Key result
Noninvasive 3D cardiac electrical imaging accurately reconstructed the ventricular activation sequence compared to invasive 3D mapping in a canine model, demonstrating a correlation coefficient of 0.74.
Why the study?
Does 3D cardiac electrical imaging accurately reconstruct ventricular activation sequences compared to intracardiac mapping in a canine model?
Does 3D cardiac electrical imaging accurately reconstruct ventricular activation sequences compared to intracardiac mapping in a canine model?
3D cardiac electrical imaging can noninvasively and accurately reconstruct 3D ventricular activation sequences and localize the origin of paced beats and ventricular tachycardia in a canine model.
Supports noninvasive mapping feasibility in canines; leaves open human translation and clinical validation.
Single-beat imaging of myocardial activation promises to aid in both cardiovascular research and clinical medicine. In the present study we validate a three-dimensional (3D) cardiac electrical imaging (3DCEI) technique with the aid of simultaneous 3D intracardiac mapping to assess its capability to localize endocardial and epicardial initiation sites and image global activation sequences during pacing and ventricular tachycardia (VT) in the canine heart. Body surface potentials were measured simultaneously with bipolar electrical recordings in a closed-chest condition in healthy canines. Computed tomography images were obtained after the mapping study to construct realistic geometry models. Data analysis was performed on paced rhythms and VTs induced by norepinephrine (NE). The noninvasively reconstructed activation sequence was in good agreement with the simultaneous measurements from 3D cardiac mapping with a correlation coefficient of 0.74 ± 0.06, a relative error of 0.29 ± 0.05, and a root mean square error of 9 ± 3 ms averaged over 460 paced beats and 96 ectopic beats including premature ventricular complexes, couplets, and nonsustained monomorphic VTs and polymorphic VTs. Endocardial and epicardial origins of paced beats were successfully predicted in 72% and 86% of cases, respectively, during left ventricular pacing. The NE-induced ectopic beats initiated in the subendocardium by a focal mechanism. Sites of initial activation were estimated to be ∼7 mm from the measured initiation sites for both the paced beats and ectopic beats. For the polymorphic VTs, beat-to-beat dynamic shifts of initiation site and activation pattern were characterized by the reconstruction. The present results suggest that 3DCEI can noninvasively image the 3D activation sequence and localize the origin of activation of paced beats and NE-induced VTs in the canine heart with good accuracy. This 3DCEI technique offers the potential to aid interventional therapeutic procedures for treating ventricular arrhythmias arising from epicardial or endocardial sites and to noninvasively assess the mechanisms of these arrhythmias.
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Han et al. (2011) studied Ventricular activation during pacing and ventricular tachycardia (n=5). 3D cardiac electrical imaging (3DCEI) vs. 3D intracardiac mapping was evaluated on Correlation coefficient between noninvasively reconstructed and invasively measured activation sequences. Noninvasive 3D cardiac electrical imaging accurately reconstructed the ventricular activation sequence compared to invasive 3D mapping in a canine model, demonstrating a correlation coefficient of 0.74.
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