Clinical evaluation of resilient denture liners. Part 2: candida count and speciation
Identifieur interne : 005357 ( Istex/Corpus ); précédent : 005356; suivant : 005358Clinical evaluation of resilient denture liners. Part 2: candida count and speciation
Auteurs : Mary E. Brosky ; Igor J. Pesun ; Brad Morrison ; James S. Hodges ; Juey H. Lai ; William LiljemarkSource :
- Journal of Prosthodontics [ 1059-941X ] ; 2003-09.
English descriptors
- KwdEn :
- Albicans, Candida, Candida albicans, Candida count, Candida growth, Candida species, Carbohydrate assimilation, Chromagar, Chromagar candida, Dent, Dentistry, Denture, Denture stomatitis, Edentulous patients, Exact mcnemar test, Fungal growth, Glabrata, Liner, Mandibular, Mandibular denture, Mandibular dentures, Minnesota school, Parapsilosis, Prosthet, Prosthet dent, Resilient, Resilient denture liner, Resilient denture liners, Trichosporon, Tropicalis.
- Teeft :
- Albicans, Candida, Candida albicans, Candida count, Candida growth, Candida species, Carbohydrate assimilation, Chromagar, Chromagar candida, Dent, Dentistry, Denture, Denture stomatitis, Edentulous patients, Exact mcnemar test, Fungal growth, Glabrata, Liner, Mandibular, Mandibular denture, Mandibular dentures, Minnesota school, Parapsilosis, Prosthet, Prosthet dent, Resilient, Resilient denture liner, Resilient denture liners, Trichosporon, Tropicalis.
Abstract
Purpose The purpose of this study was to count and to speciate Candida isolated from 2 resilient denture liners, Molloplast‐B and MPDS‐SL.
Url:
DOI: 10.1016/S1059-941X(03)00041-X
Links to Exploration step
ISTEX:A6CC008628F02F6D502793064A231EF699B826A8Le document en format XML
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Brosky DMD</name><affiliations><json:string>Division of Prosthodontics, Department of Restorative Sciences, School of Dentistry, School of Dentistry, University of Minnesota, Minneapolis, MN, USA</json:string><json:string>E-mail: brosk001@tc.umn.edu</json:string></affiliations></json:item><json:item><name>Igor J. Pesun DMD, MS, FACP</name><affiliations><json:string>Division of Prosthodontics, Department of Restorative Sciences, School of Dentistry, School of Dentistry, University of Minnesota, Minneapolis, MN, USA</json:string></affiliations></json:item><json:item><name>Brad Morrison BS</name><affiliations><json:string>School of Dentistry, School of Dentistry, University of Minnesota, Minneapolis, MN, USA</json:string></affiliations></json:item><json:item><name>James S. Hodges PhD</name><affiliations><json:string>Division of Biostatistics, School of Public Health, School of Dentistry, University of Minnesota, Minneapolis, MN, USA</json:string></affiliations></json:item><json:item><name>Juey H. Lai PhD</name><affiliations><json:string>Lai Laboratories Inc., Burnsville, MN, School of Dentistry, University of Minnesota, USA</json:string></affiliations></json:item><json:item><name>William Liljemark DDS, PhD</name><affiliations><json:string>Division of Oral Microbiology, Department of Oral Sciences, School of Dentistry, School of Dentistry, University of Minnesota, Minneapolis, MN, USA</json:string></affiliations></json:item></author><subject><json:item><lang><json:string>eng</json:string></lang><value>resilient denture liner</value></json:item><json:item><lang><json:string>eng</json:string></lang><value>Candida</value></json:item></subject><articleId><json:string>JOPR162</json:string></articleId><arkIstex>ark:/67375/WNG-65S9THGG-P</arkIstex><language><json:string>eng</json:string></language><originalGenre><json:string>miscellaneous</json:string></originalGenre><abstract>Purpose The purpose of this study was to count and to speciate Candida isolated from 2 resilient denture liners, Molloplast‐B and MPDS‐SL.</abstract><qualityIndicators><score>5.22</score><pdfWordCount>2956</pdfWordCount><pdfCharCount>19150</pdfCharCount><pdfVersion>1.3</pdfVersion><pdfPageCount>6</pdfPageCount><pdfPageSize>594 x 792 pts</pdfPageSize><refBibsNative>true</refBibsNative><abstractWordCount>22</abstractWordCount><abstractCharCount>138</abstractCharCount><keywordCount>2</keywordCount></qualityIndicators><title>Clinical evaluation of resilient denture liners. 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Lai</json:string><json:string>Igor J. Pesun</json:string><json:string>William Liljemark</json:string><json:string>Mary E. Brosky</json:string><json:string>Colleen Doyen</json:string><json:string>Brad Morrison</json:string><json:string>Donald Schneider</json:string><json:string>Speciation</json:string><json:string>James S. 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Part 2: <hi rend="italic">candida</hi> count and speciation</title></titleStmt><publicationStmt><authority>ISTEX</authority><publisher>Blackwell Publishing Ltd</publisher><pubPlace>Oxford, UK</pubPlace><date type="published" when="2003-09"></date></publicationStmt><notesStmt><note type="content-type" subtype="other" source="miscellaneous" scheme="https://content-type.data.istex.fr/ark:/67375/XTP-7474895G-0">other</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="other"><analytic><title level="a" type="main">Clinical evaluation of resilient denture liners. Part 2: <hi rend="italic">candida</hi> count and speciation</title><author xml:id="author-0000" role="corresp"><persName><forename type="first">Mary E.</forename><surname>Brosky</surname><roleName type="degree">DMD</roleName></persName><affiliation>Division of Prosthodontics, Department of Restorative Sciences, School of Dentistry, School of Dentistry, University of Minnesota, Minneapolis, MN, USA<address><country key="US"></country></address></affiliation><affiliation>*Correspondence to: Dr. Beth Brosky, University of Minnesota School of Dentistry, 9‐450 Moos Tower, 515 Delaware Street S.E., Minneapolis, MN 55455, USA; Email: brosk001@tc.umn.edu</affiliation></author><author xml:id="author-0001"><persName><forename type="first">Igor J.</forename><surname>Pesun</surname><roleName type="degree">DMD, MS, FACP</roleName></persName><affiliation>Division of Prosthodontics, Department of Restorative Sciences, School of Dentistry, School of Dentistry, University of Minnesota, Minneapolis, MN, USA<address><country key="US"></country></address></affiliation></author><author xml:id="author-0002"><persName><forename type="first">Brad</forename><surname>Morrison</surname><roleName type="degree">BS</roleName></persName><affiliation>School of Dentistry, School of Dentistry, University of Minnesota, Minneapolis, MN, USA<address><country key="US"></country></address></affiliation></author><author xml:id="author-0003"><persName><forename type="first">James S.</forename><surname>Hodges</surname><roleName type="degree">PhD</roleName></persName><affiliation>Division of Biostatistics, School of Public Health, School of Dentistry, University of Minnesota, Minneapolis, MN, USA<address><country key="US"></country></address></affiliation></author><author xml:id="author-0004"><persName><forename type="first">Juey H.</forename><surname>Lai</surname><roleName type="degree">PhD</roleName></persName><affiliation>Lai Laboratories Inc., Burnsville, MN, School of Dentistry, University of Minnesota, USA<address><country key="US"></country></address></affiliation></author><author xml:id="author-0005"><persName><forename type="first">William</forename><surname>Liljemark</surname><roleName type="degree">DDS, PhD</roleName></persName><affiliation>Division of Oral Microbiology, Department of Oral Sciences, School of Dentistry, School of Dentistry, University of Minnesota, Minneapolis, MN, USA<address><country key="US"></country></address></affiliation></author><idno type="istex">A6CC008628F02F6D502793064A231EF699B826A8</idno><idno type="ark">ark:/67375/WNG-65S9THGG-P</idno><idno type="DOI">10.1016/S1059-941X(03)00041-X</idno><idno type="unit">JOPR162</idno><idno type="toTypesetVersion">file:JOPR.JOPR162.pdf</idno></analytic><monogr><title level="j" type="main">Journal of Prosthodontics</title><title level="j" type="alt">JOURNAL OF PROSTHODONTICS</title><idno type="pISSN">1059-941X</idno><idno type="eISSN">1532-849X</idno><idno type="book-DOI">10.1111/(ISSN)1532-849X</idno><idno type="book-part-DOI">10.1111/jopr.2003.12.issue-3</idno><idno type="product">JOPR</idno><idno type="publisherDivision">ST</idno><imprint><biblScope unit="vol">12</biblScope><biblScope unit="issue">3</biblScope><biblScope unit="page" from="162">162</biblScope><biblScope unit="page" to="167">167</biblScope><biblScope unit="page-count">6</biblScope><publisher>Blackwell Publishing Ltd</publisher><pubPlace>Oxford, UK</pubPlace><date type="published" when="2003-09"></date></imprint></monogr></biblStruct></sourceDesc></fileDesc><profileDesc><abstract xml:lang="en" style="main"><p><hi rend="bold"><emph><span>Purpose</span></emph></hi> The purpose of this study was to count and to speciate <hi rend="italic">Candida</hi> isolated from 2 resilient denture liners, Molloplast‐B and MPDS‐SL.</p><p><hi rend="bold"><emph><span>Materials and Methods</span></emph></hi> A group of 20 patients each had 1 maxillary denture and 2 mandibular dentures fabricated. One mandibular denture was lined with Molloplast‐B, and 1 was lined with MPDS‐SL. Each denture was used for 3 months. At the end of the 3‐month period, the mandibular denture was surrendered, and a 5 × 5‐mm circular resilient liner sample was obtained from the tissue surface of the lingual flange. Samples were processed, and <hi rend="italic">Candida</hi> was isolated and counted. Speciation of <hi rend="italic">Candida</hi> was performed using CHROMagar Candida and API 20C AUX strips.</p><p><hi rend="bold"><emph><span>Results</span></emph></hi> Molloplast‐B had, on average, 5 times as many CFU/sample as MPDSL‐SL, but this difference was not significant (<emph><span><hi rend="italic">p</hi>= 0.26</span></emph>). A sign test gave a similar nonsignificant trend (<emph><span><hi rend="italic">p</hi>= 0.057</span></emph>). CHROMagar identified several <hi rend="italic">Candida</hi> species, and confirmation was made using API 20C AUX strips. One patient was lost to follow‐up. Of 19 Molloplast‐B samples, 7 had no growth, 4 grew <hi rend="italic">C. albicans</hi>, 3 grew <hi rend="italic">C. parapsilosis</hi>, 2 grew <hi rend="italic">C. glabrata</hi>, 1 grew <hi rend="italic">C. tropicalis</hi>, 2 grew a <hi rend="italic">Trichosporon spp.</hi>, and 2 grew a nonidentifiable colony. The analogous counts for 19 MPDS‐SL samples were 10, 4, 1, 3, 0, 1, and 1 (<emph><span><hi rend="italic">p</hi>= 0.45</span></emph> for culture positively, exact McNemar test).</p><p><hi rend="bold"><emph><span>Conclusions</span></emph></hi>
<hi rend="italic">Candida</hi> growth on Molloplast‐B was not significantly different from growth on MPDS‐SL. Several yeast species were cultured from each material. The rates of culture‐positive testing did not differ between the 2 resilient denture liners.</p></abstract><textClass><keywords xml:lang="en"><term xml:id="k1">resilient denture liner</term><term xml:id="k2"><hi rend="italic">Candida</hi></term></keywords><keywords rend="tocHeading1"><term>Basic science research</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/A6CC008628F02F6D502793064A231EF699B826A8/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)1532-849X</doi><issn type="print">1059-941X</issn><issn type="electronic">1532-849X</issn><idGroup><id type="product" value="JOPR"></id><id type="publisherDivision" value="ST"></id></idGroup><titleGroup><title type="main" sort="JOURNAL OF PROSTHODONTICS">Journal of Prosthodontics</title></titleGroup></publicationMeta><publicationMeta level="part" position="09003"><doi origin="wiley">10.1111/jopr.2003.12.issue-3</doi><numberingGroup><numbering type="journalVolume" number="12">12</numbering><numbering type="journalIssue" number="3">3</numbering></numberingGroup><coverDate startDate="2003-09">September 2003</coverDate></publicationMeta><publicationMeta level="unit" type="miscellaneous" position="0016200" status="forIssue"><doi origin="wiley">10.1016/S1059-941X(03)00041-X</doi><idGroup><id type="unit" value="JOPR162"></id></idGroup><countGroup><count type="pageTotal" number="6"></count></countGroup><titleGroup><title type="tocHeading1">Basic science research</title></titleGroup><eventGroup><event type="firstOnline" date="2004-07-26"></event><event type="publishedOnlineFinalForm" date="2004-07-26"></event><event type="xmlConverted" agent="Converter:BPG_TO_WML3G version:2.3.6 mode:FullText source:FullText result:FullText" date="2010-04-21"></event><event type="xmlConverted" agent="Converter:WILEY_ML3G_TO_WILEY_ML3GV2 version:3.8.8" date="2014-01-31"></event><event type="xmlConverted" agent="Converter:WML3G_To_WML3G version:4.1.7 mode:FullText,remove_FC" date="2014-10-30"></event></eventGroup><numberingGroup><numbering type="pageFirst" number="162">162</numbering><numbering type="pageLast" number="167">167</numbering></numberingGroup><correspondenceTo><sup>*</sup>Correspondence to: Dr. Beth Brosky, University of Minnesota School of Dentistry, 9‐450 Moos Tower, 515 Delaware Street S.E., Minneapolis, MN 55455, USA; Email: <email>brosk001@tc.umn.edu</email></correspondenceTo><linkGroup><link type="toTypesetVersion" href="file:JOPR.JOPR162.pdf"></link></linkGroup></publicationMeta><contentMeta><unparsedEditorialHistory>Accepted on March 12, 2003.</unparsedEditorialHistory><countGroup><count type="referenceTotal" number="21"></count><count type="linksCrossRef" number="35"></count><count type="formulaTotal" number="0"></count><count type="figureTotal" number="4"></count><count type="tableTotal" number="3"></count></countGroup><titleGroup><title type="main">Clinical evaluation of resilient denture liners. Part 2: <i>candida</i> count and speciation</title></titleGroup><creators><creator creatorRole="author" xml:id="cr1" affiliationRef="#a1" corresponding="yes"><personName><givenNames>Mary E.</givenNames><familyName>Brosky</familyName><degrees>DMD</degrees></personName></creator><creator creatorRole="author" xml:id="cr2" affiliationRef="#a2"><personName><givenNames>Igor J.</givenNames><familyName>Pesun</familyName><degrees>DMD, MS, FACP</degrees></personName></creator><creator creatorRole="author" xml:id="cr3" affiliationRef="#a3"><personName><givenNames>Brad</givenNames><familyName>Morrison</familyName><degrees>BS</degrees></personName></creator><creator creatorRole="author" xml:id="cr4" affiliationRef="#a4"><personName><givenNames>James S.</givenNames><familyName>Hodges</familyName><degrees>PhD</degrees></personName></creator><creator creatorRole="author" xml:id="cr5" affiliationRef="#a5"><personName><givenNames>Juey H.</givenNames><familyName>Lai</familyName><degrees>PhD</degrees></personName></creator><creator creatorRole="author" xml:id="cr6" affiliationRef="#a6"><personName><givenNames>William</givenNames><familyName>Liljemark</familyName><degrees>DDS, PhD</degrees></personName></creator></creators><affiliationGroup><affiliation xml:id="a1" countryCode="US"><unparsedAffiliation>Division of Prosthodontics, Department of Restorative Sciences, School of Dentistry, School of Dentistry, University of Minnesota, Minneapolis, MN, USA</unparsedAffiliation></affiliation><affiliation xml:id="a2" countryCode="US"><unparsedAffiliation>Division of Prosthodontics, Department of Restorative Sciences, School of Dentistry, School of Dentistry, University of Minnesota, Minneapolis, MN, USA</unparsedAffiliation></affiliation><affiliation xml:id="a3" countryCode="US"><unparsedAffiliation>School of Dentistry, School of Dentistry, University of Minnesota, Minneapolis, MN, USA</unparsedAffiliation></affiliation><affiliation xml:id="a4" countryCode="US"><unparsedAffiliation>Division of Biostatistics, School of Public Health, School of Dentistry, University of Minnesota, Minneapolis, MN, USA</unparsedAffiliation></affiliation><affiliation xml:id="a5" countryCode="US"><unparsedAffiliation>Lai Laboratories Inc., Burnsville, MN, School of Dentistry, University of Minnesota, USA</unparsedAffiliation></affiliation><affiliation xml:id="a6" countryCode="US"><unparsedAffiliation>Division of Oral Microbiology, Department of Oral Sciences, School of Dentistry, School of Dentistry, University of Minnesota, Minneapolis, MN, USA</unparsedAffiliation></affiliation></affiliationGroup><keywordGroup xml:lang="en"><keyword xml:id="k1">resilient denture liner</keyword><keyword xml:id="k2"><i>Candida</i></keyword></keywordGroup><abstractGroup><abstract type="main" xml:lang="en"><p><b><span cssStyle="text-decoration:underline">Purpose</span></b> The purpose of this study was to count and to speciate <i>Candida</i> isolated from 2 resilient denture liners, Molloplast‐B and MPDS‐SL.</p><p><b><span cssStyle="text-decoration:underline">Materials and Methods</span></b> A group of 20 patients each had 1 maxillary denture and 2 mandibular dentures fabricated. One mandibular denture was lined with Molloplast‐B, and 1 was lined with MPDS‐SL. Each denture was used for 3 months. At the end of the 3‐month period, the mandibular denture was surrendered, and a 5 × 5‐mm circular resilient liner sample was obtained from the tissue surface of the lingual flange. Samples were processed, and <i>Candida</i> was isolated and counted. Speciation of <i>Candida</i> was performed using CHROMagar Candida and API 20C AUX strips.</p><p><b><span cssStyle="text-decoration:underline">Results</span></b> Molloplast‐B had, on average, 5 times as many CFU/sample as MPDSL‐SL, but this difference was not significant (<span type="mathematics"><i>p</i>= 0.26</span>). A sign test gave a similar nonsignificant trend (<span type="mathematics"><i>p</i>= 0.057</span>). CHROMagar identified several <i>Candida</i> species, and confirmation was made using API 20C AUX strips. One patient was lost to follow‐up. Of 19 Molloplast‐B samples, 7 had no growth, 4 grew <i>C. albicans</i>, 3 grew <i>C. parapsilosis</i>, 2 grew <i>C. glabrata</i>, 1 grew <i>C. tropicalis</i>, 2 grew a <i>Trichosporon spp.</i>, and 2 grew a nonidentifiable colony. The analogous counts for 19 MPDS‐SL samples were 10, 4, 1, 3, 0, 1, and 1 (<span type="mathematics"><i>p</i>= 0.45</span> for culture positively, exact McNemar test).</p><p><b><span cssStyle="text-decoration:underline">Conclusions</span></b> <i>Candida</i> growth on Molloplast‐B was not significantly different from growth on MPDS‐SL. Several yeast species were cultured from each material. The rates of culture‐positive testing did not differ between the 2 resilient denture liners.</p></abstract></abstractGroup></contentMeta><noteGroup><note xml:id="n-fnt-1" numbered="no"><p>The substance of this report was delivered at the general session of the International Association for Dental Research, San Diego, CA, March, 2002.</p></note><note xml:id="n-fnt-2" numbered="no"><p>Supported by a grant from the University of Minnesota School of Dentistry Summer Research Fellowship Program grants from the National Institutes of Health/NIDCR (T35‐DE07098, 5R44DE11638, and P30‐DE09737), and the Minnesota Dental Research Center for Biomaterials and Biomechanics.</p></note><note xml:id="n-fnt-3" numbered="no"><p>Lai Laboratories, Inc. produced 1 of the resilient denture liners reviewed in this article. Juey Lai is the President of Lai Laboratories, Inc. The remaining authors have no financial interest in Lai Laboratories, Inc.</p></note></noteGroup></header></component></istex:document></istex:metadataXml><mods version="3.6"><titleInfo lang="en"><title>Clinical evaluation of resilient denture liners. Part 2: candida count and speciation</title></titleInfo><titleInfo type="alternative" contentType="CDATA" lang="en"><title>Clinical evaluation of resilient denture liners. Part 2: candida count and speciation</title></titleInfo><name type="personal"><namePart type="given">Mary E.</namePart><namePart type="family">Brosky</namePart><namePart type="termsOfAddress">DMD</namePart><affiliation>Division of Prosthodontics, Department of Restorative Sciences, School of Dentistry, School of Dentistry, University of Minnesota, Minneapolis, MN, USA</affiliation><affiliation>E-mail: brosk001@tc.umn.edu</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Igor J.</namePart><namePart type="family">Pesun</namePart><namePart type="termsOfAddress">DMD, MS, FACP</namePart><affiliation>Division of Prosthodontics, Department of Restorative Sciences, School of Dentistry, School of Dentistry, University of Minnesota, Minneapolis, MN, USA</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Brad</namePart><namePart type="family">Morrison</namePart><namePart type="termsOfAddress">BS</namePart><affiliation>School of Dentistry, School of Dentistry, University of Minnesota, Minneapolis, MN, USA</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">James S.</namePart><namePart type="family">Hodges</namePart><namePart type="termsOfAddress">PhD</namePart><affiliation>Division of Biostatistics, School of Public Health, School of Dentistry, University of Minnesota, Minneapolis, MN, USA</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Juey H.</namePart><namePart type="family">Lai</namePart><namePart type="termsOfAddress">PhD</namePart><affiliation>Lai Laboratories Inc., Burnsville, MN, School of Dentistry, University of Minnesota, USA</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">William</namePart><namePart type="family">Liljemark</namePart><namePart type="termsOfAddress">DDS, PhD</namePart><affiliation>Division of Oral Microbiology, Department of Oral Sciences, School of Dentistry, School of Dentistry, University of Minnesota, Minneapolis, MN, USA</affiliation><role><roleTerm type="text">author</roleTerm></role></name><typeOfResource>text</typeOfResource><genre type="article" displayLabel="miscellaneous" 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">2003-09</dateIssued><edition>Accepted on March 12, 2003.</edition><copyrightDate encoding="w3cdtf">2003</copyrightDate></originInfo><language><languageTerm type="code" authority="rfc3066">en</languageTerm><languageTerm type="code" authority="iso639-2b">eng</languageTerm></language><physicalDescription><extent unit="figures">4</extent><extent unit="tables">3</extent><extent unit="formulas">0</extent><extent unit="references">21</extent><extent unit="linksCrossRef">35</extent></physicalDescription><abstract>Purpose The purpose of this study was to count and to speciate Candida isolated from 2 resilient denture liners, Molloplast‐B and MPDS‐SL.</abstract><abstract>Materials and Methods A group of 20 patients each had 1 maxillary denture and 2 mandibular dentures fabricated. One mandibular denture was lined with Molloplast‐B, and 1 was lined with MPDS‐SL. Each denture was used for 3 months. At the end of the 3‐month period, the mandibular denture was surrendered, and a 5 × 5‐mm circular resilient liner sample was obtained from the tissue surface of the lingual flange. Samples were processed, and Candida was isolated and counted. Speciation of Candida was performed using CHROMagar Candida and API 20C AUX strips.</abstract><abstract>Results Molloplast‐B had, on average, 5 times as many CFU/sample as MPDSL‐SL, but this difference was not significant (p= 0.26). A sign test gave a similar nonsignificant trend (p= 0.057). CHROMagar identified several Candida species, and confirmation was made using API 20C AUX strips. One patient was lost to follow‐up. Of 19 Molloplast‐B samples, 7 had no growth, 4 grew C. albicans, 3 grew C. parapsilosis, 2 grew C. glabrata, 1 grew C. tropicalis, 2 grew a Trichosporon spp., and 2 grew a nonidentifiable colony. The analogous counts for 19 MPDS‐SL samples were 10, 4, 1, 3, 0, 1, and 1 (p= 0.45 for culture positively, exact McNemar test).</abstract><abstract>Conclusions Candida growth on Molloplast‐B was not significantly different from growth on MPDS‐SL. Several yeast species were cultured from each material. The rates of culture‐positive testing did not differ between the 2 resilient denture liners.</abstract><subject lang="en"><genre>keywords</genre><topic>resilient denture liner</topic><topic>Candida</topic></subject><relatedItem type="host"><titleInfo><title>Journal of Prosthodontics</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">1059-941X</identifier><identifier type="eISSN">1532-849X</identifier><identifier type="DOI">10.1111/(ISSN)1532-849X</identifier><identifier type="PublisherID">JOPR</identifier><part><date>2003</date><detail type="volume"><caption>vol.</caption><number>12</number></detail><detail type="issue"><caption>no.</caption><number>3</number></detail><extent unit="pages"><start>162</start><end>167</end><total>6</total></extent></part></relatedItem><identifier type="istex">A6CC008628F02F6D502793064A231EF699B826A8</identifier><identifier type="ark">ark:/67375/WNG-65S9THGG-P</identifier><identifier type="DOI">10.1016/S1059-941X(03)00041-X</identifier><identifier type="ArticleID">JOPR162</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/A6CC008628F02F6D502793064A231EF699B826A8/metadata/json</uri></json:item></metadata><serie></serie></istex></record>Pour manipuler ce document sous Unix (Dilib)
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