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The Biomechanical Properties of Meshed versus Perforated Acellular Dermal Matrices (ADMs)

BACKGROUND: Acellular dermal matrices (ADMs) are used for soft tissue augmentation across surgical specialties. Since allograft incorporation depends on direct opposition between the ADM and a vascular bed, seroma formation can be detrimental to incorporation. Since most ADM products are available i...

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Autores principales: Sweitzer, Keith, Carruthers, Katherine H., Blume, Lauren, Tiwari,, Pankaj, Kocak,, Ergun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7954372/
https://www.ncbi.nlm.nih.gov/pubmed/33728235
http://dx.doi.org/10.1097/GOX.0000000000003454
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author Sweitzer, Keith
Carruthers, Katherine H.
Blume, Lauren
Tiwari,, Pankaj
Kocak,, Ergun
author_facet Sweitzer, Keith
Carruthers, Katherine H.
Blume, Lauren
Tiwari,, Pankaj
Kocak,, Ergun
author_sort Sweitzer, Keith
collection PubMed
description BACKGROUND: Acellular dermal matrices (ADMs) are used for soft tissue augmentation across surgical specialties. Since allograft incorporation depends on direct opposition between the ADM and a vascular bed, seroma formation can be detrimental to incorporation. Since most ADM products are available in many meshed and perforated forms, there is a lack of consistency between manufacture designs. We set out to determine the fluid egress properties and increase in surface area resulting from common cut patterns. METHODS: Three ADM cut patterns were studied: 1 meshed and 2 perforated. We calculated the surface area of these modified ADM samples. Fluid was passed through each ADM, and time required for fluid passage was recorded. An ANOVA (P < 0.05) was used to determine if there was a significant difference in egress properties across the 3 patterns. RESULTS: Meshing in a 1:1 pattern resulted in a 97.50% increase in surface area compared with the uncut product. In comparison, only a 0.30% increase resulted from Perforation Pattern #1 and a 0.59% increase resulted from Perforation Pattern #2. There was a significant difference in egress properties across the three cut patterns (P = 0.000). The average egress time of Mesh Pattern #1 was 1.974 seconds. The average egress time of Perforation Pattern #2 was 6.504 seconds, and of Perforation Pattern #1 was 10.369 seconds. CONCLUSIONS: Quantitative comparison revealed that meshing ADM significantly improves fluid egress and increases the surface area. Therefore, the use of meshed ADM tissue could improve the incorporation of ADM with the recipient, with improved patient outcomes.
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spelling pubmed-79543722021-03-15 The Biomechanical Properties of Meshed versus Perforated Acellular Dermal Matrices (ADMs) Sweitzer, Keith Carruthers, Katherine H. Blume, Lauren Tiwari,, Pankaj Kocak,, Ergun Plast Reconstr Surg Glob Open Experimental BACKGROUND: Acellular dermal matrices (ADMs) are used for soft tissue augmentation across surgical specialties. Since allograft incorporation depends on direct opposition between the ADM and a vascular bed, seroma formation can be detrimental to incorporation. Since most ADM products are available in many meshed and perforated forms, there is a lack of consistency between manufacture designs. We set out to determine the fluid egress properties and increase in surface area resulting from common cut patterns. METHODS: Three ADM cut patterns were studied: 1 meshed and 2 perforated. We calculated the surface area of these modified ADM samples. Fluid was passed through each ADM, and time required for fluid passage was recorded. An ANOVA (P < 0.05) was used to determine if there was a significant difference in egress properties across the 3 patterns. RESULTS: Meshing in a 1:1 pattern resulted in a 97.50% increase in surface area compared with the uncut product. In comparison, only a 0.30% increase resulted from Perforation Pattern #1 and a 0.59% increase resulted from Perforation Pattern #2. There was a significant difference in egress properties across the three cut patterns (P = 0.000). The average egress time of Mesh Pattern #1 was 1.974 seconds. The average egress time of Perforation Pattern #2 was 6.504 seconds, and of Perforation Pattern #1 was 10.369 seconds. CONCLUSIONS: Quantitative comparison revealed that meshing ADM significantly improves fluid egress and increases the surface area. Therefore, the use of meshed ADM tissue could improve the incorporation of ADM with the recipient, with improved patient outcomes. Lippincott Williams & Wilkins 2021-03-11 /pmc/articles/PMC7954372/ /pubmed/33728235 http://dx.doi.org/10.1097/GOX.0000000000003454 Text en Copyright © 2021 The Authors. Published by Wolters Kluwer Health, Inc. on behalf of The American Society of Plastic Surgeons. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) , where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal.
spellingShingle Experimental
Sweitzer, Keith
Carruthers, Katherine H.
Blume, Lauren
Tiwari,, Pankaj
Kocak,, Ergun
The Biomechanical Properties of Meshed versus Perforated Acellular Dermal Matrices (ADMs)
title The Biomechanical Properties of Meshed versus Perforated Acellular Dermal Matrices (ADMs)
title_full The Biomechanical Properties of Meshed versus Perforated Acellular Dermal Matrices (ADMs)
title_fullStr The Biomechanical Properties of Meshed versus Perforated Acellular Dermal Matrices (ADMs)
title_full_unstemmed The Biomechanical Properties of Meshed versus Perforated Acellular Dermal Matrices (ADMs)
title_short The Biomechanical Properties of Meshed versus Perforated Acellular Dermal Matrices (ADMs)
title_sort biomechanical properties of meshed versus perforated acellular dermal matrices (adms)
topic Experimental
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7954372/
https://www.ncbi.nlm.nih.gov/pubmed/33728235
http://dx.doi.org/10.1097/GOX.0000000000003454
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