Arrhythmias & electrophysiology

Management of device-detected subclinical atrial fibrillation: a European Heart Rhythm Association survey

EuropacePublished Cross-sectional study

Authors' conclusion

AF screening is not routinely performed, either in primary or secondary prevention of stroke. Device-detected AF is not uncommon and generally managed based on thromboembolic risk and duration of episodes; the cut-offs of AF duration, global burden, and number of episodes are yet to be determined in terms of role and clinical value. Clinicians' approaches to subclinical AF remain heterogeneous.

Study context

Population
Physicians managing device-detected subclinical AF (DDAF), 46 countries
Participants
222 physicians · 46 countries
Outcome
Physicians' management of DDAF
Methodological detailsphysician-based survey, 24 multiple-choice questions
  • Physician-based survey
  • 24 multiple-choice questions

Main finding

As reported in the abstract

Respondents reporting DDAF in >10% of cardiac electronic devices (CIED) follow-up

37%

Initiate OAC with AF >24 h

34%

Initiate OAC with AF >6 h

26%

Initiate OAC with AF >5-6 min

15%

Observational data: associations, not effects.

Further findings

Systematic long-term AF screening with ILR after cryptogenic stroke (% of ILRs implanted for that purpose)

Regional differences in diagnostic exams and therapy

Non-European and Mediterranean European respondents more likely than North European respondents to prescribe diagnostic exams and therapy

Consumer-based devices for AF screening

Majority recommend use mainly in specific situations (undiagnosed palpitations, ischaemic stroke, AF burden monitoring), not routinely by CHA2DS2-VA or age

Original publication

Management of device-detected subclinical atrial fibrillation: a European Heart Rhythm Association survey. Europace. Published 6 November 2025. doi:10.1093/europace/euaf284

Summarised from the published abstract; every number is checked against it

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