Black-pigmenting Gram-negative bacteria in periodontal disease. II. Screening strategies for detection of P. gingivalis
The purpose of this analysis was to evaluate the feasibility of detecting P. gingivalis using selected sites and to indicate increased proportions of this organism in periodontitis patients. In 10 patients suffering from moderate to advanced periodontal disease, separate microbiological samples were...
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Veröffentlicht in: | Journal of periodontal research 1991-07, Vol.26 (4), p.308-313 |
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description | The purpose of this analysis was to evaluate the feasibility of detecting P. gingivalis using selected sites and to indicate increased proportions of this organism in periodontitis patients. In 10 patients suffering from moderate to advanced periodontal disease, separate microbiological samples were taken from the mesial, buccal, distal and oral (lingual or palatal) aspects of every tooth. This yielded a total of 927 microbiological samples, 84 to 102 per patient. Three distinct patterns of distribution and relative proportion of P. gingivalis were recognized. In one group of patients, the organism was not cultured. In a second group, few positive sites with low proportions of P. gingivalis were present. A third group of patients yielded high frequencies and proportions of P. gingivalis. The number of samples necessary to diagnose the presence of P. gingivalis at a 95% confidence level varied considerably between the three groups. In 4 patients, sampling 4 randomly selected sites was sufficient, while in the remaining 3 positive patients, 25 or more samples were required to detect the organism with equal certainty. Seven different protocols for multiple subgingival sampling were studied. When considering the number of samples needed to detect the presence of P. gingivalis and to estimate the highest proportion of this organism, selection of the deepest pocket in each quadrant was the most efficient method of sampling. |
doi_str_mv | 10.1111/j.1600-0765.1991.tb02068.x |
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II. Screening strategies for detection of P. gingivalis</title><source>MEDLINE</source><source>Wiley Online Library Journals Frontfile Complete</source><creator>Mombelli, Andrea ; McNabb, Hal ; Lang, Niklaus P.</creator><creatorcontrib>Mombelli, Andrea ; McNabb, Hal ; Lang, Niklaus P.</creatorcontrib><description>The purpose of this analysis was to evaluate the feasibility of detecting P. gingivalis using selected sites and to indicate increased proportions of this organism in periodontitis patients. In 10 patients suffering from moderate to advanced periodontal disease, separate microbiological samples were taken from the mesial, buccal, distal and oral (lingual or palatal) aspects of every tooth. This yielded a total of 927 microbiological samples, 84 to 102 per patient. Three distinct patterns of distribution and relative proportion of P. gingivalis were recognized. In one group of patients, the organism was not cultured. In a second group, few positive sites with low proportions of P. gingivalis were present. A third group of patients yielded high frequencies and proportions of P. gingivalis. The number of samples necessary to diagnose the presence of P. gingivalis at a 95% confidence level varied considerably between the three groups. In 4 patients, sampling 4 randomly selected sites was sufficient, while in the remaining 3 positive patients, 25 or more samples were required to detect the organism with equal certainty. Seven different protocols for multiple subgingival sampling were studied. 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II. Screening strategies for detection of P. gingivalis</title><title>Journal of periodontal research</title><addtitle>J Periodontal Res</addtitle><description>The purpose of this analysis was to evaluate the feasibility of detecting P. gingivalis using selected sites and to indicate increased proportions of this organism in periodontitis patients. In 10 patients suffering from moderate to advanced periodontal disease, separate microbiological samples were taken from the mesial, buccal, distal and oral (lingual or palatal) aspects of every tooth. This yielded a total of 927 microbiological samples, 84 to 102 per patient. Three distinct patterns of distribution and relative proportion of P. gingivalis were recognized. In one group of patients, the organism was not cultured. In a second group, few positive sites with low proportions of P. gingivalis were present. A third group of patients yielded high frequencies and proportions of P. gingivalis. The number of samples necessary to diagnose the presence of P. gingivalis at a 95% confidence level varied considerably between the three groups. In 4 patients, sampling 4 randomly selected sites was sufficient, while in the remaining 3 positive patients, 25 or more samples were required to detect the organism with equal certainty. Seven different protocols for multiple subgingival sampling were studied. When considering the number of samples needed to detect the presence of P. gingivalis and to estimate the highest proportion of this organism, selection of the deepest pocket in each quadrant was the most efficient method of sampling.</description><subject>Adult</subject><subject>anaerobic culture</subject><subject>Bacterial diseases</subject><subject>Bacteriological Techniques</subject><subject>Bacteroides - isolation & purification</subject><subject>Biological and medical sciences</subject><subject>Colony Count, Microbial</subject><subject>Dentistry</subject><subject>diagnosis</subject><subject>Ent and stomatologic bacterial diseases</subject><subject>Human bacterial diseases</subject><subject>Humans</subject><subject>Infectious diseases</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Periodontal Diseases - microbiology</subject><subject>Periodontal Pocket - microbiology</subject><subject>periodontitis</subject><subject>Periodontitis - microbiology</subject><subject>Porphyromonas gingivalis</subject><subject>Probability</subject><subject>Sampling Studies</subject><issn>0022-3484</issn><issn>1600-0765</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1991</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqVkF9v0zAUxS0EGmXwEZAsJHhLsGPXTnhAGtsonaaCGIhH6ya5jtzlT7Hdrfv2JEq1PeMX2zrn3Hv0I-QdZykfz8dtyhVjCdNqmfKi4GksWcZUnh6ekcWj9JwsGMuyRMhcviSvQtiy8a90cUJOeC64LPIFuf_SQnWb7FzTYR9d39CVhy7psYHo7pCWUEX0Dqjr6W58DPXQR2hp7QJCwJSu1ym9qTxiP4VD9BCxcRioHTytMWIV3dDTwdIfKW1Gj7uD1oXX5IWFNuCb431Kfn-9_HX-Lbn-vlqfn10nlZQ6TwArxZko69KOjZkVmudMosqQyywTSpSKcyEtCJGXWud5JgpgwmpZMmDKilPyYZ6788PfPYZoOhcqbFvocdgHozMmleDFaPw0Gys_hODRmp13HfgHw5mZqJutmdCaCa2ZqJsjdXMYw2-PW_Zlh_VTdMY86u-POoQKWuuhr1x4so0WuWRTic-z7961-PAfDczVz0vBpkXJPMCFiIfHAeBvjdJCL82fzcpcyQu52dxocyH-AbxnrdI</recordid><startdate>199107</startdate><enddate>199107</enddate><creator>Mombelli, Andrea</creator><creator>McNabb, Hal</creator><creator>Lang, Niklaus P.</creator><general>Blackwell Publishing Ltd</general><general>Blackwell</general><scope>BSCLL</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>199107</creationdate><title>Black-pigmenting Gram-negative bacteria in periodontal disease. 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Screening strategies for detection of P. gingivalis</title><author>Mombelli, Andrea ; McNabb, Hal ; Lang, Niklaus P.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4478-aec6103bdbf8310f371804e62e1422363b61134fa338b7788239a03f74b0a06f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1991</creationdate><topic>Adult</topic><topic>anaerobic culture</topic><topic>Bacterial diseases</topic><topic>Bacteriological Techniques</topic><topic>Bacteroides - isolation & purification</topic><topic>Biological and medical sciences</topic><topic>Colony Count, Microbial</topic><topic>Dentistry</topic><topic>diagnosis</topic><topic>Ent and stomatologic bacterial diseases</topic><topic>Human bacterial diseases</topic><topic>Humans</topic><topic>Infectious diseases</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Periodontal Diseases - microbiology</topic><topic>Periodontal Pocket - microbiology</topic><topic>periodontitis</topic><topic>Periodontitis - microbiology</topic><topic>Porphyromonas gingivalis</topic><topic>Probability</topic><topic>Sampling Studies</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mombelli, Andrea</creatorcontrib><creatorcontrib>McNabb, Hal</creatorcontrib><creatorcontrib>Lang, Niklaus P.</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of periodontal research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mombelli, Andrea</au><au>McNabb, Hal</au><au>Lang, Niklaus P.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Black-pigmenting Gram-negative bacteria in periodontal disease. II. Screening strategies for detection of P. gingivalis</atitle><jtitle>Journal of periodontal research</jtitle><addtitle>J Periodontal Res</addtitle><date>1991-07</date><risdate>1991</risdate><volume>26</volume><issue>4</issue><spage>308</spage><epage>313</epage><pages>308-313</pages><issn>0022-3484</issn><eissn>1600-0765</eissn><abstract>The purpose of this analysis was to evaluate the feasibility of detecting P. gingivalis using selected sites and to indicate increased proportions of this organism in periodontitis patients. In 10 patients suffering from moderate to advanced periodontal disease, separate microbiological samples were taken from the mesial, buccal, distal and oral (lingual or palatal) aspects of every tooth. This yielded a total of 927 microbiological samples, 84 to 102 per patient. Three distinct patterns of distribution and relative proportion of P. gingivalis were recognized. In one group of patients, the organism was not cultured. In a second group, few positive sites with low proportions of P. gingivalis were present. A third group of patients yielded high frequencies and proportions of P. gingivalis. The number of samples necessary to diagnose the presence of P. gingivalis at a 95% confidence level varied considerably between the three groups. In 4 patients, sampling 4 randomly selected sites was sufficient, while in the remaining 3 positive patients, 25 or more samples were required to detect the organism with equal certainty. Seven different protocols for multiple subgingival sampling were studied. When considering the number of samples needed to detect the presence of P. gingivalis and to estimate the highest proportion of this organism, selection of the deepest pocket in each quadrant was the most efficient method of sampling.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>1831498</pmid><doi>10.1111/j.1600-0765.1991.tb02068.x</doi><tpages>6</tpages></addata></record> |
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subjects | Adult anaerobic culture Bacterial diseases Bacteriological Techniques Bacteroides - isolation & purification Biological and medical sciences Colony Count, Microbial Dentistry diagnosis Ent and stomatologic bacterial diseases Human bacterial diseases Humans Infectious diseases Medical sciences Middle Aged Periodontal Diseases - microbiology Periodontal Pocket - microbiology periodontitis Periodontitis - microbiology Porphyromonas gingivalis Probability Sampling Studies |
title | Black-pigmenting Gram-negative bacteria in periodontal disease. II. Screening strategies for detection of P. gingivalis |
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