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Hypoglycemia in pediatric sulfonylurea poisoning: an 8-year poison center retrospective study
1Department of Clinical Pharmacy, University of California, San Francisco, California, USA. derricklung@gmail.com
Insights
Pediatric sulfonylurea poisoning can cause delayed hypoglycemia, with onset up to 18 hours after ingestion. Seizures occurred in severe, unrecognized cases.
Area of Science:
- Toxicology
- Pediatric Emergency Medicine
- Pharmacology
Background:
- Sulfonylurea medications are commonly prescribed for type 2 diabetes.
- Accidental ingestion in children can lead to significant hypoglycemia.
- Understanding the time course of hypoglycemia is crucial for effective management.
Purpose of the Study:
- To characterize the clinical effects of sulfonylurea poisoning in pediatric patients.
- To determine the time of onset and duration of hypoglycemia following ingestion.
Main Methods:
- Retrospective, descriptive study of pediatric sulfonylurea exposures (<6 years old).
- Data collected from California Poison Control System consultations (2002-2009).
- Included cases with documented hypoglycemia (glucose <60 mg/dL).
Main Results:
- 300 out of 1943 pediatric exposures resulted in hypoglycemia.
- Hypoglycemia persisted for ≥12 hours in 10% of cases.
- Prophylactic measures (food, IV glucose) delayed hypoglycemia onset up to 18 hours.
Conclusions:
- Pediatric sulfonylurea poisoning can lead to severe hypoglycemia and seizures.
- Delayed onset of hypoglycemia is possible, even with treatment.
- Prompt recognition and management are vital to prevent severe outcomes.
Objective:
The goal of this study was to describe the clinical effects and time of onset of hypoglycemia in pediatric sulfonylurea poisoning.
Methods:
This was a retrospective, descriptive study of pediatric (<6 years old) sulfonylurea exposures with hypoglycemia (glucose concentration <60 mg/dL) that were consulted on by the California Poison Control System for the 8-year period between January 1, 2002, and December 31, 2009.
Results:
Of the 1943 consultations for pediatric sulfonylurea exposure in the study period, 300 children developed hypoglycemia. Ten percent had hypoglycemia occurring or persisting ≥ 12 hours after ingestion despite receiving treatment. All 5 children with seizures experienced these before hospital presentation. The mean (SD) time to onset of hypoglycemia in children not given any prophylactic treatment was 2.0 (1.2) hours. The mean (SD) times in children receiving prophylactic food only, intravenous glucose only, and both food and intravenous glucose were 5.9 (3.9), 5.7 (2.5), and 8.9 (3.6) hours, respectively. Ranges were 1 to 18, 1.5 to 9, and 2.5 to 15 hours. Seven of 40 patients (18%) receiving prophylactic food only had an onset of hypoglycemia >8 hours after sulfonylurea ingestion.
Conclusions:
Pediatric sulfonylurea exposure can result in significant poisoning. Severe effects such as seizures occurred only in cases of unrecognized sulfonylurea ingestion. The onset of hypoglycemia after pediatric sulfonylurea ingestion can be delayed by as much as 18 hours by either free access to food or administration of intravenous glucose.
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