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Title: Computational assessment of stent durability using fatigue to fracture approach
Authors: Jovicic, Gordana
Vukicevic Arso
Filipovic, Nenad
Issue Date: 2014
Abstract: © 2014 by ASME. Stents are metal scaffold devices used to maintain lumen and restore blood flow of diseased artery. Despite they brought care of coronary diseases to a new level of efficacy, problem of stent fracture remains unclear even after global needs reached number of 5×10<sup>6</sup> devices yearly. For projected work-life of 10 years, rate of fracture occurrence in stents varies from 5% up to 25% for different designs. Analysis of such miniature devices and long-term events in realistic in vivo conditions remains impossible while experimental in vitro measurements provide limited results consuming much time and expensive equipment. The principal aim of this study was to propose procedure for numerical estimation of coronary stents durability assuming the hyperphysiological pulsatile pressure conditions. The hypothesis was whether the stent durability would be achieved safely for the projected work-life of 10 yr? The procedure was carried out within three phases: (a) initial fatigue analysis based on S-N approach; (b) fatigue lifetime assessment based on fatigue crack growth simulation using Paris power law, and (c) safe-operation, i.e., nofatigue failure (based on Kitagawa-Takahashi diagram) as well as immediate predictions of the fracture event in the stent. For considered generic stent design, results showed that the stent durability would be achieved safely. Since special diagrams were used, the fatigue risk assessment was clearer compared to the conventional fatigue lifetimes. Moreover, it was found that crack growth was stable for both small and large scale sizes of the crack. Besides the fact that the presented procedure was shown as suitable for numerical assessment of the generic stent durability under hyperphysiological pulsatile pressure conditions, it was concluded that it might be applied for any other design as well as loading conditions. Moreover, it could be efficiently combined with experimental procedures during the process of the stent design validation to reduce manufacturing and testing costs.
Type: article
DOI: 10.1115/1.4027687
ISSN: 1932-6181
SCOPUS: 2-s2.0-84922285437
Appears in Collections:Faculty of Engineering, Kragujevac

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