van Dam Peter M, Boyle Noel G, Laks Michael M, Tung Roderick
UCLA Cardiac Arrhythmia Center, UCLA Heath System, David Geffen School of Medicine at UCLA, Suite 660 Los Angeles, CA 90095, USA
UCLA Cardiac Arrhythmia Center, UCLA Heath System, David Geffen School of Medicine at UCLA, Suite 660 Los Angeles, CA 90095, USA.
Europace. 2016 Dec;18(suppl 4):iv16-iv22. doi: 10.1093/europace/euw347.
The precise localization of the site of origin of a premature ventricular contraction (PVC) prior to ablation can facilitate the planning and execution of the electrophysiological procedure. In clinical practice, the targeted ablation site is estimated from the standard 12-lead ECG. The accuracy of this qualitative estimation has limitations, particularly in the localization of PVCs originating from the papillary muscles. Clinical available electrocardiographic imaging (ECGi) techniques that incorporate patient-specific anatomy may improve the localization of these PVCs, but require body surface maps with greater specificity for the epicardium. The purpose of this report is to demonstrate that a novel cardiac isochrone positioning system (CIPS) program can accurately detect the specific location of the PVC on the papillary muscle using only a 12-lead ECG.
Cardiac isochrone positioning system uses three components: (i) endocardial and epicardial cardiac anatomy and torso geometry derived from MRI, (ii) the patient-specific electrode positions derived from an MRI model registered 3D image, and (iii) the 12-lead ECG. CIPS localizes the PVC origin by matching the anatomical isochrone vector with the ECG vector. The predicted PVC origin was compared with the site of successful ablation or stimulation. Three patients who underwent electrophysiological mapping and ablation of PVCs originating from the papillary muscles were studied. CIPS localized the PVC origin for all three patients to the correct papillary muscle and specifically to the base, mid, or apical region.
A simplified form of ECGi utilizing only 12 standard electrocardiographic leads may facilitate accurate localization of the origin of papillary muscle PVCs.
在进行消融术前精确确定室性早搏(PVC)的起源部位有助于电生理手术的规划与实施。在临床实践中,目标消融部位是根据标准12导联心电图来估计的。这种定性估计的准确性存在局限性,尤其是在定位起源于乳头肌的PVC时。结合患者特异性解剖结构的临床可用心电图成像(ECGi)技术可能会改善这些PVC的定位,但需要对心外膜具有更高特异性的体表图谱。本报告的目的是证明一种新型心脏等时线定位系统(CIPS)程序仅使用12导联心电图就能准确检测乳头肌上PVC的具体位置。
心脏等时线定位系统使用三个组件:(i)源自MRI的心内膜和心外膜心脏解剖结构及躯干几何形状,(ii)源自MRI模型配准3D图像的患者特异性电极位置,以及(iii)12导联心电图。CIPS通过将解剖等时线向量与心电图向量相匹配来定位PVC起源。将预测的PVC起源与成功消融或刺激的部位进行比较。对三名接受了起源于乳头肌的PVC电生理标测和消融的患者进行了研究。CIPS将所有三名患者的PVC起源定位到正确的乳头肌,并具体定位到基部、中部或顶端区域。
仅利用12条标准心电图导联的简化形式的ECGi可能有助于准确确定乳头肌PVC的起源部位。