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Consumer-Led Screening for Atrial Fibrillation: Frontier Review of the AF-SCREEN International Collaboration.

Authors :
Brandes, Axel
Brandes, Axel
Stavrakis, Stavros
Freedman, Ben
Antoniou, Sotiris
Boriani, Giuseppe
Camm, A
Chow, Clara
Ding, Eric
Engdahl, Johan
Gibson, Michael
Golovchiner, Gregory
Glotzer, Taya
Guo, Yutao
Healey, Jeff
Hills, Mellanie
Johnson, Linda
Lip, Gregory
Lobban, Trudie
Macfarlane, Peter
McManus, David
Neubeck, Lis
Orchard, Jessica
Perez, Marco
Schnabel, Renate
Smyth, Breda
Steinhubl, Steven
Turakhia, Mintu
Marcus, Gregory
Brandes, Axel
Brandes, Axel
Stavrakis, Stavros
Freedman, Ben
Antoniou, Sotiris
Boriani, Giuseppe
Camm, A
Chow, Clara
Ding, Eric
Engdahl, Johan
Gibson, Michael
Golovchiner, Gregory
Glotzer, Taya
Guo, Yutao
Healey, Jeff
Hills, Mellanie
Johnson, Linda
Lip, Gregory
Lobban, Trudie
Macfarlane, Peter
McManus, David
Neubeck, Lis
Orchard, Jessica
Perez, Marco
Schnabel, Renate
Smyth, Breda
Steinhubl, Steven
Turakhia, Mintu
Marcus, Gregory
Source :
Circulation; vol 146, iss 19
Publication Year :
2022

Abstract

The technological evolution and widespread availability of wearables and handheld ECG devices capable of screening for atrial fibrillation (AF), and their promotion directly to consumers, has focused attention of health care professionals and patient organizations on consumer-led AF screening. In this Frontiers review, members of the AF-SCREEN International Collaboration provide a critical appraisal of this rapidly evolving field to increase awareness of the complexities and uncertainties surrounding consumer-led AF screening. Although there are numerous commercially available devices directly marketed to consumers for AF monitoring and identification of unrecognized AF, health care professional-led randomized controlled studies using multiple ECG recordings or continuous ECG monitoring to detect AF have failed to demonstrate a significant reduction in stroke. Although it remains uncertain if consumer-led AF screening reduces stroke, it could increase early diagnosis of AF and facilitate an integrated approach, including appropriate anticoagulation, rate or rhythm management, and risk factor modification to reduce complications. Companies marketing AF screening devices should report the accuracy and performance of their products in high- and low-risk populations and avoid claims about clinical outcomes unless improvement is demonstrated in randomized clinical trials. Generally, the diagnostic yield of AF screening increases with the number, duration, and temporal dispersion of screening sessions, but the prognostic importance may be less than for AF detected by single-time point screening, which is largely permanent, persistent, or high-burden paroxysmal AF. Consumer-initiated ECG recordings suggesting possible AF always require confirmation by a health care professional experienced in ECG reading, whereas suspicion of AF on the basis of photoplethysmography must be confirmed with an ECG. Consumer-led AF screening is unlikely to be cost-effective for stroke preventi

Details

Database :
OAIster
Journal :
Circulation; vol 146, iss 19
Notes :
application/pdf, Circulation vol 146, iss 19
Publication Type :
Electronic Resource
Accession number :
edsoai.on1410326532
Document Type :
Electronic Resource