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An Electronic Algorithm to Identify Vancomycin-Associated Acute Kidney Injury
BACKGROUND: The burden of vancomycin-associated acute kidney injury (V-AKI) is unclear because it is not systematically monitored. The objective of this study was to develop and validate an electronic algorithm to identify cases of V-AKI and to determine its incidence. METHODS: Adults and children a...
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/PMC10296058/ https://www.ncbi.nlm.nih.gov/pubmed/37383251 http://dx.doi.org/10.1093/ofid/ofad264 |
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author | Cherian, Jerald P Jones, George F Bachina, Preetham Helsel, Taylor Virk, Zunaira Lee, Jae Hyoung Fiawoo, Suiyini Salinas, Alejandra Dzintars, Kate O'Shaughnessy, Elizabeth Gopinath, Ramya Tamma, Pranita D Cosgrove, Sara E Klein, Eili Y |
author_facet | Cherian, Jerald P Jones, George F Bachina, Preetham Helsel, Taylor Virk, Zunaira Lee, Jae Hyoung Fiawoo, Suiyini Salinas, Alejandra Dzintars, Kate O'Shaughnessy, Elizabeth Gopinath, Ramya Tamma, Pranita D Cosgrove, Sara E Klein, Eili Y |
author_sort | Cherian, Jerald P |
collection | PubMed |
description | BACKGROUND: The burden of vancomycin-associated acute kidney injury (V-AKI) is unclear because it is not systematically monitored. The objective of this study was to develop and validate an electronic algorithm to identify cases of V-AKI and to determine its incidence. METHODS: Adults and children admitted to 1 of 5 health system hospitals from January 2018 to December 2019 who received at least 1 dose of intravenous (IV) vancomycin were included. A subset of charts was reviewed using a V-AKI assessment framework to classify cases as unlikely, possible, or probable events. Based on review, an electronic algorithm was developed and then validated using another subset of charts. Percentage agreement and kappa coefficients were calculated. Sensitivity and specificity were determined at various cutoffs, using chart review as the reference standard. For courses ≥48 hours, the incidence of possible or probable V-AKI events was assessed. RESULTS: The algorithm was developed using 494 cases and validated using 200 cases. The percentage agreement between the electronic algorithm and chart review was 92.5% and the weighted kappa was 0.95. The electronic algorithm was 89.7% sensitive and 98.2% specific in detecting possible or probable V-AKI events. For the 11 073 courses of ≥48 hours of vancomycin among 8963 patients, the incidence of possible or probable V-AKI events was 14.0%; the V-AKI incidence rate was 22.8 per 1000 days of IV vancomycin therapy. CONCLUSIONS: An electronic algorithm demonstrated substantial agreement with chart review and had excellent sensitivity and specificity in detecting possible or probable V-AKI events. The electronic algorithm may be useful for informing future interventions to reduce V-AKI. |
format | Online Article Text |
id | pubmed-10296058 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-102960582023-06-28 An Electronic Algorithm to Identify Vancomycin-Associated Acute Kidney Injury Cherian, Jerald P Jones, George F Bachina, Preetham Helsel, Taylor Virk, Zunaira Lee, Jae Hyoung Fiawoo, Suiyini Salinas, Alejandra Dzintars, Kate O'Shaughnessy, Elizabeth Gopinath, Ramya Tamma, Pranita D Cosgrove, Sara E Klein, Eili Y Open Forum Infect Dis Major Article BACKGROUND: The burden of vancomycin-associated acute kidney injury (V-AKI) is unclear because it is not systematically monitored. The objective of this study was to develop and validate an electronic algorithm to identify cases of V-AKI and to determine its incidence. METHODS: Adults and children admitted to 1 of 5 health system hospitals from January 2018 to December 2019 who received at least 1 dose of intravenous (IV) vancomycin were included. A subset of charts was reviewed using a V-AKI assessment framework to classify cases as unlikely, possible, or probable events. Based on review, an electronic algorithm was developed and then validated using another subset of charts. Percentage agreement and kappa coefficients were calculated. Sensitivity and specificity were determined at various cutoffs, using chart review as the reference standard. For courses ≥48 hours, the incidence of possible or probable V-AKI events was assessed. RESULTS: The algorithm was developed using 494 cases and validated using 200 cases. The percentage agreement between the electronic algorithm and chart review was 92.5% and the weighted kappa was 0.95. The electronic algorithm was 89.7% sensitive and 98.2% specific in detecting possible or probable V-AKI events. For the 11 073 courses of ≥48 hours of vancomycin among 8963 patients, the incidence of possible or probable V-AKI events was 14.0%; the V-AKI incidence rate was 22.8 per 1000 days of IV vancomycin therapy. CONCLUSIONS: An electronic algorithm demonstrated substantial agreement with chart review and had excellent sensitivity and specificity in detecting possible or probable V-AKI events. The electronic algorithm may be useful for informing future interventions to reduce V-AKI. Oxford University Press 2023-05-16 /pmc/articles/PMC10296058/ /pubmed/37383251 http://dx.doi.org/10.1093/ofid/ofad264 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of Infectious Diseases Society of America. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (https://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Major Article Cherian, Jerald P Jones, George F Bachina, Preetham Helsel, Taylor Virk, Zunaira Lee, Jae Hyoung Fiawoo, Suiyini Salinas, Alejandra Dzintars, Kate O'Shaughnessy, Elizabeth Gopinath, Ramya Tamma, Pranita D Cosgrove, Sara E Klein, Eili Y An Electronic Algorithm to Identify Vancomycin-Associated Acute Kidney Injury |
title | An Electronic Algorithm to Identify Vancomycin-Associated Acute Kidney Injury |
title_full | An Electronic Algorithm to Identify Vancomycin-Associated Acute Kidney Injury |
title_fullStr | An Electronic Algorithm to Identify Vancomycin-Associated Acute Kidney Injury |
title_full_unstemmed | An Electronic Algorithm to Identify Vancomycin-Associated Acute Kidney Injury |
title_short | An Electronic Algorithm to Identify Vancomycin-Associated Acute Kidney Injury |
title_sort | electronic algorithm to identify vancomycin-associated acute kidney injury |
topic | Major Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10296058/ https://www.ncbi.nlm.nih.gov/pubmed/37383251 http://dx.doi.org/10.1093/ofid/ofad264 |
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