Trajectories of antidepressant drugs during pregnancy: A cohort study from a community-based sample.


Journal

British journal of clinical pharmacology
ISSN: 1365-2125
Titre abrégé: Br J Clin Pharmacol
Pays: England
ID NLM: 7503323

Informations de publication

Date de publication:
03 2021
Historique:
received: 22 01 2020
revised: 30 05 2020
accepted: 11 06 2020
pubmed: 6 8 2020
medline: 27 7 2021
entrez: 6 8 2020
Statut: ppublish

Résumé

The aim of this study was to monitor the trajectories of antidepressant use during pregnancy and the postpartum period among women chronically treated with antidepressants before their pregnancy, and to assess characteristics associated with each trajectory. This cohort study included all pregnant women whose data were included in the General Sample of Beneficiaries (EGB) database affiliated with the French Health Insurance System, from 2009 to 2014. Women were followed up until 6 months after childbirth. Chronic treatment was defined as exposure over the 6-month period preceding pregnancy. A group-based trajectory model (GBMT) was estimated to identify distinctive longitudinal profiles of antidepressant use. Among 760 women chronically treated with antidepressants before their pregnancy, 55.8% stopped their treatment permanently in the first trimester, 20.4% discontinued it for a minimum of 3 months and resumed it postpartum, and 23.8% maintained it throughout pregnancy and postpartum. No sociodemographic or medical characteristics were associated with any trajectory group. Women who maintained treatment presented more frequent obstetric complications and postpartum psychiatric disorders. Among women who interrupted treatment, prescription of benzodiazepines and anxiolytics decreased initially but rose postpartum to a higher level than before pregnancy. Pregnant women treated with antidepressant require a re-evaluation of psychiatric treatment. It is necessary to pay attention to obstetric complications for severely depressed women. Additionally, as relapse was associated with increased benzodiazepine use, it is important to carefully monitor all women who stop antidepressant treatment during pregnancy.

Identifiants

pubmed: 32755022
doi: 10.1111/bcp.14449
doi:

Substances chimiques

Antidepressive Agents 0
Benzodiazepines 12794-10-4

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

965-987

Commentaires et corrections

Type : CommentIn

Informations de copyright

© 2020 The British Pharmacological Society.

Références

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Auteurs

Aurélie Cabaillot (A)

Département de Médecine Générale, UFR de Médicine, Université Clermont Auvergne, Clermont-Ferrand, France.
CHU Clermont-Ferrand, Inserm, Neuro-Dol, Service de Pharmacologie médicale, Centres Addictovigilance et Pharmacovigilance, Observatoire Français des Médicaments Antalgiques (OFMA), Institut Analgesia, Université Clermont Auvergne, Clermont-Ferrand, France.

Alexandra Bourset (A)

Département de Médecine Générale, UFR de Médicine, Université Clermont Auvergne, Clermont-Ferrand, France.

Aurélien Mulliez (A)

Délégation à la recherche clinique et à l'innovation, CHU Clermont-Ferrand, Clermont-Ferrand, France.

Jessica Delorme (J)

CHU Clermont-Ferrand, Inserm, Neuro-Dol, Service de Pharmacologie médicale, Centres Addictovigilance et Pharmacovigilance, Observatoire Français des Médicaments Antalgiques (OFMA), Institut Analgesia, Université Clermont Auvergne, Clermont-Ferrand, France.

Massimiliano Orri (M)

McGill Group for Suicide Studies, Douglas Mental Health University Institute, Department of Psychiatry, McGill University, Montréal, QC, Canada.
Bordeaux Population Health Research Centre, Inserm U1219, Université de Bordeaux, Bordeaux, France.

Mathilde Vicard-Olagne (M)

Département de Médecine Générale, UFR de Médicine, Université Clermont Auvergne, Clermont-Ferrand, France.
Npsysydo, Université Clermont Auvergne, Clermont-Ferrand, France.

Marie Christine Zenut (MC)

CHU Clermont-Ferrand, Inserm, Neuro-Dol, Service de Pharmacologie médicale, Centres Addictovigilance et Pharmacovigilance, Observatoire Français des Médicaments Antalgiques (OFMA), Institut Analgesia, Université Clermont Auvergne, Clermont-Ferrand, France.

Marie Tournier (M)

Inserm, Bordeaux Population Health Research Center, Team Pharmacoepidemiology, Université de Bordeaux, Bordeaux, France.
Hospital Charles Perrens, Bordeaux, France.

Denis Gallot (D)

CNRS 6293, INSERM 1103, GReD, QC G1V 0A6 Clermont-Ferrand; Department of Obstetrics and Gynecology, CHU Clermont-Ferrand, Faculty of Medicine, Université Clermont-Auvergne, Clermont-Ferrand, France.

Nicolas Authier (N)

CHU Clermont-Ferrand, Inserm, Neuro-Dol, Service de Pharmacologie médicale, Centres Addictovigilance et Pharmacovigilance, Observatoire Français des Médicaments Antalgiques (OFMA), Institut Analgesia, Université Clermont Auvergne, Clermont-Ferrand, France.

Chouki Chenaf (C)

CHU Clermont-Ferrand, Inserm, Neuro-Dol, Service de Pharmacologie médicale, Centres Addictovigilance et Pharmacovigilance, Observatoire Français des Médicaments Antalgiques (OFMA), Institut Analgesia, Université Clermont Auvergne, Clermont-Ferrand, France.

Catherine Laporte (C)

Département de Médecine Générale, UFR de Médicine, Université Clermont Auvergne, Clermont-Ferrand, France.
Npsysydo, Université Clermont Auvergne, Clermont-Ferrand, France.

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