An extremely high blood glucose level in a child with hyperglycemic hyperosmolar state and type 1 diabetes
Ivona Butorac Ahel1, Srecko Severinski1, Kristina Lah Tomulic1
1Department of Pediatrics, Clinical Hospital Center Rijeka, Rijeka, Croatia.
Insights
Hyperglycemic hyperosmolar state (HHS) is a severe diabetes complication. Early recognition and management are crucial for better outcomes, especially in rare pediatric cases.
Area of Science:
- Pediatric Endocrinology
- Metabolic Disorders
Background:
- Hyperglycemic hyperosmolar state (HHS) is a severe acute complication of diabetes mellitus (DM).
- HHS is characterized by severe hyperglycemia and hyperosmolality without significant ketosis and acidosis.
- Pediatric cases of HHS are rare and potentially life-threatening.
Observation:
- A 7-year-old boy with Joubert syndrome presented with vomiting, polydipsia, and polyuria.
- Initial blood glucose was 115 mmol/L, with severe dehydration.
- Diagnosis of type 1 diabetes mellitus (T1DM) and HHS was made.
Findings:
- The patient received intravenous fluid resuscitation and insulin therapy.
- Discharge occurred after 10 days with no HHS-related complications.
- This case highlights the importance of recognizing HHS in children.
Implications:
- Early recognition and prompt management of HHS are critical for improving patient outcomes.
- Raising awareness of HHS in pediatric populations is essential for healthcare professionals.
- This case underscores the need for vigilance in diagnosing and treating diabetic emergencies in children with underlying conditions.
Objectives:
Hyperglycemic hyperosmolar state (HHS) is one of the most severe acute complications of diabetes mellitus (DM) characterized by severe hyperglycemia and hyperosmolality without significant ketosis and acidosis. What is new? Since HHS in the pediatric population is rare and potentially life-threatening, every reported case is very valuable for raising awareness among healthcare professionals.
Case Presentation:
A 7-year-old boy with previously diagnosed Joubert syndrome was admitted due to vomiting, polydipsia and polyuria started several days earlier. He was severely dehydrated, and the initial blood glucose level was 115 mmol/L. Based on clinical manifestations and laboratory results, he was diagnosed with T1DM and HHS. The treatment with intravenous fluid was started and insulin administration began later. He was discharged after 10 days without any complications related to HHS.
Conclusions:
Since HHS has a high mortality rate, early recognition, and proper management are necessary for a better outcome.
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