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The BinaxNOW pneumococcal antigen test: An adjunct for diagnosis of pneumococcal bacteraemia
BACKGROUND: Culture remains the diagnostic standard for Streptococcus pneumoniae bacteraemia but is limited by time to identification, prior antibiotics and bacterial autolysis. Culture-independent methods for detecting S. pneumoniae include PCR and antigen tests. We evaluated an antigen test on blo...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
AOSIS
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8378051/ https://www.ncbi.nlm.nih.gov/pubmed/34485501 http://dx.doi.org/10.4102/sajid.v36i1.244 |
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author | Tootla, Hafsah D. Bamford, Colleen Centner, Chad M. Moodley, Clinton |
author_facet | Tootla, Hafsah D. Bamford, Colleen Centner, Chad M. Moodley, Clinton |
author_sort | Tootla, Hafsah D. |
collection | PubMed |
description | BACKGROUND: Culture remains the diagnostic standard for Streptococcus pneumoniae bacteraemia but is limited by time to identification, prior antibiotics and bacterial autolysis. Culture-independent methods for detecting S. pneumoniae include PCR and antigen tests. We evaluated an antigen test on blood culture broth for the rapid detection of S. pneumoniae bacteraemia. METHOD: We collected 212 signal-positive blood cultures, with gram-positive cocci in pairs, chains or with uncertain morphology. The BinaxNOW S. pneumoniae urinary antigen test, Gram stain, culture and lytA PCR were performed on all samples. Diagnostic accuracy of the antigen test and Gram stain with gram-positive cocci in pairs were compared with culture, polymerase chain reaction (PCR) and the composite of culture and PCR. RESULTS: Streptococcus pneumoniae was isolated in 26% of samples, 66% cultured other gram-positive organisms and 8% of samples had no growth. Sensitivity and negative predictive values of the antigen test were 100%, specificity and positive predictive values were 87% – 88% and 76% – 81%, but increased to 93% – 96% and 96% – 98% when applied to subsets with gram-positive cocci in pairs, or history compatible with respiratory illness or meningitis. Sensitivity (69% – 75%) and specificity (81%) of Gram stain (gram-positive cocci in pairs) were lower than the antigen test even when applied to the same subsets. CONCLUSION: Accurate and rapid diagnosis of S. pneumoniae bacteraemia is challenging. Specificity of this antigen test is limited by cross-reactivity with other gram-positive organisms, but could be improved if Gram stain morphology and clinical history are available. The antigen test is a useful adjunct for rapid diagnosis of S. pneumoniae bacteraemia. |
format | Online Article Text |
id | pubmed-8378051 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | AOSIS |
record_format | MEDLINE/PubMed |
spelling | pubmed-83780512021-09-03 The BinaxNOW pneumococcal antigen test: An adjunct for diagnosis of pneumococcal bacteraemia Tootla, Hafsah D. Bamford, Colleen Centner, Chad M. Moodley, Clinton S Afr J Infect Dis Original Research BACKGROUND: Culture remains the diagnostic standard for Streptococcus pneumoniae bacteraemia but is limited by time to identification, prior antibiotics and bacterial autolysis. Culture-independent methods for detecting S. pneumoniae include PCR and antigen tests. We evaluated an antigen test on blood culture broth for the rapid detection of S. pneumoniae bacteraemia. METHOD: We collected 212 signal-positive blood cultures, with gram-positive cocci in pairs, chains or with uncertain morphology. The BinaxNOW S. pneumoniae urinary antigen test, Gram stain, culture and lytA PCR were performed on all samples. Diagnostic accuracy of the antigen test and Gram stain with gram-positive cocci in pairs were compared with culture, polymerase chain reaction (PCR) and the composite of culture and PCR. RESULTS: Streptococcus pneumoniae was isolated in 26% of samples, 66% cultured other gram-positive organisms and 8% of samples had no growth. Sensitivity and negative predictive values of the antigen test were 100%, specificity and positive predictive values were 87% – 88% and 76% – 81%, but increased to 93% – 96% and 96% – 98% when applied to subsets with gram-positive cocci in pairs, or history compatible with respiratory illness or meningitis. Sensitivity (69% – 75%) and specificity (81%) of Gram stain (gram-positive cocci in pairs) were lower than the antigen test even when applied to the same subsets. CONCLUSION: Accurate and rapid diagnosis of S. pneumoniae bacteraemia is challenging. Specificity of this antigen test is limited by cross-reactivity with other gram-positive organisms, but could be improved if Gram stain morphology and clinical history are available. The antigen test is a useful adjunct for rapid diagnosis of S. pneumoniae bacteraemia. AOSIS 2021-04-15 /pmc/articles/PMC8378051/ /pubmed/34485501 http://dx.doi.org/10.4102/sajid.v36i1.244 Text en © 2021. The Authors https://creativecommons.org/licenses/by/4.0/Licensee: AOSIS. This work is licensed under the Creative Commons Attribution License. |
spellingShingle | Original Research Tootla, Hafsah D. Bamford, Colleen Centner, Chad M. Moodley, Clinton The BinaxNOW pneumococcal antigen test: An adjunct for diagnosis of pneumococcal bacteraemia |
title | The BinaxNOW pneumococcal antigen test: An adjunct for diagnosis of pneumococcal bacteraemia |
title_full | The BinaxNOW pneumococcal antigen test: An adjunct for diagnosis of pneumococcal bacteraemia |
title_fullStr | The BinaxNOW pneumococcal antigen test: An adjunct for diagnosis of pneumococcal bacteraemia |
title_full_unstemmed | The BinaxNOW pneumococcal antigen test: An adjunct for diagnosis of pneumococcal bacteraemia |
title_short | The BinaxNOW pneumococcal antigen test: An adjunct for diagnosis of pneumococcal bacteraemia |
title_sort | binaxnow pneumococcal antigen test: an adjunct for diagnosis of pneumococcal bacteraemia |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8378051/ https://www.ncbi.nlm.nih.gov/pubmed/34485501 http://dx.doi.org/10.4102/sajid.v36i1.244 |
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