Jump to: Page Content, Site Navigation, Site Search,
You are seeing this message because your web browser does not support basic web standards. Find out more about why this message is appearing and what you can do to make your experience on this site better.
BMJ 2005;330:1149-1150 (14 May), doi:10.1136/bmj.330.7500.1149-b
EDITORFergusson et al report that the risk of suicide attempts is significantly greater for patients enrolled in short term randomised controlled trials of selective serotonin reuptake inhibitors (SSRIs) than with placebo (odds ratio 2.28, P < 0.02) and other interventions (not including tricyclics) (odds ratio 1.94).1 They are also one of the few groups to report that completed suicides (fatal attempts) were also higher with SSRIs than tricyclics (odds ratio 7.27 [corrected to 1.08 (0.28 to 4.09), see correction, 19 March, p 653]). This seems to have led Cipriani et al to say that there is almost a double risk of fatal and non-fatal risk of suicide for people taking SSRIs.2
An increased risk of fatal overdoses when using SSRIs is hard to understand, particularly when the comparison is tricyclics, given their acknowledged toxicity in overdose.3-5 I therefore rechecked the odds ratios from the data given by Fergusson et al and found most of them to be incorrect.
For example, they say that the odds ratio of suicide attempts in SSRIs compared with others is 1.94; but with 27 SSRI cases out of 4130 treated patients and 18 control cases out of 4233 treated patients the odds ratio is 1.54 (95% confidence interval 0.85 to 2.8)that is, non-significant. Changing the denominator to 8856 and 9059 (all trials) makes no difference to the result.
Similarly, Fergusson et al say that the odds ratio for non-fatal attempts was 2.25 whereas I calculate it at 1.89 (0.96 to 3.73), again non-significant. Perhaps most incomprehensibly regarding the odds of completed suicide and tricyclics, the number of SSRI cases is five and that of tricyclic antidepressant cases is foura non-significant difference.
In conclusion, either most of the raw data printed in table 1 are wrong or one of us has miscalculated dramatically.
Alex J Mitchell, consultant in liaison psychiatry
Leicester General Hospital, Leicester LE5 4PW alex.mitchell{at}leicspart.nhs.uk