Evidence map›Paper›PMID 42502146›Full record

ArticleJournal of thrombosis and thrombolysis2026

Early versus delayed oral anticoagulation initiation after transcatheter aortic valve replacement in patients with atrial fibrillation: a retrospective cohort study.

Muneeb Khawar, Mohab Elnashar, Mirza Muhammad Hadeed Khawar, Mohammad Azeem Malik, Shameer Iqbal Ghuman, Awon Muhammad, Mohammad Maheer Mubashir, Gul Sher Ghouri, Abdullah Shahid, Ashesh Das

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Article in Journal of thrombosis and thrombolysis, 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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5 · Who and what money

Authors and funding

10 authors.

Muneeb KhawarKing Edward Medical University, Lahore, Pakistan.
Mohab ElnasharUniversity of Arkansas for Medical Sciences, Little Rock, AR, USA.
Mirza Muhammad Hadeed KhawarServices Institute of Medical Sciences, Lahore, Pakistan.
Mohammad Azeem MalikKing Edward Medical University, Lahore, Pakistan.
Shameer Iqbal GhumanKing Edward Medical University, Lahore, Pakistan.
Awon MuhammadKing Edward Medical University, Lahore, Pakistan.
Mohammad Maheer MubashirKing Edward Medical University, Lahore, Pakistan.
Gul Sher GhouriKing Edward Medical University, Lahore, Pakistan.
Abdullah ShahidKhawaja Muhammad Safdar Medical College, Sialkot, Pakistan. shahidabdullah.1930@gmail.com.
Ashesh DasMayo Clinic, Rochester, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The optimal timing of oral anticoagulation (OAC) initiation after transcatheter aortic valve replacement (TAVR) in patients with atrial fibrillation remains uncertain. This study compared early (within 2 days) versus delayed (5-7 days) OAC initiation on clinical outcomes in this population. In this retrospective cohort study using the TriNetX US Collaborative Network (data through 2024), we identified patients aged ≥ 18 years with atrial fibrillation or flutter undergoing TAVR via percutaneous femoral approach. Patients were categorized by OAC initiation timing post-TAVR. The index date was the TAVR procedure day; outcomes were assessed at 30 days, 90 days, and 1 year. Analyses used risk ratios (RRs), hazard ratios (HRs), Kaplan-Meier curves, and log-rank tests. After 1:1 propensity score matching, 3,372 patients remained in each cohort. Early OAC was associated with lower net adverse clinical events (NACE; all-cause mortality, stroke, arterial embolism or thrombosis, or major hemorrhage including transfusion) at 30 days (RR 0.754, 95% CI 0.683-0.832, p < 0.001), 90 days (RR 0.780, 95% CI 0.719-0.846, p < 0.001), and 1 year (RR 0.839, 95% CI 0.789-0.893, p < 0.001). All-cause mortality, major hemorrhage, and acute kidney injury were also significantly reduced with early OAC across all time points. Corresponding hazard ratios confirmed sustained benefit (30-day NACE HR 0.74, 95% CI 0.66-0.82; 1-year HR 0.79, 95% CI 0.73-0.85). Early OAC initiation within 2 days after TAVR was associated with lower NACE, mortality, hemorrhage, and acute kidney injury compared with initiation at 5-7 days in patients with atrial fibrillation. Prospective trials are warranted to confirm these findings.

Indexed as

Anticoagulation timingAtrial fibrillationNet adverse clinical eventsOral anticoagulationPropensity score matchingTranscatheter aortic valve replacement

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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.