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Clinical impact of a commercially available multiplex PCR system for rapid detection of pathogens in patients with presumed sepsis

BACKGROUND: Timely identification of pathogens is crucial to minimize mortality in patients with severe infections. Detection of bacterial and fungal pathogens in blood by nucleic acid amplification promises to yield results faster than blood cultures (BC). We analyzed the clinical impact of a comme...

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Autores principales: Dierkes, Christine, Ehrenstein, Boris, Siebig, Sylvia, Linde, Hans-Jörg, Reischl, Udo, Salzberger, Bernd
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2739209/
https://www.ncbi.nlm.nih.gov/pubmed/19671147
http://dx.doi.org/10.1186/1471-2334-9-126
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author Dierkes, Christine
Ehrenstein, Boris
Siebig, Sylvia
Linde, Hans-Jörg
Reischl, Udo
Salzberger, Bernd
author_facet Dierkes, Christine
Ehrenstein, Boris
Siebig, Sylvia
Linde, Hans-Jörg
Reischl, Udo
Salzberger, Bernd
author_sort Dierkes, Christine
collection PubMed
description BACKGROUND: Timely identification of pathogens is crucial to minimize mortality in patients with severe infections. Detection of bacterial and fungal pathogens in blood by nucleic acid amplification promises to yield results faster than blood cultures (BC). We analyzed the clinical impact of a commercially available multiplex PCR system in patients with suspected sepsis. METHODS: Blood samples from patients with presumed sepsis were cultured with the Bactec 9240™ system (Becton Dickinson, Heidelberg, Germany) and aliquots subjected to analysis with the LightCycler(® )SeptiFast(® )(SF) Test (Roche Diagnostics, Mannheim, Germany) at a tertiary care centre. For samples with PCR-detected pathogens, the actual impact on clinical management was determined by chart review. Furthermore a comparison between the time to a positive blood culture result and the SF result, based on a fictive assumption that it was done either on a once or twice daily basis, was made. RESULTS: Of 101 blood samples from 77 patients, 63 (62%) yielded concordant negative results, 14 (13%) concordant positive and 9 (9%) were BC positive only. In 14 (13%) samples pathogens were detected by SF only, resulting in adjustment of antibiotic therapy in 5 patients (7,7% of patients). In 3 samples a treatment adjustment would have been made earlier resulting in a total of 8 adjustments in all 101 samples (8%). CONCLUSION: The addition of multiplex PCR to conventional blood cultures had a relevant impact on clinical management for a subset of patients with presumed sepsis.
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spelling pubmed-27392092009-09-08 Clinical impact of a commercially available multiplex PCR system for rapid detection of pathogens in patients with presumed sepsis Dierkes, Christine Ehrenstein, Boris Siebig, Sylvia Linde, Hans-Jörg Reischl, Udo Salzberger, Bernd BMC Infect Dis Research Article BACKGROUND: Timely identification of pathogens is crucial to minimize mortality in patients with severe infections. Detection of bacterial and fungal pathogens in blood by nucleic acid amplification promises to yield results faster than blood cultures (BC). We analyzed the clinical impact of a commercially available multiplex PCR system in patients with suspected sepsis. METHODS: Blood samples from patients with presumed sepsis were cultured with the Bactec 9240™ system (Becton Dickinson, Heidelberg, Germany) and aliquots subjected to analysis with the LightCycler(® )SeptiFast(® )(SF) Test (Roche Diagnostics, Mannheim, Germany) at a tertiary care centre. For samples with PCR-detected pathogens, the actual impact on clinical management was determined by chart review. Furthermore a comparison between the time to a positive blood culture result and the SF result, based on a fictive assumption that it was done either on a once or twice daily basis, was made. RESULTS: Of 101 blood samples from 77 patients, 63 (62%) yielded concordant negative results, 14 (13%) concordant positive and 9 (9%) were BC positive only. In 14 (13%) samples pathogens were detected by SF only, resulting in adjustment of antibiotic therapy in 5 patients (7,7% of patients). In 3 samples a treatment adjustment would have been made earlier resulting in a total of 8 adjustments in all 101 samples (8%). CONCLUSION: The addition of multiplex PCR to conventional blood cultures had a relevant impact on clinical management for a subset of patients with presumed sepsis. BioMed Central 2009-08-11 /pmc/articles/PMC2739209/ /pubmed/19671147 http://dx.doi.org/10.1186/1471-2334-9-126 Text en Copyright ©2009 Dierkes et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Dierkes, Christine
Ehrenstein, Boris
Siebig, Sylvia
Linde, Hans-Jörg
Reischl, Udo
Salzberger, Bernd
Clinical impact of a commercially available multiplex PCR system for rapid detection of pathogens in patients with presumed sepsis
title Clinical impact of a commercially available multiplex PCR system for rapid detection of pathogens in patients with presumed sepsis
title_full Clinical impact of a commercially available multiplex PCR system for rapid detection of pathogens in patients with presumed sepsis
title_fullStr Clinical impact of a commercially available multiplex PCR system for rapid detection of pathogens in patients with presumed sepsis
title_full_unstemmed Clinical impact of a commercially available multiplex PCR system for rapid detection of pathogens in patients with presumed sepsis
title_short Clinical impact of a commercially available multiplex PCR system for rapid detection of pathogens in patients with presumed sepsis
title_sort clinical impact of a commercially available multiplex pcr system for rapid detection of pathogens in patients with presumed sepsis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2739209/
https://www.ncbi.nlm.nih.gov/pubmed/19671147
http://dx.doi.org/10.1186/1471-2334-9-126
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