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Published on: June 11, 2012
Factors associated with neonatal hyperinsulinemic hypoglycemia, a case-control study
Thanaporn Rattanasakol1, Ratchada Kitsommart1
1Division of Neonatology, Department of Pediatrics, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand.
Insights
Fetal growth restriction and neonatal sepsis are key risk factors for hyperinsulinemic hypoglycemia in newborns. Affected infants require higher glucose support and may need diazoxide therapy.
Area of Science:
- Neonatalogy
- Pediatric Endocrinology
- Perinatal Medicine
Background:
- Hyperinsulinemic hypoglycemia (HH) is a significant neonatal condition.
- Identifying perinatal risk factors is crucial for early intervention.
Purpose of the Study:
- To identify perinatal risk factors for neonatal hyperinsulinemic hypoglycemia.
- To characterize clinical and biochemical features of affected neonates.
- To explore the duration of diazoxide treatment.
Main Methods:
- A case-control study involving 52 infants with HH and matched controls.
- Individual chart reviews were conducted for infants born between 2014 and 2021.
- Gestational age strata were used for matching cases and controls.
Main Results:
- Fetal growth restriction (FGR) and neonatal sepsis were significant risk factors for HH (aOR 8.1 and 6.3, respectively).
- Infants with HH had lower plasma glucose levels and required higher glucose infusion rates.
- The median duration of diazoxide therapy was 4 months.
Conclusions:
- FGR and neonatal sepsis are significant perinatal risk factors for HH.
- HH neonates exhibit distinct biochemical profiles requiring intensive glucose management.
- Diazoxide therapy is utilized in a substantial proportion of HH cases, with a median treatment duration of 4 months.
Objectives:
We aimed to identify perinatal risk factors associated with hyperinsulinemic hypoglycemia in neonates. Secondary objectives included an examination of clinical and biochemical characteristics at the time of diagnosis and an exploration of the duration of diazoxide therapy.
Methods:
A case-control study was conducted, involving individual chart reviews of inborn infants diagnosed with hyperinsulinemic hypoglycemia (the HH group) between 2014 and 2021. These cases were paired with controls (the non-HH group) belonging to the same gestational age (GA) strata who did not exhibit HH or only had transient postnatal hypoglycemia.
Results:
A total of 52 infants with HH were matched with corresponding controls. The mean GA in the HH group was 34.4 ± 3.1 weeks. Notably, the HH group exhibited lower mean minimum plasma glucose (PG) levels and required higher glucose infusion rates in comparison to the non-HH group (26.5 ± 15.6 vs. 49.1 ± 37.7 mg/dL and 12.9 ± 3.8 vs. 5.7 ± 2.1 mg/kg/min, respectively; p<0.001 for both). After adjusting for potential confounding factors, only two variables, fetal growth restriction (FGR) and neonatal sepsis, demonstrated significant associations with HH (adjusted odds ratio [95 % confidence interval]: 8.1 [2.1-31.0], p=0.002 and 6.3 [1.9-21.4], p=0.003, respectively). The median duration of diazoxide therapy for the HH group was 4 months.
Conclusions:
FGR and neonatal sepsis emerged as notable risk factors for HH. These infants exhibited lower PG levels and necessitated higher glucose infusion rates compared to their non-HH counterparts. Importantly, a substantial proportion of the HH group received diazoxide therapy, with a median treatment duration of 4 months.
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