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Characterization of micro-invasive trabecular bypass stents by ex vivo perfusion and computational flow modeling
Micro-invasive glaucoma surgery with the Glaukos iStent® or iStent inject® (Glaukos Corporation, Laguna Hills, CA, USA) is intended to create a bypass through the trabecular meshwork to Schlemm’s canal to improve aqueous outflow through the natural physiologic pathway. While the iStent devices have...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3956696/ https://www.ncbi.nlm.nih.gov/pubmed/24648713 http://dx.doi.org/10.2147/OPTH.S56245 |
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author | Hunter, Kendall S Fjield, Todd Heitzmann, Hal Shandas, Robin Kahook, Malik Y |
author_facet | Hunter, Kendall S Fjield, Todd Heitzmann, Hal Shandas, Robin Kahook, Malik Y |
author_sort | Hunter, Kendall S |
collection | PubMed |
description | Micro-invasive glaucoma surgery with the Glaukos iStent® or iStent inject® (Glaukos Corporation, Laguna Hills, CA, USA) is intended to create a bypass through the trabecular meshwork to Schlemm’s canal to improve aqueous outflow through the natural physiologic pathway. While the iStent devices have been evaluated in ex vivo anterior segment models, they have not previously been evaluated in whole eye perfusion models nor characterized by computational fluid dynamics. Intraocular pressure (IOP) reduction with the iStent was evaluated in an ex vivo whole human eye perfusion model. Numerical modeling, including computational fluid dynamics, was used to evaluate the flow through the stents over physiologically relevant boundary conditions. In the ex vivo model, a single iStent reduced IOP by 6.0 mmHg from baseline, and addition of a second iStent further lowered IOP by 2.9 mmHg, for a total IOP reduction of 8.9 mmHg. Computational modeling showed that simulated flow through the iStent or iStent inject is smooth and laminar at physiological flow rates. Each stent was computed to have a negligible flow resistance consistent with an expected significant decrease in IOP. The present perfusion results agree with prior clinical and laboratory studies to show that both iStent and iStent inject therapies are potentially titratable, providing clinicians with the opportunity to achieve lower target IOPs by implanting additional stents. |
format | Online Article Text |
id | pubmed-3956696 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-39566962014-03-19 Characterization of micro-invasive trabecular bypass stents by ex vivo perfusion and computational flow modeling Hunter, Kendall S Fjield, Todd Heitzmann, Hal Shandas, Robin Kahook, Malik Y Clin Ophthalmol Original Research Micro-invasive glaucoma surgery with the Glaukos iStent® or iStent inject® (Glaukos Corporation, Laguna Hills, CA, USA) is intended to create a bypass through the trabecular meshwork to Schlemm’s canal to improve aqueous outflow through the natural physiologic pathway. While the iStent devices have been evaluated in ex vivo anterior segment models, they have not previously been evaluated in whole eye perfusion models nor characterized by computational fluid dynamics. Intraocular pressure (IOP) reduction with the iStent was evaluated in an ex vivo whole human eye perfusion model. Numerical modeling, including computational fluid dynamics, was used to evaluate the flow through the stents over physiologically relevant boundary conditions. In the ex vivo model, a single iStent reduced IOP by 6.0 mmHg from baseline, and addition of a second iStent further lowered IOP by 2.9 mmHg, for a total IOP reduction of 8.9 mmHg. Computational modeling showed that simulated flow through the iStent or iStent inject is smooth and laminar at physiological flow rates. Each stent was computed to have a negligible flow resistance consistent with an expected significant decrease in IOP. The present perfusion results agree with prior clinical and laboratory studies to show that both iStent and iStent inject therapies are potentially titratable, providing clinicians with the opportunity to achieve lower target IOPs by implanting additional stents. Dove Medical Press 2014-03-11 /pmc/articles/PMC3956696/ /pubmed/24648713 http://dx.doi.org/10.2147/OPTH.S56245 Text en © 2014 Hunter et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Hunter, Kendall S Fjield, Todd Heitzmann, Hal Shandas, Robin Kahook, Malik Y Characterization of micro-invasive trabecular bypass stents by ex vivo perfusion and computational flow modeling |
title | Characterization of micro-invasive trabecular bypass stents by ex vivo perfusion and computational flow modeling |
title_full | Characterization of micro-invasive trabecular bypass stents by ex vivo perfusion and computational flow modeling |
title_fullStr | Characterization of micro-invasive trabecular bypass stents by ex vivo perfusion and computational flow modeling |
title_full_unstemmed | Characterization of micro-invasive trabecular bypass stents by ex vivo perfusion and computational flow modeling |
title_short | Characterization of micro-invasive trabecular bypass stents by ex vivo perfusion and computational flow modeling |
title_sort | characterization of micro-invasive trabecular bypass stents by ex vivo perfusion and computational flow modeling |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3956696/ https://www.ncbi.nlm.nih.gov/pubmed/24648713 http://dx.doi.org/10.2147/OPTH.S56245 |
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