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Review
. 2017 Dec;96(49):e9071.
doi: 10.1097/MD.0000000000009071.

QTc prolongation and torsades de pointes due to a coadministration of fluoxetine and amiodarone in a patient with implantable cardioverter-defibrillator: Case report and review of the literature

Affiliations
Review

QTc prolongation and torsades de pointes due to a coadministration of fluoxetine and amiodarone in a patient with implantable cardioverter-defibrillator: Case report and review of the literature

Anhua Wei et al. Medicine (Baltimore). 2017 Dec.

Abstract

Rationale: Drug-induced prolongation of the corrected QT interval (QTc) may lead to serious and potentially life-threatening ventricular tachyarrhythmia, such as torsades de pointes (Tdp), which is worthy of clinical attention. Here, we report 1 case of Tdp after a coadministration of fluoxetine and amiodarone.

Patient concerns: A 62-year-old Chinese male who placed with the implanted cardioverter-defibrillator (ICD) appeared the QTc prolongation and Tdp after the concurrent administration of fluoxetine and amiodarone.

Diagnoses: Torsades de pointes (Tdp).

Interventions: The patient was treated with magnesium and potassium immediately. Her ICD-brady pacing mode was reprogrammed to 90 bpm. Meanwhile, both of fluoxetine and amiodarone were discontinued.

Outcomes: The further episodes of Tdp were prevented. After a few days, the QTc gradually decreased without clinically significant arrhythmias.

Lessons: The present case demonstrates that a potential drug-drug interaction (DDI) may lead to a life-threatening drug adverse reaction (ADR) especially in special subjects. Therefore, clinicians should closely monitor the electrocardiogram (ECG) when QTc-prolonging agents are given to patients with cardiac abnormalities, and avoid combining 2 QTc-prolonging drugs.

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Conflict of interest statement

The authors report no conflicts of interest in this work.

Figures

Figure 1
Figure 1
(A) ECG on admission (QTc = 386 ms); (B) ECG showing QT prolongation (QTc = 501 ms); (C) The continuous ECG monitoring an episode of Tdp; (D) The continuous ECG monitoring the lapse of Tdp. (E) ECG showing pacing rhythm reprogrammed to 90 bpm (QTc = 493 ms). (F) ECG showing pacing rhythm reprogrammed to 60 bpm on discharge (QTc = 446 ms).

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References

    1. Roden DM. Drug-induced prolongation of the QT interval. N Engl J Med 2004;350:1013–22. - PubMed
    1. Tully PJ, Harrison NJ, Cheung P, et al. Anxiety and cardiovascular disease risk: a review. Curr Cardiol Rep 2016;18:120. - PubMed
    1. Castro VM, Clements CC, Murphy SN, et al. QT interval and antidepressant use: a cross sectional study of electronic health records. BMJ 2013;346:f288. - PMC - PubMed
    1. Beach SR, Kostis WJ, Celano CM, et al. Meta-analysis of selective serotonin reuptake inhibitor-associated QTc prolongation. J Clin Psychiatry 2014;75:e441–9. - PubMed
    1. Strik JJ, Honig A, Lousberg R, et al. Efficacy and safety of fluoxetine in the treatment of patients with major depression after first myocardial infarction: findings from a double-blind, placebo-controlled trial. Psychosom Med 2000;62:783–9. - PubMed

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