Colli Franzone P, Guerri L, Taccardi B
Dipartimento di Informatica e Sistemistica dell'Università di Pavia, Italy.
J Cardiovasc Electrophysiol. 1993 Aug;4(4):438-58. doi: 10.1111/j.1540-8167.1993.tb01282.x.
We present simulations of extracellular potential patterns elicited by delivering ectopic stimuli to a parallelepipedal slab of ventricular tissue represented as an anisotropic bidomain incorporating epi-endocardial fiber rotation.
Simulations were based on an eikonal model that determines wavefront shapes throughout the slab at every time instant during the depolarization phase, coupled with an approximate model of the action potential profile. The endocardial face of the slab was in contact with blood and the composite volume was surrounded by an insulating medium. The effect of a simplified Purkinje network was also studied.
(1) For all pacing depths, except endocardial pacing, a central negative area and two potential maxima were observed at QRS onset in all intramural planes parallel to the epicardium. In all planes, the axis joining the two maxima was approximately aligned with the direction of fibers in the plane of pacing. Endocardial pacing generated a different pattern, but only when blood was present; (2) During later stages of excitation, outflowing currents (from the wavefront toward the resting tissue) were always emitted, at all intramural depths, only from those portions of the wavefront that spread along fibers. At any given instant, the position of the two potential maxima in a series of planes parallel to the epicardium and intersecting the wavefront rotated as a function of depth, following the rotating direction of intramural fibers. Purkinje involvement modified the above patterns.
Epicardial and endocardial potential maps provided information on pacing site and depth and on subsequent intramural propagation by reflecting the clockwise or counter-clockwise rotation of the deep positivity. Results may be applicable to epicardial and endocardial potential maps recorded at surgery or from endocavitary probes.
我们展示了通过向一个表示为包含心外膜 - 心内膜纤维旋转的各向异性双域的心室组织平行六面体平板施加异位刺激所引发的细胞外电位模式的模拟。
模拟基于一个在去极化阶段的每个时刻确定平板内整个波前形状的程函模型,以及一个动作电位轮廓的近似模型。平板的心内膜面与血液接触,复合体积被绝缘介质包围。还研究了简化浦肯野网络的影响。
(1)对于所有起搏深度,除了心内膜起搏外,在所有与心外膜平行的壁内平面的QRS波起始处均观察到一个中央负区和两个电位最大值。在所有平面中,连接两个最大值的轴大致与起搏平面内的纤维方向对齐。心内膜起搏产生不同的模式,但仅在有血液存在时;(2)在兴奋的后期阶段,流出电流(从波前流向静息组织)总是仅在所有壁内深度处从沿纤维传播的波前部分发出。在任何给定时刻,在一系列与心外膜平行且与波前相交的平面中两个电位最大值的位置随着深度而旋转,遵循壁内纤维的旋转方向。浦肯野网络的参与改变了上述模式。
心外膜和心内膜电位图通过反映深部阳性的顺时针或逆时针旋转,提供了关于起搏部位和深度以及随后壁内传播的信息。结果可能适用于手术中记录的或来自心腔内探头的心外膜和心内膜电位图。