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Evaluation of the Sepsis Flow Chip assay for the diagnosis of blood infections

BACKGROUND: Blood infections are serious complex conditions that generally require rapid diagnosis and treatment. The big challenge is to reduce the time necessary to make a diagnosis with current clinical microbiological methods so as to improve the treatment given to patients. METHODS: In this stu...

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Autores principales: Galiana, Antonio, Coy, Javier, Gimeno, Adelina, Guzman, Noemi Marco, Rosales, Francisco, Merino, Esperanza, Royo, Gloria, Rodríguez, Juan Carlos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5436663/
https://www.ncbi.nlm.nih.gov/pubmed/28542614
http://dx.doi.org/10.1371/journal.pone.0177627
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author Galiana, Antonio
Coy, Javier
Gimeno, Adelina
Guzman, Noemi Marco
Rosales, Francisco
Merino, Esperanza
Royo, Gloria
Rodríguez, Juan Carlos
author_facet Galiana, Antonio
Coy, Javier
Gimeno, Adelina
Guzman, Noemi Marco
Rosales, Francisco
Merino, Esperanza
Royo, Gloria
Rodríguez, Juan Carlos
author_sort Galiana, Antonio
collection PubMed
description BACKGROUND: Blood infections are serious complex conditions that generally require rapid diagnosis and treatment. The big challenge is to reduce the time necessary to make a diagnosis with current clinical microbiological methods so as to improve the treatment given to patients. METHODS: In this study, we assess for the first time the Sepsis Flow Chip assay, which is a novel diagnostic assay for simultaneous rapid-detection of the vast majority of bloodstream pathogens, including Gram-positive and Gram-negative bacteria and fungi, in the same assay, and for the detection of most common antibiotic resistance genes. The SFC assay is based on multiplex PCR and low density DNA arrays. RESULTS: Positive blood cultures from 202 consecutive bacteremia patients were analyzed by SFC assay and the results were compared with the results obtained by the gold standard methodology used in clinical microbiology diagnostic laboratories (EUCAST guidelines). SFC assay overall sensitivity and specificity for bacterial identification were 93.3% and 100% respectively and sensitivity and specificity for the identification of antibiotic genetic resistance determinants were 93.6% and 100% respectively. CONCLUSIONS: This is the first evaluation of SFC assay in clinical samples. This new method appears to be very promising by combining the high number of distinct pathogens and genetic resistance determinants identified in a single assay. Further investigations should be done to evaluate the usefulness of this assay in combination with clinical multidisciplinary groups (stewardship), in order for the results to be applied appropriately to the management of patients`infectious processes.
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spelling pubmed-54366632017-05-27 Evaluation of the Sepsis Flow Chip assay for the diagnosis of blood infections Galiana, Antonio Coy, Javier Gimeno, Adelina Guzman, Noemi Marco Rosales, Francisco Merino, Esperanza Royo, Gloria Rodríguez, Juan Carlos PLoS One Research Article BACKGROUND: Blood infections are serious complex conditions that generally require rapid diagnosis and treatment. The big challenge is to reduce the time necessary to make a diagnosis with current clinical microbiological methods so as to improve the treatment given to patients. METHODS: In this study, we assess for the first time the Sepsis Flow Chip assay, which is a novel diagnostic assay for simultaneous rapid-detection of the vast majority of bloodstream pathogens, including Gram-positive and Gram-negative bacteria and fungi, in the same assay, and for the detection of most common antibiotic resistance genes. The SFC assay is based on multiplex PCR and low density DNA arrays. RESULTS: Positive blood cultures from 202 consecutive bacteremia patients were analyzed by SFC assay and the results were compared with the results obtained by the gold standard methodology used in clinical microbiology diagnostic laboratories (EUCAST guidelines). SFC assay overall sensitivity and specificity for bacterial identification were 93.3% and 100% respectively and sensitivity and specificity for the identification of antibiotic genetic resistance determinants were 93.6% and 100% respectively. CONCLUSIONS: This is the first evaluation of SFC assay in clinical samples. This new method appears to be very promising by combining the high number of distinct pathogens and genetic resistance determinants identified in a single assay. Further investigations should be done to evaluate the usefulness of this assay in combination with clinical multidisciplinary groups (stewardship), in order for the results to be applied appropriately to the management of patients`infectious processes. Public Library of Science 2017-05-18 /pmc/articles/PMC5436663/ /pubmed/28542614 http://dx.doi.org/10.1371/journal.pone.0177627 Text en © 2017 Galiana et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Galiana, Antonio
Coy, Javier
Gimeno, Adelina
Guzman, Noemi Marco
Rosales, Francisco
Merino, Esperanza
Royo, Gloria
Rodríguez, Juan Carlos
Evaluation of the Sepsis Flow Chip assay for the diagnosis of blood infections
title Evaluation of the Sepsis Flow Chip assay for the diagnosis of blood infections
title_full Evaluation of the Sepsis Flow Chip assay for the diagnosis of blood infections
title_fullStr Evaluation of the Sepsis Flow Chip assay for the diagnosis of blood infections
title_full_unstemmed Evaluation of the Sepsis Flow Chip assay for the diagnosis of blood infections
title_short Evaluation of the Sepsis Flow Chip assay for the diagnosis of blood infections
title_sort evaluation of the sepsis flow chip assay for the diagnosis of blood infections
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5436663/
https://www.ncbi.nlm.nih.gov/pubmed/28542614
http://dx.doi.org/10.1371/journal.pone.0177627
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