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Analytic solution for pulse wave propagation in flexible tubes with application to a patient-specific arterial tree

Published online by Cambridge University Press:  19 December 2023

Peishuo Wu
Affiliation:
Department of Mechanics and Engineering Science, State Key Laboratory for Turbulence and Complex Systems, Peking University, Beijing 100871, PR China
Chi Zhu*
Affiliation:
Department of Mechanics and Engineering Science, State Key Laboratory for Turbulence and Complex Systems, Peking University, Beijing 100871, PR ChinaNanchang Innovation Institute, Peking University, Nanchang 330008, PR China
*
†Email address for correspondence: chi.zhu@pku.edu.cn

Abstract

In this paper, we present an analytic solution for pulse wave propagation in a flexible arterial model with tapering, physiological boundary conditions and variable wall properties (wall elasticity and thickness). The change of wall properties follows a profile that is proportional to $r^\alpha$, where $r$ represents the lumen radius and $\alpha$ is a material coefficient. The cross-sectionally averaged velocity and pressure are obtained by solving a hyperbolic system derived from the mass and momentum conservations, and they are expressed in Bessel functions of order $(4-\alpha )/(3-\alpha )$ and $1/(3-\alpha )$, respectively. The solution is successfully validated by comparing it with numerical results from three-dimensional (3-D) fluid–structure interaction simulations. Subsequently, the solution is employed to study pulse wave propagation in an arterial model, revealing that the wall properties and the physiological outlet boundary conditions, such as the resistor–capacitor–resistor (RCR) model, play a crucial role in characterizing the input impedance and reflection coefficient. At low-frequency range, the input impedance is found to be insensitive to the wall properties and is primarily determined by the RCR parameters. At high-frequency range, the input impedance oscillates around the local characteristic impedance, and the oscillation amplitude varies non-monotonically with $\alpha$. Expressions for the input impedance at both low-frequency and high-frequency limits are presented. This analytic solution is also successfully applied to model flow inside a patient-specific arterial tree, with the maximum relative errors in pressure and flow rate never exceeding $1.6\,\%$ and $9.0\,\%$ when compared with results from 3-D numerical simulations.

Information

Type
JFM Papers
Copyright
© The Author(s), 2023. Published by Cambridge University Press
Figure 0

Figure 1.Relationship between $E h$ and lumen radius of a healthy 30-year-old human subject with $k_{1}=3 \times 10^{6}\ {\rm g} \ {\rm cm}^{-1} \ {\rm s}^{-2}$, $k_{2}=-13.5\ {\rm cm}^{-1}$, $k_{3}=5.94 \times 10^{5}\ {\rm g} \ {\rm cm}^{-1} \ {\rm s}^{-2}$ and $k_{4}=-7.8\ {\rm cm}^{-1}$ (Charlton et al.2019).

Figure 1

Figure 2.Schematic of a tapered artery model with variable wall elasticity and thickness.

Figure 2

Figure 3.The RCR boundary condition at the outlet. Here $C$ is the vascular compliance, and $R_1$, $R_2$ are the proximal and distal resistance, respectively.

Figure 3

Table 1.Parameters of tapered carotid artery model.

Figure 4

Figure 4.Comparison between the analytic solutions and 3-D simulation results for the tapered carotid with $\alpha =1$: (a) the flow rate comparison; (b) the pressure comparison.

Figure 5

Figure 5.Comparison between the analytic solutions and 1-D, 3-D simulation results for the tapered carotid with uniform wall properties. The 1-D results are extracted from Xiao et al. (2014) and $\alpha =0$, $\beta =2.1\times 10^5$.

Figure 6

Figure 6.Distribution of (a) wall properties and (b) wave velocity along the carotid artery model. Here, $\beta =2.376\times 10^5/r_0^\alpha$ so that all three cases have the same $Eh$ value at the inlet. Other parameters are from table 1.

Figure 7

Figure 7.(a) Magnitude and (b) phase of the input impedance of the tapered carotid artery model. Here, the magnitude is normalized by the characteristic impedance at the inlet, and BC refers to boundary condition. Parameters from table 1 are used.

Figure 8

Figure 8.Magnitude of the input impedance of the tapered carotid artery model with different $\alpha$. (a) Non-reflecting boundary condition is employed; (b) RCR boundary condition is employed. The shaded numbers are the asymptotic values as $\omega \rightarrow 0$ predicted by (4.7).

Figure 9

Figure 9.Pressure waves at $z=l/2$ of the tapered carotid artery model with RCR boundary condition and different $\alpha$. (a) Total pressure wave; (b) forward wave; (c) backward wave. The $y$-axis of the forward and backward waves is set to the same range to facilitate comparison.

Figure 10

Figure 10.Reflection coefficient at the inlet of the tapered carotid artery model with different $\alpha$: (a) non-reflecting boundary condition is employed; (b) RCR boundary condition is employed.

Figure 11

Figure 11.(a) Schematic of a bifurcation with splitting flow. (b) Decomposition of the bifurcation into three individual vessels. Here, the subscripts $0$ and $l$ represent the inlet and outlet of each vessel, respectively.

Figure 12

Figure 12.Patient-specific aorta model and the parameters used in the study. The dashed lines indicate all the sections of arteries used in the analytic model; AAo, ascending aorta; BCA, brachiocephalic artery; LCCA, left common carotid artery; LSUBA, left subclavian artery; DAo, descending aorta.

Figure 13

Figure 13.Comparison between the analytic solutions and 3-D simulation results for the patient-specific aorta model.