Escitalopram versus other antidepressive agents for depression

被引:118
作者
Cipriani, Andrea [1 ]
Santilli, Claudio [2 ]
Furukawa, Toshi A. [3 ]
Signoretti, Alessandra
Nakagawa, Atsuo [4 ]
McGuire, Hugh [5 ]
Churchill, Rachel [6 ]
Barbui, Corrado
机构
[1] Univ Verona, Dept Med & Publ Hlth, Sect Psychiat & Clin Psychol, Policlin GB Rossi, I-37134 Verona, Italy
[2] Univ Perugia, Dept Clin & Expt Med, I-06100 Perugia, Italy
[3] Nagoya City Univ, Dept Psychiat & Cognit Behav Med, Grad Sch Med Sci, Nagoya, Aichi, Japan
[4] Keio Univ, Sch Med, Dept Psychiat, Tokyo, Japan
[5] Natl Coordinating Ctr Women & Child Hlth, London, England
[6] Univ Bristol, Acad Unit Psychiat, Bristol, Avon, England
来源
COCHRANE DATABASE OF SYSTEMATIC REVIEWS | 2009年 / 02期
关键词
PRIMARY-CARE PATIENTS; CLINICAL-TRIALS; DOUBLE-BLIND; INDUSTRY SPONSORSHIP; 2ND-GENERATION ANTIPSYCHOTICS; STANDARD DEVIATIONS; MENTAL-HEALTH; OF-INTEREST; EFFICACY; METAANALYSIS;
D O I
10.1002/14651858.CD006532.pub2
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Although pharmacological and psychological interventions are both effective for major depression, antidepressant drugs remain the mainstay of treatment in primary and secondary care settings. During the last 20 years, antidepressant prescribing has risen dramatically in western countries, mainly because of the increasing consumption of selective serotonin reuptake inhibitors (SSRIs) and newer antidepressants, which have progressively become the most commonly prescribed antidepressants. Escitalopram is the pure S-enantiomer of the racemic citalopram. Objectives To assess the evidence for the efficacy, acceptability and tolerability of escitalopram in comparison with tricyclics, other SSRIs, heterocyclics and newer agents in the acute-phase treatment of major depression. Search strategy Electronic databases were searched up to July 2008. Trial databases of drug-approving agencies were hand-searched for published, unpublished and ongoing controlled trials. Selection criteria All randomised controlled trials comparing escitalopram against any other antidepressant (including non-conventional agents such as hypericum) for patients with major depressive disorder (regardless of the diagnostic criteria used). Data collection and analysis Data were entered by two review authors (double data entry). Responders and remitters to treatment were calculated on an intention-to-treat basis. For dichotomous data, odds ratios (ORs) were calculated with 95% confidence intervals (CI). Continuous data were analysed using standardised mean differences (with 95% CI) using the random effects model. Main results Fourteen trials compared escitalopram with another SSRI and eight compared escitalopram with a newer antidepressive agent (venlafaxine, bupropion and duloxetine). Escitalopram was shown to be significantly more effective than citalopram in achieving acute response (OR 0.67, 95% CI 0.50 to 0.87). Escitalopram was also more effective than citalopram in terms of remission (OR 0.53, 95% CI 0.30 to 0.93). Significantly fewer patients allocated to escitalopram withdrew from trials compared with patients allocated to duloxetine, for discontinuation due to any cause (OR 0.62, 95% CI 0.38 to 0.99). Authors' conclusions Some statistically significant differences favouring escitalopram over other antidepressive agents for the acute phase treatment of major depression were found, in terms of efficacy (citalopram and fluoxetine) and acceptability (duloxetine). There is insufficient evidence to detect a difference between escitalopram and other antidepressants in early response to treatment (after two weeks of treatment). Cost-effectiveness information is also needed in the field of antidepressant trials. Furthermore, as with most standard systematic reviews, the findings rely on evidence from direct comparisons. The potential for overestimation of treatment effect due to sponsorship bias should also be borne in mind.
引用
收藏
页数:252
相关论文
共 91 条
  • [1] Association of funding and conclusions in randomized drug trials - A reflection of treatment effect or adverse events?
    Als-Nielsen, B
    Chen, WD
    Gluud, C
    Kjaergard, LL
    [J]. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2003, 290 (07): : 921 - 928
  • [2] Statistics notes - Detecting skewness from summary information
    Altman, DG
    Bland, JM
    [J]. BRITISH MEDICAL JOURNAL, 1996, 313 (7066) : 1200 - 1200
  • [3] American Psychiatric Association D. S. M. T. F. & American Psychiatric Association, 2013, DIAGNOSTIC STAT MANU, V5, DOI 10.1016/B978-0-12-809324-5.05530-9
  • [4] Evidence-based guidelines for treating depressive disorders with antidepressants: a revision of the 1993 British Association for Psychopharmacology guidelines
    Anderson, IM
    Nutt, DJ
    Deakin, JFW
    [J]. JOURNAL OF PSYCHOPHARMACOLOGY, 2000, 14 (01) : 3 - 20
  • [5] [Anonymous], COCHRANE DATABASE SY
  • [6] [Anonymous], MANUAL ECDEU ASSESSM
  • [7] [Anonymous], 1991, Tenth revision of the international classification of diseases
  • [8] [Anonymous], DEPR MAN DEPR PRIM S
  • [9] [Anonymous], ANN M AM COLL NEUR D
  • [10] [Anonymous], COCHRANE DATABASE SY