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1.
Biomech Model Mechanobiol ; 17(2): 615-616, 2018 04.
Article in English | MEDLINE | ID: mdl-28933056

ABSTRACT

In the original publication of the article, Tables 2 and 3 were published with error. The correct tables are provided below (Tables 2, 3). The original version of the article has also been corrected.

2.
Biomech Model Mechanobiol ; 17(1): 111-131, 2018 02.
Article in English | MEDLINE | ID: mdl-28819758

ABSTRACT

Despite all technological innovations in esophageal stent design over the past 20 years, the association between the stent design's mechanical behavior and its effect on the clinical outcome has not yet been thoroughly explored. A parametric numerical model of a commercially available esophageal bioresorbable polymeric braided wire stent is set up, accounting for stent design aspects such as braiding angle, strut material, wire thickness, degradation and friction between the wires comprising a predictive tool on the device's mechanical behavior. Combining this tool with complex multilayered numerical models of the pathological in vivo stressed, actively contracting and buckling esophagus could provide clinicians and engineers with a patient-specific window into the mechanical aspects of stent-based esophageal intervention. This study integrates device and soft tissue mechanics in one computational framework to potentially aid in the understanding of the occurrence of specific symptoms and complications after stent placement.


Subject(s)
Computer Simulation , Esophagus/physiology , Stents , Biomechanical Phenomena , Calibration , Finite Element Analysis , Friction , Humans , Models, Theoretical , Numerical Analysis, Computer-Assisted , Peristalsis , Reproducibility of Results , Stress, Mechanical
3.
J Biomech ; 49(11): 2135-2142, 2016 07 26.
Article in English | MEDLINE | ID: mdl-26655592

ABSTRACT

The ApoE(-)(/)(-) mouse is a common small animal model to study atherosclerosis, an inflammatory disease of the large and medium sized arteries such as the carotid artery. It is generally accepted that the wall shear stress, induced by the blood flow, plays a key role in the onset of this disease. Wall shear stress, however, is difficult to derive from direct in vivo measurements, particularly in mice. In this study, we integrated in vivo imaging (micro-Computed Tomography-µCT and ultrasound) and fluid-structure interaction (FSI) modeling for the mouse-specific assessment of carotid hemodynamics and wall shear stress. Results were provided for 8 carotid bifurcations of 4 ApoE(-)(/)(-) mice. We demonstrated that accounting for the carotid elasticity leads to more realistic flow waveforms over the complete domain of the model due to volume buffering capacity in systole. The 8 simulated cases showed fairly consistent spatial distribution maps of time-averaged wall shear stress (TAWSS) and relative residence time (RRT). Zones with reduced TAWSS and elevated RRT, potential indicators of atherosclerosis-prone regions, were located mainly at the outer sinus of the external carotid artery. In contrast to human carotid hemodynamics, no flow recirculation could be observed in the carotid bifurcation region.


Subject(s)
Models, Cardiovascular , Shear Strength , Stress, Mechanical , Animals , Apolipoproteins E/deficiency , Atherosclerosis/physiopathology , Carotid Artery, External/diagnostic imaging , Carotid Artery, External/physiology , Carotid Artery, Internal/diagnostic imaging , Carotid Artery, Internal/physiology , Computer Simulation , Elasticity , Female , Hemodynamics , Mice , X-Ray Microtomography
4.
Ann Biomed Eng ; 44(2): 382-90, 2016 Feb.
Article in English | MEDLINE | ID: mdl-26703421

ABSTRACT

Bioresorbable stents represent an emerging technological development within the field of cardiovascular angioplasty. Their temporary presence avoids long-term side effects of non-degradable stents such as in-stent restenosis, late stent thrombosis and fatigue induced strut fracture. Several numerical modelling strategies have been proposed to evaluate the transitional mechanical characteristics of biodegradable stents using a continuum damage framework. However, these methods rely on an explicit finite-element integration scheme which, in combination with the quasi-static nature of many simulations involving stents and the small element size needed to model corrosion mechanisms, results in a high computational cost. To reduce the simulation times and to expand the general applicability of these degradation models, this paper investigates an implicit finite element solution method to model degradation of biodegradable stents.


Subject(s)
Computer Simulation , Models, Theoretical , Stents , Corrosion , Finite Element Analysis , Humans
5.
Comput Biol Med ; 66: 39-46, 2015 Nov 01.
Article in English | MEDLINE | ID: mdl-26378501

ABSTRACT

Among the many factors influencing the effectiveness of cardiovascular stents, tissue prolapse indicates the potential of a stent to cause restenosis. The deflection of the arterial wall between the struts of the stent and the tissue is known as a prolapse or draping. The prolapse is associated with injury and damage to the vessel wall due to the high stresses generated around the stent when it expands. The current study investigates the impact of stenosis severity and plaque morphology on prolapse in stented coronary arteries. A finite element method is applied for the stent, plaque, and artery set to quantify the tissue prolapse and the corresponding stresses in stenosed coronary arteries. The variable size of atherosclerotic plaques is considered. A plaque is modelled as a multi-layered medium with different thicknesses attached to the single layer of an arterial wall. The results reveal that the tissue prolapse is influenced by the degree of stenosis severity and the thickness of the plaque layers. Stresses are observed to be significantly different between the plaque layers and the arterial wall tissue. Higher stresses are concentrated in fibrosis layer of the plaque (the harder core), while lower stresses are observed in necrotic core (the softer core) and the arterial wall layer. Moreover, the morphology of the plaque regulates the magnitude and distribution of the stress. The fibrous cap between the necrotic core and the endothelium constitutes the most influential layer to alter the stresses. In addition, the thickness of the necrotic core and the stenosis severity affect the stresses. This study reveals that the morphology of atherosclerotic plaques needs to be considered a key parameter in designing coronary stents.


Subject(s)
Plaque, Atherosclerotic/pathology , Plaque, Atherosclerotic/therapy , Stents , Arteries/pathology , Atherosclerosis/pathology , Computer Simulation , Constriction, Pathologic , Coronary Restenosis , Coronary Vessels/pathology , Elasticity , Fibrosis/pathology , Finite Element Analysis , Humans , Imaging, Three-Dimensional , Models, Cardiovascular , Necrosis/pathology , Prolapse , Prosthesis Design , Stress, Mechanical
6.
J Biomech ; 48(10): 2012-8, 2015 Jul 16.
Article in English | MEDLINE | ID: mdl-25907549

ABSTRACT

Bioresorbable stents represent a promising technological development within the field of cardiovascular angioplasty because of their ability to avoid long-term side effects of conventional stents such as in-stent restenosis, late stent thrombosis and fatigue induced strut fracture. Finite element simulations have proven to present a useful research tool for the design and mechanical analysis of stents. However, biodegradable stents pose new challenges because of their transitional mechanical behaviour. For polymeric biodegradable stents, viscoplastic effects have to be accounted for. This paper presents a method to analyse the mechanical behaviour of polymeric bioresorbable stents using an implicit finite-element solver. As an example, we investigate the mechanical behaviour of a commercially available bioresorbable stent. We examine how, due to the visco-elastic properties of the stent material, the balloon deployment rate influences the mechanical integrity of the stent.


Subject(s)
Biocompatible Materials , Finite Element Analysis , Mechanical Phenomena , Polymers , Stents , Elasticity , Humans , Viscosity
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