Clinical and microbiological status of osseointegrated implants.
Identifieur interne : 004417 ( PubMed/Curation ); précédent : 004416; suivant : 004418Clinical and microbiological status of osseointegrated implants.
Auteurs : K. George [Suisse] ; G G Zafiropoulos ; Y. Murat ; S. Hubertus ; R J NisengardSource :
- Journal of periodontology [ 0022-3492 ] ; 1994.
Descripteurs français
- KwdFr :
- Adulte, Adulte d'âge moyen, Aggregatibacter actinomycetemcomitans (isolement et purification), Débit sécrétoire, Exsudat gingival, Facteurs temps, Femelle, Humains, Implants dentaires (effets indésirables), Implants dentaires (microbiologie), Indice d'hygiène buccodentaire, Indice de plaque dentaire, Indice parodontal, Loi du khi-deux, Mâchoire partiellement édentée (microbiologie), Mâle, Numération de colonies microbiennes, Ostéo-intégration, Parodontite (microbiologie), Parodontite (étiologie), Plaque dentaire (microbiologie), Porphyromonas gingivalis (isolement et purification), Pose d'implant dentaire endo-osseux (effets indésirables), Pose d'implant dentaire endo-osseux (microbiologie), Prevotella intermedia (isolement et purification), Prevotella intermedia (pathogénicité), Rétention de prothèse dentaire, Statistique non paramétrique, Sujet âgé.
- MESH :
- effets indésirables : Implants dentaires, Pose d'implant dentaire endo-osseux.
- isolement et purification : Aggregatibacter actinomycetemcomitans, Porphyromonas gingivalis, Prevotella intermedia.
- microbiologie : Implants dentaires, Mâchoire partiellement édentée, Parodontite, Plaque dentaire, Pose d'implant dentaire endo-osseux.
- pathogénicité : Prevotella intermedia.
- étiologie : Parodontite.
- Adulte, Adulte d'âge moyen, Débit sécrétoire, Exsudat gingival, Facteurs temps, Femelle, Humains, Indice d'hygiène buccodentaire, Indice de plaque dentaire, Indice parodontal, Loi du khi-deux, Mâle, Numération de colonies microbiennes, Ostéo-intégration, Rétention de prothèse dentaire, Statistique non paramétrique, Sujet âgé.
English descriptors
- KwdEn :
- Adult, Aged, Aggregatibacter actinomycetemcomitans (isolation & purification), Chi-Square Distribution, Colony Count, Microbial, Dental Implantation, Endosseous (adverse effects), Dental Implantation, Endosseous (microbiology), Dental Implants (adverse effects), Dental Implants (microbiology), Dental Plaque (microbiology), Dental Plaque Index, Dental Prosthesis Retention, Female, Gingival Crevicular Fluid, Humans, Jaw, Edentulous, Partially (microbiology), Male, Middle Aged, Oral Hygiene Index, Osseointegration, Periodontal Index, Periodontitis (etiology), Periodontitis (microbiology), Porphyromonas gingivalis (isolation & purification), Prevotella intermedia (isolation & purification), Prevotella intermedia (pathogenicity), Secretory Rate, Statistics, Nonparametric, Time Factors.
- MESH :
- chemical , adverse effects : Dental Implants.
- adverse effects : Dental Implantation, Endosseous.
- etiology : Periodontitis.
- isolation & purification : Aggregatibacter actinomycetemcomitans, Porphyromonas gingivalis, Prevotella intermedia.
- microbiology : Dental Implantation, Endosseous, Dental Implants, Dental Plaque, Jaw, Edentulous, Partially, Periodontitis.
- pathogenicity : Prevotella intermedia.
- Adult, Aged, Chi-Square Distribution, Colony Count, Microbial, Dental Plaque Index, Dental Prosthesis Retention, Female, Gingival Crevicular Fluid, Humans, Male, Middle Aged, Oral Hygiene Index, Osseointegration, Periodontal Index, Secretory Rate, Statistics, Nonparametric, Time Factors.
Abstract
Peri-implantitis, an inflammatory response around implants, has a poorly defined etiology and pathogenesis. To better understand the role of specific microorganisms in this disease process, clinical and microbiological parameters were examined in 24 patients with 98 osseointegrated implants. Sites were evaluated for probing depth (PD), plaque/calculus index (PI), gingival bleeding index (GBI), mobility, and crevicular fluid flow rate (CFFR). Actinobacillus actinomycetemcomitans, Porphyromonas gingivalis, and Prevotella intermedia in subgingival plaque were identified by latex agglutination assays. Clinically, a statistically significant correlation (P < 0.001) was observed between probing depth and the length of time an implant was present. Mobility was also significantly greater (P < 0.001) in the maxillary than in the mandibular implants. Subgingival sites harboring one of the three microorganisms had significantly greater PD, GBI, and CFFR than non-colonized sites. Implants in partially edentulous patients more frequently were colonized with P. gingivalis/P. intermedia than edentulous patients. The incidence of these microorganisms also correlated with fixture longevity. Implants present for 3 to 4 years had a significantly greater frequency of test microorganisms than implants present for 1 to 2 years. These findings suggest that microbial pathogens associated with periodontitis occur more commonly around implants exhibiting gingival inflammation (GBI) and may contribute to peri-implantitis.
DOI: 10.1902/jop.1994.65.8.766
PubMed: 7965553
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xml:lang="en"><term>Dental Implantation, Endosseous</term></keywords><keywords scheme="MESH" qualifier="effets indésirables" xml:lang="fr"><term>Implants dentaires</term><term>Pose d'implant dentaire endo-osseux</term></keywords><keywords scheme="MESH" qualifier="etiology" xml:lang="en"><term>Periodontitis</term></keywords><keywords scheme="MESH" qualifier="isolation & purification" xml:lang="en"><term>Aggregatibacter actinomycetemcomitans</term><term>Porphyromonas gingivalis</term><term>Prevotella intermedia</term></keywords><keywords scheme="MESH" qualifier="isolement et purification" xml:lang="fr"><term>Aggregatibacter actinomycetemcomitans</term><term>Porphyromonas gingivalis</term><term>Prevotella intermedia</term></keywords><keywords scheme="MESH" qualifier="microbiologie" xml:lang="fr"><term>Implants dentaires</term><term>Mâchoire partiellement édentée</term><term>Parodontite</term><term>Plaque dentaire</term><term>Pose d'implant dentaire endo-osseux</term></keywords><keywords 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Rate</term><term>Statistics, Nonparametric</term><term>Time Factors</term></keywords><keywords scheme="MESH" xml:lang="fr"><term>Adulte</term><term>Adulte d'âge moyen</term><term>Débit sécrétoire</term><term>Exsudat gingival</term><term>Facteurs temps</term><term>Femelle</term><term>Humains</term><term>Indice d'hygiène buccodentaire</term><term>Indice de plaque dentaire</term><term>Indice parodontal</term><term>Loi du khi-deux</term><term>Mâle</term><term>Numération de colonies microbiennes</term><term>Ostéo-intégration</term><term>Rétention de prothèse dentaire</term><term>Statistique non paramétrique</term><term>Sujet âgé</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Peri-implantitis, an inflammatory response around implants, has a poorly defined etiology and pathogenesis. To better understand the role of specific microorganisms in this disease process, clinical and microbiological parameters were examined in 24 patients with 98 osseointegrated implants. Sites were evaluated for probing depth (PD), plaque/calculus index (PI), gingival bleeding index (GBI), mobility, and crevicular fluid flow rate (CFFR). Actinobacillus actinomycetemcomitans, Porphyromonas gingivalis, and Prevotella intermedia in subgingival plaque were identified by latex agglutination assays. Clinically, a statistically significant correlation (P < 0.001) was observed between probing depth and the length of time an implant was present. Mobility was also significantly greater (P < 0.001) in the maxillary than in the mandibular implants. Subgingival sites harboring one of the three microorganisms had significantly greater PD, GBI, and CFFR than non-colonized sites. Implants in partially edentulous patients more frequently were colonized with P. gingivalis/P. intermedia than edentulous patients. The incidence of these microorganisms also correlated with fixture longevity. Implants present for 3 to 4 years had a significantly greater frequency of test microorganisms than implants present for 1 to 2 years. These findings suggest that microbial pathogens associated with periodontitis occur more commonly around implants exhibiting gingival inflammation (GBI) and may contribute to peri-implantitis.</div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">7965553</PMID><DateCompleted><Year>1994</Year><Month>12</Month><Day>06</Day></DateCompleted><DateRevised><Year>2013</Year><Month>11</Month><Day>21</Day></DateRevised><Article PubModel="Print"><Journal><ISSN IssnType="Print">0022-3492</ISSN><JournalIssue CitedMedium="Print"><Volume>65</Volume><Issue>8</Issue><PubDate><Year>1994</Year><Month>Aug</Month></PubDate></JournalIssue><Title>Journal of periodontology</Title><ISOAbbreviation>J. Periodontol.</ISOAbbreviation></Journal><ArticleTitle>Clinical and microbiological status of osseointegrated implants.</ArticleTitle><Pagination><MedlinePgn>766-70</MedlinePgn></Pagination><Abstract><AbstractText>Peri-implantitis, an inflammatory response around implants, has a poorly defined etiology and pathogenesis. To better understand the role of specific microorganisms in this disease process, clinical and microbiological parameters were examined in 24 patients with 98 osseointegrated implants. Sites were evaluated for probing depth (PD), plaque/calculus index (PI), gingival bleeding index (GBI), mobility, and crevicular fluid flow rate (CFFR). Actinobacillus actinomycetemcomitans, Porphyromonas gingivalis, and Prevotella intermedia in subgingival plaque were identified by latex agglutination assays. Clinically, a statistically significant correlation (P < 0.001) was observed between probing depth and the length of time an implant was present. Mobility was also significantly greater (P < 0.001) in the maxillary than in the mandibular implants. Subgingival sites harboring one of the three microorganisms had significantly greater PD, GBI, and CFFR than non-colonized sites. Implants in partially edentulous patients more frequently were colonized with P. gingivalis/P. intermedia than edentulous patients. The incidence of these microorganisms also correlated with fixture longevity. Implants present for 3 to 4 years had a significantly greater frequency of test microorganisms than implants present for 1 to 2 years. These findings suggest that microbial pathogens associated with periodontitis occur more commonly around implants exhibiting gingival inflammation (GBI) and may contribute to peri-implantitis.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>George</LastName><ForeName>K</ForeName><Initials>K</Initials><AffiliationInfo><Affiliation>University of Geneva, Switzerland.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Zafiropoulos</LastName><ForeName>G G</ForeName><Initials>GG</Initials></Author><Author ValidYN="Y"><LastName>Murat</LastName><ForeName>Y</ForeName><Initials>Y</Initials></Author><Author ValidYN="Y"><LastName>Hubertus</LastName><ForeName>S</ForeName><Initials>S</Initials></Author><Author ValidYN="Y"><LastName>Nisengard</LastName><ForeName>R J</ForeName><Initials>RJ</Initials></Author></AuthorList><Language>eng</Language><PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType><PublicationType UI="D013485">Research Support, Non-U.S. Gov't</PublicationType></PublicationTypeList></Article><MedlineJournalInfo><Country>United States</Country><MedlineTA>J Periodontol</MedlineTA><NlmUniqueID>8000345</NlmUniqueID><ISSNLinking>0022-3492</ISSNLinking></MedlineJournalInfo><ChemicalList><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D015921">Dental Implants</NameOfSubstance></Chemical></ChemicalList><CitationSubset>D</CitationSubset><CitationSubset>IM</CitationSubset><MeshHeadingList><MeshHeading><DescriptorName UI="D000328" MajorTopicYN="N">Adult</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D000368" MajorTopicYN="N">Aged</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D016976" MajorTopicYN="N">Aggregatibacter actinomycetemcomitans</DescriptorName><QualifierName UI="Q000302" MajorTopicYN="N">isolation & purification</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D016009" MajorTopicYN="N">Chi-Square Distribution</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D015169" MajorTopicYN="N">Colony Count, Microbial</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D003758" MajorTopicYN="N">Dental Implantation, Endosseous</DescriptorName><QualifierName UI="Q000009" MajorTopicYN="Y">adverse effects</QualifierName><QualifierName UI="Q000382" MajorTopicYN="N">microbiology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D015921" MajorTopicYN="N">Dental Implants</DescriptorName><QualifierName UI="Q000009" MajorTopicYN="N">adverse effects</QualifierName><QualifierName UI="Q000382" MajorTopicYN="Y">microbiology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D003773" MajorTopicYN="N">Dental Plaque</DescriptorName><QualifierName UI="Q000382" MajorTopicYN="Y">microbiology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D003774" MajorTopicYN="N">Dental Plaque Index</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D017268" MajorTopicYN="N">Dental Prosthesis Retention</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D005260" MajorTopicYN="N">Female</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D005883" MajorTopicYN="N">Gingival Crevicular Fluid</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D006801" MajorTopicYN="N">Humans</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D007576" MajorTopicYN="N">Jaw, Edentulous, Partially</DescriptorName><QualifierName UI="Q000382" MajorTopicYN="N">microbiology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D008297" MajorTopicYN="N">Male</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D008875" MajorTopicYN="N">Middle Aged</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D009911" MajorTopicYN="N">Oral Hygiene Index</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D016348" MajorTopicYN="N">Osseointegration</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D010512" MajorTopicYN="N">Periodontal Index</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D010518" MajorTopicYN="N">Periodontitis</DescriptorName><QualifierName UI="Q000209" MajorTopicYN="Y">etiology</QualifierName><QualifierName UI="Q000382" MajorTopicYN="N">microbiology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D016966" MajorTopicYN="N">Porphyromonas gingivalis</DescriptorName><QualifierName UI="Q000302" MajorTopicYN="N">isolation & purification</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D018713" MajorTopicYN="N">Prevotella intermedia</DescriptorName><QualifierName UI="Q000302" MajorTopicYN="N">isolation & purification</QualifierName><QualifierName UI="Q000472" MajorTopicYN="N">pathogenicity</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D012636" MajorTopicYN="N">Secretory Rate</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D018709" MajorTopicYN="N">Statistics, Nonparametric</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D013997" MajorTopicYN="N">Time Factors</DescriptorName></MeshHeading></MeshHeadingList></MedlineCitation><PubmedData><History><PubMedPubDate PubStatus="pubmed"><Year>1994</Year><Month>8</Month><Day>1</Day></PubMedPubDate><PubMedPubDate PubStatus="medline"><Year>1994</Year><Month>8</Month><Day>1</Day><Hour>0</Hour><Minute>1</Minute></PubMedPubDate><PubMedPubDate PubStatus="entrez"><Year>1994</Year><Month>8</Month><Day>1</Day><Hour>0</Hour><Minute>0</Minute></PubMedPubDate></History><PublicationStatus>ppublish</PublicationStatus><ArticleIdList><ArticleId IdType="pubmed">7965553</ArticleId><ArticleId IdType="doi">10.1902/jop.1994.65.8.766</ArticleId></ArticleIdList></PubmedData></pubmed></record>Pour manipuler ce document sous Unix (Dilib)
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