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Blood gases and retinopathy of prematurity: the ELGAN Study
Alisse K Hauspurg1, Elizabeth N Allred, Deborah K Vanderveen
1Yale University School of Medicine, New Haven, Connecticut, USA.
Insights
Preterm infants with abnormal blood gases in the first three days face higher risks of severe retinopathy of prematurity (ROP). Monitoring blood gas derangements like high PCO2, low pH, and high PaO2 is crucial for ROP risk assessment.
Area of Science:
- Neonatalogy
- Ophthalmology
- Perinatology
Background:
- Retinopathy of prematurity (ROP) is a significant cause of visual impairment in premature infants.
- Blood gas derangements in the early postnatal period are common in extremely preterm infants.
- The association between early blood gas abnormalities and ROP severity requires further investigation.
Purpose of the Study:
- To test the hypothesis that preterm infants with blood gas derangements on at least two of the first three postnatal days are at increased risk for more severe ROP.
- To identify specific blood gas parameters (PCO2, pH, PaO2) associated with ROP development and severity.
Main Methods:
- A cohort of 1,042 infants born before 28 weeks' gestational age (GA) was analyzed.
- Infants were classified as 'exposed' if their blood gas measures fell in the highest or lowest quartile for GA on at least two of the first three postnatal days.
- Multivariable models were used to adjust for potential confounders.
Main Results:
- Exposure to high partial pressure of carbon dioxide (PCO2) quartile was associated with increased odds of ROP (stage 3-5, OR=1.6; zone 1, OR=2.0).
- Low pH quartile exposure showed increased risk for ROP in zone 1 (OR=2.1) and prethreshold/threshold disease (OR=1.8).
- High partial pressure of oxygen (PaO2) quartile was linked to a doubled risk of ROP in zone 1 (OR=2.5) and prethreshold/threshold disease (OR=2.1).
Conclusions:
- Early postnatal exposure to abnormal blood gases, specifically high PCO2, low pH, and high PaO2, is associated with an increased risk of developing more severe retinopathy of prematurity.
- These findings highlight the importance of vigilant monitoring and management of blood gases in extremely preterm infants to mitigate ROP risk.
- Further research may explore targeted interventions to normalize blood gases and prevent severe ROP outcomes.
Objective:
This study tested the hypothesis that preterm infants who had a blood gas derangement on at least 2 of the first 3 postnatal days are at increased risk for more severe retinopathy of prematurity (ROP).
Method:
1,042 infants born before 28 weeks' gestational age (GA) were included. An infant was considered to be exposed if his/her blood gas measure was in the highest or lowest quartile for GA on at least 2 of the first 3 postnatal days.
Results:
Multivariable models adjusting for confounders indicate that exposure to a PCO(2) in the highest quartile predicts ROP (stage 3, 4 or 5: OR = 1.6, 95% CI = 1.1-2.3); zone 1: 2.0, 1.1-3.6; prethreshold/threshold: 1.9, 1.2-3.0; plus disease: 1.8, 1.1-2.9). Estimates are similar for a low pH for zone 1 (2.1, 1.2-3.8), prethreshold/threshold (1.8, 1.1-2.8), but did not quite achieve statistical significance for ROP stage 3, 4, or 5 (1.4, 0.9-2.0) and plus disease (1.5, 0.9-2.4). A PaO(2) in the highest quartile for GA on at least 2 of the first 3 postnatal days was associated with a doubling of the risk of ROP in zone 1 (2.5, 1.4-4.4) and of prethreshold/threshold disease (2.1, 1.4-3.3), a 70% risk increase for plus disease (1.7, 1.04-2.8), while a 40% risk increase for ROP stage 3 or higher did not achieve statistical significance (1.4, 0.96-2.0).
Conclusion:
Infants exposed to high PCO(2), low pH and high PaO(2) appear to be at increased risk of more severe ROP.
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