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2461. Carbapenem-resistant Enterobacterales reported to the National Healthcare Safety Network Multidrug-Resistant Organism & Clostridioides difficile Infection Module, January 2018 to July 2022

BACKGROUND: To describe the COVID-19 pandemic’s impact on the spread of multidrug-resistant organisms, we compared pre-pandemic and pandemic laboratory-identified carbapenem-resistant Enterobacterales (CRE) events reported to the National Healthcare Safety Network (NHSN). [Figure: see text] METHODS:...

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Autores principales: Cincotta, Samuel E, Octaria, Rany, Maroya, Walters
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10678992/
http://dx.doi.org/10.1093/ofid/ofad500.2079
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author Cincotta, Samuel E
Octaria, Rany
Maroya, Walters
author_facet Cincotta, Samuel E
Octaria, Rany
Maroya, Walters
author_sort Cincotta, Samuel E
collection PubMed
description BACKGROUND: To describe the COVID-19 pandemic’s impact on the spread of multidrug-resistant organisms, we compared pre-pandemic and pandemic laboratory-identified carbapenem-resistant Enterobacterales (CRE) events reported to the National Healthcare Safety Network (NHSN). [Figure: see text] METHODS: A CRE event was a patient’s first Escherichia coli, Klebsiella aerogenes, K. oxytoca, K. pneumoniae, or Enterobacter spp. collected on an inpatient unit in a 14-day period and resistant to ≥ 1 of the following: imipenem, meropenem, doripenem, ertapenem, meropenem/vaborbactam (as of 2021), or imipenem/relebactam (as of 2021). We included events from acute care general hospitals (ACH) performing and continuously reporting facility-wide inpatient CRE surveillance for the same specimen sources in each month, from 2018 through 2019 (Period 1) and July 2020 to July 2022 (Period 2); the first half of 2020 was excluded due to initial pandemic disruptions in reporting to the NHSN. We compared patient demographics and epidemiological changes of events between the periods using Pearson’s χ(2) or Wilcoxon rank-sum test as appropriate. RESULTS: Overall, 523 ACHs in 28 states met inclusion criteria. During Period 1, there were 5499 events from 4725 patients in 22 states compared to 5483 events from 4690 patients in 22 states in Period 2; 21 states were consistent in both periods. More facilities had ≥ 1 event in Period 1 compared to Period 2 (56% versus 51%; p< 0.001). Four public health jurisdictions with mandates to report CRE to the NHSN accounted for 86.7% of Period 1 events and 86.0% of Period 2 events. Between Periods 1 and 2, the proportion of events that were hospital onset (on or after admission day four) (54.3% to 62.6%, p< 0.001), from respiratory sources (26.3% to 31.5%, p< 0.001), and bloodstream infections (10.4% to 12.6%, p< 0.001) increased, and the median patient age decreased (66.5 to 64.6, p< 0.001) (Table 1). CONCLUSION: Despite a consistent number of events in ACHs during the two periods, we observed a shift toward events that were hospital onset, associated with invasive infection, and occurring in younger people. The timely availability of robust laboratory-based surveillance is an important public health resource for understanding potential epidemiological changes in antimicrobial resistant threats. DISCLOSURES: All Authors: No reported disclosures
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spelling pubmed-106789922023-11-27 2461. Carbapenem-resistant Enterobacterales reported to the National Healthcare Safety Network Multidrug-Resistant Organism & Clostridioides difficile Infection Module, January 2018 to July 2022 Cincotta, Samuel E Octaria, Rany Maroya, Walters Open Forum Infect Dis Abstract BACKGROUND: To describe the COVID-19 pandemic’s impact on the spread of multidrug-resistant organisms, we compared pre-pandemic and pandemic laboratory-identified carbapenem-resistant Enterobacterales (CRE) events reported to the National Healthcare Safety Network (NHSN). [Figure: see text] METHODS: A CRE event was a patient’s first Escherichia coli, Klebsiella aerogenes, K. oxytoca, K. pneumoniae, or Enterobacter spp. collected on an inpatient unit in a 14-day period and resistant to ≥ 1 of the following: imipenem, meropenem, doripenem, ertapenem, meropenem/vaborbactam (as of 2021), or imipenem/relebactam (as of 2021). We included events from acute care general hospitals (ACH) performing and continuously reporting facility-wide inpatient CRE surveillance for the same specimen sources in each month, from 2018 through 2019 (Period 1) and July 2020 to July 2022 (Period 2); the first half of 2020 was excluded due to initial pandemic disruptions in reporting to the NHSN. We compared patient demographics and epidemiological changes of events between the periods using Pearson’s χ(2) or Wilcoxon rank-sum test as appropriate. RESULTS: Overall, 523 ACHs in 28 states met inclusion criteria. During Period 1, there were 5499 events from 4725 patients in 22 states compared to 5483 events from 4690 patients in 22 states in Period 2; 21 states were consistent in both periods. More facilities had ≥ 1 event in Period 1 compared to Period 2 (56% versus 51%; p< 0.001). Four public health jurisdictions with mandates to report CRE to the NHSN accounted for 86.7% of Period 1 events and 86.0% of Period 2 events. Between Periods 1 and 2, the proportion of events that were hospital onset (on or after admission day four) (54.3% to 62.6%, p< 0.001), from respiratory sources (26.3% to 31.5%, p< 0.001), and bloodstream infections (10.4% to 12.6%, p< 0.001) increased, and the median patient age decreased (66.5 to 64.6, p< 0.001) (Table 1). CONCLUSION: Despite a consistent number of events in ACHs during the two periods, we observed a shift toward events that were hospital onset, associated with invasive infection, and occurring in younger people. The timely availability of robust laboratory-based surveillance is an important public health resource for understanding potential epidemiological changes in antimicrobial resistant threats. DISCLOSURES: All Authors: No reported disclosures Oxford University Press 2023-11-27 /pmc/articles/PMC10678992/ http://dx.doi.org/10.1093/ofid/ofad500.2079 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
Cincotta, Samuel E
Octaria, Rany
Maroya, Walters
2461. Carbapenem-resistant Enterobacterales reported to the National Healthcare Safety Network Multidrug-Resistant Organism & Clostridioides difficile Infection Module, January 2018 to July 2022
title 2461. Carbapenem-resistant Enterobacterales reported to the National Healthcare Safety Network Multidrug-Resistant Organism & Clostridioides difficile Infection Module, January 2018 to July 2022
title_full 2461. Carbapenem-resistant Enterobacterales reported to the National Healthcare Safety Network Multidrug-Resistant Organism & Clostridioides difficile Infection Module, January 2018 to July 2022
title_fullStr 2461. Carbapenem-resistant Enterobacterales reported to the National Healthcare Safety Network Multidrug-Resistant Organism & Clostridioides difficile Infection Module, January 2018 to July 2022
title_full_unstemmed 2461. Carbapenem-resistant Enterobacterales reported to the National Healthcare Safety Network Multidrug-Resistant Organism & Clostridioides difficile Infection Module, January 2018 to July 2022
title_short 2461. Carbapenem-resistant Enterobacterales reported to the National Healthcare Safety Network Multidrug-Resistant Organism & Clostridioides difficile Infection Module, January 2018 to July 2022
title_sort 2461. carbapenem-resistant enterobacterales reported to the national healthcare safety network multidrug-resistant organism & clostridioides difficile infection module, january 2018 to july 2022
topic Abstract
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10678992/
http://dx.doi.org/10.1093/ofid/ofad500.2079
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