Key result
Early DOAC initiation (≤5 days) after acute ischaemic stroke showed no significant difference in recurrent stroke (aHR 1.2; 95% CI 0.5-2.9; p=0.69) or ICH compared to late initiation (>5 days).
Why the study?
The optimal timing to start direct oral anticoagulants after acute ischaemic stroke related to atrial fibrillation remains unclear.
Does early start of DOACs (≤5 days) reduce recurrent AIS and ICH compared to late start (>5 days) in patients with acute ischaemic stroke related to non-valvular atrial fibrillation?
Observational (n=2,550)
Yes
Does early start of DOACs (≤5 days) reduce recurrent AIS and ICH compared to late start (>5 days) in patients with acute ischaemic stroke related to non-valvular atrial fibrillation?
Early initiation of DOACs (≤5 days) after an acute ischemic stroke related to atrial fibrillation appears safe and does not excessively increase the risk of intracranial hemorrhage compared to late initiation.
Answers are grounded in this paper and cite their sources.
Early DOAC start after AF-related AIS appears safe; supports but does not replace RCTs for timing guidance.
OBJECTIVE: The optimal timing to start direct oral anticoagulants (DOACs) after an acute ischaemic stroke (AIS) related to atrial fibrillation (AF) remains unclear. We aimed to compare early (≤5 days of AIS) versus late (>5 days of AIS) DOAC-start. METHODS: This is an individual patient data pooled analysis of eight prospective European and Japanese cohort studies. We included patients with AIS related to non-valvular AF where a DOAC was started within 30 days. Primary endpoints were 30-day rates of recurrent AIS and ICH. RESULTS: A total of 2550 patients were included. DOACs were started early in 1362 (53%) patients, late in 1188 (47%). During 212 patient-years, 37 patients had a recurrent AIS (1.5%), 16 (43%) before a DOAC was started; 6 patients (0.2%) had an ICH, all after DOAC-start. In the early DOAC-start group, 23 patients (1.7%) suffered from a recurrent AIS, while 2 patients (0.1%) had an ICH. In the late DOAC-start group, 14 patients (1.2%) suffered from a recurrent AIS; 4 patients (0.3%) suffered from ICH. In the propensity score-adjusted comparison of late versus early DOAC-start groups, there was no statistically significant difference in the hazard of recurrent AIS (aHR=1.2, 95% CI 0.5 to 2.9, p=0.69), ICH (aHR=6.0, 95% CI 0.6 to 56.3, p=0.12) or any stroke. CONCLUSIONS: Our results do not corroborate concerns that an early DOAC-start might excessively increase the risk of ICH. The sevenfold higher risk of recurrent AIS than ICH suggests that an early DOAC-start might be reasonable, supporting enrolment into randomised trials comparing an early versus late DOAC-start.
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Marchis et al. (2021) conducted an observational in Acute ischaemic stroke related to non-valvular atrial fibrillation (n=2,550). Early DOAC-start (≤5 days of AIS) vs. Late DOAC-start (>5 days of AIS) was evaluated on 30-day rates of recurrent AIS and ICH (aHR 1.2, 95% CI 0.5-2.9, p=0.69). Early DOAC initiation (≤5 days) after acute ischaemic stroke showed no significant difference in recurrent stroke (aHR 1.2; 95% CI 0.5-2.9; p=0.69) or ICH compared to late initiation (>5 days).
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