Percutaneous coronary intervention (PCI) is the most common revascularization procedure, in which, fibrocalcific plaques are found in 17–35% of patients undergoing PCI [1]. Numbers will rise with population aging and prolonged statin treatment. Calcifications often lead to stent under expansion and strut malapposition, with increased risk of thrombosis and in-stent restenosis [2]. Presence of calcium strongly inhibits stent performance, a well-documented metric for outcome [3]. The goal of this work is to develop the finite element models for inspecting the influence of the calcium arc extent on the stenting outcomes, such as the stress and strain distribution within the plaque, and the lumen gain following stenting. Finite element method is an effective tool to reveal the mechanism of the stent expansion and its interaction with target lesion, provide guidance for optimal clinical outcomes.
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2017 Design of Medical Devices Conference
April 10–13, 2017
Minneapolis, Minnesota, USA
ISBN:
978-0-7918-4067-2
PROCEEDINGS PAPER
Target Lesion Calcium Arc Influence the Performance of Stenting
Shengmao Lin,
Shengmao Lin
University of Nebraska-Lincoln
Xiamen University of Technology
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David L. Wilson,
David L. Wilson
Case Western Reserve University
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Hiram G. Bezerra,
Hiram G. Bezerra
University Hospitals Case Medical Center
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Linxia Gu
Linxia Gu
University of Nebraska-Lincoln
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Pengfei Dong
University of Nebraska-Lincoln
Shengmao Lin
University of Nebraska-Lincoln
Xiamen University of Technology
David L. Wilson
Case Western Reserve University
Hiram G. Bezerra
University Hospitals Case Medical Center
Linxia Gu
University of Nebraska-Lincoln
Paper No:
DMD2017-3455, V001T09A008; 2 pages
Published Online:
October 31, 2017
Citation
Dong, P, Lin, S, Wilson, DL, Bezerra, HG, & Gu, L. "Target Lesion Calcium Arc Influence the Performance of Stenting." Proceedings of the 2017 Design of Medical Devices Conference. 2017 Design of Medical Devices Conference. Minneapolis, Minnesota, USA. April 10–13, 2017. V001T09A008. ASME. https://doi.org/10.1115/DMD2017-3455
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