Detection of group A beta-hemolytic Streptococcus employing three different detection methods: culture, rapid antigen detecting test, and molecular assay

Detalhes bibliográficos
Autor(a) principal: Santos, Odimara [UNIFESP]
Data de Publicação: 2003
Outros Autores: Weckx, Luc Louis Maurice [UNIFESP], Pignatari, Antonio Carlos Campos [UNIFESP], Pignatari, Shirley Shizue Nagata [UNIFESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNIFESP
Texto Completo: http://repositorio.unifesp.br/handle/11600/1885
http://dx.doi.org/10.1590/S1413-86702003000500003
Resumo: In order to study the prevalence of Group A beta-hemolytic Streptococcus (GABHS) pharyngotonsillitis in our pediatric population and to compare different sampling methods of GABHS detection, oropharyngeal swabs from 50 children with acute pharyngotonsillitis, between 1 and 12 years old, were used simultaneously for culture, molecular assay and rapid GABHS antigen detection tests. All children were clinically examined at the Division of Pediatric Otorhinolaryngology of the Federal University of São Paulo. Diagnostic criteria were based on signs and symptoms, including sore throat, fever and oropharyngeal purulent secretion. Children that had been treated with antibiotics were excluded. Overall, combining the three methods, the prevalence of GABHS was 34%. GABHS was diagnosed in 30% of the bacterial cultures, in 25% of the samples tested with the molecular nucleic acid hybridization method and in 26% of the cases tested with the rapid antigen detection test. There was no significant difference between these three methods.
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spelling Santos, Odimara [UNIFESP]Weckx, Luc Louis Maurice [UNIFESP]Pignatari, Antonio Carlos Campos [UNIFESP]Pignatari, Shirley Shizue Nagata [UNIFESP]Universidade Federal de São Paulo (UNIFESP)2015-06-14T13:30:10Z2015-06-14T13:30:10Z2003-10-01Brazilian Journal of Infectious Diseases. Brazilian Society of Infectious Diseases, v. 7, n. 5, p. 297-300, 2003.1413-8670http://repositorio.unifesp.br/handle/11600/1885http://dx.doi.org/10.1590/S1413-86702003000500003S1413-86702003000500003.pdfS1413-8670200300050000310.1590/S1413-86702003000500003In order to study the prevalence of Group A beta-hemolytic Streptococcus (GABHS) pharyngotonsillitis in our pediatric population and to compare different sampling methods of GABHS detection, oropharyngeal swabs from 50 children with acute pharyngotonsillitis, between 1 and 12 years old, were used simultaneously for culture, molecular assay and rapid GABHS antigen detection tests. All children were clinically examined at the Division of Pediatric Otorhinolaryngology of the Federal University of São Paulo. Diagnostic criteria were based on signs and symptoms, including sore throat, fever and oropharyngeal purulent secretion. Children that had been treated with antibiotics were excluded. Overall, combining the three methods, the prevalence of GABHS was 34%. GABHS was diagnosed in 30% of the bacterial cultures, in 25% of the samples tested with the molecular nucleic acid hybridization method and in 26% of the cases tested with the rapid antigen detection test. There was no significant difference between these three methods.Federal University of São Paulo Division of Pediatric OtolaryngologyUNIFESP, Division of Pediatric OtolaryngologySciELO297-300engBrazilian Society of Infectious DiseasesBrazilian Journal of Infectious DiseasesAcute pharyngotonsillitisGABHSlaboratory detectionDetection of group A beta-hemolytic Streptococcus employing three different detection methods: culture, rapid antigen detecting test, and molecular assayinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESPORIGINALS1413-86702003000500003.pdfapplication/pdf20111${dspace.ui.url}/bitstream/11600/1885/1/S1413-86702003000500003.pdf42e4aff0f41d8641b7328d2c801d7b2aMD51open accessTEXTS1413-86702003000500003.pdf.txtS1413-86702003000500003.pdf.txtExtracted texttext/plain14669${dspace.ui.url}/bitstream/11600/1885/21/S1413-86702003000500003.pdf.txt09717c94d921156757ebe007415dbf13MD521open accessTHUMBNAILS1413-86702003000500003.pdf.jpgS1413-86702003000500003.pdf.jpgIM Thumbnailimage/jpeg6388${dspace.ui.url}/bitstream/11600/1885/23/S1413-86702003000500003.pdf.jpg9baee780f97eb5019d51611d91054c69MD523open access11600/18852023-06-05 19:29:47.188open accessoai:repositorio.unifesp.br:11600/1885Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestopendoar:34652023-06-05T22:29:47Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false
dc.title.en.fl_str_mv Detection of group A beta-hemolytic Streptococcus employing three different detection methods: culture, rapid antigen detecting test, and molecular assay
title Detection of group A beta-hemolytic Streptococcus employing three different detection methods: culture, rapid antigen detecting test, and molecular assay
spellingShingle Detection of group A beta-hemolytic Streptococcus employing three different detection methods: culture, rapid antigen detecting test, and molecular assay
Santos, Odimara [UNIFESP]
Acute pharyngotonsillitis
GABHS
laboratory detection
title_short Detection of group A beta-hemolytic Streptococcus employing three different detection methods: culture, rapid antigen detecting test, and molecular assay
title_full Detection of group A beta-hemolytic Streptococcus employing three different detection methods: culture, rapid antigen detecting test, and molecular assay
title_fullStr Detection of group A beta-hemolytic Streptococcus employing three different detection methods: culture, rapid antigen detecting test, and molecular assay
title_full_unstemmed Detection of group A beta-hemolytic Streptococcus employing three different detection methods: culture, rapid antigen detecting test, and molecular assay
title_sort Detection of group A beta-hemolytic Streptococcus employing three different detection methods: culture, rapid antigen detecting test, and molecular assay
author Santos, Odimara [UNIFESP]
author_facet Santos, Odimara [UNIFESP]
Weckx, Luc Louis Maurice [UNIFESP]
Pignatari, Antonio Carlos Campos [UNIFESP]
Pignatari, Shirley Shizue Nagata [UNIFESP]
author_role author
author2 Weckx, Luc Louis Maurice [UNIFESP]
Pignatari, Antonio Carlos Campos [UNIFESP]
Pignatari, Shirley Shizue Nagata [UNIFESP]
author2_role author
author
author
dc.contributor.institution.none.fl_str_mv Universidade Federal de São Paulo (UNIFESP)
dc.contributor.author.fl_str_mv Santos, Odimara [UNIFESP]
Weckx, Luc Louis Maurice [UNIFESP]
Pignatari, Antonio Carlos Campos [UNIFESP]
Pignatari, Shirley Shizue Nagata [UNIFESP]
dc.subject.eng.fl_str_mv Acute pharyngotonsillitis
GABHS
laboratory detection
topic Acute pharyngotonsillitis
GABHS
laboratory detection
description In order to study the prevalence of Group A beta-hemolytic Streptococcus (GABHS) pharyngotonsillitis in our pediatric population and to compare different sampling methods of GABHS detection, oropharyngeal swabs from 50 children with acute pharyngotonsillitis, between 1 and 12 years old, were used simultaneously for culture, molecular assay and rapid GABHS antigen detection tests. All children were clinically examined at the Division of Pediatric Otorhinolaryngology of the Federal University of São Paulo. Diagnostic criteria were based on signs and symptoms, including sore throat, fever and oropharyngeal purulent secretion. Children that had been treated with antibiotics were excluded. Overall, combining the three methods, the prevalence of GABHS was 34%. GABHS was diagnosed in 30% of the bacterial cultures, in 25% of the samples tested with the molecular nucleic acid hybridization method and in 26% of the cases tested with the rapid antigen detection test. There was no significant difference between these three methods.
publishDate 2003
dc.date.issued.fl_str_mv 2003-10-01
dc.date.accessioned.fl_str_mv 2015-06-14T13:30:10Z
dc.date.available.fl_str_mv 2015-06-14T13:30:10Z
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dc.identifier.citation.fl_str_mv Brazilian Journal of Infectious Diseases. Brazilian Society of Infectious Diseases, v. 7, n. 5, p. 297-300, 2003.
dc.identifier.uri.fl_str_mv http://repositorio.unifesp.br/handle/11600/1885
http://dx.doi.org/10.1590/S1413-86702003000500003
dc.identifier.issn.none.fl_str_mv 1413-8670
dc.identifier.file.none.fl_str_mv S1413-86702003000500003.pdf
dc.identifier.scielo.none.fl_str_mv S1413-86702003000500003
dc.identifier.doi.none.fl_str_mv 10.1590/S1413-86702003000500003
identifier_str_mv Brazilian Journal of Infectious Diseases. Brazilian Society of Infectious Diseases, v. 7, n. 5, p. 297-300, 2003.
1413-8670
S1413-86702003000500003.pdf
S1413-86702003000500003
10.1590/S1413-86702003000500003
url http://repositorio.unifesp.br/handle/11600/1885
http://dx.doi.org/10.1590/S1413-86702003000500003
dc.language.iso.fl_str_mv eng
language eng
dc.relation.ispartof.none.fl_str_mv Brazilian Journal of Infectious Diseases
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dc.format.none.fl_str_mv 297-300
dc.publisher.none.fl_str_mv Brazilian Society of Infectious Diseases
publisher.none.fl_str_mv Brazilian Society of Infectious Diseases
dc.source.none.fl_str_mv reponame:Repositório Institucional da UNIFESP
instname:Universidade Federal de São Paulo (UNIFESP)
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