Key result
VKA use in coronary embolism with AF is linked to ~90% higher adverse outcomes versus DOACs.
Why the study?
Coronary embolism is an uncommon cause of acute myocardial infarction and the optimal post-discharge antithrombotic strategy remains uncertain.
Does stratification of antithrombotic therapy (DOAC vs VKA in AF; antiplatelet vs OAC in non-OAC indicated) improve long-term outcomes in patients with coronary embolism?
Cohort (n=489)
Yes
Does stratification of antithrombotic therapy (DOAC vs VKA in AF; antiplatelet vs OAC in non-OAC indicated) improve long-term outcomes in patients with coronary embolism?
Hazard Ratio: 1.9 (95% CI 1.02–3.5)
Absolute Event Rate: 40% vs 18%
p-value: p=0.04
In patients with coronary embolism, DOACs yield better long-term outcomes than VKAs for those with atrial fibrillation, while antiplatelet therapy is superior to oral anticoagulation for those without an explicit OAC indication.
May support DOAC over VKA in AF-related coronary embolism; hypothesis-generating for non-OAC patients.
Background Coronary embolism (CE) is an uncommon cause of acute myocardial infarction, and the optimal post-discharge antithrombotic strategy remains uncertain. Methods Retrospective multicenter study including patients with definite or probable CE. Three groups of patients were identified: i) requiring with specific management, ii) with atrial fibrillation (AF), and iii) with no indication for oral anticoagulation (OAC). The latter two groups were further classified according to the antithrombotic treatment received, and long-term outcomes (composite of recurrent CE, stroke, systemic embolism, cardiovascular or all cause death and major bleeding at 5 years) were subsequently evaluated Results A total of 489 patients were considered. Among 189 patients with AF, 85 received direct oral anticoagulants (DOAC) and 104 vitamin K antagonists (VKAs). VKA users showed a higher rate of the composite endpoint compared with DOACs (40% vs. 18%, p < 0.001) with the difference primarily driven by all-cause mortality. In multivariable analysis, VKA therapy remained independently associated with worse outcomes (HR 1.9, 95% CI 1.02–3.5; p=0.04). In the 182 patients without an indication for anticoagulation, 115 received antiplatelet therapy and 67 OAC. Those treated with OAC had a higher incidence of the composite outcome (16% vs. 7%, p=0.049) with the difference primarily driven by all-cause mortality. Multivariable analysis confirmed OAC as an independent predictor of adverse prognosis (HR 3.4 (95%CI 1.2-9.7;p=0.02). Conclusions In patients with CE, stratification based on underlying etiology and embolic risk before hospital discharge might serve as a decision-making approach for determining optimal antithrombotic strategies and improved clinical outcomes
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Vera et al. (2026) conducted a cohort in Coronary embolism (n=489). Vitamin K antagonists vs. Direct oral anticoagulants (DOACs) was evaluated on Composite of recurrent CE, stroke, systemic embolism, cardiovascular or all cause death and major bleeding at 5 years (HR 1.9, 95% CI 1.02-3.5, p=0.04). Vitamin K antagonist use in coronary embolism patients with atrial fibrillation was associated with higher adverse outcomes than DOACs (40% vs. 18%; HR 1.9, 95% CI 1.02-3.5, p=0.04).
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