Bone Graft Healing in Reconstruction of Maxillary Atrophy
Identifieur interne : 001496 ( Istex/Corpus ); précédent : 001495; suivant : 001497Bone Graft Healing in Reconstruction of Maxillary Atrophy
Auteurs : Mats Sjöström ; Lars Sennerby ; Stefan LundgrenSource :
- Clinical Implant Dentistry and Related Research [ 1523-0899 ] ; 2013-06.
English descriptors
- KwdEn :
- Alveolar ridge augmentation, Anterior maxilla, Autogenous, Biopsy, Blood samples, Body mass index, Bone, Bone graft, Bone graft healing, Bone grafts, Bone metabolism, Bone mineral density, Bone volume fraction, Cancellous, Clin, Clinical implant dentistry, Clinical study, Donor site, Endosteal implants, Fascia lata, Femoral, Femoral neck, Glucocorticoid, Glucocorticoid medication, Graft, Graft volume change, Grafted, Grafted bone, Healing, Hematologic, Hematologic factors, Iliac, Iliac crest, Implant, Implant failure, Implant failures, Implant placement, Implant stability, Implant stability quotient, Implant survival, Initial healing, Internal table, Lumbar vertebrae, Maxilla, Maxillary, Maxillary reconstruction, Maxillofac, Multiple implant failures, Normal range, Normal ranges, Onlay, Onlay bone graft, Onlay bone grafts, Oral maxillofac implants, Oral maxillofac surg, Osteoporosis, Pearson correlation test, Present study, Resonance frequency analysis, Resorption, Sinus, Surg, Total body, Univariate analysis, Vertebra, Volume change, Volume changes.
- Teeft :
- Alveolar ridge augmentation, Anterior maxilla, Autogenous, Biopsy, Blood samples, Body mass index, Bone, Bone graft, Bone graft healing, Bone grafts, Bone metabolism, Bone mineral density, Bone volume fraction, Cancellous, Clin, Clinical implant dentistry, Clinical study, Donor site, Endosteal implants, Fascia lata, Femoral, Femoral neck, Glucocorticoid, Glucocorticoid medication, Graft, Graft volume change, Grafted, Grafted bone, Healing, Hematologic, Hematologic factors, Iliac, Iliac crest, Implant, Implant failure, Implant failures, Implant placement, Implant stability, Implant stability quotient, Implant survival, Initial healing, Internal table, Lumbar vertebrae, Maxilla, Maxillary, Maxillary reconstruction, Maxillofac, Multiple implant failures, Normal range, Normal ranges, Onlay, Onlay bone graft, Onlay bone grafts, Oral maxillofac implants, Oral maxillofac surg, Osteoporosis, Pearson correlation test, Present study, Resonance frequency analysis, Resorption, Sinus, Surg, Total body, Univariate analysis, Vertebra, Volume change, Volume changes.
Abstract
Purpose: Evaluate correlations between volume change for iliac crest bone grafts in maxillary reconstruction (graft volume change [GVC]) and bone mineral density (BMD), bone volume fraction (BVF), hematologic bone metabolic factors (I), and identify indicators of implant failure (II).
Url:
DOI: 10.1111/j.1708-8208.2011.00368.x
Links to Exploration step
ISTEX:2B0A85BF9759EFC7D77E7669D269E3EF59C38B8DLe document en format XML
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sortKey="Sjostrom, Mats" sort="Sjostrom, Mats" uniqKey="Sjostrom M" first="Mats" last="Sjöström">Mats Sjöström</name><affiliation><mods:affiliation>Professor, Department of Oral & Maxillofacial Surgery, Umeå University, Umeå, Sweden;</mods:affiliation></affiliation><affiliation><mods:affiliation>E-mail: mats.sjostrom@odont.umu.se</mods:affiliation></affiliation></author><author><name sortKey="Sennerby, Lars" sort="Sennerby, Lars" uniqKey="Sennerby L" first="Lars" last="Sennerby">Lars Sennerby</name><affiliation><mods:affiliation>Professor, Department of Oral & Maxillofacial Surgery, Umeå University, Umeå, Sweden;</mods:affiliation></affiliation><affiliation><mods:affiliation>professor, Department of Biomaterials/Handicap Research Institute for Surgical Sciences, Gothenburg University, Sweden</mods:affiliation></affiliation></author><author><name sortKey="Lundgren, Stefan" sort="Lundgren, Stefan" uniqKey="Lundgren S" first="Stefan" last="Lundgren">Stefan 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xml:lang="en"><term>Alveolar ridge augmentation</term><term>Anterior maxilla</term><term>Autogenous</term><term>Biopsy</term><term>Blood samples</term><term>Body mass index</term><term>Bone</term><term>Bone graft</term><term>Bone graft healing</term><term>Bone grafts</term><term>Bone metabolism</term><term>Bone mineral density</term><term>Bone volume fraction</term><term>Cancellous</term><term>Clin</term><term>Clinical implant dentistry</term><term>Clinical study</term><term>Donor site</term><term>Endosteal implants</term><term>Fascia lata</term><term>Femoral</term><term>Femoral neck</term><term>Glucocorticoid</term><term>Glucocorticoid medication</term><term>Graft</term><term>Graft volume change</term><term>Grafted</term><term>Grafted bone</term><term>Healing</term><term>Hematologic</term><term>Hematologic factors</term><term>Iliac</term><term>Iliac crest</term><term>Implant</term><term>Implant failure</term><term>Implant failures</term><term>Implant placement</term><term>Implant stability</term><term>Implant stability quotient</term><term>Implant survival</term><term>Initial healing</term><term>Internal table</term><term>Lumbar vertebrae</term><term>Maxilla</term><term>Maxillary</term><term>Maxillary reconstruction</term><term>Maxillofac</term><term>Multiple implant failures</term><term>Normal range</term><term>Normal ranges</term><term>Onlay</term><term>Onlay bone graft</term><term>Onlay bone grafts</term><term>Oral maxillofac implants</term><term>Oral maxillofac surg</term><term>Osteoporosis</term><term>Pearson correlation test</term><term>Present study</term><term>Resonance frequency analysis</term><term>Resorption</term><term>Sinus</term><term>Surg</term><term>Total body</term><term>Univariate analysis</term><term>Vertebra</term><term>Volume change</term><term>Volume changes</term></keywords><keywords scheme="Teeft" xml:lang="en"><term>Alveolar ridge augmentation</term><term>Anterior maxilla</term><term>Autogenous</term><term>Biopsy</term><term>Blood samples</term><term>Body mass index</term><term>Bone</term><term>Bone graft</term><term>Bone graft healing</term><term>Bone grafts</term><term>Bone metabolism</term><term>Bone mineral density</term><term>Bone volume fraction</term><term>Cancellous</term><term>Clin</term><term>Clinical implant dentistry</term><term>Clinical study</term><term>Donor site</term><term>Endosteal implants</term><term>Fascia lata</term><term>Femoral</term><term>Femoral neck</term><term>Glucocorticoid</term><term>Glucocorticoid medication</term><term>Graft</term><term>Graft volume change</term><term>Grafted</term><term>Grafted bone</term><term>Healing</term><term>Hematologic</term><term>Hematologic factors</term><term>Iliac</term><term>Iliac crest</term><term>Implant</term><term>Implant failure</term><term>Implant failures</term><term>Implant placement</term><term>Implant stability</term><term>Implant stability quotient</term><term>Implant survival</term><term>Initial healing</term><term>Internal table</term><term>Lumbar vertebrae</term><term>Maxilla</term><term>Maxillary</term><term>Maxillary reconstruction</term><term>Maxillofac</term><term>Multiple implant failures</term><term>Normal range</term><term>Normal ranges</term><term>Onlay</term><term>Onlay bone graft</term><term>Onlay bone grafts</term><term>Oral maxillofac implants</term><term>Oral maxillofac surg</term><term>Osteoporosis</term><term>Pearson correlation test</term><term>Present study</term><term>Resonance frequency analysis</term><term>Resorption</term><term>Sinus</term><term>Surg</term><term>Total body</term><term>Univariate analysis</term><term>Vertebra</term><term>Volume change</term><term>Volume changes</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract">Purpose: Evaluate correlations between volume change for iliac crest bone grafts in maxillary reconstruction (graft volume change [GVC]) and bone mineral density (BMD), bone volume fraction (BVF), hematologic bone metabolic 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DDS, PhD</name><affiliations><json:string>Professor, Department of Oral & Maxillofacial Surgery, Umeå University, Umeå, Sweden;</json:string><json:string>E-mail: mats.sjostrom@odont.umu.se</json:string></affiliations></json:item><json:item><name>Lars Sennerby DDS, PhD</name><affiliations><json:string>Professor, Department of Oral & Maxillofacial Surgery, Umeå University, Umeå, Sweden;</json:string><json:string>professor, Department of Biomaterials/Handicap Research Institute for Surgical Sciences, Gothenburg University, Sweden</json:string></affiliations></json:item><json:item><name>Stefan Lundgren DDS, PhD</name><affiliations><json:string>Professor, Department of Oral & Maxillofacial Surgery, Umeå University, Umeå, Sweden;</json:string></affiliations></json:item></author><subject><json:item><lang><json:string>eng</json:string></lang><value>autogenous bone graft</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>bone metabolic factors</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>bone mineral density</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>donor bone quality</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>edentulous atrophic maxilla</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>graft volume change</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>implant stability</value></json:item></subject><articleId><json:string>CID368</json:string></articleId><arkIstex>ark:/67375/WNG-SF6HQK98-H</arkIstex><language><json:string>eng</json:string></language><originalGenre><json:string>article</json:string></originalGenre><abstract>Purpose: Evaluate correlations between volume change for iliac crest bone grafts in maxillary reconstruction (graft volume change [GVC]) and bone mineral density (BMD), bone volume fraction (BVF), hematologic bone metabolic factors (I), and identify indicators of implant failure (II).</abstract><qualityIndicators><score>7.468</score><pdfWordCount>5460</pdfWordCount><pdfCharCount>35445</pdfCharCount><pdfVersion>1.3</pdfVersion><pdfPageCount>13</pdfPageCount><pdfPageSize>585 x 783 pts</pdfPageSize><refBibsNative>true</refBibsNative><abstractWordCount>39</abstractWordCount><abstractCharCount>285</abstractCharCount><keywordCount>7</keywordCount></qualityIndicators><title>Bone Graft Healing in Reconstruction of Maxillary Atrophy</title><pmid><json:string>21745329</json:string></pmid><genre><json:string>article</json:string></genre><host><title>Clinical Implant Dentistry and Related Research</title><language><json:string>unknown</json:string></language><doi><json:string>10.1111/(ISSN)1708-8208</json:string></doi><issn><json:string>1523-0899</json:string></issn><eissn><json:string>1708-8208</json:string></eissn><publisherId><json:string>CID</json:string></publisherId><volume>15</volume><issue>3</issue><pages><first>367</first><last>379</last><total>13</total></pages><genre><json:string>journal</json:string></genre><subject><json:item><value>ARTICLE</value></json:item></subject></host><namedEntities><unitex><date><json:string>2013</json:string></date><geogName></geogName><orgName><json:string>Umeå University Hospital, Department of Clinical Chemistry</json:string><json:string>SPSS Inc., Chicago</json:string><json:string>Umeå University</json:string><json:string>Related Research, Volume</json:string><json:string>Integration Diagnostics</json:string><json:string>Lunar Co</json:string></orgName><orgName_funder></orgName_funder><orgName_provider></orgName_provider><persName><json:string>Stefan Lundgren</json:string><json:string>Philips Tomoscan</json:string></persName><placeName><json:string>Germany</json:string><json:string>NY</json:string><json:string>Helsinki</json:string><json:string>York</json:string><json:string>Wetzlar</json:string><json:string>Sweden</json:string></placeName><ref_url></ref_url><ref_bibl><json:string>Smolka et al.</json:string><json:string>Östman et al.</json:string><json:string>Nyström et al.</json:string><json:string>Sjöström et al.</json:string><json:string>Sbordone et al. 2009</json:string><json:string>Johansson et al. 2001a</json:string><json:string>Kan et al.</json:string><json:string>Hollinger et al.</json:string><json:string>Riebel et al.</json:string><json:string>Blomqvist et al.</json:string><json:string>Miyamoto et al.</json:string></ref_bibl><bibl></bibl></unitex></namedEntities><ark><json:string>ark:/67375/WNG-SF6HQK98-H</json:string></ark><categories><wos><json:string>1 - science</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 - dentistry</json:string></scienceMetrix><scopus><json:string>1 - Health Sciences</json:string><json:string>2 - Dentistry</json:string><json:string>3 - General Dentistry</json:string><json:string>1 - Health Sciences</json:string><json:string>2 - Dentistry</json:string><json:string>3 - Oral Surgery</json:string></scopus></categories><publicationDate>2013</publicationDate><copyrightDate>2013</copyrightDate><doi><json:string>10.1111/j.1708-8208.2011.00368.x</json:string></doi><id>2B0A85BF9759EFC7D77E7669D269E3EF59C38B8D</id><score>1</score><fulltext><json:item><extension>pdf</extension><original>true</original><mimetype>application/pdf</mimetype><uri>https://api.istex.fr/document/2B0A85BF9759EFC7D77E7669D269E3EF59C38B8D/fulltext/pdf</uri></json:item><json:item><extension>zip</extension><original>false</original><mimetype>application/zip</mimetype><uri>https://api.istex.fr/document/2B0A85BF9759EFC7D77E7669D269E3EF59C38B8D/fulltext/zip</uri></json:item><istex:fulltextTEI uri="https://api.istex.fr/document/2B0A85BF9759EFC7D77E7669D269E3EF59C38B8D/fulltext/tei"><teiHeader><fileDesc><titleStmt><title level="a" type="main">Bone Graft Healing in Reconstruction of Maxillary Atrophy</title></titleStmt><publicationStmt><authority>ISTEX</authority><publisher>Blackwell Publishing Ltd</publisher><pubPlace>Oxford, UK</pubPlace><availability><licence>© 2011 Wiley Periodicals, Inc.</licence></availability><date type="published" when="2013-06"></date></publicationStmt><notesStmt><note type="content-type" subtype="article" source="article" scheme="https://content-type.data.istex.fr/ark:/67375/XTP-6N5SZHKN-D">article</note><note type="publication-type" subtype="journal" scheme="https://publication-type.data.istex.fr/ark:/67375/JMC-0GLKJH51-B">journal</note></notesStmt><sourceDesc><biblStruct type="article"><analytic><title level="a" type="main">Bone Graft Healing in Reconstruction of Maxillary Atrophy</title><title level="a" type="short">Bone Graft Healing</title><author xml:id="author-0000" role="corresp"><persName><forename type="first">Mats</forename><surname>Sjöström</surname><roleName type="degree">DDS, PhD</roleName></persName><affiliation>Professor, Department of Oral & Maxillofacial Surgery, Umeå University, Umeå, Sweden;<address><country key="SE"></country></address></affiliation><affiliation>Consultant Mats Sjöström, Department of Oral & Maxillofacial Surgery, Umeå University, SE 901 87 Umeå, Sweden; e‐mail: mats.sjostrom@odont.umu.se</affiliation></author><author xml:id="author-0001"><persName><forename type="first">Lars</forename><surname>Sennerby</surname><roleName type="degree">DDS, PhD</roleName></persName><affiliation>Professor, Department of Oral & Maxillofacial Surgery, Umeå University, Umeå, Sweden;<address><country key="SE"></country></address></affiliation><affiliation>professor, Department of Biomaterials/Handicap Research Institute for Surgical Sciences, Gothenburg University, Sweden<address><country key="SE"></country></address></affiliation></author><author xml:id="author-0002"><persName><forename type="first">Stefan</forename><surname>Lundgren</surname><roleName type="degree">DDS, PhD</roleName></persName><affiliation>Professor, Department of Oral & Maxillofacial Surgery, Umeå University, Umeå, Sweden;<address><country key="SE"></country></address></affiliation></author><idno type="istex">2B0A85BF9759EFC7D77E7669D269E3EF59C38B8D</idno><idno type="ark">ark:/67375/WNG-SF6HQK98-H</idno><idno type="DOI">10.1111/j.1708-8208.2011.00368.x</idno><idno type="unit">CID368</idno><idno type="toTypesetVersion">file:CID.CID368.pdf</idno></analytic><monogr><title level="j" type="main">Clinical Implant Dentistry and Related Research</title><title level="j" type="alt">CLINICAL IMPLANT DENTISTRY RELATED RESEARCH</title><idno type="pISSN">1523-0899</idno><idno type="eISSN">1708-8208</idno><idno type="book-DOI">10.1111/(ISSN)1708-8208</idno><idno type="book-part-DOI">10.1111/cid.2013.15.issue-3</idno><idno type="product">CID</idno><idno type="publisherDivision">ST</idno><imprint><biblScope unit="vol">15</biblScope><biblScope unit="issue">3</biblScope><biblScope unit="page" from="367">367</biblScope><biblScope unit="page" to="379">379</biblScope><biblScope unit="page-count">13</biblScope><publisher>Blackwell Publishing Ltd</publisher><pubPlace>Oxford, UK</pubPlace><date type="published" when="2013-06"></date></imprint></monogr></biblStruct></sourceDesc></fileDesc><profileDesc><abstract xml:lang="en" style="main"><head>ABSTRACT</head><p><hi rend="bold">Purpose:</hi> Evaluate correlations between volume change for iliac crest bone grafts in maxillary reconstruction (graft volume change [GVC]) and bone mineral density (BMD), bone volume fraction (BVF), hematologic bone metabolic factors (I), and identify indicators of implant failure (II).</p><p><hi rend="bold">Material and Methods:</hi> Forty‐six consecutive patients had their edentulous atrophic maxilla reconstructed with free autogenous bone grafts from anterior iliac crest. Endosteal implants were placed 6 months after graft healing. Computer tomography was performed after 3 weeks and 6 months after grafting. Bone biopsies were taken from the internal table of donor site for calculation (BVF), and blood samples were collected. Implant stability was measured at placement with resonance frequency analysis and expressed as implant stability quotient (ISQ). Implant failure was registered.</p><p><hi rend="bold">Results:</hi> GVC in onlay bone graft was 37%. The BVF in iliac crest biopsies was 32%. Serum‐IGFBP3 differed with 79% of the samples over normal range. Fifteen patients had one or more implant failures prior to loading (early failures). Forty‐two patients were followed for a minimum of 3 years after implant loading and, in addition, 6/42 patients had one or more implants removed during the follow‐up (late failures). GVC correlated to decreased BMD of lumbar vertebrae L2‐L4 (Kruskal–Wallis test, <hi rend="italic">p</hi> = .017). No correlation was found between GVC and hematologic factors (Pearson correlation test) or between GVC and BVF (Kruskal–Wallis test). No correlation was found between ISQ and GVC (Pearson correlation test, <hi rend="italic">p</hi> = .865). The association between implant failures and the described factors were evaluated, and no significant correlations were found (unconditional logistic regression).</p><p><hi rend="bold">Conclusion:</hi> Onlay bone grafts decrease 37% during initial healing period, which correlate to BMD of lumbar vertebrae L2‐L4. No other evaluated parameters could explain GVC. The evaluated factors could not explain implant failure.</p></abstract><textClass><keywords xml:lang="en"><term xml:id="k1">autogenous bone graft</term><term xml:id="k2">bone metabolic factors</term><term xml:id="k3">bone mineral density</term><term xml:id="k4">donor bone quality</term><term xml:id="k5">edentulous atrophic maxilla</term><term xml:id="k6">graft volume change</term><term xml:id="k7">implant stability</term></keywords><keywords rend="tocHeading1"><term>ARTICLES</term></keywords><keywords rend="articleCategory"><term>ARTICLE</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/2B0A85BF9759EFC7D77E7669D269E3EF59C38B8D/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)1708-8208</doi><issn type="print">1523-0899</issn><issn type="electronic">1708-8208</issn><idGroup><id type="product" value="CID"></id><id type="publisherDivision" value="ST"></id></idGroup><titleGroup><title type="main" sort="CLINICAL IMPLANT DENTISTRY RELATED RESEARCH">Clinical Implant Dentistry and Related Research</title></titleGroup></publicationMeta><publicationMeta level="part" position="06103"><doi>10.1111/cid.2013.15.issue-3</doi><copyright ownership="publisher">Copyright © 2013 Wiley Periodicals, Inc.</copyright><numberingGroup><numbering number="15" type="journalVolume">15</numbering><numbering type="journalIssue">3</numbering></numberingGroup><coverDate startDate="2013-06">June 2013</coverDate></publicationMeta><publicationMeta level="unit" type="article" position="70" status="forIssue"><doi origin="wiley">10.1111/j.1708-8208.2011.00368.x</doi><idGroup><id type="unit" value="CID368"></id></idGroup><countGroup><count type="pageTotal" number="13"></count></countGroup><titleGroup><title type="tocHeading1">ARTICLES</title><title type="articleCategory">ARTICLE</title></titleGroup><copyright>© 2011 Wiley Periodicals, Inc.</copyright><eventGroup><event type="xmlConverted" agent="Converter:BPG_TO_WML3G version:3.2.2 mode:FullText" date="2013-05-22"></event><event date="2013-05-22" type="xmlCorrected"></event><event type="publishedOnlineEarlyUnpaginated" date="2011-07-11"></event><event type="firstOnline" date="2011-07-11"></event><event type="publishedOnlineFinalForm" date="2013-06-04"></event><event type="xmlConverted" agent="Converter:WILEY_ML3G_TO_WILEY_ML3GV2 version:3.8.8" date="2014-01-15"></event><event type="xmlConverted" agent="Converter:WML3G_To_WML3G version:4.6.4 mode:FullText" date="2015-10-03"></event></eventGroup><numberingGroup><numbering type="pageFirst">367</numbering><numbering type="pageLast">379</numbering></numberingGroup><correspondenceTo>Consultant Mats Sjöström, Department of Oral & Maxillofacial Surgery, Umeå University, SE 901 87 Umeå, Sweden; e‐mail: <email>mats.sjostrom@odont.umu.se</email></correspondenceTo><linkGroup><link type="toTypesetVersion" href="file:CID.CID368.pdf"></link></linkGroup></publicationMeta><contentMeta><countGroup><count type="figureTotal" number="10"></count><count type="tableTotal" number="4"></count><count type="formulaTotal" number="0"></count><count type="referenceTotal" number="58"></count><count type="wordTotal" number="6563"></count><count type="linksPubMed" number="0"></count><count type="linksCrossRef" number="0"></count></countGroup><titleGroup><title type="main">Bone Graft Healing in Reconstruction of Maxillary Atrophy</title><title type="shortAuthors">Clinical Implant Dentistry and Related Research, Volume *, Number *, 2011</title><title type="short">Bone Graft Healing</title></titleGroup><creators><creator creatorRole="author" xml:id="cr1" affiliationRef="#a1" corresponding="yes"><personName><givenNames>Mats</givenNames><familyName>Sjöström</familyName><degrees>DDS, PhD</degrees></personName></creator><creator creatorRole="author" xml:id="cr2" affiliationRef="#a1 #a2"><personName><givenNames>Lars</givenNames><familyName>Sennerby</familyName><degrees>DDS, PhD</degrees></personName></creator><creator creatorRole="author" xml:id="cr3" affiliationRef="#a1"><personName><givenNames>Stefan</givenNames><familyName>Lundgren</familyName><degrees>DDS, PhD</degrees></personName></creator></creators><affiliationGroup><affiliation xml:id="a1" countryCode="SE"><unparsedAffiliation>Professor, Department of Oral & Maxillofacial Surgery, Umeå University, Umeå, Sweden;</unparsedAffiliation></affiliation><affiliation xml:id="a2" countryCode="SE"><unparsedAffiliation>professor, Department of Biomaterials/Handicap Research Institute for Surgical Sciences, Gothenburg University, Sweden</unparsedAffiliation></affiliation></affiliationGroup><keywordGroup xml:lang="en"><keyword xml:id="k1">autogenous bone graft</keyword><keyword xml:id="k2">bone metabolic factors</keyword><keyword xml:id="k3">bone mineral density</keyword><keyword xml:id="k4">donor bone quality</keyword><keyword xml:id="k5">edentulous atrophic maxilla</keyword><keyword xml:id="k6">graft volume change</keyword><keyword xml:id="k7">implant stability</keyword></keywordGroup><abstractGroup><abstract type="main" xml:lang="en"><title type="main">ABSTRACT</title><p><b>Purpose:</b> Evaluate correlations between volume change for iliac crest bone grafts in maxillary reconstruction (graft volume change [GVC]) and bone mineral density (BMD), bone volume fraction (BVF), hematologic bone metabolic factors (I), and identify indicators of implant failure (II).</p><p><b>Material and Methods:</b> Forty‐six consecutive patients had their edentulous atrophic maxilla reconstructed with free autogenous bone grafts from anterior iliac crest. Endosteal implants were placed 6 months after graft healing. Computer tomography was performed after 3 weeks and 6 months after grafting. Bone biopsies were taken from the internal table of donor site for calculation (BVF), and blood samples were collected. Implant stability was measured at placement with resonance frequency analysis and expressed as implant stability quotient (ISQ). Implant failure was registered.</p><p><b>Results:</b> GVC in onlay bone graft was 37%. The BVF in iliac crest biopsies was 32%. Serum‐IGFBP3 differed with 79% of the samples over normal range. Fifteen patients had one or more implant failures prior to loading (early failures). Forty‐two patients were followed for a minimum of 3 years after implant loading and, in addition, 6/42 patients had one or more implants removed during the follow‐up (late failures). GVC correlated to decreased BMD of lumbar vertebrae L2‐L4 (Kruskal–Wallis test, <i>p</i> = .017). No correlation was found between GVC and hematologic factors (Pearson correlation test) or between GVC and BVF (Kruskal–Wallis test). No correlation was found between ISQ and GVC (Pearson correlation test, <i>p</i> = .865). The association between implant failures and the described factors were evaluated, and no significant correlations were found (unconditional logistic regression).</p><p><b>Conclusion:</b> Onlay bone grafts decrease 37% during initial healing period, which correlate to BMD of lumbar vertebrae L2‐L4. No other evaluated parameters could explain GVC. The evaluated factors could not explain implant failure.</p></abstract></abstractGroup></contentMeta></header></component></istex:document></istex:metadataXml><mods version="3.6"><titleInfo lang="en"><title>Bone Graft Healing in Reconstruction of Maxillary Atrophy</title></titleInfo><titleInfo type="abbreviated" lang="en"><title>Bone Graft Healing</title></titleInfo><titleInfo type="alternative" contentType="CDATA" lang="en"><title>Bone Graft Healing in Reconstruction of Maxillary Atrophy</title></titleInfo><name type="personal"><namePart type="given">Mats</namePart><namePart type="family">Sjöström</namePart><namePart type="termsOfAddress">DDS, PhD</namePart><affiliation>Professor, Department of Oral & Maxillofacial Surgery, Umeå University, Umeå, Sweden;</affiliation><affiliation>E-mail: mats.sjostrom@odont.umu.se</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Lars</namePart><namePart type="family">Sennerby</namePart><namePart type="termsOfAddress">DDS, PhD</namePart><affiliation>Professor, Department of Oral & Maxillofacial Surgery, Umeå University, Umeå, Sweden;</affiliation><affiliation>professor, Department of Biomaterials/Handicap Research Institute for Surgical Sciences, Gothenburg University, Sweden</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Stefan</namePart><namePart type="family">Lundgren</namePart><namePart type="termsOfAddress">DDS, PhD</namePart><affiliation>Professor, Department of Oral & Maxillofacial Surgery, Umeå University, Umeå, 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">2013-06</dateIssued><copyrightDate encoding="w3cdtf">2013</copyrightDate></originInfo><language><languageTerm type="code" authority="rfc3066">en</languageTerm><languageTerm type="code" authority="iso639-2b">eng</languageTerm></language><physicalDescription><extent unit="figures">10</extent><extent unit="tables">4</extent><extent unit="formulas">0</extent><extent unit="references">58</extent><extent unit="linksCrossRef">0</extent><extent unit="words">6563</extent></physicalDescription><abstract>Purpose: Evaluate correlations between volume change for iliac crest bone grafts in maxillary reconstruction (graft volume change [GVC]) and bone mineral density (BMD), bone volume fraction (BVF), hematologic bone metabolic factors (I), and identify indicators of implant failure (II).</abstract><abstract>Material and Methods: Forty‐six consecutive patients had their edentulous atrophic maxilla reconstructed with free autogenous bone grafts from anterior iliac crest. Endosteal implants were placed 6 months after graft healing. Computer tomography was performed after 3 weeks and 6 months after grafting. Bone biopsies were taken from the internal table of donor site for calculation (BVF), and blood samples were collected. Implant stability was measured at placement with resonance frequency analysis and expressed as implant stability quotient (ISQ). Implant failure was registered.</abstract><abstract>Results: GVC in onlay bone graft was 37%. The BVF in iliac crest biopsies was 32%. Serum‐IGFBP3 differed with 79% of the samples over normal range. Fifteen patients had one or more implant failures prior to loading (early failures). Forty‐two patients were followed for a minimum of 3 years after implant loading and, in addition, 6/42 patients had one or more implants removed during the follow‐up (late failures). GVC correlated to decreased BMD of lumbar vertebrae L2‐L4 (Kruskal–Wallis test, p = .017). No correlation was found between GVC and hematologic factors (Pearson correlation test) or between GVC and BVF (Kruskal–Wallis test). No correlation was found between ISQ and GVC (Pearson correlation test, p = .865). The association between implant failures and the described factors were evaluated, and no significant correlations were found (unconditional logistic regression).</abstract><abstract>Conclusion: Onlay bone grafts decrease 37% during initial healing period, which correlate to BMD of lumbar vertebrae L2‐L4. No other evaluated parameters could explain GVC. The evaluated factors could not explain implant failure.</abstract><subject lang="en"><genre>keywords</genre><topic>autogenous bone graft</topic><topic>bone metabolic factors</topic><topic>bone mineral density</topic><topic>donor bone quality</topic><topic>edentulous atrophic maxilla</topic><topic>graft volume change</topic><topic>implant stability</topic></subject><relatedItem type="host"><titleInfo><title>Clinical Implant Dentistry and Related 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><subject><genre>article-category</genre><topic>ARTICLE</topic></subject><identifier type="ISSN">1523-0899</identifier><identifier type="eISSN">1708-8208</identifier><identifier type="DOI">10.1111/(ISSN)1708-8208</identifier><identifier type="PublisherID">CID</identifier><part><date>2013</date><detail type="volume"><caption>vol.</caption><number>15</number></detail><detail type="issue"><caption>no.</caption><number>3</number></detail><extent unit="pages"><start>367</start><end>379</end><total>13</total></extent></part></relatedItem><identifier type="istex">2B0A85BF9759EFC7D77E7669D269E3EF59C38B8D</identifier><identifier type="ark">ark:/67375/WNG-SF6HQK98-H</identifier><identifier type="DOI">10.1111/j.1708-8208.2011.00368.x</identifier><identifier type="ArticleID">CID368</identifier><accessCondition type="use and reproduction" contentType="copyright">Copyright © 2013 Wiley Periodicals, Inc.© 2011 Wiley Periodicals, Inc.</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/2B0A85BF9759EFC7D77E7669D269E3EF59C38B8D/metadata/json</uri></json:item></metadata><serie></serie></istex></record>Pour manipuler ce document sous Unix (Dilib)
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