Why the study?
Females with AF taking vitamin K antagonists face higher risks of SSE, bleeding, and death than males, prompting investigation of sex differences in a contemporary anticoagulated cohort.
Does female sex influence the risk of stroke, bleeding, or death in patients with atrial fibrillation receiving oral anticoagulants?
Does female sex influence the risk of stroke, bleeding, or death in patients with atrial fibrillation receiving oral anticoagulants?
In a contemporary cohort of AF patients on oral anticoagulants, women had a significantly lower risk of all-cause death compared to men, with similar rates of stroke and major bleeding.
May warrant closer monitoring of females on VKA; leaves open whether NOACs mitigate sex disparities in contemporary AF cohorts.
BACKGROUND AND OBJECTIVES: In patients with atrial fibrillation (AF), females taking vitamin K antagonist are at higher risk of stroke or systemic embolism (SSE), bleeding and all-cause death than males. This study investigated the relationship between sex and adverse clinical events in a contemporary AF patient cohort taking anticoagulation. METHODS: -VAscore ≥1) and receiving oral anticoagulation therapy. Adverse clinical outcomes, including SSE, bleeding, death were evaluated in patients stratified by sex and anticoagulation patterns. RESULTS: percentiles) follow-up of 30 (24, 38) months, the incidence rate and risk of SSE (0.7 in women vs. 0.7 in men per 100 person-years) and major bleeding (0.1 in women vs. 0.1 in men per 100 person-years) were not different between the sexes. However, women had a lower all-cause death rate (0.4 in women vs. 0.6 in men per 100 person-years, hazard ratio: 0.48, 95% confidence interval: 0.25-0.91, p=0.025) than men. CONCLUSIONS: In contemporary anticoagulation for AF, SSE and major bleeding risks did not differ between sexes. However, women showed a lower risk of all-cause death rate than men, indicating that the use of oral anticoagulants for treating AF in females does not appear to be a risk factor for adverse clinical events. TRIAL REGISTRATION: ClinicalTrials.gov Identifier: NCT02786095.
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Kim et al. (2022) studied this question.
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