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Direct matrix-assisted laser desorption ionization time-of-flight mass spectrometry and real-time PCR in a combined protocol for diagnosis of bloodstream infections: a turnaround time approach

Bloodstream infections (BSIs) are serious infections associated with high rates of morbidity and mortality. Every hour delay in initiation of an effective antibiotic increases mortality due to sepsis by 7%. Turnaround time (TAT) for conventional blood cultures takes 48 h, forcing physicians to strea...

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Autores principales: Quiles, Milene Gonçalves, Boettger, Bruno Cruz, Inoue, Fernanda Matsiko, Monteiro, Jussimara, Santos, Daniel Wagner, Ponzio, Vinicius, Carlesse, Fabianne, Cappellano, Paola, Carvalhaes, Cecilia Godoy, Pignatari, Antonio Carlos Campos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9428233/
https://www.ncbi.nlm.nih.gov/pubmed/31175842
http://dx.doi.org/10.1016/j.bjid.2019.05.005
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author Quiles, Milene Gonçalves
Boettger, Bruno Cruz
Inoue, Fernanda Matsiko
Monteiro, Jussimara
Santos, Daniel Wagner
Ponzio, Vinicius
Carlesse, Fabianne
Cappellano, Paola
Carvalhaes, Cecilia Godoy
Pignatari, Antonio Carlos Campos
author_facet Quiles, Milene Gonçalves
Boettger, Bruno Cruz
Inoue, Fernanda Matsiko
Monteiro, Jussimara
Santos, Daniel Wagner
Ponzio, Vinicius
Carlesse, Fabianne
Cappellano, Paola
Carvalhaes, Cecilia Godoy
Pignatari, Antonio Carlos Campos
author_sort Quiles, Milene Gonçalves
collection PubMed
description Bloodstream infections (BSIs) are serious infections associated with high rates of morbidity and mortality. Every hour delay in initiation of an effective antibiotic increases mortality due to sepsis by 7%. Turnaround time (TAT) for conventional blood cultures takes 48 h, forcing physicians to streamline therapy by exposing patients to broad-spectrum antimicrobials. Our objective was (1) to evaluate the accuracy and TAT of an optimized workflow combining direct matrix-assisted laser desorption ionization time-of-flight mass spectrometry (MALDI-TOF MS) and in-house real-time polymerase chain reaction (PCR) for bacterial identification and antimicrobial resistance profiling directly from positive blood bottles for diagnosing bloodstream infections and (2) to verify the effect of reporting results to medical staff. A total of 103 BSI episodes from 91 patients admitted to three hospitals in São Paulo, Brazil were included. TAT from molecular versus conventional methods was measured and compared. Our protocol showed an overall agreement of 93.5% for genus and 78.5% for species identification; 74.2% for methicillin resistance detection, 89.2% for extended-spectrum β-lactamase profiling, 77.8% for metallo-β-lactamase profiling, and 100% for carbapenemase profile and vancomycin-resistance detection when compared with conventional testing. TAT of molecular sample processing according to our protocol was 38 h shorter than conventional methods. Antimicrobial interventions were possible in 27 BSI episodes. Antimicrobial discontinuation was achieved in 12 BSI episodes while escalation of therapy occurred in 15 episodes. Antimicrobial therapy was inadequate in three (12%) BSI episodes diagnosed using results of molecular testing. Our in-house rapid protocol for identifying both bacteria and antimicrobial resistance provided rapid and accurate results, having good agreement with conventional testing results. These results could contribute to faster antimicrobial therapy interventions in BSI episodes.
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spelling pubmed-94282332022-09-01 Direct matrix-assisted laser desorption ionization time-of-flight mass spectrometry and real-time PCR in a combined protocol for diagnosis of bloodstream infections: a turnaround time approach Quiles, Milene Gonçalves Boettger, Bruno Cruz Inoue, Fernanda Matsiko Monteiro, Jussimara Santos, Daniel Wagner Ponzio, Vinicius Carlesse, Fabianne Cappellano, Paola Carvalhaes, Cecilia Godoy Pignatari, Antonio Carlos Campos Braz J Infect Dis Original Article Bloodstream infections (BSIs) are serious infections associated with high rates of morbidity and mortality. Every hour delay in initiation of an effective antibiotic increases mortality due to sepsis by 7%. Turnaround time (TAT) for conventional blood cultures takes 48 h, forcing physicians to streamline therapy by exposing patients to broad-spectrum antimicrobials. Our objective was (1) to evaluate the accuracy and TAT of an optimized workflow combining direct matrix-assisted laser desorption ionization time-of-flight mass spectrometry (MALDI-TOF MS) and in-house real-time polymerase chain reaction (PCR) for bacterial identification and antimicrobial resistance profiling directly from positive blood bottles for diagnosing bloodstream infections and (2) to verify the effect of reporting results to medical staff. A total of 103 BSI episodes from 91 patients admitted to three hospitals in São Paulo, Brazil were included. TAT from molecular versus conventional methods was measured and compared. Our protocol showed an overall agreement of 93.5% for genus and 78.5% for species identification; 74.2% for methicillin resistance detection, 89.2% for extended-spectrum β-lactamase profiling, 77.8% for metallo-β-lactamase profiling, and 100% for carbapenemase profile and vancomycin-resistance detection when compared with conventional testing. TAT of molecular sample processing according to our protocol was 38 h shorter than conventional methods. Antimicrobial interventions were possible in 27 BSI episodes. Antimicrobial discontinuation was achieved in 12 BSI episodes while escalation of therapy occurred in 15 episodes. Antimicrobial therapy was inadequate in three (12%) BSI episodes diagnosed using results of molecular testing. Our in-house rapid protocol for identifying both bacteria and antimicrobial resistance provided rapid and accurate results, having good agreement with conventional testing results. These results could contribute to faster antimicrobial therapy interventions in BSI episodes. Elsevier 2019-06-05 /pmc/articles/PMC9428233/ /pubmed/31175842 http://dx.doi.org/10.1016/j.bjid.2019.05.005 Text en © 2019 Sociedade Brasileira de Infectologia. Published by Elsevier España, S.L.U. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
Quiles, Milene Gonçalves
Boettger, Bruno Cruz
Inoue, Fernanda Matsiko
Monteiro, Jussimara
Santos, Daniel Wagner
Ponzio, Vinicius
Carlesse, Fabianne
Cappellano, Paola
Carvalhaes, Cecilia Godoy
Pignatari, Antonio Carlos Campos
Direct matrix-assisted laser desorption ionization time-of-flight mass spectrometry and real-time PCR in a combined protocol for diagnosis of bloodstream infections: a turnaround time approach
title Direct matrix-assisted laser desorption ionization time-of-flight mass spectrometry and real-time PCR in a combined protocol for diagnosis of bloodstream infections: a turnaround time approach
title_full Direct matrix-assisted laser desorption ionization time-of-flight mass spectrometry and real-time PCR in a combined protocol for diagnosis of bloodstream infections: a turnaround time approach
title_fullStr Direct matrix-assisted laser desorption ionization time-of-flight mass spectrometry and real-time PCR in a combined protocol for diagnosis of bloodstream infections: a turnaround time approach
title_full_unstemmed Direct matrix-assisted laser desorption ionization time-of-flight mass spectrometry and real-time PCR in a combined protocol for diagnosis of bloodstream infections: a turnaround time approach
title_short Direct matrix-assisted laser desorption ionization time-of-flight mass spectrometry and real-time PCR in a combined protocol for diagnosis of bloodstream infections: a turnaround time approach
title_sort direct matrix-assisted laser desorption ionization time-of-flight mass spectrometry and real-time pcr in a combined protocol for diagnosis of bloodstream infections: a turnaround time approach
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9428233/
https://www.ncbi.nlm.nih.gov/pubmed/31175842
http://dx.doi.org/10.1016/j.bjid.2019.05.005
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