Trends and racial differences in hypoxic ischemic encephalopathy-related mortality in newborns in the United States, 2007–2022
BackgroundHypoxic ischemic encephalopathy (HIE) is a significant cause of morbidity and mortality. However, the changes in HIE-related mortality and its associated racial differences, if any, have not been extensively studied. We examined the population-based temporal trends and any racial differences in the HIE-related infant mortality rate (HIE-IMR) in the United States from 2007 through 2022.MethodsThis was a retrospective cross-sectional analysis of linked birth and infant death records data from the CDC WONDER from 2007-2022. We evaluated all infants born at ≥35 weeks gestational age (GA) who died within the first year of life with HIE (ICD-10 codes P91.6 and P21) as the underlying cause of death. The exposure was the year of death, and the outcomes were the changes in overall HIE-IMR and then stratified by race. HIE-IMR was calculated as per 100,000 live births. Linear regression was used for trend analysis.ResultsAmong 59,117,761 live births, 3998 infants with GA ≥ 35 weeks died from HIE (6.7 per 100,000). The overall HIE-IMR increased significantly from 5.2 to 9.6 per 100,000 (<i>p</i> < .001). The rate increased significantly in White (5.3 to 7.2; <i>p</i> < .001) and Black (5.2 to 8.1; <i>p</i> = .005) infants. The overall HIE-IMR was significantly higher in Black infants (7.3) than in White infants (7.2) [<i>p</i> = .02].ConclusionThe HIE-IMR rate increased significantly, and the rate was higher in Black than in White infants. The drivers behind these changes require further examination in future studies.
Authors
- Fredrick Dapaah‐Siakwan (ORCID: https://orcid.org/0000-0002-0563-0437)
- Henry Pulido
Institutions
- Children's Hospital Central California (US)
Publication Details
- Journal
- Journal of Neonatal-Perinatal Medicine
- Published
- 2025-03-04
- DOI
- https://doi.org/10.1177/19345798251325496
- Primary Topic
- Neonatal and fetal brain pathology
- Type
- article
- Field-Weighted Citation Impact
- 0.00