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Frequency and etiology of persistent neonatal hypoglycemia using the more stringent 2015 Pediatric Endocrine Society
Rozeanna Skovrlj1, Seth D Marks1,2, Celia Rodd1,2
1Department of Pediatrics and Child Health, Rady Faculty of Health Sciences, University of Manitoba, Winnipeg, Manitoba.
Insights
The 2015 guidelines for persistent neonatal hypoglycemia led to a significant increase in endocrine consultations. Hyperinsulinism was the primary cause, with diazoxide treatment generally effective but requiring careful monitoring for adverse effects.
Area of Science:
- Neonatal Medicine
- Pediatric Endocrinology
- Clinical Guidelines
Background:
- Persistent neonatal hypoglycemia poses significant health risks.
- The 2015 Pediatric Endocrine Society guidelines introduced more stringent criteria for diagnosis and management.
- Evaluating the impact of guideline changes on clinical practice is crucial.
Purpose of the Study:
- To assess the impact of the 2015 guidelines on endocrine consultation rates for persistent neonatal hypoglycemia.
- To identify the primary etiologies and management patterns for infants with persistent hypoglycemia under the new guidelines.
Main Methods:
- Retrospective chart review of infants with hypoglycemia persisting beyond 72 hours.
- Data collected included demographics, clinical parameters, and treatment details.
- Interrupted time series analysis was used to evaluate changes post-guideline implementation.
Main Results:
- A significant increase in endocrine consultations was observed after the 2015 guidelines (P<0.03).
- Hyperinsulinism was the most common etiology (52/58 infants).
- Diazoxide was used in approximately 56% of hyperinsulinism cases, with a median treatment duration of 91 days; two infants developed pulmonary hypertension.
Conclusions:
- The 2015 guidelines resulted in a higher number of diagnosed persistent neonatal hypoglycemia cases.
- Prolonged hyperinsulinism is a key driver, often managed effectively with medication.
- Caution is advised regarding diazoxide's adverse effects, particularly pulmonary hypertension.
Objective:
To determine if there was a significant increase in Endocrine consultations postinitiation of the more stringent 2015 guidelines for persistent neonatal hypoglycemia.
Methods:
A retrospective chart review was conducted using data from November 2011 to October 2016. All infants with persistent hypoglycemia past 72 hours of life were included. Data included age, critical sample values, anthropometric measures, and maternal health. Descriptive statistical analyses were performed as was an interrupted time series analysis assuming a Poisson distribution.
Results:
Fifty-eight infants were evaluated. Postintervention, there was a significant increase in the number of consults (P<0.03, 95% confidence interval [CI]: 1.14 to 8.93). Most infants with hypoglycemia persisting >72 hours were hypoglycemic shortly after birth. Half had intrauterine growth restriction; 75% were male. The median age for investigation was 8.3 days. Hyperinsulinism was the most common etiology (52/58 infants); diazoxide treatment was utilized in roughly half (29/52 to 56%) with a median duration of treatment for 91 days. The phenotype of the infants and duration of diazoxide pre- and post-Pediatric Endocrine Society protocol did not differ; two infants on diazoxide developed pulmonary hypertension. Mothers were typically of lower socioeconomic status.
Conclusion:
Not surprisingly, there was significant increase in the number of infants with persistent hypoglycemia using the 2015 guidelines. Prolonged hyperinsulinism was the major cause; medical management was typically sufficient and typically well tolerated. Care to reduce adverse effects of diazoxide is advised. We postulate that infants diagnosed using the more stringent 2015 guidelines have real disease based on the protracted medical management required.
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