Neonatal Hypoxic-Ischemic Encephalopathy Spectrum: Severity-Stratified Analysis of Neuroimaging Modalities and Association with Neurodevelopmental Outcomes

医学 缺氧缺血性脑病 磁共振成像 模式 神经影像学 脑病 联想(心理学) 儿科 重症监护医学 神经科学 放射科 心理治疗师 心理学 社会科学 精神科 社会学 生物
作者
Mehmet Nevzat Çizmeci,Diane Wilson,Maya Singhal,Amr El Shahed,Brian T. Kalish,Emily Tam,Vann Chau,Linh Ly,Vanna Kazazian,Cecil D. Hahn,Helen M. Branson,Steven P. Miller
出处
期刊:The Journal of Pediatrics [Elsevier BV]
卷期号:266: 113866-113866 被引量:4
标识
DOI:10.1016/j.jpeds.2023.113866
摘要

Objective

To compare hypoxic-ischemic injury on early cranial ultrasonography (cUS) and post-rewarming brain magnetic resonance imaging (MRI) in newborn infants with hypoxic-ischemic encephalopathy (HIE) and to correlate that neuroimaging with neurodevelopmental outcomes.

Study design

This was a retrospective cohort study of infants with mild, moderate, and severe HIE treated with therapeutic hypothermia and evaluated with early cUS and postrewarming MRI. Validated scoring systems were used to compare the severity of brain injury on cUS and MRI. Neurodevelopmental outcomes were assessed at 18 months of age.

Results

Among the 149 included infants, abnormal white matter (WM) and deep gray matter (DGM) hyperechogenicity on cUS in the first 48 hours after birth were more common in the severe HIE group than the mild HIE group (81% vs 39% and 50% vs 0%, respectively; P < .001). In infants with a normal cUS, 95% had normal or mildly abnormal brain MRIs. In infants with severely abnormal cUS, none had normal and 83% had severely abnormal brain MRIs. Total abnormality scores on cUS were higher in neonates with near-total brain injury on MRI than in neonates with normal MRI or WM-predominant injury pattern (adjusted P < .001 for both). In the multivariable model, a severely abnormal MRI was the only independent risk factor for adverse outcomes (OR: 19.9, 95% CI: 4.0-98.1; P < .001).

Conclusion

The present study shows the complementary utility of cUS in the first 48 hours after birth as a predictive tool for the presence of hypoxic-ischemic injury on brain MRI.
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