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The Concept of a Rupture Risk Envelope for the Cochleo-Saccular Membranes
Introduction Alterations in endolymphatic pressure have long been suspected of being associated with the development of endolymphatic hydrops and rupture of the membranous labyrinth. More recently, there has been a focus on how membrane mechanics might contribute to membrane rupture. This is suspec...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Thieme Revinter Publicações Ltda.
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9668410/ https://www.ncbi.nlm.nih.gov/pubmed/36405472 http://dx.doi.org/10.1055/s-0042-1742331 |
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author | Pender, Daniel J. |
author_facet | Pender, Daniel J. |
author_sort | Pender, Daniel J. |
collection | PubMed |
description | Introduction Alterations in endolymphatic pressure have long been suspected of being associated with the development of endolymphatic hydrops and rupture of the membranous labyrinth. More recently, there has been a focus on how membrane mechanics might contribute to membrane rupture. This is suspected to involve the viscoelastoplastic properties of these membranes. Objective To construct a rupture risk envelope for the cochleo-saccular membranes based on viscoelastoplasticity to provide insight into lesion behavior in Meniere disease. Methods Reported deformation data from a collagen model of the cochleo-saccular membranes was utilized. Yield stress was defined as 80% of ultimate failure stress. The yield points at various strain rates were used to construct a rupture risk envelope for the membranes. Results The rupture risk envelope was found to be downward sloping in configuration. At the highest strain rate of 385% per minute, the membrane yield was associated with greater stress (7.0 kPa) and lesser strain (30%); while at the lowest strain rate of 19.2% per minute, there was substantially less membrane yield stress (4.3 kPa) but it was associated with greater strain (44%). Conclusion The concept of a rupture risk envelope based on viscoelastoplasticity provides insight into hydropic lesion behavior in Meniere disease. This concept helps to explain how variations in membrane distensibility might occur as suspected in the double hit theory of lesion generation in Meniere disease. Slowly developing lesions would appear have a lower rupture risk while rapidly developing lesions would appear to have a greater risk of early membrane rupture. |
format | Online Article Text |
id | pubmed-9668410 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Thieme Revinter Publicações Ltda. |
record_format | MEDLINE/PubMed |
spelling | pubmed-96684102022-11-17 The Concept of a Rupture Risk Envelope for the Cochleo-Saccular Membranes Pender, Daniel J. Int Arch Otorhinolaryngol Introduction Alterations in endolymphatic pressure have long been suspected of being associated with the development of endolymphatic hydrops and rupture of the membranous labyrinth. More recently, there has been a focus on how membrane mechanics might contribute to membrane rupture. This is suspected to involve the viscoelastoplastic properties of these membranes. Objective To construct a rupture risk envelope for the cochleo-saccular membranes based on viscoelastoplasticity to provide insight into lesion behavior in Meniere disease. Methods Reported deformation data from a collagen model of the cochleo-saccular membranes was utilized. Yield stress was defined as 80% of ultimate failure stress. The yield points at various strain rates were used to construct a rupture risk envelope for the membranes. Results The rupture risk envelope was found to be downward sloping in configuration. At the highest strain rate of 385% per minute, the membrane yield was associated with greater stress (7.0 kPa) and lesser strain (30%); while at the lowest strain rate of 19.2% per minute, there was substantially less membrane yield stress (4.3 kPa) but it was associated with greater strain (44%). Conclusion The concept of a rupture risk envelope based on viscoelastoplasticity provides insight into hydropic lesion behavior in Meniere disease. This concept helps to explain how variations in membrane distensibility might occur as suspected in the double hit theory of lesion generation in Meniere disease. Slowly developing lesions would appear have a lower rupture risk while rapidly developing lesions would appear to have a greater risk of early membrane rupture. Thieme Revinter Publicações Ltda. 2022-02-04 /pmc/articles/PMC9668410/ /pubmed/36405472 http://dx.doi.org/10.1055/s-0042-1742331 Text en Fundação Otorrinolaringologia. This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commecial purposes, or adapted, remixed, transformed or built upon. ( https://creativecommons.org/licenses/by-nc-nd/4.0/ ) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License, which permits unrestricted reproduction and distribution, for non-commercial purposes only; and use and reproduction, but not distribution, of adapted material for non-commercial purposes only, provided the original work is properly cited. |
spellingShingle | Pender, Daniel J. The Concept of a Rupture Risk Envelope for the Cochleo-Saccular Membranes |
title | The Concept of a Rupture Risk Envelope for the Cochleo-Saccular Membranes |
title_full | The Concept of a Rupture Risk Envelope for the Cochleo-Saccular Membranes |
title_fullStr | The Concept of a Rupture Risk Envelope for the Cochleo-Saccular Membranes |
title_full_unstemmed | The Concept of a Rupture Risk Envelope for the Cochleo-Saccular Membranes |
title_short | The Concept of a Rupture Risk Envelope for the Cochleo-Saccular Membranes |
title_sort | concept of a rupture risk envelope for the cochleo-saccular membranes |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9668410/ https://www.ncbi.nlm.nih.gov/pubmed/36405472 http://dx.doi.org/10.1055/s-0042-1742331 |
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