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Published in: BMC Psychiatry 1/2019

Open Access 01-12-2019 | Antidepressant Drugs | Debate

Guidelines for the pharmacological acute treatment of major depression: conflicts with current evidence as demonstrated with the German S3-guidelines

Authors: Martin Plöderl, Michael P. Hengartner

Published in: BMC Psychiatry | Issue 1/2019

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Abstract

Several international guidelines for the acute treatment of moderate to severe unipolar depression recommend a first-line treatment with antidepressants (AD). This is based on the assumption that AD obviously outperform placebo, at least in the case of severe depression. The efficacy of AD for severe depression can only be definitely clarified with individual patient data, but corresponding studies have only been available recently. In this paper, we point out discrepancies between the content of guidelines and the scientific evidence by taking a closer look at the German S3-guidelines for the treatment of depression. Based on recent studies and a systematic review of studies using individual patient data, it turns out that AD are marginally superior to placebo in both moderate and severe depression. The clinical significance of this small drug-placebo-difference is questionable, even in the most severe forms of depression. In addition, the modest efficacy is likely an overestimation of the true efficacy due to systematic method biases. There is no related discussion in the S3-guidelines, despite substantial empirical evidence confirming these biases. In light of recent data and with their underlying biases, the recommendations in the S3-guidelines are in contradiction with the current evidence. The risk-benefit ratio of AD for severe depression may be similar to the one estimated for mild depression and thus could be unfavorable. Downgrading of the related grade of recommendation would be a logical consequence.
Footnotes
1
All quotations from the S3-guidelines were translated into English by the authors.
 
2
Unfortunately, the NICE guidelines did not justify the different definitions of clinical significance. Three different criteria for clinical significance were defined: First, a ≥ 3 points difference between AD and placebo on the HAMD scale (or the BDI scale). Second, an effect-size of d ≥ 0.5 (equivalent to approximately 3.8 points difference on the HAMD scale [17]). Third, a risk-ratio (RR) of RR ≤ 0.8 for response rates. Of note, these criteria are an absolute minimum, corresponding to a “no improvement” clinical judgment, but this is not mentioned. Furthermore, the three criteria are not equivalent, leading to contradictory conclusions. For example, the average effect-size in a recent meta-analysis [20] was d = 0.3 (clearly below the required d = 0.5), corresponding to a 2.4 HAMD points difference (below the required 3 points), but to a risk ratio of RR = 0.8 (only just fulfilling the criterion).
 
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Metadata
Title
Guidelines for the pharmacological acute treatment of major depression: conflicts with current evidence as demonstrated with the German S3-guidelines
Authors
Martin Plöderl
Michael P. Hengartner
Publication date
01-12-2019
Publisher
BioMed Central
Published in
BMC Psychiatry / Issue 1/2019
Electronic ISSN: 1471-244X
DOI
https://doi.org/10.1186/s12888-019-2230-4

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