Pathmanathan Pras, Gray Richard A
U.S. Food and Drug Administration, 10903 New Hampshire Avenue (WO 62), Silver Spring, MD 20993, USA.
Biomed Res Int. 2015;2015:720575. doi: 10.1155/2015/720575. Epub 2015 Oct 26.
The mechanisms underlying ventricular fibrillation (VF) are not well understood. The electrical activity on the heart surface during VF has been recorded extensively in the experimental setting and in some cases clinically; however, corresponding transmural activation patterns are prohibitively difficult to measure. In this paper, we use a high-resolution biventricular heart model to study three-dimensional electrical activity during fibrillation, focusing on the driving sources of VF: "filaments," the organising centres of unstable reentrant scroll waves. We show, for the first time, specific 3D filament dynamics during simulated VF in a whole heart geometry that includes fine-scale anatomical structures. Our results suggest that transmural activity is much more complex than what would be expected from surface observations alone. We present examples of complex intramural activity, including filament breakup and reattachment, anchoring to the thin right ventricular apex; rapid transitions among various filament shapes; and filament lengths much greater than wall thickness. We also present evidence for anatomy playing a major role in VF development and coronary vessels and trabeculae influencing filament dynamics. Overall, our results indicate that intramural activity during simulated VF is extraordinarily complex and suggest that further investigation of 3D filaments is necessary to fully comprehend recorded surface patterns.
室颤(VF)的潜在机制尚未完全明确。在实验环境以及某些临床病例中,已经广泛记录了室颤期间心脏表面的电活动;然而,相应的透壁激活模式极难测量。在本文中,我们使用高分辨率双心室心脏模型来研究颤动期间的三维电活动,重点关注室颤的驱动源:“细丝”,即不稳定折返涡旋波的组织中心。我们首次展示了在包含精细解剖结构的全心几何模型中模拟室颤期间特定的三维细丝动态。我们的结果表明,透壁活动比仅从表面观察所预期的要复杂得多。我们展示了复杂的壁内活动示例,包括细丝断裂和重新附着、锚定在右心室薄心尖;各种细丝形状之间的快速转变;以及细丝长度远大于壁厚。我们还提供了证据表明解剖结构在室颤发展中起主要作用,冠状动脉血管和小梁影响细丝动态。总体而言,我们的结果表明模拟室颤期间的壁内活动极其复杂,并表明有必要进一步研究三维细丝以充分理解所记录的表面模式。