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Case–case–control study of risk factors for carbapenem-resistant Enterobacterales infections among hospitalized patients

OBJECTIVE: To identify important risk factors for carbapenem-resistant Enterobacterales (CRE) infections among hospitalized patients. DESIGN: We utilized a case–case–control design that compared patients with CRE infections to patients with carbapenem-susceptible Enterobacterales (CSE) infections an...

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Autores principales: Stuever, David M., Ferketich, Amy K., Lee, Jiyoung, Stevenson, Kurt B., Wittum, Thomas E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cambridge University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9726559/
https://www.ncbi.nlm.nih.gov/pubmed/36483348
http://dx.doi.org/10.1017/ash.2022.244
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author Stuever, David M.
Ferketich, Amy K.
Lee, Jiyoung
Stevenson, Kurt B.
Wittum, Thomas E.
author_facet Stuever, David M.
Ferketich, Amy K.
Lee, Jiyoung
Stevenson, Kurt B.
Wittum, Thomas E.
author_sort Stuever, David M.
collection PubMed
description OBJECTIVE: To identify important risk factors for carbapenem-resistant Enterobacterales (CRE) infections among hospitalized patients. DESIGN: We utilized a case–case–control design that compared patients with CRE infections to patients with carbapenem-susceptible Enterobacterales (CSE) infections and randomly selected controls during the period from January 2011 through December 2016. SETTING: The study population was selected from patients at a large metropolitan tertiary-care and instructional medical center. PATIENTS: Cases of CRE were defined as initial admission of adults diagnosed with a bacterial infection of an Enterobacterales species resistant clinically or through sensitivity testing to carbapenems 48 hours or more after admission. Cases of CSE were selected from the same patient population as the CRE cases within a 30-day window for admission, with diagnostic pathogens identified as susceptible to carbapenems. Controls were defined as adult patients admitted to any service within a 30-day window from a CRE case for >48 hours who did not meet either of the above case definitions during that admission. RESULTS: Antibiotic exposure within 90 days prior to admission and length of hospital stay were both associated with increased odds of CRE and CSE infections compared to controls. Patients with CRE infections had >18 times greater odds of prior antibiotic exposure compared to patients with CSE infections. CONCLUSIONS: Antibiotic exposure and increased length of hospital stay may result in increased patient risk of developing an infection resistant to carbapenems and other β-lactams.
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spelling pubmed-97265592022-12-07 Case–case–control study of risk factors for carbapenem-resistant Enterobacterales infections among hospitalized patients Stuever, David M. Ferketich, Amy K. Lee, Jiyoung Stevenson, Kurt B. Wittum, Thomas E. Antimicrob Steward Healthc Epidemiol Original Article OBJECTIVE: To identify important risk factors for carbapenem-resistant Enterobacterales (CRE) infections among hospitalized patients. DESIGN: We utilized a case–case–control design that compared patients with CRE infections to patients with carbapenem-susceptible Enterobacterales (CSE) infections and randomly selected controls during the period from January 2011 through December 2016. SETTING: The study population was selected from patients at a large metropolitan tertiary-care and instructional medical center. PATIENTS: Cases of CRE were defined as initial admission of adults diagnosed with a bacterial infection of an Enterobacterales species resistant clinically or through sensitivity testing to carbapenems 48 hours or more after admission. Cases of CSE were selected from the same patient population as the CRE cases within a 30-day window for admission, with diagnostic pathogens identified as susceptible to carbapenems. Controls were defined as adult patients admitted to any service within a 30-day window from a CRE case for >48 hours who did not meet either of the above case definitions during that admission. RESULTS: Antibiotic exposure within 90 days prior to admission and length of hospital stay were both associated with increased odds of CRE and CSE infections compared to controls. Patients with CRE infections had >18 times greater odds of prior antibiotic exposure compared to patients with CSE infections. CONCLUSIONS: Antibiotic exposure and increased length of hospital stay may result in increased patient risk of developing an infection resistant to carbapenems and other β-lactams. Cambridge University Press 2022-07-14 /pmc/articles/PMC9726559/ /pubmed/36483348 http://dx.doi.org/10.1017/ash.2022.244 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
Stuever, David M.
Ferketich, Amy K.
Lee, Jiyoung
Stevenson, Kurt B.
Wittum, Thomas E.
Case–case–control study of risk factors for carbapenem-resistant Enterobacterales infections among hospitalized patients
title Case–case–control study of risk factors for carbapenem-resistant Enterobacterales infections among hospitalized patients
title_full Case–case–control study of risk factors for carbapenem-resistant Enterobacterales infections among hospitalized patients
title_fullStr Case–case–control study of risk factors for carbapenem-resistant Enterobacterales infections among hospitalized patients
title_full_unstemmed Case–case–control study of risk factors for carbapenem-resistant Enterobacterales infections among hospitalized patients
title_short Case–case–control study of risk factors for carbapenem-resistant Enterobacterales infections among hospitalized patients
title_sort case–case–control study of risk factors for carbapenem-resistant enterobacterales infections among hospitalized patients
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9726559/
https://www.ncbi.nlm.nih.gov/pubmed/36483348
http://dx.doi.org/10.1017/ash.2022.244
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