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Experimentally validated simulation of coronary stents considering different dogboning ratios and asymmetric stent positioning
In-stent restenosis remains a major problem of arteriosclerosis treatment by stenting. Expansion-optimized stents could reduce this problem. With numerical simulations, stent designs/ expansion behaviours can be effectively analyzed. For reasons of efficiency, simplified models of balloon-expandable...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6799901/ https://www.ncbi.nlm.nih.gov/pubmed/31626662 http://dx.doi.org/10.1371/journal.pone.0224026 |
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author | Wiesent, Lisa Schultheiß, Ulrich Schmid, Christof Schratzenstaller, Thomas Nonn, Aida |
author_facet | Wiesent, Lisa Schultheiß, Ulrich Schmid, Christof Schratzenstaller, Thomas Nonn, Aida |
author_sort | Wiesent, Lisa |
collection | PubMed |
description | In-stent restenosis remains a major problem of arteriosclerosis treatment by stenting. Expansion-optimized stents could reduce this problem. With numerical simulations, stent designs/ expansion behaviours can be effectively analyzed. For reasons of efficiency, simplified models of balloon-expandable stents are often used, but their accuracy must be challenged due to insufficient experimental validation. In this work, a realistic stent life-cycle simulation has been performed including balloon folding, stent crimping and free expansion of the balloon-stent-system. The successful simulation and validation of two stent designs with homogenous and heterogeneous stent stiffness and an asymmetrically positioned stent on the balloon catheter confirm the universal applicability of the simulation approach. Dogboning ratio, as well as the final dimensions of the folded balloon, the crimped and expanded stent, correspond well to the experimental dimensions with only slight deviations. In contrast to the detailed stent life-cycle simulation, a displacement-controlled simulation can not predict the transient stent expansion, but is suitable to reproduce the final expanded stent shape and the associated stress states. The detailed stent life-cycle simulation is thus essential for stent expansion analysis/optimization, whereas for reasons of computational efficiency, the displacement-controlled approach can be considered in the context of pure stress analysis. |
format | Online Article Text |
id | pubmed-6799901 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-67999012019-10-25 Experimentally validated simulation of coronary stents considering different dogboning ratios and asymmetric stent positioning Wiesent, Lisa Schultheiß, Ulrich Schmid, Christof Schratzenstaller, Thomas Nonn, Aida PLoS One Research Article In-stent restenosis remains a major problem of arteriosclerosis treatment by stenting. Expansion-optimized stents could reduce this problem. With numerical simulations, stent designs/ expansion behaviours can be effectively analyzed. For reasons of efficiency, simplified models of balloon-expandable stents are often used, but their accuracy must be challenged due to insufficient experimental validation. In this work, a realistic stent life-cycle simulation has been performed including balloon folding, stent crimping and free expansion of the balloon-stent-system. The successful simulation and validation of two stent designs with homogenous and heterogeneous stent stiffness and an asymmetrically positioned stent on the balloon catheter confirm the universal applicability of the simulation approach. Dogboning ratio, as well as the final dimensions of the folded balloon, the crimped and expanded stent, correspond well to the experimental dimensions with only slight deviations. In contrast to the detailed stent life-cycle simulation, a displacement-controlled simulation can not predict the transient stent expansion, but is suitable to reproduce the final expanded stent shape and the associated stress states. The detailed stent life-cycle simulation is thus essential for stent expansion analysis/optimization, whereas for reasons of computational efficiency, the displacement-controlled approach can be considered in the context of pure stress analysis. Public Library of Science 2019-10-18 /pmc/articles/PMC6799901/ /pubmed/31626662 http://dx.doi.org/10.1371/journal.pone.0224026 Text en © 2019 Wiesent et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Wiesent, Lisa Schultheiß, Ulrich Schmid, Christof Schratzenstaller, Thomas Nonn, Aida Experimentally validated simulation of coronary stents considering different dogboning ratios and asymmetric stent positioning |
title | Experimentally validated simulation of coronary stents considering different dogboning ratios and asymmetric stent positioning |
title_full | Experimentally validated simulation of coronary stents considering different dogboning ratios and asymmetric stent positioning |
title_fullStr | Experimentally validated simulation of coronary stents considering different dogboning ratios and asymmetric stent positioning |
title_full_unstemmed | Experimentally validated simulation of coronary stents considering different dogboning ratios and asymmetric stent positioning |
title_short | Experimentally validated simulation of coronary stents considering different dogboning ratios and asymmetric stent positioning |
title_sort | experimentally validated simulation of coronary stents considering different dogboning ratios and asymmetric stent positioning |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6799901/ https://www.ncbi.nlm.nih.gov/pubmed/31626662 http://dx.doi.org/10.1371/journal.pone.0224026 |
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