Association between citalopram, escitalopram and QTc prolongation in a real-world geriatric setting.


Journal

Journal of affective disorders
ISSN: 1573-2517
Titre abrégé: J Affect Disord
Pays: Netherlands
ID NLM: 7906073

Informations de publication

Date de publication:
01 05 2019
Historique:
received: 13 10 2018
revised: 17 01 2019
accepted: 25 02 2019
pubmed: 17 3 2019
medline: 30 6 2019
entrez: 17 3 2019
Statut: ppublish

Résumé

Although the US Food and Drug Administration (FDA) recommended upper limits for citalopram dosing in older adults due to risk of corrected-QT (QTc) prolongation, which was adopted, and extended to escitalopram by Health Canada, the scientific basis is unclear. The objective of this study was to assess the relationship between citalopram/escitalopram dosages and QTc interval in a real-world geriatric setting. We reviewed electronic health records at a university-affiliated geriatric health care center, over a 7-year period, to identify patients prescribed citalopram and escitalopram, who had an ECG within 90 days of initiation or dosage change. Linear regression analyses were conducted to assess the relationship between antidepressant dosage and QTc interval. 137 patients were identified (citalopram=97, escitalopram=40). No association was found between citalopram, escitalopram and QTc, in unadjusted or adjusted analyses. Among covariates, older age was significantly associated with QTc prolongation in the escitalopram group. Limitations to the current study include its retrospective design and the small sample size. These data do not support the FDA or Health Canada's recommended maximum dosages of citalopram or escitalopram in the elderly. Therefore, for patients already on higher doses of these medications, the risk of QTc prolongation may not always outweigh the risk of dose lowering, such as relapse. Until larger prospective studies become available, the decision to comply or not with these federal agencies' recommendations should be weighed on an individual basis, taking into consideration all potential risk factors.

Sections du résumé

BACKGROUND
Although the US Food and Drug Administration (FDA) recommended upper limits for citalopram dosing in older adults due to risk of corrected-QT (QTc) prolongation, which was adopted, and extended to escitalopram by Health Canada, the scientific basis is unclear. The objective of this study was to assess the relationship between citalopram/escitalopram dosages and QTc interval in a real-world geriatric setting.
METHODS
We reviewed electronic health records at a university-affiliated geriatric health care center, over a 7-year period, to identify patients prescribed citalopram and escitalopram, who had an ECG within 90 days of initiation or dosage change. Linear regression analyses were conducted to assess the relationship between antidepressant dosage and QTc interval.
RESULTS
137 patients were identified (citalopram=97, escitalopram=40). No association was found between citalopram, escitalopram and QTc, in unadjusted or adjusted analyses. Among covariates, older age was significantly associated with QTc prolongation in the escitalopram group.
LIMITATIONS
Limitations to the current study include its retrospective design and the small sample size.
CONCLUSIONS
These data do not support the FDA or Health Canada's recommended maximum dosages of citalopram or escitalopram in the elderly. Therefore, for patients already on higher doses of these medications, the risk of QTc prolongation may not always outweigh the risk of dose lowering, such as relapse. Until larger prospective studies become available, the decision to comply or not with these federal agencies' recommendations should be weighed on an individual basis, taking into consideration all potential risk factors.

Identifiants

pubmed: 30877856
pii: S0165-0327(18)32053-6
doi: 10.1016/j.jad.2019.02.060
pii:
doi:

Substances chimiques

Serotonin Uptake Inhibitors 0
Citalopram 0DHU5B8D6V

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

341-345

Informations de copyright

Copyright © 2019. Published by Elsevier B.V.

Auteurs

Gabrielle Crépeau-Gendron (G)

Département de psychiatrie et d'addictologie, Division de gérontopsychiatrie, Université de Montréal; Hôpital en santé mentale Albert-Prévost, Montréal, Québec, Canada. Electronic address: gabrielle.crepeau-gendron@umontreal.ca.

Hilary K Brown (HK)

Interdisciplinary Centre for Health & Society, University of Toronto Scarborough and Dalla Lana School of Public Health, University of Toronto; Women's College Research Institute, Women's College Hospital, Canada.

Carrie Shorey (C)

Rotman Research Institute, Baycrest Health Sciences Centre, Canada.

Robert Madan (R)

Department of Psychiatry, Baycrest Health Sciences Centre; Department of Psychiatry, Division of Geriatric Psychiatry, University of Toronto, Canada.

Claudia Szabuniewicz (C)

Rotman Research Institute, Baycrest Health Sciences Centre, Canada.

Samantha Koh (S)

Rotman Research Institute, Baycrest Health Sciences Centre, Canada.

Shelley Veinish (S)

Geriatric and Internal Medicine, Baycrest Health Sciences Centre; Department of Medicine, University of Toronto, Canada.

Linda Mah (L)

Department of Psychiatry, Baycrest Health Sciences Centre; Department of Psychiatry, Division of Geriatric Psychiatry, University of Toronto, Canada; Rotman Research Institute, Baycrest Health Sciences Centre; Department of Psychiatry, Division of Geriatric Psychiatry, University of Toronto, Canada. Electronic address: lmah@research.baycrest.org.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH