Literature DB >> 16968586

Remission, dropouts, and adverse drug reaction rates in major depressive disorder: a meta-analysis of head-to-head trials.

Márcio Machado1, Michael Iskedjian, Inés Ruiz, Thomas R Einarson.   

Abstract

OBJECTIVE: To summarize remission rates and dropouts due to adverse drug reactions (ADRs) or lack of efficacy (LoE) of serotonin-norepinephrine reuptake inhibitors (SNRIs), selective serotonin-reuptake inhibitors (SSRIs), and tricyclic antidepressants (TCAs) in treating major depressive disorder.
METHODS: We searched MEDLINE, EMBASE, IPA, and the Cochrane International Library from 1980-2005. Meta-analysis summarized outcomes from head-to-head randomized clinical trials comparing >or= 2 drugs from three antidepressants classes (SNRIs, and/or SSRIs, and/or TCAs) followed by >or= 6 weeks of treatment. Remission was a final Hamilton Depression Rating Scale (HAMD) score <or= 7 or Montgomery-Asberg Depression Rating Scale (MADRS) <or= 12. Intent-to-treat data were combined across study arms using random effects models, producing point estimates with 95% confidence intervals.
RESULTS: We obtained data from 30 arms of 15 head-to-head trials with 2458 patients. SNRIs had the highest ITT remission rate (49.0%), then TCAs (44.1%), and SSRIs (37.7%) (p > 0.05 for SNRIs versus TCAs; p < 0.001 for TCAs versus SSRIs and SNRIs versus SSRIs). When categorized as inpatients (n = 582) and outpatients (n = 1613), SNRIs had the highest remission rates (52.0% for 144 inpatients and 49.3% for 559 outpatients). SNRIs had lowest overall dropouts (26.1%), followed by SSRIs (28.4%), and TCAs (35.7%). Dropouts due to ADRs and LoE were 10.3% and 6.2% for SNRIs, 8.3% and 7.2% for SSRIs, and 19.8% and 9.9% for TCAs, respectively (p > 0.05 for ADR dropouts only). One limitation was the inclusion of only venlafaxine-XR; results may not be the same for immediate release forms. In addition, few studies reported remission rates.
CONCLUSIONS: SNRIs had the highest efficacy remission rates (statistically significant for inpatients and outpatients), and the lowest overall dropout rates, suggesting clinical superiority in treating major depression.

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Year:  2006        PMID: 16968586     DOI: 10.1185/030079906X132415

Source DB:  PubMed          Journal:  Curr Med Res Opin        ISSN: 0300-7995            Impact factor:   2.580


  36 in total

Review 1.  Systematic Review and Meta-Analysis: Dose-Response Relationship of Selective Serotonin Reuptake Inhibitors in Major Depressive Disorder.

Authors:  Ewgeni Jakubovski; Anjali L Varigonda; Nicholas Freemantle; Matthew J Taylor; Michael H Bloch
Journal:  Am J Psychiatry       Date:  2015-11-10       Impact factor: 18.112

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

Authors:  S Weinmann; T Becker; M Koesters
Journal:  Psychopharmacology (Berl)       Date:  2007-10-23       Impact factor: 4.530

3.  Early adverse events and attrition in selective serotonin reuptake inhibitor treatment: a suicide assessment methodology study report.

Authors:  Diane Warden; Madhukar H Trivedi; Stephen R Wisniewski; Benji Kurian; Sidney Zisook; Susan G Kornstein; Edward S Friedman; Sachiko Miyahara; Andrew F Leuchter; Maurizio Fava; A John Rush
Journal:  J Clin Psychopharmacol       Date:  2010-06       Impact factor: 3.153

4.  Remission with venlafaxine extended release or selective serotonin reuptake inhibitors in depressed patients: a randomized, open-label study.

Authors:  Michael E Thase; Philip T Ninan; Jeff J Musgnung; Madhukar H Trivedi
Journal:  Prim Care Companion CNS Disord       Date:  2011

5.  Response to sertraline is influenced by GNβ3 gene G-350A variant in patients with major depressive disorder.

Authors:  Dena Firouzabadi; Negar Firouzabadi; Kiana Kalani; Kamyar Zomorrodian; Elham Shirazi Tehrani
Journal:  Eur J Clin Pharmacol       Date:  2018-10-15       Impact factor: 2.953

6.  Antidepressant effects on serotonin 1A/1B receptors in the rat brain using a gene x environment model.

Authors:  Stal Saurav Shrestha; Daniel S Pine; David A Luckenbaugh; Katarina Varnäs; Ioline D Henter; Robert B Innis; Aleksander A Mathé; Per Svenningsson
Journal:  Neurosci Lett       Date:  2013-11-25       Impact factor: 3.046

7.  Olanzapine and fluoxetine combination therapy for treatment-resistant depression: review of efficacy, safety, and study design issues.

Authors:  William V Bobo; Richard C Shelton
Journal:  Neuropsychiatr Dis Treat       Date:  2009-07-02       Impact factor: 2.570

8.  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

Review 9.  A systematic approach to pharmacotherapy for geriatric major depression.

Authors:  Benoit H Mulsant; Daniel M Blumberger; Zahinoor Ismail; Kiran Rabheru; Mark J Rapoport
Journal:  Clin Geriatr Med       Date:  2014-06-14       Impact factor: 3.076

10.  The economic impact of introducing serotonin-noradrenaline reuptake inhibitors into the Brazilian national drug formulary: cost-effectiveness and budget-impact analyses.

Authors:  Márcio Machado; Michael Iskedjian; Inés A Ruiz; Thomas R Einarson
Journal:  Pharmacoeconomics       Date:  2007       Impact factor: 4.981

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