How was it found? (the evidence differs) Device- or wearable-detected only
af-device-detectedNo one has reached this rule yetConfirm on an ECG first; anticoagulation is a narrower call (NOAH-AFNET 6 / ARTESiA)
No clinician has signed off this rule yet. It reflects our reading of the guidelines cited below, which has not been independently checked.
Word for word, as generated for the example person below. Figures in the text are theirs.
Your atrial fibrillation was picked up by a device rather than diagnosed clinically, and that genuinely changes the calculation. The first step is confirming it on a proper ECG.
Brief high-rate episodes caught by a watch or an implanted monitor are not the same condition as clinically diagnosed AF, even though they share a name. The two trials that tested anticoagulation in exactly this situation — NOAH-AFNET 6 and ARTESiA — found the untreated stroke rate was only about 1% a year, and pooling them gives roughly a 32% reduction in stroke against roughly a 62% increase in major bleeding. That is a much narrower margin than in clinical AF, and it is why this is a genuine discussion rather than an automatic prescription. Episode length matters to that discussion, so bring the actual recordings.
Outcome-provenTested in randomised trials measuring heart attacks, strokes, or death, not a stand-in for them.· Class 2b· Level A· checked 2026-09-12
Meta-analysis of NOAH-AFNET 6 and ARTESiA — anticoagulation for device-detected atrial fibrillation (Circulation) · Class 2b — individualized decision
“Atrial fibrillation from a smartwatch” — an illustrative profile, not a real user.
Asked after: Atrial fibrillation
Cited by the recommendations above.
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Runs in lib/engine/afPathway.ts as af-device-detected.