Dofetilide use is not associated with increased mortality in patients with left ventricular hypertrophy and atrial

Daniel G Wann1, Brent S Medoff1, Noor-Ul-Huda A Mehdi2

  • 1Center for Atrial Fibrillation, Heart and Vascular Institute, University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania, USA.

Insights

Dofetilide did not increase mortality in patients with left ventricular hypertrophy (LVH) and atrial fibrillation (AF). This study suggests dofetilide may be a safe option for managing symptomatic AF in this patient group.

Area of Science:

  • Cardiology
  • Clinical Pharmacology
  • Electrophysiology

Background:

  • Left ventricular hypertrophy (LVH) is common in atrial fibrillation (AF) patients.
  • Antiarrhythmic drugs (AADs) are often contraindicated in LVH.
  • US guidelines advise against dofetilide in LVH due to safety concerns, despite limited clinical data.

Purpose of the Study:

  • To investigate the association between dofetilide use and mortality in patients with AF and LVH.
  • To evaluate the safety of dofetilide in a population where it is typically avoided.

Main Methods:

  • Propensity matching was used to compare patients with AF and LVH treated with dofetilide versus those not on AADs.
  • The study included 718 patients (359 per group) with LVH ≥1.4 cm.
  • Primary outcome was all-cause mortality at 3 years; secondary outcomes included hospitalizations.

Main Results:

  • Dofetilide use was not associated with increased all-cause mortality at 3 years (7% vs. 12% in control group; HR 0.90).
  • Total hospitalizations were higher in the control group.
  • Hospitalizations specifically for AF were similar between the dofetilide and control groups.

Conclusions:

  • Dofetilide use was not linked to increased mortality in a propensity-matched cohort of patients with AF and LVH.
  • Findings support the safety of dofetilide in this population, challenging current guideline recommendations.
  • Dofetilide may be a viable treatment option for symptomatic AF management in patients with LVH.
Abstract

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