Literature DB >> 19165525

The effect of venlafaxine compared with other antidepressants and placebo in the treatment of major depression: a meta-analysis.

Michael Bauer1, Puvan Tharmanathan, Hans-Peter Volz, Hans-Juergen Moeller, Nick Freemantle.   

Abstract

OBJECTIVE: Meta-analysis of all available trials of Venlafaxine in the treatment of major depressive disorders, including treatment resistant depression and long-term relapse prevention.
METHODS: We conducted a meta-analysis comparing venlafaxine and tricyclics, or selective serotonin reuptake inhibitors (SSRIs), in major depression. We also included trials comparing venlafaxine and alternative antidepressants in subjects with treatment resistant depression, or compared with placebo in long-term relapse prevention. Trials were identified through searches of Medline, Embase, Cochrane Library and through accessing unpublished trials held by the manufacturer. Results based on intention to treat analyses where available, were pooled using theoretically exact conditional maximum likelihood methods for fixed effects (primary analyses), and numerical simulation using a Gibbs sampler for full random effects.
RESULTS: Compared to all SSRIs for the treatment of major depression (fluoxetine, paroxetine, sertraline, citalopram, escitalopram and fluvoxamine), venlafaxine was associated with a greater response [odds ratio 1.15 (95% CI 1.02-1.29)] and remission [odds ratio 1.19 (95% CI 1.06-1.34)]. Overall drop out rates appeared similar for SSRIs and venlafaxine. Compared to tricyclics, response to venlafaxine was estimated to be greater by exact method, odds ratio 1.21 (95% CI 1.03-1.43), but not statistically significantly different, using a full random effects method odds ratio 1.22 (95% CI 0.96-1.54). We observed no difference in remission rates (odds ratio 1.06 (95% CI 0.74-1.63)). Tricyclics were less well tolerated with higher overall drop out rates. Compared to alternative antidepressants in treatment resistant depression (trials included comparison with sertraline, bupropion, fluoxetine, citalopram, and one with a range of agents-mostly SSRIs), the odds ratio for response was 1.35 (95% CI 1.19-1.54). The odds ratio for remission was 1.35 (95% CI 1.20-1.52). Compared to placebo the odds ratio for relapse prevention with venlafaxine was 0.37 (95% CI 0.27-0.51).
CONCLUSION: This meta analysis provides evidence of the clinical efficacy of venlafaxine in achieving therapeutic response and remission in patients with major depression. Venlafaxine appears more effective than SSRIs, and at least as effective as tricyclic antidepressants, in the treatment of major depressive episode. Venlafaxine appeared more effective than comparators in treatment resistant depression. In addition, venlafaxine effective in reducing relapse when given long term after major depressive episode.

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Year:  2009        PMID: 19165525     DOI: 10.1007/s00406-008-0849-0

Source DB:  PubMed          Journal:  Eur Arch Psychiatry Clin Neurosci        ISSN: 0940-1334            Impact factor:   5.270


  51 in total

1.  Increased remission rates with venlafaxine compared with fluoxetine in hospitalized patients with major depression and melancholia.

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2.  The efficacy and tolerability of venlafaxine and paroxetine in outpatients with depressive disorder or dysthymia.

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5.  Venlafaxine XR demonstrates higher rates of sustained remission compared to fluoxetine, paroxetine or placebo.

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7.  A randomized, double-blind comparison of a rapidly escalating dose of venlafaxine and imipramine in inpatients with major depression and melancholia.

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8.  Randomized, double-blind comparison of venlafaxine and fluoxetine in outpatients with major depression.

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9.  Long-term safety and clinical acceptability of venlafaxine and imipramine in outpatients with major depression.

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10.  Bupropion-SR, sertraline, or venlafaxine-XR after failure of SSRIs for depression.

Authors:  A John Rush; Madhukar H Trivedi; Stephen R Wisniewski; Jonathan W Stewart; Andrew A Nierenberg; Michael E Thase; Louise Ritz; Melanie M Biggs; Diane Warden; James F Luther; Kathy Shores-Wilson; George Niederehe; Maurizio Fava
Journal:  N Engl J Med       Date:  2006-03-23       Impact factor: 91.245

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  34 in total

1.  How close is evidence to truth in evidence-based treatment of mental disorders?

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Journal:  Eur Arch Psychiatry Clin Neurosci       Date:  2011-11-22       Impact factor: 5.270

2.  Use of antidepressants during pregnancy and the risk of spontaneous abortion.

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Review 3.  How should primary care doctors select which antidepressants to administer?

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4.  Treatment of Resistant Depression in Adolescents (TORDIA): week 24 outcomes.

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Review 5.  The efficacy and tolerability of bupropion in the treatment of major depressive disorder.

Authors:  Ricardo Moreira
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Review 6.  [Psychotherapy of depressive disorders: Evidence in chronic depression and comorbidities].

Authors:  M Härter; A Jansen; M Berger; H Baumeister; T Bschor; T Harfst; M Hautzinger; L Kriston; C Kühner; H Schauenburg; S G Schorr; F Schneider; R Meister
Journal:  Nervenarzt       Date:  2018-03       Impact factor: 1.214

7.  Evidence-based medicine in psychopharmacotherapy: possibilities, problems and limitations.

Authors:  Hans-Jürgen Möller; Wolfgang Maier
Journal:  Eur Arch Psychiatry Clin Neurosci       Date:  2010-02       Impact factor: 5.270

8.  [Pharmacotherapy of depression in the elderly].

Authors:  V Holthoff
Journal:  Z Gerontol Geriatr       Date:  2013-02       Impact factor: 1.281

9.  Development of potent dopamine-norepinephrine uptake inhibitors (DNRIs) based on a (2S,4R,5R)-2-benzhydryl-5-((4-methoxybenzyl)amino)tetrahydro-2H-pyran-4-ol molecular template.

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Journal:  Bioorg Med Chem       Date:  2014-12-25       Impact factor: 3.641

10.  Milnacipran and venlafaxine at flexible doses (up to 200 mg/day) in the outpatient treatment of adults with moderate-to-severe major depressive disorder: a 24-week randomized, double-blind exploratory study.

Authors:  Jean-Pierre Olié; David Gourion; Agnès Montagne; Michel Rostin; Marie-France Poirier
Journal:  Neuropsychiatr Dis Treat       Date:  2010-04-07       Impact factor: 2.570

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