Abstract 4139536: Incidence of Severe QT Prolongation and the Assoicated Risk of Ventricular Arrhythmias and Sudden Cardiac Death in Patients Taking Antipsychotics or Antidepressants

Background: Limited data exist on the incidence of severe QT prolongation (SQTP) in patients using antipsychotics or antidepressants and the associated risk of ventricular arrhythmias (VA) and sudden cardiac death (SCD). Aims: This study aimed to investigate the incidence, risk factors, and outcomes of SQTP in patients using antipsychotics or antidepressants. Methods: Electronic medical records from a multicenter healthcare system in Taiwan were analyzed to identify patients using antipsychotics or antidepressants with baseline and follow-up electrocardiograms. SQTP was defined as a corrected QT interval exceeding 500 ms post-treatment or an increase of >60 ms compared to baseline. Risk factors for SQTP development and associated risks of VA and SCD were assessed using multivariate logistic regression. Results: Following antipsychotic use (n = 28,892) and antidepressant use (n = 14,634), mean corrected QT interval increases were +7.7 ± 39.0 ms and +6.7 ± 36.1 ms, respectively. Over 10% of patients using haloperidol, amisulpride, olanzapine, quetiapine, or risperidone experienced SQTP. Antipsychotics with a known or conditional risk of torsades de pointes and antidepressants with a known risk of torsades de pointes had a higher likelihood of SQTP compared to alprazolam control. Risk factors for SQTP included age >65 years, electrolyte imbalances, renal insufficiency, amiodarone use, left ventricular ejection fraction <50%, and the use of drugs with known torsades de pointes risk. In antipsychotic users, SQTP was significantly associated with increased risks of VA (odds ratio 2.91; 95% CI 2.29–3.70) and SCD (odds ratio 2.16; 95% CI 1.50–3.12). Similarly, in antidepressant users, SQTP was significantly linked to VA risks (odds ratio 2.78; 95% CI 1.63–4.74). Subgroup analyses for females and patients aged 18-50 years yielded consistent results. Conclusions: Over 10% of patients on certain antipsychotics experienced SQTP, often with related risk factors. SQTP was significantly associated with elevated risks of VA and SCD in antipsychotic users, and increased VA risk in antidepressant users. Clinicians should be alert to SQTP in patients taking antipsychotics or antidepressants.

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Publication Details

Journal
Circulation
Published
2024-11-12
DOI
https://doi.org/10.1161/circ.150.suppl_1.4139536
Primary Topic
Cardiac electrophysiology and arrhythmias
Type
article
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article

Abstract 4139536: Incidence of Severe QT Prolongation and the Assoicated Risk of Ventricular Arrhythmias and Sudden Cardiac Death in Patients Taking Antipsychotics or Antidepressants

Yu‐Tung Huang, Chang Shang-Hung, Victor Chien‐Chia Wu, Chunli Wang
Circulation
Cardiac electrophysiology and arrhythmias
article

Abstract 4139536: Incidence of Severe QT Prolongation and the Assoicated Risk of Ventricular Arrhythmias and Sudden Cardiac Death in Patients Taking Antipsychotics or Antidepressants

Yu‐Tung Huang, Chang Shang-Hung, Victor Chien‐Chia Wu, Chunli Wang
article en

Abstract

Background: Limited data exist on the incidence of severe QT prolongation (SQTP) in patients using antipsychotics or antidepressants and the associated risk of ventricular arrhythmias (VA) and sudden cardiac death (SCD). Aims: This study aimed to investigate the incidence, risk factors, and outcomes of SQTP in patients using antipsychotics or antidepressants. Methods: Electronic medical records from a multicenter healthcare system in Taiwan were analyzed to identify patients using antipsychotics or antidepressants with baseline and follow-up electrocardiograms. SQTP was defined as a corrected QT interval exceeding 500 ms post-treatment or an increase of >60 ms compared to baseline. Risk factors for SQTP development and associated risks of VA and SCD were assessed using multivariate logistic regression. Results: Following antipsychotic use (n = 28,892) and antidepressant use (n = 14,634), mean corrected QT interval increases were +7.7 ± 39.0 ms and +6.7 ± 36.1 ms, respectively. Over 10% of patients using haloperidol, amisulpride, olanzapine, quetiapine, or risperidone experienced SQTP. Antipsychotics with a known or conditional risk of torsades de pointes and antidepressants with a known risk of torsades de pointes had a higher likelihood of SQTP compared to alprazolam control. Risk factors for SQTP included age >65 years, electrolyte imbalances, renal insufficiency, amiodarone use, left ventricular ejection fraction <50%, and the use of drugs with known torsades de pointes risk. In antipsychotic users, SQTP was significantly associated with increased risks of VA (odds ratio 2.91; 95% CI 2.29–3.70) and SCD (odds ratio 2.16; 95% CI 1.50–3.12). Similarly, in antidepressant users, SQTP was significantly linked to VA risks (odds ratio 2.78; 95% CI 1.63–4.74). Subgroup analyses for females and patients aged 18-50 years yielded consistent results. Conclusions: Over 10% of patients on certain antipsychotics experienced SQTP, often with related risk factors. SQTP was significantly associated with elevated risks of VA and SCD in antipsychotic users, and increased VA risk in antidepressant users. Clinicians should be alert to SQTP in patients taking antipsychotics or antidepressants.

CirculationVol. 150(Suppl_1)
Taoyuan Chang Gung Memorial Hospital (TW)
Good health and well-being
Openalex Percentile: Top 62%
Cardiac electrophysiology and arrhythmias
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