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Impact of three dimensional atrial fibrosis on development and stability of rotational and focal sources in atrial fibrillation — A 3D simulation and clinical high-density mapping study in persistent atrial fibrillation

机译:三维房颤对房颤中旋转和局灶性源的发展和稳定性的影响—持续性房颤的3D模拟和临床高密度标测研究

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The arrhythmogenic mechanisms of atrial fibrillation (AF) are still not well understood. Increased atrial fibrosis is a structural hallmark in patients with persistent AF. We assessed the electrogram signature rotational activity and their spatial relationship to low voltage areas in patients with persistent AF. Computer simulations implicating 3-dimensional atrial tissue with different amount of atrial fibrosis were used to assess development and stability of rotational activities during AF. Rotor anchoring occurred at the borderzone between fibrosis and healthy atrial tissue with 12 consecutive rotations prior to rotor extinction. Rotational activity in fibrotic tissue resulted in fractionated signals and were overlapped with large negative electrograms in unipolar recording mode from neighboring healthy tissue — impressing as a focal source. Necessary conditions for development and stability of rotational activities around fibrosis were on the one hand a minimum size of atrial fibrosis area equal or larger than 10mm × 10mm and on the other hand the degree of atrial fibrosis of 40%. Clinical data showed that AF termination sites were located within low voltage areas (displaying <0,5mV in AF on the multielectrode mapping catheter) in 80% and at their borderzones in 20% of cases.
机译:心房颤动(AF)的心律失常机制仍然不甚了解。持续性房颤患者心房纤维化增加是其结构特征。我们评估了持续性房颤患者的电图签名旋转活动及其与低压区域的空间关系。涉及具有不同量的心房纤维化的三维心房组织的计算机模拟被用来评估房颤期间旋转活动的发展和稳定性。转子锚定发生在纤维化和健康的心房组织之间的边界区域,并在转子熄灭之前连续12次旋转。纤维化组织中的旋转活动导致信号分离,并与邻近健康组织的单极记录模式下的大负电图重叠,给人留下了深刻的印象。纤维化周围旋转活动发展和稳定的必要条件,一方面是房颤纤维化区域的最小尺寸等于或大于10mm×10mm,另一方面房颤纤维化的程度为40%。临床数据显示,在80%的病例中,AF终止位点位于低压区域内(在多电极标测导管上的AF中显示<0.5mV),在20%的病例位于其边界区。

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