Preliminary Report of Immediately Loaded Altiva Natural Tooth Replacement Dental Implants
Identifieur interne : 006178 ( Istex/Corpus ); précédent : 006177; suivant : 006179Preliminary Report of Immediately Loaded Altiva Natural Tooth Replacement Dental Implants
Auteurs : Andre U. Buchs ; Laurence Levine ; Peter MoySource :
- Clinical Implant Dentistry and Related Research [ 1523-0899 ] ; 2001-04.
English descriptors
- KwdEn :
- Alpha omegan, Bicuspid, Biomed mater, Bone ingrowth, Bone mill, Bone quality, Branemark adell, Central incisor, Clin, Clin orthop, Clinical implant dentistry, Dense bone, Dent, Dental implants, Dental prostheses, Edentulous, Edentulous area, Endosseous implant, Final impression, Final restoration, First bicuspid, First molar, Healing period, Immediate load, Immediate loading, Immediate restoration, Implant, Implant design, Implant failure, Implant length, Implant material, Implant placement, Implant stability, Implant survival, Incisor, Integral part, Interdental papilla, Lateral incisor, Mandible, Maxilla, Maxillofac, Molar, Natural tooth replacement, Oral implantol, Oral maxillofac implants, Osseointegrated implants, Osseointegration, Patient acceptance, Periapical radiographs, Periodontics restor dent, Plast reconstr surg, Primary stability, Prospective study, Prosthesis, Prosthetic posts, Provisional restoration, Reference point, Restorative collar, Restorative collars, Restorative dentist, Restorative tissue collars, Second bicuspid, Second molar, Successful outcome, Surgical placement, Temporary prosthesis, Thread design, Tissue integration, Tissue punch, Titanium, Titanium implants, Undisturbed healing, Vertical bone loss, Weeks postoperatively, Wide implants.
- Teeft :
- Alpha omegan, Bicuspid, Biomed mater, Bone ingrowth, Bone mill, Bone quality, Branemark adell, Central incisor, Clin, Clin orthop, Clinical implant dentistry, Dense bone, Dent, Dental implants, Dental prostheses, Edentulous, Edentulous area, Endosseous implant, Final impression, Final restoration, First bicuspid, First molar, Healing period, Immediate load, Immediate loading, Immediate restoration, Implant, Implant design, Implant failure, Implant length, Implant material, Implant placement, Implant stability, Implant survival, Incisor, Integral part, Interdental papilla, Lateral incisor, Mandible, Maxilla, Maxillofac, Molar, Natural tooth replacement, Oral implantol, Oral maxillofac implants, Osseointegrated implants, Osseointegration, Patient acceptance, Periapical radiographs, Periodontics restor dent, Plast reconstr surg, Primary stability, Prospective study, Prosthesis, Prosthetic posts, Provisional restoration, Reference point, Restorative collar, Restorative collars, Restorative dentist, Restorative tissue collars, Second bicuspid, Second molar, Successful outcome, Surgical placement, Temporary prosthesis, Thread design, Tissue integration, Tissue punch, Titanium, Titanium implants, Undisturbed healing, Vertical bone loss, Weeks postoperatively, Wide implants.
Abstract
Background: Osseointegration may be described as a direct contact between living bone and an alloplastic implant. It is thought that a period of undisturbed healing is required to ensure osseointegration. The length of the healing period is dependent on a number of factors, such as implant material, surface configuration, site preparation technique, bone quality, healing capacity of the osteotomy, and implant design. Elimination of the healing period offers distinct advantages in terms of cost of therapy and convenience to patients. Recently, a new one‐piece implant design was proposed that provides improved stability of the implant to allow immediate support of an interim prosthesis. Purpose: This article presents the initial clinical experiences when the Altiva Natural Tooth Replacement one‐piece implant was used in a human clinical trial. Materials and Methods: This was a prospective multicenter study of the placement and immediate loading of the one‐piece implant. A total of 142 implants were placed in the jaws of 93 patients. Implants were placed consecutively and were followed at specified intervals in three private clinical practices. Clinical performance was recorded relative to implant survival and prosthesis support. Results: The implant survival rate was 93.7%, with similar responses in the maxilla (95.0%) and the mandible (92.7%). When implant failure occurred, it was observed as mobility without infection within 3 to 5 weeks of implant insertion. Conclusions: On the basis of this trial, there is promising evidence that this implant design can succeed at rates similar to other designs that require conventional healing times.
Url:
DOI: 10.1111/j.1708-8208.2001.tb00237.x
Links to Exploration step
ISTEX:C4B72AA1D056FCA3A984CDEA5D3A35ACC7E1A2D4Le document en format XML
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Buchs</name><affiliation><mods:affiliation>Adjunct Professor, Oral Surgery, University of Pennsylvania, Philadelphia, Pennsylvania</mods:affiliation></affiliation></author><author><name sortKey="Levine, Laurence" sort="Levine, Laurence" uniqKey="Levine L" first="Laurence" last="Levine">Laurence Levine</name><affiliation><mods:affiliation>Private Practice, Fort Lauderdale, Florida, California</mods:affiliation></affiliation></author><author><name sortKey="Moy, Peter" sort="Moy, Peter" uniqKey="Moy P" first="Peter" last="Moy">Peter Moy</name><affiliation><mods:affiliation>Co‐Director, Implant Program, UCLA, Los Angeles, California</mods:affiliation></affiliation><affiliation><mods:affiliation>E-mail: pkmoy@ucla.edu</mods:affiliation></affiliation></author></analytic><monogr></monogr><series><title level="j" type="main">Clinical Implant Dentistry and Related Research</title><title level="j" type="alt">CLINICAL IMPLANT DENTISTRY RELATED RESEARCH</title><idno 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prostheses</term><term>Edentulous</term><term>Edentulous area</term><term>Endosseous implant</term><term>Final impression</term><term>Final restoration</term><term>First bicuspid</term><term>First molar</term><term>Healing period</term><term>Immediate load</term><term>Immediate loading</term><term>Immediate restoration</term><term>Implant</term><term>Implant design</term><term>Implant failure</term><term>Implant length</term><term>Implant material</term><term>Implant placement</term><term>Implant stability</term><term>Implant survival</term><term>Incisor</term><term>Integral part</term><term>Interdental papilla</term><term>Lateral incisor</term><term>Mandible</term><term>Maxilla</term><term>Maxillofac</term><term>Molar</term><term>Natural tooth replacement</term><term>Oral implantol</term><term>Oral maxillofac implants</term><term>Osseointegrated implants</term><term>Osseointegration</term><term>Patient acceptance</term><term>Periapical radiographs</term><term>Periodontics restor dent</term><term>Plast reconstr surg</term><term>Primary stability</term><term>Prospective study</term><term>Prosthesis</term><term>Prosthetic posts</term><term>Provisional restoration</term><term>Reference point</term><term>Restorative collar</term><term>Restorative collars</term><term>Restorative dentist</term><term>Restorative tissue collars</term><term>Second bicuspid</term><term>Second molar</term><term>Successful outcome</term><term>Surgical placement</term><term>Temporary prosthesis</term><term>Thread design</term><term>Tissue integration</term><term>Tissue punch</term><term>Titanium</term><term>Titanium implants</term><term>Undisturbed healing</term><term>Vertical bone loss</term><term>Weeks postoperatively</term><term>Wide implants</term></keywords><keywords scheme="Teeft" xml:lang="en"><term>Alpha omegan</term><term>Bicuspid</term><term>Biomed mater</term><term>Bone ingrowth</term><term>Bone mill</term><term>Bone quality</term><term>Branemark adell</term><term>Central 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implants</term><term>Osseointegrated implants</term><term>Osseointegration</term><term>Patient acceptance</term><term>Periapical radiographs</term><term>Periodontics restor dent</term><term>Plast reconstr surg</term><term>Primary stability</term><term>Prospective study</term><term>Prosthesis</term><term>Prosthetic posts</term><term>Provisional restoration</term><term>Reference point</term><term>Restorative collar</term><term>Restorative collars</term><term>Restorative dentist</term><term>Restorative tissue collars</term><term>Second bicuspid</term><term>Second molar</term><term>Successful outcome</term><term>Surgical placement</term><term>Temporary prosthesis</term><term>Thread design</term><term>Tissue integration</term><term>Tissue punch</term><term>Titanium</term><term>Titanium implants</term><term>Undisturbed healing</term><term>Vertical bone loss</term><term>Weeks postoperatively</term><term>Wide implants</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Background: Osseointegration may be described as a direct contact between living bone and an alloplastic implant. It is thought that a period of undisturbed healing is required to ensure osseointegration. The length of the healing period is dependent on a number of factors, such as implant material, surface configuration, site preparation technique, bone quality, healing capacity of the osteotomy, and implant design. Elimination of the healing period offers distinct advantages in terms of cost of therapy and convenience to patients. Recently, a new one‐piece implant design was proposed that provides improved stability of the implant to allow immediate support of an interim prosthesis. Purpose: This article presents the initial clinical experiences when the Altiva Natural Tooth Replacement one‐piece implant was used in a human clinical trial. Materials and Methods: This was a prospective multicenter study of the placement and immediate loading of the one‐piece implant. A total of 142 implants were placed in the jaws of 93 patients. Implants were placed consecutively and were followed at specified intervals in three private clinical practices. Clinical performance was recorded relative to implant survival and prosthesis support. Results: The implant survival rate was 93.7%, with similar responses in the maxilla (95.0%) and the mandible (92.7%). When implant failure occurred, it was observed as mobility without infection within 3 to 5 weeks of implant insertion. Conclusions: On the basis of this trial, there is promising evidence that this implant design can succeed at rates similar to other designs that require conventional healing times.</div></front></TEI><istex><corpusName>wiley</corpusName><keywords><teeft><json:string>implant</json:string><json:string>prosthesis</json:string><json:string>bicuspid</json:string><json:string>mandible</json:string><json:string>maxilla</json:string><json:string>implant design</json:string><json:string>osseointegration</json:string><json:string>maxillofac</json:string><json:string>clin</json:string><json:string>oral maxillofac implants</json:string><json:string>incisor</json:string><json:string>implant placement</json:string><json:string>healing period</json:string><json:string>bone quality</json:string><json:string>provisional restoration</json:string><json:string>dental implants</json:string><json:string>molar</json:string><json:string>restorative dentist</json:string><json:string>second bicuspid</json:string><json:string>first bicuspid</json:string><json:string>edentulous area</json:string><json:string>immediate loading</json:string><json:string>second molar</json:string><json:string>first molar</json:string><json:string>final impression</json:string><json:string>lateral incisor</json:string><json:string>central incisor</json:string><json:string>titanium implants</json:string><json:string>implant survival</json:string><json:string>edentulous</json:string><json:string>titanium</json:string><json:string>plast reconstr surg</json:string><json:string>periodontics restor dent</json:string><json:string>final restoration</json:string><json:string>implant stability</json:string><json:string>restorative collar</json:string><json:string>temporary prosthesis</json:string><json:string>oral implantol</json:string><json:string>integral part</json:string><json:string>prosthetic posts</json:string><json:string>weeks postoperatively</json:string><json:string>restorative tissue collars</json:string><json:string>interdental papilla</json:string><json:string>periapical radiographs</json:string><json:string>vertical bone loss</json:string><json:string>natural tooth replacement</json:string><json:string>tissue punch</json:string><json:string>bone mill</json:string><json:string>patient acceptance</json:string><json:string>clin orthop</json:string><json:string>wide implants</json:string><json:string>reference point</json:string><json:string>implant length</json:string><json:string>successful outcome</json:string><json:string>implant material</json:string><json:string>thread design</json:string><json:string>primary stability</json:string><json:string>clinical implant dentistry</json:string><json:string>dental prostheses</json:string><json:string>surgical placement</json:string><json:string>branemark adell</json:string><json:string>osseointegrated implants</json:string><json:string>dense bone</json:string><json:string>endosseous implant</json:string><json:string>immediate restoration</json:string><json:string>tissue integration</json:string><json:string>prospective study</json:string><json:string>undisturbed healing</json:string><json:string>implant failure</json:string><json:string>alpha omegan</json:string><json:string>immediate load</json:string><json:string>bone ingrowth</json:string><json:string>biomed mater</json:string><json:string>restorative collars</json:string><json:string>dent</json:string></teeft></keywords><author><json:item><name>Andre U. Buchs DDS</name><affiliations><json:string>Adjunct Professor, Oral Surgery, University of Pennsylvania, Philadelphia, Pennsylvania</json:string></affiliations></json:item><json:item><name>Laurence Levine DDS</name><affiliations><json:string>Private Practice, Fort Lauderdale, Florida, California</json:string></affiliations></json:item><json:item><name>Peter Moy DMD</name><affiliations><json:string>Co‐Director, Implant Program, UCLA, Los Angeles, California</json:string><json:string>E-mail: pkmoy@ucla.edu</json:string></affiliations></json:item></author><subject><json:item><lang><json:string>eng</json:string></lang><value>immediate load</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>implant design</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>implant survival</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>one‐piece implant</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>osseointegration</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>single stage</value></json:item></subject><articleId><json:string>CID97</json:string></articleId><arkIstex>ark:/67375/WNG-RQQP19D2-X</arkIstex><language><json:string>eng</json:string></language><originalGenre><json:string>article</json:string></originalGenre><abstract>Background: Osseointegration may be described as a direct contact between living bone and an alloplastic implant. It is thought that a period of undisturbed healing is required to ensure osseointegration. The length of the healing period is dependent on a number of factors, such as implant material, surface configuration, site preparation technique, bone quality, healing capacity of the osteotomy, and implant design. Elimination of the healing period offers distinct advantages in terms of cost of therapy and convenience to patients. Recently, a new one‐piece implant design was proposed that provides improved stability of the implant to allow immediate support of an interim prosthesis. Purpose: This article presents the initial clinical experiences when the Altiva Natural Tooth Replacement one‐piece implant was used in a human clinical trial. Materials and Methods: This was a prospective multicenter study of the placement and immediate loading of the one‐piece implant. A total of 142 implants were placed in the jaws of 93 patients. Implants were placed consecutively and were followed at specified intervals in three private clinical practices. Clinical performance was recorded relative to implant survival and prosthesis support. Results: The implant survival rate was 93.7%, with similar responses in the maxilla (95.0%) and the mandible (92.7%). When implant failure occurred, it was observed as mobility without infection within 3 to 5 weeks of implant insertion. Conclusions: On the basis of this trial, there is promising evidence that this implant design can succeed at rates similar to other designs that require conventional healing times.</abstract><qualityIndicators><score>8.816</score><pdfWordCount>3828</pdfWordCount><pdfCharCount>24608</pdfCharCount><pdfVersion>1.4</pdfVersion><pdfPageCount>10</pdfPageCount><pdfPageSize>594 x 792 pts</pdfPageSize><refBibsNative>true</refBibsNative><abstractWordCount>249</abstractWordCount><abstractCharCount>1664</abstractCharCount><keywordCount>6</keywordCount></qualityIndicators><title>Preliminary Report of Immediately Loaded Altiva Natural Tooth Replacement Dental Implants</title><pmid><json:string>11472656</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>3</volume><issue>2</issue><pages><first>97</first><last>106</last><total>10</total></pages><genre><json:string>journal</json:string></genre></host><namedEntities><unitex><date><json:string>2001</json:string></date><geogName></geogName><orgName><json:string>Altiva Corp., Minneapolis</json:string><json:string>BC Decker Inc</json:string></orgName><orgName_funder></orgName_funder><orgName_provider></orgName_provider><persName><json:string>Laurence Levine</json:string><json:string>Pilliar</json:string><json:string>Schnitman</json:string><json:string>Tarnow</json:string><json:string>Salama</json:string><json:string>Peter Moy</json:string></persName><placeName><json:string>Los Angeles</json:string><json:string>San Vicente</json:string><json:string>CA</json:string></placeName><ref_url></ref_url><ref_bibl></ref_bibl><bibl></bibl></unitex></namedEntities><ark><json:string>ark:/67375/WNG-RQQP19D2-X</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><inist><json:string>1 - sciences appliquees, technologies et medecines</json:string><json:string>2 - sciences biologiques et medicales</json:string><json:string>3 - sciences medicales</json:string><json:string>4 - chirurgie (generalites). transplantations, greffes d'organes et de tissus. pathologie des greffons</json:string></inist></categories><publicationDate>2001</publicationDate><copyrightDate>2001</copyrightDate><doi><json:string>10.1111/j.1708-8208.2001.tb00237.x</json:string></doi><id>C4B72AA1D056FCA3A984CDEA5D3A35ACC7E1A2D4</id><score>1</score><fulltext><json:item><extension>pdf</extension><original>true</original><mimetype>application/pdf</mimetype><uri>https://api.istex.fr/document/C4B72AA1D056FCA3A984CDEA5D3A35ACC7E1A2D4/fulltext/pdf</uri></json:item><json:item><extension>zip</extension><original>false</original><mimetype>application/zip</mimetype><uri>https://api.istex.fr/document/C4B72AA1D056FCA3A984CDEA5D3A35ACC7E1A2D4/fulltext/zip</uri></json:item><istex:fulltextTEI uri="https://api.istex.fr/document/C4B72AA1D056FCA3A984CDEA5D3A35ACC7E1A2D4/fulltext/tei"><teiHeader><fileDesc><titleStmt><title level="a" type="main">Preliminary Report of Immediately Loaded Altiva Natural Tooth Replacement Dental Implants</title></titleStmt><publicationStmt><authority>ISTEX</authority><publisher>Blackwell Publishing Ltd</publisher><pubPlace>Oxford, UK</pubPlace><date type="published" when="2001-04"></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">Preliminary Report of Immediately Loaded Altiva Natural Tooth Replacement Dental Implants</title><author xml:id="author-0000"><persName><forename type="first">Andre U.</forename><surname>Buchs</surname><roleName type="degree">DDS</roleName></persName><affiliation>Adjunct Professor, Oral Surgery, University of Pennsylvania, Philadelphia, Pennsylvania<address><country key="US"></country></address></affiliation></author><author xml:id="author-0001"><persName><forename type="first">Laurence</forename><surname>Levine</surname><roleName type="degree">DDS</roleName></persName><affiliation>Private Practice, Fort Lauderdale, Florida, California</affiliation></author><author xml:id="author-0002" role="corresp"><persName><forename type="first">Peter</forename><surname>Moy</surname><roleName type="degree">DMD</roleName></persName><affiliation>Co‐Director, Implant Program, UCLA, Los Angeles, California<address><country key="US"></country></address></affiliation><affiliation>Reprint requests: Peter Moy, DMD, 11980 San Vicente Blvd., Suite 503, Los Angeles, CA 90049‐6603; e‐mail: pkmoy@ucla.edu</affiliation></author><idno type="istex">C4B72AA1D056FCA3A984CDEA5D3A35ACC7E1A2D4</idno><idno type="ark">ark:/67375/WNG-RQQP19D2-X</idno><idno type="DOI">10.1111/j.1708-8208.2001.tb00237.x</idno><idno type="unit">CID97</idno><idno type="toTypesetVersion">file:CID.CID97.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.2001.3.issue-2</idno><idno type="product">CID</idno><idno type="publisherDivision">ST</idno><imprint><biblScope unit="vol">3</biblScope><biblScope unit="issue">2</biblScope><biblScope unit="page" from="97">97</biblScope><biblScope unit="page" to="106">106</biblScope><biblScope unit="page-count">10</biblScope><publisher>Blackwell Publishing Ltd</publisher><pubPlace>Oxford, UK</pubPlace><date type="published" when="2001-04"></date></imprint></monogr></biblStruct></sourceDesc></fileDesc><profileDesc><abstract xml:lang="en" style="main"><head>Abstract:</head><p>
<hi rend="italic">Background</hi>: Osseointegration may be described as a direct contact between living bone and an alloplastic implant. It is thought that a period of undisturbed healing is required to ensure osseointegration. The length of the healing period is dependent on a number of factors, such as implant material, surface configuration, site preparation technique, bone quality, healing capacity of the osteotomy, and implant design. Elimination of the healing period offers distinct advantages in terms of cost of therapy and convenience to patients. Recently, a new one‐piece implant design was proposed that provides improved stability of the implant to allow immediate support of an interim prosthesis.</p><p>
<hi rend="italic">Purpose</hi>: This article presents the initial clinical experiences when the Altiva Natural Tooth Replacement one‐piece implant was used in a human clinical trial.</p><p>
<hi rend="italic">Materials and Methods</hi>: This was a prospective multicenter study of the placement and immediate loading of the one‐piece implant. A total of 142 implants were placed in the jaws of 93 patients. Implants were placed consecutively and were followed at specified intervals in three private clinical practices. Clinical performance was recorded relative to implant survival and prosthesis support.</p><p>
<hi rend="italic">Results</hi>: The implant survival rate was 93.7%, with similar responses in the maxilla (95.0%) and the mandible (92.7%). When implant failure occurred, it was observed as mobility without infection within 3 to 5 weeks of implant insertion.</p><p>
<hi rend="italic">Conclusions</hi>: On the basis of this trial, there is promising evidence that this implant design can succeed at rates similar to other designs that require conventional healing times.</p></abstract><textClass><keywords xml:lang="en"><term xml:id="k1">immediate load</term><term xml:id="k2">implant design</term><term xml:id="k3">implant survival</term><term xml:id="k4">one‐piece implant</term><term xml:id="k5">osseointegration</term><term xml:id="k6">single stage</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/C4B72AA1D056FCA3A984CDEA5D3A35ACC7E1A2D4/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="04002"><doi origin="wiley">10.1111/cid.2001.3.issue-2</doi><numberingGroup><numbering type="journalVolume" number="3">3</numbering><numbering type="journalIssue" number="2">2</numbering></numberingGroup><coverDate startDate="2001-04">April 2001</coverDate></publicationMeta><publicationMeta level="unit" type="article" position="0009700" status="forIssue"><doi origin="wiley">10.1111/j.1708-8208.2001.tb00237.x</doi><idGroup><id type="unit" value="CID97"></id></idGroup><countGroup><count type="pageTotal" number="10"></count></countGroup><eventGroup><event type="firstOnline" date="2007-04-10"></event><event type="publishedOnlineFinalForm" date="2007-04-10"></event><event type="xmlConverted" agent="Converter:BPG_TO_WML3G version:2.3.2 mode:FullText source:HeaderRef result:HeaderRef" date="2010-03-13"></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:4.1.7 mode:FullText,remove_FC" date="2014-10-16"></event></eventGroup><numberingGroup><numbering type="pageFirst" number="97">97</numbering><numbering type="pageLast" number="106">106</numbering></numberingGroup><correspondenceTo>Reprint requests: Peter Moy, DMD, 11980 San Vicente Blvd., Suite 503, Los Angeles, CA 90049‐6603; e‐mail: <email>pkmoy@ucla.edu</email></correspondenceTo><linkGroup><link type="toTypesetVersion" href="file:CID.CID97.pdf"></link></linkGroup></publicationMeta><contentMeta><countGroup><count type="referenceTotal" number="41"></count><count type="linksCrossRef" number="4"></count></countGroup><titleGroup><title type="main">Preliminary Report of Immediately Loaded Altiva Natural Tooth Replacement Dental Implants</title></titleGroup><creators><creator creatorRole="author" xml:id="cr1" affiliationRef="#a1"><personName><givenNames>Andre U.</givenNames><familyName>Buchs</familyName><degrees>DDS</degrees></personName></creator><creator creatorRole="author" xml:id="cr2" affiliationRef="#a2"><personName><givenNames>Laurence</givenNames><familyName>Levine</familyName><degrees>DDS</degrees></personName></creator><creator creatorRole="author" xml:id="cr3" affiliationRef="#a3" corresponding="yes"><personName><givenNames>Peter</givenNames><familyName>Moy</familyName><degrees>DMD</degrees></personName></creator></creators><affiliationGroup><affiliation xml:id="a1" countryCode="US"><unparsedAffiliation>Adjunct Professor, Oral Surgery, University of Pennsylvania, Philadelphia, Pennsylvania</unparsedAffiliation></affiliation><affiliation xml:id="a2"><unparsedAffiliation>Private Practice, Fort Lauderdale, Florida, California</unparsedAffiliation></affiliation><affiliation xml:id="a3" countryCode="US"><unparsedAffiliation>Co‐Director, Implant Program, UCLA, Los Angeles, California</unparsedAffiliation></affiliation></affiliationGroup><keywordGroup xml:lang="en"><keyword xml:id="k1">immediate load</keyword><keyword xml:id="k2">implant design</keyword><keyword xml:id="k3">implant survival</keyword><keyword xml:id="k4">one‐piece implant</keyword><keyword xml:id="k5">osseointegration</keyword><keyword xml:id="k6">single stage</keyword></keywordGroup><abstractGroup><abstract type="main" xml:lang="en"><title type="main">Abstract:</title><p> <i>Background</i>: Osseointegration may be described as a direct contact between living bone and an alloplastic implant. It is thought that a period of undisturbed healing is required to ensure osseointegration. The length of the healing period is dependent on a number of factors, such as implant material, surface configuration, site preparation technique, bone quality, healing capacity of the osteotomy, and implant design. Elimination of the healing period offers distinct advantages in terms of cost of therapy and convenience to patients. Recently, a new one‐piece implant design was proposed that provides improved stability of the implant to allow immediate support of an interim prosthesis.</p><p> <i>Purpose</i>: This article presents the initial clinical experiences when the Altiva Natural Tooth Replacement one‐piece implant was used in a human clinical trial.</p><p> <i>Materials and Methods</i>: This was a prospective multicenter study of the placement and immediate loading of the one‐piece implant. A total of 142 implants were placed in the jaws of 93 patients. Implants were placed consecutively and were followed at specified intervals in three private clinical practices. Clinical performance was recorded relative to implant survival and prosthesis support.</p><p> <i>Results</i>: The implant survival rate was 93.7%, with similar responses in the maxilla (95.0%) and the mandible (92.7%). When implant failure occurred, it was observed as mobility without infection within 3 to 5 weeks of implant insertion.</p><p> <i>Conclusions</i>: On the basis of this trial, there is promising evidence that this implant design can succeed at rates similar to other designs that require conventional healing times.</p></abstract></abstractGroup></contentMeta></header></component></istex:document></istex:metadataXml><mods version="3.6"><titleInfo lang="en"><title>Preliminary Report of Immediately Loaded Altiva Natural Tooth Replacement Dental Implants</title></titleInfo><titleInfo type="alternative" contentType="CDATA" lang="en"><title>Preliminary Report of Immediately Loaded Altiva Natural Tooth Replacement Dental Implants</title></titleInfo><name type="personal"><namePart type="given">Andre U.</namePart><namePart type="family">Buchs</namePart><namePart type="termsOfAddress">DDS</namePart><affiliation>Adjunct Professor, Oral Surgery, University of Pennsylvania, Philadelphia, Pennsylvania</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Laurence</namePart><namePart type="family">Levine</namePart><namePart type="termsOfAddress">DDS</namePart><affiliation>Private Practice, Fort Lauderdale, Florida, California</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Peter</namePart><namePart type="family">Moy</namePart><namePart type="termsOfAddress">DMD</namePart><affiliation>Co‐Director, Implant Program, UCLA, Los Angeles, California</affiliation><affiliation>E-mail: pkmoy@ucla.edu</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">2001-04</dateIssued><copyrightDate encoding="w3cdtf">2001</copyrightDate></originInfo><language><languageTerm type="code" authority="rfc3066">en</languageTerm><languageTerm type="code" authority="iso639-2b">eng</languageTerm></language><physicalDescription><extent unit="references">41</extent><extent unit="linksCrossRef">4</extent></physicalDescription><abstract lang="en">Background: Osseointegration may be described as a direct contact between living bone and an alloplastic implant. It is thought that a period of undisturbed healing is required to ensure osseointegration. The length of the healing period is dependent on a number of factors, such as implant material, surface configuration, site preparation technique, bone quality, healing capacity of the osteotomy, and implant design. Elimination of the healing period offers distinct advantages in terms of cost of therapy and convenience to patients. Recently, a new one‐piece implant design was proposed that provides improved stability of the implant to allow immediate support of an interim prosthesis. Purpose: This article presents the initial clinical experiences when the Altiva Natural Tooth Replacement one‐piece implant was used in a human clinical trial. Materials and Methods: This was a prospective multicenter study of the placement and immediate loading of the one‐piece implant. A total of 142 implants were placed in the jaws of 93 patients. Implants were placed consecutively and were followed at specified intervals in three private clinical practices. Clinical performance was recorded relative to implant survival and prosthesis support. Results: The implant survival rate was 93.7%, with similar responses in the maxilla (95.0%) and the mandible (92.7%). When implant failure occurred, it was observed as mobility without infection within 3 to 5 weeks of implant insertion. Conclusions: On the basis of this trial, there is promising evidence that this implant design can succeed at rates similar to other designs that require conventional healing times.</abstract><subject lang="en"><genre>keywords</genre><topic>immediate load</topic><topic>implant design</topic><topic>implant survival</topic><topic>one‐piece implant</topic><topic>osseointegration</topic><topic>single stage</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><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>2001</date><detail type="volume"><caption>vol.</caption><number>3</number></detail><detail type="issue"><caption>no.</caption><number>2</number></detail><extent unit="pages"><start>97</start><end>106</end><total>10</total></extent></part></relatedItem><identifier type="istex">C4B72AA1D056FCA3A984CDEA5D3A35ACC7E1A2D4</identifier><identifier type="ark">ark:/67375/WNG-RQQP19D2-X</identifier><identifier type="DOI">10.1111/j.1708-8208.2001.tb00237.x</identifier><identifier type="ArticleID">CID97</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>Blackwell Publishing Ltd</recordOrigin></recordInfo></mods><json:item><extension>json</extension><original>false</original><mimetype>application/json</mimetype><uri>https://api.istex.fr/document/C4B72AA1D056FCA3A984CDEA5D3A35ACC7E1A2D4/metadata/json</uri></json:item></metadata><serie></serie></istex></record>Pour manipuler ce document sous Unix (Dilib)
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