Maxillary sinus floor elevation surgery with BioOss® mixed with a bone marrow concentrate or autogenous bone: test of principle on implant survival and clinical performance.
Identifieur interne : 000979 ( PubMed/Curation ); précédent : 000978; suivant : 000980Maxillary sinus floor elevation surgery with BioOss® mixed with a bone marrow concentrate or autogenous bone: test of principle on implant survival and clinical performance.
Auteurs : D. Rickert [Pays-Bas] ; A. Vissink [Pays-Bas] ; W J Slot [Pays-Bas] ; S. Sauerbier [Allemagne] ; H J A. Meijer [Pays-Bas] ; G M Raghoebar [Pays-Bas]Source :
- International journal of oral and maxillofacial surgery [ 1399-0020 ] ; 2014.
Descripteurs français
- KwdFr :
- Adulte d'âge moyen, Complications postopératoires (épidémiologie), Céphalométrie, Femelle, Humains, Implants dentaires, Indice de plaque dentaire, Indice parodontal, Minéraux (usage thérapeutique), Mâchoire édentée (), Mâchoire édentée (imagerie diagnostique), Mâle, Méthode en double aveugle, Pose d'implant dentaire endo-osseux (), Péri-implantite (épidémiologie), Radiographie panoramique, Rehaussement du plancher du sinus (), Résultat thérapeutique, Satisfaction du patient, Substituts osseux (usage thérapeutique), Sujet âgé, Transplantation de moelle osseuse, Transplantation osseuse (), Échec de restauration dentaire.
- MESH :
- imagerie diagnostique : Mâchoire édentée.
- usage thérapeutique : Minéraux, Substituts osseux.
- épidémiologie : Complications postopératoires, Péri-implantite.
- Adulte d'âge moyen, Céphalométrie, Femelle, Humains, Implants dentaires, Indice de plaque dentaire, Indice parodontal, Mâchoire édentée, Mâle, Méthode en double aveugle, Pose d'implant dentaire endo-osseux, Radiographie panoramique, Rehaussement du plancher du sinus, Résultat thérapeutique, Satisfaction du patient, Sujet âgé, Transplantation de moelle osseuse, Transplantation osseuse, Échec de restauration dentaire.
English descriptors
- KwdEn :
- Aged, Bone Marrow Transplantation, Bone Substitutes (therapeutic use), Bone Transplantation (methods), Cephalometry, Dental Implantation, Endosseous (methods), Dental Implants, Dental Plaque Index, Dental Restoration Failure, Double-Blind Method, Female, Humans, Jaw, Edentulous (diagnostic imaging), Jaw, Edentulous (surgery), Male, Middle Aged, Minerals (therapeutic use), Patient Satisfaction, Peri-Implantitis (epidemiology), Periodontal Index, Postoperative Complications (epidemiology), Radiography, Panoramic, Sinus Floor Augmentation (methods), Treatment Outcome.
- MESH :
- chemical , therapeutic use : Bone Substitutes, Minerals.
- diagnostic imaging : Jaw, Edentulous.
- epidemiology : Peri-Implantitis, Postoperative Complications.
- methods : Bone Transplantation, Dental Implantation, Endosseous, Sinus Floor Augmentation.
- surgery : Jaw, Edentulous.
- Aged, Bone Marrow Transplantation, Cephalometry, Dental Implants, Dental Plaque Index, Dental Restoration Failure, Double-Blind Method, Female, Humans, Male, Middle Aged, Patient Satisfaction, Periodontal Index, Radiography, Panoramic, Treatment Outcome.
Abstract
The purpose of this study was to assess implant survival and 1-year clinical performance of implants placed in the posterior maxilla that had been subjected to maxillary sinus floor elevation surgery with bovine bone mineral (BioOss®) mixed with autogenous bone marrow concentrate or autogenous bone. In a randomized, controlled, split-mouth design study, a bilateral sinus floor augmentation procedure was performed in 12 edentulous patients. At random, one side was treated with BioOss® seeded with an iliac crest bone marrow concentrate enriched in mesenchymal stem cells (test side) and the other with BioOss® mixed with autogenous bone (control side). Three to four months after augmentation, 66 implants were placed. Implant survival, plaque, gingival, and bleeding indices, probing depth, and peri-implant radiographic bone levels were assessed at baseline and 12 months after functional loading. During osseointegration, three implants failed on the test side (two patients) and no implants failed on the control side, resulting in 3-month survival rates of 91% and 100%, respectively. No implants were lost after functional loading and no differences in soft tissue parameters or peri-implant bone loss were observed between the control and test sides. After 1 year in function, no clinically relevant differences were observed regarding soft tissue parameters or peri-implant bone loss.
DOI: 10.1016/j.ijom.2013.09.006
PubMed: 24183511
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Electronic address: a.vissink@umcg.nl.</nlm:affiliation><country xml:lang="fr">Pays-Bas</country><wicri:regionArea>Department of Oral and Maxillofacial Surgery, University Medical Center Groningen, Groningen</wicri:regionArea></affiliation></author><author><name sortKey="Slot, W J" sort="Slot, W J" uniqKey="Slot W" first="W J" last="Slot">W J Slot</name><affiliation wicri:level="1"><nlm:affiliation>Department of Oral and Maxillofacial Surgery, University Medical Center Groningen, Groningen, The Netherlands; Department of Prosthodontics, Academic Center for Oral Health, University Medical Center Groningen, Groningen, The Netherlands.</nlm:affiliation><country xml:lang="fr">Pays-Bas</country><wicri:regionArea>Department of Oral and Maxillofacial Surgery, University Medical Center Groningen, Groningen, The Netherlands; Department of Prosthodontics, Academic Center for Oral Health, University Medical Center Groningen, Groningen</wicri:regionArea></affiliation></author><author><name sortKey="Sauerbier, S" sort="Sauerbier, S" uniqKey="Sauerbier S" first="S" last="Sauerbier">S. 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xml:lang="fr">Pays-Bas</country><wicri:regionArea>Department of Oral and Maxillofacial Surgery, University Medical Center Groningen, Groningen</wicri:regionArea></affiliation></author></analytic><series><title level="j">International journal of oral and maxillofacial surgery</title><idno type="eISSN">1399-0020</idno><imprint><date when="2014" type="published">2014</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Aged</term><term>Bone Marrow Transplantation</term><term>Bone Substitutes (therapeutic use)</term><term>Bone Transplantation (methods)</term><term>Cephalometry</term><term>Dental Implantation, Endosseous (methods)</term><term>Dental Implants</term><term>Dental Plaque Index</term><term>Dental Restoration Failure</term><term>Double-Blind Method</term><term>Female</term><term>Humans</term><term>Jaw, Edentulous (diagnostic imaging)</term><term>Jaw, Edentulous (surgery)</term><term>Male</term><term>Middle Aged</term><term>Minerals (therapeutic use)</term><term>Patient Satisfaction</term><term>Peri-Implantitis (epidemiology)</term><term>Periodontal Index</term><term>Postoperative Complications (epidemiology)</term><term>Radiography, Panoramic</term><term>Sinus Floor Augmentation (methods)</term><term>Treatment Outcome</term></keywords><keywords scheme="KwdFr" xml:lang="fr"><term>Adulte d'âge moyen</term><term>Complications postopératoires (épidémiologie)</term><term>Céphalométrie</term><term>Femelle</term><term>Humains</term><term>Implants dentaires</term><term>Indice de plaque dentaire</term><term>Indice parodontal</term><term>Minéraux (usage thérapeutique)</term><term>Mâchoire édentée ()</term><term>Mâchoire édentée (imagerie diagnostique)</term><term>Mâle</term><term>Méthode en double aveugle</term><term>Pose d'implant dentaire endo-osseux ()</term><term>Péri-implantite (épidémiologie)</term><term>Radiographie panoramique</term><term>Rehaussement du plancher du sinus ()</term><term>Résultat thérapeutique</term><term>Satisfaction du patient</term><term>Substituts osseux (usage thérapeutique)</term><term>Sujet âgé</term><term>Transplantation de moelle osseuse</term><term>Transplantation osseuse ()</term><term>Échec de restauration dentaire</term></keywords><keywords scheme="MESH" type="chemical" qualifier="therapeutic use" xml:lang="en"><term>Bone Substitutes</term><term>Minerals</term></keywords><keywords scheme="MESH" qualifier="diagnostic imaging" xml:lang="en"><term>Jaw, Edentulous</term></keywords><keywords scheme="MESH" qualifier="epidemiology" xml:lang="en"><term>Peri-Implantitis</term><term>Postoperative Complications</term></keywords><keywords scheme="MESH" qualifier="imagerie diagnostique" xml:lang="fr"><term>Mâchoire édentée</term></keywords><keywords scheme="MESH" qualifier="methods" xml:lang="en"><term>Bone Transplantation</term><term>Dental Implantation, Endosseous</term><term>Sinus Floor Augmentation</term></keywords><keywords scheme="MESH" qualifier="surgery" xml:lang="en"><term>Jaw, Edentulous</term></keywords><keywords scheme="MESH" qualifier="usage thérapeutique" xml:lang="fr"><term>Minéraux</term><term>Substituts osseux</term></keywords><keywords scheme="MESH" qualifier="épidémiologie" xml:lang="fr"><term>Complications postopératoires</term><term>Péri-implantite</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Aged</term><term>Bone Marrow Transplantation</term><term>Cephalometry</term><term>Dental Implants</term><term>Dental Plaque Index</term><term>Dental Restoration Failure</term><term>Double-Blind Method</term><term>Female</term><term>Humans</term><term>Male</term><term>Middle Aged</term><term>Patient Satisfaction</term><term>Periodontal Index</term><term>Radiography, Panoramic</term><term>Treatment Outcome</term></keywords><keywords scheme="MESH" xml:lang="fr"><term>Adulte d'âge moyen</term><term>Céphalométrie</term><term>Femelle</term><term>Humains</term><term>Implants dentaires</term><term>Indice de plaque dentaire</term><term>Indice parodontal</term><term>Mâchoire édentée</term><term>Mâle</term><term>Méthode en double aveugle</term><term>Pose d'implant dentaire endo-osseux</term><term>Radiographie panoramique</term><term>Rehaussement du plancher du sinus</term><term>Résultat thérapeutique</term><term>Satisfaction du patient</term><term>Sujet âgé</term><term>Transplantation de moelle osseuse</term><term>Transplantation osseuse</term><term>Échec de restauration dentaire</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">The purpose of this study was to assess implant survival and 1-year clinical performance of implants placed in the posterior maxilla that had been subjected to maxillary sinus floor elevation surgery with bovine bone mineral (BioOss®) mixed with autogenous bone marrow concentrate or autogenous bone. In a randomized, controlled, split-mouth design study, a bilateral sinus floor augmentation procedure was performed in 12 edentulous patients. At random, one side was treated with BioOss® seeded with an iliac crest bone marrow concentrate enriched in mesenchymal stem cells (test side) and the other with BioOss® mixed with autogenous bone (control side). Three to four months after augmentation, 66 implants were placed. Implant survival, plaque, gingival, and bleeding indices, probing depth, and peri-implant radiographic bone levels were assessed at baseline and 12 months after functional loading. During osseointegration, three implants failed on the test side (two patients) and no implants failed on the control side, resulting in 3-month survival rates of 91% and 100%, respectively. No implants were lost after functional loading and no differences in soft tissue parameters or peri-implant bone loss were observed between the control and test sides. After 1 year in function, no clinically relevant differences were observed regarding soft tissue parameters or peri-implant bone loss.</div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">24183511</PMID><DateCompleted><Year>2014</Year><Month>11</Month><Day>04</Day></DateCompleted><DateRevised><Year>2016</Year><Month>11</Month><Day>25</Day></DateRevised><Article PubModel="Print-Electronic"><Journal><ISSN IssnType="Electronic">1399-0020</ISSN><JournalIssue CitedMedium="Internet"><Volume>43</Volume><Issue>2</Issue><PubDate><Year>2014</Year><Month>Feb</Month></PubDate></JournalIssue><Title>International journal of oral and maxillofacial surgery</Title><ISOAbbreviation>Int J Oral Maxillofac Surg</ISOAbbreviation></Journal><ArticleTitle>Maxillary sinus floor elevation surgery with BioOss® mixed with a bone marrow concentrate or autogenous bone: test of principle on implant survival and clinical performance.</ArticleTitle><Pagination><MedlinePgn>243-7</MedlinePgn></Pagination><ELocationID EIdType="doi" ValidYN="Y">10.1016/j.ijom.2013.09.006</ELocationID><ELocationID EIdType="pii" ValidYN="Y">S0901-5027(13)01091-6</ELocationID><Abstract><AbstractText>The purpose of this study was to assess implant survival and 1-year clinical performance of implants placed in the posterior maxilla that had been subjected to maxillary sinus floor elevation surgery with bovine bone mineral (BioOss®) mixed with autogenous bone marrow concentrate or autogenous bone. In a randomized, controlled, split-mouth design study, a bilateral sinus floor augmentation procedure was performed in 12 edentulous patients. At random, one side was treated with BioOss® seeded with an iliac crest bone marrow concentrate enriched in mesenchymal stem cells (test side) and the other with BioOss® mixed with autogenous bone (control side). Three to four months after augmentation, 66 implants were placed. Implant survival, plaque, gingival, and bleeding indices, probing depth, and peri-implant radiographic bone levels were assessed at baseline and 12 months after functional loading. During osseointegration, three implants failed on the test side (two patients) and no implants failed on the control side, resulting in 3-month survival rates of 91% and 100%, respectively. No implants were lost after functional loading and no differences in soft tissue parameters or peri-implant bone loss were observed between the control and test sides. After 1 year in function, no clinically relevant differences were observed regarding soft tissue parameters or peri-implant bone loss.</AbstractText><CopyrightInformation>Copyright © 2013 International Association of Oral and Maxillofacial Surgeons. Published by Elsevier Ltd. All rights reserved.</CopyrightInformation></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Rickert</LastName><ForeName>D</ForeName><Initials>D</Initials><AffiliationInfo><Affiliation>Department of Oral and Maxillofacial Surgery, University Medical Center Groningen, Groningen, The Netherlands.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Vissink</LastName><ForeName>A</ForeName><Initials>A</Initials><AffiliationInfo><Affiliation>Department of Oral and Maxillofacial Surgery, University Medical Center Groningen, Groningen, The Netherlands. Electronic address: a.vissink@umcg.nl.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Slot</LastName><ForeName>W J</ForeName><Initials>WJ</Initials><AffiliationInfo><Affiliation>Department of Oral and Maxillofacial Surgery, University Medical Center Groningen, Groningen, The Netherlands; Department of Prosthodontics, Academic Center for Oral Health, University Medical Center Groningen, Groningen, The Netherlands.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Sauerbier</LastName><ForeName>S</ForeName><Initials>S</Initials><AffiliationInfo><Affiliation>Department of Oral and Craniomaxillofacial Surgery, University Hospital Freiburg, Freiburg, Germany.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Meijer</LastName><ForeName>H J A</ForeName><Initials>HJ</Initials><AffiliationInfo><Affiliation>Department of Oral and Maxillofacial Surgery, University Medical Center Groningen, Groningen, The Netherlands; Department of Prosthodontics, Academic Center for Oral Health, University Medical Center Groningen, Groningen, The Netherlands.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Raghoebar</LastName><ForeName>G M</ForeName><Initials>GM</Initials><AffiliationInfo><Affiliation>Department of Oral and Maxillofacial Surgery, University Medical Center Groningen, Groningen, The Netherlands.</Affiliation></AffiliationInfo></Author></AuthorList><Language>eng</Language><PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType><PublicationType UI="D016449">Randomized Controlled Trial</PublicationType><PublicationType UI="D013485">Research Support, Non-U.S. Gov't</PublicationType></PublicationTypeList><ArticleDate DateType="Electronic"><Year>2013</Year><Month>10</Month><Day>30</Day></ArticleDate></Article><MedlineJournalInfo><Country>Denmark</Country><MedlineTA>Int J Oral Maxillofac Surg</MedlineTA><NlmUniqueID>8605826</NlmUniqueID><ISSNLinking>0901-5027</ISSNLinking></MedlineJournalInfo><ChemicalList><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="C077540">Bio-Oss</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D018786">Bone Substitutes</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D015921">Dental Implants</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D008903">Minerals</NameOfSubstance></Chemical></ChemicalList><CitationSubset>D</CitationSubset><CitationSubset>IM</CitationSubset><MeshHeadingList><MeshHeading><DescriptorName UI="D000368" MajorTopicYN="N">Aged</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D016026" MajorTopicYN="N">Bone Marrow Transplantation</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D018786" MajorTopicYN="N">Bone Substitutes</DescriptorName><QualifierName UI="Q000627" MajorTopicYN="Y">therapeutic use</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D016025" MajorTopicYN="N">Bone Transplantation</DescriptorName><QualifierName UI="Q000379" MajorTopicYN="Y">methods</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D002508" MajorTopicYN="N">Cephalometry</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D003758" MajorTopicYN="N">Dental Implantation, Endosseous</DescriptorName><QualifierName UI="Q000379" MajorTopicYN="Y">methods</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D015921" MajorTopicYN="Y">Dental Implants</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D003774" MajorTopicYN="N">Dental Plaque Index</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D019232" MajorTopicYN="N">Dental Restoration Failure</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D004311" MajorTopicYN="N">Double-Blind Method</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D005260" MajorTopicYN="N">Female</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D006801" MajorTopicYN="N">Humans</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D007575" MajorTopicYN="N">Jaw, Edentulous</DescriptorName><QualifierName UI="Q000000981" MajorTopicYN="N">diagnostic imaging</QualifierName><QualifierName UI="Q000601" MajorTopicYN="Y">surgery</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D008297" MajorTopicYN="N">Male</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D008875" MajorTopicYN="N">Middle Aged</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D008903" MajorTopicYN="N">Minerals</DescriptorName><QualifierName UI="Q000627" MajorTopicYN="Y">therapeutic use</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D017060" MajorTopicYN="N">Patient Satisfaction</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D057873" MajorTopicYN="N">Peri-Implantitis</DescriptorName><QualifierName UI="Q000453" MajorTopicYN="N">epidemiology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D010512" MajorTopicYN="N">Periodontal Index</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D011183" MajorTopicYN="N">Postoperative Complications</DescriptorName><QualifierName UI="Q000453" MajorTopicYN="N">epidemiology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D011862" MajorTopicYN="N">Radiography, Panoramic</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D059546" MajorTopicYN="N">Sinus Floor Augmentation</DescriptorName><QualifierName UI="Q000379" MajorTopicYN="Y">methods</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D016896" MajorTopicYN="N">Treatment Outcome</DescriptorName></MeshHeading></MeshHeadingList><KeywordList Owner="NOTNLM"><Keyword MajorTopicYN="N">autogenous bone</Keyword><Keyword MajorTopicYN="N">bone marrow concentrate</Keyword><Keyword MajorTopicYN="N">dental implants</Keyword><Keyword MajorTopicYN="N">maxillary sinus floor elevation</Keyword></KeywordList></MedlineCitation><PubmedData><History><PubMedPubDate PubStatus="received"><Year>2013</Year><Month>01</Month><Day>30</Day></PubMedPubDate><PubMedPubDate PubStatus="revised"><Year>2013</Year><Month>07</Month><Day>01</Day></PubMedPubDate><PubMedPubDate PubStatus="accepted"><Year>2013</Year><Month>09</Month><Day>10</Day></PubMedPubDate><PubMedPubDate PubStatus="entrez"><Year>2013</Year><Month>11</Month><Day>5</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="pubmed"><Year>2013</Year><Month>11</Month><Day>5</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="medline"><Year>2014</Year><Month>11</Month><Day>5</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate></History><PublicationStatus>ppublish</PublicationStatus><ArticleIdList><ArticleId IdType="pubmed">24183511</ArticleId><ArticleId IdType="pii">S0901-5027(13)01091-6</ArticleId><ArticleId IdType="doi">10.1016/j.ijom.2013.09.006</ArticleId></ArticleIdList></PubmedData></pubmed></record>Pour manipuler ce document sous Unix (Dilib)
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|texte= Maxillary sinus floor elevation surgery with BioOss® mixed with a bone marrow concentrate or autogenous bone: test of principle on implant survival and clinical performance.
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