Abdominal wall reinforcement: biologic vs. degradable synthetic devices
Background New biodegradable synthetic and biologic hernia implants have been promoted for rapid integration and tissue reinforcement in challenging repairs, e.g. at the hiatus or in contaminated wound fields. Interestingly, experimental data to support or falsify this assumption is scarce. Methods...
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Veröffentlicht in: | Hernia : the journal of hernias and abdominal wall surgery 2017-04, Vol.21 (2), p.305-315 |
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container_title | Hernia : the journal of hernias and abdominal wall surgery |
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creator | Gruber-Blum, S. Brand, J. Keibl, C. Fortelny, R. H. Redl, H. Mayer, F. Petter-Puchner, A. H. |
description | Background
New biodegradable synthetic and biologic hernia implants have been promoted for rapid integration and tissue reinforcement in challenging repairs, e.g. at the hiatus or in contaminated wound fields. Interestingly, experimental data to support or falsify this assumption is scarce.
Methods
Synthetic (BioA
®
) and biologic implants (porcine and bovine collagen matrices Strattice
®
and Veritas
®
) have been tested in experimental onlay hernia repair in rats in observation periods of 30 and 60 days. The key outcome parameters were mesh integration and reinforcement of the tissue at the implant site over sutured and sealed defects as well as comparison to native abdominal wall. Macroscopic assessment, biomechanical analysis and histology with haematoxylin/eosin staining, collagen staining and van Willebrand factor staining for detection of neovascularization were performed.
Results
BioA
®
was well integrated. Although the matrices were already fragmented at 60 days follow-up, hernia sites treated with synthetic scaffolds showed a significantly enhanced tissue deflection and resistance to burst force when compared to the native abdominal wall. In porcine and bovine matrices, tissue integration and shrinkage were significantly inferior to BioA
®
. Histology revealed a lack of fibroblast ingrowth through mesh interstices in biologic samples, whereas BioA
®
was tightly connected to the underlying tissue by reticular collagen fibres.
Conclusions
Strattice
®
and Veritas
®
yielded reduced tissue integration and significant shrinkage, prohibiting further biomechanical tests. The synthetic BioA
®
provides little inherent strength but reticular collagen remodelling led to an augmentation of the scar due to significantly higher burst force resistance in comparison to native tissue. |
doi_str_mv | 10.1007/s10029-016-1556-9 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1881759765</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>4321036457</sourcerecordid><originalsourceid>FETCH-LOGICAL-c405t-82f4c0056bae117f5038cb07fa0977fd6304964ab5a3b4501d1d82b46d66c9033</originalsourceid><addsrcrecordid>eNqNkclKBDEQhoMo7g_gRRq8eOmxks7qTQY3ELzoOWTrsYdeNOlRfHvTjIoIgpdKQX31B-pD6AjDDAOIs5QrUSVgXmLGeKk20C4mVJaKAN2ces5KqoDvoL2UlgAgKZfbaIdIwAQqsouuL6wfuqY3bfFm2raIoenrIbrQhX48L2wztMOiccVrmhU-LKLxxrahSO_9-BTGPPDhtXEhHaCt2rQpHH6---jx6vJhflPe3V_fzi_uSkeBjaUkNXUAjFsTMBY1g0o6C6I2oISoPa-AKk6NZaaylAH22EtiKfecOwVVtY9O17nPcXhZhTTqrkkutK3pw7BKGkuJBVOCs3-gjAjJOZ3Qk1_ocljFfJSJEqqSNB8uU3hNuTikFEOtn2PTmfiuMehJiF4L0VmInoRolXeOP5NXtgv-e-PLQAbIGkh51C9C_PH1n6kf2Y2TlA</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1879384846</pqid></control><display><type>article</type><title>Abdominal wall reinforcement: biologic vs. degradable synthetic devices</title><source>MEDLINE</source><source>SpringerLink Journals</source><creator>Gruber-Blum, S. ; Brand, J. ; Keibl, C. ; Fortelny, R. H. ; Redl, H. ; Mayer, F. ; Petter-Puchner, A. H.</creator><creatorcontrib>Gruber-Blum, S. ; Brand, J. ; Keibl, C. ; Fortelny, R. H. ; Redl, H. ; Mayer, F. ; Petter-Puchner, A. H.</creatorcontrib><description>Background
New biodegradable synthetic and biologic hernia implants have been promoted for rapid integration and tissue reinforcement in challenging repairs, e.g. at the hiatus or in contaminated wound fields. Interestingly, experimental data to support or falsify this assumption is scarce.
Methods
Synthetic (BioA
®
) and biologic implants (porcine and bovine collagen matrices Strattice
®
and Veritas
®
) have been tested in experimental onlay hernia repair in rats in observation periods of 30 and 60 days. The key outcome parameters were mesh integration and reinforcement of the tissue at the implant site over sutured and sealed defects as well as comparison to native abdominal wall. Macroscopic assessment, biomechanical analysis and histology with haematoxylin/eosin staining, collagen staining and van Willebrand factor staining for detection of neovascularization were performed.
Results
BioA
®
was well integrated. Although the matrices were already fragmented at 60 days follow-up, hernia sites treated with synthetic scaffolds showed a significantly enhanced tissue deflection and resistance to burst force when compared to the native abdominal wall. In porcine and bovine matrices, tissue integration and shrinkage were significantly inferior to BioA
®
. Histology revealed a lack of fibroblast ingrowth through mesh interstices in biologic samples, whereas BioA
®
was tightly connected to the underlying tissue by reticular collagen fibres.
Conclusions
Strattice
®
and Veritas
®
yielded reduced tissue integration and significant shrinkage, prohibiting further biomechanical tests. The synthetic BioA
®
provides little inherent strength but reticular collagen remodelling led to an augmentation of the scar due to significantly higher burst force resistance in comparison to native tissue.</description><identifier>ISSN: 1265-4906</identifier><identifier>EISSN: 1248-9204</identifier><identifier>DOI: 10.1007/s10029-016-1556-9</identifier><identifier>PMID: 28012032</identifier><language>eng</language><publisher>Paris: Springer Paris</publisher><subject>Abdominal Surgery ; Abdominal Wall - surgery ; Absorbable Implants ; Animals ; Biocompatible Materials - administration & dosage ; Biological Products - administration & dosage ; Cattle ; Collagen - administration & dosage ; Fibrin Tissue Adhesive ; Hernia, Ventral - physiopathology ; Hernia, Ventral - surgery ; Herniorrhaphy - methods ; Incisional Hernia - physiopathology ; Incisional Hernia - surgery ; Male ; Medicine ; Medicine & Public Health ; Original Article ; Rats ; Rats, Sprague-Dawley ; Surgical Mesh ; Swine ; Tissue Scaffolds ; Wound Healing - physiology</subject><ispartof>Hernia : the journal of hernias and abdominal wall surgery, 2017-04, Vol.21 (2), p.305-315</ispartof><rights>Springer-Verlag France 2016</rights><rights>Hernia is a copyright of Springer, 2017.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c405t-82f4c0056bae117f5038cb07fa0977fd6304964ab5a3b4501d1d82b46d66c9033</citedby><cites>FETCH-LOGICAL-c405t-82f4c0056bae117f5038cb07fa0977fd6304964ab5a3b4501d1d82b46d66c9033</cites><orcidid>0000-0003-3449-7855</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s10029-016-1556-9$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s10029-016-1556-9$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,41488,42557,51319</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28012032$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gruber-Blum, S.</creatorcontrib><creatorcontrib>Brand, J.</creatorcontrib><creatorcontrib>Keibl, C.</creatorcontrib><creatorcontrib>Fortelny, R. H.</creatorcontrib><creatorcontrib>Redl, H.</creatorcontrib><creatorcontrib>Mayer, F.</creatorcontrib><creatorcontrib>Petter-Puchner, A. H.</creatorcontrib><title>Abdominal wall reinforcement: biologic vs. degradable synthetic devices</title><title>Hernia : the journal of hernias and abdominal wall surgery</title><addtitle>Hernia</addtitle><addtitle>Hernia</addtitle><description>Background
New biodegradable synthetic and biologic hernia implants have been promoted for rapid integration and tissue reinforcement in challenging repairs, e.g. at the hiatus or in contaminated wound fields. Interestingly, experimental data to support or falsify this assumption is scarce.
Methods
Synthetic (BioA
®
) and biologic implants (porcine and bovine collagen matrices Strattice
®
and Veritas
®
) have been tested in experimental onlay hernia repair in rats in observation periods of 30 and 60 days. The key outcome parameters were mesh integration and reinforcement of the tissue at the implant site over sutured and sealed defects as well as comparison to native abdominal wall. Macroscopic assessment, biomechanical analysis and histology with haematoxylin/eosin staining, collagen staining and van Willebrand factor staining for detection of neovascularization were performed.
Results
BioA
®
was well integrated. Although the matrices were already fragmented at 60 days follow-up, hernia sites treated with synthetic scaffolds showed a significantly enhanced tissue deflection and resistance to burst force when compared to the native abdominal wall. In porcine and bovine matrices, tissue integration and shrinkage were significantly inferior to BioA
®
. Histology revealed a lack of fibroblast ingrowth through mesh interstices in biologic samples, whereas BioA
®
was tightly connected to the underlying tissue by reticular collagen fibres.
Conclusions
Strattice
®
and Veritas
®
yielded reduced tissue integration and significant shrinkage, prohibiting further biomechanical tests. The synthetic BioA
®
provides little inherent strength but reticular collagen remodelling led to an augmentation of the scar due to significantly higher burst force resistance in comparison to native tissue.</description><subject>Abdominal Surgery</subject><subject>Abdominal Wall - surgery</subject><subject>Absorbable Implants</subject><subject>Animals</subject><subject>Biocompatible Materials - administration & dosage</subject><subject>Biological Products - administration & dosage</subject><subject>Cattle</subject><subject>Collagen - administration & dosage</subject><subject>Fibrin Tissue Adhesive</subject><subject>Hernia, Ventral - physiopathology</subject><subject>Hernia, Ventral - surgery</subject><subject>Herniorrhaphy - methods</subject><subject>Incisional Hernia - physiopathology</subject><subject>Incisional Hernia - surgery</subject><subject>Male</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Original Article</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Surgical Mesh</subject><subject>Swine</subject><subject>Tissue Scaffolds</subject><subject>Wound Healing - physiology</subject><issn>1265-4906</issn><issn>1248-9204</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNqNkclKBDEQhoMo7g_gRRq8eOmxks7qTQY3ELzoOWTrsYdeNOlRfHvTjIoIgpdKQX31B-pD6AjDDAOIs5QrUSVgXmLGeKk20C4mVJaKAN2ces5KqoDvoL2UlgAgKZfbaIdIwAQqsouuL6wfuqY3bfFm2raIoenrIbrQhX48L2wztMOiccVrmhU-LKLxxrahSO_9-BTGPPDhtXEhHaCt2rQpHH6---jx6vJhflPe3V_fzi_uSkeBjaUkNXUAjFsTMBY1g0o6C6I2oISoPa-AKk6NZaaylAH22EtiKfecOwVVtY9O17nPcXhZhTTqrkkutK3pw7BKGkuJBVOCs3-gjAjJOZ3Qk1_ocljFfJSJEqqSNB8uU3hNuTikFEOtn2PTmfiuMehJiF4L0VmInoRolXeOP5NXtgv-e-PLQAbIGkh51C9C_PH1n6kf2Y2TlA</recordid><startdate>20170401</startdate><enddate>20170401</enddate><creator>Gruber-Blum, S.</creator><creator>Brand, J.</creator><creator>Keibl, C.</creator><creator>Fortelny, R. H.</creator><creator>Redl, H.</creator><creator>Mayer, F.</creator><creator>Petter-Puchner, A. H.</creator><general>Springer Paris</general><general>Springer Nature B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7T5</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>H94</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-3449-7855</orcidid></search><sort><creationdate>20170401</creationdate><title>Abdominal wall reinforcement: biologic vs. degradable synthetic devices</title><author>Gruber-Blum, S. ; Brand, J. ; Keibl, C. ; Fortelny, R. H. ; Redl, H. ; Mayer, F. ; Petter-Puchner, A. H.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c405t-82f4c0056bae117f5038cb07fa0977fd6304964ab5a3b4501d1d82b46d66c9033</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Abdominal Surgery</topic><topic>Abdominal Wall - surgery</topic><topic>Absorbable Implants</topic><topic>Animals</topic><topic>Biocompatible Materials - administration & dosage</topic><topic>Biological Products - administration & dosage</topic><topic>Cattle</topic><topic>Collagen - administration & dosage</topic><topic>Fibrin Tissue Adhesive</topic><topic>Hernia, Ventral - physiopathology</topic><topic>Hernia, Ventral - surgery</topic><topic>Herniorrhaphy - methods</topic><topic>Incisional Hernia - physiopathology</topic><topic>Incisional Hernia - surgery</topic><topic>Male</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Original Article</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Surgical Mesh</topic><topic>Swine</topic><topic>Tissue Scaffolds</topic><topic>Wound Healing - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gruber-Blum, S.</creatorcontrib><creatorcontrib>Brand, J.</creatorcontrib><creatorcontrib>Keibl, C.</creatorcontrib><creatorcontrib>Fortelny, R. H.</creatorcontrib><creatorcontrib>Redl, H.</creatorcontrib><creatorcontrib>Mayer, F.</creatorcontrib><creatorcontrib>Petter-Puchner, A. H.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Immunology Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><jtitle>Hernia : the journal of hernias and abdominal wall surgery</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gruber-Blum, S.</au><au>Brand, J.</au><au>Keibl, C.</au><au>Fortelny, R. H.</au><au>Redl, H.</au><au>Mayer, F.</au><au>Petter-Puchner, A. H.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Abdominal wall reinforcement: biologic vs. degradable synthetic devices</atitle><jtitle>Hernia : the journal of hernias and abdominal wall surgery</jtitle><stitle>Hernia</stitle><addtitle>Hernia</addtitle><date>2017-04-01</date><risdate>2017</risdate><volume>21</volume><issue>2</issue><spage>305</spage><epage>315</epage><pages>305-315</pages><issn>1265-4906</issn><eissn>1248-9204</eissn><abstract>Background
New biodegradable synthetic and biologic hernia implants have been promoted for rapid integration and tissue reinforcement in challenging repairs, e.g. at the hiatus or in contaminated wound fields. Interestingly, experimental data to support or falsify this assumption is scarce.
Methods
Synthetic (BioA
®
) and biologic implants (porcine and bovine collagen matrices Strattice
®
and Veritas
®
) have been tested in experimental onlay hernia repair in rats in observation periods of 30 and 60 days. The key outcome parameters were mesh integration and reinforcement of the tissue at the implant site over sutured and sealed defects as well as comparison to native abdominal wall. Macroscopic assessment, biomechanical analysis and histology with haematoxylin/eosin staining, collagen staining and van Willebrand factor staining for detection of neovascularization were performed.
Results
BioA
®
was well integrated. Although the matrices were already fragmented at 60 days follow-up, hernia sites treated with synthetic scaffolds showed a significantly enhanced tissue deflection and resistance to burst force when compared to the native abdominal wall. In porcine and bovine matrices, tissue integration and shrinkage were significantly inferior to BioA
®
. Histology revealed a lack of fibroblast ingrowth through mesh interstices in biologic samples, whereas BioA
®
was tightly connected to the underlying tissue by reticular collagen fibres.
Conclusions
Strattice
®
and Veritas
®
yielded reduced tissue integration and significant shrinkage, prohibiting further biomechanical tests. The synthetic BioA
®
provides little inherent strength but reticular collagen remodelling led to an augmentation of the scar due to significantly higher burst force resistance in comparison to native tissue.</abstract><cop>Paris</cop><pub>Springer Paris</pub><pmid>28012032</pmid><doi>10.1007/s10029-016-1556-9</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0003-3449-7855</orcidid></addata></record> |
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issn | 1265-4906 1248-9204 |
language | eng |
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source | MEDLINE; SpringerLink Journals |
subjects | Abdominal Surgery Abdominal Wall - surgery Absorbable Implants Animals Biocompatible Materials - administration & dosage Biological Products - administration & dosage Cattle Collagen - administration & dosage Fibrin Tissue Adhesive Hernia, Ventral - physiopathology Hernia, Ventral - surgery Herniorrhaphy - methods Incisional Hernia - physiopathology Incisional Hernia - surgery Male Medicine Medicine & Public Health Original Article Rats Rats, Sprague-Dawley Surgical Mesh Swine Tissue Scaffolds Wound Healing - physiology |
title | Abdominal wall reinforcement: biologic vs. degradable synthetic devices |
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