, A ;
Wetzel, H ;
Staab, HJ ;
Meister, W ;
Philipp, M .
ACTA PSYCHIATRICA SCANDINAVICA, 1997, 95 (04) :288-296
[5]
Bernardo M, 2003, ACTAS ESP PSIQUIATRI, V31, P31
[6]
Trajectories of treatment response in late-life depression - Psychosocial and clinical correlates [J].
Gildengers, AG ;
Houck, PR ;
Mulsant, BH ;
Dew, MA ;
Aizenstein, HJ ;
Jones, BL ;
Greenhouse, J ;
Pollock, BG ;
Reynolds, CF .
JOURNAL OF CLINICAL PSYCHOPHARMACOLOGY, 2005, 25 (04) :S8-S13
[7]
Fluoxetine 40-60 mg versus fluoxetine 20 mg in the treatment of children and adolescents with a less-than-complete response to nine-week treatment with fluoxetine 10-20 mg: A pilot study [J].
Heiligenstein, JH ;
Hoog, SL ;
Wagner, KD ;
Findling, RL ;
Galil, N ;
Kaplan, S ;
Busner, J ;
Nilsson, ME ;
Brown, EB ;
Jacobson, JG .
JOURNAL OF CHILD AND ADOLESCENT PSYCHOPHARMACOLOGY, 2006, 16 (1-2) :207-217
[8]
Onset and early behavioral effects of pharmacologically different antidepressants and placebo in depression [J].
Katz, MM ;
Tekell, JL ;
Bowden, CL ;
Brannan, S ;
Houston, JP ;
Berman, N ;
Frazer, A .
NEUROPSYCHOPHARMACOLOGY, 2004, 29 (03) :566-579
[9]
'Delay' hypothesis of onset of antidepressant action [J].
Katz, MM ;
Frazer, A ;
Bowden, CL .
BRITISH JOURNAL OF PSYCHIATRY, 2006, 188 :586-586
[10]
THE TIMING, SPECIFICITY AND CLINICAL-PREDICTION OF TRICYCLIC DRUG EFFECTS IN DEPRESSION [J].
KATZ, MM ;
KOSLOW, SH ;
MAAS, JW ;
FRAZER, A ;
BOWDEN, CL ;
CASPER, R ;
CROUGHAN, J ;
KOCSIS, J ;
REDMOND, E .
PSYCHOLOGICAL MEDICINE, 1987, 17 (02) :297-309