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Journal Article

Citation

Curtin F, Schulz P. Br. Med. J. BMJ 2005; 330(7500): 1148; author reply 1148-9.

Affiliation

Clinical Psychopharmacology Unit, University Hospital of Geneva, Geneva, Switzerland. francoiscurtin@compuserve.com

Copyright

(Copyright © 2005, BMJ Publishing Group)

DOI

10.1136/bmj.330.7500.1148

PMID

15891236

PMCID

PMC557907

Abstract

Gunnell et al's report on suicide risk with selective serotonin reuptake inhibitors (SSRIs) raises several issues. Firstly, clinicians have observed that the first weeks of treatment of severe depression with an antidepressant are accompanied by a higher risk of suicide because of a drug induced motor disinhibition that is not yet accompanied by mood improvement. Secondly, the authors' finding of a trend towards a protective effect of SSRIs against suicidal thoughts (odds ratio 0.77) compared with a trend towards an increased risk of self harm (odds ratio 1.57) is paradoxical. More surprising is the heterogeneity of results among SSRIs. Why would sertraline show a protective effect for suicidal thoughts and simultaneously increase the risk of self harm? The risk difference between citalopram and its active S-enantiomere, escitalopram, is also strange. No strong biological rationale can explain such heterogeneity among drugs with the same mechanism of action.

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