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Hypercapnia: An Added Culprit in Gray Matter Injury in Preterm Neonates

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AbstractOver the last decade, there has been increased recognition of diverse forms of primary gray matter injury (GMI) in postpreterm neonates. In this study, we aimed to assess whether early neonatal hypercapnia in the preterm infant was associated with GMI on magnetic resonance imaging (MRI) at term equivalent age (TEA). All blood gases taken during the first 2 weeks of life were analyzed for hypercapnia. MRI was performed at TEA postpreterm infants using a unique neonatal MRI 1T scanner. The neonatal MRI scans were assessed using a standardized scoring system, the Kidokoro scoring system, a method used to assess abnormal brain metrics and the presence and severity of brain abnormalities. Subscores are assigned for different regions of the brain. Twenty-nine infants were studied, about half of whom had evidence of some gray matter abnormality. Fifteen of the infants were hypercapnic. The hypercapnic infants had significantly higher deep gray matter abnormality readings as compared with the nonhypercapnic infants (12 [11; 12] vs. 10 [8; 11], respectively; p = 0.0106). Correlations were observed between peak pCO2 over the first 2 weeks of life and the overall gray matter abnormality score (GMAS) at TEA, and between the percentage of hypercapnic blood gases during the first 2 weeks of life and the GMAS. All of the infants in our population who had severe GMI at TEA were hypercapnic in the first 2 weeks of life. In conclusion, our data show a correlation between early hypercapnia in preterm neonates and GMI at TEA.
Title: Hypercapnia: An Added Culprit in Gray Matter Injury in Preterm Neonates
Description:
AbstractOver the last decade, there has been increased recognition of diverse forms of primary gray matter injury (GMI) in postpreterm neonates.
In this study, we aimed to assess whether early neonatal hypercapnia in the preterm infant was associated with GMI on magnetic resonance imaging (MRI) at term equivalent age (TEA).
All blood gases taken during the first 2 weeks of life were analyzed for hypercapnia.
MRI was performed at TEA postpreterm infants using a unique neonatal MRI 1T scanner.
The neonatal MRI scans were assessed using a standardized scoring system, the Kidokoro scoring system, a method used to assess abnormal brain metrics and the presence and severity of brain abnormalities.
Subscores are assigned for different regions of the brain.
Twenty-nine infants were studied, about half of whom had evidence of some gray matter abnormality.
Fifteen of the infants were hypercapnic.
The hypercapnic infants had significantly higher deep gray matter abnormality readings as compared with the nonhypercapnic infants (12 [11; 12] vs.
10 [8; 11], respectively; p = 0.
0106).
Correlations were observed between peak pCO2 over the first 2 weeks of life and the overall gray matter abnormality score (GMAS) at TEA, and between the percentage of hypercapnic blood gases during the first 2 weeks of life and the GMAS.
All of the infants in our population who had severe GMI at TEA were hypercapnic in the first 2 weeks of life.
In conclusion, our data show a correlation between early hypercapnia in preterm neonates and GMI at TEA.

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