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DOI 10.1161/jaha.125.046966

Медицинская библиотека · Journal of the American Heart Association · 2026

Impact of Atrial Fibrillation Pattern on Edoxaban Antithrombotic Therapy in Patients With Atrial Fibrillation and Stable Coronary Artery Disease: A Secondary Analysis of the EPIC-CAD Randomized Clinical Trial.

Yu Jae-Sung, Cho Min-Soo, Kang Do-Yoon, Ahn Jung-Min, Lee Jung-Bok, Oh Yong-Seog, Lee Chang-Hoon, Choi Eue-Keun, Lee Ji-Hyun, Kwon Chang-Hee, Park Gyung-Min, Choi Hyung-Oh, Park Kyung-Ha, Park Kyoung-Min, Hwang Jong-Min, Yoo Ki-Dong, Cho Young-Rak, Kim Ji-Hyun, Hwang Ki-Won, Jin Eun-Sun, Kwon Osung, Kim Ki-Hun, Park Seung-Jung, Nam Gi-Byoung, Park Duk-Woo, EPIC‐CAD Investigators

СтатьяРандомизированное исследованиеМногоцентровое исследованиеПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

BACKGROUND

Paroxysmal atrial fibrillation (AF) is associated with a risk of stroke or systemic embolism similar to nonparoxysmal (persistent or permanent) AF. However, whether the optimal antithrombotic strategy in patients with AF and stable coronary artery disease differs by AF pattern remains uncertain.

METHODS

This prespecified substudy of the EPIC-CAD (Edoxaban Antithrombotic Therapy for Atrial Fibrillation and Stable Coronary Artery Disease) trial compared edoxaban monotherapy with dual antithrombotic therapy (edoxaban plus a single antiplatelet agent) in patients with AF and stable coronary artery disease. Stratified analyses were performed by AF pattern. The primary outcome was net adverse clinical events, defined as a composite of all-cause death, myocardial infarction, stroke, systemic embolism, unplanned urgent revascularization, major bleeding, or clinically relevant nonmajor bleeding within 12 months.

RESULTS

Among 1040 patients, 575 (55.3%) had paroxysmal and 465 (44.7%) had nonparoxysmal AF. The 12-month primary outcome rate was similar between paroxysmal and nonparoxysmal AF (10.3% versus 12.2%; adjusted hazard ratio [HR], 1.15 [95% CI, 0.79-1.68]). Edoxaban monotherapy was associated with a significantly lower risk of the primary outcome than dual antithrombotic therapy in both paroxysmal AF (4.6% versus 16.2%; adjusted HR, 0.23 [95% CI, 0.12-0.42]) and nonparoxysmal AF (9.3% versus 15.0%; adjusted HR, 0.56 [95% CI, 0.32-0.87]). No significant interaction was observed between antithrombotic strategy and AF pattern (P for interaction=0.10).

CONCLUSIONS

In patients with AF and stable coronary artery disease, edoxaban monotherapy significantly reduced net adverse clinical events at 12 months compared with dual antithrombotic therapy, irrespective of AF pattern.

REGISTRATION: URL: https://www.ClinicalTrials.gov; Unique identifier: NCT03718559.

Для цитирования: Yu Jae-Sung, Cho Min-Soo, Kang Do-Yoon, Ahn Jung-Min, Lee Jung-Bok, Oh Yong-Seog, Lee Chang-Hoon, Choi Eue-Keun, Lee Ji-Hyun, Kwon Chang-Hee, Park Gyung-Min, Choi Hyung-Oh, Park Kyung-Ha, Park Kyoung-Min, Hwang Jong-Min, Yoo Ki-Dong, Cho Young-Rak, Kim Ji-Hyun, Hwang Ki-Won, Jin Eun-Sun, Kwon Osung, Kim Ki-Hun, Park Seung-Jung, Nam Gi-Byoung, Park Duk-Woo, EPIC‐CAD Investigators. Impact of Atrial Fibrillation Pattern on Edoxaban Antithrombotic Therapy in Patients With Atrial Fibrillation and Stable Coronary Artery Disease: A Secondary Analysis of the EPIC-CAD Randomized Clinical Trial.. Journal of the American Heart Association. 2026. DOI: 10.1161/jaha.125.046966.

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