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Assessment and Evaluation of the High Risk Neonate: The NICU Network Neurobehavioral Scale
Published on: August 25, 2014
Cumulative Hydrocortisone Exposure and Early Brain Volumetrics in Very Low Birth Weight Infants: Associations with
Min Soo Kim1, Moon-Yeon Oh1, Emi Tomita2
1Department of Pediatrics, Seoul St. Mary's Hospital, College of Medicine, The Catholic University of Korea, 222 Banpo-daero, Seocho-gu, Seoul 06591, Republic of Korea.
Insights
High doses of systemic hydrocortisone (HCS) in very low birth weight (VLBW) infants are linked to reduced brain volume and poorer neurodevelopmental outcomes. Careful HCS dose monitoring is crucial for VLBW infants to mitigate potential risks.
Area of Science:
- Neonatal Medicine
- Pediatric Neurology
- Developmental Pediatrics
Background:
- Systemic hydrocortisone (HCS) is frequently used for very low birth weight (VLBW) infants to manage hypotension or prevent bronchopulmonary dysplasia.
- The long-term neurodevelopmental effects of postnatal HCS exposure in VLBW infants require further investigation.
Purpose of the Study:
- To evaluate the association between postnatal HCS exposure and neurodevelopmental outcomes in VLBW infants.
- To compare regional brain volumes at term-equivalent age (TEA) with early infancy neurodevelopmental assessments.
Main Methods:
- Retrospective cohort study of VLBW infants (2013-2019) admitted to a neonatal intensive care unit (NICU).
- Recorded cumulative HCS dose and analyzed regional brain volumes via magnetic resonance imaging at TEA.
- Assessed neurodevelopmental outcomes at 18-24 months corrected age.
Main Results:
- Infants receiving high HCS doses (>90 mg/kg) showed higher rates of bronchopulmonary dysplasia, periventricular leukomalacia, and sepsis.
- High HCS exposure correlated with reduced brain volumes at TEA.
- The high HCS group had significantly more cases of cerebral palsy, neurodevelopmental impairment, and small head circumference at follow-up.
Conclusions:
- High cumulative hydrocortisone exposure in VLBW infants is associated with reduced brain volume and adverse neurodevelopmental outcomes.
- Independent associations were found between HCS > 90 mg/kg and cerebral palsy and reduced head circumference.
- Judicious monitoring of HCS dose and duration is essential to balance treatment benefits against potential neurodevelopmental risks.
Abstract:
Background/Objectives: Systemic hydrocortisone (HCS) in very low birth weight (VLBW) infants is commonly used to treat early hypotension or prevent bronchopulmonary dysplasia. This study evaluated the associations between postnatal HCS exposure and neurodevelopment in VLBW infants by comparing regional brain volume at term-equivalent age (TEA) with neurodevelopmental outcomes in early infancy. Methods: This retrospective cohort study included VLBW infants admitted to a neonatal intensive care unit (NICU) between 2013 and 2019. The cumulative HCS dose during hospitalization was recorded, and regional brain volumes were analyzed using magnetic resonance imaging at TEA. Neurodevelopmental outcomes were assessed at a corrected age for prematurity of 18-24 months. Results: Among 146 infants, 57 were classified in the high HCS group (>90 mg/kg) and 89 in the low HCS group (≤90 mg/kg HCS). Bronchopulmonary dysplasia, periventricular leukomalacia, and sepsis were more frequent in the high HCS group. Ninety-five infants underwent magnetic resonance imaging, which revealed reduced brain volumes in the high HCS group. At follow-up, cerebral palsy (35.9% vs. 9.1%, p = 0.003), neurodevelopmental impairment (54.0% vs. 23.6%, p = 0.002), and head circumference <10th percentile (64.3% vs. 19.5%, p < 0.001) were more common in the high HCS group. After adjustment, HCS > 90 mg/kg remained independently associated with cerebral palsy (adjusted odds ratio [aOR] 5.44, p = 0.016) and reduced head circumference (aOR 4.45, p = 0.016). Conclusions: High cumulative HC exposure correlated with reduced brain volume at TEA and adverse neurodevelopmental outcomes at 24 months of age. Careful monitoring of dose and treatment duration is essential to balance therapeutic benefits against potential risks.
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