Key result
Dofetilide or sotalol in HFpEF linked to ~134% higher VT risk but not sudden cardiac arrest.
Why the study?
While HFrEF is a known risk factor for drug-induced arrhythmias, it is unknown whether HFpEF also increases this risk in patients prescribed dofetilide or sotalol.
Does dofetilide or sotalol increase the risk of ventricular tachycardia and sudden cardiac arrest in patients with HFpEF compared to those with HFrEF or no HF?
Cohort (n=639,729)
Yes
Does dofetilide or sotalol increase the risk of ventricular tachycardia and sudden cardiac arrest in patients with HFpEF compared to those with HFrEF or no HF?
Effect estimate: HR 2.34 (95% CI 1.11-4.95)
Dofetilide or sotalol use in patients with HFpEF is associated with an increased risk of ventricular tachycardia, similar to the known risk in HFrEF, but does not significantly increase the risk of sudden cardiac arrest.
May warrant caution with dofetilide/sotalol in HFpEF; extends known VT risk from HFrEF but leaves SCA association open.
Background: Heart failure (HF) with reduced ejection fraction (HFrEF) is a risk factor for drug-induced arrhythmias. It is unknown whether HF with preserved ejection fraction (HFpEF) also increases the risk. Objectives: The purpose of this study was to determine if the risk of ventricular tachycardia (VT) and sudden cardiac arrest (SCA) is increased in patients with HFpEF prescribed dofetilide or sotalol. Methods: Using Medicare claims and pharmacy benefits from 2014 to 2016, we identified patients taking dofetilide or sotalol and non-dofetilide/sotalol users among 3 groups: HFrEF (n = 26,176), HFpEF (n = 33,304), and no HF (n = 580,249). Multinomial propensity score matching was performed. We compared baseline characteristics using Cochran-Mantel-Haenszel statistics and standardized differences, and tested associations of VT and SCA among dofetilide/sotalol users and those with HFpEF, HFrEF, or no HF using a generalized Cox proportional hazards model. Results: VT and SCA occurred 166 (10.68%) and 16 (1.03%) of 1,554 dofetilide/sotalol users with HFpEF, 543 (38.76%) and 40 (2.86%) of 1,401 dofetilide/sotalol users with HFrEF, and 245 (5.06%) and 13 (0.27%) of 4,839 dofetilide/sotalol users without HF. Overall VT risk was increased in HFrEF and HFpEF patients (HR: 7.00 [95% CI: 6.10-8.02] and 1.99 [95% CI: 1.70-2.32], respectively). The risk of VT in patients prescribed dofetilide/sotalol was increased in HFrEF and HFpEF patients (1.53 [95% CI: 1.07-2.20] and 2.34 [95% CI: 1.11-4.95], respectively). While the overall SCA risk was increased in HFrEF and HFpEF patients (5.19 [95% CI: 4.10-6.57] and 2.53 [95% CI: 1.98-3.23], respectively), dofetilide/sotalol use was not associated with an increased SCA risk. Conclusions: In patients with HF who are prescribed dofetilide or sotalol, the risk of VT, but not SCA, was increased.
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Huang et al. (2024) conducted a cohort in Heart Failure (HFpEF and HFrEF) (n=639,729). Dofetilide or sotalol vs. Non-users of dofetilide or sotalol was evaluated on Ventricular tachycardia in HFpEF patients taking dofetilide/sotalol vs HFpEF not taking dofetilide/sotalol (HR 2.34, 95% CI 1.11-4.95). Dofetilide or sotalol use in patients with heart failure with preserved ejection fraction significantly increased the risk of ventricular tachycardia (HR 2.34) but not sudden cardiac arrest.
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