Key result
Apixaban yields an absolute ~1.6% reduction in stroke or systemic embolism vs. aspirin.
Why the study?
Does accounting for death and atrial fibrillation progression as competing events alter the estimated absolute risk reduction of apixaban compared with aspirin for stroke and systemic embolism in patients with subclinical atrial fibrillation?
Does accounting for death and atrial fibrillation progression as competing events alter the estimated absolute risk reduction of apixaban compared with aspirin for stroke and systemic embolism in patients with subclinical atrial fibrillation?
Answers are grounded in this paper and cite their sources.
Accounting for competing risks of death and AF progression reduces the estimated 3.5-year absolute risk reduction of apixaban versus aspirin in subclinical AF from 1.94% to 1.62%, providing a more realistic estimate of therapeutic benefit.
In the ARTESIA trial, apixaban reduced stroke and systemic embolism compared with aspirin in patients with subclinical atrial fibrillation (AF), but the primary analysis treated death and AF progression as censoring rather than competing events. We estimated the absolute risk reduction (ARR) at 3.5 years treating death and AF progression as competing events. We used event-level data reconstructed from published Kaplan-Meier curves to probabilistically impute status and timing of competing events. The ARR was 1.94% when treating death and AF progression as censoring events vs. 1.62% treating them as competing events (difference 0.33 percentage points; 95% CI 0.04 to 0.62). Absolute benefit estimates depend on how competing events are handled. Competing risk analyses can provide more realistic estimates of expected therapeutic benefit at the point of treatment decisions when competing events are common.
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Lo et al. (2026) studied Subclinical atrial fibrillation. Apixaban (competing risk reanalysis) vs. Aspirin (censoring vs. competing risk analysis) was evaluated on Stroke and systemic embolism (ARR 1.62%). Apixaban vs aspirin yielded an ARR in stroke/systemic embolism of 1.62% accounting for competing risks vs 1.94% with censoring.
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