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Meta-Analysis
. 2008 Mar;196(4):511-20; discussion 521-2.
doi: 10.1007/s00213-007-0975-9. Epub 2007 Oct 23.

Re-evaluation of the efficacy and tolerability of venlafaxine vs SSRI: meta-analysis

Affiliations
Meta-Analysis

Re-evaluation of the efficacy and tolerability of venlafaxine vs SSRI: meta-analysis

S Weinmann et al. Psychopharmacology (Berl). 2008 Mar.

Abstract

Rationale: A number of reviews have claimed that the selective serotonin and noradrenalin re-uptake inhibitor venlafaxine is more effective than selective serotonin re-uptake inhibitors (SSRIs) in achieving remission and symptom reduction in major depression.

Objectives: The aim of this study was to systematically review studies on the efficacy of venlafaxine vs SSRI and to evaluate the influence of methodological issues on the effect sizes.

Materials and methods: Following a systematic literature search, we pooled data on depression scores, response, remission and dropout rates. We also performed sub-group analyses.

Results: Seventeen studies were included. We found no significant superiority in remission rates (risk ratio [RR] = 1.07, 95% confidence intervals [95%CI] = 0.99 to 1.15, numbers needed to treat [NNT] = 34) and a small superiority in response rates (RR = 1.06, 95%CI = 1.01 to 1.12, NNT = 27) over SSRIs. There was a small advantage to venlafaxine in change scores (effect size = -0.09, 95%CI = -0.16 to -0.02, p = 0.013), which did not reach significance when post-treatment scores were used (effect size = -0.06, 95%CI = -0.13 to 0.00). Discontinuation rates due to adverse events were 45% higher in the venlafaxine group. The main reasons for the differences between this analysis and previous reviews were the exclusion of studies with methodological limitations, avoiding to pool selectively reported study results and exclusion of studies available as abstracts only.

Conclusions: Our analysis does not support a clinically significant superiority of venlafaxine over SSRIs. Differences between our study and previous reviews were not accounted for by technical aspects of data synthesis, but rather by study selection and choice of outcome parameters.

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Comment in

  • The review by Weinmann and colleagues.
    Freemantle N. Freemantle N. Psychopharmacology (Berl). 2008 Jul;199(1):131-2; author reply 133-4. doi: 10.1007/s00213-008-1106-y. Epub 2008 May 28. Psychopharmacology (Berl). 2008. PMID: 18504557 No abstract available.

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References

    1. Int Clin Psychopharmacol. 2000 Jan;15(1):29-34 - PubMed
    1. Br J Psychiatry. 2004 May;184:452-3 - PubMed
    1. Arch Gen Psychiatry. 1991 Sep;48(9):851-5 - PubMed
    1. J Clin Psychopharmacol. 2005 Aug;25(4 Suppl 1):S1-7 - PubMed
    1. Acta Psychiatr Scand Suppl. 2002;(415):24-30 - PubMed

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