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1015. A multicenter evaluation of antimicrobial utilization in hospitalized bone marrow transplant (BMT) and T-cell therapy (CAR-T) patients, and the impact on rates of C. difficile infection (CDI)

BACKGROUND: Benchmarking antimicrobial utilization through the National Healthcare Safety Network (NHSN) will be a CMS requirement in 2024. NHSN benchmarking is available for some hospitalized populations, but there are currently no benchmarking capabilities for BMT units. Additionally, there are no...

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Autores principales: Nagel, Jerod, Boeser, Kimberly D, Hale, Cory, Harris, Alyssa, Jain, Rupali, Postelnick, Mike, Spivak, Emily S
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10678188/
http://dx.doi.org/10.1093/ofid/ofad500.046
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author Nagel, Jerod
Boeser, Kimberly D
Hale, Cory
Harris, Alyssa
Jain, Rupali
Postelnick, Mike
Spivak, Emily S
author_facet Nagel, Jerod
Boeser, Kimberly D
Hale, Cory
Harris, Alyssa
Jain, Rupali
Postelnick, Mike
Spivak, Emily S
author_sort Nagel, Jerod
collection PubMed
description BACKGROUND: Benchmarking antimicrobial utilization through the National Healthcare Safety Network (NHSN) will be a CMS requirement in 2024. NHSN benchmarking is available for some hospitalized populations, but there are currently no benchmarking capabilities for BMT units. Additionally, there are no published manuscripts describing antimicrobial utilization in BMT hospitals. Intra-Hospital BMT Antimicrobial Utilization [Figure: see text] Data from the Vizient Clinical Data Base used with permission of Vizient, Inc. All rights reserved. METHODS: This retrospective multicenter study was conducted by the Vizient Pharmacy Network AMS Committee. Antimicrobial utilization was evaluated for Vizient-member hospitals that treat at least 50 BMT patients per year. Vizient Clinical Database was used to identify patients via ICD10 codes for allogeneic transplant, autologous stem cell transplant and CAR-T therapy. Total antimicrobial days of therapy (DOTs) per 1,000 patient days was evaluated across all hospitals for each type of transplant, and for 9 different groups of antimicrobials (anti-pseudomonal beta-lactams, carbapenems, MDRO gram-negatives, fluoroquinolones, MRSA-active agents, antifungals, CMV-active agents, high-risk C. difficile agents, and C. difficile treatments). ANOVA was used to compare antimicrobial utilization across hospitals and across antimicrobial types. RESULTS: A total of 90 hospitals and 63,379 patient encounters were included in the analysis from 2018-2021. The median total antimicrobial utilization for allogeneic, autologous, and CAR-T patients were 2,562, 2,083, and 2,187 DOTs per 1,000 patient days, respectively. Figure 1 describes the variability in intra-hospital prescribing for 9 antimicrobial categories. Hospitals with higher antimicrobial utilization rates in allogenic transplant patients were associated with a higher incidence of CDI in this population (p=0.0368). CONCLUSION: Significant variation in intra-hospital antimicrobial utilization exists for allogeneic transplant, autologous stem cell transplant, and CAR-T patients; and across 9 different categories of antimicrobials! Increasing rates of antimicrobial utilization were associated with increases in C. difficile infections in allogeneic transplants. Benchmarking antimicrobial utilization in BMT patients may help improve systematic approaches to minimize unnecessary antimicrobial exposure. DISCLOSURES: All Authors: No reported disclosures
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spelling pubmed-106781882023-11-27 1015. A multicenter evaluation of antimicrobial utilization in hospitalized bone marrow transplant (BMT) and T-cell therapy (CAR-T) patients, and the impact on rates of C. difficile infection (CDI) Nagel, Jerod Boeser, Kimberly D Hale, Cory Harris, Alyssa Jain, Rupali Postelnick, Mike Spivak, Emily S Open Forum Infect Dis Abstract BACKGROUND: Benchmarking antimicrobial utilization through the National Healthcare Safety Network (NHSN) will be a CMS requirement in 2024. NHSN benchmarking is available for some hospitalized populations, but there are currently no benchmarking capabilities for BMT units. Additionally, there are no published manuscripts describing antimicrobial utilization in BMT hospitals. Intra-Hospital BMT Antimicrobial Utilization [Figure: see text] Data from the Vizient Clinical Data Base used with permission of Vizient, Inc. All rights reserved. METHODS: This retrospective multicenter study was conducted by the Vizient Pharmacy Network AMS Committee. Antimicrobial utilization was evaluated for Vizient-member hospitals that treat at least 50 BMT patients per year. Vizient Clinical Database was used to identify patients via ICD10 codes for allogeneic transplant, autologous stem cell transplant and CAR-T therapy. Total antimicrobial days of therapy (DOTs) per 1,000 patient days was evaluated across all hospitals for each type of transplant, and for 9 different groups of antimicrobials (anti-pseudomonal beta-lactams, carbapenems, MDRO gram-negatives, fluoroquinolones, MRSA-active agents, antifungals, CMV-active agents, high-risk C. difficile agents, and C. difficile treatments). ANOVA was used to compare antimicrobial utilization across hospitals and across antimicrobial types. RESULTS: A total of 90 hospitals and 63,379 patient encounters were included in the analysis from 2018-2021. The median total antimicrobial utilization for allogeneic, autologous, and CAR-T patients were 2,562, 2,083, and 2,187 DOTs per 1,000 patient days, respectively. Figure 1 describes the variability in intra-hospital prescribing for 9 antimicrobial categories. Hospitals with higher antimicrobial utilization rates in allogenic transplant patients were associated with a higher incidence of CDI in this population (p=0.0368). CONCLUSION: Significant variation in intra-hospital antimicrobial utilization exists for allogeneic transplant, autologous stem cell transplant, and CAR-T patients; and across 9 different categories of antimicrobials! Increasing rates of antimicrobial utilization were associated with increases in C. difficile infections in allogeneic transplants. Benchmarking antimicrobial utilization in BMT patients may help improve systematic approaches to minimize unnecessary antimicrobial exposure. DISCLOSURES: All Authors: No reported disclosures Oxford University Press 2023-11-27 /pmc/articles/PMC10678188/ http://dx.doi.org/10.1093/ofid/ofad500.046 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
Nagel, Jerod
Boeser, Kimberly D
Hale, Cory
Harris, Alyssa
Jain, Rupali
Postelnick, Mike
Spivak, Emily S
1015. A multicenter evaluation of antimicrobial utilization in hospitalized bone marrow transplant (BMT) and T-cell therapy (CAR-T) patients, and the impact on rates of C. difficile infection (CDI)
title 1015. A multicenter evaluation of antimicrobial utilization in hospitalized bone marrow transplant (BMT) and T-cell therapy (CAR-T) patients, and the impact on rates of C. difficile infection (CDI)
title_full 1015. A multicenter evaluation of antimicrobial utilization in hospitalized bone marrow transplant (BMT) and T-cell therapy (CAR-T) patients, and the impact on rates of C. difficile infection (CDI)
title_fullStr 1015. A multicenter evaluation of antimicrobial utilization in hospitalized bone marrow transplant (BMT) and T-cell therapy (CAR-T) patients, and the impact on rates of C. difficile infection (CDI)
title_full_unstemmed 1015. A multicenter evaluation of antimicrobial utilization in hospitalized bone marrow transplant (BMT) and T-cell therapy (CAR-T) patients, and the impact on rates of C. difficile infection (CDI)
title_short 1015. A multicenter evaluation of antimicrobial utilization in hospitalized bone marrow transplant (BMT) and T-cell therapy (CAR-T) patients, and the impact on rates of C. difficile infection (CDI)
title_sort 1015. a multicenter evaluation of antimicrobial utilization in hospitalized bone marrow transplant (bmt) and t-cell therapy (car-t) patients, and the impact on rates of c. difficile infection (cdi)
topic Abstract
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10678188/
http://dx.doi.org/10.1093/ofid/ofad500.046
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