Key result
The presence of cerebral microbleeds in patients with cardiogenic cerebral embolism due to nonvalvular atrial fibrillation did not significantly increase the risk of cerebral hemorrhage events (HR 2.349) or all-cause death following antithrombotic therapy.
Why the study?
The impact of cerebral microbleeds on the safety of antithrombotic therapy in patients with cardiogenic cerebral embolism due to nonvalvular atrial fibrillation was uncertain.
Does antithrombotic therapy increase the risk of cerebral hemorrhage and all-cause death in patients with cerebral microbleeds and cardiogenic cerebral embolism due to nonvalvular atrial fibrillation compared to those without cerebral microbleeds?
Cohort (n=232)
No
Does antithrombotic therapy increase the risk of cerebral hemorrhage and all-cause death in patients with cerebral microbleeds and cardiogenic cerebral embolism due to nonvalvular atrial fibrillation compared to those without cerebral microbleeds?
Antithrombotic therapy in patients with cerebral microbleeds and cardiogenic cerebral embolism due to nonvalvular atrial fibrillation does not increase the overall risk of cerebral hemorrhage or all-cause death, though close follow-up is needed for those with a history of hypertension or prior cerebral hemorrhage.
Antithrombotic therapy may continue despite cerebral microbleeds; leaves open need for randomized confirmation in nonvalvular AF embolism.
BACKGROUND: The impact of cerebral microbleeds on the safety of antithrombotic therapy has recently received considerable attention. We investigated the safety of antithrombotic therapy in patients with cerebral microbleeds and cardiogenic cerebral embolism caused by nonvalvular atrial fibrillation. METHODS: This retrospective study enrolled patients with acute cardiogenic cerebral embolism due to nonvalvular atrial fibrillation in the stroke unit of the Department of Neurology at the Beijing Tiantan Hospital, the Capital Medical University, from January 2015 to January 2018. General clinical data, magnetic resonance imaging data, and data regarding the use of antithrombotic medications were collected. The main adverse events were cerebral hemorrhage and all-cause death. RESULTS: According to the susceptibility-weighted imaging sequence, patients were divided into a cerebral microbleeds group and a non-cerebral microbleeds group. Patients with cerebral microbleeds were more likely to be male and to have a history of hypertension and diabetes, and they were less likely to have received anticoagulant therapy (49.1% vs. 71.3%, P = 0.001). However, no significant differences were found in the event-free time, the occurrence of cerebral hemorrhage events and all-cause death. Cox regression analysis showed that the risk of all-cause death in patients with a cerebral hemorrhage history and cerebral microbleeds increased 2.773-fold (HR = 2.773, 95%CI 1.056-7.280, P = 0.019), and the risk of a cerebral hemorrhage event in patients with cerebral microbleeds and a hypertension history (HR = 3.451, 95%CI 1.947-6.119, P = 0.045) or a cerebral hemorrhage history (HR = 2.443, 1.078-5.536, P = 0.006) was increased 3.451-fold and 2.443-fold, respectively. CONCLUSIONS: Antithrombotic therapy in patients with CMBs and cardiogenic cerebral embolism due to nonvalvular atrial fibrillation did not have increased risks of a cerebral hemorrhage event and all-cause death. CMBs were probably not a crucial predictor of whether patients were prescribed antithrombotic medicine. Patients with CMBs and a hypertension history or cerebral hemorrhage history should receive a close follow-up after antithrombotic therapy.
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Wang et al. (2019) conducted a cohort in Acute cardiogenic cerebral embolism due to nonvalvular atrial fibrillation (n=232). Cerebral microbleeds vs. No cerebral microbleeds was evaluated on Cerebral hemorrhage events (HR 2.349, 95% CI 0.945-5.840, p=0.066). The presence of cerebral microbleeds in patients with cardiogenic cerebral embolism due to nonvalvular atrial fibrillation did not significantly increase the risk of cerebral hemorrhage events (HR 2.349) or all-cause death following antithrombotic therapy.
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