CHARACTERIZATION OF BLOOD FLOW AROUND A STENTED CORONARY
ARTERY
Cíntia Soares1, Adrieli T. O. Dal´Toé1, Sérgio R. Janesch1, Luismar M. Porto1
1
Chemical and Food Engineering Department, Federal University of Santa Catarina,
Florinópolis (SC), Integrated Tecnologies Laboratory (Intelab), Brazil
E-mail: {cintia, adrieli, sergio, luismar}@intelab.ufsc.br
Abstract. In the cardiovascular system, altered flow conditions, such as regions of separation and reverse flow
have a strong influence on the development of cardiovascular disease. One of the most common diseases is
atherosclerosis, which reduces the size of the lumen through a plaque formation and arterial wall thickening.
Traditional treatments were limited to “open heart” surgery until the advent of therapies based on the use of
catheters and stents. The stent is defined as an expandable mesh tube (usually of metals, especially nitinol),
which is inserted into the artery to treat narrow or weak arteries and to prevent the obstruction of the flow.
Based on these statements, local changes in the flow caused by the presence of a metallic stent were simulated
using computational fluid dynamics techniques. The values of shear stresses at the implant site were evaluated
since there is a direct relationship between restenosis (reoccurrence of the initial injury) and this characteristic
parameter of the flow. Different geometries have been defined in order to verity the effects of the stent strut
spacing on the flow patterns adjacent to the artery. The results showed that the stents generate a complex flow
pattern at the implant site. The presence of the stent also has a strong implication in the value of shear stress
near the strut. These low values are associated with a thickening in the arterial wall and are the main cause of
restenosis, which is common in about 30% of cases of stent implantation.
Key-words: Stent, Coronary artery, Shear stress, Restenosis.
1. INTRODUCTION
Coronary artery disease occurs due to the build up of plaque in the coronary arteries
which supply fresh blood to the constantly active heart muscle [Murphy and Boyle, 2006],
especially in regions of separation and reverse flow. The plaque is known as atherosclerosis, a
common disorder of the arteries, characterized by accumulation of cells, lipids, connective
tissue, calcium, and other substances inside the inner lining of the arterial wall, resulting in
the arterial wall thickening [Kious, 2008].
Atherosclerosis has the propensity to occur in arteries bifurcations involving the outer
edges of the vessel [Malek, Alper and Izumo, 1999] and is directly affected by hemodynamics
factors. In these areas, the blood flow presents low levels of wall shear stress with high levels
of oscillating amplitude, hypothesis proposed by Caro et al. [1971 apud Chaniotis et al., 2010,
p. 2], and validated by subsequent studies [Zarins et al., 1983; Asakura and Karino, 1990;
Bharadvaj, Mabon and Giddens, 1982; Motomiya and Karino, 1984].
Traditional treatments were limited to “open heart” surgery, the most invasive
procedure, until the advent of therapies based on the use of catheters and stents, considered
minimally invasive techniques. The stent is defined as an expandable mesh tube with the
priorities functions to holds the artery open, preserving the lumen cylindrical [Frank, Walsh
and Moore, 2002], and restore the blood flow, in order to suit perfusion to the cardiac tissue.
However, the interaction between stent-strut and artery cause injuries in the vessel wall,
contributing to neointimal growth, phenomenon known as restenosis [Garasic et al., 2000],
which is straight related with stent design [LaDisa et al., 2005]. Restenosis has a considerable
recurrence in patients of about 10% to 30%, requiring new revascularization procedures
[Centemero et al., 2004].
The aim of this study was to assess local changes in the flow caused by the presence
of a metallic stent making use of computational fluid dynamics (CFD) models. The values of
shear stress at the implant site were evaluated since there is a direct relationship between
restenosis and this characteristic parameter of the flow. Different geometries have been
defined in order to verity the effects of the stent strut spacing on the flow patterns adjacent to
the artery. All the studies were carried out on COMSOL Multiphysics® 4.3.
2. METHODOLOGY
A free model stent provided by the project available in Open Stent Design
[Bonsignore, 2012] was taken as model for the simulations. As an open design, with copyleft
license, modifications in drawings could be done in order to study the influence of altered
designs in the flow profile. The differences in each stent design are presented in Table 1 and
Fig. 1.
Table 1 – Differences between the stent geometries.
Variables
Stent A
Stent B
Stent C
Columns
Struts
6
12
6
18
6
24
Bridges
2
3
4
Figure 1 - Models of stents used in the numerical evaluation.
The simulations were implemented on a stented coronary artery using a 2D axisymmetric domain for the geometries presented in Fig. 1. The aim was to investigate the
effects of the stent struts on the flow pattern, considering velocity and pressure fields and
shear stress profile. To better visualize the results, a standard domain representing the artery
without the stent was add to the simulations.
Stent A
Stent B
Stent C
Standard
Figure 2 – Physical domains considered in the simulations.
The blood properties and flow parameters needed to the problem implementation in
COMSOL Multiphysics 4.3 are presented in Table 2. The artery diameter was obtained
based on studies carried out by Funabashi et al. (2003) and Dodge et al. (1992), whereas the
blood properties were taken from Frank, Walsh and Moore (2002). The maximum velocity in
the coronary artery at peak of systole was available in Chuchard et al. (2011).
Table 2 - Physical parameters used in the simulation.
Parameter
Value
Artery diameter (mm)
3.5
Blood density (kgm-3)
1,055
Viscosity (Pas)
0.0035
Maximum velocity (ms-1)
0.29179
The mathematical model used was a single-phase model, presenting a laminar flow
and steady-state condition. Blood was treated as an incompressible, homogenous and
Newtonian fluid. The transport equation involved in the model to predict the flow in the
stented coronary artery can be written as follows:
Mass conservation equation:
𝜌∇ ∙ 𝐮 = 0
(1)
Momentum conservation equation:
𝜌(𝐮 ∙ ∇)𝐮 = ∇ ∙ [−𝜌𝐈 + 𝜇(∇𝐮 + (∇𝐮)𝑇 )] + 𝐅
(2)
where ρ is the density (Kg.m-3), u is the velocity field (m.s-1), I is a 3x3 identity matrix, µ is
the dynamic viscosity (Pa.s) and F are the body forces field (N).
In this study, the vessel was considered being rigid, hence the wall and stent are not
moving due to the heart contraction. Thus, the no-slip boundary condition was specified at the
vessel wall and at the struts. The effect of the fluid-structure interaction was not taken under
consideration as the aim was to analyze the behavior of flow near the struts. The remaining
boundaries conditions were constant pressure as outlet, and a parabolic blood velocity profile
(Fig. 3) as inlet condition. As the condition of symmetry is being used, only a half of the
velocity curve is used in the inlet. The software uses a finite element analysis to solve
equations, satisfying conservation of mass and momentum.
0,3
0,25
Velocity (m/s)
0,2
0,15
0,1
0,05
0
0
0,5
1
1,5
2
Radius (mm)
2,5
3
3,5
Figure 3 - Velocity profile of blood flow in a coronary artery.
3. RESULTS AND DISCUSSION
3.1
Velocity Profile
The velocity profile, represented by Fig. 4, shows the behavior of the blood flow in the
presence of a stent. When contrasting the stented cases and the standard, a deviation of the
laminar velocity layers was noticed as the flow reaches the stent struts. It is possible to
observe that for Stent A, this disturbance was greater, being lower in Stent B and even more
in C. Another analysis that can be made in Fig. 4 is that the enlargement of the spacing
between the struts effectively reduces the disturbance experienced by the flow.
The flow patterns can be deeper investigated visualizing the flow streamlines,
presented in Fig. 5 for all cases analyzed. The flow field in the vicinity of the struts
demonstrated the presence of stagnation zones localized in the regions upstream and
downstream of the struts, where the velocity is a small fraction of the velocities found in a
distance above the struts, where their influence is not significant. This stagnation zones are
higher forward the strut and smaller afterward for all the stent cases. In other words, the
stagnation zones magnitude depends on the flow direction, which is upwards. This flow
behavior was also obtained by Berry et al. (2000).
Stent A
Stent B
Stent C
Stantard
Figure 4. Velocity profile for each stent.
Stent A
Stent B
Stent C
Figure 5. Flow streamlines for each stent.
As can be seen, the disturbance suffered by the flow is directly related with the stent
geometry. Depending on the width and height of the strut, stagnation zones appear bigger or
smaller.
3.2
Pressure
The pressure drop along the stented artery is showed in Fig. 6. The pressure drop for
the standard was obtained using the same conditions as for the stented cases. Comparing the
results, it can be seen that exists a pressure drop in stented cases.
Stent A
Stent B
Stent C
Standard
Figure 6. Pressure drop along the stented section.
Normal coronary arteries provide no resistance to blood flow. Therefore, optimum
coronary stenting should at least result a minimal pressure drop within the respective
coronary segment. Also, the presence of a persistent pressure gradient across the stented
segment indicates an abnormal blood flow pattern with heterogeneous and abnormal low
shear stress [Pijls et al., 2002].
3.3
Shear Stress
From the velocity fields, the shear stress distribution was computed. The results,
presented in Fig. 7, showed that wall shear stress (WSS) distribution was sensitive to stent
strut spacing, as obtained by Dehlaghi, Shadpoor and Najarian (2008). In all the simulations,
excepted for the standard, lower WSS values were localized between the wires, very close to
vessel wall, independent of the strut width, thickness, number, or stent-to-vessel diameter
ratio. In contrast, the highest WSS values were noticed over the surface of stent struts, as
observed by Murphy and Boyle (2006) and Sanmartín et al. (2006). The standard case
presented a higher WSS along the vessel, and thereby, it can be seen the magnitude of the
stent influence on the hemodynamic conditions in the artery.
Stent A
Stent B
Stent C
Standard
Figure 7. Shear stress distribution.
Figure 8 shows an enlargement of shear stress distribution presented on Fig. 7 in order
to enable an accurate view of this parameter near the struts. A comparison between the cases
shows that the increase in strut-strut spacing tends to smooth the variation in shear stress next
the vessel wall. In summary, the change in face structures creates changes in the shear stress
field indicating that the number, width, and thickness of stent struts cause distinctive patterns
of WSS, as obtained by Ladisa Jr et al. (2003). Hence, the difference of shear stress field is
particularly obvious between the input area of stent and the stagnation zones related to the
stent geometry [Bénard, Coisne and Perrault, 2001].
Stent A
Stent B
Figure 8. Shear stress distribution enlargement.
Stent C
As mentioned, stagnation zones appearance is directly related to the strut geometry. In
this case is not different, as the shear stress is very small near the wall. So it can be concluded
that small shear stress and stagnation zones are related, and both contribute to thrombus
accumulation by inhibiting the removal of platelets and others substances from the wall
[Berry et al., 2000]. This fact backs to the issue of restenosis that limits the efficiency of the
artery stenting in long term.
An evidence of the WSS influence in the cellular proliferation is the in vivo human
model study developed by Sanmartín et al. (2006) that found there is a negative correlation
between wall shear stress and neointimal growth. In other words, regions with lowest values
of WSS presented higher degree of cell proliferation.
The study presented demonstrated the importance of understanding the factors
involved in hemodynamic alterations occurred due to the stent presence in the artery. The
determination of the flow patterns disturbances related to a given stent is crucial to the
optimization of stent design and stent-placement protocols, as well as to limit vascular injury
and perhaps reduce restenosis [Rogers et al., 1999].
As can be seen, arteries are living organs that can adapt to and change with the
varying hemodynamic conditions. According to Glagov et al. [1988 apud Ku, 1997, p. 417]
decreased flow rates, presented in stagnation zones, as well as, lower WSS, will cause the
intimal layer to thicken to reestablish a normal wall shear stress.
4. CONCLUSION
Computational tools are useful to predict, when there is not enough data available, or
verify, when an experimental data exists, the behavior of a physical issue. In this case, the
local hemodynamic and flow pattern, changed due to the presence of stent, were qualitatively
provided by computational fluid dynamics, and the results were consistent with the studies
available in the literature.
A disturbance of normal blood flow in an artery occurs in the presence of the stent.
What determinates the magnitude and significance of this disturbance is the geometry of the
stent, since the blood properties do not change. The existence of lower shear stress near the
arterial wall was verified, which contributes to restenosis, a problem that still achieves a high
proportion of treated patients.
Thus, it is understood that such investigations are important because it is possible to
optimize the stent design in order to minimize effects on the flow, avoiding health problems
such as restenosis.
5. ACKNOWLEDGEMENTS
The authors acknowledge financial support from FAPESC (Fundação de Amparo à
Pesquisa e Inovação do Estado de Santa Catarina) and CAPES (Coordenação de
Aperfeiçoamento de Pessoal de Nível Superior).
REFERENCES
Asakura, T. and Karino, T. (1990), “Flow Patterns and Spatial Distribution of Atherosclerotic Lesions In Human
Coronary Arteries”, Circ. Res., 66, 1045–1066.
Bharadvaj, B.K., Mabon, R.F. and Giddens, D.P. (1982), “Steady Flow in a Model of the Human Carotid
Bifurcation. Part I – Flow Visualization”, J. Biomech., 15, 349–362.
Bénard, N., Coisne, D. and Perrault, R. (2001), “Experimental Study of Blood Laminar Flow Through a Stented
Artery”, Annual Reports of the Research Reactor Institute, Kyoto University, 83-85.
Berry, J. L., Santamarina, A., Moore Jr, J. E., Roychowdhury, S. and Routh, W. D. (2000), “Experimental and
Computational Flow Evaluation of Coronary Stents”, Biomedical Engineering Society, 28, 386-398.
Bonsignore, C. (2012), “Open Stent Design”. Enable at http://nitinoluniversity.com/open-stentdesign/ Access:
10 jan. 2012.
Centemero, M. P., Sousa, A. G. M. R., Tanajura, L. F., Chaves, A., Faria, C. F., Feres, F., Abizaid, A. and
Sousa, J. (2004), “Reestenose Intra-Stent: Como Diagnosticar, Quando Tratar e Qual o Prognóstico?”, Revista
Brasileira de Cardiologia Invasiva, 12, 185-192.
Chaniotis, A. K., Kaiktsis, L., Katritsis, D., Efstathopoulos, E., Pantos, I. and Marmarellis, V. (2010),
“Computational Study of Pulsatile Blood Flow in Prototype Vessel Geometries of Coronary Segments”, Phys.
Med., 26, 140-156.
Chuchard, P., Wiwatanapataphee, B., Puapansawat, T. and Siriapisith, T. (2011), “Numerical Simulation of
Blood Flow in the System of Human Coronary Arteries with Stenosis”, 4th WSEAS International Conference on
Finite Differences – Finite Elements – Finite Volumes – Boundary Elements.
Dehlaghi, V., Shadpoor, M. T. and Najarian, S. (2008), “Analysis of Wall Shear Stress in Stented Coronary
Artery Using 3D Computational, Fluid Dynamics Modeling”, Journal of Materials Processing Technology, 197,
174-181.
Dodge Jr, J. T., Brown, B. G., Bolson, E. L. and Dodge, H. T. (1992), “Lumen Diameter of Normal Human
Coronary Arteries. Influence of Age, Sex, Anatomic Variation and Left Ventricular Hypertrophy or Dilation”,
Circulation, 86, 232-246.
Frank, A. O., Walsh, P. W. and Moore, J. E. (2002), “Computational Fluid Dynamics and Stent Design”,
Artificial Organs, 26, 614-621.
Funabashi, N., Kobayashi, Y., Perlroth, M. and Rubin, G. D. (2003), “Coronary Artery: Quantitative Evaluation
of Normal Diameter Determined with Electron-beam CT Compared with Cine Coronary Angiography – Initial
Experience”, Radiology, 226, 263-271.
Garasic, J. M., Edelman, E. R., Squire, J. C., Seifert, P., Williams, M. S. and Rogers, C. (2000), “Stent and
Artery Geometry Determine Intimal Thickening Independent of Arterial Injury”, Circulation, 101, 812-818.
Kious, D. E. (2008), “Biomechanical and Computational Modeling of Atherosclerotic Arteries”, Dissertation,
Graz University of Technology, Institute for Biomechanics.
Ku, D. N. (1997), “Blood Flow in Arteries”, Annu. Rev. Fluid Mech, 29, 399-434.
Ladisa Jr, J. F., Warltiers, D. C., Guler, I., Kersten, J. R. and Pagel, P. S. (2003), “Stent Geometry and
Deployment Ratio Influence Distributions of Wall Shear Stress: Three-Dimensional Numerical Simulations
Exploiting Properties of an Implanted Stent”, Summer Bioengineering Conference, Sonesta Beach Resort in Key
Biscayne, Florida, 25-29.
Ladisa Jr, J. F., Olson, L. E., Hettrick, D. A., Warltier, D. C., Kersten, J. R. and Pagel, P. S. (2005), “Axial Stent
Strut Angel Influences Wall Shear Stress After Stent Implantation: Analysis Using 3D Computational Fluid
Dynamics Models of Stent Foreshortening”, Biomedical Engineering Online.
Malek, A. M., Alper, S. L. and Izumo, S. (1999), “Hemodynamic Shear Stress and Its Role in Atherosclerosis”,
JAMA, 282, 2035-2042.
Motomiya, M. and Karino, T. (1984), “Flow Patterns in the Human Carotid Artery Bifurcation”, Stroke, 15, 50–
56.
Murphy, J. and Boyle, F. (2006), “Application of Advanced Computational Modelling in the Numerical
Prediction of the Haemodynamic Impact of Coronary Stent Implantation”, WSEAS Transations on Computer
Research .
Pijls, N. H. J., Klauss, V., Siebert, U., Powers, E., Takazawa, K., Fearon, W. F., Escaned, J., Tsurumi, Y.,
Akasaka, T., Samady, H. and Bruyne, B. (2002), “Coronary Pressure Measurement After Stenting Predicts
Adverse Events at Follow-Up: A Multicenter Registry”, Circulation, 105, 2950-2954.
Rogers, C., Tseng, D. Y., Squire, J. C. and Edelman, E. R. (1999), “Balloon-Artery Interactions During Stent
Placement: A Finite Element Analysis Approach to Pressure, Compliance, and Stent Design as Contributors to
Vascular Injury”, Circ. Res., 84, 378-383.
Sanmartín, M., Goicolea, J., García, C., García, J., Crespo, A., Rodríguez. J. and Goicolea, J. M. (2006),
“Influence of Shear Stress on In-Stent Restenosis: In Vivo Study Using 3D Reconstruction and Computational
Fluid Dynamics”, Rev Esp Cardiol, 59, 20-27.
Zarins, C.K., Giddens, D. P., Bharadvaj, B. K., Sottinurai, V.S., Mabon, R.F. and Glagov, S. (1983), “Carotid
Bifurcation Atherosclerosis. Quantitative Correlation of Plaque Localization with Flow Velocity Profiles and
Wall Shear Stress”, Circ. Res., 53, 502-514.
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