Copyright
©The Author(s) 2026.
World J Cardiol. Jan 26, 2026; 18(1): 111882
Published online Jan 26, 2026. doi: 10.4330/wjc.v18.i1.111882
Published online Jan 26, 2026. doi: 10.4330/wjc.v18.i1.111882
Table 1 Comparison of key attributes of two recent randomized controlled trials on use of oral anticoagulation in subclinical atrial fibrillation
| ARTESIA | NOAH AFNET 6 | |
| Population size | 4012 | 2536 |
| SCAF duration | 6 minutes-24 hours | > 6 minutes |
| Longest duration of SCAF (median) | 1.5 hours | 2.8 hours |
| Drug used | Apixaban 5 mg BD | Edoxaban 60 mg OD |
| Comparator | Aspirin | Aspirin/placebo |
| Mean CHA2DS2VaSc score | 3.9 ± 1.1 | 4 |
| Mean age (years) | 76 ± 7.6 | 78 |
| Females (%) | 36.1 | 37.4 |
| Follow up (years) | 3.5 ± 1.8 | 1.8 |
| Primary efficacy end point | Stroke or SE (intention-to-treat analysis) | Cardiovascular death, stroke, or SE (time-to-event analysis) |
| Primary safety end point | Major bleeding | Death from any cause or major bleeding |
| Trial completion | Completed | Premature termination |
- Citation: Pradhan A, Shah S, Vishwakarma P, Singh AK. Subclinical atrial fibrillation: Implications of recent trials for guideline updates? World J Cardiol 2026; 18(1): 111882
- URL: https://www.wjgnet.com/1949-8462/full/v18/i1/111882.htm
- DOI: https://dx.doi.org/10.4330/wjc.v18.i1.111882
