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Regions of High Dominant Frequency in Chronic Atrial Fibrillation Anchored to Areas of Atrial Fibrosis

机译:慢性心房纤颤高频率区域锚定于心房纤维化区域

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Regions within the atria with sustained rapid reentrant or focal activity have been defined as a mechanism of persistent atrial fibrillation (AF). However, the mechanism behind the anchoring of these sites and their stability over time is unknown. We tested the hypothesis that fibrosis anchors sites of high frequency activation during AF and that these sites can be non-invasively determined using cardiac T1 Mapping with MRI.A canine rapid atrial paced model of persistent AF was used (n=12, including 6 controls) for the study. Whole heart T1 Mapping was performed prior to an electrical mapping study. Spatial maps of high dominant frequency (DF) probability were constructed to determine stability of the highest DF sites. These sites were then correlated with fibrotic regions determined by T1 Mapping.The chronic AF animals had at least one site of stable, high DF for at least 22.5 (75%) of 30 minutes of AF. Regions of stable high DF bordered regions offibrosis as determined by T1 Mapping MRI 82% of the time (p<0.05).Heterogeneous atrial remodeling, specifically fibrosis, arising from chronic AF may provide a substrate that anchors sites of high DF. Cardiac T1 Mapping with MRI may determine such sites non-invasively.
机译:心房内持续快速折返或局灶性活动的区域已被定义为持续性心房颤动(AF)的机制。但是,这些位点的锚定机制及其随时间的稳定性尚不清楚。我们测试了纤维化锚定房颤期间高频激活部位的假设,并且可以使用心脏T1映射和MRI来无创地确定这些部位。使用了犬持续性房颤的快速心房起搏模型(n = 12,包括6个对照)进行研究。在进行电测绘研究之前,进行了全心T1测绘。构建高主频(DF)概率的空间图,以确定最高DF站点的稳定性。然后将这些位点与通过T1映射确定的纤维化区域相关联。慢性AF动物在30分钟的AF中至少有22.5(75%)个处于稳定,高DF的位点。通过T1映射MRI确定的稳定高DF区域毗邻纤维化区域,时间为82%(p <0.05)。慢性房颤引起的非均质心房重构,特别是纤维化可能提供了固定高DF部位的基质。 MRI的心脏T1定位可以无创地确定此类部位。

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