<?xml version="1.0" encoding="UTF-8"?><!DOCTYPE article  PUBLIC "-//NLM//DTD Journal Publishing DTD v3.0 20080202//EN" "http://dtd.nlm.nih.gov/publishing/3.0/journalpublishing3.dtd"><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" dtd-version="3.0" xml:lang="en" article-type="research article"><front><journal-meta><journal-id journal-id-type="publisher-id">JBiSE</journal-id><journal-title-group><journal-title>Journal of Biomedical Science and Engineering</journal-title></journal-title-group><issn pub-type="epub">1937-6871</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/jbise.2013.69112</article-id><article-id pub-id-type="publisher-id">JBiSE-37152</article-id><article-categories><subj-group subj-group-type="heading"><subject>Articles</subject></subj-group><subj-group subj-group-type="Discipline-v2"><subject>Biomedical&amp;Life Sciences</subject></subj-group></article-categories><title-group><article-title>
 
 
  Aortic endovascular repair modeling using the finite element method
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>hizlane</surname><given-names>Mouktadiri</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref><xref ref-type="corresp" rid="cor1"><sup>*</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Benyebka</surname><given-names>Bou-Saïd</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref><xref ref-type="corresp" rid="cor1"><sup>*</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Hélène</surname><given-names>Walter-Le-Berre</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib></contrib-group><aff id="aff1"><addr-line>Université de Lyon, CNRS INSA-Lyon, LaMCoS, UMR5259, F-69621, Lyon, France</addr-line></aff><author-notes><corresp id="cor1">* E-mail:<email>ghizlane.mouktadiri@hotmail.fr(HM)</email>;<email>benyebka.bou-said@insa-lyon.fr(BB)</email>;</corresp></author-notes><pub-date pub-type="epub"><day>29</day><month>08</month><year>2013</year></pub-date><volume>06</volume><issue>09</issue><fpage>917</fpage><lpage>927</lpage><history><date date-type="received"><day>16</day>	<month>July</month>	<year>2013</year></date><date date-type="rev-recd"><day>25</day>	<month>August</month>	<year>2013</year>	</date><date date-type="accepted"><day>12</day>	<month>September</month>	<year>2013</year></date></history><permissions><copyright-statement>&#169; Copyright  2014 by authors and Scientific Research Publishing Inc. </copyright-statement><copyright-year>2014</copyright-year><license><license-p>This work is licensed under the Creative Commons Attribution International License (CC BY). http://creativecommons.org/licenses/by/4.0/</license-p></license></permissions><abstract><p>
 
 
  Aim: The goal is to simulate different stages of the endovascular procedure in the preoperative phase. Methods: We have developed a numerical model of the endovascular treatment of abdominal aortic aneurysms (AAA) using finite element analysis (FEA), we took into account the geometry of the biological region reconstructed from scans, a local characterization of the guidewire/catheter mechanical properties, a mapping of material properties depending on the degree of calcification, a real behavior of the vascular walls, and a projection of the aorta environment. Results: Our results present the endovascular system navigation from the femoral artery to the neck of the aneurysm, predict the deformation of femoral, iliac and aortic arteries while driving flexible and stiff endovascular devices, and detect stress concentration due to tortuous and calcified artery zones. A given group of patients with very angulated and calcified arteries were validated, based on a tuning between clinical data and our endovascular simulation. Conclusion: Our model allows controlling with accuracy the delivery system rise during surgery, predicting the feasibility of the surgery with reliability as well as choose the best guide for each patient, taking into account the risk of rupture of calcified areas in the case of high angulations, and using planning simulated images with deformation of artery walls to propose stent sizing. 
     
 
</p></abstract><kwd-group><kwd>AAA; Endovascular Repair; FEA; Composite; Nonlinearity</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. INTRODUCTION</title><p>The Abdominal Aorta Aneurysm (AAA) is a cardiovascular disease that affects 6% - 7% of the Western population and its incidence increases with age [1-3]. At least 90% of AAA is affected by atherosclerosis because of high cholesterol, inflammation, infection or tobacco [<xref ref-type="bibr" rid="scirp.37152-ref4">4</xref>]. Most of these aneurysms are located near bifurcation [<xref ref-type="bibr" rid="scirp.37152-ref5">5</xref>]. The rupture of the aneurysm is a dangerous and potentially fatal accident whose incidence is increased by arterial hypertension [<xref ref-type="bibr" rid="scirp.37152-ref2">2</xref>].</p><p>For over 50 years, open surgery was the only treatment of AAA. This is a major procedure with considerable risk of cardiac complications (myocardial infarction), respiratory problems, bleeding, renal difficulties, as well as infection and colic (risk of ischemic colitis) [<xref ref-type="bibr" rid="scirp.37152-ref2">2</xref>]. However, since 1991, a new mini-invasive surgical procedure has been introduced. The endovascular procedure involves dragging a stent through a release device of the femoral artery to the level of the aneurysm.&#160;</p><p>This technique has several advantages such as shorter hospital stay, smaller incisions, and faster recovery. However, current clinical results in the long term are not significantly different when compared to conventional surgery [<xref ref-type="bibr" rid="scirp.37152-ref6">6</xref>], and have failed to show that these procedures can be performed with lower morbidity and mortality [<xref ref-type="bibr" rid="scirp.37152-ref7">7</xref>].&#160;</p><p>However, due to complications arising from their implementation, the reliability of these new methods of treatment remains a subject for discussion [<xref ref-type="bibr" rid="scirp.37152-ref8">8</xref>]. The main complications that can occur are:&#160;</p><p>• During the surgery: difficulties of navigation of the guidewire and catheter, resulting from strong tortuous form of the arteries and significant calcification of the arterial walls…, may cause stress concentration and, consequently, a risk of rupture [9-11].</p><p>• After the surgery: the phenomena of migration and endoleaks [12-16] related to poor design of the stent are not yet fully mastered [<xref ref-type="bibr" rid="scirp.37152-ref17">17</xref>]. Not taking into account the deformation of the artery under the action of the release device may be the cause of poor sizing, positioning and choice of the stent [18-20].</p><p>Numerous research scientists have attempted to understand the biomechanics of the diagnosis or clinical treatment [21-23] and to make improvements to this intervention. Let us recall that it is minimally invasive and can treat complex arterial pathologies (aneurysms, stenosis, embolisms, etc.), using an endovascular guidewire, the catheter containing the stent and a sheath. Despite major progress in this technology (new devices and techniques), anatomical factors of specific patients make handling of the catheter very difficult and require considerable technical skill. The more we are confronted with complex cases, the more ambitious the endovascular procedure becomes, and mastering of endovascular skills becomes difficult [<xref ref-type="bibr" rid="scirp.37152-ref24">24</xref>].</p><p>For this purpose, we have developed a numerical simulation tool to assist the surgery. It contributes to the improvement of therapeutic endovascular procedures in terms of accuracy and optimizes the intervention strategy.&#160;</p><p>This tool takes into account: 1) the actual biological geometry reconstructed from preoperative clinical images on a specific group of patients with a tortuous artery surface and calcification, 2) local characterization of mechanical properties of the endovascular system, 3) mapping of mechanical properties of soft tissue based on its degree of calcification (safe, calcified, thrombus), 4) projection of the real environment of the artery on the simulated model for each patient, 5) pre-stress, and 6) the material and geometric non-linearity of the composite model for the wall artery.&#160;</p><p>The main objectives of this complete modeling of the endovascular procedure are:</p><p>• Simulation of all treatment steps using patient specific data.</p><p>• Specifying control of the endovascular system navigation and stent deployment during the surgery procedure.</p><p>• Detecting the risks of perforation due to tortuous and calcified areas while transporting the more rigid endovascular devices.</p><p>• Providing augmented reality tools to surgeons for the 3D geometry of deformed artery with calcified and tortuous walls for pre-operative treatment during surgery.</p><p>• Determining deformation of the anatomical structure under the action of the deployment device (stiff guidewire and catheter with stent).</p><p>• Verifying the presence of endoleaks and migration using planning images with and without deformation after stent deployment.</p><p>• Study of the biological tissue flexibility by the navigation of various surgical tools (flexible and rigid), for better choices of guidewire and catheter.</p></sec><sec id="s2"><title>2. MATERIALS AND METHODS</title><sec id="s2_1"><title>2.1. Nano-Biomechanical Characterization of the Anatomical Structure</title><p>Numerical modeling of endovascular treatment of AAA requires knowing the biomechanical properties of arterial vessels throughout the path traveled by guidewire catheter device from the femoral to the abdominal aorta. Due to the lack of data on the mechanical properties due to the degree of calcification [<xref ref-type="bibr" rid="scirp.37152-ref25">25</xref>], we propose to perform mechanical testing of human arterial tissue that allows distinguishing calcified walls, pathological or healthy, and to integrate these mechanical characteristics according to the degree of calcification in numerical model.</p><p>Femoral, iliac and aortic samples of aged patients were tested after being stored and dissected <xref ref-type="fig" rid="fig1">Figure 1</xref>. The dissection is performed as a function of parietal quality: data scanners that contain indications as “grid level” on</p><p>the state of arterial tissue were translated in terms of mechanical properties.</p><p>For this purpose, an atomic force microscope (AFM), a tribometer and rheometer were used to characterize the mechanical behavior in compression, shearing and friction of different layers of arteries <xref ref-type="fig" rid="fig2">Figure 2</xref> as function of the degree of calcification. A large number of samples (474) were tested in a liquid environment (Phosphate buffered saline PBS pH 7.4) at room temperature.</p><p><xref ref-type="fig" rid="fig3">Figure 3</xref>(a) depicts the number of events as a function of adhesion force to verify the low bond strength hypothesis in the theory of contact. Thereafter, for each sample, we measured the indentation force as a function of depth for different speeds. Compression and decompression paths do not always overlap. This explains the effect of some visco-plastic arterial walls properties <xref ref-type="fig" rid="fig3">Figure 3</xref>(b). Only the elastic part is retained for the measurement of mechanical properties, using AFM tools, we measured the normal load as function of the indentation. However, different theories of elastic contact have been proposed to improve the description of contact between two solid bodies: Hertz [26,27] [<xref ref-type="bibr" rid="scirp.37152-ref1889">1889</xref>], Sneddon [<xref ref-type="bibr" rid="scirp.37152-ref1965">1965</xref>], Johnson, Kendall and Roberts (JKR) in [<xref ref-type="bibr" rid="scirp.37152-ref1971">1971</xref>], Derjaguin, Muller and Toporov (DMT) in [<xref ref-type="bibr" rid="scirp.37152-ref1975">1975</xref>]. The Hertz model, in a liquid medium with the assumption of weak Vander-Waals intermolecular adhesion forces (capillarity), was adapted to characterize the tip-sample contact:</p><p>Thus, the relationship Equation (1) between force F<sub>n</sub> and indentation δ for a sphere of radius R is:</p><disp-formula id="scirp.37152-formula147646"><label>(1)</label><graphic position="anchor" xlink:href="8-9101683\45110c06-a34d-47e8-841b-4e02a29bf032.jpg"  xlink:type="simple"/></disp-formula><p>For a cone of half-tip angle ϕ, we find Equation (2):</p><disp-formula id="scirp.37152-formula147647"><label>(2)</label><graphic position="anchor" xlink:href="8-9101683\c1466613-c234-41d2-97bb-a75736c5b339.jpg"  xlink:type="simple"/></disp-formula><p>E: Elastic modulus and ν: Poisson coefficient.</p><p>An example is shown below of test results on an internal and external layer of a fatty artery. We find that the outer layer is more rigid than the inner layer <xref ref-type="fig" rid="fig4">Figure 4</xref>(a), and that the viscoelastic effect at the nanoscale is negligible, because the modulus of elasticity is not strongly</p><p>affected by the indentation velocity <xref ref-type="fig" rid="fig4">Figure 4</xref>(b).</p><p>One of the test results concerns measuring tangential forces and deducing the friction coefficient depending on the degree of calcification for the internal layer of a highly calcified artery. This coefficient is the ratio between the normal force that is imposed by gravity and the tangential force that is measured. The variation of this coefficient is recorded with time. <xref ref-type="fig" rid="fig5">Figure 5</xref> represents the surface topography of the involved sample. Thus, the friction curve shows positive and negative parts, each corresponding to an alternating displacement. The friction coefficient remains stable over time. It is</p><p>about 0.5 for very calcified areas.&#160;</p><p>The assessment of tests on different human arterial samples has led to a determination of nano-mechanical properties of different layers as a function of the degree of calcification. This was done through preoperative images of the wall artery as shown in <xref ref-type="fig" rid="fig6">Figure 6</xref>. We connected each grid point to a mechanical property such as elastic modulus and friction coefficient.</p>• 2.2. Local Mechanical Characterization of the Guidewire and Catheter<p>• The guidewire In this section, our goal is to make a local characterization of the mechanical properties of the guidewire catheter device, as input to a numerical endovascular model predicting the deformation of the anatomical</p><p>structure under the action of this device.&#160;</p><p>• The folding stent: Catheter This system contains the stent; it has a 0.889 mm internal diameter, that allows its navigation in interaction with the guide. It is also composed of several areas: the tip with variable diameter, the area containing the stent, the tubular area, and the sheath. It is of variable construction (platinum-iridium, nickel, nitinol, polyester, etc.).&#160;</p><p>To create a model and to understand the mechanical behavior of the guidewire and catheter devices, tests were conducted for each region, considering the variation of mechanical properties according to various medical tools. The 3D image correlation was found to be the best tool to follow this variation.&#160;</p><p>The tests were performed on the tensile machine. A speckled black on white is applied to the tested sample. This is then subjected to uniaxial quasi-static tension and is fixed between the two jaws of the LFPlus machine, which is connected to an image acquisition system, lighting and 3D correlation <xref ref-type="fig" rid="fig7">Figure 7</xref>.</p><p>The results were obtained through a local characterization (3D correlation and extensometer) and global one. The curves in <xref ref-type="fig" rid="fig8">Figure 8</xref> show one example of mechanical tests results on the catheter tip. We measured stress versus strain to obtain value of Young’s modulus. <xref ref-type="fig" rid="fig9">Figure 9</xref> is an example of a summary of mechanical properties (elastic modulus and Poisson’s ratio) as a function of</p><p>position on the endovascular system (guidewire and catheter).</p><p>We note a very significant stiffness gradient between the tip and the stiff zone of the guide, which is added gradually in the transition area. The tips of different guides used in the clinical setting have a stiffness between 700 to 2000 MPa. The purpose is to make easier the navigation of the guidewire in vessels without pain and improve the contact between the guide head and blood vessels, while the rigid part is in the range of 11,800 to 19,000 MPa to make the artery straight.&#160;</p></sec><sec id="s2_2"><title>2.3. Finite Element Analysis Model</title><p>After creating a functional relation for the mechanical properties of biological tissues and surgical tools, a simulation is possible to predict all steps of endovascular treatment using patient specific data and the behavior of arterial walls under the action of the guidewire and the catheter system.&#160;</p><p>Creating a model of the complete system guidewire/ catheter/aortic/femoral/iliac/aneurysm/environment of the artery requires the separate modeling of its different components. The originality of this study is as follows:</p><p>Consideration of a realistic geometry of the biological system reconstructed from preoperative clinical images on a specific group of patients with high tortuosity and calcification.</p><p>Accounting for the environment of the artery, the degree of calcification, the reference geometry with preload, and the nonlinear behavior of materials and geometry.&#160;</p><p>Considering frictional contact behavior between arterial walls and the surgical tools, and between the tools themselves.&#160;</p><p>A composite model for biological tissue including fiber orientation.</p><p>The computer code used is Abaqus 6.10-1. We used Updated Lagrangian description due to large deformations. The arterial walls were modeled using thin shell theory with Kirchhoff approach. The delivery system was modeled using Timoshenko beam elements.&#160;</p><p>Considering the strong nonlinearity of the problem, the explicit time integration scheme is a relatively easy numerical scheme to implement and less expensive in terms of computation time [28,29]. Thus we adopted the method β-2, which allows the introduction of a numerical damping coefficient that removes the high frequencies [<xref ref-type="bibr" rid="scirp.37152-ref30">30</xref>]. The contact between the tools and biological tissues was managed by unilateral penalty conditions, which consist of increasing the functional of total energy by a penalty function [<xref ref-type="bibr" rid="scirp.37152-ref31">31</xref>]. This contact represents the interaction between tools and soft tissues by a spring with a stiffness depending on the penetration. Femoral, iliac, and aortic wall thickness models have been introduced, varying from 1 to 2 mm.</p><p>The models were created using preoperative individual patient data. A three-dimensional scan of the patient is performed with a contrast injection to reveal the arrangement of blood vessels located around the area of interest <xref ref-type="fig" rid="fig1">Figure 1</xref>0.&#160;</p><p>Initially, a manual step is necessary. It consists of extracting the vessel centerline, the lumen of the artery by splines, and the planes orthogonal to the neutral line depending on the degree of curvature of the artery wall.</p><p>Then a reconstruction of the aneurysm is done, including bifurcations. The iliac and tortuous femoral artery is the final geometry to be used for&#160; simulation <xref ref-type="fig" rid="fig1">Figure 1</xref>1.</p><p>This technique has the advantage of generating a geometry which is very close to the real one.&#160;</p><p>In order to overcome convergence difficulties due to the complex geometry, and problems arising from the contact between the endovascular tools and the arterial walls; only the aorta, femoral and internal iliac used for endovascular instruments navigation are included in the analysis. The external iliac and secondary vessels are taken into account using appropriate boundary conditions.&#160;</p><p>- The artery was modeled using composite materials. It is considered as a matrix material with three layers that are reinforced by two families of fibers. Therefore its mechanical properties depend on both directions of the fibers. The orientation of collagen fibers was observed by microscopy in the layers of the human aorta, on the order of 10˚ on average for the collagen fibers in the</p><p>media, and 40˚ in the adventitia have been found [<xref ref-type="bibr" rid="scirp.37152-ref32">32</xref>]. These results are in accordance with the histologic findings of a general human abdominal aortic media.</p><p>- Environmental information of the artery was taken into from the data of the scanner images. We extracted the list of the nearest points of the spline, the centerline and secondary branches of the artery. Thus, we have represented this environment by elastic supports <xref ref-type="fig" rid="fig1">Figure 1</xref>2(a).</p><p>- Information on the condition of the arterial wall was described in the numerical model. Information related to the distribution of the degree of calcification, which can differentiate healthy areas from aneurysmal and calcified regions was projected in the numerical model <xref ref-type="fig" rid="fig1">Figure 1</xref>2(b).</p><p>Environmental information of the artery was taken into</p><p>- Information on the condition of the arterial wall was described in the numerical model. Information related to the distribution of the degree of calcification, which can differentiate healthy areas from aneurysmal and calcified regions was projected in the numerical model <xref ref-type="fig" rid="fig1">Figure 1</xref>2</p><p>Healthy and aneurysmal areas were modeled as a hyper-elastic material with Mooney-Rivlin constitutive Equation (3), while calcified areas have been considered as linear elastic <xref ref-type="fig" rid="fig1">Figure 1</xref>3:</p><disp-formula id="scirp.37152-formula147648"><label>(3)</label><graphic position="anchor" xlink:href="8-9101683\401e9605-fa32-4cfc-8156-497c0f6f796e.jpg"  xlink:type="simple"/></disp-formula><p>where</p><disp-formula id="scirp.37152-formula147649"><label>(4)</label><graphic position="anchor" xlink:href="8-9101683\9070aa25-cf85-4366-911e-8492abaf9644.jpg"  xlink:type="simple"/></disp-formula><p>with W is the energy density of Mooney-Rivlin, I<sub>1</sub>, I<sub>2</sub>, I<sub>3</sub> are the strain invariants, I<sub>41</sub> and I<sub>42</sub> describe the square</p><p>stretching fibers, characterized by the directions a<sub>1</sub> and a<sub>2</sub> (anisotropy terms), a<sub>01</sub> and a<sub>10</sub> are the constants parameters of Mooney-Rivlin, [C] Cauchy Green tensor, k<sub>1</sub> and k<sub>3</sub> are material parameters, k<sub>2</sub> and k<sub>4</sub> are dimensionless parameters, generated by two families of fibers and k is the bulk modulus.</p><p>The Mooney-Rivlin anisotropy terms present the energy stored in the fibers, they are described by exponential functions.</p><p>In their normal physiological condition, the arteries are in a state of longitudinal elongation and generally subject to internal pressure. This means that the stress straint is non-zero when the vascular smooth muscle is inactive. This hypothesis was justified by several experimental studies on normal and decellularized arteries and revealed the existence of significant residual stresses within the arterial wall [33,34]. In our model, we considered the reference state of the artery corresponding to the nonzero stress state when the intravascular pressure is zero. This pre-stress was estimated from a state of unknown geometry, subjected to a positive pressure that can reproduce the real reference geometry extracted from the preoperative data.&#160; &#160;</p></sec></sec><sec id="s3"><title>3. RESULTS AND DISCUSSIONS</title><p>The finite element simulation of endovascular aortic aneurysm treatment of a selected patients group with a very strong angulation and calcification has enabled 3D visualization of the guidewire and catheter navigation from the incision area to the neck of the aneurysm. Surgical tools are initially positioned at the entrance to the femoral, in the direction of the neutral line, and then a displacement is applied to the lower base of the guide and the catheter.</p><p>Here are the results of one insertion of the guidewire and the catheter within a guide, for a given position of the endovascular tools including wall deformation at all treatment steps <xref ref-type="fig" rid="fig1">Figure 1</xref>4, movie1.</p><p>The main objective of this simulation is to control the navigation of the medical device, in order to have virtual 3D images in real time of the manipulation of the guide. The guide is interacting with the arterial walls. The catheter interacts with the entire system. Thus we obtain the stress state at each step of navigation. Therefore it is possible to locate the stress peaks, and predict the risk of rupture due to curvature and calcification of the iliac and femoral artery. <xref ref-type="fig" rid="fig1">Figure 1</xref>5 shows the stress distribution throughout the endovascular procedure. It allows the evaluation of the critical areas at the time of the ascent of the device and analyzes the maximum stress value with reference to failure models already established in the literature.</p><p>The numerical model was also used to simulate various endovascular devices most commonly used in the clinical environment. However, this simulation provides</p><p>useful information for surgeons, to determine during the preoperative phase, the difficulties they may face. Thus, it allows refining the selection of a best guide for each patient. <xref ref-type="fig" rid="fig1">Figure 1</xref>6 shows the flexibility of arterial walls under the action of different types of guide. It is observed that the behavior of blood vessels towards the flexible guide remains the same. The guide tends to warp and follow the path of the artery without distortion. As for the stiff guide, it stiffens and straightens the artery.&#160;</p><p>In order to get a biologically realistic simulation, the model has been validated by comparing the simulation results with preoperative clinical findings. Radiographs were performed to observe the final position of artery walls and deployment tools during injections of contrast. From these images, a projection of the simulation results in the same plane of the clinical images was used to compare the final geometry of the guide obtained by the simulation. The position of the guide in the preoperative phase obtained by surgeons is shown <xref ref-type="fig" rid="fig1">Figure 1</xref>7(a). The</p><p>comparison between the results of the first simulation before tuning and clinical data show a significant difference.</p><p>However, the inaccuracy is due to not taking into account the environment of the artery. This is why other simulations were performed to gradually approach clinical reality. Elastic supports with the environment of the artery have been added in the numerical model <xref ref-type="fig" rid="fig1">Figure 1</xref>7(b). Thus the final result is quite satisfactory <xref ref-type="fig" rid="fig1">Figure 1</xref>7(c), and allows us to validate our numerical model of endovascular treatment of AAA.&#160;</p><p>The validation was done on a very specific group of patients, selected with a high degree of tortuosity and calcification. Thus, the clinical results match well with the simulated results.</p></sec><sec id="s4"><title>4. CONCLUSIONS</title><p>The analysis of the results from endovascular treatment AAA using FEA for real patients-specific complicated geometry in terms of angulation and calcification demonstrates its potential impact:</p><p>• Precise control in real-time and with 3D visualization during the different stages of endovascular treatment of AAA.</p><p>• A feasibility study of endovascular surgery, and therefore an assessment of the state of stress in pre-</p><p>dicting the risk of damaging very tortuous and calcified arteries during simulation of the rise of endovascular tools.</p><p>• Assistance in the surgery, such as a better choice of surgical tools for each patient, and therefore a decrease in the number of endovascular tools used, and the radiation dose.</p><p>In addition, this model may be useful in the design of stents from the information given by the deformed state of the artery. At the current state of the technology, stent sizing using planning images without deformation does not take into account the morphological changes experienced by vessels during surgery, and therefore may bring an inaccuracy to the results. However, the present numerical model can contribute to understanding the causes of endoleaks and migration of stents and improving the outcome for many patients.</p><p>Future research should assess how this simulation can implement the present in vitro results to in vivo.</p></sec><sec id="s5"><title>5. ACKNOWLEDGEMENTS</title><p>The authors would like to thank Dr Ana Maria Sfarghiu for her help to the experimental part. 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