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1209. Let’s take a time-out: Implementing a standardized process to assess the clinical use of vancomycin for pharmacists
BACKGROUND: Vancomycin is often started empirically for its reliability with gram-positive pathogens, particularly Methicillin Resistant Staph aureus (MRSA). Consequently, it is often over-prescribed. Antimicrobial stewardship programs (ASP) have used time-outs to ensure therapies are tailored to th...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10678660/ http://dx.doi.org/10.1093/ofid/ofad500.1049 |
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author | Oderinde, Jennifer Chiang, Anthony Juska, Alicia ADEYEMI, O L U W A D A M I L O L A A |
author_facet | Oderinde, Jennifer Chiang, Anthony Juska, Alicia ADEYEMI, O L U W A D A M I L O L A A |
author_sort | Oderinde, Jennifer |
collection | PubMed |
description | BACKGROUND: Vancomycin is often started empirically for its reliability with gram-positive pathogens, particularly Methicillin Resistant Staph aureus (MRSA). Consequently, it is often over-prescribed. Antimicrobial stewardship programs (ASP) have used time-outs to ensure therapies are tailored to the patient with proper indication and coverage. This study aims to evaluate the impact of a standardized vancomycin time-out to optimize utilization and safety. METHODS: This is a pre-/post-implementation study conducted at a community teaching hospital. The study was separated into a pre-implementation phase (July-September 2022), implementation/teaching phase (October 2022), and post-implementation phase (November 2022-February 2023). Study subjects included inpatient adults on vancomycin for longer than 48 hours. Patients who are immunocompromised, hospice, or on a vancomycin regimen prior to admission were excluded. Primary outcomes include (1) percent appropriate vancomycin continued after time-out, (2) percent inappropriate vancomycin discontinued during time-out, and (3) time to de-escalation. Additional outcomes include vancomycin days of therapy (DOT) per 1000 patient days, hospital length of stay, and acute kidney injury (AKI) incidence rate. This study looked at 182 patients in the retrospective arm and 214 patients in the prospective arm. Preliminary data was initially presented at the Illinois Pharmacy Residency Conference when only 195 total patients had been reviewed. RESULTS: There was a statistically significant difference seen in percent appropriate vancomycin continued after time-out, with 57% and 40.2% seen in the prospective and retrospective arm respectively. The percent inappropriate vancomycin discontinued during time-out was also statistically significant with 69.9% and 38.8% respectively. With a time-out, average days to discontinuation for continued inappropriate regimens, and overall vancomycin DOT were decreased. There was no significant difference seen in safety outcomes including AKI incidence rates. CONCLUSION: Pharmacy driven time-outs are useful for promoting antimicrobial stewardship and can contribute to decreased vancomycin use, DISCLOSURES: All Authors: No reported disclosures |
format | Online Article Text |
id | pubmed-10678660 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-106786602023-11-27 1209. Let’s take a time-out: Implementing a standardized process to assess the clinical use of vancomycin for pharmacists Oderinde, Jennifer Chiang, Anthony Juska, Alicia ADEYEMI, O L U W A D A M I L O L A A Open Forum Infect Dis Abstract BACKGROUND: Vancomycin is often started empirically for its reliability with gram-positive pathogens, particularly Methicillin Resistant Staph aureus (MRSA). Consequently, it is often over-prescribed. Antimicrobial stewardship programs (ASP) have used time-outs to ensure therapies are tailored to the patient with proper indication and coverage. This study aims to evaluate the impact of a standardized vancomycin time-out to optimize utilization and safety. METHODS: This is a pre-/post-implementation study conducted at a community teaching hospital. The study was separated into a pre-implementation phase (July-September 2022), implementation/teaching phase (October 2022), and post-implementation phase (November 2022-February 2023). Study subjects included inpatient adults on vancomycin for longer than 48 hours. Patients who are immunocompromised, hospice, or on a vancomycin regimen prior to admission were excluded. Primary outcomes include (1) percent appropriate vancomycin continued after time-out, (2) percent inappropriate vancomycin discontinued during time-out, and (3) time to de-escalation. Additional outcomes include vancomycin days of therapy (DOT) per 1000 patient days, hospital length of stay, and acute kidney injury (AKI) incidence rate. This study looked at 182 patients in the retrospective arm and 214 patients in the prospective arm. Preliminary data was initially presented at the Illinois Pharmacy Residency Conference when only 195 total patients had been reviewed. RESULTS: There was a statistically significant difference seen in percent appropriate vancomycin continued after time-out, with 57% and 40.2% seen in the prospective and retrospective arm respectively. The percent inappropriate vancomycin discontinued during time-out was also statistically significant with 69.9% and 38.8% respectively. With a time-out, average days to discontinuation for continued inappropriate regimens, and overall vancomycin DOT were decreased. There was no significant difference seen in safety outcomes including AKI incidence rates. CONCLUSION: Pharmacy driven time-outs are useful for promoting antimicrobial stewardship and can contribute to decreased vancomycin use, DISCLOSURES: All Authors: No reported disclosures Oxford University Press 2023-11-27 /pmc/articles/PMC10678660/ http://dx.doi.org/10.1093/ofid/ofad500.1049 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 Oderinde, Jennifer Chiang, Anthony Juska, Alicia ADEYEMI, O L U W A D A M I L O L A A 1209. Let’s take a time-out: Implementing a standardized process to assess the clinical use of vancomycin for pharmacists |
title | 1209. Let’s take a time-out: Implementing a standardized process to assess the clinical use of vancomycin for pharmacists |
title_full | 1209. Let’s take a time-out: Implementing a standardized process to assess the clinical use of vancomycin for pharmacists |
title_fullStr | 1209. Let’s take a time-out: Implementing a standardized process to assess the clinical use of vancomycin for pharmacists |
title_full_unstemmed | 1209. Let’s take a time-out: Implementing a standardized process to assess the clinical use of vancomycin for pharmacists |
title_short | 1209. Let’s take a time-out: Implementing a standardized process to assess the clinical use of vancomycin for pharmacists |
title_sort | 1209. let’s take a time-out: implementing a standardized process to assess the clinical use of vancomycin for pharmacists |
topic | Abstract |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10678660/ http://dx.doi.org/10.1093/ofid/ofad500.1049 |
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