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Echogenicity as a surrogate for bioresorbable everolimus-eluting scaffold degradation: analysis at 1-, 3-, 6-, 12- 18, 24-, 30-, 36- and 42-month follow-up in a porcine model
The objective of the study is to validate intravascular quantitative echogenicity as a surrogate for molecular weight assessment of poly-l-lactide-acid (PLLA) bioresorbable scaffold (Absorb BVS, Abbott Vascular, Santa Clara, California). We analyzed at 9 time points (from 1- to 42-month follow-up) a...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Netherlands
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4368838/ https://www.ncbi.nlm.nih.gov/pubmed/25627777 http://dx.doi.org/10.1007/s10554-015-0591-4 |
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author | Campos, Carlos M. Ishibashi, Yuki Eggermont, Jeroen Nakatani, Shimpei Cho, Yun Kyeong Dijkstra, Jouke Reiber, Johan H. C. Sheehy, Alexander Lane, Jennifer Kamberi, Marika Rapoza, Richard Perkins, Laura Garcia-Garcia, Hector M. Onuma, Yoshinobu Serruys, Patrick W. |
author_facet | Campos, Carlos M. Ishibashi, Yuki Eggermont, Jeroen Nakatani, Shimpei Cho, Yun Kyeong Dijkstra, Jouke Reiber, Johan H. C. Sheehy, Alexander Lane, Jennifer Kamberi, Marika Rapoza, Richard Perkins, Laura Garcia-Garcia, Hector M. Onuma, Yoshinobu Serruys, Patrick W. |
author_sort | Campos, Carlos M. |
collection | PubMed |
description | The objective of the study is to validate intravascular quantitative echogenicity as a surrogate for molecular weight assessment of poly-l-lactide-acid (PLLA) bioresorbable scaffold (Absorb BVS, Abbott Vascular, Santa Clara, California). We analyzed at 9 time points (from 1- to 42-month follow-up) a population of 40 pigs that received 97 Absorb scaffolds. The treated regions were analyzed by echogenicity using adventitia as reference, and were categorized as more (hyperechogenic or upperechogenic) or less bright (hypoechogenic) than the reference. The volumes of echogenicity categories were correlated with the measurements of molecular weight (Mw) by gel permeation chromatography. Scaffold struts appeared as high echogenic structures. The quantification of grey level intensity in the scaffold-vessel compartment had strong correlation with the scaffold Mw: hyperechogenicity (correlation coefficient = 0.75; P < 0.01), upperechogenicity (correlation coefficient = 0.63; P < 0.01) and hyper + upperechogenicity (correlation coefficient = 0.78; P < 0.01). In the linear regression, the R(2) for high echogenicity and Mw was 0.57 for the combination of hyper and upper echogenicity. IVUS high intensity grey level quantification is correlated to Absorb BVS residual molecular weight and can be used as a surrogate for the monitoring of the degradation of semi-crystalline polymers scaffolds. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s10554-015-0591-4) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4368838 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Springer Netherlands |
record_format | MEDLINE/PubMed |
spelling | pubmed-43688382015-03-26 Echogenicity as a surrogate for bioresorbable everolimus-eluting scaffold degradation: analysis at 1-, 3-, 6-, 12- 18, 24-, 30-, 36- and 42-month follow-up in a porcine model Campos, Carlos M. Ishibashi, Yuki Eggermont, Jeroen Nakatani, Shimpei Cho, Yun Kyeong Dijkstra, Jouke Reiber, Johan H. C. Sheehy, Alexander Lane, Jennifer Kamberi, Marika Rapoza, Richard Perkins, Laura Garcia-Garcia, Hector M. Onuma, Yoshinobu Serruys, Patrick W. Int J Cardiovasc Imaging Original Paper The objective of the study is to validate intravascular quantitative echogenicity as a surrogate for molecular weight assessment of poly-l-lactide-acid (PLLA) bioresorbable scaffold (Absorb BVS, Abbott Vascular, Santa Clara, California). We analyzed at 9 time points (from 1- to 42-month follow-up) a population of 40 pigs that received 97 Absorb scaffolds. The treated regions were analyzed by echogenicity using adventitia as reference, and were categorized as more (hyperechogenic or upperechogenic) or less bright (hypoechogenic) than the reference. The volumes of echogenicity categories were correlated with the measurements of molecular weight (Mw) by gel permeation chromatography. Scaffold struts appeared as high echogenic structures. The quantification of grey level intensity in the scaffold-vessel compartment had strong correlation with the scaffold Mw: hyperechogenicity (correlation coefficient = 0.75; P < 0.01), upperechogenicity (correlation coefficient = 0.63; P < 0.01) and hyper + upperechogenicity (correlation coefficient = 0.78; P < 0.01). In the linear regression, the R(2) for high echogenicity and Mw was 0.57 for the combination of hyper and upper echogenicity. IVUS high intensity grey level quantification is correlated to Absorb BVS residual molecular weight and can be used as a surrogate for the monitoring of the degradation of semi-crystalline polymers scaffolds. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s10554-015-0591-4) contains supplementary material, which is available to authorized users. Springer Netherlands 2015-01-28 2015 /pmc/articles/PMC4368838/ /pubmed/25627777 http://dx.doi.org/10.1007/s10554-015-0591-4 Text en © The Author(s) 2015 https://creativecommons.org/licenses/by/4.0/ Open AccessThis article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited. |
spellingShingle | Original Paper Campos, Carlos M. Ishibashi, Yuki Eggermont, Jeroen Nakatani, Shimpei Cho, Yun Kyeong Dijkstra, Jouke Reiber, Johan H. C. Sheehy, Alexander Lane, Jennifer Kamberi, Marika Rapoza, Richard Perkins, Laura Garcia-Garcia, Hector M. Onuma, Yoshinobu Serruys, Patrick W. Echogenicity as a surrogate for bioresorbable everolimus-eluting scaffold degradation: analysis at 1-, 3-, 6-, 12- 18, 24-, 30-, 36- and 42-month follow-up in a porcine model |
title | Echogenicity as a surrogate for bioresorbable everolimus-eluting scaffold degradation: analysis at 1-, 3-, 6-, 12- 18, 24-, 30-, 36- and 42-month follow-up in a porcine model |
title_full | Echogenicity as a surrogate for bioresorbable everolimus-eluting scaffold degradation: analysis at 1-, 3-, 6-, 12- 18, 24-, 30-, 36- and 42-month follow-up in a porcine model |
title_fullStr | Echogenicity as a surrogate for bioresorbable everolimus-eluting scaffold degradation: analysis at 1-, 3-, 6-, 12- 18, 24-, 30-, 36- and 42-month follow-up in a porcine model |
title_full_unstemmed | Echogenicity as a surrogate for bioresorbable everolimus-eluting scaffold degradation: analysis at 1-, 3-, 6-, 12- 18, 24-, 30-, 36- and 42-month follow-up in a porcine model |
title_short | Echogenicity as a surrogate for bioresorbable everolimus-eluting scaffold degradation: analysis at 1-, 3-, 6-, 12- 18, 24-, 30-, 36- and 42-month follow-up in a porcine model |
title_sort | echogenicity as a surrogate for bioresorbable everolimus-eluting scaffold degradation: analysis at 1-, 3-, 6-, 12- 18, 24-, 30-, 36- and 42-month follow-up in a porcine model |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4368838/ https://www.ncbi.nlm.nih.gov/pubmed/25627777 http://dx.doi.org/10.1007/s10554-015-0591-4 |
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