TY - JOUR
T1 - Clinical utility and prognostic implications of the novel 4S-AF scheme to characterize and evaluate patients with atrial fibrillation
T2 - a report from ESC-EHRA EORP-AF Long-Term General Registry
AU - Atrial fibrillation (AF)
AU - Ding, Wern Yew
AU - Proietti, Marco
AU - Boriani, Giuseppe
AU - Fauchier, Laurent
AU - Blomström-Lundqvist, Carina
AU - Marin, Francisco
AU - Potpara, Tatjana S.
AU - Lip, Gregory Y.H.
AU - Tavazzi, L.
AU - Maggioni, A. P.
AU - Lip, G. Y.H.
AU - Potpara, T.
AU - Nabauer, M.
AU - Marin, F.
AU - Kalarus, Z.
AU - Fauchier, L.
AU - Goda, A.
AU - Mairesse, G.
AU - Shalganov, T.
AU - Antoniades, L.
AU - Taborsky, M.
AU - Riahi, S.
AU - Muda, P.
AU - García Bolao, I.
AU - Piot, O.
AU - Nabauer, M.
AU - Etsadashvili, K.
AU - Simantirakis, E.
AU - Haim, M.
AU - Azhari, A.
AU - Najafian, J.
AU - Santini, M.
AU - Mirrakhimov, E.
AU - Kulzida, K. A.
AU - Erglis, A.
AU - Poposka, L.
AU - Burg, M.
AU - Crijns, H.
AU - Erküner,
AU - Atar, D.
AU - Lenarczyk, R.
AU - Martins Oliveira, M.
AU - Shah, D.
AU - Dan, G. A.
AU - Serdechnaya, E.
AU - Potpara, T.
AU - Diker, E.
AU - Lip, G. Y.H.
AU - Lane, D.
AU - Zëra, E.
N1 - Publisher Copyright:
© 2021 Published on behalf of the European Society of Cardiology. All rights reserved.
PY - 2022/5/1
Y1 - 2022/5/1
N2 - 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.
AB - 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.
KW - 4S-AF
KW - Atrial fibrillation
KW - Bleeding
KW - Characterization
KW - Classification
KW - EORP-AF registry
KW - Mortality
KW - Prognostic implications
KW - Stroke
KW - Thromboembolism
KW - Validation
UR - http://www.scopus.com/inward/record.url?scp=85130863248&partnerID=8YFLogxK
U2 - 10.1093/europace/euab280
DO - 10.1093/europace/euab280
M3 - Article
C2 - 35446354
AN - SCOPUS:85130863248
SN - 1099-5129
VL - 24
SP - 721
EP - 728
JO - Europace
JF - Europace
IS - 5
ER -