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The WATCHMAN Left Atrial Appendage Closure Device for Atrial Fibrillation
Published on: February 28, 2012
Early Versus Later Anticoagulation for Acute Ischemic Stroke in Patients With Atrial Fibrillation: A Systematic
Marwah Nasir Ahmad1, Arooj Waheed2, Nayan Manish Gandhi3
1Medicine Department Batterjee Medical College Jeddah Saudi Arabia.
Background:
The optimal timing for initiating oral anticoagulation in patients with atrial fibrillation after acute ischemic stroke remains uncertain. This systematic review and meta-analysis aims to compare early versus later initiation of oral anticoagulants in this patient population.
Methods:
We systematically searched multiple databases, including MEDLINE, Embase, CENTRAL, and ClinicalTrials.gov, up to January 2026. We included randomized controlled trials (RCTs) comparing early (≤ 4 days, post-stroke) versus later (> 5 days) direct oral anticoagulation (DOAC) initiation in patients with atrial fibrillation and acute ischemic stroke. Our main outcomes were a primary composite outcome of ischemic stroke, sICH, or unclassified stroke and the primary composite outcome, or all-cause mortality.
Results:
Four RCTs were included with a total of 6722 patients. Our meta-analysis revealed no significant difference between early and later DOAC initiation for the primary composite outcome (RR: 0.84, 95% CI: 0.64-1.10), primary composite outcome or mortality (RR: 0.99; 95% CI: 0.82-1.19), ischemic stroke (RR: 0.78, 95% CI: 0.54-1.12), symptomatic intracranial hemorrhage (RR: 1.00, 95% CI: 0.48-2.06), all-cause mortality (RR: 0.96, 95% CI: 0.80-1.14), or major bleeding (RR: 0.72, 95% CI: 0.33-1.60).
Conclusion:
Early initiation of anticoagulants appears to be comparable to later initiation in terms of stroke recurrence, bleeding risks, and mortality in patients with atrial fibrillation. These findings support a more individualized approach to anticoagulation timing, balancing ischemic and hemorrhagic risks based on patient characteristics. Further high-quality trials are needed to refine clinical guidelines and optimize anticoagulation strategies in this population.
Trial Registration:
CRD42024629570 [PROSPERO].
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