Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2019
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
_version_ 1783488178312708096
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
work_keys_str_mv AT vandriestsaral acutekidneyinjuryriskbasedscreeninginpediatricinpatientsapragmaticrandomizedtrial
AT wangli acutekidneyinjuryriskbasedscreeninginpediatricinpatientsapragmaticrandomizedtrial
AT mclemoremichaelf acutekidneyinjuryriskbasedscreeninginpediatricinpatientsapragmaticrandomizedtrial
AT bridgesbrianc acutekidneyinjuryriskbasedscreeninginpediatricinpatientsapragmaticrandomizedtrial
AT fleminggeoffreym acutekidneyinjuryriskbasedscreeninginpediatricinpatientsapragmaticrandomizedtrial
AT mcgregortracyl acutekidneyinjuryriskbasedscreeninginpediatricinpatientsapragmaticrandomizedtrial
AT jonesdeborahp acutekidneyinjuryriskbasedscreeninginpediatricinpatientsapragmaticrandomizedtrial
AT shireyricejana acutekidneyinjuryriskbasedscreeninginpediatricinpatientsapragmaticrandomizedtrial
AT gattocheryll acutekidneyinjuryriskbasedscreeninginpediatricinpatientsapragmaticrandomizedtrial
AT gayjamesc acutekidneyinjuryriskbasedscreeninginpediatricinpatientsapragmaticrandomizedtrial
AT byrnedanielw acutekidneyinjuryriskbasedscreeninginpediatricinpatientsapragmaticrandomizedtrial
AT weitkampasli acutekidneyinjuryriskbasedscreeninginpediatricinpatientsapragmaticrandomizedtrial
AT rodendanm acutekidneyinjuryriskbasedscreeninginpediatricinpatientsapragmaticrandomizedtrial
AT bernardgordon acutekidneyinjuryriskbasedscreeninginpediatricinpatientsapragmaticrandomizedtrial