Fluid–structure interaction study for biomechanics and risk factors in Stanford type A aortic dissection

主动脉 心脏病学 医学 主动脉夹层 人口 胸主动脉 升主动脉 内科学 动脉瘤 解剖(医学) 主动脉弓 血流 主动脉破裂 主动脉瘤 放射科 环境卫生
作者
Xiaochen Wang,Mergen H. Ghayesh,Andrei Kotousov,Anthony C. Zander,Joseph Dawson,Peter J. Psaltis
出处
期刊:International Journal for Numerical Methods in Biomedical Engineering [Wiley]
卷期号:39 (8): e3736-e3736 被引量:15
标识
DOI:10.1002/cnm.3736
摘要

Abstract Aortic dissection is a life‐threatening condition with a rising prevalence in the elderly population, possibly as a consequence of the increasing population life expectancy. Untreated aortic dissection can lead to myocardial infarction, aortic branch malperfusion or occlusion, rupture, aneurysm formation and death. This study aims to assess the potential of a biomechanical model in predicting the risks of a non‐dilated thoracic aorta with Stanford type A dissection. To achieve this, a fully coupled fluid–structure interaction model was developed under realistic blood flow conditions. This model of the aorta was developed by considering three‐dimensional artery geometry, multiple artery layers, hyperelastic artery wall, in vivo‐based physiological time‐varying blood velocity profiles, and non‐Newtonian blood behaviours. The results demonstrate that in a thoracic aorta with Stanford type A dissection, the wall shear stress (WSS) is significantly low in the ascending aorta and false lumen, leading to potential aortic dilation and thrombus formation. The results also reveal that the WSS is highly related to blood flow patterns. The aortic arch region near the brachiocephalic and left common carotid artery is prone to rupture, showing a good agreement with the clinical reports. The results have been translated into their potential clinical relevance by revealing the role of the stress state, WSS and flow characteristics as the main parameters affecting lesion progression, including rupture and aneurysm. The developed model can be tailored for patient‐specific studies and utilised as a predictive tool to estimate aneurysm growth and initiation of wall rupture inside the human thoracic aorta.
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