Establishing a surveillance network for severe lower respiratory tract infections in Korean infants and young children
Identifieur interne : 000177 ( Istex/Corpus ); précédent : 000176; suivant : 000178Establishing a surveillance network for severe lower respiratory tract infections in Korean infants and young children
Auteurs : J.-K. Chun ; J.-H. Lee ; H.-S. Kim ; H.-M. Cheong ; K. S. Kim ; C. Kang ; D. S. KimSource :
- European Journal of Clinical Microbiology & Infectious Diseases [ 0934-9723 ] ; 2009-07-01.
Abstract
Abstract: To reduce morbidity and mortality through integrated case management, a pilot study to detect respiratory viruses in patients with acute lower respiratory infections (ALRIs) was designed as part of a nationwide surveillance for this disease in Korea. The study population consisted of hospitalized patients under the age of 5 years with bronchiolitis, pneumonia, croup, or acute respiratory distress syndrome. A prospective 6-month study was performed. Two hundred and ninety-seven nasopharyngeal secretions were collected and multiplex reverse transcriptase polymerase chain reactions (RT-PCR)/polymerase chain reactions (PCR) were performed to detect respiratory viruses. If there were any positive RT-PCR/PCR results, viral cultures were proceeded for confirmation. Respiratory viruses were identified in 49.6% of 296 patients. The detection rates were as follows: respiratory syncytial virus (RSV) was the most commonly detected in 52.7% (87/165), human metapneumovirus (hMPV) in 15.8%, human corona virus (hCoV) in 5.5%, adenovirus in 9.7%, human bocavirus (hBoV) in 5.5%, parainfluenza virus (PIV) in 3.6%, rhinovirus (RV) in 4.2%, and the influenza virus in 3% of the patients with ALRIs. The consistent rate of positive results between RT-PCR and viral culture was 92% (105/114). Using our methods to detect viral causes seemed to be acceptable for the national surveillance of severe acute respiratory infections in infants and children.
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DOI: 10.1007/s10096-009-0701-0
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Chun</name><affiliation><mods:affiliation>Department of Pediatrics, Yonsei University College of Medicine, Severance Children’s Hospital, 250 Seongsanno, Seodaemun-gu, 120-752, Seoul, South Korea</mods:affiliation></affiliation></author><author><name sortKey="Lee, J H" sort="Lee, J H" uniqKey="Lee J" first="J.-H." last="Lee">J.-H. Lee</name><affiliation><mods:affiliation>Department of Laboratory Medicine, Yonsei University College of Medicine, Severance Hospital, 250 Seongsanno, Seodaemun-gu, 120-752, Seoul, South Korea</mods:affiliation></affiliation></author><author><name sortKey="Kim, H S" sort="Kim, H S" uniqKey="Kim H" first="H.-S." last="Kim">H.-S. Kim</name><affiliation><mods:affiliation>Department of Laboratory Medicine, Yonsei University College of Medicine, Severance Hospital, 250 Seongsanno, Seodaemun-gu, 120-752, Seoul, South Korea</mods:affiliation></affiliation></author><author><name sortKey="Cheong, H M" sort="Cheong, H M" uniqKey="Cheong H" first="H.-M." last="Cheong">H.-M. Cheong</name><affiliation><mods:affiliation>Division of Influenza and Respiratory viruses, Korea Centers for Disease Control and Prevention, 194 Tongil-Lo Eunpyong-Gu, 122-701, Seoul, South Korea</mods:affiliation></affiliation></author><author><name sortKey="Kim, K S" sort="Kim, K S" uniqKey="Kim K" first="K. S." last="Kim">K. S. Kim</name><affiliation><mods:affiliation>Division of Influenza and Respiratory viruses, Korea Centers for Disease Control and Prevention, 194 Tongil-Lo Eunpyong-Gu, 122-701, Seoul, South Korea</mods:affiliation></affiliation></author><author><name sortKey="Kang, C" sort="Kang, C" uniqKey="Kang C" first="C." last="Kang">C. 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Kim</name><affiliation><mods:affiliation>Department of Pediatrics, Yonsei University College of Medicine, Severance Children’s Hospital, 250 Seongsanno, Seodaemun-gu, 120-752, Seoul, South Korea</mods:affiliation></affiliation><affiliation><mods:affiliation>E-mail: dskim6634@yuhs.ac</mods:affiliation></affiliation></author></analytic><monogr></monogr><series><title level="j">European Journal of Clinical Microbiology & Infectious Diseases</title><title level="j" type="abbrev">Eur J Clin Microbiol Infect Dis</title><idno type="ISSN">0934-9723</idno><idno type="eISSN">1435-4373</idno><imprint><publisher>Springer-Verlag</publisher><pubPlace>Berlin/Heidelberg</pubPlace><date type="published" when="2009-07-01">2009-07-01</date><biblScope unit="volume">28</biblScope><biblScope unit="issue">7</biblScope><biblScope unit="page" from="841">841</biblScope><biblScope unit="page" to="844">844</biblScope></imprint><idno type="ISSN">0934-9723</idno></series></biblStruct></sourceDesc><seriesStmt><idno type="ISSN">0934-9723</idno></seriesStmt></fileDesc><profileDesc><textClass></textClass><langUsage><language ident="en">en</language></langUsage></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Abstract: To reduce morbidity and mortality through integrated case management, a pilot study to detect respiratory viruses in patients with acute lower respiratory infections (ALRIs) was designed as part of a nationwide surveillance for this disease in Korea. The study population consisted of hospitalized patients under the age of 5 years with bronchiolitis, pneumonia, croup, or acute respiratory distress syndrome. A prospective 6-month study was performed. Two hundred and ninety-seven nasopharyngeal secretions were collected and multiplex reverse transcriptase polymerase chain reactions (RT-PCR)/polymerase chain reactions (PCR) were performed to detect respiratory viruses. If there were any positive RT-PCR/PCR results, viral cultures were proceeded for confirmation. Respiratory viruses were identified in 49.6% of 296 patients. The detection rates were as follows: respiratory syncytial virus (RSV) was the most commonly detected in 52.7% (87/165), human metapneumovirus (hMPV) in 15.8%, human corona virus (hCoV) in 5.5%, adenovirus in 9.7%, human bocavirus (hBoV) in 5.5%, parainfluenza virus (PIV) in 3.6%, rhinovirus (RV) in 4.2%, and the influenza virus in 3% of the patients with ALRIs. 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A prospective 6-month study was performed. Two hundred and ninety-seven nasopharyngeal secretions were collected and multiplex reverse transcriptase polymerase chain reactions (RT-PCR)/polymerase chain reactions (PCR) were performed to detect respiratory viruses. If there were any positive RT-PCR/PCR results, viral cultures were proceeded for confirmation. Respiratory viruses were identified in 49.6% of 296 patients. The detection rates were as follows: respiratory syncytial virus (RSV) was the most commonly detected in 52.7% (87/165), human metapneumovirus (hMPV) in 15.8%, human corona virus (hCoV) in 5.5%, adenovirus in 9.7%, human bocavirus (hBoV) in 5.5%, parainfluenza virus (PIV) in 3.6%, rhinovirus (RV) in 4.2%, and the influenza virus in 3% of the patients with ALRIs. The consistent rate of positive results between RT-PCR and viral culture was 92% (105/114). 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The study population consisted of hospitalized patients under the age of 5 years with bronchiolitis, pneumonia, croup, or acute respiratory distress syndrome. A prospective 6-month study was performed. Two hundred and ninety-seven nasopharyngeal secretions were collected and multiplex reverse transcriptase polymerase chain reactions (RT-PCR)/polymerase chain reactions (PCR) were performed to detect respiratory viruses. If there were any positive RT-PCR/PCR results, viral cultures were proceeded for confirmation. Respiratory viruses were identified in 49.6% of 296 patients. The detection rates were as follows: respiratory syncytial virus (RSV) was the most commonly detected in 52.7% (87/165), human metapneumovirus (hMPV) in 15.8%, human corona virus (hCoV) in 5.5%, adenovirus in 9.7%, human bocavirus (hBoV) in 5.5%, parainfluenza virus (PIV) in 3.6%, rhinovirus (RV) in 4.2%, and the influenza virus in 3% of the patients with ALRIs. The consistent rate of positive results between RT-PCR and viral culture was 92% (105/114). Using our methods to detect viral causes seemed to be acceptable for the national surveillance of severe acute respiratory infections in infants and children.</p></abstract><textClass><keywords scheme="Journal Subject"><list><head>Biomedicine</head><item><term>Medical Microbiology</term></item><item><term>Internal Medicine</term></item></list></keywords></textClass></profileDesc><revisionDesc><change when="2008-10-28">Created</change><change when="2009-07-01">Published</change></revisionDesc></teiHeader></istex:fulltextTEI><json:item><extension>txt</extension><original>false</original><mimetype>text/plain</mimetype><uri>https://api.istex.fr/ark:/67375/VQC-XXX3NNRJ-7/fulltext.txt</uri></json:item></fulltext><metadata><istex:metadataXml wicri:clean="corpus springer-journals not found" wicri:toSee="no header"><istex:xmlDeclaration>version="1.0" encoding="UTF-8"</istex:xmlDeclaration><istex:docType PUBLIC="-//Springer-Verlag//DTD A++ V2.4//EN" 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DisplayOrder="Western"><GivenName>K.</GivenName><GivenName>S.</GivenName><FamilyName>Kim</FamilyName></AuthorName></Author><Author AffiliationIDS="Aff3"><AuthorName DisplayOrder="Western"><GivenName>C.</GivenName><FamilyName>Kang</FamilyName></AuthorName></Author><Author AffiliationIDS="Aff1" CorrespondingAffiliationID="Aff1"><AuthorName DisplayOrder="Western"><GivenName>D.</GivenName><GivenName>S.</GivenName><FamilyName>Kim</FamilyName></AuthorName><Contact><Phone>+82-2-22282050</Phone><Fax>+82-2-3939118</Fax><Email>dskim6634@yuhs.ac</Email></Contact></Author><Affiliation ID="Aff1"><OrgDivision>Department of Pediatrics</OrgDivision><OrgName>Yonsei University College of Medicine, Severance Children’s Hospital</OrgName><OrgAddress><Street>250 Seongsanno, Seodaemun-gu</Street><City>Seoul</City><Postcode>120-752</Postcode><Country Code="KR">South Korea</Country></OrgAddress></Affiliation><Affiliation ID="Aff2"><OrgDivision>Department of Laboratory Medicine</OrgDivision><OrgName>Yonsei University College of Medicine, Severance Hospital</OrgName><OrgAddress><Street>250 Seongsanno, Seodaemun-gu</Street><City>Seoul</City><Postcode>120-752</Postcode><Country Code="KR">South Korea</Country></OrgAddress></Affiliation><Affiliation ID="Aff3"><OrgDivision>Division of Influenza and Respiratory viruses</OrgDivision><OrgName>Korea Centers for Disease Control and Prevention</OrgName><OrgAddress><Street>194 Tongil-Lo Eunpyong-Gu</Street><City>Seoul</City><Postcode>122-701</Postcode><Country Code="KR">South Korea</Country></OrgAddress></Affiliation></AuthorGroup><Abstract ID="Abs1" Language="En"><Heading>Abstract</Heading><Para>To reduce morbidity and mortality through integrated case management, a pilot study to detect respiratory viruses in patients with acute lower respiratory infections (ALRIs) was designed as part of a nationwide surveillance for this disease in Korea. The study population consisted of hospitalized patients under the age of 5 years with bronchiolitis, pneumonia, croup, or acute respiratory distress syndrome. A prospective 6-month study was performed. Two hundred and ninety-seven nasopharyngeal secretions were collected and multiplex reverse transcriptase polymerase chain reactions (RT-PCR)/polymerase chain reactions (PCR) were performed to detect respiratory viruses. If there were any positive RT-PCR/PCR results, viral cultures were proceeded for confirmation. Respiratory viruses were identified in 49.6% of 296 patients. The detection rates were as follows: respiratory syncytial virus (RSV) was the most commonly detected in 52.7% (87/165), human metapneumovirus (hMPV) in 15.8%, human corona virus (hCoV) in 5.5%, adenovirus in 9.7%, human bocavirus (hBoV) in 5.5%, parainfluenza virus (PIV) in 3.6%, rhinovirus (RV) in 4.2%, and the influenza virus in 3% of the patients with ALRIs. The consistent rate of positive results between RT-PCR and viral culture was 92% (105/114). Using our methods to detect viral causes seemed to be acceptable for the national surveillance of severe acute respiratory infections in infants and children.</Para></Abstract></ArticleHeader><NoBody></NoBody></Article></Issue></Volume></Journal></Publisher></istex:document></istex:metadataXml><mods version="3.6"><titleInfo lang="en"><title>Establishing a surveillance network for severe lower respiratory tract infections in Korean infants and young children</title></titleInfo><titleInfo type="alternative" contentType="CDATA"><title>Establishing a surveillance network for severe lower respiratory tract infections in Korean infants and young children</title></titleInfo><name type="personal"><namePart type="given">J.-K.</namePart><namePart type="family">Chun</namePart><affiliation>Department of Pediatrics, Yonsei University College of Medicine, Severance Children’s Hospital, 250 Seongsanno, Seodaemun-gu, 120-752, Seoul, South Korea</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">J.-H.</namePart><namePart type="family">Lee</namePart><affiliation>Department of Laboratory Medicine, Yonsei University College of Medicine, Severance Hospital, 250 Seongsanno, Seodaemun-gu, 120-752, Seoul, South Korea</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">H.-S.</namePart><namePart type="family">Kim</namePart><affiliation>Department of Laboratory Medicine, Yonsei University College of Medicine, Severance Hospital, 250 Seongsanno, Seodaemun-gu, 120-752, Seoul, South Korea</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">H.-M.</namePart><namePart type="family">Cheong</namePart><affiliation>Division of Influenza and Respiratory viruses, Korea Centers for Disease Control and Prevention, 194 Tongil-Lo Eunpyong-Gu, 122-701, Seoul, South Korea</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">K.</namePart><namePart type="given">S.</namePart><namePart type="family">Kim</namePart><affiliation>Division of Influenza and Respiratory viruses, Korea Centers for Disease Control and Prevention, 194 Tongil-Lo Eunpyong-Gu, 122-701, Seoul, South Korea</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">C.</namePart><namePart type="family">Kang</namePart><affiliation>Division of Influenza and Respiratory viruses, Korea Centers for Disease Control and Prevention, 194 Tongil-Lo Eunpyong-Gu, 122-701, Seoul, South Korea</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal" displayLabel="corresp"><namePart type="given">D.</namePart><namePart type="given">S.</namePart><namePart type="family">Kim</namePart><affiliation>Department of Pediatrics, Yonsei University College of Medicine, Severance Children’s Hospital, 250 Seongsanno, Seodaemun-gu, 120-752, Seoul, South Korea</affiliation><affiliation>E-mail: dskim6634@yuhs.ac</affiliation><role><roleTerm type="text">author</roleTerm></role></name><typeOfResource>text</typeOfResource><genre type="research-article" displayLabel="Report" authority="ISTEX" authorityURI="https://content-type.data.istex.fr" valueURI="https://content-type.data.istex.fr/ark:/67375/XTP-1JC4F85T-7">research-article</genre><originInfo><publisher>Springer-Verlag</publisher><place><placeTerm type="text">Berlin/Heidelberg</placeTerm></place><dateCreated encoding="w3cdtf">2008-10-28</dateCreated><dateIssued encoding="w3cdtf">2009-07-01</dateIssued><copyrightDate encoding="w3cdtf">2009</copyrightDate></originInfo><language><languageTerm type="code" authority="rfc3066">en</languageTerm><languageTerm type="code" authority="iso639-2b">eng</languageTerm></language><abstract lang="en">Abstract: To reduce morbidity and mortality through integrated case management, a pilot study to detect respiratory viruses in patients with acute lower respiratory infections (ALRIs) was designed as part of a nationwide surveillance for this disease in Korea. The study population consisted of hospitalized patients under the age of 5 years with bronchiolitis, pneumonia, croup, or acute respiratory distress syndrome. A prospective 6-month study was performed. Two hundred and ninety-seven nasopharyngeal secretions were collected and multiplex reverse transcriptase polymerase chain reactions (RT-PCR)/polymerase chain reactions (PCR) were performed to detect respiratory viruses. If there were any positive RT-PCR/PCR results, viral cultures were proceeded for confirmation. Respiratory viruses were identified in 49.6% of 296 patients. The detection rates were as follows: respiratory syncytial virus (RSV) was the most commonly detected in 52.7% (87/165), human metapneumovirus (hMPV) in 15.8%, human corona virus (hCoV) in 5.5%, adenovirus in 9.7%, human bocavirus (hBoV) in 5.5%, parainfluenza virus (PIV) in 3.6%, rhinovirus (RV) in 4.2%, and the influenza virus in 3% of the patients with ALRIs. The consistent rate of positive results between RT-PCR and viral culture was 92% (105/114). Using our methods to detect viral causes seemed to be acceptable for the national surveillance of severe acute respiratory infections in infants and children.</abstract><note>Brief Report</note><relatedItem type="host"><titleInfo><title>European Journal of Clinical Microbiology & Infectious Diseases</title></titleInfo><titleInfo type="abbreviated"><title>Eur J Clin Microbiol Infect Dis</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><originInfo><publisher>Springer</publisher><dateIssued encoding="w3cdtf">2009-06-09</dateIssued><copyrightDate encoding="w3cdtf">2009</copyrightDate></originInfo><subject><genre>Biomedicine</genre><topic>Medical Microbiology</topic><topic>Internal Medicine</topic></subject><identifier type="ISSN">0934-9723</identifier><identifier type="eISSN">1435-4373</identifier><identifier type="JournalID">10096</identifier><identifier type="IssueArticleCount">26</identifier><identifier type="VolumeIssueCount">12</identifier><part><date>2009</date><detail type="volume"><number>28</number><caption>vol.</caption></detail><detail type="issue"><number>7</number><caption>no.</caption></detail><extent unit="pages"><start>841</start><end>844</end></extent></part><recordInfo><recordOrigin>Springer-Verlag, 2009</recordOrigin></recordInfo></relatedItem><identifier type="istex">42245AACDF7BB7F55E7FB72E4B033A37C09B6324</identifier><identifier type="ark">ark:/67375/VQC-XXX3NNRJ-7</identifier><identifier type="DOI">10.1007/s10096-009-0701-0</identifier><identifier type="ArticleID">701</identifier><identifier type="ArticleID">s10096-009-0701-0</identifier><accessCondition type="use and reproduction" contentType="copyright">Springer-Verlag, 2009</accessCondition><recordInfo><recordContentSource authority="ISTEX" authorityURI="https://loaded-corpus.data.istex.fr" valueURI="https://loaded-corpus.data.istex.fr/ark:/67375/XBH-3XSW68JL-F">springer</recordContentSource><recordOrigin>Springer-Verlag, 2009</recordOrigin></recordInfo></mods><json:item><extension>json</extension><original>false</original><mimetype>application/json</mimetype><uri>https://api.istex.fr/ark:/67375/VQC-XXX3NNRJ-7/record.json</uri></json:item></metadata><serie></serie></istex></record>Pour manipuler ce document sous Unix (Dilib)
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