Evidence map›Paper›PMID 40395561›Full record

ReviewEuropean cardiology2025

Comparative Analysis of the Net Clinical Benefit of Direct Oral Anticoagulants in Atrial Fibrillation: Systematic Review and Network Meta-analysis of Randomised Controlled Trials.

Ton Duy Mai, Tri Huynh Quang Ho, Sy Van Hoang, Hoai Thi Thu Nguyen, Jeyaraj Pandian, Tan Van Nguyen, Khoa Tien Vu, Giang Song Tran, Viet Phuong Dao, Minh Cong Tran and 1 more

Abstract readReview
In one paragraph

Review in European cardiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. A double paradox: end-stage renal disease-high thromboembolic and bleeding risk management using a device with risks of thromboembolism and bleeding.Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology · 2025
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Ton Duy MaiStroke Centre, Bach Mai Hospital Hanoi, Vietnam.ORCID https://orcid.org/0000-0002-7210-3522
Tri Huynh Quang HoHeart Institute Ho Chi Minh City, Vietnam.ORCID https://orcid.org/0000-0002-5226-5372
Sy Van HoangDepartment of Internal Medicine, University of Medicine and Pharmacy at Ho Chi Minh City Ho Chi Minh City, Vietnam.ORCID https://orcid.org/0000-0002-3984-648X
Hoai Thi Thu NguyenDepartment of Internal Medicine, VNU University of Medicine and Pharmacy Hanoi, Vietnam.ORCID https://orcid.org/0000-0003-1742-3061
Jeyaraj PandianDepartment of Neurology, Christian Medical College Ludhiana, India.ORCID https://orcid.org/0000-0003-0028-1968
Tan Van NguyenDepartment of Geriatrics and Gerontology, University of Medicine and Pharmacy at Ho Chi Minh City Ho Chi Minh City, Vietnam.ORCID https://orcid.org/0000-0002-0234-6596
Khoa Tien VuMedical Affairs Department, Bayer Vietnam Ho Chi Minh City, Vietnam.ORCID https://orcid.org/0009-0000-6350-8416
Giang Song TranVietnam National Heart Institute, Bach Mai Hospital Hanoi, Vietnam.
Viet Phuong DaoStroke Centre, Bach Mai Hospital Hanoi, Vietnam.
Minh Cong TranNuffield Department of Clinical Neuroscience, University of Oxford Oxford, UK.ORCID https://orcid.org/0000-0003-2622-1365
Hung Manh PhamDepartment of Cardiology, Ha Noi Medical University Hanoi, Vietnam.ORCID https://orcid.org/0000-0001-8943-3248

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Direct oral anticoagulants (DOACs) are the standard treatment for stroke prevention in AF. However, high-quality head-to-head comparisons of DOACs are lacking. This study compared oral anticoagulants in patients with AF. Methods: Data were retrieved from eligible randomised controlled trials (RCTs). Interventions were ranked using the surface under the cumulative ranking curve (SUCRA) and the frequentist random effects model was applied. Efficacy outcomes included stroke, systemic embolism, MI, and all-cause mortality; the safety outcome was major bleeding. A composite outcome of efficacy and net clinical benefit was also evaluated. Results: From 23,152 records, 11 eligible RCTs were identified and included in the study. Rivaroxaban was superior to vitamin K antagonists (VKA) in net clinical benefit (RR 0.75; 95% CI [0.59-0.94]; p=0.0133), but there were no significant differences between other DOACs and VKA or among the DOACs themselves. Rivaroxaban reduced the risk of the composite outcome of efficacy compared with dabigatran (RR 0.85; 95% CI [0.75-0.98]; p=0.02) and edoxaban (RR 0.84; 95% CI [0.75-0.95]; p=0.0051), but not apixaban (RR 0.89; 95% CI [0.89-1.02]; p=0.087). All DOACs showed superiority over VKA in efficacy, without an increased risk of major bleeding. Based on the SUCRA, rivaroxaban showed a favourable risk-benefit profile compared with the other anticoagulants. Conclusion: This study showed that DOACs are superior to VKA in efficacy without increasing major bleeding risk, with rivaroxaban demonstrating the most balanced risk-benefit profile. Well-designed RCTs are needed to validate these findings.

Indexed as

AFbleedingdirect oral anticoagulantstrokevitamin K antagonist

Identifiers

PMID40395561
PMCPMC12090073

What Socratic holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

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 Socratic graph.