Tissue integration of non‐submerged implants. l‐year results of a prospective study with 100 ITI hollow‐cylinder and hollow‐screw implants.
Identifieur interne : 006776 ( Istex/Corpus ); précédent : 006775; suivant : 006777Tissue integration of non‐submerged implants. l‐year results of a prospective study with 100 ITI hollow‐cylinder and hollow‐screw implants.
Auteurs : D. Buser ; H. Weber ; N. P. LangSource :
- Clinical Oral Implants Research [ 0905-7161 ] ; 1990-12.
Abstract
It has been postulated that the wound healing in a closed submerged location is one of the prerequisites for osseointegration of dental implants. The purpose of the present study was to evaluate the tissue integration of intentionally non‐submerged titanium implants inserted by a one‐stage surgical procedure. 100 ITI implants were consecutively placed in 70 partially edentulous patients. After a healing period free of masticatory loading for at least 3 months, the implants were examined. The clinical status showed for all implants neither detectable mobility nor signs of a peri‐implant infection. Therefore, prosthetic abutments were inserted, and the patients were restored with fixed partial dentures. All patients were regularly recalled at 3‐month intervals, and no patient dropped out of the study. Thus, all 100 implants were re‐evaluated 12 months following implantation. Plaque‐ and sulcus bleeding indices, probing depth, clinical attachment level, width of keratinized mucosa, and periotest scores were assessed. In addition, standardized radiographs were analyzed for the presence of peri‐implant radiolucencies and for the location of alveolar bone levels around the implants. Based on predefined criteria, the implants were classified as successful or failing. 98 implants were considered successful, and 1 implant failing. The remaining implant exhibited a peri‐implant infection requiring local and systemic antimicrobial treatment. The results of this short‐term study indicate that intentionally non‐submerged ITI implants yield a high predictability for successful tissue integration.
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DOI: 10.1034/j.1600-0501.1990.010105.x
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Lang</name><affiliation><mods:affiliation>University of Berne, School of Dental Medicine, Bern/Switzerland and Harvard School of Dental Medicine, Boston MA, USA</mods:affiliation></affiliation></author></analytic><monogr></monogr><series><title level="j" type="main">Clinical Oral Implants Research</title><title level="j" type="alt">CLINICAL ORAL IMPLANTS RESEARCH</title><idno type="ISSN">0905-7161</idno><idno type="eISSN">1600-0501</idno><imprint><biblScope unit="vol">1</biblScope><biblScope unit="issue">1</biblScope><biblScope unit="page" from="33">33</biblScope><biblScope unit="page" to="40">40</biblScope><publisher>Munksgaard International Publishers</publisher><pubPlace>Copenhagen</pubPlace><date type="published" when="1990-12">1990-12</date></imprint><idno type="ISSN">0905-7161</idno></series></biblStruct></sourceDesc><seriesStmt><idno type="ISSN">0905-7161</idno></seriesStmt></fileDesc><profileDesc><textClass></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">It has been postulated that the wound healing in a closed submerged location is one of the prerequisites for osseointegration of dental implants. The purpose of the present study was to evaluate the tissue integration of intentionally non‐submerged titanium implants inserted by a one‐stage surgical procedure. 100 ITI implants were consecutively placed in 70 partially edentulous patients. After a healing period free of masticatory loading for at least 3 months, the implants were examined. The clinical status showed for all implants neither detectable mobility nor signs of a peri‐implant infection. Therefore, prosthetic abutments were inserted, and the patients were restored with fixed partial dentures. All patients were regularly recalled at 3‐month intervals, and no patient dropped out of the study. Thus, all 100 implants were re‐evaluated 12 months following implantation. Plaque‐ and sulcus bleeding indices, probing depth, clinical attachment level, width of keratinized mucosa, and periotest scores were assessed. In addition, standardized radiographs were analyzed for the presence of peri‐implant radiolucencies and for the location of alveolar bone levels around the implants. Based on predefined criteria, the implants were classified as successful or failing. 98 implants were considered successful, and 1 implant failing. The remaining implant exhibited a peri‐implant infection requiring local and systemic antimicrobial treatment. The results of this short‐term study indicate that intentionally non‐submerged ITI implants yield a high predictability for successful tissue integration.</div></front></TEI><istex><corpusName>wiley</corpusName><author><json:item><name>D. Buser</name><affiliations><json:string>University of Berne, School of Dental Medicine, Bern/Switzerland and Harvard School of Dental Medicine, Boston MA, USA</json:string></affiliations></json:item><json:item><name>H.‐P. 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Lang</name><affiliations><json:string>University of Berne, School of Dental Medicine, Bern/Switzerland and Harvard School of Dental Medicine, Boston MA, USA</json:string></affiliations></json:item></author><subject><json:item><lang><json:string>eng</json:string></lang><value>annual examination</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>criteria of success</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>ITI implants‐one‐stage procedure</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>non‐submerged implants</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>tissue integration</value></json:item></subject><articleId><json:string>CLR010105</json:string></articleId><arkIstex>ark:/67375/WNG-626R0RQF-2</arkIstex><language><json:string>eng</json:string></language><originalGenre><json:string>article</json:string></originalGenre><abstract>It has been postulated that the wound healing in a closed submerged location is one of the prerequisites for osseointegration of dental implants. 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In addition, standardized radiographs were analyzed for the presence of peri‐implant radiolucencies and for the location of alveolar bone levels around the implants. Based on predefined criteria, the implants were classified as successful or failing. 98 implants were considered successful, and 1 implant failing. The remaining implant exhibited a peri‐implant infection requiring local and systemic antimicrobial treatment. 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P.</forename><surname>Lang</surname></persName><affiliation>University of Berne, School of Dental Medicine, Bern/Switzerland and Harvard School of Dental Medicine, Boston MA, USA<address><country key="US"></country></address></affiliation></author><idno type="istex">D07A5E59643033F2BDF63F78F7DA108A5FBCC99C</idno><idno type="ark">ark:/67375/WNG-626R0RQF-2</idno><idno type="DOI">10.1034/j.1600-0501.1990.010105.x</idno><idno type="unit">CLR010105</idno><idno type="supplier"></idno><idno type="toTypesetVersion">file:CLR.CLR010105.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.1990.1.issue-1</idno><idno type="product">CLR</idno><idno type="publisherDivision">ST</idno><imprint><biblScope unit="vol">1</biblScope><biblScope unit="issue">1</biblScope><biblScope unit="page" from="33">33</biblScope><biblScope unit="page" to="40">40</biblScope><publisher>Munksgaard International Publishers</publisher><pubPlace>Copenhagen</pubPlace><date type="published" when="1990-12"></date></imprint></monogr></biblStruct></sourceDesc></fileDesc><profileDesc><abstract xml:lang="en" style="main"><p>It has been postulated that the wound healing in a closed submerged location is one of the prerequisites for osseointegration of dental implants. The purpose of the present study was to evaluate the tissue integration of intentionally non‐submerged titanium implants inserted by a one‐stage surgical procedure. 100 ITI implants were consecutively placed in 70 partially edentulous patients. After a healing period free of masticatory loading for at least 3 months, the implants were examined. The clinical status showed for all implants neither detectable mobility nor signs of a peri‐implant infection. Therefore, prosthetic abutments were inserted, and the patients were restored with fixed partial dentures. All patients were regularly recalled at 3‐month intervals, and no patient dropped out of the study. Thus, all 100 implants were re‐evaluated 12 months following implantation. Plaque‐ and sulcus bleeding indices, probing depth, clinical attachment level, width of keratinized mucosa, and periotest scores were assessed. In addition, standardized radiographs were analyzed for the presence of peri‐implant radiolucencies and for the location of alveolar bone levels around the implants. Based on predefined criteria, the implants were classified as successful or failing. 98 implants were considered successful, and 1 implant failing. The remaining implant exhibited a peri‐implant infection requiring local and systemic antimicrobial treatment. The results of this short‐term study indicate that intentionally non‐submerged ITI implants yield a high predictability for successful tissue integration.</p></abstract><textClass><keywords xml:lang="en"><term xml:id="k1">annual examination</term><term xml:id="k2">criteria of success</term><term xml:id="k3">ITI implants‐one‐stage procedure</term><term xml:id="k4">non‐submerged implants</term><term xml:id="k5">tissue integration</term></keywords><keywords rend="tocHeading1"><term>Original Articles</term></keywords></textClass><langUsage><language ident="en"></language></langUsage></profileDesc><revisionDesc><change>undefined</change><change>[object Object]</change></revisionDesc></teiHeader></istex:fulltextTEI><json:item><extension>txt</extension><original>false</original><mimetype>text/plain</mimetype><uri>https://api.istex.fr/document/D07A5E59643033F2BDF63F78F7DA108A5FBCC99C/fulltext/txt</uri></json:item></fulltext><metadata><istex:metadataXml wicri:clean="Wiley component found"><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>Munksgaard International Publishers</publisherName><publisherLoc>Copenhagen</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="12001"><doi origin="wiley">10.1111/clr.1990.1.issue-1</doi><numberingGroup><numbering type="journalVolume" number="1">1</numbering><numbering type="journalIssue" number="1">1</numbering></numberingGroup><coverDate startDate="1990-12">December 1990</coverDate></publicationMeta><publicationMeta level="unit" type="article" position="0003300" status="forIssue"><doi origin="wiley">10.1034/j.1600-0501.1990.010105.x</doi><idGroup><id type="unit" value="CLR010105"></id><id type="supplier" value=""></id></idGroup><titleGroup><title type="tocHeading1">Original Articles</title></titleGroup><eventGroup><event type="firstOnline" date="2002-02-27"></event><event type="publishedOnlineFinalForm" date="2002-02-27"></event><event type="xmlConverted" agent="Converter:BPG_TO_WML3G version:2.3.2 mode:FullText source:Header result:Header" date="2010-03-15"></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="33">33</numbering><numbering type="pageLast" number="40">40</numbering></numberingGroup><correspondenceTo>Daniel Buser, Department of Oral Surgery, School of Dental Medicine, Freiburgstrasse 7, CH‐3010 Bern/Switzerland</correspondenceTo><linkGroup><link type="toTypesetVersion" href="file:CLR.CLR010105.pdf"></link></linkGroup></publicationMeta><contentMeta><unparsedEditorialHistory>Accepted for publication 6 September 1990</unparsedEditorialHistory><countGroup><count type="linksPubMed" number="0"></count><count type="linksCrossRef" number="0"></count></countGroup><titleGroup><title type="main">Tissue integration of non‐submerged implants. l‐year results of a prospective study with 100 ITI hollow‐cylinder and hollow‐screw implants.</title><title type="shortAuthors">Buser et al.</title><title type="short">Tissue integration of non‐submerged implants</title></titleGroup><creators><creator creatorRole="author" xml:id="cr1" affiliationRef="#a1"><personName><givenNames>D.</givenNames><familyName>Buser</familyName></personName></creator><creator creatorRole="author" xml:id="cr2" affiliationRef="#a1"><personName><givenNames>H.‐P.</givenNames><familyName>Weber</familyName></personName></creator><creator creatorRole="author" xml:id="cr3" affiliationRef="#a1"><personName><givenNames>N. P.</givenNames><familyName>Lang</familyName></personName></creator></creators><affiliationGroup><affiliation xml:id="a1" countryCode="US"><unparsedAffiliation>University of Berne, School of Dental Medicine, Bern/Switzerland and Harvard School of Dental Medicine, Boston MA, USA</unparsedAffiliation></affiliation></affiliationGroup><keywordGroup xml:lang="en"><keyword xml:id="k1">annual examination</keyword><keyword xml:id="k2">criteria of success</keyword><keyword xml:id="k3">ITI implants‐one‐stage procedure</keyword><keyword xml:id="k4">non‐submerged implants</keyword><keyword xml:id="k5">tissue integration</keyword></keywordGroup><abstractGroup><abstract type="main" xml:lang="en"><p>It has been postulated that the wound healing in a closed submerged location is one of the prerequisites for osseointegration of dental implants. The purpose of the present study was to evaluate the tissue integration of intentionally non‐submerged titanium implants inserted by a one‐stage surgical procedure. 100 ITI implants were consecutively placed in 70 partially edentulous patients. After a healing period free of masticatory loading for at least 3 months, the implants were examined. The clinical status showed for all implants neither detectable mobility nor signs of a peri‐implant infection. Therefore, prosthetic abutments were inserted, and the patients were restored with fixed partial dentures. All patients were regularly recalled at 3‐month intervals, and no patient dropped out of the study. Thus, all 100 implants were re‐evaluated 12 months following implantation. Plaque‐ and sulcus bleeding indices, probing depth, clinical attachment level, width of keratinized mucosa, and periotest scores were assessed. In addition, standardized radiographs were analyzed for the presence of peri‐implant radiolucencies and for the location of alveolar bone levels around the implants. Based on predefined criteria, the implants were classified as successful or failing. 98 implants were considered successful, and 1 implant failing. The remaining implant exhibited a peri‐implant infection requiring local and systemic antimicrobial treatment. The results of this short‐term study indicate that intentionally non‐submerged ITI implants yield a high predictability for successful tissue integration.</p></abstract></abstractGroup></contentMeta></header></component></istex:document></istex:metadataXml><mods version="3.6"><titleInfo lang="en"><title>Tissue integration of non‐submerged implants. l‐year results of a prospective study with 100 ITI hollow‐cylinder and hollow‐screw implants.</title></titleInfo><titleInfo type="abbreviated" lang="en"><title>Tissue integration of non‐submerged implants</title></titleInfo><titleInfo type="alternative" contentType="CDATA" lang="en"><title>Tissue integration of non‐submerged implants. l‐year results of a prospective study with 100 ITI hollow‐cylinder and hollow‐screw implants.</title></titleInfo><name type="personal"><namePart type="given">D.</namePart><namePart type="family">Buser</namePart><affiliation>University of Berne, School of Dental Medicine, Bern/Switzerland and Harvard School of Dental Medicine, Boston MA, USA</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">H.‐P.</namePart><namePart type="family">Weber</namePart><affiliation>University of Berne, School of Dental Medicine, Bern/Switzerland and Harvard School of Dental Medicine, Boston MA, USA</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">N. P.</namePart><namePart type="family">Lang</namePart><affiliation>University of Berne, School of Dental Medicine, Bern/Switzerland and Harvard School of Dental Medicine, Boston MA, USA</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>Munksgaard International Publishers</publisher><place><placeTerm type="text">Copenhagen</placeTerm></place><dateIssued encoding="w3cdtf">1990-12</dateIssued><edition>Accepted for publication 6 September 1990</edition><copyrightDate encoding="w3cdtf">1990</copyrightDate></originInfo><language><languageTerm type="code" authority="rfc3066">en</languageTerm><languageTerm type="code" authority="iso639-2b">eng</languageTerm></language><physicalDescription><extent unit="linksCrossRef">0</extent></physicalDescription><abstract lang="en">It has been postulated that the wound healing in a closed submerged location is one of the prerequisites for osseointegration of dental implants. The purpose of the present study was to evaluate the tissue integration of intentionally non‐submerged titanium implants inserted by a one‐stage surgical procedure. 100 ITI implants were consecutively placed in 70 partially edentulous patients. After a healing period free of masticatory loading for at least 3 months, the implants were examined. The clinical status showed for all implants neither detectable mobility nor signs of a peri‐implant infection. Therefore, prosthetic abutments were inserted, and the patients were restored with fixed partial dentures. All patients were regularly recalled at 3‐month intervals, and no patient dropped out of the study. Thus, all 100 implants were re‐evaluated 12 months following implantation. Plaque‐ and sulcus bleeding indices, probing depth, clinical attachment level, width of keratinized mucosa, and periotest scores were assessed. In addition, standardized radiographs were analyzed for the presence of peri‐implant radiolucencies and for the location of alveolar bone levels around the implants. Based on predefined criteria, the implants were classified as successful or failing. 98 implants were considered successful, and 1 implant failing. The remaining implant exhibited a peri‐implant infection requiring local and systemic antimicrobial treatment. The results of this short‐term study indicate that intentionally non‐submerged ITI implants yield a high predictability for successful tissue integration.</abstract><subject lang="en"><genre>keywords</genre><topic>annual examination</topic><topic>criteria of success</topic><topic>ITI implants‐one‐stage procedure</topic><topic>non‐submerged implants</topic><topic>tissue integration</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>1990</date><detail type="volume"><caption>vol.</caption><number>1</number></detail><detail type="issue"><caption>no.</caption><number>1</number></detail><extent unit="pages"><start>33</start><end>40</end></extent></part></relatedItem><identifier type="istex">D07A5E59643033F2BDF63F78F7DA108A5FBCC99C</identifier><identifier type="ark">ark:/67375/WNG-626R0RQF-2</identifier><identifier type="DOI">10.1034/j.1600-0501.1990.010105.x</identifier><identifier type="ArticleID">CLR010105</identifier><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>Munksgaard International Publishers</recordOrigin></recordInfo></mods><json:item><extension>json</extension><original>false</original><mimetype>application/json</mimetype><uri>https://api.istex.fr/document/D07A5E59643033F2BDF63F78F7DA108A5FBCC99C/metadata/json</uri></json:item></metadata><serie></serie></istex></record>Pour manipuler ce document sous Unix (Dilib)
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|texte= Tissue integration of non‐submerged implants. l‐year results of a prospective study with 100 ITI hollow‐cylinder and hollow‐screw implants.
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