Using soft vinyl stents to facilitate augmentation of maxillary anterior atrophic ridges with hydroxyapatite.
Identifieur interne : 005300 ( PubMed/Corpus ); précédent : 005299; suivant : 005301Using soft vinyl stents to facilitate augmentation of maxillary anterior atrophic ridges with hydroxyapatite.
Auteurs : C P Torres ; L M Shimoda ; A F ShernoffSource :
- The Journal of prosthetic dentistry [ 0022-3913 ] ; 1986.
English descriptors
- KwdEn :
- Alveolar Ridge Augmentation (instrumentation), Alveolar Ridge Augmentation (methods), Alveoloplasty (instrumentation), Atrophy, Bone Resorption (surgery), Durapatite, Equipment Design, Humans, Hydroxyapatites, Jaw, Edentulous (surgery), Maxilla (pathology), Maxilla (surgery), Oral Surgical Procedures, Preprosthetic (instrumentation), Prostheses and Implants, Vinyl Compounds.
- MESH :
- chemical : Durapatite, Hydroxyapatites, Vinyl Compounds.
- instrumentation : Alveolar Ridge Augmentation, Alveoloplasty, Oral Surgical Procedures, Preprosthetic.
- methods : Alveolar Ridge Augmentation.
- pathology : Maxilla.
- surgery : Bone Resorption, Jaw, Edentulous, Maxilla.
- Atrophy, Equipment Design, Humans, Prostheses and Implants.
Abstract
A technique has been described for fabrication of a surgical template made of soft vinyl mouthguard material. Use of this stent at the time of surgery can be of great value to the oral surgeon and the prosthodontist. The risk of excessive augmentation and migration of the particulate hydroxyapatite to an undesired area will be minimized if the stent is used as a matrix. Uniform results in size and form of the ridge can be obtained from the surgical procedure when the stent is used. The denture-bearing area of the maxillary anterior ridge will improve significantly, enabling the dentist to make a maxillary complete denture.
PubMed: 3018237
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Use of this stent at the time of surgery can be of great value to the oral surgeon and the prosthodontist. The risk of excessive augmentation and migration of the particulate hydroxyapatite to an undesired area will be minimized if the stent is used as a matrix. Uniform results in size and form of the ridge can be obtained from the surgical procedure when the stent is used. The denture-bearing area of the maxillary anterior ridge will improve significantly, enabling the dentist to make a maxillary complete denture.</div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">3018237</PMID><DateCompleted><Year>1986</Year><Month>10</Month><Day>21</Day></DateCompleted><DateRevised><Year>2013</Year><Month>11</Month><Day>21</Day></DateRevised><Article PubModel="Print"><Journal><ISSN IssnType="Print">0022-3913</ISSN><JournalIssue CitedMedium="Print"><Volume>56</Volume><Issue>3</Issue><PubDate><Year>1986</Year><Month>Sep</Month></PubDate></JournalIssue><Title>The Journal of prosthetic dentistry</Title><ISOAbbreviation>J Prosthet Dent</ISOAbbreviation></Journal><ArticleTitle>Using soft vinyl stents to facilitate augmentation of maxillary anterior atrophic ridges with hydroxyapatite.</ArticleTitle><Pagination><MedlinePgn>326-9</MedlinePgn></Pagination><Abstract><AbstractText>A technique has been described for fabrication of a surgical template made of soft vinyl mouthguard material. Use of this stent at the time of surgery can be of great value to the oral surgeon and the prosthodontist. The risk of excessive augmentation and migration of the particulate hydroxyapatite to an undesired area will be minimized if the stent is used as a matrix. Uniform results in size and form of the ridge can be obtained from the surgical procedure when the stent is used. The denture-bearing area of the maxillary anterior ridge will improve significantly, enabling the dentist to make a maxillary complete denture.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Torres</LastName><ForeName>C P</ForeName><Initials>CP</Initials></Author><Author ValidYN="Y"><LastName>Shimoda</LastName><ForeName>L M</ForeName><Initials>LM</Initials></Author><Author ValidYN="Y"><LastName>Shernoff</LastName><ForeName>A F</ForeName><Initials>AF</Initials></Author></AuthorList><Language>eng</Language><PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType></PublicationTypeList></Article><MedlineJournalInfo><Country>United States</Country><MedlineTA>J Prosthet Dent</MedlineTA><NlmUniqueID>0376364</NlmUniqueID><ISSNLinking>0022-3913</ISSNLinking></MedlineJournalInfo><ChemicalList><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D006882">Hydroxyapatites</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D014753">Vinyl Compounds</NameOfSubstance></Chemical><Chemical><RegistryNumber>91D9GV0Z28</RegistryNumber><NameOfSubstance UI="D017886">Durapatite</NameOfSubstance></Chemical></ChemicalList><CitationSubset>D</CitationSubset><CitationSubset>IM</CitationSubset><MeshHeadingList><MeshHeading><DescriptorName UI="D000540" MajorTopicYN="N">Alveolar Ridge Augmentation</DescriptorName><QualifierName UI="Q000295" MajorTopicYN="Y">instrumentation</QualifierName><QualifierName UI="Q000379" MajorTopicYN="N">methods</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D000543" MajorTopicYN="N">Alveoloplasty</DescriptorName><QualifierName UI="Q000295" MajorTopicYN="Y">instrumentation</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D001284" MajorTopicYN="N">Atrophy</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D001862" MajorTopicYN="N">Bone Resorption</DescriptorName><QualifierName UI="Q000601" MajorTopicYN="N">surgery</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D017886" MajorTopicYN="N">Durapatite</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D004867" MajorTopicYN="N">Equipment Design</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D006801" MajorTopicYN="N">Humans</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D006882" MajorTopicYN="Y">Hydroxyapatites</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D007575" MajorTopicYN="N">Jaw, Edentulous</DescriptorName><QualifierName UI="Q000601" MajorTopicYN="N">surgery</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D008437" MajorTopicYN="N">Maxilla</DescriptorName><QualifierName UI="Q000473" MajorTopicYN="N">pathology</QualifierName><QualifierName UI="Q000601" MajorTopicYN="Y">surgery</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D013516" MajorTopicYN="N">Oral Surgical Procedures, Preprosthetic</DescriptorName><QualifierName UI="Q000295" MajorTopicYN="Y">instrumentation</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D019736" MajorTopicYN="Y">Prostheses and Implants</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D014753" MajorTopicYN="N">Vinyl Compounds</DescriptorName></MeshHeading></MeshHeadingList></MedlineCitation><PubmedData><History><PubMedPubDate PubStatus="pubmed"><Year>1986</Year><Month>9</Month><Day>1</Day></PubMedPubDate><PubMedPubDate PubStatus="medline"><Year>1986</Year><Month>9</Month><Day>1</Day><Hour>0</Hour><Minute>1</Minute></PubMedPubDate><PubMedPubDate PubStatus="entrez"><Year>1986</Year><Month>9</Month><Day>1</Day><Hour>0</Hour><Minute>0</Minute></PubMedPubDate></History><PublicationStatus>ppublish</PublicationStatus><ArticleIdList><ArticleId IdType="pubmed">3018237</ArticleId></ArticleIdList></PubmedData></pubmed></record>Pour manipuler ce document sous Unix (Dilib)
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