Skip navigation.

  ASMEDL.ORG »  Journals »  J. Biomech. Eng. »  Volume 131 »  pp. 21010
Adjust text size: Decrease font size Increase font size

Journal of Biomechanical Engineering
Volume: Page/CID:

Previous Article
Invariant-Based Anisotropic Constitutive Models of the Healthy and Aneurysmal Abdominal Aortic Wall
The arterial wall is a complex fiber-reinforced composite. Pathological conditions, such as aneurysms, significantly alter the mechanical response of the arterial wall, resulting in a loss of elastici...
Next Article
Load Transfer Mechanism for Different Metatarsal Geometries: A Finite Element Study
The load transfer mechanism across the skeleton of the human foot is very important to understand its biomechanical function. In this work, we develop several computational models to compare the biome...

Three-Dimensional Computational Modeling of Subject-Specific Cerebrospinal Fluid Flow in the Subarachnoid Space

J. Biomech. Eng.  -- February 2009 --  Volume 131,  Issue 2, 021010 (11 pages)
doi:10.1115/1.3005171

You are not logged into the ASME Digital Library.
Log in

Author(s):
Sumeet Gupta
Laboratory of Thermodynamics in Emerging Technologies, Department of Mechanical and Process Engineering, ETH Zurich, 8092 Zurich, Switzerland

Michaela Soellinger and Peter Boesiger
Institute for Biomedical Engineering, University of Zurich, CH-8006 Zurich, Switzerland; ETH Zurich, 8092 Zurich, Switzerland

Dimos Poulikakos and Vartan Kurtcuoglu
Laboratory of Thermodynamics in Emerging Technologies, Department of Mechanical and Process Engineering, ETH Zurich, 8092 Zurich, Switzerland
This study aims at investigating three-dimensional subject-specific cerebrospinal fluid (CSF) dynamics in the inferior cranial space, the superior spinal subarachnoid space (SAS), and the fourth cerebral ventricle using a combination of a finite-volume computational fluid dynamics (CFD) approach and magnetic resonance imaging (MRI) experiments. An anatomically accurate 3D model of the entire SAS of a healthy volunteer was reconstructed from high resolution T2 weighted MRI data. Subject-specific pulsatile velocity boundary conditions were imposed at planes in the pontine cistern, cerebellomedullary cistern, and in the spinal subarachnoid space. Velocimetric MRI was used to measure the velocity field at these boundaries. A constant pressure boundary condition was imposed at the interface between the aqueduct of Sylvius and the fourth ventricle. The morphology of the SAS with its complex trabecula structures was taken into account through a novel porous media model with anisotropic permeability. The governing equations were solved using finite-volume CFD. We observed a total pressure variation from −42  Pa  to  40  Pa within one cardiac cycle in the investigated domain. Maximum CSF velocities of about 15  cm/s occurred in the inferior section of the aqueduct, 14  cm/s in the left foramen of Luschka, and 9  cm/s in the foramen of Magendie. Flow velocities in the right foramen of Luschka were found to be significantly lower than in the left, indicating three-dimensional brain asymmetries. The flow in the cerebellomedullary cistern was found to be relatively diffusive with a peak Reynolds number (Re)=72, while the flow in the pontine cistern was primarily convective with a peak Re=386. The net volumetric flow rate in the spinal canal was found to be negligible despite CSF oscillation with substantial amplitude with a maximum volumetric flow rate of 109  ml/min. The observed transient flow patterns indicate a compliant behavior of the cranial subarachnoid space. Still, the estimated deformations were small owing to the large parenchymal surface. We have integrated anatomic and velocimetric MRI data with computational fluid dynamics incorporating the porous SAS morphology for the subject-specific reconstruction of cerebrospinal fluid flow in the subarachnoid space. This model can be used as a basis for the development of computational tools, e.g., for the optimization of intrathecal drug delivery and computer-aided evaluation of cerebral pathologies such as syrinx development in syringomelia.

©2009 American Society of Mechanical Engineers

History: Received 23 October 2007; revised 25 August 2008; published 10 December 2008
doi: http://dx.doi.org/10.1115/1.3005171

KEYWORDS and PACS

Keywords
PACS
  • 87.85.gf
    Fluid mechanics and rheology (biomechanics in biomedical engineering)
  • 47.11.Df
    Finite volume methods in fluid dynamics
  • 87.61.-c
    Medical magnetic resonance imaging
  • 87.85.gp
    Mechanical systems (biomechanics in biomedical engineering)
  • 47.63.-b
    Biological fluid dynamics
  • 87.19.U-
    Haemodynamics
  • YEAR: 2009

RELATED DATABASES


To view database links for this article,
you need to log in.
To view database links for this article,
you need to log in.

PUBLICATION DATA

Coden:
JBENDY
ISSN:
0148-0731 (print)   1528-8951 (online)
Publisher:
AIP is a member of CrossRef ASME

REFERENCES (53)

For access to fully linked references, you need to log in. For access to fully linked references, you need to Log in.

CITING ARTICLES

For access to citing articles, you need to log in.
For access to citing articles, you need to Log in.