Table 2.
Antiarrhythmic drug therapy for atrial fibrillation in heart failure
Guidelines | Agent | Class | Safety | Efficacy |
---|---|---|---|---|
Recommended | Amiodarone | Mixed channel blockade | Risks of toxicity, including thyroid, hepatic, pulmonary, and neurological.78 | Superior efficacy for maintenance of sinus rhythm vs. placebo: odds ratio 0.15 (95% CI 0.10–0.22).79 |
Dofetilide | III | Requires inpatient stay for loading. Risk of torsades 0.8–3.3%. Not approved in EU. | Lower risk of all-cause rehospitalization in patients with AF at baseline vs. placebo: relative risk 0.70 (95% CI 0.56–0.89).80 | |
Caution required | Dronedarone | Mixed channel blockade | Increased mortality in patients with HF and permanent AF.15,81 | Decreased risk of CV hospitalization or death in patients with AF and no recent HF decompensation vs. placebo: 0.76 (95% CI 0.69–0.84).82 |
Sotalol | III | Concern for excess proarrhythmia in patients with acute myocardial infarction or LVEF ≤40%: relative risk 1.65 (95% CI 1.15–2.36) for all-cause mortality.83a | Sotalol was inferior to amiodarone in patients with AF (28% had NYHA class I/II HF).84 | |
Contraindicated | Flecainide and Propafenone | I | Flecainide, encainide and moracizine increased mortality in patients with myocardial infarction.85 Propafenone can precipitate decompensated HF, particularly in CYP 2D6 slow-metabolizers. |
aSWORD evaluated d-sotalol rather than d,l-sotalol.