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

Author:

Artola Arita Vicente1ORCID,Van De Lande Martijn E1ORCID,Khalilian Ekrami Neda1,Nguyen Bao-Oanh1ORCID,Van Melle Joost M1ORCID,Geelhoed Bastiaan1,De With Ruben R1,Weberndörfer Vanessa23ORCID,Erküner Ömer23ORCID,Hillege Hans14ORCID,Linz Dominik23567ORCID,Ten Cate Hugo8910ORCID,Spronk Henri M H8910ORCID,Koldenhof Tim111ORCID,Tieleman Robert G111ORCID,Schotten Ulrich35ORCID,Crijns Harry J G M23ORCID,Van Gelder Isabelle C1,Rienstra Michiel1ORCID

Affiliation:

1. Department of Cardiology, University of Groningen, University Medical Centre Groningen , Hanzeplein 1, Groningen , The Netherlands

2. Department of Cardiology, Maastricht University Medical Centre + , Maastricht , The Netherlands

3. Cardiovascular Research Institute Maastricht (CARIM), Maastricht University , Maastricht , The Netherlands

4. Department of Epidemiology, University Medical Centre Groningen, University of Groningen , Groningen , The Netherlands

5. Department of Cardiology, Radboud University Medical Centre , Nijmegen , The Netherlands

6. Centre for Heart Rhythm Disorders, University of Adelaide and Royal Adelaide Hospital , Adelaide , Australia

7. Department of Biomedical Sciences, Faculty of Health and Medical Sciences, University of Copenhagen , Copenhagen , Denmark

8. Thrombosis Expertise Center (TEC) Maastricht, Departments of Biochemistry , Maastricht , The Netherlands

9. Internal Medicine, Cardiovascular Research Institute Maastricht (CARIM), Maastricht University , Maastricht , The Netherlands

10. Maastricht University Medical Center+ , Maastricht , The Netherlands

11. Department of Cardiology, Martini Hospital , Groningen , The Netherlands

Abstract

AbstractAimsThe 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 resultsWe 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 CHA2DS2-VASc (the CHA2DS2–VASc score assesses thromboembolic risk. C, congestive heart failure/left ventricular dysfunction; H, hypertension; A2, age ≥ 75 years; D, diabetes mellitus; S2, 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.ConclusionsIn 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 numbersClinicaltrials.gov NCT02726698 for RACE V

Publisher

Oxford University Press (OUP)

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine

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