| dc.contributor.author | Bailey, Lynn | |
| dc.contributor.author | Markham, Peter | |
| dc.contributor.author | Costa, Marco | |
| dc.contributor.author | Ware, James | |
| dc.contributor.author | O'Brien, Caroline C. | |
| dc.contributor.author | Lopes Jr, Augusto Celso de Araujo | |
| dc.contributor.author | Kolandaivelu, Kumaran | |
| dc.contributor.author | Kunio, Mie | |
| dc.contributor.author | Brown, Jonathan | |
| dc.contributor.author | Kolachalama, Vijaya Bhasker | |
| dc.contributor.author | Conway, Claire | |
| dc.contributor.author | Edelman, Elazer R | |
| dc.date.accessioned | 2017-02-17T17:28:49Z | |
| dc.date.available | 2017-02-17T17:28:49Z | |
| dc.date.issued | 2016-01 | |
| dc.date.submitted | 2015-08 | |
| dc.identifier.issn | 0090-6964 | |
| dc.identifier.issn | 1573-9686 | |
| dc.identifier.uri | http://hdl.handle.net/1721.1/106983 | |
| dc.description.abstract | Up to 80% of all endovascular stents have malapposed struts, and while some impose catastrophic events others are inconsequential. Thirteen stents were implanted in coronary arteries of seven healthy Yorkshire pigs, using specially-designed cuffed balloons inducing controlled stent malapposition and under-expansion. Optical coherence tomography (OCT) imaging confirmed that 25% of struts were malapposed (strut-wall distance <strut thickness) to variable extent (max. strut-wall distance malapposed group 0.51 ± 0.05 mm vs. apposed group 0.09 ± 0.05 mm, p = 2e−3). Imaging at follow-up revealed malapposition acutely resolved (<1% of struts remained malapposed at day 5), with strong correlation between lumen and the stent cross-sectional areas (slope = 0.86, p < 0.0001, R[superscript 2] = 0.94). OCT in three of the most significantly malapposed vessels at baseline showed high correlation of elastic lamina area and lumen area (R[superscript 2] = 0.96) suggesting all lumen loss was related to contraction of elastic lamina with negligible plaque/intimal hyperplasia growth. Simulation showed this vascular recoil could be partially explained by the non-uniform strain environment created from sub-optimal expansion of device and balloon, and the inability of stent support in the malapposed region to resist recoil. Malapposition as a result of stent under-expansion is resolved acutely in healthy normal arteries, suggesting existing animal models are limited in replicating clinically observed persistent stent malapposition. | en_US |
| dc.description.sponsorship | National Institutes of Health (U.S.) (R01 GM-49039) | en_US |
| dc.description.sponsorship | American Heart Association (FTF Award (12FTF12080241)) | en_US |
| dc.publisher | Springer US | en_US |
| dc.relation.isversionof | http://dx.doi.org/10.1007/s10439-015-1518-x | en_US |
| dc.rights | Creative Commons Attribution-Noncommercial-Share Alike | en_US |
| dc.rights.uri | http://creativecommons.org/licenses/by-nc-sa/4.0/ | en_US |
| dc.source | Springer US | en_US |
| dc.title | Vascular Response to Experimental Stent Malapposition and Under-Expansion | en_US |
| dc.type | Article | en_US |
| dc.identifier.citation | O’Brien, Caroline C., Augusto C. Lopes, Kumaran Kolandaivelu, Mie Kunio, Jonathan Brown, Vijaya B. Kolachalama, Claire Conway, et al. “Vascular Response to Experimental Stent Malapposition and Under-Expansion.” Ann Biomed Eng 44, no. 7 (January 5, 2016): 2251–2260. | en_US |
| dc.contributor.department | Massachusetts Institute of Technology. Institute for Medical Engineering & Science | en_US |
| dc.contributor.department | Harvard University--MIT Division of Health Sciences and Technology | en_US |
| dc.contributor.department | Massachusetts Institute of Technology. School of Engineering | en_US |
| dc.contributor.mitauthor | O'Brien, Caroline C. | |
| dc.contributor.mitauthor | Lopes Jr, Augusto Celso de Araujo | |
| dc.contributor.mitauthor | Kolandaivelu, Kumaran | |
| dc.contributor.mitauthor | Kunio, Mie | |
| dc.contributor.mitauthor | Brown, Jonathan | |
| dc.contributor.mitauthor | Kolachalama, Vijaya Bhasker | |
| dc.contributor.mitauthor | Conway, Claire | |
| dc.contributor.mitauthor | Edelman, Elazer R | |
| dc.relation.journal | Annals of Biomedical Engineering | en_US |
| dc.eprint.version | Author's final manuscript | en_US |
| dc.type.uri | http://purl.org/eprint/type/JournalArticle | en_US |
| eprint.status | http://purl.org/eprint/status/PeerReviewed | en_US |
| dc.date.updated | 2016-06-30T12:07:56Z | |
| dc.language.rfc3066 | en | |
| dc.rights.holder | Biomedical Engineering Society | |
| dspace.orderedauthors | O’Brien, Caroline C.; Lopes, Augusto C.; Kolandaivelu, Kumaran; Kunio, Mie; Brown, Jonathan; Kolachalama, Vijaya B.; Conway, Claire; Bailey, Lynn; Markham, Peter; Costa, Marco; Ware, James; Edelman, Elazer R. | en_US |
| dspace.embargo.terms | N | en |
| dc.identifier.orcid | https://orcid.org/0000-0002-2890-2319 | |
| dc.identifier.orcid | https://orcid.org/0000-0003-0525-4723 | |
| dc.identifier.orcid | https://orcid.org/0000-0003-4236-2280 | |
| dc.identifier.orcid | https://orcid.org/0000-0002-7832-7156 | |
| mit.license | OPEN_ACCESS_POLICY | en_US |