Association between citalopram, escitalopram and QTc prolongation in a real-world geriatric setting.
Aged
Arrhythmias, Cardiac
Citalopram
/ administration & dosage
Electrocardiography
/ drug effects
Electronic Health Records
Female
Health Services for the Aged
Humans
Long QT Syndrome
/ chemically induced
Male
Retrospective Studies
Risk Factors
Selective Serotonin Reuptake Inhibitors
/ administration & dosage
Antidepressants
Citalopram
Escitalopram
Geriatric psychiatry
QTc interval
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
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
341-345Informations de copyright
Copyright © 2019. Published by Elsevier B.V.