Sinus lift with guided bone regeneration or anorganic bovine bone: 1-year post-loading results of a pilot randomised clinical trial.
Identifieur interne : 001A80 ( PubMed/Corpus ); précédent : 001A79; suivant : 001A81Sinus lift with guided bone regeneration or anorganic bovine bone: 1-year post-loading results of a pilot randomised clinical trial.
Auteurs : Marco Esposito ; Maurizio Piattelli ; Roberto Pistilli ; Gerardo Pellegrino ; Pietro FeliceSource :
- European journal of oral implantology [ 1756-2406 ] ; 2010.
English descriptors
- KwdEn :
- Absorbable Implants, Adult, Alveolar Bone Loss (etiology), Alveolar Ridge Augmentation (methods), Bone Matrix (transplantation), Bone Substitutes (therapeutic use), Dental Implantation, Endosseous, Dental Implants, Dental Prosthesis, Implant-Supported, Dental Restoration Failure, Denture, Partial, Temporary, Female, Follow-Up Studies, Guided Tissue Regeneration, Periodontal (instrumentation), Guided Tissue Regeneration, Periodontal (methods), Humans, Iatrogenic Disease, Jaw, Edentulous, Partially (rehabilitation), Jaw, Edentulous, Partially (surgery), Male, Maxilla (surgery), Maxillary Sinus (surgery), Membranes, Artificial, Metal Ceramic Alloys (chemistry), Middle Aged, Minerals (therapeutic use), Mucous Membrane (injuries), Periodontitis (etiology), Pilot Projects, Postoperative Complications, Treatment Outcome.
- MESH :
- chemical , chemistry : Metal Ceramic Alloys.
- chemical , therapeutic use : Bone Substitutes, Minerals.
- etiology : Alveolar Bone Loss, Periodontitis.
- injuries : Mucous Membrane.
- instrumentation : Guided Tissue Regeneration, Periodontal.
- methods : Alveolar Ridge Augmentation, Guided Tissue Regeneration, Periodontal.
- rehabilitation : Jaw, Edentulous, Partially.
- surgery : Jaw, Edentulous, Partially, Maxilla, Maxillary Sinus.
- transplantation : Bone Matrix.
- Absorbable Implants, Adult, Dental Implantation, Endosseous, Dental Implants, Dental Prosthesis, Implant-Supported, Dental Restoration Failure, Denture, Partial, Temporary, Female, Follow-Up Studies, Humans, Iatrogenic Disease, Male, Membranes, Artificial, Middle Aged, Pilot Projects, Postoperative Complications, Treatment Outcome.
Abstract
To compare the efficacy of two different techniques for maintaining the space beneath a maxillary lining lifted using a lateral window approach: rigid synthetic resorbable barriers versus granular anorganic bovine bone.
PubMed: 21180682
Links to Exploration step
pubmed:21180682Le document en format XML
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<author><name sortKey="Esposito, Marco" sort="Esposito, Marco" uniqKey="Esposito M" first="Marco" last="Esposito">Marco Esposito</name>
<affiliation><nlm:affiliation>Department of Biomaterials, The Sahlgrenska Academy at Göteborg University, Sweden. espositomarco@hotmail.com</nlm:affiliation>
</affiliation>
</author>
<author><name sortKey="Piattelli, Maurizio" sort="Piattelli, Maurizio" uniqKey="Piattelli M" first="Maurizio" last="Piattelli">Maurizio Piattelli</name>
</author>
<author><name sortKey="Pistilli, Roberto" sort="Pistilli, Roberto" uniqKey="Pistilli R" first="Roberto" last="Pistilli">Roberto Pistilli</name>
</author>
<author><name sortKey="Pellegrino, Gerardo" sort="Pellegrino, Gerardo" uniqKey="Pellegrino G" first="Gerardo" last="Pellegrino">Gerardo Pellegrino</name>
</author>
<author><name sortKey="Felice, Pietro" sort="Felice, Pietro" uniqKey="Felice P" first="Pietro" last="Felice">Pietro Felice</name>
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<sourceDesc><biblStruct><analytic><title xml:lang="en">Sinus lift with guided bone regeneration or anorganic bovine bone: 1-year post-loading results of a pilot randomised clinical trial.</title>
<author><name sortKey="Esposito, Marco" sort="Esposito, Marco" uniqKey="Esposito M" first="Marco" last="Esposito">Marco Esposito</name>
<affiliation><nlm:affiliation>Department of Biomaterials, The Sahlgrenska Academy at Göteborg University, Sweden. espositomarco@hotmail.com</nlm:affiliation>
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<author><name sortKey="Piattelli, Maurizio" sort="Piattelli, Maurizio" uniqKey="Piattelli M" first="Maurizio" last="Piattelli">Maurizio Piattelli</name>
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<author><name sortKey="Pistilli, Roberto" sort="Pistilli, Roberto" uniqKey="Pistilli R" first="Roberto" last="Pistilli">Roberto Pistilli</name>
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<author><name sortKey="Pellegrino, Gerardo" sort="Pellegrino, Gerardo" uniqKey="Pellegrino G" first="Gerardo" last="Pellegrino">Gerardo Pellegrino</name>
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<author><name sortKey="Felice, Pietro" sort="Felice, Pietro" uniqKey="Felice P" first="Pietro" last="Felice">Pietro Felice</name>
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<series><title level="j">European journal of oral implantology</title>
<idno type="ISSN">1756-2406</idno>
<imprint><date when="2010" type="published">2010</date>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Absorbable Implants</term>
<term>Adult</term>
<term>Alveolar Bone Loss (etiology)</term>
<term>Alveolar Ridge Augmentation (methods)</term>
<term>Bone Matrix (transplantation)</term>
<term>Bone Substitutes (therapeutic use)</term>
<term>Dental Implantation, Endosseous</term>
<term>Dental Implants</term>
<term>Dental Prosthesis, Implant-Supported</term>
<term>Dental Restoration Failure</term>
<term>Denture, Partial, Temporary</term>
<term>Female</term>
<term>Follow-Up Studies</term>
<term>Guided Tissue Regeneration, Periodontal (instrumentation)</term>
<term>Guided Tissue Regeneration, Periodontal (methods)</term>
<term>Humans</term>
<term>Iatrogenic Disease</term>
<term>Jaw, Edentulous, Partially (rehabilitation)</term>
<term>Jaw, Edentulous, Partially (surgery)</term>
<term>Male</term>
<term>Maxilla (surgery)</term>
<term>Maxillary Sinus (surgery)</term>
<term>Membranes, Artificial</term>
<term>Metal Ceramic Alloys (chemistry)</term>
<term>Middle Aged</term>
<term>Minerals (therapeutic use)</term>
<term>Mucous Membrane (injuries)</term>
<term>Periodontitis (etiology)</term>
<term>Pilot Projects</term>
<term>Postoperative Complications</term>
<term>Treatment Outcome</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="chemistry" xml:lang="en"><term>Metal Ceramic Alloys</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="etiology" xml:lang="en"><term>Alveolar Bone Loss</term>
<term>Periodontitis</term>
</keywords>
<keywords scheme="MESH" qualifier="injuries" xml:lang="en"><term>Mucous Membrane</term>
</keywords>
<keywords scheme="MESH" qualifier="instrumentation" xml:lang="en"><term>Guided Tissue Regeneration, Periodontal</term>
</keywords>
<keywords scheme="MESH" qualifier="methods" xml:lang="en"><term>Alveolar Ridge Augmentation</term>
<term>Guided Tissue Regeneration, Periodontal</term>
</keywords>
<keywords scheme="MESH" qualifier="rehabilitation" xml:lang="en"><term>Jaw, Edentulous, Partially</term>
</keywords>
<keywords scheme="MESH" qualifier="surgery" xml:lang="en"><term>Jaw, Edentulous, Partially</term>
<term>Maxilla</term>
<term>Maxillary Sinus</term>
</keywords>
<keywords scheme="MESH" qualifier="transplantation" xml:lang="en"><term>Bone Matrix</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Absorbable Implants</term>
<term>Adult</term>
<term>Dental Implantation, Endosseous</term>
<term>Dental Implants</term>
<term>Dental Prosthesis, Implant-Supported</term>
<term>Dental Restoration Failure</term>
<term>Denture, Partial, Temporary</term>
<term>Female</term>
<term>Follow-Up Studies</term>
<term>Humans</term>
<term>Iatrogenic Disease</term>
<term>Male</term>
<term>Membranes, Artificial</term>
<term>Middle Aged</term>
<term>Pilot Projects</term>
<term>Postoperative Complications</term>
<term>Treatment Outcome</term>
</keywords>
</textClass>
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<front><div type="abstract" xml:lang="en">To compare the efficacy of two different techniques for maintaining the space beneath a maxillary lining lifted using a lateral window approach: rigid synthetic resorbable barriers versus granular anorganic bovine bone.</div>
</front>
</TEI>
<pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">21180682</PMID>
<DateCompleted><Year>2011</Year>
<Month>03</Month>
<Day>24</Day>
</DateCompleted>
<DateRevised><Year>2010</Year>
<Month>12</Month>
<Day>24</Day>
</DateRevised>
<Article PubModel="Print"><Journal><ISSN IssnType="Print">1756-2406</ISSN>
<JournalIssue CitedMedium="Print"><Volume>3</Volume>
<Issue>4</Issue>
<PubDate><Year>2010</Year>
<Season>Winter</Season>
</PubDate>
</JournalIssue>
<Title>European journal of oral implantology</Title>
<ISOAbbreviation>Eur J Oral Implantol</ISOAbbreviation>
</Journal>
<ArticleTitle>Sinus lift with guided bone regeneration or anorganic bovine bone: 1-year post-loading results of a pilot randomised clinical trial.</ArticleTitle>
<Pagination><MedlinePgn>297-305</MedlinePgn>
</Pagination>
<Abstract><AbstractText Label="PURPOSE" NlmCategory="OBJECTIVE">To compare the efficacy of two different techniques for maintaining the space beneath a maxillary lining lifted using a lateral window approach: rigid synthetic resorbable barriers versus granular anorganic bovine bone.</AbstractText>
<AbstractText Label="MATERIALS AND METHODS" NlmCategory="METHODS">Ten partially edentulous patients having bilaterally 1 to 5 mm of residual bone height and at least 5 mm bone width below the maxillary sinuses, were randomised in a split-mouth study design, to receive a rigid Inion GTR Biodegradable Membrane System barrier without any graft on one side and 100% loosely packed granular Bio-Oss on the contralateral side following a lateral window, two-stage, sinus lift procedure. After 6 months, two or three implants were inserted at each side and submerged for 4 months. Implants were loaded with provisional acrylic prostheses and replaced, after 4 months, by definitive metal-ceramic prostheses cemented with provisional cement. Outcome measures were implant and prosthetic failures, any complication and peri-implant marginal bone level changes assessed by a blinded outcome assessor. All patients were followed up to 1 year after loading.</AbstractText>
<AbstractText Label="RESULTS" NlmCategory="RESULTS">One patient dropped out after implant placement. One distal implant failed at the Inion side just before delivery of the definitive prosthesis, which was cut and maintained as a single crown. Four complications occurred in three patients at Inion sites (two sinus lining perforations, one fracture of the ceramic cusp of the definitive prosthesis, one iatrogenic peri-implantitis) versus two complications at Bio-Oss sites (one sinus lining perforation and one iatrogenic peri-implantitis). There were no differences for failures or complications between groups; however, in one of the patients where a perforation occurred at the Inion site, at implant placement, the sinus was filled two-thirds with soft tissue and the site was retreated with Bio-Oss. There were no statistically significant differences in bone loss between groups. One year after loading, Inion sides lost an average of 1.5 mm of periimplant bone and Bio-Oss sides about 1.7 mm.</AbstractText>
<AbstractText Label="CONCLUSIONS" NlmCategory="CONCLUSIONS">A bone graft may not be needed to augment atrophic maxillary sinuses since it is sufficient to keep space with a rigid barrier; however, it may be simpler to fill sinuses with a bone substitute than positioning a rigid barrier to maintain space.</AbstractText>
</Abstract>
<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Esposito</LastName>
<ForeName>Marco</ForeName>
<Initials>M</Initials>
<AffiliationInfo><Affiliation>Department of Biomaterials, The Sahlgrenska Academy at Göteborg University, Sweden. espositomarco@hotmail.com</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Piattelli</LastName>
<ForeName>Maurizio</ForeName>
<Initials>M</Initials>
</Author>
<Author ValidYN="Y"><LastName>Pistilli</LastName>
<ForeName>Roberto</ForeName>
<Initials>R</Initials>
</Author>
<Author ValidYN="Y"><LastName>Pellegrino</LastName>
<ForeName>Gerardo</ForeName>
<Initials>G</Initials>
</Author>
<Author ValidYN="Y"><LastName>Felice</LastName>
<ForeName>Pietro</ForeName>
<Initials>P</Initials>
</Author>
</AuthorList>
<Language>eng</Language>
<PublicationTypeList><PublicationType UI="D003160">Comparative Study</PublicationType>
<PublicationType UI="D016428">Journal Article</PublicationType>
<PublicationType UI="D016449">Randomized Controlled Trial</PublicationType>
<PublicationType UI="D013485">Research Support, Non-U.S. Gov't</PublicationType>
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<MedlineJournalInfo><Country>England</Country>
<MedlineTA>Eur J Oral Implantol</MedlineTA>
<NlmUniqueID>101473719</NlmUniqueID>
<ISSNLinking>1756-2406</ISSNLinking>
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<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="D008567">Membranes, Artificial</NameOfSubstance>
</Chemical>
<Chemical><RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="D016876">Metal Ceramic Alloys</NameOfSubstance>
</Chemical>
<Chemical><RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="D008903">Minerals</NameOfSubstance>
</Chemical>
</ChemicalList>
<CitationSubset>D</CitationSubset>
<CitationSubset>IM</CitationSubset>
<MeshHeadingList><MeshHeading><DescriptorName UI="D020341" MajorTopicYN="N">Absorbable Implants</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D000328" MajorTopicYN="N">Adult</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D016301" MajorTopicYN="N">Alveolar Bone Loss</DescriptorName>
<QualifierName UI="Q000209" MajorTopicYN="N">etiology</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D000540" MajorTopicYN="N">Alveolar Ridge Augmentation</DescriptorName>
<QualifierName UI="Q000379" MajorTopicYN="Y">methods</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D001857" MajorTopicYN="N">Bone Matrix</DescriptorName>
<QualifierName UI="Q000637" MajorTopicYN="Y">transplantation</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D018786" MajorTopicYN="N">Bone Substitutes</DescriptorName>
<QualifierName UI="Q000627" MajorTopicYN="Y">therapeutic use</QualifierName>
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<MeshHeading><DescriptorName UI="D003758" MajorTopicYN="N">Dental Implantation, Endosseous</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D015921" MajorTopicYN="N">Dental Implants</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D019094" MajorTopicYN="N">Dental Prosthesis, Implant-Supported</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D019232" MajorTopicYN="N">Dental Restoration Failure</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D003833" MajorTopicYN="N">Denture, Partial, Temporary</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D005260" MajorTopicYN="N">Female</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D005500" MajorTopicYN="N">Follow-Up Studies</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D016557" MajorTopicYN="N">Guided Tissue Regeneration, Periodontal</DescriptorName>
<QualifierName UI="Q000295" MajorTopicYN="N">instrumentation</QualifierName>
<QualifierName UI="Q000379" MajorTopicYN="Y">methods</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D006801" MajorTopicYN="N">Humans</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D007049" MajorTopicYN="N">Iatrogenic Disease</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D007576" MajorTopicYN="N">Jaw, Edentulous, Partially</DescriptorName>
<QualifierName UI="Q000534" MajorTopicYN="N">rehabilitation</QualifierName>
<QualifierName UI="Q000601" MajorTopicYN="N">surgery</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D008297" MajorTopicYN="N">Male</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D008437" MajorTopicYN="N">Maxilla</DescriptorName>
<QualifierName UI="Q000601" MajorTopicYN="Y">surgery</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D008443" MajorTopicYN="N">Maxillary Sinus</DescriptorName>
<QualifierName UI="Q000601" MajorTopicYN="Y">surgery</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D008567" MajorTopicYN="N">Membranes, Artificial</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D016876" MajorTopicYN="N">Metal Ceramic Alloys</DescriptorName>
<QualifierName UI="Q000737" MajorTopicYN="N">chemistry</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D008875" MajorTopicYN="N">Middle Aged</DescriptorName>
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<QualifierName UI="Q000627" MajorTopicYN="N">therapeutic use</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D009092" MajorTopicYN="N">Mucous Membrane</DescriptorName>
<QualifierName UI="Q000293" MajorTopicYN="N">injuries</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D010518" MajorTopicYN="N">Periodontitis</DescriptorName>
<QualifierName UI="Q000209" MajorTopicYN="N">etiology</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D010865" MajorTopicYN="N">Pilot Projects</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D011183" MajorTopicYN="N">Postoperative Complications</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D016896" MajorTopicYN="N">Treatment Outcome</DescriptorName>
</MeshHeading>
</MeshHeadingList>
</MedlineCitation>
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