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Published on: November 20, 2015
Early Neonatal Hyperglycemia, Risk Factors, and Adverse Outcomes in Extremely Preterm Infants: A Propensity-Matched
Safaa M G A Alsayigh1, Nuha Nimeri1,2, Alaa Almashhadani1,3
1Neonatal Intensive Care Unit, Women's Wellness and Research Center, Hamad Medical Corporation, Doha 3050, Qatar.
Insights
Neonatal hyperglycemia in extremely preterm infants is linked to increased respiratory issues and severe retinopathy of prematurity. This early metabolic complication serves as a significant risk marker in this vulnerable population.
Area of Science:
- Neonatology
- Perinatal Medicine
- Metabolic Disorders
Background:
- Neonatal hyperglycemia is a frequent complication in extremely preterm (EP) infants.
- Early risk factors and outcomes of neonatal hyperglycemia in EP infants require further elucidation.
Purpose of the Study:
- To investigate the association between neonatal hyperglycemia within the first postnatal week and significant neonatal morbidities in EP infants.
- To assess the early neurodevelopmental risk associated with neonatal hyperglycemia in EP infants.
Main Methods:
- A retrospective cohort study included EP infants born between 2018-2019.
- Neonatal hyperglycemia was defined as blood glucose > 8.3 mmol/L.
- Propensity score matching was utilized to control for baseline differences.
Main Results:
- Over half (58.2%) of EP infants experienced neonatal hyperglycemia.
- Hyperglycemia correlated with increased ventilator-associated pneumonia, prolonged invasive ventilation, and higher rates of severe retinopathy of prematurity (ROP).
- A trend towards moderate-to-severe bronchopulmonary dysplasia was observed, with no significant difference in mortality.
Conclusions:
- Early neonatal hyperglycemia in EP infants is significantly associated with heightened respiratory morbidity and severe ROP.
- Neonatal hyperglycemia is a clinically relevant early risk marker in EP infants.
- Further prospective and interventional studies are warranted to explore these associations.
Background:
Neonatal hyperglycemia is a common metabolic complication in extremely preterm (EP) infants; however, early risk factors and associated outcomes remain incompletely defined.
Objective:
To evaluate the association between neonatal hyperglycemia in the first postnatal week and key neonatal morbidities including early neurodevelopmental risk in EP infants.
Methods:
We conducted a retrospective cohort study of EP infants born in 2018-2019 at the Women's Wellness and Research Center. Neonatal hyperglycemia was defined as a blood glucose level > 8.3 mmol/L. Maternal factors, delivery room interventions, early physiological markers, neonatal morbidities, and follow-up outcomes were compared. Propensity score matching was applied to balance the baseline demographic and perinatal differences.
Results:
Among 225 EP infants, 131 (58.2%) developed neonatal hyperglycemia in the first week (mild, 21.4%; moderate, 42%; severe, 36.6%). Before matching, infants with neonatal hyperglycemia had lower gestational age and birth weight and required more delivery-room surfactant, and their mothers had lower rates of premature rupture of membranes. After matching, neonatal hyperglycemia was associated with higher rates of ventilator-associated pneumonia (1.45 vs. 0.37; IRR 6.2, 95% CI 1.4-27.6), longer duration of invasive ventilation (19.8 ± 25.3 vs. 8.9 ± 24.8 days; mean difference -10.9 days; p = 0.042), higher postnatal steroid exposure (18.2% vs. 5.5%; OR 4.6, 95% CI 1.6-14.4; p = 0.040), and severe retinopathy of prematurity (ROP) (21.6% vs. 6.4%; OR 4.0, 95% CI 1.0-15.5; p = 0.032). A trend toward moderate-to-severe bronchopulmonary dysplasia was observed (33.3% vs. 15.9%; p = 0.054). Mortality did not differ significantly between groups; however, among non-survivors, age at death was higher in the neonatal hyperglycemia group.
Conclusions:
In EP infants, early neonatal hyperglycemia is associated with higher respiratory morbidity and severe ROP even after propensity score matching. These findings support neonatal hyperglycemia as a clinically relevant early risk marker and justify further prospective and interventional studies.
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