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Patient-specific risk factors contributing to blood culture contamination

OBJECTIVE: Contaminated blood cultures result in extended hospital stays and unnecessary antibiotic therapy. Patient-specific factors associated with blood culture contamination remain largely unexplored. Identifying patients at higher risk of blood culture contamination could alert healthcare provi...

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Autores principales: Liaquat, Sidra, Baccaglini, Lorena, Haynatzki, Gleb, Medcalf, Sharon J., Rupp, Mark E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cambridge University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9614848/
https://www.ncbi.nlm.nih.gov/pubmed/36310794
http://dx.doi.org/10.1017/ash.2022.22
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author Liaquat, Sidra
Baccaglini, Lorena
Haynatzki, Gleb
Medcalf, Sharon J.
Rupp, Mark E.
author_facet Liaquat, Sidra
Baccaglini, Lorena
Haynatzki, Gleb
Medcalf, Sharon J.
Rupp, Mark E.
author_sort Liaquat, Sidra
collection PubMed
description OBJECTIVE: Contaminated blood cultures result in extended hospital stays and unnecessary antibiotic therapy. Patient-specific factors associated with blood culture contamination remain largely unexplored. Identifying patients at higher risk of blood culture contamination could alert healthcare providers to take extra precautionary measures to limit contamination in these patients, and thereby prevent associated adverse outcomes. We sought to identify patient-related factors that contribute to blood culture contamination in hospitalized patients. DESIGN AND SETTING: We conducted a secondary data analysis of a retrospective cohort study at an academic medical center. PATIENTS: Study participants included 19,255 adult patients who had blood culture(s) performed during a hospital admission between June 2014 and December 2016. METHODS: Data were analyzed to evaluate risk factors for blood culture contamination using logistic regression. RESULTS: Among adult patients, we identified 464 contaminated episodes and 11,010 negative blood-culture episodes. Chronic obstructive pulmonary disease (adjusted odds ratio [AOR], 1.67; 95% confidence interval [CI], 1.20–2.34) and stay in an intensive care unit (ICU) during an admission (AOR, 1.41; 95% CI, 1.14–1.74) were associated with blood culture contamination. Other risk factors included race, body mass index, and admission from the emergency department. Subgroup analyses of patients admitted from the emergency department showed similar results. CONCLUSIONS: We identified patient-specific factors that increase the odds of false-positive blood cultures. By introducing mitigation strategies to limit contamination in patients with these risk factors, it may be possible to reduce the adverse clinical impact of blood culture contamination.
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spelling pubmed-96148482022-10-29 Patient-specific risk factors contributing to blood culture contamination Liaquat, Sidra Baccaglini, Lorena Haynatzki, Gleb Medcalf, Sharon J. Rupp, Mark E. Antimicrob Steward Healthc Epidemiol Original Article OBJECTIVE: Contaminated blood cultures result in extended hospital stays and unnecessary antibiotic therapy. Patient-specific factors associated with blood culture contamination remain largely unexplored. Identifying patients at higher risk of blood culture contamination could alert healthcare providers to take extra precautionary measures to limit contamination in these patients, and thereby prevent associated adverse outcomes. We sought to identify patient-related factors that contribute to blood culture contamination in hospitalized patients. DESIGN AND SETTING: We conducted a secondary data analysis of a retrospective cohort study at an academic medical center. PATIENTS: Study participants included 19,255 adult patients who had blood culture(s) performed during a hospital admission between June 2014 and December 2016. METHODS: Data were analyzed to evaluate risk factors for blood culture contamination using logistic regression. RESULTS: Among adult patients, we identified 464 contaminated episodes and 11,010 negative blood-culture episodes. Chronic obstructive pulmonary disease (adjusted odds ratio [AOR], 1.67; 95% confidence interval [CI], 1.20–2.34) and stay in an intensive care unit (ICU) during an admission (AOR, 1.41; 95% CI, 1.14–1.74) were associated with blood culture contamination. Other risk factors included race, body mass index, and admission from the emergency department. Subgroup analyses of patients admitted from the emergency department showed similar results. CONCLUSIONS: We identified patient-specific factors that increase the odds of false-positive blood cultures. By introducing mitigation strategies to limit contamination in patients with these risk factors, it may be possible to reduce the adverse clinical impact of blood culture contamination. Cambridge University Press 2022-03-18 /pmc/articles/PMC9614848/ /pubmed/36310794 http://dx.doi.org/10.1017/ash.2022.22 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution and reproduction, provided the original article is properly cited.
spellingShingle Original Article
Liaquat, Sidra
Baccaglini, Lorena
Haynatzki, Gleb
Medcalf, Sharon J.
Rupp, Mark E.
Patient-specific risk factors contributing to blood culture contamination
title Patient-specific risk factors contributing to blood culture contamination
title_full Patient-specific risk factors contributing to blood culture contamination
title_fullStr Patient-specific risk factors contributing to blood culture contamination
title_full_unstemmed Patient-specific risk factors contributing to blood culture contamination
title_short Patient-specific risk factors contributing to blood culture contamination
title_sort patient-specific risk factors contributing to blood culture contamination
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9614848/
https://www.ncbi.nlm.nih.gov/pubmed/36310794
http://dx.doi.org/10.1017/ash.2022.22
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