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Acute kidney injury risk-based screening in pediatric inpatients: A pragmatic randomized trial
BACKGROUND: Pediatric acute kidney injury (AKI) is common and associated with increased morbidity, mortality, and length of stay. We performed a pragmatic randomized trial testing the hypothesis that AKI risk alerts increase AKI screening. METHODS: All intensive care and ward admissions of children...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6962531/ https://www.ncbi.nlm.nih.gov/pubmed/31454829 http://dx.doi.org/10.1038/s41390-019-0550-1 |
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author | Van Driest, Sara L. Wang, Li McLemore, Michael F. Bridges, Brian C. Fleming, Geoffrey M. McGregor, Tracy L. Jones, Deborah P. Shirey-Rice, Jana Gatto, Cheryl L. Gay, James C. Byrne, Daniel W. Weitkamp, Asli Roden, Dan M. Bernard, Gordon |
author_facet | Van Driest, Sara L. Wang, Li McLemore, Michael F. Bridges, Brian C. Fleming, Geoffrey M. McGregor, Tracy L. Jones, Deborah P. Shirey-Rice, Jana Gatto, Cheryl L. Gay, James C. Byrne, Daniel W. Weitkamp, Asli Roden, Dan M. Bernard, Gordon |
author_sort | Van Driest, Sara L. |
collection | PubMed |
description | BACKGROUND: Pediatric acute kidney injury (AKI) is common and associated with increased morbidity, mortality, and length of stay. We performed a pragmatic randomized trial testing the hypothesis that AKI risk alerts increase AKI screening. METHODS: All intensive care and ward admissions of children aged 28 days through 21 years without chronic kidney disease from 12/6/2016 to 11/1/2017 were included. The intervention alert displayed if calculated AKI risk >50% and no serum creatinine (SCr) was ordered within 24 hours. The primary outcome was SCr testing within 48 hours of AKI risk >50%. RESULTS: Among intensive care admissions, 973/1,909 (51%) were randomized to the intervention. Among those at risk, more SCr tests were ordered for the intervention group than for controls (418/606, 69% vs. 361/597, 60%, p=0.002). AKI incidence and severity were the same in intervention and control groups. Among ward admissions, 5,492/10,997 (50%) were randomized to the intervention, and there were no differences between groups in SCr testing, AKI incidence, or severity of AKI. CONCLUSIONS: Alerts based on real-time prediction of AKI risk increased screening rates in intensive care but not pediatric ward settings. Pragmatic clinical trials provide the opportunity to assess clinical decision support and potentially eliminate ineffective alerts. |
format | Online Article Text |
id | pubmed-6962531 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
record_format | MEDLINE/PubMed |
spelling | pubmed-69625312020-02-27 Acute kidney injury risk-based screening in pediatric inpatients: A pragmatic randomized trial Van Driest, Sara L. Wang, Li McLemore, Michael F. Bridges, Brian C. Fleming, Geoffrey M. McGregor, Tracy L. Jones, Deborah P. Shirey-Rice, Jana Gatto, Cheryl L. Gay, James C. Byrne, Daniel W. Weitkamp, Asli Roden, Dan M. Bernard, Gordon Pediatr Res Article BACKGROUND: Pediatric acute kidney injury (AKI) is common and associated with increased morbidity, mortality, and length of stay. We performed a pragmatic randomized trial testing the hypothesis that AKI risk alerts increase AKI screening. METHODS: All intensive care and ward admissions of children aged 28 days through 21 years without chronic kidney disease from 12/6/2016 to 11/1/2017 were included. The intervention alert displayed if calculated AKI risk >50% and no serum creatinine (SCr) was ordered within 24 hours. The primary outcome was SCr testing within 48 hours of AKI risk >50%. RESULTS: Among intensive care admissions, 973/1,909 (51%) were randomized to the intervention. Among those at risk, more SCr tests were ordered for the intervention group than for controls (418/606, 69% vs. 361/597, 60%, p=0.002). AKI incidence and severity were the same in intervention and control groups. Among ward admissions, 5,492/10,997 (50%) were randomized to the intervention, and there were no differences between groups in SCr testing, AKI incidence, or severity of AKI. CONCLUSIONS: Alerts based on real-time prediction of AKI risk increased screening rates in intensive care but not pediatric ward settings. Pragmatic clinical trials provide the opportunity to assess clinical decision support and potentially eliminate ineffective alerts. 2019-08-27 2020-01 /pmc/articles/PMC6962531/ /pubmed/31454829 http://dx.doi.org/10.1038/s41390-019-0550-1 Text en http://www.nature.com/authors/editorial_policies/license.html#terms Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Van Driest, Sara L. Wang, Li McLemore, Michael F. Bridges, Brian C. Fleming, Geoffrey M. McGregor, Tracy L. Jones, Deborah P. Shirey-Rice, Jana Gatto, Cheryl L. Gay, James C. Byrne, Daniel W. Weitkamp, Asli Roden, Dan M. Bernard, Gordon Acute kidney injury risk-based screening in pediatric inpatients: A pragmatic randomized trial |
title | Acute kidney injury risk-based screening in pediatric inpatients: A pragmatic randomized trial |
title_full | Acute kidney injury risk-based screening in pediatric inpatients: A pragmatic randomized trial |
title_fullStr | Acute kidney injury risk-based screening in pediatric inpatients: A pragmatic randomized trial |
title_full_unstemmed | Acute kidney injury risk-based screening in pediatric inpatients: A pragmatic randomized trial |
title_short | Acute kidney injury risk-based screening in pediatric inpatients: A pragmatic randomized trial |
title_sort | acute kidney injury risk-based screening in pediatric inpatients: a pragmatic randomized trial |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6962531/ https://www.ncbi.nlm.nih.gov/pubmed/31454829 http://dx.doi.org/10.1038/s41390-019-0550-1 |
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