# Mechanical response of cardiovascular stents under vascular dynamic bending

- Jiang Xu
^{1}, - Jie Yang
^{1}Email author, - Nan Huang
^{2}, - Christopher Uhl
^{3}, - Yihua Zhou
^{4}and - Yaling Liu
^{1, 3, 4}

**Received: **15 October 2015

**Accepted: **2 February 2016

**Published: **20 February 2016

## Abstract

### Backround

Currently, the effect of vascular dynamic bending (VDB) has not been fully considered when studying cardiovascular stents’ long-term mechanical properties, as the previous studies about stent’s mechanical properties mostly focus on the effect of vascular pulsation (VP). More and more clinical reports suggested that the effect of VDB have a significant impact on stent.

### Methods

In this paper, an explicit-implicit coupling simulation method was applied to analyze the mechanical responses of cardiovascular stents considering the effect of VDB. The effect of VP on stent mechanical properties was also studied and compared to the effect of VDB.

### Results

The results showed that the dynamic bending deformation occurred in stents due to the effect of VDB. The effects of VDB and VP resulted in alternating stress states of the stent, while the VDB alternate stresses effective on the stent were almost three times larger than that of the VP. The stress concentration under VDB mainly occurred in bridge struts and the maximal stress was located in the middle loops of the stent. However, the stress distributed uniformly in the stents under the effect of VP. Stent fracture occurred more frequently as a result of VDB with the predicted fracture position located in the bridging struts of the stent. These results are consistent with the reported data in clinical literatures. The stress of the vessel under VDB was higher, than that caused by VP.

### Conclusions

The results showed that the effect of VDB has a significant impact on the stent’s stress distribution, fatigue performance and overall stress on the vessel, thus it is necessary to be considered when analyzing stent’s long-term mechanical properties. Meanwhile, the results showed that the explicit-implicit coupling simulation can be applied to analyze stent mechanical properties.

### Keywords

Cardiovascular stent Vascular dynamic bending (VDB) Vascular pulsation (VP) Stent fatigue Explicit-implicit coupling simulation method## Background

Vascular stenting, with its advantages of slight trauma and effective treatment, has been widely used in clinic [1]. The mechanical behavior of a coronary stent in the human body affects short-term and long-term therapeutic effects of vascular stenting [2, 3]. Thus, analyzing stent mechanical properties is of great importance for further improvement of stent design and effective treatment.

Currently, finite element method (FEM) is widely used to study stents’ mechanical properties. FEM studies about the stent solid mechanical properties are mainly categorized into two types: the first investigates mechanical properties of the stent during the process of free expansion without any external constraints; the other studies mechanical properties of stents surrounded by blood vessels. The first type is mainly applied to obtain the stent’s expanding pressure, axial contraction, flexibility, radial recoil rate, strain distribution in stent ends, uniformity of expansion, the “dog bone” phenomenon, fatigue of the stent and so on [4–12]. Its main purpose is to provide guidance for stent design and optimization. The second type is mainly for studying the interaction between the stent and the vessel. It aims to understand the clinical complications of stent implantation [i.e. in-stent restenosis (ISR) and stent fracture (SF)], while also providing technical support for stent surgery optimization [13–28].

Many clinical results have shown that stent fracture is one of the most important factors for serious complications (i.e. ISR) after stent implantation. Most stent fractures happened in the mid-late service time, although a few of them immediately fractured after implantation. Nakazawa et al. [29] found that stent complications occurred in 78 % of serious stent fracture cases. The statistical data from Umeda et al. [30] showed the restenosis rate increased from 3 to 15 % after stent fracture. The restenosis rate before and after stent fracture from Aoki et al. [31] was 12.4 and 37.5 % respectively. Lee et al. [32] claimed that stent restenosis was more likely to happen after stent fracture, because the fractured stent promoted neointimal or smooth muscle hyperplasia.

The fatigue of coronary artery stents is mainly caused by contractions of the heart (the systolic and diastolic function) where the main effects on the stent’s mechanical properties are the pulsation of vessels and vascular movement. Currently, the pulsation force of the vasculature has been applied to study the stent fatigue. Marrey et al. [33] investigated the development of micro cracks in stents and predicted the life of stents under the vascular pulse conditions based on fracture mechanics. Li et al. [34] analyzed the pulse pressure applied on stents by computational fluid dynamics. Making use of computational fluid dynamics, the pulsation force was calculated and then converted into a stress by the group. The stress was then used in conjunction with the S–N curve for the material in order to determine the expected lifespan of the stent in terms of cycles. Zhi et al. [35] studied the fatigue life of NiTi stents, which simplified the pulse pressure to a harmonic load on the inner surface of the stents. Others also analyzed the coronary stent’s fatigue performance, such as Weiß et al. [36] tested the coronary stent’s fatigue performance based on the stent test standard, H.A.F. Argente et al. [37] studied a balloon stent’s fatigue life based on a two-scale continuum damage mechanics model. H. M. Hsiao et al. [38, 39] studied the fatigue properties of renal artery stent in which the effect of VP and VDB was considered. Among these studies about cardiovascular stent’s mechanical performance only the effect of VP was being considered, the effect of vascular movement on stent fatigue performance has not been fully studied.

However, more and more clinical results have revealed that the movement of vascular has an important impact on stent fatigue. Lee et al. [40], Shaikh et al. [41] and Umeda et al. [30] suggested that deformations of the vasculature such as bending, tensile, shear, and torsion, which were caused by heart contractions, lead to alternating stress states in the stent. This alternating state of stress is one of the main reasons for stent fracture. Marrey et al. [33] demonstrated that during the alternation between systolic and diastolic states of the heart, the stent underwent reciprocating conditions, which included stent fatigue and stent fracture. Doi et al. [42] found that during the transition from the systolic to the diastolic state of the heart, the twist of the coronary artery was one of the major reasons for stent fatigue and fracture.

Thus, the vascular movement during the beating of the heart influences the stent mechanical properties (i.e. the fatigue and fracture). Among studies of stent mechanical properties, only the effect of vascular pulsation (VP) caused by heart contractions has been studied, without any consideration for the effect of vascular movement. So it is necessary to determine whether the motion of the artery during heart contractions, negatively impacts stent mechanical performance or not.

The movement of the coronary artery caused by heart contractions is complex, comprised of rigid motion, dynamic twists and dynamic bending. The rigid motion of the coronary artery was neglected because it only changed the position of the stents and artery without changing the stress in the stents or artery. The effect of vessel dynamic twist (VDT) was also ignored accordingly, because anatomical studies proved that coronary arteries undergo important curvature changes throughout the cardiac cycle [43].

In this study, structural FE models were implemented to simulate stent expansion in curved vessel and to investigate the effects of VDB on the long-term mechanical properties of the stent. The aim of this work was to provide a mechanical explanation for the increased risks of stent failure after being implanted in the body. Furthermore, the effect of VDB was explored for its relative importance during mechanical analysis of coronary stents and was to determine whether the motion of the artery during heart contractions, negatively impacts stent mechanical performance or not. The effect of VP on stent mechanical properties was also studied and compared to the effect of VDB.

## Methods

In order to compare the effect of VDB and VP on stent’s mechanical properties, two simulation models were built. The only differences in these two models were the boundary conditions. Details of the simulation models are described as follows.

### Stent model

Material properties of Co alloy

Young’s modulus E (GPa) | 0.2 % offset yield strength σ | Ultimate tensile strength | Fatigue endurance strength |
---|---|---|---|

243 | 547 | 1449 | 207 |

### The balloon model

The balloon had a length of 18 mm, diameter of 3 mm, and thickness of 0.05 mm when it was fully deflated. The balloon was an isotropic, linear-elastic material with a Young’s modulus of 900 MPa, a Poisson’s ratio of 0.30 and a density of 2000 kg/m^{3} [44].

The balloon was meshed using 4-node membrane elements with reduced integration and hourglass control (Abaqus element type M3D4R). The total number of elements for the balloon was 12,120 based on mesh sensitivity studies.

### Coronary model

*λ*

_{ i }are the principal stretches and

*J*is the total volume ratio.

Coefficients of the strain energy density function for each layer of the coronary artery

C | C | C | C | C | C | |
---|---|---|---|---|---|---|

Plaque | 2.38e−3 | 1.89e−1 | −3.88e−1 | 3.73 | −2.54 | 5.73e−1 |

Intima | 6.79e−03 | 5.40e−01 | −1.11 | 10.65 | −7.27 | 1.63 |

Media | 6.52e−03 | 4.89e−02 | 9.26e−03 | 0.76 | −0.43 | 8.69e−02 |

Adventitia | 8.27e−03 | 1.20e−02 | 5.20e−01 | −5.63 | 21.44 | 0.00 |

_{0}was set as 30 mm, parameter δ was 0.15, and T as 0.75 s.

### Numerical model

In this work, the simulation as two major mechanical processes: the stent expansion in a curved vessel and the stent working in the curved vessel (the stent under the effect of VDB or VP). The stent expansion process was simulated using the explicit dynamics method (Abaqus/Explicit) and the second one was simulated using the implicit method (Abaqus/Standard). A data (mainly include the stresses of stent and artery after stent implanted) transfer process was carried out between two different mechanical processes, which is referred to as a typical explicit-implicit continuous analysis method.

In order to compare the effect of vascular dynamic curvature with that of vascular pulsation, two different simulation models were carried out: Model-1 was the VDB effect simulation and Model-2 was the VP effect simulation.

The details of each step are defined below for Model-1.

#### Step1: Compressing the stent to the folded balloon and bending stent and folded balloon

This step was a pre-treatment step which include two process: compressing the stent to the folded balloon and bending stent and folded balloon to meet the initial curvature of the artery. For the compressing stent process, the balloon was constrained; two ends of the stent were constrained in the circumferential direction and a radial displacement of 0.3 mm was applied on the outer surface of the stent to compress it. After being released, the radial displacement of outer and inner stent was about 1.3 mm. For the bending stent process, the stent and balloon was free, a rigid catheter was imposed in the outer surface of stent and balloon, the bending deformation of stent and balloon is driven by the configure change of the rigid catheter set by the displacement boundary conditions. This method for bending stent and balloon had been applied to study stent’s mechanical properties by F. Auricchio et al. [48].

#### Step2: Expansion of the stent in the curved vessel and release of the pressure applied on balloon

In this step, two processes were simulated: expansion of the stent in the curved vessel followed by the release of the pressure. A load of 1.0 MPa was initially applied on the inner surface of balloon for expansion. When the stent was completely expanded under a full load of 1.0 MPa, the load was gradually decreased from 1.0 to 0 MPa. Two ends of the balloon and coronary artery were constrained in all directions and two ends of the stent were constrained in the circumferential direction.

Due to the high nonlinear compression/expansion of the balloon and stent in Step1 and Step2, a quasi-static analysis was performed using Abaqus/Explicit. In order to control the ratio of kinetic energy to the total strain energy under 5 % in each step, the simulation time was set as 5 s in Step1 and 13 s in Step2.

#### Step3: Transferring mechanical information from Abaqus/Explicit to Abaqus/Standard

When the load applied on the inner surface of balloon was released completely, the mechanical information (i.e. displacement U, stress σ) of the stent and the artery was transferred from the Abaqus/Explicit module to the Abaqus/Standard module. The residual stresses after stent expansion were being considered to analyze stent’s mechanical properties under the effect VDB or VP. The transferred information would be set as the initial conditions of Step4. In this step, the balloon was withdrawn from the simulation model. The boundary conditions of the stent and coronary artery were the same as in Step2.

#### Step4: Applying the VDB on the stent

A spatial displacement function described in section “Coronary model” was applied to the outer surface of the artery to simulate its bending. The stent was set free in all directions.

For Model-2, the boundary conditions in Step1, Step2 and Step3 were the same as those in Model-1, with the only differences occurring in Step4 of the two modules. In Step4, different values of cyclic pressure ranging from 80 mmHg (diastolic) to 120 mmHg (systolic) were applied on the inner surface of the stent to simulate the pulsation of vessels caused by the beating of the heart. The load was regarded as harmonic, with the period of the load being 0.75 s, which was equal to the cardiac cycle. It was considered to be the same as the load in the work by Zhi et al. [35]. The two ends of the artery were constrained in all directions and the stent was set free in all directions.

In this work, a surface to surface contact algorithm is selected to model the nonlinear contacts in Step1, Step2 and Step4. The coulomb friction model is used to model the frictional contacts between the balloon and stent, balloon and artery as well as the stent and artery. This contact method was used in many of the works about the interactions between stents and vessels [8, 11, 17, 19–21, 23, 25]. A value of 0.1 was selected in the whole simulation [19, 20].

### The explicit-implicit coupling method

- 1.
The deformed configure of stent and artery at the end time of stent expansion process in Explicit module was imported to the Standard module and it was set as the initial configure of the stent and artery for analyzing stent response under VDB and VP.

- 2.
The residua stresses of stent and artery (the balloon had been removed from the simulation model) after stent implanted was set as the initial stress conditions of the implicit simulation. The plastic strain of stent during the expansion process was omitted due to under the effect of VDB or VP the mechanical properties of stent were in the elastic state.

### Post-processing

Here, *σ*
_{
m
} is the effective mean stress, *σ*
_{
a
} is the effective alternate stress, *S*
_{
u
} is the ultimate stress and *S*
_{
a
} is the endurance limit for zero mean stress. Associated with the ultimate tensile strength and endurance strength of the Co alloy stent material, respectively; actual values used in the current analysis are listed in Table 2.

*σ*

_{1},

*σ*

_{2}and

*σ*

_{3}) at each node, the effective mean and alternate stresses were calculated using the following equations:

*σ*

_{1m },

*σ*

_{2m }and

*σ*

_{3m }are principal mean stresses, while the

*σ*

_{1a },

*σ*

_{2a }and

*σ*

_{3a }are principal alternate stresses. These values were used to build Goodman diagrams that are commonly used to quantify the combined effect of mean and alternating stresses on the fatigue life of a material.

## Results

### The validity of simulation results

### The deformation and stress of vessel under the effect of VDB

### The bending deformation of stent under the effect of VDB

The displacement of Point 13 and Point 7 relative to the cardiac cycle is shown in Fig. 9b. The displacement difference between Point 13 and Point 7 was caused by the dynamic curvature of the stent during the process of VDB. The maximal bending deformation of the stent occurred at half of a cardiac cycle. During the process of VDB, the stent was in a state of dynamic bending deformation. Under this dynamic bending deformation state, the stent experienced alternating stress states, which would cause the fatigue and failure of the stent.

### The stress of stent during the process of VDB

## Discussions

### The safety of the stent

In the process of VDB, the stent experienced dynamic bending deformation; the stress placed on the stent was an alternating stress. This was a main contributing factor to stent fatigue. As discussed in the introduction, the VP was another main trigger for stent fatigue which has been considered in previous studies. As a result, the effect of VP on stent fatigue performance was also studied and compared to the effect of VDB.

The maximal effective alternate stresses occurred in bridge struts as the result of both the VDB and VP. A concentration in the middle loops of the stent was observed where the bending deformation was greater than that in other positions. Also, the effective alternate stress in the bridge struts was higher than that in the main struts with regards to VDB. In terms of VP, the effective alternate stress uniformly distributed along the stent axially and the effective alternate stresses in the bridge struts was similar to that in the main struts. This occurred because the dynamic bending deformation appeared in the stent under the effect of VDB, therefore the main bearing load portion was the bridge struts. Also in terms of VP, the load was uniformly applied on the inner surface of the stent, the deformation of the stent was in the state of dynamic expansion and recoil, therefore the effective alternate stresses in the bridge struts was similar to that in the main struts.

^{8}cycles under both fatigue loading conditions. These results fitted favorably with those results reported in the literature [30, 33]. When comparing two Goodman diagrams under different loads, the effect of VDB on the stent’s FSF was lower than that caused by VP. As shown in Fig. 14, the FEM results of the VDB were closer to the Goodman curve than those of the VP.

### The impact of the stent on the vessel

During the process of stent implantation, the maximal effective mean stress of the vessel caused by the stent was 248.77 kPa. Considering VP, the maximal stress of the vessel caused by the stent was 355.35 kPa. Considering VDB, the maximal stress of the vessel caused by the stent was 497.55 kPa. The stress level of the vessel caused by the stent was higher under VDB than that under VP or during stent expansion; this suggested that more injury occurred as a result of VDB. It indicated that in the analysis model of stent’s mechanical properties, the effect of VDB caused by the beating heart should be considered.

### Discussion of the simulation method used

For the previous studies on stent mechanical properties, the implicit simulation method was used more widely in early works [4–7, 13–19]. However, only simplified models could be solved using this method because it was difficult to solve the highly nonlinear problem [8]. Since 2008, the explicit method was more and more widely used [9–12, 21–28] in most studies about stent mechanical properties. Up until now, a combination of explicit and implicit methods has never been utilized to analyze the stent mechanical properties.

In fact, the explicit method was a dynamic solution method and the results included inertial effect and kinetic energy, while the static analysis was contrary to it. If the explicit method was applied to solve static problem (the quasi static problem), it was necessary to reduce effect of the kinetic energy of system on the simulation results. A common strategy in previous studies was to increase the loading time and to achieve the purpose of reducing the kinetic energy. At the same time the simulation time also increased with the increase of loading time.

In addition, the stable increment time of the explicit method is.very small after the stent has been meshed. Based on this increment time, a long simulation time is needed. Instead, a mass scale method is used to artificially increase the stable time, however the kinetic energy of the system must also correspondingly be artificially increased. It was very important to find a balance between the kinetic energy of system and the simulation time. But for the implicit method, there was not this limitation. So using the implicit method the simulation time could be saved and the results were more reliable than that using the explicit method.

Here, a novel way to simulate a stent’s mechanical responses was provided. The stent expansion process was simulated using the explicit dynamics method (Abaqus/Explicit), due to the fact that the problem was highly nonlinear. The stent mechanical properties under the effect of VDB and VP, were simulated using the implicit method (Abaqus/Standard) to save computational time. A data transfer process was carried out between two different mechanical processes, which is referred to as a typical explicit-implicit continuous analysis method. From the simulation results, it was concluded that this method can be applied to study stent’s mechanical properties. In this work, we describe the explicit-implicit continuous analysis method in order to simulate the stent’s mechanical properties with the application of this method on other problems to be explored in the future.

## Conclusion

In this work, an explicit-implicit coupling finite element simulation was employed to investigate the coronary stent’s mechanical properties considering the effect of VDB after the stent was expanded in a curved vessel. Compared with the mechanical properties of a coronary stent with regards to VP, the following conclusion can be drawn.

Under the effect of VDB, the predicted worst case of stent fracture was mainly located in the bridge struts of the middle loops, which matches well with the results reported in the literature in which the stent fracture was confirmed by medical images. For the effect of VP on the stent, the predicted worst-case of stent fracture was also located in the bridge struts rather than in the middle loops. The result for the effect of VDB was consistent with clinical observations. The effect of VDB was a reason for the increased risk of long-term stent fracture.

Under the effect of VDB, the stent was in a bending deformation state, where the deformation of the stent under VDB was larger than that under VP, which caused a higher alternating stress level under VDB (the effective alternate stresses were 159.25 MPa under VDB vs. 59.37 under VP). The fatigue failure of the stent under VDB occurred more easily than that under VP (the fatigue safety factor of the stent was lower for the VDB than for the VP, which is mainly caused by the higher alternating stress induced by the VDB). Under VDB, the stress in the vessel was greater than that under VP. During stent expansion, it was suggested that more vascular injury occurs as a result of VDB. The effect of VDB during the beating of the heart would negatively impact stent mechanical performance. Thus, in the analysis model for the coronary stent, the mechanical performance should be considered.

Meanwhile an explicit-implicit coupling method was employed to analyze the long term stent mechanical properties. The results showed that this method is feasible and effective to study stent mechanical properties.

## Declarations

### Authors’ contributions

JX participated in the design and development of the model, performed finite element simulations and drafted the article. JY participated in the design and development of the model and drafting the article. NH performed finite element simulation, developed the simulation methods and drafted the article. CU contributed to design the simulation model and heart motion model and drafting the article. YZ performed finite element simulations and drafted the article. YL contributed to develop simulation model and drafting the article and contributed for intellectual content. All authors read and approved the final manuscript.

### Acknowledgements

This work was supported by a grant from National High-Tech Program of China (2006AA02A139), NSFC (No.11372257and1330031.) for J. Y., National Science Foundation Grant CBET-1113040, and National Institute of Health grant EB015105 for Y. L. and doctorial innovation fund of SWJTU for J. Xu.

### Competing interests

The authors declare that they have no competing interests.

**Open Access**This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

## Authors’ Affiliations

## References

- Garg S, Serruys PW. Coronary Stents: current status. J Am Coll Cardiol. 2010;56(10 Supplement):S1–42.View ArticleGoogle Scholar
- Sangiorgi G, Melzi G, Agostoni P, Cola C, Clementi F, Romitelli P, Virmani R, Colombo A. Engineering aspects of stents design and their translation into clinical practice. Ann Ist Super Sanita. 2007;43(1):89–100.Google Scholar
- Katz G, Harchandani B, Shah B. Drug-eluting stents: the past, present, and future. Curr Atheroscler Rep. 2015;17(3):485.View ArticleGoogle Scholar
- Etave F, Finet G, Boivin M, Boyer J-C, Rioufol G, Thollet G. Mechanical properties of coronary stents determined by using finite element analysis. J Biomech. 2001;34(8):1065–75.View ArticleGoogle Scholar
- Migliavacca F, Petrini L, Colombo M, Auricchio F, Pietrabissa R. Mechanical behavior of coronary stents investigated through the finite element method. J Biomech. 2002;35(6):803–11.View ArticleGoogle Scholar
- Petrini L, Migliavacca F, Auricchio F, Dubini G. Numerical investigation of the intravascular coronary stent flexibility. J Biomech. 2004;37(4):495–501.View ArticleGoogle Scholar
- Wu W, Yang DZ, Qi M, Wang WQ. An FEA method to study flexibility of expanded coronary stents. J Mater Process Technol. 2007;184(1–3):447–50.View ArticleGoogle Scholar
- De Beule M, Mortier P, Carlier SG, Verhegghe B, Van Impe R, Verdonck P. Realistic finite element-based stent design: the impact of balloon folding. J Biomech. 2008;41(2):383–9.View ArticleGoogle Scholar
- J. Yang MBL, N. Huang, Q.X. Du. Simulation of stent expansion by finite element method. In ICBBE 3rd International Conference on Bioinformatics and Biomedical Engineering. Beijing: IEEE CFP0929C-CDR, 1–4; 2009.Google Scholar
- Li N, Zhang H, Ouyang H. Shape optimization of coronary artery stent based on a parametric model. Finite Elem Anal Des. 2009;45(6–7):468–75.View ArticleGoogle Scholar
- García A, Peña E, Martínez MA. Influence of geometrical parameters on radial force during self-expanding stent deployment. Application for a variable radial stiffness stent. J Mech Behav Biomed Mater. 2012;10:166–75.View ArticleGoogle Scholar
- Azaouzi M, Makradi A, Petit J, Belouettar S, Polit O. On the numerical investigation of cardiovascular balloon-expandable stent using finite element method. Comput Mater Sci. 2013;79:326–35.View ArticleGoogle Scholar
- David Chua SN, MacDonald BJ, Hashmi MSJ. Finite element simulation of slotted tube (stent) with the presence of plaque and artery by balloon expansion. J Mater Process Technol. 2004;155–156:1772–9.View ArticleGoogle Scholar
- Lally C, Dolan F, Prendergast PJ. Cardiovascular stent design and vessel stresses: a finite element analysis. J Biomech. 2005;38(8):1574–81.View ArticleGoogle Scholar
- Liang DK, Yang DZ, Qi M, Wang WQ. Finite element analysis of the implantation of a balloon-expandable stent in a stenosed artery. Int J Cardiol. 2005;104(3):314–8.View ArticleGoogle Scholar
- Wu W, Wang W-Q, Yang D-Z, Qi M. Stent expansion in curved vessel and their interactions: a finite element analysis. J Biomech. 2007;40(11):2580–5.View ArticleGoogle Scholar
- Pericevic I, Lally C, Toner D, Kelly DJ. The influence of plaque composition on underlying arterial wall stress during stent expansion: the case for lesion-specific stents. Med Eng Phys. 2009;31(4):428–33.View ArticleGoogle Scholar
- Hyun Kim J, Jin Kang T, Yu WR. Simulation of mechanical behavior of temperature-responsive braided stents made of shape memory polyurethanes. J Biomech. 2010;43(4):632–43.View ArticleGoogle Scholar
- Schievano S, Taylor AM. Patient specific finite element analysis results in more accurate prediction of stent fractures: application to percutaneous pulmonary valve implantation. J Biomech. 2010;43(4):687–93.View ArticleGoogle Scholar
- Zahedmanesh H, John Kelly D, Lally C. Simulation of a balloon expandable stent in a realistic coronary artery—Determination of the optimum modelling strategy. J Biomech. 2010;43(11):2126–32.View ArticleGoogle Scholar
- Gu L, Zhao S, Muttyam AK, Hammel JM. The relation between the arterial stress and restenosis rate after coronary stenting. J Med Devices. 2010;4(3):031005–031005.View ArticleGoogle Scholar
- De Bock S, Iannaccone F, De Santis G, De Beule M, Van Loo D, Devos D, Vermassen F, Segers P, Verhegghe B. Virtual evaluation of stent graft deployment: a validated modeling and simulation study. J Mech Behav Biomed Mater. 2012;13:129–39.View ArticleGoogle Scholar
- Hsiao H-M, Chiu Y-H, Lee K-H, Lin C-H. Computational modeling of effects of intravascular stent design on key mechanical and hemodynamic behavior. Comput Aided Des. 2012;44(8):757–65.View ArticleGoogle Scholar
- De Bock S, Iannaccone F, De Santis G, De Beule M, Mortier P, Verhegghe B, Segers P. Our capricious vessels: the influence of stent design and vessel geometry on the mechanics of intracranial aneurysm stent deployment. J Biomech. 2012;45(8):1353–9.View ArticleGoogle Scholar
- Morlacchi S, Pennati G, Petrini L, Dubini G, Migliavacca F. Influence of plaque calcifications on coronary stent fracture: a numerical fatigue life analysis including cardiac wall movement. J Biomech. 2014;47(4):899–907.View ArticleGoogle Scholar
- Huang Y, Teng Z, Sadat U, Graves MJ, Bennett MR, Gillard JH. The influence of computational strategy on prediction of mechanical stress in carotid atherosclerotic plaques: comparison of 2D structure-only, 3D structure-only, one-way and fully coupled fluid-structure interaction analyses. J Biomech. 2014;47(6):1465–71.View ArticleGoogle Scholar
- Li J, Zheng F, Qiu X, Wan P, Tan L, Yang K. Finite element analyses for optimization design of biodegradable magnesium alloy stent. Mater Sci Eng C. 2014;42:705–14.View ArticleGoogle Scholar
- Douglas GR, Phani AS, Gagnon J. Analyses and design of expansion mechanisms of balloon expandable vascular stents. J Biomech. 2014;47(6):1438–46.View ArticleGoogle Scholar
- Nakazawa G, Finn AV, Vorpahl M, Ladich E, Kutys R, Balazs I, Kolodgie FD, Virmani R. Incidence and predictors of drug-eluting stent fracture in human coronary artery: a pathologic analysis. J Am Coll Cardiol. 2009;54(21):1924–31.View ArticleGoogle Scholar
- Umeda H, Gochi T, Iwase M, Izawa H, Shimizu T, Ishiki R, Inagaki H, Toyama J, Yokota M, Murohara T. Frequency, predictors and outcome of stent fracture after sirolimus-eluting stent implantation. Int J Cardiol. 2009;133(3):321–6.View ArticleGoogle Scholar
- Aoki J, Nakazawa G, Tanabe K, Hoye A, Yamamoto H, Nakayama T, Onuma Y, Higashikuni Y, Otsuki S, Yagishita A, et al. Incidence and clinical impact of coronary stent fracture after sirolimus-eluting stent implantation. Catheter Cardiovasc Interv. 2007;69(3):380–6.View ArticleGoogle Scholar
- Lee S-H, Park J-S, Shin D-G, Kim Y-J, Hong G-R, Kim W, Shim B-S. Frequency of stent fracture as a cause of coronary restenosis after sirolimus-eluting stent implantation. Am J Cardiol. 2007;100(4):627–30.View ArticleGoogle Scholar
- Marrey RV, Burgermeister R, Grishaber RB, Ritchie RO. Fatigue and life prediction for cobalt-chromium stents: a fracture mechanics analysis. Biomaterials. 2006;27(9):1988–2000.View ArticleGoogle Scholar
- Li H, Zhang Y, Wang X. Analysis of stent expansion, blood flow and fatigue life based on finite element method. J Med Biomech. 2012;27(2):178–85.Google Scholar
- Zhi Y, Shi X. Fatigue and fracture behavior of Nitinol cardiovascular stents. J Med Biomech. 2011;26(1):1–6.Google Scholar
- Weiß S, Szymczak H, Meißner A. Fatigue and endurance of coronary stents. Materialwiss Werkstofftech. 2009;40(1–2):61–4.View ArticleGoogle Scholar
- Argente dos Santos HAF, Auricchio F, Conti M. Fatigue life assessment of cardiovascular balloon-expandable stents: a two-scale plasticity–damage model approach. J Mech Behav Biomed Mater. 2012;15:78–92.View ArticleGoogle Scholar
- Hsiao HM, Nikanorov A, Prabhu S, Razavi MK. Respiration-induced kidney motion on cobalt-chromium stent fatigue resistance. J Biomed Mater Res B Appl Biomater. 2009;91(2):508–16.View ArticleGoogle Scholar
- Hsiao HM, Prabhu S, Nikanorov A, Razavi M. Renal artery stent bending fatigue analysis. J Med Devices. 2007;1(2):113–8.View ArticleGoogle Scholar
- Lee MS, Jurewitz D, Aragon J, Forrester J, Makkar RR, Kar S. Stent fracture associated with drug-eluting stents: clinical characteristics and implications. Catheter Cardiovasc Interv. 2007;69(3):387–94.View ArticleGoogle Scholar
- Shaikh F, Maddikunta R, Djelmami-Hani M, Solis J, Allaqaband S, Bajwa T. Stent fracture, an incidental finding or a significant marker of clinical in-stent restenosis? Catheter Cardiovasc Interv. 2008;71(5):614–8.View ArticleGoogle Scholar
- Doi H, Maehara A, Mintz GS, Tsujita K, Kubo T, Castellanos C, Liu J, Yang J, Oviedo C, Aoki J, et al. Classification and potential mechanisms of intravascular ultrasound patterns of stent fracture. Am J Cardiol. 2009;103(6):818–23.View ArticleGoogle Scholar
- Liao R, Chen SYJ, Messenger JC, Groves BM, Burchenal JEB, Carroll JD. Four-dimensional analysis of cyclic changes in coronary artery shape. Catheter Cardiovasc Interv. 2002;55(3):344–54.View ArticleGoogle Scholar
- Gervaso F, Capelli C, Petrini L, Lattanzio S, Di Virgilio L, Migliavacca F. On the effects of different strategies in modelling balloon-expandable stenting by means of finite element method. J Biomech. 2008;41(6):1206–12.View ArticleGoogle Scholar
- Weydahl ES, Moore JE. Dynamic curvature strongly affects wall shear rates in a coronary artery bifurcation model. J Biomech. 2001;34(9):1189–96.View ArticleGoogle Scholar
- Holzapfel GA, Sommer G, Gasser CT, Regitnig P. Determination of layer-specific mechanical properties of human coronary arteries with nonatherosclerotic intimal thickening and related constitutive modeling. Am J Physiol Heart Circ Physiol. 2005;289(5):H2048–58.View ArticleGoogle Scholar
- Moore JE, Weydahl ES, Santamarina A. Frequency dependence of dynamic curvature effects on flow through coronary arteries. J Biomech Eng. 2001;123(2):129–33.View ArticleGoogle Scholar
- Auricchio F, Conti M, De Beule M, De Santis G, Verhegghe B. Carotid artery stenting simulation: from patient-specific images to finite element analysis. Med Eng Phys. 2011;33(3):281–9.View ArticleGoogle Scholar
- Wang J, Li J, Tang J, Lu S, Xi T. A Long Term Accelerating Corrosion Fatigue Texting of Coronary Stents in Vitro. J Biomed Eng. 2008;25(2):398–401.Google Scholar