Evaluation of QTc prolongation and dosage effect with citalopram
- PMID: 29955465
- PMCID: PMC6007721
- DOI: 10.9740/mhc.2016.07.165
Evaluation of QTc prolongation and dosage effect with citalopram
Abstract
Introduction: Recently, controversy has surrounded a 2011 Food and Drug Administration warning against using citalopram at doses >40 mg/day due to QTc prolonging effects.
Methods: Patients ≥18 years old at the VA North Texas Health Care System were included in this retrospective review if they had received at least 1 prescription for a 30-day supply of citalopram between January 1, 2007, and February 29, 2012, and had a baseline electrocardiogram (ECG) within 1 year before initiation or dose increase of citalopram and at least 1 repeat ECG within 3 months after citalopram initiation or dose increase. The primary endpoint was the prevalence of QTc prolongation (QTc interval ≥470 ms for men and ≥480 ms for women) after initiation or a dose increase of citalopram. For secondary objectives, Fisher exact tests were used determine if there was a dose-dependent difference in prevalence of QTc prolongation among the whole study sample and among the subgroup of patients ≥60 years old.
Results: Among the entire study sample, QTc prolongation was identified in 12 patients (16.4%) after initiation or a dose increase of citalopram. In the subgroup of patients ≥60 years old, QTc prolongation was identified in 7 patients (21.9%). Prevalence of QTc prolongation increased with dose in the entire study population (P = .016) and in patients ≥60 years (not significant).
Discussion: This retrospective study suggests that citalopram produces a dose-dependent increase in QTc interval.
Keywords: QT interval; QTc prolongation; SSRI; antidepressant; citalopram; elderly; ventricular arrhythmia.
Conflict of interest statement
Disclosures: The authors have no disclosures of interest.
Figures
References
-
- FDA [Internet]. Silver Spring (MD): FDA. FDA Drug Safety Communication: abnormal heart rhythms associated with high doses of Celexa (citalopram hydrobromide) . August 24, 2011. Available from: http://www.fda.gov/Drugs/DrugSafety/ucm269086.htm.
-
- FDA [Internet]. Silver Spring (MD): FDA. FDA Drug Safety Communication: Revised recommendations for Celexa (citalopram hydrobromide) related to a potential risk of abnormal heart rhythms with high doses; March 28, 2012. Available from: http://www.fda.gov/Drugs/DrugSafety/ucm297391.htm.
-
- Howland RH. . A critical evaluation of the cardiac toxicity of citalopram: part 1. J Psychosoc Nurs Ment Health Ser. 2011; 49 11: 13- 6. DOI: 10.3928/02793695-20111011-01. PubMed PMID: 22007855. - DOI - PubMed
-
- Committee for proprietary medicinal products (CPMP) [Internet]. Silver Spring (MD): FDA. Points to consider. The assessment of the potential for QT interval prolongation by non-cardiovascular medicinal products. Available from: http://www.fda.gov/ohrms/dockets/ac/03/briefing/pubs/cpmp.pdf.
-
- Kanjanauthai S, Kanluen T, Chareonthaitawee P. . Citalopram induced torsade de pointes, a rare life threatening side effect. Int J Cardiol. 2008; 131 1: e33- 4. DOI: 10.1016/j.ijcard.2007.08.006. PubMed PMID: 17919753. - DOI - PubMed
LinkOut - more resources
Full Text Sources
Other Literature Sources