Abstract: TH-OR099
AKI in Neonates in the Modern Era: Preliminary Results from the Multinational AWAKEN 2.0 Cohort
Session Information
- Shaping Pediatric Kidney Disease: Developmental Insights, Stem Cell Systems, Novel Biomarkers, and More
October 22, 2026 | Location: Room 603, Convention Center
Abstract Time: 05:50 PM - 06:00 PM
Category: Pediatric Nephrology
- 1800 Pediatric Nephrology
Authors
- Starr, Michelle C., Indiana University School of Medicine, Indianapolis, Indiana, United States
- Kumar, Hanush, Indiana University School of Medicine, Indianapolis, Indiana, United States
- Baeta Baptista, Rute, Indiana University School of Medicine, Indianapolis, Indiana, United States
- Askenazi, David J., University of Alabama at Birmingham Health System, Birmingham, Alabama, United States
- Charlton, Jennifer R., University of Virginia School of Medicine, Charlottesville, Virginia, United States
- Forbes, Thomas A., Murdoch Children's Research Institute, Parkville, Victoria, Australia
- Harer, Matthew W., University of Wisconsin-Madison, Madison, Wisconsin, United States
- Sanderson, Keia, The University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, United States
- Slagle, Cara L., Indiana University School of Medicine, Indianapolis, Indiana, United States
- Selewski, David T., University of Arkansas for Medical Sciences, Little Rock, Arkansas, United States
Group or Team Name
- AWAKEN 2.0 Collaborative Study Group
Background
Neonatal acute kidney injury (AKI) is associated with increased mortality and prolonged neonatal intensive care unit (NICU) admission. Since the original AWAKEN study, AKI definitions and practices have evolved. We aimed to determine incidence and outcomes associated with neonatal AKI using the 2026 KDIGO criteria in a multinational cohort.
Methods
In this multicenter, multinational, retrospective cohort, neonates admitted to NICUs 1/1-3/31/19 were screened. Eligible neonates received intravenous fluids >48h. Exclusion criteria: admission ≥14d, congenital heart disease with surgery within 7d, lethal chromosomal anomalies, or death within 48h. AKI was defined according to the 2026 neonatal KDIGO criteria (increase in SCr ≥0.3mg/dL [26.5umol/L] within 48h, SCr ≥1.5x baseline within 7d, or urine output. AKI severity was staged using either creatinine or urine output. Multivariable models were used to evaluate associations between AKI and mortality and length of stay after adjustment for gestational age, birth weight, illness severity, and center.
Results
Of the 2,134 infants included in this preliminary analysis (27 of 106 enrolling sites, 8 countries), 1,972 had sufficient data to determine AKI status. Of those, 461 (23.4%) developed AKI. AKI incidence varied by gestational age: <29 weeks 40.9% (115/281); ≥29 to <36 weeks 15.6% (123/786); and ≥36 weeks 24.6% (223/907). Stage distribution: stage 1 AKI in 238 (12.1%), stage 2 in 112 (5.7%), and stage 3 in 111(5.6%) infants. Infants with AKI had higher mortality compared with those without AKI (53/461 [11.5%] vs 22/1511 [1.5%]; aOR 6.41, 95% CI 3.54–11.93; p<0.0001). AKI was independently associated with longer NICU stay (adjusted parameter estimate 19.3 days, 95% CI 10.82–27.85; p<0.0001). Additional analyses between AKI and outcomes, both short- and long-term are ongoing, with an anticipated sample size of >8,000 by Kidney Week.
Conclusion
AKI occurs in nearly one-quarter of critically ill neonates using contemporary neonatal-specific KDIGO criteria and is independently associated with mortality and prolonged hospitalization. These findings support the need for standardized AKI surveillance in neonatal intensive care.
Table 1. Clinical Outcomes by AKI Status
Funding
- NIDDK Support