Cargando…

Clinical utility of the 4S-AF scheme in predicting progression of atrial fibrillation: data from the RACE V study

AIMS: The recent 4S-AF (scheme proposed by the 2020 ESC AF guidelines to address stroke risk, symptom severity, severity of AF burden and substrate of AF to provide a structured phenotyping of AF patients in clinical practice to guide therapy and assess prognosis) scheme has been proposed as a struc...

Descripción completa

Detalles Bibliográficos
Autores principales: Artola Arita, Vicente, Van De Lande, Martijn E, Khalilian Ekrami, Neda, Nguyen, Bao-Oanh, Van Melle, Joost M, Geelhoed, Bastiaan, De With, Ruben R, Weberndörfer, Vanessa, Erküner, Ömer, Hillege, Hans, Linz, Dominik, Ten Cate, Hugo, Spronk, Henri M H, Koldenhof, Tim, Tieleman, Robert G, Schotten, Ulrich, Crijns, Harry J G M, Van Gelder, Isabelle C, Rienstra, Michiel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10105835/
https://www.ncbi.nlm.nih.gov/pubmed/36857318
http://dx.doi.org/10.1093/europace/euac268
_version_ 1785026295310057472
author Artola Arita, Vicente
Van De Lande, Martijn E
Khalilian Ekrami, Neda
Nguyen, Bao-Oanh
Van Melle, Joost M
Geelhoed, Bastiaan
De With, Ruben R
Weberndörfer, Vanessa
Erküner, Ömer
Hillege, Hans
Linz, Dominik
Ten Cate, Hugo
Spronk, Henri M H
Koldenhof, Tim
Tieleman, Robert G
Schotten, Ulrich
Crijns, Harry J G M
Van Gelder, Isabelle C
Rienstra, Michiel
author_facet Artola Arita, Vicente
Van De Lande, Martijn E
Khalilian Ekrami, Neda
Nguyen, Bao-Oanh
Van Melle, Joost M
Geelhoed, Bastiaan
De With, Ruben R
Weberndörfer, Vanessa
Erküner, Ömer
Hillege, Hans
Linz, Dominik
Ten Cate, Hugo
Spronk, Henri M H
Koldenhof, Tim
Tieleman, Robert G
Schotten, Ulrich
Crijns, Harry J G M
Van Gelder, Isabelle C
Rienstra, Michiel
author_sort Artola Arita, Vicente
collection PubMed
description AIMS: The recent 4S-AF (scheme proposed by the 2020 ESC AF guidelines to address stroke risk, symptom severity, severity of AF burden and substrate of AF to provide a structured phenotyping of AF patients in clinical practice to guide therapy and assess prognosis) scheme has been proposed as a structured scheme to characterize patients with atrial fibrillation (AF). We aimed to assess whether the 4S-AF scheme predicts AF progression in patients with self-terminating AF. METHODS AND RESULTS: We analysed 341 patients with self-terminating AF included in the well-phenotyped Reappraisal of Atrial Fibrillation: Interaction between HyperCoagulability, Electrical remodelling, and Vascular Destabilization in the Progression of AF (RACE V) study. Patients had continuous monitoring with implantable loop recorders or pacemakers. AF progression was defined as progression to persistent or permanent AF or progression of self-terminating AF with >3% burden increase. Progression of AF was observed in 42 patients (12.3%, 5.9% per year). Patients were given a score based on the components of the 4S-AF scheme. Mean age was 65 [interquartile range (IQR) 58–71] years, 149 (44%) were women, 103 (49%) had heart failure, 276 (81%) had hypertension, and 38 (11%) had coronary artery disease. Median CHA(2)DS(2)-VASc (the CHA(2)DS(2)–VASc score assesses thromboembolic risk. C, congestive heart failure/left ventricular dysfunction; H, hypertension; A(2), age ≥ 75 years; D, diabetes mellitus; S(2), stroke/transient ischaemic attack/systemic embolism; V, vascular disease; A, age 65–74 years; Sc, sex category (female sex)) score was 2 (IQR 2–3), and median follow-up was 2.1 (1.5–2.6) years. The average score of the 4S-AF scheme was 4.6 ± 1.4. The score points from the 4S-AF scheme did not predict the risk of AF progression [odds ratio (OR) 1.1 95% CI 0.88–1.41, C-statistic 0.53]. However, excluding the symptoms domain, resulting in the 3S-AF (4S-AF scheme without the domain symptom severity, only including stroke risk, severity of AF burden and substrate of AF) scheme, predicted the risk of progression (OR 1.59 95% CI 1.15–2.27, C-statistic 0.62) even after adjusting for sex and age. CONCLUSIONS: In self-terminating AF patients, the 4S-AF scheme does not predict AF progression. The 3S-AF scheme, excluding the symptom domain, may be a more appropriate score to predict AF progression. TRIAL REGISTRATION NUMBERS: Clinicaltrials.gov NCT02726698 for RACE V
format Online
Article
Text
id pubmed-10105835
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-101058352023-04-17 Clinical utility of the 4S-AF scheme in predicting progression of atrial fibrillation: data from the RACE V study Artola Arita, Vicente Van De Lande, Martijn E Khalilian Ekrami, Neda Nguyen, Bao-Oanh Van Melle, Joost M Geelhoed, Bastiaan De With, Ruben R Weberndörfer, Vanessa Erküner, Ömer Hillege, Hans Linz, Dominik Ten Cate, Hugo Spronk, Henri M H Koldenhof, Tim Tieleman, Robert G Schotten, Ulrich Crijns, Harry J G M Van Gelder, Isabelle C Rienstra, Michiel Europace Clinical Research AIMS: The recent 4S-AF (scheme proposed by the 2020 ESC AF guidelines to address stroke risk, symptom severity, severity of AF burden and substrate of AF to provide a structured phenotyping of AF patients in clinical practice to guide therapy and assess prognosis) scheme has been proposed as a structured scheme to characterize patients with atrial fibrillation (AF). We aimed to assess whether the 4S-AF scheme predicts AF progression in patients with self-terminating AF. METHODS AND RESULTS: We analysed 341 patients with self-terminating AF included in the well-phenotyped Reappraisal of Atrial Fibrillation: Interaction between HyperCoagulability, Electrical remodelling, and Vascular Destabilization in the Progression of AF (RACE V) study. Patients had continuous monitoring with implantable loop recorders or pacemakers. AF progression was defined as progression to persistent or permanent AF or progression of self-terminating AF with >3% burden increase. Progression of AF was observed in 42 patients (12.3%, 5.9% per year). Patients were given a score based on the components of the 4S-AF scheme. Mean age was 65 [interquartile range (IQR) 58–71] years, 149 (44%) were women, 103 (49%) had heart failure, 276 (81%) had hypertension, and 38 (11%) had coronary artery disease. Median CHA(2)DS(2)-VASc (the CHA(2)DS(2)–VASc score assesses thromboembolic risk. C, congestive heart failure/left ventricular dysfunction; H, hypertension; A(2), age ≥ 75 years; D, diabetes mellitus; S(2), stroke/transient ischaemic attack/systemic embolism; V, vascular disease; A, age 65–74 years; Sc, sex category (female sex)) score was 2 (IQR 2–3), and median follow-up was 2.1 (1.5–2.6) years. The average score of the 4S-AF scheme was 4.6 ± 1.4. The score points from the 4S-AF scheme did not predict the risk of AF progression [odds ratio (OR) 1.1 95% CI 0.88–1.41, C-statistic 0.53]. However, excluding the symptoms domain, resulting in the 3S-AF (4S-AF scheme without the domain symptom severity, only including stroke risk, severity of AF burden and substrate of AF) scheme, predicted the risk of progression (OR 1.59 95% CI 1.15–2.27, C-statistic 0.62) even after adjusting for sex and age. CONCLUSIONS: In self-terminating AF patients, the 4S-AF scheme does not predict AF progression. The 3S-AF scheme, excluding the symptom domain, may be a more appropriate score to predict AF progression. TRIAL REGISTRATION NUMBERS: Clinicaltrials.gov NCT02726698 for RACE V Oxford University Press 2023-03-01 /pmc/articles/PMC10105835/ /pubmed/36857318 http://dx.doi.org/10.1093/europace/euac268 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of the European Society of Cardiology. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Clinical Research
Artola Arita, Vicente
Van De Lande, Martijn E
Khalilian Ekrami, Neda
Nguyen, Bao-Oanh
Van Melle, Joost M
Geelhoed, Bastiaan
De With, Ruben R
Weberndörfer, Vanessa
Erküner, Ömer
Hillege, Hans
Linz, Dominik
Ten Cate, Hugo
Spronk, Henri M H
Koldenhof, Tim
Tieleman, Robert G
Schotten, Ulrich
Crijns, Harry J G M
Van Gelder, Isabelle C
Rienstra, Michiel
Clinical utility of the 4S-AF scheme in predicting progression of atrial fibrillation: data from the RACE V study
title Clinical utility of the 4S-AF scheme in predicting progression of atrial fibrillation: data from the RACE V study
title_full Clinical utility of the 4S-AF scheme in predicting progression of atrial fibrillation: data from the RACE V study
title_fullStr Clinical utility of the 4S-AF scheme in predicting progression of atrial fibrillation: data from the RACE V study
title_full_unstemmed Clinical utility of the 4S-AF scheme in predicting progression of atrial fibrillation: data from the RACE V study
title_short Clinical utility of the 4S-AF scheme in predicting progression of atrial fibrillation: data from the RACE V study
title_sort clinical utility of the 4s-af scheme in predicting progression of atrial fibrillation: data from the race v study
topic Clinical Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10105835/
https://www.ncbi.nlm.nih.gov/pubmed/36857318
http://dx.doi.org/10.1093/europace/euac268
work_keys_str_mv AT artolaaritavicente clinicalutilityofthe4safschemeinpredictingprogressionofatrialfibrillationdatafromtheracevstudy
AT vandelandemartijne clinicalutilityofthe4safschemeinpredictingprogressionofatrialfibrillationdatafromtheracevstudy
AT khalilianekramineda clinicalutilityofthe4safschemeinpredictingprogressionofatrialfibrillationdatafromtheracevstudy
AT nguyenbaooanh clinicalutilityofthe4safschemeinpredictingprogressionofatrialfibrillationdatafromtheracevstudy
AT vanmellejoostm clinicalutilityofthe4safschemeinpredictingprogressionofatrialfibrillationdatafromtheracevstudy
AT geelhoedbastiaan clinicalutilityofthe4safschemeinpredictingprogressionofatrialfibrillationdatafromtheracevstudy
AT dewithrubenr clinicalutilityofthe4safschemeinpredictingprogressionofatrialfibrillationdatafromtheracevstudy
AT weberndorfervanessa clinicalutilityofthe4safschemeinpredictingprogressionofatrialfibrillationdatafromtheracevstudy
AT erkuneromer clinicalutilityofthe4safschemeinpredictingprogressionofatrialfibrillationdatafromtheracevstudy
AT hillegehans clinicalutilityofthe4safschemeinpredictingprogressionofatrialfibrillationdatafromtheracevstudy
AT linzdominik clinicalutilityofthe4safschemeinpredictingprogressionofatrialfibrillationdatafromtheracevstudy
AT tencatehugo clinicalutilityofthe4safschemeinpredictingprogressionofatrialfibrillationdatafromtheracevstudy
AT spronkhenrimh clinicalutilityofthe4safschemeinpredictingprogressionofatrialfibrillationdatafromtheracevstudy
AT koldenhoftim clinicalutilityofthe4safschemeinpredictingprogressionofatrialfibrillationdatafromtheracevstudy
AT tielemanrobertg clinicalutilityofthe4safschemeinpredictingprogressionofatrialfibrillationdatafromtheracevstudy
AT schottenulrich clinicalutilityofthe4safschemeinpredictingprogressionofatrialfibrillationdatafromtheracevstudy
AT crijnsharryjgm clinicalutilityofthe4safschemeinpredictingprogressionofatrialfibrillationdatafromtheracevstudy
AT vangelderisabellec clinicalutilityofthe4safschemeinpredictingprogressionofatrialfibrillationdatafromtheracevstudy
AT rienstramichiel clinicalutilityofthe4safschemeinpredictingprogressionofatrialfibrillationdatafromtheracevstudy