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1657. Evaluating the Effectiveness of Biofire® FilmArray® BCID2 Sepsis Panel in Pediatric Antibiotic Stewardship Program: Less time and more control

BACKGROUND: The use of molecular biology tools has allowed for a decrease in the time required for effective therapy in bacteremia. Integrating these tools into Antimicrobial Stewardship Programs (ASP) can improve clinical outcomes. The aim of this study is to describe the impact of using a molecula...

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Autores principales: Londono-Ruiz, Juan Pablo, Betancur, Juan Pablo, Casadiego-Payares, Stephanie, Castellanos-Leguizamon, Daniela, Gutierrez-Tobar, Ivan Felipe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10678358/
http://dx.doi.org/10.1093/ofid/ofad500.1490
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author Londono-Ruiz, Juan Pablo
Betancur, Juan Pablo
Casadiego-Payares, Stephanie
Castellanos-Leguizamon, Daniela
Gutierrez-Tobar, Ivan Felipe
author_facet Londono-Ruiz, Juan Pablo
Betancur, Juan Pablo
Casadiego-Payares, Stephanie
Castellanos-Leguizamon, Daniela
Gutierrez-Tobar, Ivan Felipe
author_sort Londono-Ruiz, Juan Pablo
collection PubMed
description BACKGROUND: The use of molecular biology tools has allowed for a decrease in the time required for effective therapy in bacteremia. Integrating these tools into Antimicrobial Stewardship Programs (ASP) can improve clinical outcomes. The aim of this study is to describe the impact of using a molecular biology platform for sepsis as part of an ASP in a pediatric hospital. METHODS: This descriptive study collected data from positive blood cultures that underwent Biofire® FilmArray® BCID2 testing for sepsis from January 2021 to February 2023. In our hospital, taking this molecular test is indicated in all blood cultures positive for Gram-negative bacilli, in Gram-positive cocci only when there is a pyogenic focus or both sets are positives, additionally in patients with immunosuppression or who present with septic shock. Clinical and microbiological characteristics of the samples were described, along with the impact of the ASP after receiving the test results. Data analysis was performed using the R program. RESULTS: A total of 119 positive blood culture bottles were included in the study, in which the molecular test was performed. Gram-positive cocci were identified in 82 (68.9%) bottles, while Gram-negative bacilli were identified in 37 (31.1%). The mean detection time for Gram-positive cocci was 13 hours and 33 minutes (range: 11-18 h), while for Gram-negative bacilli it was 11 hours and 30 minutes (range: 9-13 h). The most frequently detected germs are presented in Table 1. Among the 119 patients, the FilmArray test result prompted a change in antibiotic therapy in 54 cases (45.3%). In an additional 28 cases (23%), a change was made after the final culture result. Only 6 patients (5%) experienced clinical deterioration after the FilmArray® test, requiring changes prior to the definitive culture result. [Figure: see text] CONCLUSION: In conclusion, our study demonstrates that the use of molecular tools in positive blood culture bottles, guided by an ASP, allowed for rapid changes in nearly half of the cases. Few patients experienced deterioration after the completion of the FilmArray® test, requiring empirical changes in the antibiotic. These findings suggest that incorporating molecular tests into ASPs can significantly improve the management of bacteremia, leading to more effective and timely treatment decisions. DISCLOSURES: All Authors: No reported disclosures
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spelling pubmed-106783582023-11-27 1657. Evaluating the Effectiveness of Biofire® FilmArray® BCID2 Sepsis Panel in Pediatric Antibiotic Stewardship Program: Less time and more control Londono-Ruiz, Juan Pablo Betancur, Juan Pablo Casadiego-Payares, Stephanie Castellanos-Leguizamon, Daniela Gutierrez-Tobar, Ivan Felipe Open Forum Infect Dis Abstract BACKGROUND: The use of molecular biology tools has allowed for a decrease in the time required for effective therapy in bacteremia. Integrating these tools into Antimicrobial Stewardship Programs (ASP) can improve clinical outcomes. The aim of this study is to describe the impact of using a molecular biology platform for sepsis as part of an ASP in a pediatric hospital. METHODS: This descriptive study collected data from positive blood cultures that underwent Biofire® FilmArray® BCID2 testing for sepsis from January 2021 to February 2023. In our hospital, taking this molecular test is indicated in all blood cultures positive for Gram-negative bacilli, in Gram-positive cocci only when there is a pyogenic focus or both sets are positives, additionally in patients with immunosuppression or who present with septic shock. Clinical and microbiological characteristics of the samples were described, along with the impact of the ASP after receiving the test results. Data analysis was performed using the R program. RESULTS: A total of 119 positive blood culture bottles were included in the study, in which the molecular test was performed. Gram-positive cocci were identified in 82 (68.9%) bottles, while Gram-negative bacilli were identified in 37 (31.1%). The mean detection time for Gram-positive cocci was 13 hours and 33 minutes (range: 11-18 h), while for Gram-negative bacilli it was 11 hours and 30 minutes (range: 9-13 h). The most frequently detected germs are presented in Table 1. Among the 119 patients, the FilmArray test result prompted a change in antibiotic therapy in 54 cases (45.3%). In an additional 28 cases (23%), a change was made after the final culture result. Only 6 patients (5%) experienced clinical deterioration after the FilmArray® test, requiring changes prior to the definitive culture result. [Figure: see text] CONCLUSION: In conclusion, our study demonstrates that the use of molecular tools in positive blood culture bottles, guided by an ASP, allowed for rapid changes in nearly half of the cases. Few patients experienced deterioration after the completion of the FilmArray® test, requiring empirical changes in the antibiotic. These findings suggest that incorporating molecular tests into ASPs can significantly improve the management of bacteremia, leading to more effective and timely treatment decisions. DISCLOSURES: All Authors: No reported disclosures Oxford University Press 2023-11-27 /pmc/articles/PMC10678358/ http://dx.doi.org/10.1093/ofid/ofad500.1490 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of Infectious Diseases Society of America. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Abstract
Londono-Ruiz, Juan Pablo
Betancur, Juan Pablo
Casadiego-Payares, Stephanie
Castellanos-Leguizamon, Daniela
Gutierrez-Tobar, Ivan Felipe
1657. Evaluating the Effectiveness of Biofire® FilmArray® BCID2 Sepsis Panel in Pediatric Antibiotic Stewardship Program: Less time and more control
title 1657. Evaluating the Effectiveness of Biofire® FilmArray® BCID2 Sepsis Panel in Pediatric Antibiotic Stewardship Program: Less time and more control
title_full 1657. Evaluating the Effectiveness of Biofire® FilmArray® BCID2 Sepsis Panel in Pediatric Antibiotic Stewardship Program: Less time and more control
title_fullStr 1657. Evaluating the Effectiveness of Biofire® FilmArray® BCID2 Sepsis Panel in Pediatric Antibiotic Stewardship Program: Less time and more control
title_full_unstemmed 1657. Evaluating the Effectiveness of Biofire® FilmArray® BCID2 Sepsis Panel in Pediatric Antibiotic Stewardship Program: Less time and more control
title_short 1657. Evaluating the Effectiveness of Biofire® FilmArray® BCID2 Sepsis Panel in Pediatric Antibiotic Stewardship Program: Less time and more control
title_sort 1657. evaluating the effectiveness of biofire® filmarray® bcid2 sepsis panel in pediatric antibiotic stewardship program: less time and more control
topic Abstract
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10678358/
http://dx.doi.org/10.1093/ofid/ofad500.1490
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