Massively Parallel Models of the Human Circulatory System

被引:32
|
作者
Randles, Amanda [1 ,2 ]
Draeger, Erik W. [1 ]
Oppelstrup, Tomas [1 ]
Krauss, Liam [1 ]
Gunnels, John A. [3 ]
机构
[1] Lawrence Livermore Natl Lab, 7000 East Ave, Livermore, CA 94550 USA
[2] Duke Univ, Durham, NC USA
[3] IBM Corp, TJ Watson Res Ctr, Yorktown Hts, NY 10598 USA
关键词
Category:; time-to-solution; ANKLE-BRACHIAL INDEX; INTERMITTENT CLAUDICATION; BLOOD-FLOW; ARTERIAL; RISK; CORONARY; DISEASE; HEMODYNAMICS; SIMULATIONS; MORTALITY;
D O I
10.1145/2807591.2807676
中图分类号
TP301 [理论、方法];
学科分类号
081202 ;
摘要
The potential impact of blood flow simulations on the diagnosis and treatment of patients suffering from vascular disease is tremendous. Empowering models of the full arterial tree can provide insight into diseases such as arterial hypertension and enables the study of the influence of local factors on global hemodynamics. We present a new, highly scalable implementation of the lattice Boltzmann method which addresses key challenges such as multiscale coupling, limited memory capacity and bandwidth, and robust load balancing in complex geometries. We demonstrate the strong scaling of a three-dimensional, high-resolution simulation of hemodynamics in the systemic arterial tree on 1,572,864 cores of Blue Gene/Q. Faster calculation of flow in full arterial networks enables unprecedented risk stratification on a perpatient basis. In pursuit of this goal, we have introduced computational advances that significantly reduce time-tosolution for biofluidic simulations.
引用
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页数:11
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