Soto-Becerra Richard, Bazan Victor, Bautista William, Malavassi Federico, Altamar Jhancarlo, Ramirez Juan David, Everth Arlen, Callans David J, Marchlinski Francis E, Rodríguez Diego, García Fermin C, Sáenz Luis C
From the International Arrhythmia Center at CardioInfantil Foundation-Cardiac Institute, Bogotá, Colombia (R.S.-B., W.B., F.M., J.A., J.D.R., A.E., D.R., L.C.S.); Electrophysiology Unit, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain (V.B.); and Division of Cardiology, Electrophysiology Program, Hospital of the University of Pennsylvania, Philadelphia (D.J.C., F.E.M., F.C.G.).
Circ Arrhythm Electrophysiol. 2017 Nov;10(11). doi: 10.1161/CIRCEP.116.004950.
Chagasic cardiomyopathy (CC) is the most frequent nonischemic substrate causing left ventricular (LV) tachycardia in Latin America. Systematic characterization of the LV epicardial/endocardial scar distribution and density in CC has not been performed. Additionally, the usefulness of unipolar endocardial electroanatomic mapping to identify epicardial scar has not been assessed in this setting.
Nineteen patients with CC undergoing detailed epicardial and endocardial LV tachycardia mapping and ablation were included. A total of 8494 epicardial and 6331 endocardial voltage signals and 314 epicardial/endocardial matched pairs of points were analyzed. Basal lateral LV scar involvement was observed in 18 of 19 patients. Bipolar voltage mapping demonstrated larger epicardial than endocardial scar and core-dense (≤0.5 mV) scar areas (28 [20-36] versus 19 [15-26] and 21 [2-49] versus 4 [0-7] cm; =0.049 and =0.004, respectively). Bipolar epicardial and endocardial voltages within scar were low (0.4 [0.2-0.55] and 0.54 [0.33-0.87] mV, respectively) and confluent, indicating a dense/transmural scarring process in CC. The endocardial unipolar voltage value (with a newly proposed ≤4-mV cutoff) predicted the presence and extent of epicardial bipolar scar (<0.001).
CC causes a unique ventricular tachycardia substrate concentrated to the basal lateral LV, with marked epicardial predominance. The scar pattern is particularly dense and transmural as compared with the more erratic/patchy scar patterns seen in other nonischemic cardiomyopathies. Endocardial unipolar voltage mapping serves to characterize epicardial scar in this setting.
恰加斯心肌病(CC)是拉丁美洲导致左心室(LV)心动过速最常见的非缺血性病因。尚未对CC患者左心室心外膜/心内膜瘢痕分布及密度进行系统特征分析。此外,在此情况下,尚未评估单极心内膜电解剖标测识别心外膜瘢痕的效用。
纳入19例接受详细的心外膜和心内膜LV心动过速标测及消融的CC患者。共分析了8494个心外膜和6331个心内膜电压信号以及314个心外膜/心内膜匹配点对。19例患者中有18例观察到左心室基底部外侧瘢痕累及。双极电压标测显示心外膜瘢痕大于心内膜瘢痕以及核心致密(≤0.5 mV)瘢痕区域(分别为28 [20 - 36] 对19 [15 - 26] 以及21 [2 - 49] 对4 [0 - 7] cm;P分别为0.049和0.004)。瘢痕内心外膜和心内膜双极电压均较低(分别为0.4 [0.2 - 0.55] 和0.54 [0.33 - 0.87] mV)且呈融合状态,表明CC存在致密/透壁性瘢痕形成过程。心内膜单极电压值(采用新提出的≤4 - mV截止值)可预测心外膜双极瘢痕的存在及范围(P<0.001)。
CC导致一种独特的室性心动过速基质,集中于左心室基底部外侧,心外膜占明显优势。与其他非缺血性心肌病中更不规则/片状的瘢痕模式相比,CC的瘢痕模式特别致密且透壁。在此情况下,心内膜单极电压标测有助于描绘心外膜瘢痕特征。