Literature DB >> 12918001

A comparison of active drugs for the treatment of dysthymia.

M Silva de Lima1, M Hotopf.   

Abstract

BACKGROUND: Many drug treatments have been proposed for the treatment of dysthymia, but with so many potential comparisons it is not possible at the present time to determine which is the treatment of choice. There is a need to know whether the different classes of antidepressants have similar efficacy. In addition, the tolerability of treatments may be even more important, since dysthymia is a chronic condition characterised by less severe symptoms than major depression.
OBJECTIVES: To conduct a systematic review of all randomised controlled trials comparing two or more active drug treatments for dysthymia. SEARCH STRATEGY: Electronic searches of Cochrane Library, EMBASE, MEDLINE, PsycLIT and LILACS, Biological Abstracts; reference searching; personal communication; unpublished trials from pharmaceutical industry. SELECTION CRITERIA: Only randomised and quasi-randomised controlled trials were included. Trials had to compare at least two active drug treatments in the treatment of dysthymia. Exclusion criteria were: non-randomised studies, studies which included patients with mixed major depression/dysthymia and studies on depression/dysthymia secondary to other disorders (e.g. substance abuse). DATA COLLECTION AND ANALYSIS: The reviewers extracted the data independently and odds ratios, weighted mean difference and number needed to treat were estimated. The reviewers assumed that people who died or dropped out had no improvement and tested the sensitivity of the final results to this assumption. MAIN
RESULTS: A total of 14 trials were eligible for inclusion in the review. All studied drugs promoted similar clinical responses, although with different side effect profiles. The evidence for TCAs and SSRIs was the most robust, considering the number of trials and participants. REVIEWER'S
CONCLUSIONS: The conclusion is that the choice of drug must be made based on consideration of drug-specific side effect properties.

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Year:  2003        PMID: 12918001      PMCID: PMC6986692          DOI: 10.1002/14651858.CD004047

Source DB:  PubMed          Journal:  Cochrane Database Syst Rev        ISSN: 1361-6137


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