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Change in Methicillin-Resistant Staphylococcus aureus Testing in the Intensive Care Unit as an Antimicrobial Stewardship Initiative

Background: Methicillin-resistant Staphylococcus aureus (MRSA)–associated infections are a cause of morbidity and mortality in the intensive care unit (ICU). Vancomycin is a treatment option but is not without risks. Methods: A MRSA testing change—the switch from culture to polymerase chain reaction...

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Autores principales: Smith, Hayden L., DuMontier, Samuel P., Bushman, Amanda M., Hurdelbrink, Jonathan R., Yost, William J., Craig, Steven R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Academic Division of Ochsner Clinic Foundation 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10262952/
https://www.ncbi.nlm.nih.gov/pubmed/37323512
http://dx.doi.org/10.31486/toj.22.0103
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author Smith, Hayden L.
DuMontier, Samuel P.
Bushman, Amanda M.
Hurdelbrink, Jonathan R.
Yost, William J.
Craig, Steven R.
author_facet Smith, Hayden L.
DuMontier, Samuel P.
Bushman, Amanda M.
Hurdelbrink, Jonathan R.
Yost, William J.
Craig, Steven R.
author_sort Smith, Hayden L.
collection PubMed
description Background: Methicillin-resistant Staphylococcus aureus (MRSA)–associated infections are a cause of morbidity and mortality in the intensive care unit (ICU). Vancomycin is a treatment option but is not without risks. Methods: A MRSA testing change—the switch from culture to polymerase chain reaction—was implemented at 2 adult (tertiary and community) ICUs located in a Midwestern US health system. Data from 2016 to 2020 were included in the study, and the median change in time to test results was examined. Results: During the study period, 71% of 19,975 patients seen at the 2 ICUs received MRSA testing. In the preintervention period, 91% and 99% of patients at the tertiary and community hospitals received testing via culture, respectively. Culture testing was used 1% and ∼0% of the time at the tertiary and community hospitals, respectively, in the postintervention period. A counterfactual estimate showed 36 (95% credible interval [CrI], 35, 37) and 32 (95% CrI, 31, 33) fewer hours until results were available at the tertiary and community hospitals, respectively. Conclusion: After the testing change, MRSA results were available in less time. Obtaining results sooner can assist with antimicrobial stewardship through the potential delay in initiating therapies such as vancomycin and/or quicker de-escalation of such therapies.
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spelling pubmed-102629522023-06-15 Change in Methicillin-Resistant Staphylococcus aureus Testing in the Intensive Care Unit as an Antimicrobial Stewardship Initiative Smith, Hayden L. DuMontier, Samuel P. Bushman, Amanda M. Hurdelbrink, Jonathan R. Yost, William J. Craig, Steven R. Ochsner J Original Research Background: Methicillin-resistant Staphylococcus aureus (MRSA)–associated infections are a cause of morbidity and mortality in the intensive care unit (ICU). Vancomycin is a treatment option but is not without risks. Methods: A MRSA testing change—the switch from culture to polymerase chain reaction—was implemented at 2 adult (tertiary and community) ICUs located in a Midwestern US health system. Data from 2016 to 2020 were included in the study, and the median change in time to test results was examined. Results: During the study period, 71% of 19,975 patients seen at the 2 ICUs received MRSA testing. In the preintervention period, 91% and 99% of patients at the tertiary and community hospitals received testing via culture, respectively. Culture testing was used 1% and ∼0% of the time at the tertiary and community hospitals, respectively, in the postintervention period. A counterfactual estimate showed 36 (95% credible interval [CrI], 35, 37) and 32 (95% CrI, 31, 33) fewer hours until results were available at the tertiary and community hospitals, respectively. Conclusion: After the testing change, MRSA results were available in less time. Obtaining results sooner can assist with antimicrobial stewardship through the potential delay in initiating therapies such as vancomycin and/or quicker de-escalation of such therapies. Academic Division of Ochsner Clinic Foundation 2023 2023 /pmc/articles/PMC10262952/ /pubmed/37323512 http://dx.doi.org/10.31486/toj.22.0103 Text en ©2023 by the author(s); Creative Commons Attribution License (CC BY) https://creativecommons.org/licenses/by/4.0/©2023 by the author(s); licensee Ochsner Journal, Ochsner Clinic Foundation, New Orleans, LA. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (creativecommons.org/licenses/by/4.0/legalcode) that permits unrestricted use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.
spellingShingle Original Research
Smith, Hayden L.
DuMontier, Samuel P.
Bushman, Amanda M.
Hurdelbrink, Jonathan R.
Yost, William J.
Craig, Steven R.
Change in Methicillin-Resistant Staphylococcus aureus Testing in the Intensive Care Unit as an Antimicrobial Stewardship Initiative
title Change in Methicillin-Resistant Staphylococcus aureus Testing in the Intensive Care Unit as an Antimicrobial Stewardship Initiative
title_full Change in Methicillin-Resistant Staphylococcus aureus Testing in the Intensive Care Unit as an Antimicrobial Stewardship Initiative
title_fullStr Change in Methicillin-Resistant Staphylococcus aureus Testing in the Intensive Care Unit as an Antimicrobial Stewardship Initiative
title_full_unstemmed Change in Methicillin-Resistant Staphylococcus aureus Testing in the Intensive Care Unit as an Antimicrobial Stewardship Initiative
title_short Change in Methicillin-Resistant Staphylococcus aureus Testing in the Intensive Care Unit as an Antimicrobial Stewardship Initiative
title_sort change in methicillin-resistant staphylococcus aureus testing in the intensive care unit as an antimicrobial stewardship initiative
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10262952/
https://www.ncbi.nlm.nih.gov/pubmed/37323512
http://dx.doi.org/10.31486/toj.22.0103
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