Evaluation of a diagnostic polymerase chain reaction assay for Neisseria meningitidis in North America and field experience during an outbreak
Meningococcal infection has a high public profile because of its dramatic presentation, high fatality rate, and propensity to occur in outbreaks and clusters of cases. Use of a diagnostic polymerase chain reaction (PCR) assay could enhance laboratory confirmation of cases and guide the public health...
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Veröffentlicht in: | Archives of pathology & laboratory medicine (1976) 2002-10, Vol.126 (10), p.1209-1215 |
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creator | Pollard, Andrew J Probe, Gary Trombley, Colleen Castell, Annette Whitehead, Sue Bigham, J Mark Champagne, Sylvie Isaac-Renton, Judy Tan, Rusung Guiver, Malcolm Borrow, Ray Speert, David P Thomas, Eva |
description | Meningococcal infection has a high public profile because of its dramatic presentation, high fatality rate, and propensity to occur in outbreaks and clusters of cases. Use of a diagnostic polymerase chain reaction (PCR) assay could enhance laboratory confirmation of cases and guide the public health response in North America.
To assess the performance of a PCR assay for the diagnosis of meningococcal disease after its implementation in a North American setting and to evaluate sensitivity and specificity of the assay for the detection of prevalent bacterial isolates.
Laboratory evaluation of the sensitivity and specificity of a PCR assay for Neisseria meningitidis and observational study of a series of cases comparing molecular diagnosis against the criterion standard of conventional laboratory diagnostic tests.
A Canadian province with a population of 4 million people.
Children and adults presenting with suspected meningococcal disease in British Columbia.
The sensitivity and specificity of the PCR assay when compared against standard laboratory methods.
The PCR assay correctly identified all of 38 Canadian isolates of Neisseria meningitidis and correctly assigned the serogroup to each isolate. None of 57 other gram-positive or gram-negative bacteria or yeasts were detected by the PCR assay. In a clinical evaluation, for diagnosis of meningococcal disease, the PCR assay had a sensitivity and specificity of 91% and 76%, respectively, against conventional methods of diagnosis. Use of the PCR assay increased the laboratory confirmation of clinically suspected cases by 36%. During an outbreak, the PCR assay allowed serogroup determination in 3 of 7 cases, aiding in the public health decision to launch an immunization campaign.
The PCR assay is more sensitive than conventional methods for the diagnosis of meningococcal disease, and enhanced surveillance may help direct the public health response to the changing epidemiology of disease in North America. |
doi_str_mv | 10.5858/2002-126-1209-EOADPC |
format | Article |
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To assess the performance of a PCR assay for the diagnosis of meningococcal disease after its implementation in a North American setting and to evaluate sensitivity and specificity of the assay for the detection of prevalent bacterial isolates.
Laboratory evaluation of the sensitivity and specificity of a PCR assay for Neisseria meningitidis and observational study of a series of cases comparing molecular diagnosis against the criterion standard of conventional laboratory diagnostic tests.
A Canadian province with a population of 4 million people.
Children and adults presenting with suspected meningococcal disease in British Columbia.
The sensitivity and specificity of the PCR assay when compared against standard laboratory methods.
The PCR assay correctly identified all of 38 Canadian isolates of Neisseria meningitidis and correctly assigned the serogroup to each isolate. None of 57 other gram-positive or gram-negative bacteria or yeasts were detected by the PCR assay. In a clinical evaluation, for diagnosis of meningococcal disease, the PCR assay had a sensitivity and specificity of 91% and 76%, respectively, against conventional methods of diagnosis. Use of the PCR assay increased the laboratory confirmation of clinically suspected cases by 36%. During an outbreak, the PCR assay allowed serogroup determination in 3 of 7 cases, aiding in the public health decision to launch an immunization campaign.
The PCR assay is more sensitive than conventional methods for the diagnosis of meningococcal disease, and enhanced surveillance may help direct the public health response to the changing epidemiology of disease in North America.</description><identifier>ISSN: 0003-9985</identifier><identifier>ISSN: 1543-2165</identifier><identifier>EISSN: 1543-2165</identifier><identifier>DOI: 10.5858/2002-126-1209-EOADPC</identifier><identifier>PMID: 12296761</identifier><identifier>CODEN: APLMAS</identifier><language>eng</language><publisher>United States: College of American Pathologists</publisher><subject>Adolescent ; Adult ; Aged ; Analysis ; British Columbia - epidemiology ; Child ; Child, Preschool ; Disease Outbreaks ; DNA Primers - chemistry ; DNA, Bacterial - blood ; DNA, Bacterial - classification ; Epidemiology ; Female ; Humans ; Infant ; Male ; Meningitis, Meningococcal - diagnosis ; Meningitis, Meningococcal - microbiology ; Meningitis, Meningococcal - mortality ; Microbiological Techniques ; Neisseria meningitidis ; Neisseria meningitidis - genetics ; Neisseria meningitidis - growth & development ; Neisseria meningitidis - isolation & purification ; Patient outcomes ; Polymerase chain reaction ; Polymerase Chain Reaction - methods ; Public health ; Sensitivity and Specificity ; Survival Rate</subject><ispartof>Archives of pathology & laboratory medicine (1976), 2002-10, Vol.126 (10), p.1209-1215</ispartof><rights>COPYRIGHT 2002 College of American Pathologists</rights><rights>Copyright College of American Pathologists Oct 2002</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c438t-80ae7f666e5a1bce6b06e9d5a8502c613114428c4648ed0081b5f0a40a114cff3</citedby><cites>FETCH-LOGICAL-c438t-80ae7f666e5a1bce6b06e9d5a8502c613114428c4648ed0081b5f0a40a114cff3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,781,785,27928,27929</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12296761$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Pollard, Andrew J</creatorcontrib><creatorcontrib>Probe, Gary</creatorcontrib><creatorcontrib>Trombley, Colleen</creatorcontrib><creatorcontrib>Castell, Annette</creatorcontrib><creatorcontrib>Whitehead, Sue</creatorcontrib><creatorcontrib>Bigham, J Mark</creatorcontrib><creatorcontrib>Champagne, Sylvie</creatorcontrib><creatorcontrib>Isaac-Renton, Judy</creatorcontrib><creatorcontrib>Tan, Rusung</creatorcontrib><creatorcontrib>Guiver, Malcolm</creatorcontrib><creatorcontrib>Borrow, Ray</creatorcontrib><creatorcontrib>Speert, David P</creatorcontrib><creatorcontrib>Thomas, Eva</creatorcontrib><title>Evaluation of a diagnostic polymerase chain reaction assay for Neisseria meningitidis in North America and field experience during an outbreak</title><title>Archives of pathology & laboratory medicine (1976)</title><addtitle>Arch Pathol Lab Med</addtitle><description>Meningococcal infection has a high public profile because of its dramatic presentation, high fatality rate, and propensity to occur in outbreaks and clusters of cases. Use of a diagnostic polymerase chain reaction (PCR) assay could enhance laboratory confirmation of cases and guide the public health response in North America.
To assess the performance of a PCR assay for the diagnosis of meningococcal disease after its implementation in a North American setting and to evaluate sensitivity and specificity of the assay for the detection of prevalent bacterial isolates.
Laboratory evaluation of the sensitivity and specificity of a PCR assay for Neisseria meningitidis and observational study of a series of cases comparing molecular diagnosis against the criterion standard of conventional laboratory diagnostic tests.
A Canadian province with a population of 4 million people.
Children and adults presenting with suspected meningococcal disease in British Columbia.
The sensitivity and specificity of the PCR assay when compared against standard laboratory methods.
The PCR assay correctly identified all of 38 Canadian isolates of Neisseria meningitidis and correctly assigned the serogroup to each isolate. None of 57 other gram-positive or gram-negative bacteria or yeasts were detected by the PCR assay. In a clinical evaluation, for diagnosis of meningococcal disease, the PCR assay had a sensitivity and specificity of 91% and 76%, respectively, against conventional methods of diagnosis. Use of the PCR assay increased the laboratory confirmation of clinically suspected cases by 36%. During an outbreak, the PCR assay allowed serogroup determination in 3 of 7 cases, aiding in the public health decision to launch an immunization campaign.
The PCR assay is more sensitive than conventional methods for the diagnosis of meningococcal disease, and enhanced surveillance may help direct the public health response to the changing epidemiology of disease in North America.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Analysis</subject><subject>British Columbia - epidemiology</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Disease Outbreaks</subject><subject>DNA Primers - chemistry</subject><subject>DNA, Bacterial - blood</subject><subject>DNA, Bacterial - classification</subject><subject>Epidemiology</subject><subject>Female</subject><subject>Humans</subject><subject>Infant</subject><subject>Male</subject><subject>Meningitis, Meningococcal - diagnosis</subject><subject>Meningitis, Meningococcal - microbiology</subject><subject>Meningitis, Meningococcal - mortality</subject><subject>Microbiological Techniques</subject><subject>Neisseria meningitidis</subject><subject>Neisseria meningitidis - genetics</subject><subject>Neisseria meningitidis - growth & development</subject><subject>Neisseria meningitidis - isolation & purification</subject><subject>Patient outcomes</subject><subject>Polymerase chain reaction</subject><subject>Polymerase Chain Reaction - methods</subject><subject>Public health</subject><subject>Sensitivity and Specificity</subject><subject>Survival Rate</subject><issn>0003-9985</issn><issn>1543-2165</issn><issn>1543-2165</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNptkl2PEyEUhonRuHX1HxhDvNi7WYEZmJnLptaPZLPrhV6TU-bQsjJQYcbYP-FvltomfmRDCOGc533Dx0vIS86uZSe7N4IxUXGhymR9tb5bvv20ekQWXDZ1JbiSj8mCMVZXfd_JC_Is5_uy7YXgT8kFF6JXreIL8nP9HfwMk4uBRkuBDg62IebJGbqP_jBigozU7MAFmhDMbxJyhgO1MdFbdDljckBHDC5s3eQGl2mBb2OadnRZDJwBCmGg1qEfKP7YlxIGg3SYU5GUHo3ztCnuX5-TJxZ8xhfn9ZJ8ebf-vPpQ3dy9_7ha3lSmqbup6hhga5VSKIFvDKoNU9gPEjrJhFG85rxpRGca1XQ4MNbxjbQMGgalYaytL8nVyXef4rcZ86RHlw16DwHjnHUrOG9bIQr4-j_wPs4plLPpgvR1XTNVoOoEbcGjdsHGKYHZYiiP52NA60p5KWXbMsVEW_jrB_gyBhydeVBw9Zdgh-CnXY5-Pn5G_hdsTqBJMeeEVu-TGyEdNGf6GBt9jI0usdHH2OhTbIrs1fmW82bE4Y_onJP6F19Qvi0</recordid><startdate>200210</startdate><enddate>200210</enddate><creator>Pollard, Andrew J</creator><creator>Probe, Gary</creator><creator>Trombley, Colleen</creator><creator>Castell, Annette</creator><creator>Whitehead, Sue</creator><creator>Bigham, J Mark</creator><creator>Champagne, Sylvie</creator><creator>Isaac-Renton, Judy</creator><creator>Tan, Rusung</creator><creator>Guiver, Malcolm</creator><creator>Borrow, Ray</creator><creator>Speert, David P</creator><creator>Thomas, Eva</creator><general>College of American Pathologists</general><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>3V.</scope><scope>4T-</scope><scope>4U-</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88I</scope><scope>8AF</scope><scope>8AO</scope><scope>8C1</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB0</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope></search><sort><creationdate>200210</creationdate><title>Evaluation of a diagnostic polymerase chain reaction assay for Neisseria meningitidis in North America and field experience during an outbreak</title><author>Pollard, Andrew J ; Probe, Gary ; Trombley, Colleen ; Castell, Annette ; Whitehead, Sue ; Bigham, J Mark ; Champagne, Sylvie ; Isaac-Renton, Judy ; Tan, Rusung ; Guiver, Malcolm ; Borrow, Ray ; Speert, David P ; Thomas, Eva</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c438t-80ae7f666e5a1bce6b06e9d5a8502c613114428c4648ed0081b5f0a40a114cff3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Aged</topic><topic>Analysis</topic><topic>British Columbia - epidemiology</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Disease Outbreaks</topic><topic>DNA Primers - chemistry</topic><topic>DNA, Bacterial - blood</topic><topic>DNA, Bacterial - classification</topic><topic>Epidemiology</topic><topic>Female</topic><topic>Humans</topic><topic>Infant</topic><topic>Male</topic><topic>Meningitis, Meningococcal - diagnosis</topic><topic>Meningitis, Meningococcal - microbiology</topic><topic>Meningitis, Meningococcal - mortality</topic><topic>Microbiological Techniques</topic><topic>Neisseria meningitidis</topic><topic>Neisseria meningitidis - genetics</topic><topic>Neisseria meningitidis - growth & development</topic><topic>Neisseria meningitidis - isolation & purification</topic><topic>Patient outcomes</topic><topic>Polymerase chain reaction</topic><topic>Polymerase Chain Reaction - methods</topic><topic>Public health</topic><topic>Sensitivity and Specificity</topic><topic>Survival Rate</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pollard, Andrew J</creatorcontrib><creatorcontrib>Probe, Gary</creatorcontrib><creatorcontrib>Trombley, Colleen</creatorcontrib><creatorcontrib>Castell, Annette</creatorcontrib><creatorcontrib>Whitehead, Sue</creatorcontrib><creatorcontrib>Bigham, J Mark</creatorcontrib><creatorcontrib>Champagne, Sylvie</creatorcontrib><creatorcontrib>Isaac-Renton, Judy</creatorcontrib><creatorcontrib>Tan, Rusung</creatorcontrib><creatorcontrib>Guiver, Malcolm</creatorcontrib><creatorcontrib>Borrow, Ray</creatorcontrib><creatorcontrib>Speert, David P</creatorcontrib><creatorcontrib>Thomas, Eva</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Docstoc</collection><collection>University Readers</collection><collection>Nursing & Allied Health Database</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>STEM Database</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database</collection><collection>Biological Science Database</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><jtitle>Archives of pathology & laboratory medicine (1976)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pollard, Andrew J</au><au>Probe, Gary</au><au>Trombley, Colleen</au><au>Castell, Annette</au><au>Whitehead, Sue</au><au>Bigham, J Mark</au><au>Champagne, Sylvie</au><au>Isaac-Renton, Judy</au><au>Tan, Rusung</au><au>Guiver, Malcolm</au><au>Borrow, Ray</au><au>Speert, David P</au><au>Thomas, Eva</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Evaluation of a diagnostic polymerase chain reaction assay for Neisseria meningitidis in North America and field experience during an outbreak</atitle><jtitle>Archives of pathology & laboratory medicine (1976)</jtitle><addtitle>Arch Pathol Lab Med</addtitle><date>2002-10</date><risdate>2002</risdate><volume>126</volume><issue>10</issue><spage>1209</spage><epage>1215</epage><pages>1209-1215</pages><issn>0003-9985</issn><issn>1543-2165</issn><eissn>1543-2165</eissn><coden>APLMAS</coden><abstract>Meningococcal infection has a high public profile because of its dramatic presentation, high fatality rate, and propensity to occur in outbreaks and clusters of cases. Use of a diagnostic polymerase chain reaction (PCR) assay could enhance laboratory confirmation of cases and guide the public health response in North America.
To assess the performance of a PCR assay for the diagnosis of meningococcal disease after its implementation in a North American setting and to evaluate sensitivity and specificity of the assay for the detection of prevalent bacterial isolates.
Laboratory evaluation of the sensitivity and specificity of a PCR assay for Neisseria meningitidis and observational study of a series of cases comparing molecular diagnosis against the criterion standard of conventional laboratory diagnostic tests.
A Canadian province with a population of 4 million people.
Children and adults presenting with suspected meningococcal disease in British Columbia.
The sensitivity and specificity of the PCR assay when compared against standard laboratory methods.
The PCR assay correctly identified all of 38 Canadian isolates of Neisseria meningitidis and correctly assigned the serogroup to each isolate. None of 57 other gram-positive or gram-negative bacteria or yeasts were detected by the PCR assay. In a clinical evaluation, for diagnosis of meningococcal disease, the PCR assay had a sensitivity and specificity of 91% and 76%, respectively, against conventional methods of diagnosis. Use of the PCR assay increased the laboratory confirmation of clinically suspected cases by 36%. During an outbreak, the PCR assay allowed serogroup determination in 3 of 7 cases, aiding in the public health decision to launch an immunization campaign.
The PCR assay is more sensitive than conventional methods for the diagnosis of meningococcal disease, and enhanced surveillance may help direct the public health response to the changing epidemiology of disease in North America.</abstract><cop>United States</cop><pub>College of American Pathologists</pub><pmid>12296761</pmid><doi>10.5858/2002-126-1209-EOADPC</doi><tpages>7</tpages></addata></record> |
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source | MEDLINE; Allen Press Journals; EZB-FREE-00999 freely available EZB journals |
subjects | Adolescent Adult Aged Analysis British Columbia - epidemiology Child Child, Preschool Disease Outbreaks DNA Primers - chemistry DNA, Bacterial - blood DNA, Bacterial - classification Epidemiology Female Humans Infant Male Meningitis, Meningococcal - diagnosis Meningitis, Meningococcal - microbiology Meningitis, Meningococcal - mortality Microbiological Techniques Neisseria meningitidis Neisseria meningitidis - genetics Neisseria meningitidis - growth & development Neisseria meningitidis - isolation & purification Patient outcomes Polymerase chain reaction Polymerase Chain Reaction - methods Public health Sensitivity and Specificity Survival Rate |
title | Evaluation of a diagnostic polymerase chain reaction assay for Neisseria meningitidis in North America and field experience during an outbreak |
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