2004
DOI: 10.1111/j.1540-8159.2004.00581.x
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Evolution of Mapping and Anatomic Imaging of Cardiac Arrhythmias

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Cited by 13 publications
(12 citation statements)
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“…38 Within the border zone of the scar, abnormal myocardial fibrils are interspersed among fibrotic tissue, causing electrical activity to proceed in a slow and roundabout manner. [44][45][46] Every time the catheter touches the endocardium, the exact catheter tip position within the 3D model, as well as the local uni-or bipolar EGMs including voltage and local activation time (compared with a reference point), is recorded and added to the map. [39][40][41] To facilitate catheter ablation, real-time electroanatomical maps are created using 3D mapping systems (i.e., Carto 3D Mapping System, Biosense Webster, Diamond Bar, CA; EnSite NavX, St. Jude Medical, Inc., Saint Paul, MN) 42,43 These systems allow for exact localization and orientation of the catheter tip inside a virtual 3D reconstruction of the ventricular cavities.…”
Section: Mappingmentioning
confidence: 99%
“…38 Within the border zone of the scar, abnormal myocardial fibrils are interspersed among fibrotic tissue, causing electrical activity to proceed in a slow and roundabout manner. [44][45][46] Every time the catheter touches the endocardium, the exact catheter tip position within the 3D model, as well as the local uni-or bipolar EGMs including voltage and local activation time (compared with a reference point), is recorded and added to the map. [39][40][41] To facilitate catheter ablation, real-time electroanatomical maps are created using 3D mapping systems (i.e., Carto 3D Mapping System, Biosense Webster, Diamond Bar, CA; EnSite NavX, St. Jude Medical, Inc., Saint Paul, MN) 42,43 These systems allow for exact localization and orientation of the catheter tip inside a virtual 3D reconstruction of the ventricular cavities.…”
Section: Mappingmentioning
confidence: 99%
“…The present available electrophysiological models, ranging from single cell (Noble & Rudy, 2001; ten Tusscher et al 2004; Fenton et al 2005; ten Tusscher & Panfilov 2006) to tissue level (Henriquez & Papazoglou 1996; Pollard & Barr, 1991; Pollard et al 1993) and organ level (Noble, 2004, 2007; Trayanova, 2006; Vigmond et al 2008 a ), have proved sufficiently accurate to model complex processes, including ion kinetics in healthy and pathological conditions. In many cases, cardiac modelling can be used to investigate phenomena such as drug effects on the electromechanical response and arrhythmogenesis (Henriquez & Papazoglou, 1996; Packer, 2004; Rodriguez et al 2005), which are difficult to study in vivo .…”
Section: Electrophysiological Analysismentioning
confidence: 99%
“…This limitation has provided the incentive for the development of computer‐based mapping that chronicles both the temporal and spatial characteristics of cardiac activation. This development has also been driven by the need for increasing accuracy in arrhythmia localization as required for catheter ablation 1 …”
Section: Introductionmentioning
confidence: 99%