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Discontinuation of antidepressant treatment: a retrospective cohort study on more than 20,000 participants

Abstract:
Background: Factors influencing antidepressant treatment discontinuation are poorly understood. In the present study, we aimed to estimate the prevalence of antidepressant treatment discontinuation and identify demographic characteristics, psychiatric comorbidities, and specific side effects associated with treatment discontinuation. Methods: We leveraged data from the Australian Genetics of Depression Study (AGDS; N = 20,941) to perform a retrospective cohort study on antidepressant treatment discontinuation. Participants were eligible if they were over 18 years of age, had taken antidepressants in the past 4 years, and provided informed consent. Results: Among the ten antidepressants studied, the highest discontinuation rates were observed for Mirtazapine (57.3%) and Amitriptyline (51.6%). Discontinuation rates were comparable across sexes except for Mirtazapine, for which women were more likely to discontinue. The two most common side effects, reduced sexual function and weight gain, were not associated with increased odds of treatment discontinuation. Anxiety, agitation, suicidal thoughts, vomiting, and rashes were associated with higher odds for treatment discontinuation, as were lifetime diagnoses of PTSD, ADHD, and a higher neuroticism score. Educational attainment showed a negative (protective) association with discontinuation across medications. Conclusions: Our study suggests that not all side effects contribute equally to discontinuation. Common side effects such as reduced sexual function and weight gain may not necessarily increase the risk of treatment discontinuation. Side effects linked to discontinuation can be divided into two groups, psychopathology related and allergy/intolerance.
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1186/s12991-023-00480-z

Authors

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Role:
Author
ORCID:
0000-0003-4731-6558
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Role:
Author
ORCID:
0000-0002-9491-7797
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Role:
Author
ORCID:
0000-0003-1382-380X
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Institution:
University of Oxford
Role:
Author
ORCID:
0000-0001-7421-3357


Publisher:
BioMed Central
Journal:
Annals of General Psychiatry More from this journal
Volume:
22
Issue:
1
Pages:
49-49
Article number:
49
Publication date:
2023-11-24
DOI:
EISSN:
1744-859X
ISSN:
1744-859X


Language:
English
Keywords:
Pubs id:
1577514
Local pid:
pubs:1577514
Source identifiers:
W4388972558
Deposit date:
2026-06-04
ARK identifier:
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