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Antidepressants and risk of suicide or self-harm in Canadian youth: A study involving common data models in Quebec and British Columbia

Published online by Cambridge University Press:  15 April 2020

Y. Moride
Affiliation:
Université de Montréal, Faculté de pharmacie, Canada
T. Lynd
Affiliation:
University of British Columbia, Canada
H. Ducruet
Affiliation:
Université de Montréal, Faculté de pharmacie, Canada
H. Li
Affiliation:
University of British Columbia, Canada
M. Tournier*
Affiliation:
Université de Bordeaux, Inserm U657, Bordeaux Department of Psychiatry, Montreal Children Hospital, Montreal, Quebec, Canada
B. Greenield
Affiliation:
Université de Bordeaux, Inserm U657, Bordeaux Department of Psychiatry, Montreal Children Hospital, Montreal, Quebec, Canada
*
*E-mail address: mtournier@ch-perrens.fr (M. Tournier)

Abstract

Introduction

The use of antidepressants (AD) in children and adolescents has become controversial due to a possible increased risk of suicide, revised evidence about effectiveness, and growing usage. Several studies have been conducted through healthcare databases, mainly restricted to hospitalized cases.

Objective

To evaluate the rate of self-harm among children (10–14 years) and adolescents (15–19 years) who use AD and to compare rates between classes of AD, using a common data model.

Methods

A retrospective cohort study was conducted in children and adolescents, age 10–19, members of the Quebec (QC) public drug plan or residents of British Columbia (BC), and who received a new AD treatment in 1997–2008 (QC) and 1997–2006 (BC). Self-harm (fatal or non-fatal) was the main outcome. Data sources consisted of prescription, medical services, and hospitalization databases. AD were categorized into: fluoxetine (only AD approved for paediatric use for depression in Canada), non-fluoxetine SSRIs, TCAs, and others. Multivariate logistic regression analyses were conducted using high dimensional propensity scores.

Results

Were included 51,868 and 28,200 AD users from BC and QC, respectively: 70% were females, and 60% had received a diagnosis of depression. Risk of hospitalization for self-harm was 38.15 and 19.23/1000 person-years in BC and QC, respectively. Rates were higher among adolescents (BC: 47.52; QC: 21.36) than children (BC: 17.00, QC: 12.99). For both hospitalized and non-hospitalized cases, while there was no statistically significant difference in risk associated with fluoxetine relative to non-fluoxetine SSRIs, TCAs were associated with a lower risk in BC (OR = 0.47; 95% CI: 0.31–0.72) and Quebec (OR = 0.41; 95% CI: 0.30–0.46).

Conclusion

In two independent large cohorts, there was no apparent differences in risk across ADs. Lower risk of TCAs may be due to residual confounding by indication.

Type
Congrès français de psychiatrie: Rencontres avec l’expert
Copyright
Copyright © European Psychiatric Association 2015

Disclosure of interest

MT a reçu des honoraires comme orateur par Janssen, BMS, AstraZeneca. YM, LL, BG et TD travaillent comme consultants pour les autorités de régulation et l’industrie pharmaceutique.

References

Further reading

Isacsson, GRich, CL. Antidepressant drugs and the risk of suicide in children and adolescents. Paediatr Drugs 2014;16(2):115–22.CrossRefGoogle ScholarPubMed
Miller, MPate, VSwanson, SAAzrael, DWhite, AStürmer, T. Antidepressant class, age, and the risk of deliberate self-harm: a propensity score matched cohort study of SSRI and SNRI users in the USA. CNS Drugs 2014;28 (1):7988.CrossRefGoogle ScholarPubMed
Stone, MLaughren, TJones, MLLevenson, MHolland, PCHughes, A, et al. Risk of suicidality in clinical trials of antidepressants in adults: analysis of proprietary data submitted to US Food and Drug Administration. BMJ 2009;339:b2880.CrossRefGoogle ScholarPubMed
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