4.6 Article

Acute kidney injury risk-based screening in pediatric inpatients: a pragmatic randomized trial

Journal

PEDIATRIC RESEARCH
Volume 87, Issue 1, Pages 118-124

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/s41390-019-0550-1

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Funding

  1. CTSA from the National Center for Advancing Translational Sciences (NCATS) [UL1 TR000445]
  2. Vanderbilt Institute for Clinical and Translational Research Learning Healthcare System Platform
  3. NIH/NCATS [UL1 TR000445, KL2 TR000446]
  4. Burroughs Wellcome Foundation
  5. Doris Duke Foundation
  6. NIH/National Institute of Child Health and Development [K23 HD000001]
  7. BWF [1015006]
  8. DDF [2017075]
  9. NIH/NICHD [K23 HD000001]

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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 was > 50% and no serum creatinine (SCr) was ordered within 24 h. The primary outcome was SCr testing within 48 h of AKI risk > 50%. RESULTS: Among intensive care admissions, 973/1909 (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, 5492/10997 (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.

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