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
Hauptverfasser: 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
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container_end_page 1215
container_issue 10
container_start_page 1209
container_title Archives of pathology & laboratory medicine (1976)
container_volume 126
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.
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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. 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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. 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development</subject><subject>Neisseria meningitidis - isolation &amp; 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 ; 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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. 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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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