Key result
OAC in AF with prior ICH reduces ischemic stroke and mortality without increasing ICH recurrence.
Why the study?
The benefit of resuming anticoagulation in atrial fibrillation patients with prior intracranial haemorrhage and the optimal anticoagulant choice remain controversial.
Does oral anticoagulation reduce ischaemic stroke and mortality without increasing ICH recurrence in atrial fibrillation patients with prior intracranial haemorrhage?
Meta-Analysis (n=17,600)
Does oral anticoagulation reduce ischaemic stroke and mortality without increasing ICH recurrence in atrial fibrillation patients with prior intracranial haemorrhage?
Hazard Ratio: 0.85 (95% CI 0.57–1.25)
p-value: p=0.41
In AF patients with prior ICH, resuming OAC (especially NOACs) reduces ischemic stroke and mortality without increasing ICH recurrence, despite an increased risk of major bleeding.
May support individualized OAC decisions in AF post-ICH; leaves open need for RCTs to confirm net benefit.
BACKGROUND: The benefit of resuming anticoagulation in atrial fibrillation (AF) patients with prior intracranial haemorrhage (ICH) and which anticoagulant to choose are controversial. SUMMARY OF REVIEW: PubMed, Embase, Web of Science and the Cochrane Library were searched from their inception until 13 February 2022. Thirteen eligible articles (17 600 participants) were collected, including 11 real-world studies (n=17 296) and 2 randomised controlled trials (RCTs) (n=304). Compared with no anticoagulants, oral anticoagulation (OAC) was not associated with an increased risk of ICH recurrence (HR 0.85 (95% CI 0.57 to 1.25), p=0.41), but with a significantly increased risk of major bleeding (HR 1.66 (95% CI 1.20 to 2.30), p<0.01). Meanwhile, OAC was associated with a reduced risk of ischaemic stroke/systemic thromboembolism (IS/SE) (HR 0.54 (95% CI 0.42 to 0.70), p<0.01) and all-cause death (HR 0.38 (95% CI 0.28 to 0.52), p<0.01) compared with no anticoagulants. Furthermore, compared with warfarin, non-vitamin K antagonist oral anticoagulants (NOACs) were associated with a significant reduction of ICH recurrence (HR 0.64 (95% CI 0.49 to 0.85), p<0.01), while the risk of IS/SE and all-cause mortality were comparable between warfarin and NOACs. CONCLUSIONS: For patients with AF with prior ICH, OAC is associated with a significant reduction in IS/SE and all-cause mortality without increasing ICH recurrence, but may increase major bleeding risk. Compared with warfarin, NOACs had a better safety profile and comparable efficacy. Further larger RCTs are warranted to validate these findings.
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Cai et al. (2023) conducted a meta-analysis in Atrial fibrillation with prior intracranial haemorrhage (n=17,600). Oral anticoagulation (OAC) vs. No anticoagulants was evaluated on ICH recurrence (HR 0.85, 95% CI 0.57-1.25, p=0.41). Oral anticoagulation in AF patients with prior ICH did not increase ICH recurrence (HR 0.85; 95% CI 0.57-1.25) but reduced ischemic stroke and mortality compared with no anticoagulants.
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