Modeling of non-Newtonian blood rheology with applications to arterial flow simulations

Date
2015
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University of Delaware
Abstract
This thesis aims at improving the accuracy of blood flow simulations by offering a faithful representation of the human blood rheology. A central component of this work has been the establishment of a connection between the physiological conditions in blood and the exhibited rheology. This connection, along with the macroscopic approach which is adopted so as to describe the structural changes within blood that dictate the key rheological properties, namely the viscosity and yield stress, can be a powerful tool in the hands of physicians and medical scientists who might require detailed and reliable information of the exhibited hemodynamics in the arterial network. Thus, this work can be potentially used for the improvement of diagnostic methods in cardiovascular-related diseases. Throughout this thesis particular emphasis has been placed on adhering to a systematic approach, a practice that is warranted for the modeling of systems as complex, and highly coupled, as the flow of blood in the human arterial network. The first step has been the development of a parametric model for the description of the steady state rheology in simple shear flows. Under physiological conditions, we have shown that the Casson constitutive equation describes best the rheology of blood. The proposed model connects the involved parameters, the Casson viscosity and yield stress, to the physiological conditions, the hematocrit, temperature and fibrinogen concentration. Yield stress has been modeled as critical, percolation type phenomenon with an onset that corresponds to a critical hematocrit. The highlight of this work has been the quantification of the dependence of yield stress, and the critical hematocrit, on the fibrinogen concentration. Following the development of the parametric Casson model for physiological conditions we extended our analysis to pathological cases, whereby we examined the effect of both high and low values of cholesterol and triglycerides to the steady shear flow properties. We showed that while the Casson model continues to describe well the blood rheology, its model parameters, i.e. the yield stress and model viscosity, need to be significantly modified from their physiological expressions. The new parametrization involves indices, formed from the supplied cholesterol and triglycerides information. Namely, we found that the indices of interest are all ratios: total cholesterol to high density lipoproteins (HDL), low density lipoproteins (LDL) to HDL, and total triglyceride to HDL. While these indices arose naturally in the fitting of the data, they all have been previously identified as important in medical evaluations of CVDs. Upon completion of the steady state analysis, we focused on the modeling of blood in transient shear flows. We have developed a scalar, structural, parameter thixotropic model capable of describing the transient shear rheology. The thixotropic model introduces only three additional parameters, with a specific physical meaning (a zero shear rate maximum strain, and two kinematic coefficients) and a known order of magnitude. Even more importantly, at steady state the thixotropic model reduces to the parametric Casson for low and moderate shear rates, therefore ensuring the previously emphasized systematic analysis, while at high shear rates it reduces to a Newtonian model, which is consistent with data from literature that have, however, never been predicted theoretically. The thixotropic model has been extensively validated against triangular step-change, rectangular step-change, and large amplitude oscillatory (LAOS) data, and it offers, at a minimum, a reasonable, semi-quantitative fit. Finally, we have examined the impact of the described rheology on simulations of arterial flow. Namely, we have carried out CFD simulations of blood flow in the left coronary artery (LCA), considering two separate cases: a healthy LCA artery, and a pathological one with a stenosis causing ~82% blockage in the left anterior descending (LAD) branch of the LCA. In this study we further developed a previously proposed methodology for the proper implementation of outflow boundary conditions (OBCs) in simulations of arterial flow, while also applying a numerical analysis technique which accelerated significantly the convergence rate of the proposed scheme. The results were presented via two comparative cases. For the healthy LCA artery, we compared the predictions of a Newtonian-based simulation to those that resulted from the application of the Casson parametric model. The obtained pressure and flow profiles, as well as the wall shear stress (WSS), which is the most important parameter in CVD related hematological studies, were shown to be significantly different in the two cases. This highlights the importance of incorporating the rheology of blood in CFD simulations. Then, for the pathological geometry we compared the results obtained with and without the application of the proposed scheme for the proper implementation of OBCs. Again, the marked differences in the simulation output in the two cases highlights the need for adopting the proposed methodology in arterial flow simulations.
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