期刊论文详细信息
His electrogram alternans reveal dual-wavefront inputs into and longitudinal dissociation within the bundle of his
Article
关键词: NODAL REENTRANT TACHYCARDIA;    ATRIOVENTRICULAR NODE;    CONDUCTION;    PATHWAY;    POSTERIOR;    ABLATION;    HEART;   
DOI  :  10.1161/hc3301.092804
来源: SCIE
【 摘 要 】

Background-His electrogram (HE) amplitude and morphology changes were observed in our previous studies during transition from fast to slow atrioventricular nodal (AVN) conduction. This phenomenon and its significance for the dual-AVN electrophysiology are not well recognized and have not been studied. Methods and Results-Experiments were performed on 17 healthy rabbit atrial-AVN preparations during standard programmed electrical pacing. HEs were mapped along the His bundle with roving surface electrodes, along with recording of cellular action potentials (APs). HEs recorded from the superior margin of the His bundle were of greater amplitude during basic beats and decreased substantially, by 42 +/- 19% (P <0.01), when premature A(1)A(2) shortened to 178 +/- 20 ms. In contrast, the HEs from the inferior margin increased dramatically, 2.9 +/-1.7 times (P <0.01), during short A(1)A(2) and remained high until AVN block occurred. In addition, during long A(1)A(2), the superior HEs consistently preceded the inferior by 1.9 +/-0.7 ms. In contrast, at short A(1)A(2), the superior HEs occurred 2.7 +/-0.8 ms after the inferior. Cellular AP recordings demonstrated clearly the presence of and the transition between early (fast) and late (slow) excitation wavefronts that accompanied HE alternans. Conclusions-The morphological-electrophysiological evidence from the AV junction suggests that fast and slow wavefronts reach the His bundle differently, producing functional longitudinal dissociation into 2 domains. The characteristic HE alternans recorded from these domains are a new sensitive tool to determine the presence of distinctly different wavefronts and their participation in the conduction during reentrant or other arrhythmias. These findings provide further understanding of the mechanisms of dual-AVN electrophysiology.

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