Evidence map›Paper›PMID 42038682›Full record

ArticleHeart rhythm O22026

OPTIA-AF trial: A randomized study of rhythm-guided antithrombotic strategy after atrial fibrillation ablation in patients with prior drug-eluting stent implantation.

Dong-Hyeok Kim, Yeji Kim, Seung Woo Lee, Jungmin Kang, Junbeom Park, OPTIA-AF investigators

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Article in Heart rhythm O2, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Dong-Hyeok KimDivision of Cardiology, Ewha Womans University Seoul Hospital, Seoul, South Korea.
Yeji KimDivision of Cardiology, Ewha Womans University Seoul Hospital, Seoul, South Korea.
Seung Woo LeeDivision of Cardiology, Ewha Womans University Mokdong Hospital, Seoul, South Korea.
Jungmin KangDivision of Cardiology, Ewha Womans University Mokdong Hospital, Seoul, South Korea.
Junbeom ParkDivision of Cardiology, Ewha Womans University Mokdong Hospital, Seoul, South Korea.
OPTIA-AF investigators

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Recent randomized studies suggest that oral anticoagulation may be safely discontinued in carefully selected patients who maintain durable sinus rhythm (SR) after atrial fibrillation (AF) ablation. However, patients with previous drug-eluting stent (DES) implantation represent a distinct population in whom residual coronary ischemic risk persists and long-term antiplatelet therapy remains clinically relevant. The optimal antithrombotic strategy in this setting remains uncertain. Objective: The Optimal Postablation Therapy for Ischemic and Arrhythmic Risk in Atrial Fibrillation (OPTIA-AF) trial was designed to evaluate whether discontinuation of non-vitamin K antagonist oral anticoagulation (NOAC) with transition to single antiplatelet therapy is noninferior to continued NOAC therapy in patients with durable SR after AF ablation and previous DES implantation. Methods: OPTIA-AF is a prospective, multicenter, randomized controlled trial enrolling patients with nonvalvular AF who have maintained ≥12 months of documented SR after catheter ablation and are ≥12 months removed from DES implantation. Participants are randomized 1:1 to continued NOAC therapy or NOAC discontinuation with single antiplatelet therapy. Structured rhythm surveillance using electrocardiography and ambulatory monitoring is mandated throughout follow-up. Results: The primary end point is a 24-month net clinical outcome composite of ischemic stroke, systemic embolism, myocardial infarction, definite or probable stent thrombosis, cardiovascular death, and major bleeding. Key secondary end points include individual components of the composite endpoint, clinically relevant nonmajor bleeding, AF recurrence, AF burden, arrhythmia-related hospitalization, and repeat ablation. Approximately 1000 patients will be enrolled to provide adequate power for noninferiority testing. Conclusion: OPTIA-AF will provide randomized evidence to inform a rhythm-guided, individualized antithrombotic strategy after AF ablation in patients with concomitant coronary artery disease and previous DES implantation.

Indexed as

Antithrombotic therapyAtrial fibrillationCatheter ablationDrug-eluting stent (DES)Noninferiority trialNon–vitamin K antagonist oral anticoagulant (NOAC)Rhythm-guided strategySingle antiplatelet therapy (SAPT)

Identifiers

PMID42038682
PMCPMC13107038

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.