Key result
Early DOAC initiation cuts composite cardiovascular events ~19% vs. delayed initiation after stroke in AF.
Why the study?
The optimal timing for direct oral anticoagulant initiation after acute ischaemic stroke in atrial fibrillation patients is clinically debated, with uncertainty about balancing prevention of haemorrhagic transformation and recurrent embolic events.
Does early DOAC initiation reduce recurrent ischaemic stroke, systemic embolism, and all-cause mortality compared to delayed initiation in patients with atrial fibrillation and acute ischaemic stroke?
Meta-Analysis (n=6,210)
Does early DOAC initiation reduce recurrent ischaemic stroke, systemic embolism, and all-cause mortality compared to delayed initiation in patients with atrial fibrillation and acute ischaemic stroke?
Relative Risk: 0.81 (95% CI 0.66–0.98)
p-value: p=0.03
Early initiation of DOACs within 4 days of acute ischemic stroke in patients with atrial fibrillation reduces composite ischemic outcomes and mortality without increasing symptomatic intracranial hemorrhage compared to delayed initiation.
Supports immediate DOAC initiation after AF ischaemic stroke; challenges delayed-start consensus and prior practice.
Background and Aims The optimal timing for direct oral anticoagulant (DOAC) initiation following acute ischaemic stroke in atrial fibrillation (AF) patients is clinically debated. While traditional practice favoured delayed initiation to prevent haemorrhagic transformation, recent trials suggest earlier therapy may reduce recurrent embolic events. This meta-analysis evaluates the efficacy and safety of early versus delayed DOAC initiation. Methods Systematic review of randomised controlled trials based on PRISMA 2020 Guideline was performed, including ELAN, TIMING, and OPTIMAS. Early initiation was defined as ≤4 days and delayed as 5–14 days post-stroke. The primary efficacy outcome was a composite of recurrent ischaemic stroke, systemic embolism, and all-cause mortality. The primary safety outcome was symptomatic intracranial haemorrhage (sICH). Statistical analysis was performed using RStudio with the meta package, employing a random-effects model to calculate pooled Risk Ratios (RR). Results Data from 6,210 participants showed early DOAC initiation significantly reduced the composite primary outcome (RR 0.81; 95% CI 0.66–0.98; p=0.03) compared to delayed initiation. Recurrent ischaemic stroke risk was numerically lower in the early group. Safety analysis revealed no significant increase in sICH (RR 1.02; 95% CI 0.44–2.37), regardless of stroke severity or prior reperfusion therapy. One-year follow-up confirmed a sustained safety profile. Conclusion Early DOAC initiation within 4 days of ischaemic stroke in AF patients is superior for preventing composite cardiovascular events and is safe across all stroke severities. These findings support early anticoagulation as the standard of care in acute stroke management.
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Nurisma et al. (2026) conducted a meta-analysis in Acute ischaemic stroke in atrial fibrillation (AF) patients (n=6,210). Early DOAC initiation (≤4 days post-stroke) vs. Delayed DOAC initiation (5–14 days post-stroke) was evaluated on Composite of recurrent ischaemic stroke, systemic embolism, and all-cause mortality (RR 0.81, 95% CI 0.66-0.98, p=0.03). Early DOAC initiation (≤4 days) post-ischaemic stroke in AF patients was superior to delayed initiation for preventing composite cardiovascular events (RR 0.81; 95% CI 0.66-0.98; p=0.03).
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