The importance of coronary microcirculatory perfusion is highlighted by the severe impact of microvascular diseases such as diabetes and hypertension on heart function. Recently, highly-detailed three-dimensional (3D) data on ex vivo coronary microvascular structure have become available. However, hemodynamic information in individual myocardial capillaries cannot yet be obtained using current in vivo imaging techniques. In this thesis, a novel data-driven modelling framework is developed to predict tissue-scale flow properties from discrete anatomical data, which can in future be used to aid interpretation of coarse-scale perfusion imaging data in healthy and diseased states. Mathematical models are parametrised by the 3D anatomical data set of Lee (2009) from the rat myocardium, and tested using flow measurements in two-dimensional rat mesentery networks. Firstly, algorithmic and statistical tools are developed to separate branching arterioles and venules from mesh-like capillaries, and then to extract geometrical properties of the 3D capillary network. The multi-scale asymptotic homogenisation approach of Shipley and Chapman (2010) is adapted to derive a continuum model of coronary capillary fluid transport incorporating a non-Newtonian viscosity term. Tissue-scale flow is captured by Darcy's Law whose coefficient, the permeability tensor, transmits the volume-averaged capillary-scale flow variations to the tissue-scale equation. This anisotropic permeability tensor is explicitly calculated by solving the capillary-scale fluid mechanics problem on synthetic, stochastically-generated periodic networks parametrised by the geometrical data statistics, and a thorough sensitivity analysis is conducted. Permeability variations across the myocardium are computed by parametrising synthetic networks with transmurally-dependent data statistics, enabling the hypothesis that subendocardial permeability is much higher in diastole to compensate for severely-reduced systolic blood flow to be tested. The continuum Darcy flow model is parametrised by purely structural information to provide tissue-scale perfusion metrics, with the hypothesis that this model is less sensitive and more reliably parametrised than an alternative, estimated discrete network flow solution.
| Identifer | oai:union.ndltd.org:bl.uk/oai:ethos.bl.uk:604462 |
| Date | January 2013 |
| Creators | Smith, Amy |
| Contributors | Shipley, Rebecca; Smith, Nicolas P.; Chapman, S. Jon |
| Publisher | University of Oxford |
| Source Sets | Ethos UK |
| Detected Language | English |
| Type | Electronic Thesis or Dissertation |
| Source | http://ora.ox.ac.uk/objects/uuid:e6f576a2-75d9-4778-a640-a1e8551141a6 |
Page generated in 0.0018 seconds