Why the study?
Outcomes of device-detected AF remain unclear in individuals without a prior history of AF.
Does device-detected atrial fibrillation increase the risk of clinical AF, thromboembolism, and mortality in individuals with no prior history of AF?
Population
Individuals with no prior history of AF
Comparison
Device-detected AF vs no device-detected AF
Design
Systematic review and meta-analysis
Key result
Device-detected atrial high-rate episodes significantly increased the risk of clinical atrial fibrillation (RR 3.33) and thromboembolic events (RR 2.21) in patients with no prior history of AF.
Authors
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Supports intensified monitoring for clinical AF and thromboembolism; confirms associations and leaves optimal anticoagulation strategies open.
Meta-Analysis (n=7,440)
Does device-detected atrial fibrillation increase the risk of clinical AF, thromboembolism, and mortality in individuals with no prior history of AF?
Effect estimate: RR 3.33 (95% CI 1.99-5.57)
p-value: p=<0.0001
Device-detected atrial high-rate episodes in patients without prior AF are associated with a significantly increased risk of subsequent clinical AF and thromboembolism, particularly when episodes last >24 hours.
Ahmed et al. (2024) conducted a meta-analysis in Device-detected Atrial High-rate Episodes (AHREs) without prior history of Atrial Fibrillation (n=7,440). Device-detected Atrial High-rate Episodes (AHREs) vs. No device-detected Atrial High-rate Episodes was evaluated on Clinical Atrial Fibrillation (RR 3.33, 95% CI 1.99-5.57, p=<0.0001). Device-detected atrial high-rate episodes significantly increased the risk of clinical atrial fibrillation (RR 3.33) and thromboembolic events (RR 2.21) in patients with no prior history of AF.
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