Computational hemodynamics framework for the analysis of cerebral aneurysms

被引:90
作者
Mut, Fernando [1 ]
Loehner, Rainald [1 ]
Chien, Aichi [2 ]
Tateshima, Satoshi [2 ]
Vinuela, Fernando [2 ]
Putman, Christopher [3 ]
Cebral, Juan R. [1 ]
机构
[1] George Mason Univ, Dept Computat & Data Sci, Ctr Computat Fluid Dynam, Fairfax, VA 22030 USA
[2] Univ Calif Los Angeles, UCLA Med Ctr, Los Angeles, CA USA
[3] Inova Fairfax Hosp, Falls Church, VA USA
基金
美国国家卫生研究院;
关键词
cerebral aneurysms; hemodynamics; rupture risk; patient-specific modeling; BLOOD-FLOW; INTRACRANIAL ANEURYSMS; VERTEBRAL ARTERIES; NITRIC-OXIDE; MODELS; SIMULATION; APOPTOSIS; DYNAMICS; WILLIS; CIRCLE;
D O I
10.1002/cnm.1424
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Assessing the risk of rupture of intracranial aneurysms is important for clinicians because the natural rupture risk can be exceeded by the small but significant risk carried by current treatments. To this end numerous investigators have used image-based computational fluid dynamics models to extract patient-specific hemodynamics information, but there is no consensus on which variables or hemodynamic characteristics are the most important. This paper describes a computational framework to study and characterize the hemodynamic environment of cerebral aneurysms in order to relate it to clinical events, such as growth or rupture. In particular, a number of hemodynamic quantities are proposed to describe the most salient features of these hemodynamic environments. Application to a patient population indicates that ruptured aneurysms tend to have concentrated inflows, concentrated wall shear stress distributions, high maximal wall shear stress, and smaller viscous dissipation ratios than unruptured aneurysms. Furthermore, these statistical associations are largely unaffected by the choice of physiologic flow conditions. This confirms the notion that hemodynamic information derived from image-based computational models can be used to assess aneurysm rupture risk, to test hypotheses about the mechanisms responsible for aneurysm formation, progression, and rupture, and to answer specific clinical questions. Copyright (C) 2010 John Wiley & Sons, Ltd.
引用
收藏
页码:822 / 839
页数:18
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