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Clinical utility and prognostic implications of the novel 4S-AF scheme to characterize and evaluate patients with atrial fibrillation: a report from ESC-EHRA EORP-AF Long-Term General Registry
Univ Liverpool, Liverpool Ctr Cardiovasc Sci, Liverpool, Merseyside, England.;Liverpool Heart & Chest Hosp, Liverpool, Merseyside, England..
Univ Liverpool, Liverpool Ctr Cardiovasc Sci, Liverpool, Merseyside, England.;Liverpool Heart & Chest Hosp, Liverpool, Merseyside, England.;Univ Milan, Dept Clin Sci & Community Hlth, Milan, Italy.;IRCCS Ist Clin Scientif Maugeri, Geriatr Unit, Milan, Italy..
Univ Modena & Reggio Emilia, Dept Biomed Metab & Neural Sci, Cardiol Div, Policlin Modena, Modena, Italy..
Ctr Hosp Univ Trousseau, Serv Cardiol, Tours, France..
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2022 (English)In: Europace, ISSN 1099-5129, E-ISSN 1532-2092, Vol. 24, no 5, p. 721-728Article in journal (Refereed) Published
Abstract [en]

Aims: The 4S-AF classification scheme comprises of four domains: stroke risk (St), symptoms (Sy), severity of atrial fibrillation (AF) burden (Sb), and substrate (Su). We sought to examine the implementation of the 4S-AF scheme in the EORP-AF General Long-Term Registry and compare outcomes in AF patients according to the 4S-AF-led decision-making process.

Methods and results: Atrial fibrillation patients from 250 centres across 27 European countries were included. A 4S-AF score was calculated as the sum of each domain with a maximum score of 9. Of 6321 patients, 8.4% had low (St), 47.5% EHRA I (Sy), 40.5% newly diagnosed or paroxysmal AF (Sb), and 5.1% no cardiovascular risk factors or left atrial enlargement (Su). Median follow-up was 24 months. Using multivariable Cox regression analysis, independent predictors of all-cause mortality were (St) [adjusted hazard ratio (aHR) 8.21, 95% confidence interval (CI): 2.60-25.9], (Sb) (aHR 1.21, 95% CI: 1.08-1.35), and (Su) (aHR 1.27, 95% CI: 1.14-1.41). For CV mortality and any thromboembolic event, only (Su) (aHR 1.73, 95% CI: 1.45-2.06) and (Sy) (aHR 1.29, 95% CI: 1.00-1.66) were statistically significant, respectively. None of the domains were independently linked to ischaemic stroke or major bleeding. Higher 4S-AF score was related to a significant increase in all-cause mortality, CV mortality, any thromboembolic event, and ischaemic stroke but not major bleeding. Treatment of all 4S-AF domains was associated with an independent decrease in all-cause mortality (aHR 0.71, 95% CI: 0.55-0.92). For each 4S-AF domain left untreated, the risk of all-cause mortality increased substantially (aHR 1.35, 95% CI: 1.16-1.56).

Conclusion: Implementation of the novel 4S-AF scheme is feasible, and treatment decisions based on this scheme improve mortality rates in AF.

Place, publisher, year, edition, pages
Oxford University Press (OUP) Oxford University Press, 2022. Vol. 24, no 5, p. 721-728
Keywords [en]
Atrial fibrillation, 4S-AF, Characterization, Classification, EORP-AF registry, Validation, Prognostic implications, Mortality, Thromboembolism, Stroke, Bleeding
National Category
Cardiology and Cardiovascular Disease
Identifiers
URN: urn:nbn:se:uu:diva-479419DOI: 10.1093/europace/euab280ISI: 000785553500001PubMedID: 35446354OAI: oai:DiVA.org:uu-479419DiVA, id: diva2:1679195
Funder
AstraZenecaEli Lilly and CompanyAvailable from: 2022-06-30 Created: 2022-06-30 Last updated: 2025-02-10Bibliographically approved

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Blomström-Lundqvist, Carina

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