## Abstract

Coronary flow is governed by a number of determinants including network anatomy, systemic afterload and the mechanical interaction with the myocardium throughout the cardiac cycle. The range of spatial scales and multi-physics nature of coronary perfusion highlights a need for a multiscale framework that captures the relevant details at each level of the network. The goal of this review is to provide a compact and accessible introduction to the methodology and current state of the art application of the modelling frameworks that have been used to study the coronary circulation. We begin with a brief description of the seminal experimental observations that have motivated the development of mechanistic frameworks for understanding how myocardial mechanics influences coronary flow. These concepts are then linked to an overview of the lumped parameter models employed to test these hypotheses. We then outline the full and reduced-order (3D and 1D) continuum mechanics models based on the Navier–Stokes equations and highlight, with examples, their application regimes. At the smaller spatial scales the case for the importance of addressing the microcirculation is presented, with an emphasis on the poroelastic approach that is well-suited to bridge an existing gap in the development of an integrated whole heart model. Finally, the recent accomplishments of the wave intensity analysis and related approaches are presented and the clinical outlook for coronary flow modelling discussed.

### Similar content being viewed by others

Avoid common mistakes on your manuscript.

## Introduction

Over the past decades, technological and clinical driving forces have fuelled significant advancements in modelling of blood flow in the coronary vessels of the heart. However, while the governing models and numerical solution techniques are now well-established, the complexities introduced by the anatomy and the dynamic mechanical environment produced by heart contraction present a number of further technical challenges. As emergent models of large-scale coronary circulation have demonstrated, a multiscale modelling approach in which heterogeneous modelling strategies are employed at different network scales has the potential to be both physiologically accurate and computationally effective. This review aims to provide a compact summary of selected past and recent state of the art in coronary modelling, extending over full and reduced-dimensional approaches relevant for constructing a multiscale model and where appropriate, link these developments to clinical applications. For the benefit of the general audience, readers may refer to the basic coronary anatomy (Fig. 1) and hemodynamic characteristics (Table 1, Fig. 2) as background to this review.

The majority of early coronary models employed lumped parameter frameworks to postulate and test the key mechanisms by which flow is determined. Often closely integrated with experimental work, these studies set the stage for initial understanding of the origins behind the pulsatile and phasic nature of the coronary flow and hemodynamic forces governing it. In particular, these pioneering research efforts reinforced the importance of the coronary-myocardial coupling (termed by some as ‘crosstalk’) and that, in order to understand the coronary circulation, an integrated quantitative approach is indispensible.

The more recent models of the coronary circulation have increasingly leveraged the parallel developments in structural and functional imaging technology that provided increasingly detailed computational domains and boundary conditions, as well as the improved solution algorithms and computing power. These technologies have enabled the construction and solution of larger integrated models through the application of three broadly different approaches reviewed herein (see Fig. 3). The first of these is one-dimensional network modelling, often employed to study wave propagation phenomena in a spatially distributed coronary bed, which is, in turn, significantly affected by the transmural variation in myocardial interaction. The second approach builds upon the ongoing computational advances that have rendered detailed three-dimensional computational fluid dynamics (CFD) increasingly tractable, and is relevant to image-based diagnosis and interventional planning as well as exploring factors underlying atherosclerosis development. Finally, the poroelastic modelling approach has received less attention than the previous modelling frameworks, but is well suited for studying the bilateral interaction between coronary flow and myocardial deformation, thus readily lending itself for whole-heart cardiac function modelling.

Although clinical applications of the above-mentioned methodologies have only recently become a major focus for the modelling community, those based on wave intensity analysis have already yielded successful outcomes. As described below, the current established measure for functional diagnosis of stenosis severity (fractional flow reserve) has seen limited uptake in clinics in spite of the overwhelming clinical supporting evidences, owing to its practical difficulties. A new index (instantaneous wave-free ratio) based on the theory of wave intensity analysis introduced recently appears well-posed to address some of these drawbacks, and serves as a noteworthy example of bench-to-bedside translation.

This review is organised as follows. First, the key historical developments in lumped-parameter modelling of coronary flow are reviewed, with an emphasis on the experimental findings which motivated the development of specific frameworks. Progressing from this historical context, three different continuum mechanics approaches are described, including the one-dimensional and three-dimensional computational fluid dynamics, and poroelastic modelling of blood flow in tissues. Finally, the role wave intensity analysis has played in clinical developments is visited as a contemporary example of the potential of modelling technology, and a motivation for its developmental outlook.

## Earlier Concepts in Coronary Modelling

The coronary circulation is distinguished from other vascular networks by its phasic flow pattern.81 Most of the coronary arterial flow occurs in diastole, while during systole the arterial flow may slow down or even reverse, while the venous flow accelerates. These out-of-phase transient changes are not caused by fluctuations in the coronary perfusion pressure but, rather, are broadly attributed to the interaction of coronary flow with cardiac contraction termed ‘mechanical crosstalk’. The exact mechanisms of crosstalk had been under much investigation (For comprehensive reviews of the mechanisms, refer to Spaan89 and Westerhof *et al.*
109). Earlier attempts to understand the mechanical determinants of coronary flow deployed single predominant mechanism in a lumped-parameter model to explain the then-available experimental data. A selection of ideas which steered the major developments in the field is reviewed below.

### Waterfall and Intramyocardial Pump Models

The concept that distal vessels collapse due to the compression of the surrounding myocardium led to the vascular waterfall model.28 Based on the previous work on flow in collapsible tubes,40 it was assumed that when a vessel partially collapses, the flow is no longer a function of the pressure gradient between the arterial and venous pressures; but rather it is the gradient between arterial pressure and the intravascular pressure at the collapse point that determines the flow. With a 4-transmural layer lumped elements, this simple model was able to reproduce the measured arterial inflow. However, the shortcomings of the waterfall model are apparent when the venous flow is considered. In its proposed form, when the vessel collapses the flow eventually halts completely without exhibiting the experimentally-observed inflow reversal or outflow augmentation. To address this issue, the intramyocardial pump model90 was proposed to characterize the mechanism of systolic vascular compression leading to displacement of fluid. This model highlighted the importance of the vascular capacitance which serves to store the fluid during diastole which then is actively pumped away by the myocardial contraction. Many subsequent models were proposed based on the waterfall and intramyocardial pump mechanisms.2,11,12,18,113,114

### Varying Elastance Model

Most of the models mentioned above share the common assumption that the pressure to which the vessels are subjected within the myocardium (intramyocardial pressure or IMP), decreases linearly from the left ventricular pressure (LVP) at the endocardium to zero pressure at epicardium. This association of LVP to vascular compression was debated on grounds that measured IMP may sometimes exceed LVP,56 IMP is confounded by the compartmentalization of pressures in various microstructures within the tissue and also depends on the local venular emptying rate.89,110 Subsequently, the pivotal evidence which supplanted the assumptions underpinning these previous models was provided by the experiments which compared coronary flow in a contracting myocardium with pressurised (isovolumic) or non-pressurised (isobaric) ventricular chambers. That the flow in either case was similar, in both isolated54,55 and *in situ*
102 setups, indicated that another mechanism must be responsible for the systolic flow impediment. This led to the introduction of vascular varying elastance model,54 based on the concepts originally applied to the cardiac chambers.92 In this model, the increased stiffness of the myocardium during systole was postulated to drive the coronary flow through modulating the compliance and resistive properties of the embedded vessels. At low levels of LVP, the contracting ventricle was observed to prevent the LVP from being transmitted in the myocardial wall, thereby shielding the intramural coronary vessels from compression.53,71 Further experiments confirmed the dissociation between LVP and systolic impediment by conversely showing that, with an impaired regional cardiac contraction (*via* application of lidocaine) coronary flow exhibits a considerable dependence on the peak LVP.27

### Lumped Parameter Models and Integrated Modelling

While each of the above experimental studies has contributed elegant mechanistic hypotheses to explain the origin of coronary flow impediment, collectively they show that no single measurable index or mechanism is solely responsible for the phasic flow patterns. This determinant is now understood to be the summed contributions from coronary pressure, the direct (myocardium-vascular interaction) and the indirect (through IMP generation) crosstalk, modulated by contractility, transmural position, afterload, heart rate and the diastolic time interval. Accordingly the lumped parameter models proposed following these seminal studies have been integrative, for example, coupling LV mechanics, coronary flow and fluid and mass transport to test the mechanisms of coronary compression,113 or the shielding effects of vasculature at low LVP.9 Also, the integrative approach has been used to investigate aortic stenosis.34

With a few exceptions, the majority of recent coronary modelling studies have employed a continuum mechanics approach, which is discussed in subsequent sections. Nevertheless, the lumped-parameter approach remains a useful element in the multiscale vascular modelling for retaining the computational tractability, as demonstrated by a number of recent works.30,49,51,67,87,88,101

## One Dimensional Flow Modelling

The key feature of the one dimensional modelling over the lumped parameter approach is the ability to incorporate wave propagation phenomenon. Through a comparative 1D vs. lumped parameter model study, the importance of the wave phenomenon has been demonstrated, particularly pertaining to systolic compression.38 The 1D model also offers significant computational savings compared to simulating full 3D CFD, while capturing the pulse wave characteristics of long wavelength and cross-sectionally averaged flow and pressure in deformable vessels. It is therefore the currently preferred approach for vascular modelling in networks of many vessels. In the following sections, key aspects of the 1D approach are reviewed.

### The Standard Model

The standard 1D flow equations used in many models14,32,60,68,70,77,83,84,88,104 to describe the conservation of mass and momentum can be obtained by averaging the Navier–Stokes equations over the cross-section of an axisymmetric circular cylinder,88 or derived from first principles.83 A characteristic analysis of the governing PDE system shows that it is hyperbolic, with forward and backward traveling waves.32 As these equations model the flow in a deformable vessel, the interaction between fluid and vessel wall warrants further description, requiring an additional equation. The system closure is usually achieved by assuming an algebraic form of the pressure-area (p-A) relationship, derived from a linearly elastic shell model32,83—which will “blow out” at high pressures, but is deemed valid for physiological operating conditions—or otherwise empirically formulated.88 Several forms of the p-A relations were also proposed for the collapsed regime, exhibiting large compliance at first but becoming rapidly stiff toward total collapse point.38,88 The viscous momentum loss in this system is often represented as a force term, which is often derived from an assumed shape of velocity profile across the cross section.88 Alternatively, a flat profile with a linear boundary layer has also been used.70

### Boundary Conditions

The inflow conditions in many 1D modelling studies use waveforms directly measured from experiments38,88 or generated by a simplified model of the heart,68 presuming a dominant role of aortic pressure over coronary perfusion. In contrast, much attention has been paid to formulating the outflow condition, which must capture the characteristics of the distal microcirculation network. The simplest outflow condition is to directly prescribe a pressure or pressure-dependent flow at the distal terminal. However, this is undesirable since it introduces spurious reflections back into the computational domain, fails to reproduce the phase lag between the reflected pressure and flow, and ignores the considerable compliance of the microcirculation. A windkessel outflow condition (reviewed in Westerhof111) offers improvements by incorporating compliance as well as resistance and thus exhibits the frequency-dependent reflection coefficients, although not necessarily in a physiological fashion particularly at higher frequencies. To address these issues, an alternative approach was proposed where the input impedance of the distal network was derived using a generalized branching network.10,70 This model was shown to reproduce the correct impedance behavior across a wider range of frequencies. Numerically consistent ways to incorporate such downstream conditions within the 1D model has also been investigated.104 However, these methods require additional derivations and modifications to the implementation that are not always straightforward to apply. Therefore, a simpler solution of using a single tapered vessel as the outflow condition was proposed recently.68 This approach requires no additional implementation. The tapered vessel model has been used previously to approximate a whole arterial tree,29 and has the useful property of producing a series of reflected waves which are attenuated distally in a graded manner, as can be expected from a vascular tree.

Finally, in the standard model, the coupling of the vessel segments at a junction is normally achieved by two sets of equations. One imposes the conservation of mass and total pressure. These are supplemented by conditions on Riemann invariants of the 1D system83 or “compatibility” equations32 which prescribe appropriate conditions on the characteristics.

### Experimental Validation

The validity of using the 1D model for wave propagation studies in arteries has been investigated using a silicon experimental phantom of the systemic circulation, comprising 37 segments.66 Using measured rather than fitted material parameters, the 1D flow model yielded errors of less than 4% pressure and 19% flow for 70 measurements obtained over the network. Interestingly, the model was able to faithfully reproduce the frequency of the non-physiological oscillations introduced by the simple resistive boundary conditions. Further investigations revealed that the error in amplitude of the oscillations was not corrected by adding peripheral compliance, inertance or energy loss at branching junctions to the model. These authors suggested that the underdamping may be produced by neglecting the viscoelasticity of the tube walls, and later provided supporting evidences using a visco-elastic model of the network.1 This study was performed on a phantom, and its scale was significantly different to that of the coronary vessels. Nevertheless, its *in vitro* validation reasserts that the flow in an elastic tube network can be adequately modelled using the 1D model.

### Viscoelasticity of the Vessel Walls

It has long been established that vascular walls exhibit viscoelastic properties as evidenced by its typical hysteresis behaviour in load-unload cycles. The degree to which viscoelasticity plays a role in coronary flow remains to be fully ascertained; however, to date, modelling studies have offered several insights into this aspect. Pontrelli 77 used a coupled 1D-lumped outflow model to conduct a linearised wave propagation analysis. With periodical forcing, it showed that varying the elasticity coefficient modified the amplitude of the oscillation but had no effect on its frequency, while the viscosity of the wall played a predominant role in attenuating the high frequency wave components. This result lends support to the conclusion reached by the authors of the aforementioned *in vitro* experiment of Matthys66 and their more recent modelling work.1 An extended analysis was offered in Canic *et al.*
15 in which a more complete model description of viscoelastic vascular fluid–structure interaction was presented. Using the techniques of asymptotic homogenization, 3D Navier–Stokes and linear viscoelastic membrane equations were reduced to three systems of parabolic-hyperbolic equations, each of which required the computational complexity of a 1D system, but taken together, captured two-dimensional descriptions of axisymmetric flow features. In particular, the more complete description of the fluid viscous terms allowed the velocity profile in the viscoelastic vessel to be calculated as part of the solution. The model showed that the hysteresis behavior observed in the loading cycle of an artery is solely due to the viscosity of the wall, independent of the fluid viscosity. In addition, the in-depth treatment of the fluid viscous forces appears to indicate a greater contribution of fluid viscous effects to oscillation damping than was suggested by simpler models. Regrettably, this work lacked the description of junction coupling of vessels, limiting its usage so far to a single segment. Further developments in this direction would be useful in bridging the gap between full CFD and 1D models.

### Coronary System Modelling

Surprisingly, to date there has only been a limited number of attempts to study the transient pulsatile flow in a distributed 1D coronary network. An example of such an analysis is provided by Smith *et al.*,87,88 in which the regional myocardial stresses calculated with an anisotropic finite deformation model of the beating heart69 was applied on the vessels. The extravascular pressure applied to the vessels was calculated as the average radial stress on the local vessel. This approach unified the contributions from intramyocardial pump and varying elastance mechanisms (see *Earlier concepts* section), and contrasted the varying significance of each during diastole and systole. The phase difference between arterial and venous flow, and diameter variations of arterioles and venules corresponding to experimental observations in different myocardial layers were also reproduced.

However, although the above analysis captured the broad characteristics of coronary flow and its mechanical determinants, it was limited by two key aspects. The first is in its treatment of the microcirculation, which lumped the complex interaction between the flow-contraction crosstalk into a 0D resistance–capacitance model. The model did however capture their spatial distribution (and thus corresponding variation of myocardial stress) throughout the myocardial layers, as each lumped model was attached to the termini of the distal vessels. Secondly, due to imaging limitation (see next section) and thus the availability of anatomical data at the time of study, the vascular network used was stochastically generated rather than obtained from a sample. This may detract from the strength of the conclusions regarding the transmural variability of crosstalk mechanisms. Efforts to address both of these shortcomings are currently underway, with the poroelastic models reviewed below, and new advances in imaging of microcirculation (as previously reviewed61).

### Computational Solution Techniques

The numerical solution of the 1D flow equation system has been achieved using both finite difference14,88 and finite element techniques.68,84,106 Although the Lax-Wendroff finite difference method applied in previous studies14,88 achieved a good balance between accuracy and solution speed, the finite element method has been preferentially applied in more recent studies. Of note is the spectral/hp technique83 which is known to yield good dispersion and diffusion error properties well-suited for modelling wave propagation, and exponential ideal convergence rate.48 Techniques which can decouple the solution in each vessel have also been of particular interest, since they have the attractive property of avoiding large matrix inversion. In these schemes the information between vessels at a junction is passed through inter-element flux terms. Techniques of this type so far have employed discontinuous Galerkin84 and locally-conservative Galerkin formulations.68,97 With a nonlinear flow model, these methods may require an explicit time integration scheme to retain efficient segment decoupling. Additionally, if an inviscid flow is assumed, it is possible to decouple the mass and momentum equations into scalar equations by re-expressing them in terms of characteristic variables.32

## Poroelastic Modelling of Perfusion

In terms of both structure and function, it may be argued that the microvascular compartment is the most fundamental component of the coronary circulation. It is the site of major resistance (~70% with normal vasomotor tone20) and regulation of flow52 that is largely responsible for the coronary reserve which allows 4 to 5-fold increase in maximal flow rate during exercise. It is well-established that disease outcome correlates better with functional indicators (assessed by regional perfusion efficacy) than anatomical indices.98 The loss of vasodilatory capacity of the microcirculation (microvascular dysfunction) itself has been identified as a strong predictor of disease outcome and has emerged as a new therapeutic target.13,64 But while these factors strongly suggest that the coronary microcirculation deserves closer attention, modelling literature has been limited to date.

To model the spatiotemporal flow features in microcirculation with the approaches presented so far would be difficult; the acquisition of large and complex microvascular anatomy is onerous and would make the model computationally intractable. These difficulties motivate the application of a poroelastic modelling approach,23 which can capture the essential features of heterogeneous and anisotropic flow patterns without having to model the individual vessels. Furthermore, the approach naturally provides a framework to incorporate solid–fluid interactions i.e., direct and indirect crosstalk mechanisms at the microscale. The key idea underlying poroelasticity is in its treatment of mixtures which replaces the complex fluid–structure interaction with a superposition of both fluid and solid components. Using this framework a model description is obtained in terms of each homogenised component that now occupies a fraction of the volume in every point of the material. This can be achieved through a formal averaging process,112 which enables simpler geometrical descriptions and aggregates the microscopic interactions. Since its original development in soil mechanics,3,4 the poroelastic modelling approach has found its way into various applications in soft tissue mechanics. On the contrary, since the pioneering whole-heart poroelastic models of Huyghe *et al.*
42,47 only a limited number of studies have been proposed in the cardiac literature.

### Multicompartment Formulation

As mentioned above, in poroelasticity the microscopic variations of pressure and flow are averaged over a number of nearby pores. For a vascular system however this approach is inadequate since it would average together the pressures in the arterioles, capillaries and venules (typically in close proximity) meaning they would be impossible to distinguish. In order to address this issue an extended formulation has been proposed,43–46 using a “hierarchic parameter” which reflected the hierarchical position of the vessel segment with a normalised scale between zero and one. A prescribed interval of this parameter would then define a particular vascular compartment. Carrying this formalism through the derivation, the new set of fluid equations obtained additional coupling terms between the inter- and intra-compartmental flows. These new terms allowed the inter-compartmental pressure gradient to drive the intra-compartmental flows, and conversely intra-compartmental pressure gradient to drive the inter-compartmental flows.

Using the above formulation, Vankan *et al.*
103 conducted a numerical comparison between a finite element perfusion model and an explicit network flow solution obtained using the Poiseuille equation in a computer-generated vascular bed. Two alternative definitions for the hierarchic parameter were used, based on the vessel diameter or the pressure calculated from the solution of network flow. While qualitative agreements were found between the network and FEM model with either choice of the hierarchic parameter, the diameter-based compartmentalization resulted in a poor quantitative comparison. The requirement that vascular pressures must be known *a priori*, and the high sensitivity of the solution to this parameter present some practical difficulties. In a more recent multi-compartmental porous flow model22 a simpler formulation based on a double-porosity model23 was used. This model has the advantage of computational efficiency due to the collapsing of the hierarchical dimension to a few discrete lumped compartments, at the cost of providing a less general description. Despite this, a good agreement of spatial and compartmental pressure distribution was found between the network model and the continuum finite element model, applied in a pig left ventricular perfusion sub-region. Currently, the investigation to characterize the sensitivity and robustness of the approach is continuing.

### Calculation of Permeability

In porous perfusion models, the relationship between flow and pressure is usually expressed using the Darcy equation, which defines a linear proportionality between flow and pressure gradient. The proportionality constant (or function) is the permeability of the porous medium which is inversely proportional to the fluid viscosity. It is a tensorial quantity which is anisotropic for a typical vascular network, reflecting the material’s preferred directions of flow. A method to derive the multi-compartment permeability tensors from a set of circular, curved cylinders in arbitrary orientations was presented previously, along with their transformation under finite strain of the porous skeleton.46 It was assumed that fluid volume increase was distributed equally over the whole cylinder irrespective of its orientation. Additionally, as the hierarchical porous flow framework was used in its derivation, the permeability was a four-dimensional quantity that included off-diagonal terms to couple the intra- and inter-compartmental pressure gradients and flow. In comparison, an alternative approach was outlined,22 whereby multi-compartment permeabilities were calculated using a technique based on principal component analysis of straight cylinder networks. This method has useful properties such as guaranteed symmetry and positive definiteness, required for physical flow solutions, and also provides ease of extension, e.g., to diameter-dependent viscosity. Further extensions should elucidate the dependency on the averaging volume and shape, provide a validation of the multi-compartment flow and characterize the transformation of permeability under direct and indirect crosstalk with surrounding myocytes.

### Constitutive Behaviors

In the standard theory of hyperelasticity, the stress–strain relationship of the solid can be derived from a strain energy function. In a similar manner, thermodynamic analysis of poroelastic media leads to a free energy function from which state laws of solid (stress–strain) and fluid (mass-porosity) can be derived.23 Together, the equations describe the interaction between the solid and fluid phases. Chapelle *et al.*,19 developed a large strain poroelastic constitutive law to model cardiac perfusion, and presented a procedure to manage the singularity arising in the case where both solid and fluid phases are incompressible. Coupling this with an active stress generation model, an empty beating left ventricle was simulated that showed the effects of systolic flow impediment. In Cookson *et al.*,22 a large strain law was applied to simulate the stiffening behavior of the cardiac tissue with increased blood content. As the incompressibilities of solid and fluid phases were dealt with by using a Lagrange multiplier solution scheme, no specific procedure to address the singularity was required. Both of these constitutive laws are isotropic and empirical—currently a constitutive law which captures the fiber-sheet structure of the cardiac tissue62 and its inter-relationship with the embedded vasculature is not available. To develop a finite strain poroelastic law based on the cardiac microstructure, that is thermodynamically consistent, remains a major challenge for future applications of the porous modelling approach.

## Three-Dimensional and Multiscale Models of Coronary Flow

Although mechanical crosstalk and perfusion have comprised the central theme of this review so far, there are important reasons to examine the detailed local flow features in larger vessels of the coronary network. After all, atherosclerotic plaques are found most commonly in the proximal vessels, and localised to major bifurcations and inner walls of curved segments. The correlation between low and oscillatory wall shear stress (WSS) and atherosclerosis16 has been the subject of intense research. As the shear stress distribution is highly sensitive to individual vessel geometry, detailed CFD approaches have been employed to characterize WSS distribution and reveal potential sites and determinants of vulnerability. The state of the art in large multiscale image-based modelling of arterial networks has been detailed in recent reviews.36,96 Although most of these applications were in non-coronary vessels, the tools and techniques applied therein are directly relevant to the coronary circulation. On the other hand, the dynamic motion of the myocardium and fluid–structure interaction with surrounding myocytes introduce increased computational challenges in coronary CFD models.

### Patient Specific Coronary Modelling

Unfortunately the scope of this review does not permit an in-depth description of mechanistic CFD studies in the coronary vessels, however, an increasing number of work in recent years have employed CFD to examine patient-specific flow characteristics in coronary arteries. Biplane-cineangiography has been commonly used to reconstruct 3D coronary geometries, and can be acquired during a routine catheterization procedure with no additional equipment or training. Coronary CFD has been combined with a surface area based categorization of WSS (akin to the ideas expressed previously33,91) and statistical analysis in a small set of patients to discriminate between healthy, obstructive or aneurysmatic coronary artery disease with high accuracy.107,108 Also, a completely non-invasive subject-specific imaging-based CFD study was recently performed.99 The vessel geometry, dynamic motion and proximal velocity waveforms were all acquired using custom designed MR protocols. CFD based on an arbitrary Lagrangian–Eulerian formulation yielded consistent results with previous literature which demonstrated the potential of MRI in patient specific coronary CFD modelling. Unfortunately however, the study was severely limited by its long image acquisition time (7 scanning sessions in total), inordinate even for routine research work. Although MRI-based coronary CFD remains a feasibility-only study for now, new advances in MR coronary imaging could be expected to broaden its scope in future.21

### Integrated Multiscale Modelling

Owing to the enormous computational demands of the 3D CFD models, the brute force simulation of a complete coronary circulation is currently intractable, and will remain so in foreseeable future. A recent study which compared 3D and 1D simulations of 50 intracranial arteries37 reported a 24 h running time on 256 cores per cardiac cycle for the full model. In comparison the 1D counterpart required only 20 min per eight cardiac cycles on a single-core desktop, which is a ratio of approximately 150,000. There are also questions as to whether a model that includes all individual vessels of the microcirculation can be correctly parameterised, and whether experimental and modelling assumptions made at various stages will begin to dominate the outcome. A solution to the tractability problem was first proposed soon after image-based blood flow modelling began. It involved the use of a heterogeneous set of 3D, 1D and lumped parameter models that were coupled as a means to tackle the hierarchical vascular flow.32 This idea has been applied in many subsequent studies,8,57,67,100,101 including those which included 3D coronary vessel flow as part of a closed-circuit whole body circulation.50 The mathematics of coupling the multidimensional models (e.g., parabolic-hyperbolic PDEs in the case of 3D-1D coupling or PDE-ODE for 3D-0D coupling) is non-trivial, as incompatible models at the interface may introduce discontinuities in the solution variables. Additional assumptions must also be made to address the degeneracy between the full 3D field and averaged quantities of the reduced-order model at the interface. The well-posedness of the 3D-0D coupling has been previously analyzed,80 while numerous approaches for the 3D-1D problem have been proposed, beginning with the iterative coupling strategy of Formaggia *et al.*
30,31 This work was followed by an implicit coupling strategy, in which the downstream impedances were taken into account through a Dirichlet-to-Neumann mapping105 that provided more stable convergence behavior at the cost of modifications to the governing equations. A further generalization was made in an extended variational formulation,6 which was applied in subsequent numerical simulation studies.7,8

## Wave Intensity Analysis and Real-Time Clinical Application

While multiscale models of coronary flow have yet to make a significant impact in the clinical environments, recent achievements exploiting the wave intensity analysis (WIA) techniques serve as an exemplar and an elegant demonstration of application of modelling in real-time clinical diagnosis. Although WIA shares common theoretical foundations with the1D fluid models, its philosophy can be contrasted with the multiscale approaches presented so far, as it is applied to analyze waveforms acquired in a point-wise manner in practice. The applications of WIA in coronary circulation and its role in clinical developments are briefly described below.

### Wave Intensity Analysis

Wave intensity analysis is a time-domain analysis technique which is applied to arterial pressure and velocity waveforms. Pioneered close to 25 years ago by Parker *et al.*,73,74 the theoretical background of WIA and an overview of its subsequent applications can also be found in recent reviews.41,72 The application of WIA in the coronary circulation has a relatively recent history, but has yielded substantial new understandings. By building upon theoretical foundations of method of characteristics, WIA has provided a series of insights relating the pressure and velocity waveforms to the propagation speed and intensity, and allowed a separation of forward and backward traveling waves.72 By separating the forward and backward wave components, Sun *et al*.93 demonstrated that epicardial flow can be interpreted in terms of the interplay between upstream (aortic, forward-traveling) and downstream (microvascular, backward-traveling) sources of wave origination. Various cardiac events such as opening/closing of the aortic valve or the onset of systole/diastole would generate a propagating pulse wave which increases or decreases the arterial pressure and velocity. This concept has been extended to an animal study to draw a quantitative relationship between backward compression wave intensity and systolic impediment.94 A later study offered a more comprehensive description, characterising the human coronary circulation with six predominating waves.24 It also found that 94% of the forward acceleration was due to two waves generated by LV ejection (forward) and microvascular de-compression (traveling backwards toward aortic sinus). Interestingly, the latter ‘backward-traveling suction wave’ was found to be responsible for a much larger portion of the anterograde flow acceleration.

### Fractional Flow Reserve and Instantaneous Wave-Free Ratio

Fractional flow reserve (FFR) is a clinical index acquired during a catherization procedure that estimates the functional severity of a coronary stenosis. It is a strong indicator of ischemia, and was developed to overcome the poor diagnostic values of purely anatomical measures in assessing the functional consequences of stenoses, particularly those with intermediate severity.5,26 It is defined as the ratio of maximal blood flow in a diseased artery to maximal flow if that same artery was to be normal.76 One of the assumptions critical to FFR is the invariant resistance of the microvascular bed supplied by the artery, between healthy and diseased states. To ensure this condition, vasodilating agents such as adenosine are administered during catheterization. Although its theoretical foundation is dependent on a number of idealised assumptions, a substantial body of clinical evidence has validated its value in guiding whether a coronary intervention should be carried out for improved patient outcomes.98 Despite this, the clinical adoption rate had been poor, owing mainly to the need for adenosine-induced hyperemia, which increases the procedure time and cost.

The instantaneous wave-free ratio (iFR) has recently been proposed as an alternative stenosis severity index which requires no pharmacological administration. iFR is defined as the instantaneous ratio of translesional pressures, acquired during a specific period of diastole, named the wave-free period. A recently completed pilot clinical study82 provided evidence that during the wave-free period, microvascular resistance is similar to that achieved using pharmacological means. iFR acquired during this period was found to be strongly correlated with FFR, exhibiting high positive and negative predictive values and reproducibility. WIA has also contributed to the usage of iFR in practice in ancillary ways, though the development of a new wave velocity estimation method. In applying WIA in a vessel, an estimate of the wave velocity is required. In a vessel as short as the coronary segment, the traditional two-point foot-to-foot measurement method can be difficult to apply in a reliable manner. The development of a one-point wave speed measurement technique,25 which uses the recently developed dual pressure–velocity sensor guidewire,86 was instrumental in addressing this issue.

## Conclusions and Future Outlook

Building upon the concepts of coronary-cardiac interaction established by earlier studies, the one-dimensional flow modelling has reinforced the importance of wave propagation phenomena and contributed a number of additional insights into the factors governing coronary flow. Further efforts are continuing in detailed CFD and multiscale models, which gained recent momentum, to produce models that are both subject-specific and predictive. However, it must be stated again that even though the techniques reviewed here set the stage for multiscale flow modelling, coronary flow cannot be studied in isolation to the rest of cardiac function. Specifically, the studies of mechanical crosstalk will require regional and quantitative descriptions of myocardial stresses, which currently is attainable only through a model simulation. Thus an integrated cardiac model including myocardial contraction, systemic circulation, ventricular fluid–structure interaction and electromechanical coupling59 are of paramount importance to the simulation of coronary flow. The continuum description adopted by the poroelastic approach is well-suited to the existing framework of integrated cardiac modelling. Future efforts should also address the flow in coronary microcirculation as much remains unknown regarding the precise role and etiology of microcirculation in diseases. Modelling flow in the microcirculation presents a new series of challenges including autoregulatory responses,65 rheological complexities78 and structural adaptation and angiogenesis75 in addition to anatomy and crosstalk. Relevant modelling studies in the microcirculation have been outlined in a previous review.61

Regarding clinical translation, the wave intensity analysis technique has undoubtedly made profound contributions to diagnosis of coronary heart disease within a relatively short time. However it must be reminded that such progress was enabled by over two decades of prior research, and that these developments do not represent the end point; WIA is a globally aggregated approach and thus cannot be used to study regional or transmurally varying coronary phenomena. As commented previously,85 the ability of WIA in assessing myocardial perfusion has not yet been established. It would appear that the application of coronary models to clinically-oriented studies remains limited in comparison to other vascular models e.g., carotid,58,95 cerebral aneurysms17,79 and abdominal aortic aneurysms.63 While the causes for this are multifactorial, the present inability of the imaging technology to access the small intramyocardial vessels and the complex physiology of the heart are undoubtedly contributing factors. On both accounts we see forthcoming opportunities—the new advances in MRI technology is poised to attain the elusive *in vivo* non-invasive imaging of the regional perfusion assessments,35,39 while the need to understand the physiological and pathophysiological mechanisms will propel new joint efforts between modellers and experimentalists in basic science. Furthermore, we remark that in order for multiscale coronary modelling to gain clinical momentum the lessons of iFR—that a degree of crudeness in modelling can be tolerated and still achieve useful real life applications—need to be heeded, and encourage further translational applications of the modelling technology in this vein.

## References

Alastruey, J., A. W. Khir, K. S. Matthys, P. Segers, S. J. Sherwin, P. R. Verdonck, K. P. Parker, Joaquim. Pulse wave propagation in a model human arterial network: assessment of 1-D visco-elastic simulations against in vitro measurements.

*J. Biomech*. 44:2250-2258; 2011.Beyar, R., R. Caminker, D. Manor, and S. Sideman. Coronary flow patterns in normal and ischemic hearts: transmyocardial and artery to vein distribution.

*Ann. Biomed. Eng*. 21(4):435–458, 1993.Biot, M. A. Theory of elasticity and consolidation for a porous anisotropic solid.

*J. Appl. Phys.*26(2):182, 1955.Biot, M. A. Theory of finite deformations of porous solids.

*Indiana Univ. Math. J.*21(7):597–620, 1972.Bishop, A. H., and H. Samady. Fractional flow reserve: critical review of an important physiologic adjunct to angiography.

*Am. Heart J.*147:792–802, 2004.Blanco, P., R. Feijoo, and S. Urquiza. A unified variational approach for coupling 3D-1D models and its blood flow applications.

*Comput. Methods Appl. Mech. Eng.*196:4391–4410, 2007.Blanco, P. J., M. R. Pivello, S. A. Urquiza, and R. A. Feijóo. On the potentialities of 3D-1D coupled models in hemodynamics simulations.

*J. Biomech.*42:919–930, 2009.Blanco, P., S. Urquiza, and R. Feijóo. Assessing the influence of heart rate in local hemodynamics through coupled 3D-1D-0D models.

*Int. J. Numer. Methods Biomed. Eng.*26:890–903, 2010.Bovendeerd, P. H. M., P. Borsje, T. Arts, and F. N. van De Vosse. Dependence of intramyocardial pressure and coronary flow on ventricular loading and contractility: a model study.

*Ann. Biomed. Eng.*34:1833–1845, 2006.Brown, D. Input impedance and reflection coefficient in fractal-like models of asymmetrically branching compliant tubes.

*IEEE Trans. Biomed. Eng.*43(7):715–722, 1996.Bruinsma, P., T. Arts, J. Dankelman, and J. A. E. Spaan. Model of the coronary circulation based on pressure dependence of coronary resistance and compliance.

*Basic Res. Cardiol.*83:510–524, 1988.Burattini, R., P. Sipkema, G. A. van Huis, and N. Westerhof. Identification of canine coronary resistance and intramyocardial compliance on the basis of the waterfall model.

*Ann. Biomed. Eng.*13:385–404, 1985.Camici, P. G., and F. Crea. Coronary microvascular dysfunction.

*NEJM*356:830–840, 2007.Čanić, S. Blood flow through compliant vessels after endovascular repair: wall deformations induced by the discontinuous wall properties.

*Comput. Vis. Sci.*4:147–155, 2002.Canić, S., C. J. Hartley, D. Rosenstrauch, J. Tambaca, G. Guidoboni, and A. Mikelić. Blood flow in compliant arteries: an effective viscoelastic reduced model, numerics, and experimental validation.

*Ann. Biomed. Eng.*34:575–592, 2006.Caro, C., J. Fitz-Gerald, and R. Schoter. Atheroma and arterial wall shear observation, correlation and proposal of a shear dependent mass transfer mechanism for atherogenesis.

*Proc. R. Soc. B: Biol. Sci*. 177(1046):109–133, 1971.Cebral, J. R., M. A. Castro, J. E. Burgess, R. S. Pergolizzi, M. J. Sheridan, and C. M. Putman. Characterization of cerebral aneurysms for assessing risk of rupture by using patient-specific computational hemodynamics models.

*Am. J. Neurorad.*26:2550–2559, 2005.Chadwick, R. S., A. Tedgui, J. B. Michael, J. Ohayon, and B. I. Levy. Phasic regional myocardial inflow and outflow: comparison of theory and experiments.

*Am. J. Physiol*. 27:H1687–H1698, 1990.Chapelle, D., J.-F. Gerbeau, J. Sainte-Marie, and I. E. Vignon-Clementel. A poroelastic model valid in large strains with applications to perfusion in cardiac modeling.

*Comput. Mech.*46:91–101, 2009.Chilian, W. M., S. M. Layne, E. C. Klausner, C. L. Eastham, and M. L. Marcus. Redistribution of coronary microvascular resistance produced by dipyridamole.

*Am. J. Physiol.*256:H383–H390, 1989.Chiribiri, A., M. Ishida, E. Nagel, and R. M. Botnar. Coronary imaging with cardiovascular magnetic resonance: current state of the art.

*Prog. Cardiovasc. Dis.*54:240–252, 2011.Cookson, A., J. Lee, C. Michler, R. Chabiniok, E. Hyde, D. Nordsletten, M. Sinclair, M. Siebes, and N. Smith. A novel porous mechanical framework for modelling the interaction between coronary perfusion and myocardial mechanics.

*J. Biomech*. 45(5):850–855, 2012.Coussy, O. Poromechanics. Chichester: John Wiley & Sons Ltd, 2004.

Davies, J. E., Z. I. Whinnett, D. P. Francis, C. H. Manisty, J. Aguado-Sierra, K. Willson, R. A. Foale, I. S. Malik, A. D. Hughes, K. H. Parker,

*et al*. Evidence of a dominant backward-propagating “suction” wave responsible for diastolic coronary filling in humans, attenuated in left ventricular hypertrophy.*Circulation*113:1768–1778, 2006.Davies, J. E., Z. I. Whinnett, D. P. Francis, K. Willson, R. A. Foale, I. S. Malik, A. D. Hughes, K. H. Parker, J. Mayet, E. Justin,

*et al*. Use of simultaneous pressure and velocity measurements to estimate arterial wave speed at a single site in humans.*Am. J. Phys*. 59–61, 2006.De Bruyne, B., and J. Sarma. Fractional flow reserve: a review: invasive imaging.

*Heart (British Cardiac Society)*94:949–959, 2008.Doucette, J., M. Goto, A. Flynn, R. J. Austin, W. Husseini, and J. I. Hoffman. Effects of cardiac contraction and cavity pressure on myocardial blood flow.

*Am. J. Physiol.*265:H1342–H1352, 1993.Downey, J. M., and E. S. Kirk. Inhibition of coronary blood flow by a vascular waterfall mechanism.

*Circ. Res.*36:753–760, 1975.Einav, S., S. Aharoni, and M. Manoach. Exponentially tapered transmission line model of the arterial system.

*IEEE Trans. Biomed. Eng.*35(5):333–339, 1988.Formaggia, L., J. F. Gerbeau, F. Nobile, and A. Quarteroni. On the coupling of 3D and 1D Navier-Stokes equations for flow problems in compliant vessels.

*Comput. Methods Appl. Mech. Eng.*191:561–582, 2001.Formaggia, L., J. F. Gerbeau, F. Nobile, and A. Quarteroni. Numerical treatment of defective boundary conditions for the Navier-Stokes equations.

*SIAM J. Numer. Anal.*40(1):376–401, 2002.Formaggia, L., F. Nobile, A. Quarteroni, and A. Veneziani. Multiscale modelling of the circulatory system: a preliminary analysis.

*Comput. Vis. Sci.*2:75–83, 1999.Friedman, M. H., H. A. Himburg, and J. A. LaMack. Statistical hemodynamics: a tool for evaluating the effect of fluid dynamic forces on vascular biology in vivo.

*J. Biomech. Eng.*128:965–968, 2006.Garcia, D., P. G. Camici, L. G. Durand, K. Rajappan, E. Gaillard, O. E. Rimoldi, and P. Pibarot. Impairment of coronary flow reserve in aortic stenosis.

*J. Appl. Physiol.*106:113, 2009.Greenwood, J. P., N. Maredia, J. F. Younger, J. M. Brown, J. Nixon, C. C. Everett, P. Bijsterveld, J. P. Ridgway, A. Radjenovic, C. J. Dickinson,

*et al*. Cardiovascular magnetic resonance and single-photon emission computed tomography for diagnosis of coronary heart disease (CE-MARC): a prospective trial.*Lancet*379:453–460, 2011.Grinberg, L., T. Anor, J. R. Madsen, A. Yakhot, and G. E. Karniadakis. Large-scale simulation of the human arterial tree.

*Clin. Exp. Pharm. Physiol.*36:194–205, 2009.Grinberg, L., E. Cheever, T. Anor, J. R. Madsen, and G. E. Karniadakis. Modeling blood flow circulation in intracranial arterial networks: a comparative 3D/1D simulation study.

*Ann. Biomed. Eng*. 2010.Guiot, C., P. G. Piantà, C. Cancelli, and T. J. Pedley. Prediction of coronary blood flow with a numerical model based on collapsible tube dynamics.

*Am. J. Physiol.*258:H1606–H1614, 1990.Hautvast, G. L. T. F., A. Chiribiri, T. Lockie, M. Breeuwer, E. Nagel, and S. Plein. Quantitative analysis of transmural gradients in myocardial perfusion magnetic resonance images.

*Magn. Res. Med.*66(5):1477–1487, 2011.Holt, J. Flow through collapsible tubes and through in situ veins.

*IEEE Trans. Biomed. Eng.*16:274–283, 1969.Hughes, A., K. Parker, and J. Davies. Waves in arteries: a review of wave intensity analysis in the systemic and coronary circulations.

*Artery Res.*2:51–59, 2008.Huyghe, J. M., T. Arts, D. H. Van Campen, and R. S. Reneman. Porous medium finite element model of the beating left ventricle.

*Am. J. Physiol.*262(31):H1256–H1267, 1992.Huyghe, J. M., J. A. F. Oomen, and D. H. Van Campen. Low Reynolds number steady state flow through a branching network of rigid vessels: II. A finite element mixture model.

*Biorheology*26:73–84, 1989.Huyghe, J. M., J. A. F. Oomen, D. H. Van Campen, and R. M. Heethaar. Low Reynolds number steady state flow through a branching network of rigid vessels: I. A mixture theory.

*Biorheology*26(1):55–71, 1989.Huyghe, J., and D. H. van Campen. Finite deformation theory of hierarchically arranged porous solids-I. Balance of mass and momentum.

*Int. J. Eng. Sci.*33:1861–1871, 1995.Huyghe, J. M., and D. H. van Campen. Finite deformation theory of hierarchically arranged porous solids-II. Constitutive behaviour.

*Int. J. Eng. Sci.*33:1873–1886, 1995.Huyghe, J. M., D. H. van Campen, T. Arts, and R. M. Heethaar. A two-phase finite element model of the diastolic left ventricle.

*J. Biomech.*24:527–538, 1991.Karniadakis, G. E., and S. J. Sherwin. Spectral/hp Element Methods for Computational Fluid Dynamics. Oxford: Oxford University Press, 2005.

Kim, H. J., K. E. Jansen, and C. A. Taylor. Incorporating autoregulatory mechanisms of the cardiovascular system in three-dimensional finite element models of arterial blood flow.

*Ann. Biomed. Eng.*38:2314–2330, 2010.Kim, H. J., I. E. Vignon-Clementel, J. S. Coogan, C. A. Figueroa, K. E. Jansen, and C. A. Taylor. Patient-specific modeling of blood flow and pressure in human coronary arteries.

*Ann. Biomed. Eng.*38:3195–3209, 2010.Kim, H. J., I. E. Vignon-Clementel, C. A. Figueroa, J. F. LaDisa, K. E. Jansen, J. A. Feinstein, and C. A. Taylor. On coupling a lumped parameter heart model and a three-dimensional finite element aorta model.

*Ann. Biomed. Eng.*37:2153–2169, 2009.Komaru, T., H. Kanatsuka, and K. Shirato. Coronary microcirculation: physiology and pharmacology.

*Pharm. Ther.*86:217–261, 2000.Kouwenhoven, E., I. Vergroesen, Y. Han, and J. A. Spaan. Retrograde coronary flow is limited by time-varying elastance.

*Am. J. Physiol.*263:H484–H490, 1992.Krams, R., P. Sipkema, and N. Westerhof. Varying elastance concept may explain coronary systolic flow impediment.

*Am. J. Physiol.*257:H1471–H1479, 1989.Krams, R., P. Sipkema, J. Zegers, and N. Westerhof. Contractility is the main determinant of coronary systolic flow impediment.

*Am. J. Physiol.*257:H1936–H1944, 1989.Kresh, J. Y., M. A. Cobanoglu, and S. K. Brockman. The intramyocardial pressure: a parameter of heart contractility.

*J. Heart Transp.*4(2):241–246, 1985.Lagana, K., R. Balossino, F. Migliavacca, G. Pennati, E. L. Bove, M. R. D. Leval, and G. Dubini. Multiscale modeling of the cardiovascular system: application to the study of pulmonary and coronary perfusions in the univentricular circulation.

*J. Biomech.*38:1129–1141, 2005.Lee, S.-W., L. Antiga, J. D. Spence, and D. A. Steinman. Geometry of the carotid bifurcation predicts its exposure to disturbed flow.

*Stroke*39:2341–2347, 2008.Lee, J., S. Niederer, D. Nordsletten, I. Le Grice, B. Smaill, B. Smail, D. Kay, and N. Smith. Coupling contraction, excitation, ventricular and coronary blood flow across scale and physics in the heart.

*Phil. Trans. Ser. A. Math. Phys. Eng. Sci.*367:2311–2331, 2009.Lee, J., and N. Smith. Development and application of a one-dimensional blood flow model for microvascular networks.

*Proc. Inst. Mech. Eng. Part H: J. Eng. Med.*222:487–512, 2008.Lee, J., and N. P. Smith. Theoretical modeling in hemodynamics of microcirculation.

*Microcirculation*15:699–714, 2008.Legrice, I., B. Smaill, L. Z. Chai, S. G. Edgar, J. B. Gavin, and P. J. Hunter. Laminar structure of the heart: ventricular myocyte arrangement and connective tissue architecture in the dog.

*Am. J. Physiol.*269(38):H571–H582, 1995.Les, A. S., S. C. Shadden, C. A. Figueroa, J. M. Park, M. M. Tedesco, R. J. Herfkens, R. L. Dalman, and C. A. Taylor. Quantification of hemodynamics in abdominal aortic aneurysms during rest and exercise using magnetic resonance imaging and computational fluid dynamics.

*Ann. Biomed. Eng.*38:1288–1313, 2010.Leung, D. Y., and M. Leung. Non-invasive/invasive imaging: significance and assessment of coronary microvascular dysfunction.

*Heart (British Cardiac Society)*97:587–595, 2011.Liu, Y., and D. D. Gutterman. Vascular control in humans: focus on the coronary microcirculation.

*Basic Res. Cardiol.*104:211–227, 2009.Matthys, K. S., J. Alastruey, J. Peiró, A. W. Khir, P. Segers, P. R. Verdonck, K. H. Parker, and S. J. Sherwin. Pulse wave propagation in a model human arterial network: assessment of 1-D numerical simulations against in vitro measurements.

*J. Biomech.*40:3476–3486, 2007.Migliavacca, F., R. Balossino, G. Pennati, G. Dubini, T.-Y. Hsia, M. R. D. Leval, and E. L. Bove. Multiscale modelling in biofluidynamics: application to reconstructive paediatric cardiac surgery.

*J. Biomech.*39:1010–1020, 2006.Mynard, J., and P. Nithiarasu. A 1D arterial blood flow model incorporating ventricular pressure, aortic valve and regional coronary flow using the locally conservative Galerkin (LCG) method.

*Commun. Numer. Methods Eng.*24:367–417, 2008.Nash, M. P., and P. J. Hunter. Computational mechanics of the heart.

*J. Elas.*61:113–141, 2000.Olufsen, M. S. Structured tree outflow condition for blood flow in larger systemic arteries.

*Am. J. Physiol.*45:H257–H268, 1999.Pagliaro, P., D. Gattullo, R. Linden, G. Losano, and N. Westerhof. Systolic coronary flow impediment in the dog: role of ventricular pressure and contractility.

*Exp. Physiol.*83:821–831, 1998.Parker, K. H. An introduction to wave intensity analysis.

*Med. Biol. Eng. Comput.*47:175–188, 2009.Parker, K., and C. Jones. Forward and backward running waves in the arteries: analysis using the method of characteristics.

*Trans. ASME*112:322–326, 1990.Parker, K., C. Jones, J. Dawson, and D. Gibson. What stops the flow of blood from the heart?

*Heart Vessels*4:241–245, 1988.Peirce, S. M. Computational and mathematical modeling of angiogenesis.

*Microcirculation*15:739–751, 2008.Pijls, N. H., J. van Son, R. Kirkeeide, B. De Bruyne, and K. Gould. Experimental basis of determining maximum coronary, myocardial, and collateral blood flow by pressure measurements for assessing functional stenosis severity before and after percutaneous transluminal coronary angioplasty.

*Circulation*87:1354–1367, 1993.Pontrelli, G. Numerical modelling of the pressure wave propagation in the arterial flow.

*Int. J. Numer. Methods Fluids*671:651–671, 2003.Pries, A. R., and T. W. Secomb. Rheology of the microcirculation.

*Clin. Hemorheol. Microcirc.*29:143–148, 2003.Qian, Y., H. Takao, and M. Umezu. Risk analysis of unruptured aneurysms using computational fluid dynamics technology.

*Am. J. Neurorad*. 2011.Quarteroni, A., and A. Veneziani. Analysis of a geometrical multiscale model based on the coupling of ODE and PDE for blood flow simulations.

*Multiscale Model Simul.*1:173, 2003.Sabiston, D. C., and D. E. Gregg. Effect of cardiac contraction coronary blood flow.

*Circulation*15(1):14–20, 1957.Sen, S., J. Escaned, I. S. Malik, G. W. Mikhail, R. A. Foale, R. Mila, J. Tarkin, R. Petraco, C. Broyd, R. Jabbour, A. Sethi,

*et al*. Development and validation of a new adenosine-independent index of stenosis severity from coronary wave–intensity analysis.*JACC*2011.Sherwin, S. J., V. Franke, J. Peiró, and K. Parker. One-dimensional modelling of a vascular network in space-time.

*J. Eng. Math*. 47:217–250, 2003.Sherwin, S., L. Formaggia, J. Peiro, and V. Franke. Computational modelling of 1D blood flow with variable mechanical properties and its application to the simulation of wave propagation in the human arterial system.

*Int. J. Numer. Methods Fluids*2003Siebes, M., C. Kolyva, B. Verhoeff, J. J. Piek, and J. A. Spaan. Potential and limitations of wave intensity analysis in coronary arteries.

*Med. Biol. Eng. Comput.*47:233–239, 2009.Siebes, M., B. Verhoeff, M. Meuwissen, R. J. de Winter, J. A. Spaan, and J. J. Piek. Single-wire pressure and flow velocity measurement to quantify coronary stenosis hemodynamics and effects of percutaneous interventions.

*Circulation*109:756–762, 2004.Smith, N. P. A computational study of the interaction between coronary blood flow and myocardial mechanics.

*Physiol. Meas.*25:863–877, 2004.Smith, N. P., A. J. Pullan, and P. J. Hunter. An anatomically based model of transient coronary blood flow in the heart.

*SIAM J. Appl. Math.*62:990–1018, 2002.Spaan, J. A. Mechanical determinants of myocardial perfusion.

*Basic Res. Cardiol.*90:89–102, 1995.Spaan, J. A., N. P. Breuls, and J. D. Laird. Diastolic-systolic coronary flow differences are caused by intramyocardial pump action in the anesthetized dog.

*Circ. Res.*49:584–593, 1981.Stone, P. H., A. U. Coskun, S. Kinlay, M. E. Clark, M. Sonka, A. Wahle, O. J. Ilegbusi, Y. Yeghiazarians, J. J. Popma, J. Orav,

*et al*. Effect of endothelial shear stress on the progression of coronary artery disease, vascular remodeling, and in-stent restenosis in humans: in vivo 6-month follow-up study.*Circulation*108:438–444, 2003.Suga, H., K. Sagawa, and A. Shouka. Load independence of the instantaneous pressure-volume ratio of the canine left ventricle and effects of epinephrine and heart rate on the ratio.

*Circ. Res.*32:314–322, 1973.Sun, Y. H., T. J. Anderson, K. H. Parker, and J. V. Tyberg. Wave-intensity analysis: a new approach to coronary hemodynamics.

*J. Appl. Physiol.*89:1636–1644, 2000.Sun, Y. H., T. J. Anderson, K. Parker, and J. V. Tyberg. Effects of left ventricular contractility and coronary vascular resistance on coronary dynamics.

*Am. J. Physiol.*286:H1590–H1595, 2004.Tang, D., C. Yang, S. Mondal, F. Liu, G. Canton, T. S. Hatsukami, and C. Yuan. A negative correlation between human carotid atherosclerotic plaque progression and plaque wall stress: in vivo MRI-based 2D/3D FSI models.

*J. Biomech.*41:727–736, 2008.Taylor, C. A., and D. A. Steinman. Image-based modeling of blood flow and vessel wall dynamics: applications, methods and future directions: sixth international bio-fluid mechanics symposium and workshop, March 28–30, 2008 Pasadena, California.

*Ann. Biomed. Eng.*38:1188–1203, 2010.Thomas, C., P. Nithiarasu, and R. L. T. Bevan. The locally conservative Galerkin (LCG) method for solving the incompressible Navier–Stokes equations.

*Int. J. Numer. Methods Fluids*57:1771–1792, 2008.Tonino, P. A. L., W. F. Fearon, B. De Bruyne, K. G. Oldroyd, M. A. Leesar, P. N. Ver Lee, P. A. Maccarthy, M. Van’t Veer, and N. H. J. Pijls. Angiographic versus functional severity of coronary artery stenoses in the FAME study fractional flow reserve versus angiography in multivessel evaluation.

*JACC*55:2816–2821, 2010.Torii, R., J. Keegan, N. B. Wood, A. W. Dowsey, A. D. Hughes, G.-Z. Yang, D. N. Firmin, S. A. M. Thom, and X. Y. Xu. MR image-based geometric and hemodynamic investigation of the right coronary artery with dynamic vessel motion.

*Ann. Biomed. Eng.*38:2606–2620, 2010.Torii, R., M. Oshima, T. Kobayashi, K. Takagi, and T. E. Tezduyar. Computer modeling of cardiovascular fluid–structure interactions with the deforming-spatial-domain/stabilized space–time formulation.

*Comput. Methods Appl. Mech. Eng.*195:1885–1895, 2006.Urquiza, S., P. Blanco, M. Venere, and R. Feijoo. Multidimensional modelling for the carotid artery blood flow.

*Comput. Methods Appl. Mech. Eng.*195:4002–4017, 2006.van Winkle, D., A. J. Swafford, and J. M. Downey. Subendocardial coronary compression in beating dog hearts is independent of pressure in the ventricular lumen.

*Am. J. Physiol.*261:H500–H505, 1991.Vankan, J., J. M. Huyghe, D. Janssen, A. Huson, W. J. G. Hacking, and W. Schreiner. Finite element analysis of blood flow through biological tissue.

*Int. J. Eng. Sci.*35:375–385, 1997.Vignon, I., and C. Taylor. Outflow boundary conditions for one-dimensional finite element modeling of blood flow and pressure waves in arteries.

*Wave Motion*39:361–374, 2004.Vignon-clementel, I. E., C. A. Figueroa, K. E. Jansen, and C. A. Taylor. Outflow boundary conditions for three-dimensional finite element modeling of blood flow and pressure in arteries.

*Comput. Methods Appl. Mech. Eng.*195:3776–3796, 2005.Wan, J., B. Steele, S. A. Spicer, S. Strohband, G. R. Feijóo, T. J. R. Hughes, and C. A. Taylor. A one-dimensional finite element method for simulation-based medical planning for cardiovascular disease.

*Comput. Methods. Biomech. Biomed. Eng.*5:195–206, 2002.Wellnhofer, E., L. Goubergrits, U. Kertzscher, K. Affeld, and E. Fleck. Novel non-dimensional approach to comparison of wall shear stress distributions in coronary arteries of different groups of patients.

*Atherosclerosis*202:483–490, 2009.Wellnhofer, E., J. Osman, U. Kertzscher, K. Affeld, E. Fleck, and L. Goubergrits. Non-dimensional modeling in flow simulation studies of coronary arteries including side-branches: a novel diagnostic tool in coronary artery disease.

*Atherosclerosis*216:277–282, 2011.Westerhof, N., C. Boer, R. R. Lamberts, and P. Sipkema. Cross-talk between cardiac muscle and coronary vasculature.

*Physiol. Rev*. 86(4):1263–1308, 2006.Westerhof, N. Physiological hypotheses—intramyocardial pressure. A new concept, suggestions for measurement.

*Basic Res. Cardiol.*85:105–119, 1990.Westerhof, N., J. Lankhaar, and B. Westerhof. The arterial windkessel.

*Med. Biol. Eng. Comput.*47:131–141, 2009.Whitaker, S. Flow in porous media I: a theoretical derivation of Darcy’s law.

*Transp. Porous Media*1:3–25, 1986.Zinemanas, D., R. Beyar, and S. Sideman. Effects of myocardial contraction on coronary blood flow: an integrated model.

*Ann. Biomed. Eng.*22:638–652, 1994.Zinemanas, D., R. Beyar, and S. Sideman. An integrated model of LV muscle mechanics, coronary flow, and fluid and mass transport.

*Am. J. Physiol.*268:H633–H645, 1995.

## Acknowledgments

The authors would like to acknowledge support from the EPSRC under grant (EP/G007527/2) and the Centre of Excellence in Medical Engineering funded by the Wellcome Trust and EPSRC under grant number WT 088641/Z/09/Z.

### Open Access

This article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.

## Author information

### Authors and Affiliations

### Corresponding author

## Additional information

Associate Editor Michael R. King oversaw the review of this article.

## Rights and permissions

**Open Access** This article is distributed under the terms of the Creative Commons Attribution 2.0 International License (https://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

## About this article

### Cite this article

Lee, J., Smith, N.P. The Multi-Scale Modelling of Coronary Blood Flow.
*Ann Biomed Eng* **40**, 2399–2413 (2012). https://doi.org/10.1007/s10439-012-0583-7

Received:

Accepted:

Published:

Issue Date:

DOI: https://doi.org/10.1007/s10439-012-0583-7