Guided bone generation in a rabbit mandible model after periosteal expansion with an osmotic tissue expander
Identifieur interne : 007537 ( Istex/Corpus ); précédent : 007536; suivant : 007538Guided bone generation in a rabbit mandible model after periosteal expansion with an osmotic tissue expander
Auteurs : Peter Abrahamsson ; Sten Isaksson ; Gunilla AnderssonSource :
- Clinical Oral Implants Research [ 0905-7161 ] ; 2011-11.
English descriptors
- KwdEn :
- Abrahamsson, Augmentation, Autogenous, Autogenous bone, Autogenous bone graft, Autologous bone, Bone, Bone augmentation, Bone formation, Bone generation, Bone graft, Bone mineral, Bone regeneration, Clin, Clinical orthopaedics, Collagen, Collagen membrane, Cortical bone layer, Dbbm, Dbbm area, Dbbm particles, Dehiscence, Direct contact, Expander, Experimental study, Graft, Grafted, Grafted area, Impl, Implant, Implant placement, Implants research, Ingrowth, International journal, John wiley sons, Lateral border, Mandible, Maxillofacial, Maxillofacial surgery, Membrane, Mesh, Mesh area, Mineralized, Mineralized bone, Mineralized bone area, Oral impl, Osmotic tissue expander, Other studies, Periosteal, Periosteal expansion, Periosteum, Present study, Rabbit mandible, Rabbit mandible model, Recipient site, Reconstructive surgery, Regeneration, Soft tissue, Soft tissue expander, Soft tissue expansion, Soft tissue ingrowth, Tissue expander, Titanium, Titanium mesh, Titanium micromesh, Total area, Total bone area.
- Teeft :
- Abrahamsson, Augmentation, Autogenous, Autogenous bone, Autogenous bone graft, Autologous bone, Bone, Bone augmentation, Bone formation, Bone generation, Bone graft, Bone mineral, Bone regeneration, Clin, Clinical orthopaedics, Collagen, Collagen membrane, Cortical bone layer, Dbbm, Dbbm area, Dbbm particles, Dehiscence, Direct contact, Expander, Experimental study, Graft, Grafted, Grafted area, Impl, Implant, Implant placement, Implants research, Ingrowth, International journal, John wiley sons, Lateral border, Mandible, Maxillofacial, Maxillofacial surgery, Membrane, Mesh, Mesh area, Mineralized, Mineralized bone, Mineralized bone area, Oral impl, Osmotic tissue expander, Other studies, Periosteal, Periosteal expansion, Periosteum, Present study, Rabbit mandible, Rabbit mandible model, Recipient site, Reconstructive surgery, Regeneration, Soft tissue, Soft tissue expander, Soft tissue expansion, Soft tissue ingrowth, Tissue expander, Titanium, Titanium mesh, Titanium micromesh, Total area, Total bone area.
Abstract
Objectives: To evaluate the space‐maintaining capacity of titanium mesh covered by a collagen membrane after soft tissue expansion on the lateral border of the mandible in rabbits, and to assess bone quantity and quality using autogenous particulate bone or bone‐substitute (Bio‐Oss®), and if soft tissue ingrowth can be avoided by covering the mesh with a collagen membrane.
Url:
DOI: 10.1111/j.1600-0501.2010.02108.x
Links to Exploration step
ISTEX:EC9BCBE42A373AF3C33BFE8D7615B0114216F464Le document en format XML
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orthopaedics</json:string><json:string>implant placement</json:string><json:string>titanium micromesh</json:string><json:string>other studies</json:string><json:string>autogenous bone graft</json:string><json:string>osmotic tissue expander</json:string><json:string>reconstructive surgery</json:string><json:string>mesh area</json:string><json:string>bone</json:string><json:string>membrane</json:string></teeft></keywords><author><json:item><name>Peter Abrahamsson</name><affiliations><json:string>Department of Maxillofacial Surgery, Maxillofacial Unit, Länssjukhuset, Halmstad, Sweden</json:string><json:string>Department of Oral and Maxillofacial Surgery and Oral Medicine, Faculty of Odontology, Malmö University, Malmö, Sweden</json:string></affiliations></json:item><json:item><name>Sten Isaksson</name><affiliations><json:string>Department of Maxillofacial Surgery, Maxillofacial Unit, Länssjukhuset, Halmstad, Sweden</json:string><json:string>Department of Oral and Maxillofacial Surgery and Oral Medicine, Faculty of Odontology, Malmö University, Malmö, Sweden</json:string></affiliations></json:item><json:item><name>Gunilla Andersson</name><affiliations><json:string>Department of Oral and Maxillofacial Surgery and Oral Medicine, Faculty of Odontology, Malmö University, Malmö, Sweden</json:string></affiliations></json:item></author><subject><json:item><lang><json:string>eng</json:string></lang><value>animal study</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>bone graft</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>bone regeneration</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>bone substitutes</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>deproteinized bovine bone</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>soft‐tissue 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membrane.</abstract><qualityIndicators><refBibsNative>true</refBibsNative><abstractWordCount>57</abstractWordCount><abstractCharCount>375</abstractCharCount><keywordCount>7</keywordCount><score>7.684</score><pdfWordCount>5038</pdfWordCount><pdfCharCount>30567</pdfCharCount><pdfVersion>1.3</pdfVersion><pdfPageCount>7</pdfPageCount><pdfPageSize>595.276 x 782.362 pts</pdfPageSize></qualityIndicators><title>Guided bone generation in a rabbit mandible model after periosteal expansion with an osmotic tissue expander</title><pmid><json:string>21985285</json:string></pmid><genre><json:string>article</json:string></genre><host><title>Clinical Oral Implants Research</title><language><json:string>unknown</json:string></language><doi><json:string>10.1111/(ISSN)1600-0501</json:string></doi><issn><json:string>0905-7161</json:string></issn><eissn><json:string>1600-0501</json:string></eissn><publisherId><json:string>CLR</json:string></publisherId><volume>22</volume><issue>11</issue><pages><first>1282</first><last>1288</last><total>7</total></pages><genre><json:string>journal</json:string></genre></host><namedEntities><unitex><date><json:string>2011</json:string></date><geogName></geogName><orgName><json:string>Orion Corporation</json:string><json:string>Dentsply Ltd</json:string><json:string>Department of Oral and Maxillofacial Surgery</json:string><json:string>Malmo University</json:string><json:string>Sweden/Domitor Orion Corporation, Esboo, Finland</json:string></orgName><orgName_funder></orgName_funder><orgName_provider></orgName_provider><persName><json:string>Lisbeth Lindbergh</json:string><json:string>G. Andersson</json:string><json:string>John Wiley</json:string><json:string>Andy Brown</json:string><json:string>S. 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2001</json:string><json:string>Wang & Boyapati 2006</json:string><json:string>Abrahamsson et al. 2010</json:string><json:string>Eyre-Brook 1984</json:string><json:string>Strong et al. 2003</json:string><json:string>von See et al. 2010</json:string><json:string>Degidi et al. 2003</json:string><json:string>Zhang et al. 2008</json:string><json:string>Slotte et al. 2003</json:string><json:string>Abrahamsson et al. 2009</json:string><json:string>Sencimen et al. 2007</json:string><json:string>Hammerle et al. 2008</json:string><json:string>Abrahamsson et al</json:string><json:string>Zeiter et al. 1998</json:string><json:string>Van Steenberghe et al. 2003</json:string><json:string>Horn & Garrett 2004</json:string><json:string>Schmid et al. 1994</json:string><json:string>Pieri et al. 2008</json:string><json:string>Proussaefs & Lozada 2006</json:string><json:string>Xie et al. 2007</json:string><json:string>Allen et al. 2004</json:string><json:string>Adeyemo et al. 2008</json:string><json:string>Dahlin et al. 1991</json:string><json:string>Gutta et al. 2009</json:string><json:string>Hallman et al. 2001</json:string><json:string>Schonmeyr et al. 2009</json:string><json:string>Kim et al. 2009</json:string><json:string>Roccuzzo et al. 2007</json:string><json:string>von Arx & Kurt 1999</json:string><json:string>Elshahat et al. 2005</json:string><json:string>LaTrenta et al. 1988</json:string><json:string>Chiapasco et al. 1999</json:string><json:string>Araujo et al. 2008</json:string></ref_bibl><bibl></bibl></unitex></namedEntities><ark><json:string>ark:/67375/WNG-11QD1K8M-J</json:string></ark><categories><wos><json:string>1 - science</json:string><json:string>2 - engineering, biomedical</json:string><json:string>2 - dentistry, oral surgery & medicine</json:string></wos><scienceMetrix><json:string>1 - health sciences</json:string><json:string>2 - clinical medicine</json:string><json:string>3 - 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xml:id="author-0000"><persName><forename type="first">Peter</forename><surname>Abrahamsson</surname></persName><affiliation>Department of Maxillofacial Surgery, Maxillofacial Unit, Länssjukhuset, Halmstad, Sweden<address><country key="SE"></country></address></affiliation><affiliation>Department of Oral and Maxillofacial Surgery and Oral Medicine, Faculty of Odontology, Malmö University, Malmö, Sweden<address><country key="SE"></country></address></affiliation></author><author xml:id="author-0001"><persName><forename type="first">Sten</forename><surname>Isaksson</surname></persName><affiliation>Department of Maxillofacial Surgery, Maxillofacial Unit, Länssjukhuset, Halmstad, Sweden<address><country key="SE"></country></address></affiliation><affiliation>Department of Oral and Maxillofacial Surgery and Oral Medicine, Faculty of Odontology, Malmö University, Malmö, Sweden<address><country key="SE"></country></address></affiliation></author><author xml:id="author-0002"><persName><forename type="first">Gunilla</forename><surname>Andersson</surname></persName><affiliation>Department of Oral and Maxillofacial Surgery and Oral Medicine, Faculty of Odontology, Malmö University, Malmö, Sweden<address><country key="SE"></country></address></affiliation></author><idno type="istex">EC9BCBE42A373AF3C33BFE8D7615B0114216F464</idno><idno type="ark">ark:/67375/WNG-11QD1K8M-J</idno><idno type="DOI">10.1111/j.1600-0501.2010.02108.x</idno><idno type="unit">CLR2108</idno><idno type="supplier">2108</idno><idno type="toTypesetVersion">file:CLR.CLR2108.pdf</idno></analytic><monogr><title level="j" type="main">Clinical Oral Implants Research</title><title level="j" type="alt">CLINICAL ORAL IMPLANTS RESEARCH</title><idno type="pISSN">0905-7161</idno><idno type="eISSN">1600-0501</idno><idno type="book-DOI">10.1111/(ISSN)1600-0501</idno><idno type="book-part-DOI">10.1111/clr.2011.22.issue-11</idno><idno type="product">CLR</idno><idno type="publisherDivision">ST</idno><imprint><biblScope unit="vol">22</biblScope><biblScope unit="issue">11</biblScope><biblScope unit="page" from="1282">1282</biblScope><biblScope unit="page" to="1288">1288</biblScope><biblScope unit="page-count">7</biblScope><publisher>Blackwell Publishing Ltd</publisher><pubPlace>Oxford, UK</pubPlace><date type="published" when="2011-11"></date></imprint></monogr></biblStruct></sourceDesc></fileDesc><profileDesc><abstract xml:lang="en" style="main"><head>Abstract</head><p><hi rend="bold">Objectives: </hi> To evaluate the space‐maintaining capacity of titanium mesh covered by a collagen membrane after soft tissue expansion on the lateral border of the mandible in rabbits, and to assess bone quantity and quality using autogenous particulate bone or bone‐substitute (Bio‐Oss<hi rend="superscript">®</hi>), and if soft tissue ingrowth can be avoided by covering the mesh with a collagen membrane.</p><p><hi rend="bold">Material and methods: </hi> In 11 rabbits, a self‐inflatable soft tissue expander was placed under the lateral mandibular periosteum via an extra‐oral approach. After 2 weeks, the expanders were removed and a particulated onlay bone graft and deproteinized bovine bone mineral (DBBM) (Bio‐Oss<hi rend="superscript">®</hi>) were placed in the expanded area and covered by a titanium mesh. The bone and DBBM were separated in two compartments under the mesh with a collagen membrane in between. The mesh was then covered with a collagen membrane. After 3 months, the animals were sacrificed and specimens were collected for histology.</p><p><hi rend="bold">Results: </hi> The osmotic soft tissue expander created a subperiosteal pocket and a ridge of new bone formed at the edges of the expanded periosteum in all sites. After the healing period of 3 months, no soft tissue dehiscence was recorded. The mean bone fill was 58.1±18% in the bone grafted area and 56.9±13.7% in the DBBM area. There was no significant difference between the autologous bone graft and the DDBM under the titanium mesh with regard to the total bone area or the mineralized bone area. Scanning electron microscopy showed that new bone was growing in direct contact with the DBBM particles and the titanium mesh. There is a soft tissue ingrowth even after soft tissue expansion and protection of the titanium mesh with a collagen membrane.</p><p><hi rend="bold">Conclusion: </hi> This study confirms that an osmotic soft tissue expander creates a surplus of periosteum and soft tissue, and that new bone can subsequently be generated under a titanium mesh with the use of an autologous bone graft or DBBM.</p><p><hi rend="bold">To cite this article:</hi>
Abrahamsson P, Isaksson S, Andersson G. Guided bone generation in a rabbit mandible model after periosteal expansion with an osmotic tissue expander.
<hi rend="italic">Clin. Oral Impl. Res</hi>. <hi rend="bold">22</hi>, 2011; 1282–1288.
doi: 10.1111/j.1600‐0501.2010.02108.x</p></abstract><textClass><keywords xml:lang="en"><term xml:id="k1">animal study</term><term xml:id="k2">bone graft</term><term xml:id="k3">bone regeneration</term><term xml:id="k4">bone substitutes</term><term xml:id="k5">deproteinized bovine bone</term><term xml:id="k6">soft‐tissue expansion</term><term xml:id="k7">titanium mesh</term></keywords><keywords rend="tocHeading1"><term>Original Articles</term></keywords></textClass><langUsage><language ident="en"></language></langUsage></profileDesc></teiHeader></istex:fulltextTEI><json:item><extension>txt</extension><original>false</original><mimetype>text/plain</mimetype><uri>https://api.istex.fr/document/EC9BCBE42A373AF3C33BFE8D7615B0114216F464/fulltext/txt</uri></json:item></fulltext><metadata><istex:metadataXml wicri:clean="Wiley, elements deleted: body"><istex:xmlDeclaration>version="1.0" encoding="UTF-8" standalone="yes"</istex:xmlDeclaration><istex:document><component version="2.0" type="serialArticle" xml:lang="en"><header><publicationMeta level="product"><publisherInfo><publisherName>Blackwell Publishing Ltd</publisherName><publisherLoc>Oxford, UK</publisherLoc></publisherInfo><doi origin="wiley" registered="yes">10.1111/(ISSN)1600-0501</doi><issn type="print">0905-7161</issn><issn type="electronic">1600-0501</issn><idGroup><id type="product" value="CLR"></id><id type="publisherDivision" value="ST"></id></idGroup><titleGroup><title type="main" sort="CLINICAL ORAL IMPLANTS RESEARCH">Clinical Oral Implants Research</title></titleGroup></publicationMeta><publicationMeta level="part" position="11111"><doi origin="wiley">10.1111/clr.2011.22.issue-11</doi><numberingGroup><numbering type="journalVolume" number="22">22</numbering><numbering type="journalIssue" number="11">11</numbering></numberingGroup><coverDate startDate="2011-11">November 2011</coverDate></publicationMeta><publicationMeta level="unit" type="article" position="12" status="forIssue"><doi origin="wiley">10.1111/j.1600-0501.2010.02108.x</doi><idGroup><id type="unit" value="CLR2108"></id><id type="supplier" value="2108"></id></idGroup><countGroup><count type="pageTotal" number="7"></count></countGroup><titleGroup><title type="tocHeading1">Original Articles</title></titleGroup><copyright>© 2011 John Wiley & Sons A/S</copyright><eventGroup><event type="xmlConverted" agent="Converter:BPG_TO_WML3G version:2.10 mode:FullText" date="2011-10-10"></event><event type="publishedOnlineEarlyUnpaginated" date="2011-02-24"></event><event type="firstOnline" date="2011-02-24"></event><event type="publishedOnlineFinalForm" date="2011-10-10"></event><event type="xmlConverted" agent="Converter:WILEY_ML3G_TO_WILEY_ML3GV2 version:4.0.1" date="2014-03-12"></event><event type="xmlConverted" agent="Converter:WML3G_To_WML3G version:4.1.7 mode:FullText,remove_FC" date="2014-10-16"></event></eventGroup><numberingGroup><numbering type="pageFirst" number="1282">1282</numbering><numbering type="pageLast" number="1288">1288</numbering></numberingGroup><correspondenceTo><b>Corresponding author:</b>
<i>Peter Abrahamsson</i>
Department of Maxillofacial Surgery
Maxillofacial Unit
Länssjukhuset
SE‐30185 Halmstad
Sweden
Tel.:+46 0 35 134 000
Fax:+46 0 35 215 159
e‐mail: <email normalForm="peter.abrahamsson@lthalland.se">peter.abrahamsson@lthalland.se</email></correspondenceTo><linkGroup><link type="toTypesetVersion" href="file:CLR.CLR2108.pdf"></link></linkGroup></publicationMeta><contentMeta><unparsedEditorialHistory><b>Date:</b> , Accepted 24 September 2010</unparsedEditorialHistory><countGroup><count type="figureTotal" number="7"></count><count type="tableTotal" number="1"></count><count type="formulaTotal" number="0"></count><count type="referenceTotal" number="37"></count><count type="wordTotal" number="6134"></count><count type="linksCrossRef" number="52"></count></countGroup><titleGroup><title type="main">Guided bone generation in a rabbit mandible model after periosteal expansion with an osmotic tissue expander</title><title type="shortAuthors">Abrahamsson et al.</title><title type="short">Guided bone generation in a rabbit mandible model</title></titleGroup><creators><creator creatorRole="author" xml:id="cr1" affiliationRef="#a1 #a2"><personName><givenNames>Peter</givenNames><familyName>Abrahamsson</familyName></personName></creator><creator creatorRole="author" xml:id="cr2" affiliationRef="#a1 #a2"><personName><givenNames>Sten</givenNames><familyName>Isaksson</familyName></personName></creator><creator creatorRole="author" xml:id="cr3" affiliationRef="#a2"><personName><givenNames>Gunilla</givenNames><familyName>Andersson</familyName></personName></creator></creators><affiliationGroup><affiliation xml:id="a1" countryCode="SE"><unparsedAffiliation>Department of Maxillofacial Surgery, Maxillofacial Unit, Länssjukhuset, Halmstad, Sweden</unparsedAffiliation></affiliation><affiliation xml:id="a2" countryCode="SE"><unparsedAffiliation>Department of Oral and Maxillofacial Surgery and Oral Medicine, Faculty of Odontology, Malmö University, Malmö, Sweden</unparsedAffiliation></affiliation></affiliationGroup><keywordGroup xml:lang="en"><keyword xml:id="k1">animal study</keyword><keyword xml:id="k2">bone graft</keyword><keyword xml:id="k3">bone regeneration</keyword><keyword xml:id="k4">bone substitutes</keyword><keyword xml:id="k5">deproteinized bovine bone</keyword><keyword xml:id="k6">soft‐tissue expansion</keyword><keyword xml:id="k7">titanium mesh</keyword></keywordGroup><abstractGroup><abstract type="main" xml:lang="en"><title type="main">Abstract</title><p><b>Objectives: </b> To evaluate the space‐maintaining capacity of titanium mesh covered by a collagen membrane after soft tissue expansion on the lateral border of the mandible in rabbits, and to assess bone quantity and quality using autogenous particulate bone or bone‐substitute (Bio‐Oss<sup>®</sup>), and if soft tissue ingrowth can be avoided by covering the mesh with a collagen membrane.</p><p><b>Material and methods: </b> In 11 rabbits, a self‐inflatable soft tissue expander was placed under the lateral mandibular periosteum via an extra‐oral approach. After 2 weeks, the expanders were removed and a particulated onlay bone graft and deproteinized bovine bone mineral (DBBM) (Bio‐Oss<sup>®</sup>) were placed in the expanded area and covered by a titanium mesh. The bone and DBBM were separated in two compartments under the mesh with a collagen membrane in between. The mesh was then covered with a collagen membrane. After 3 months, the animals were sacrificed and specimens were collected for histology.</p><p><b>Results: </b> The osmotic soft tissue expander created a subperiosteal pocket and a ridge of new bone formed at the edges of the expanded periosteum in all sites. After the healing period of 3 months, no soft tissue dehiscence was recorded. The mean bone fill was 58.1±18% in the bone grafted area and 56.9±13.7% in the DBBM area. There was no significant difference between the autologous bone graft and the DDBM under the titanium mesh with regard to the total bone area or the mineralized bone area. Scanning electron microscopy showed that new bone was growing in direct contact with the DBBM particles and the titanium mesh. There is a soft tissue ingrowth even after soft tissue expansion and protection of the titanium mesh with a collagen membrane.</p><p><b>Conclusion: </b> This study confirms that an osmotic soft tissue expander creates a surplus of periosteum and soft tissue, and that new bone can subsequently be generated under a titanium mesh with the use of an autologous bone graft or DBBM.</p><p><b>To cite this article:</b>
Abrahamsson P, Isaksson S, Andersson G. Guided bone generation in a rabbit mandible model after periosteal expansion with an osmotic tissue expander.
<i>Clin. Oral Impl. Res</i>. <b>22</b>, 2011; 1282–1288.
doi: 10.1111/j.1600‐0501.2010.02108.x</p></abstract></abstractGroup></contentMeta></header></component></istex:document></istex:metadataXml><mods version="3.6"><titleInfo lang="en"><title>Guided bone generation in a rabbit mandible model after periosteal expansion with an osmotic tissue expander</title></titleInfo><titleInfo type="abbreviated" lang="en"><title>Guided bone generation in a rabbit mandible model</title></titleInfo><titleInfo type="alternative" contentType="CDATA" lang="en"><title>Guided bone generation in a rabbit mandible model after periosteal expansion with an osmotic tissue expander</title></titleInfo><name type="personal"><namePart type="given">Peter</namePart><namePart type="family">Abrahamsson</namePart><affiliation>Department of Maxillofacial Surgery, Maxillofacial Unit, Länssjukhuset, Halmstad, Sweden</affiliation><affiliation>Department of Oral and Maxillofacial Surgery and Oral Medicine, Faculty of Odontology, Malmö University, Malmö, Sweden</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Sten</namePart><namePart type="family">Isaksson</namePart><affiliation>Department of Maxillofacial Surgery, Maxillofacial Unit, Länssjukhuset, Halmstad, Sweden</affiliation><affiliation>Department of Oral and Maxillofacial Surgery and Oral Medicine, Faculty of Odontology, Malmö University, Malmö, Sweden</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Gunilla</namePart><namePart type="family">Andersson</namePart><affiliation>Department of Oral and Maxillofacial Surgery and Oral Medicine, Faculty of Odontology, Malmö University, Malmö, Sweden</affiliation><role><roleTerm type="text">author</roleTerm></role></name><typeOfResource>text</typeOfResource><genre type="article" displayLabel="article" authority="ISTEX" authorityURI="https://content-type.data.istex.fr" valueURI="https://content-type.data.istex.fr/ark:/67375/XTP-6N5SZHKN-D">article</genre><originInfo><publisher>Blackwell Publishing Ltd</publisher><place><placeTerm type="text">Oxford, UK</placeTerm></place><dateIssued encoding="w3cdtf">2011-11</dateIssued><edition>Date: , Accepted 24 September 2010</edition><copyrightDate encoding="w3cdtf">2011</copyrightDate></originInfo><language><languageTerm type="code" authority="rfc3066">en</languageTerm><languageTerm type="code" authority="iso639-2b">eng</languageTerm></language><physicalDescription><extent unit="figures">7</extent><extent unit="tables">1</extent><extent unit="formulas">0</extent><extent unit="references">37</extent><extent unit="linksCrossRef">52</extent><extent unit="words">6134</extent></physicalDescription><abstract>Objectives: To evaluate the space‐maintaining capacity of titanium mesh covered by a collagen membrane after soft tissue expansion on the lateral border of the mandible in rabbits, and to assess bone quantity and quality using autogenous particulate bone or bone‐substitute (Bio‐Oss®), and if soft tissue ingrowth can be avoided by covering the mesh with a collagen membrane.</abstract><abstract>Material and methods: In 11 rabbits, a self‐inflatable soft tissue expander was placed under the lateral mandibular periosteum via an extra‐oral approach. After 2 weeks, the expanders were removed and a particulated onlay bone graft and deproteinized bovine bone mineral (DBBM) (Bio‐Oss®) were placed in the expanded area and covered by a titanium mesh. The bone and DBBM were separated in two compartments under the mesh with a collagen membrane in between. The mesh was then covered with a collagen membrane. After 3 months, the animals were sacrificed and specimens were collected for histology.</abstract><abstract>Results: The osmotic soft tissue expander created a subperiosteal pocket and a ridge of new bone formed at the edges of the expanded periosteum in all sites. After the healing period of 3 months, no soft tissue dehiscence was recorded. The mean bone fill was 58.1±18% in the bone grafted area and 56.9±13.7% in the DBBM area. There was no significant difference between the autologous bone graft and the DDBM under the titanium mesh with regard to the total bone area or the mineralized bone area. Scanning electron microscopy showed that new bone was growing in direct contact with the DBBM particles and the titanium mesh. There is a soft tissue ingrowth even after soft tissue expansion and protection of the titanium mesh with a collagen membrane.</abstract><abstract>Conclusion: This study confirms that an osmotic soft tissue expander creates a surplus of periosteum and soft tissue, and that new bone can subsequently be generated under a titanium mesh with the use of an autologous bone graft or DBBM.</abstract><abstract>To cite this article:
Abrahamsson P, Isaksson S, Andersson G. Guided bone generation in a rabbit mandible model after periosteal expansion with an osmotic tissue expander.
Clin. Oral Impl. Res. 22, 2011; 1282–1288.
doi: 10.1111/j.1600‐0501.2010.02108.x</abstract><subject lang="en"><genre>keywords</genre><topic>animal study</topic><topic>bone graft</topic><topic>bone regeneration</topic><topic>bone substitutes</topic><topic>deproteinized bovine bone</topic><topic>soft‐tissue expansion</topic><topic>titanium mesh</topic></subject><relatedItem type="host"><titleInfo><title>Clinical Oral Implants Research</title></titleInfo><genre type="journal" authority="ISTEX" authorityURI="https://publication-type.data.istex.fr" valueURI="https://publication-type.data.istex.fr/ark:/67375/JMC-0GLKJH51-B">journal</genre><identifier type="ISSN">0905-7161</identifier><identifier type="eISSN">1600-0501</identifier><identifier type="DOI">10.1111/(ISSN)1600-0501</identifier><identifier type="PublisherID">CLR</identifier><part><date>2011</date><detail type="volume"><caption>vol.</caption><number>22</number></detail><detail type="issue"><caption>no.</caption><number>11</number></detail><extent unit="pages"><start>1282</start><end>1288</end><total>7</total></extent></part></relatedItem><identifier type="istex">EC9BCBE42A373AF3C33BFE8D7615B0114216F464</identifier><identifier type="ark">ark:/67375/WNG-11QD1K8M-J</identifier><identifier type="DOI">10.1111/j.1600-0501.2010.02108.x</identifier><identifier type="ArticleID">CLR2108</identifier><accessCondition type="use and reproduction" contentType="copyright">© 2011 John Wiley & Sons A/S</accessCondition><recordInfo><recordContentSource authority="ISTEX" authorityURI="https://loaded-corpus.data.istex.fr" valueURI="https://loaded-corpus.data.istex.fr/ark:/67375/XBH-L0C46X92-X">wiley</recordContentSource><recordOrigin>Blackwell Publishing Ltd</recordOrigin></recordInfo></mods><json:item><extension>json</extension><original>false</original><mimetype>application/json</mimetype><uri>https://api.istex.fr/document/EC9BCBE42A373AF3C33BFE8D7615B0114216F464/metadata/json</uri></json:item></metadata><serie></serie></istex></record>Pour manipuler ce document sous Unix (Dilib)
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