Key result
Amiodarone is linked to ~140% higher all-cause mortality versus other AADs in AF without structural heart disease.
Why the study?
Amiodarone is commonly prescribed for AF but its impact on all-cause mortality in patients with structurally normal hearts was unclear.
Cohort (n=2,077)
No
Hazard Ratio: 2.41
p-value: p=0.012
Should not yet change amiodarone use in AF without SHD; hypothesis-generating and requires randomized confirmation.
BACKGROUND: Amiodarone is often prescribed in the management of atrial fibrillation (AF) but is known to cause significant end-organ toxicities. In this study, we examined the impact of amiodarone on all-cause mortality in AF patients with structurally normal hearts. METHODS: We performed a retrospective cohort analysis of all AF patients with structurally normal hearts who were prescribed antiarrhythmic drugs (AAD) for rhythm control of AF at our institution from 2006 to 2013 (n = 2,077). Baseline differences between the amiodarone (AMIO: n = 403) and other AADs (NON-AMIO: n = 1,674) groups were corrected for using propensity score matching. RESULTS: Amiodarone use as first-line therapy decreased significantly with a higher degree of prescriber specialization in arrhythmia management (31%, 22%, and 9% for primary care physicians, general cardiologists and cardiac electrophysiologists, respectively, p < 0.001). After propensity score matching, baseline comorbidities were balanced between the AMIO and NON-AMIO groups. Over a median follow-up of 28.2 months (range 6.0-100.9 months), amiodarone was associated with increased all-cause (HR 2.41, p = 0.012) and non-cardiac (HR 3.55, p = 0.008) mortality, but not cardiac mortality. AF recurrence and cardiac hospitalizations were similar between the two study groups. CONCLUSIONS: Amiodarone treatment of AF is associated with increased mortality in patients without structural heart disease and therefore should be avoided or only used as a second-line therapy, when other AF therapies fail. Adherence to guideline recommendations in the management of AF patients impacts clinical outcome.
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Qin et al. (2015) conducted a cohort in Atrial fibrillation without structural heart disease (n=2,077). Amiodarone vs. Other antiarrhythmic drugs (dronedarone, dofetilide, flecainide, propafenone, or sotalol) was evaluated on All-cause mortality (HR 2.41, p=0.012). Amiodarone therapy was associated with a significantly increased risk of all-cause mortality (HR 2.41) compared to other antiarrhythmic drugs in atrial fibrillation patients without structural heart disease.
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