Key result
Beta-blockers linked to ~53% lower 30-day mortality vs amiodarone in new-onset AF.
Why the study?
New onset atrial fibrillation (NOAF) is common in critically ill patients and associated with adverse outcomes, but whether commonly used beta-blockers and amiodarone differ in clinical benefits remained to be determined.
Does beta-blocker therapy reduce 30-day and 90-day all-cause mortality compared with amiodarone in critically ill patients who develop new onset atrial fibrillation?
Cohort (n=3,451)
Yes
Does beta-blocker therapy reduce 30-day and 90-day all-cause mortality compared with amiodarone in critically ill patients who develop new onset atrial fibrillation?
In critically ill patients with new-onset atrial fibrillation, beta-blocker therapy was associated with significantly lower 30-day and 90-day all-cause mortality compared to amiodarone in a propensity-matched cohort.
May support beta-blocker preference over amiodarone for new-onset AF in critical illness; leaves open confirmation in randomized trials.
Background and objectives New onset atrial fibrillation (NOAF) is common in critically ill patients and is associated with increased adverse outcomes such as death, stroke, and myocardial infarction. While beta-blockers and amiodarone are both commonly used in the management of NOAF, there remains a need to determine whether these treatment strategies differ in terms of clinical benefits. Methods The TriNetX Global Collaborative Network was used to define two cohorts of patients who developed NOAF within 2 weeks of receiving critical care services and were treated with either beta-blockers or amiodarone, excluding patients with concomitant calcium channel blocker or digoxin treatment and prior beta-blocker use in the past 3 months. The primary outcome was all-cause mortality at 30 and 90 days. Analyses were performed before and after propensity score matching (PSM). Results Before PSM, the beta-blocker group (N=2841, age=71.9 ± 13.1) was older with fewer comorbidities, including hypertension, ischemic heart disease, and heart failure, when compared to the amiodarone group (N=610, age=69.8 ± 12.5). After PSM (matched N=577), patients in the beta-blocker group had a lower risk of 30-day (HR: 0.47, 95% CI: 0.32, 0.69) and 90-day all-cause mortality (HR: 0.60, 95% CI: 0.43, 0.83). Subgroup analyses were mainly consistent with the primary findings. Conclusion Beta-blocker therapy was associated with significantly lower 30-day and 90-day mortality compared with amiodarone in patients receiving critical care services who subsequently developed NOAF. However, the lack of a surrogate for acute disease severity limits interpretation of observed associations. Prospective randomised controlled trials are warranted to better define the optimal therapeutic strategy for patients who develop NOAF in the critical care setting.
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Ahmadzadeh et al. (2026) conducted a cohort in New onset atrial fibrillation in critically ill patients (n=3,451). Beta-blockers vs. Amiodarone was evaluated on All-cause mortality at 30 and 90 days (HR 0.47 (30-day); HR 0.60 (90-day), 95% CI 0.32-0.69 (30-day); 0.43-0.83 (90-day)). Beta-blocker therapy was associated with lower 30-day (HR 0.47; 95% CI 0.32-0.69) and 90-day mortality (HR 0.60; 95% CI 0.43-0.83) vs amiodarone in critically ill patients with new-onset AF.
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