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Abstract
Fragmented QRS (fQRS) is an electrocardiographic (ECG) marker of myocardial conduction abnormality, characterized by additional notches in the QRS complex. The presence of fQRS has been associated with an increased risk of all-cause mortality and arrhythmia in patients with cardiovascular disease. However, current binary visual analysis is prone to intra- and inter-observer variability and different definitions are problematic in clinical practice. Therefore, objective quantification of fQRS is needed and could further improve risk stratification of these patients. We present an automated method for fQRS detection and quantification. First, a novel robust QRS complex segmentation strategy is proposed, which combines multi-lead information and excludes abnormal heartbeats automatically. Afterwards extracted features, based on variational mode decomposition (VMD), phase-rectified signal averaging (PRSA) and the number of baseline-crossings of the ECG, were used to train a machine learning classifier (Support Vector Machine) to discriminate fragmented from non-fragmented ECG-traces using multi-center data and combining different fQRS criteria used in clinical settings. The best model was trained on the combination of two independent previously annotated datasets and, compared to these visual fQRS annotations, achieved Kappa scores of 0.68 and 0.44, respectively. We also show that the algorithm might be used in both regular sinus rhythm and irregular beats during atrial fibrillation. These results demonstrate that the proposed approach could be relevant for clinical practice by objectively assessing and quantifying fQRS. The study sets the path for further clinical application of the developed automated fQRS algorithm.
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1 STADIUS Center for Dynamical Systems, Signal Processing and Data Analytics, Department of Electrical Engineering (ESAT), KU Leuven, Belgium (GRID:grid.5596.f) (ISNI:0000 0001 0668 7884)
2 Experimental Cardiology, Department of Cardiovascular Diseases, KU Leuven, Belgium (GRID:grid.5596.f) (ISNI:0000 0001 0668 7884); Libin Cardiovascular Institute, Cumming School of Medicine, University of Calgary, Department of Cardiac Sciences, Calgary, Canada (GRID:grid.22072.35) (ISNI:0000 0004 1936 7697)
3 Research Unit of Internal Medicine, Medical Research Center Oulu, University of Oulu and Oulu University Hospital, Oulu, Finland (GRID:grid.10858.34) (ISNI:0000 0001 0941 4873)
4 Experimental Cardiology, Department of Cardiovascular Diseases, KU Leuven, Belgium (GRID:grid.5596.f) (ISNI:0000 0001 0668 7884)
5 Heart Center, University of Göttingen Medical Center, Department of Cardiology and Pneumology, Göttingen, Germany (GRID:grid.7450.6) (ISNI:0000 0001 2364 4210)
6 University Medical Center Göttingen, Department of Medical Statistics, Göttingen, Germany (GRID:grid.411984.1) (ISNI:0000 0001 0482 5331); DZHK (German Center of Cardiovascular Research), partner site Göttingen, Göttingen, Germany (GRID:grid.452396.f) (ISNI:0000 0004 5937 5237)
7 University of Basel Hospital, Division of Cardiology, Basel, Switzerland (GRID:grid.410567.1)
8 University Medical Center Utrecht, Department of Cardiology, Utrecht, Netherlands (GRID:grid.7692.a) (ISNI:0000000090126352)
9 National Heart and Lung Institute, Imperial College, London, UK (GRID:grid.7445.2) (ISNI:0000 0001 2113 8111); Masaryk University, Department of Internal Medicine and Cardiology, Brno, Czech Republic (GRID:grid.10267.32) (ISNI:0000 0001 2194 0956)
10 STADIUS Center for Dynamical Systems, Signal Processing and Data Analytics, Department of Electrical Engineering (ESAT), KU Leuven, Belgium (GRID:grid.5596.f) (ISNI:0000 0001 0668 7884); Microgravity Research Center, Université Libre de Bruxelles, Brussels, Belgium (GRID:grid.4989.c) (ISNI:0000 0001 2348 0746)