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Recognition, assessment and management of hypoglycaemia in childhood
Arunabha Ghosh1, Indraneel Banerjee2, Andrew A M Morris1
1Paediatric Inherited Metabolic Disease, Manchester Centre for Genomic Medicine, St Mary's Hospital, Manchester, UK.
Insights
Prompt management of paediatric hypoglycaemia is crucial to prevent brain injury. This review covers causes like diabetes mellitus and idiopathic ketotic hypoglycaemia (IKH), alongside endocrine disorders and inborn errors of metabolism (IEMs).
Area of Science:
- Pediatric Endocrinology
- Metabolic Disorders
- Clinical Diagnostics
Background:
- Hypoglycaemia is a common and serious condition in children, necessitating prompt intervention to avert neurological damage.
- While diabetes mellitus and idiopathic ketotic hypoglycaemia (IKH) are frequent causes, other conditions such as endocrine disorders and inborn errors of metabolism (IEMs) must be considered.
Purpose of the Study:
- To review the diagnosis and management of hypoglycaemia in children beyond the neonatal period.
- To highlight the differential diagnoses, diagnostic approaches, and specific treatments for various causes of paediatric hypoglycaemia.
Main Methods:
- Diagnostic strategies include investigations during hypoglycaemic episodes, biochemical testing between episodes, dynamic endocrine tests, and molecular genetics.
- Management strategies are tailored to the underlying cause, ranging from specific treatments like hormone replacement to dietary modifications.
Main Results:
- Accurate diagnosis relies on a combination of clinical presentation and targeted investigations.
- Treatment varies significantly, with some conditions requiring specific medical or surgical interventions, while others are managed through dietary adjustments.
Conclusions:
- Effective management of paediatric hypoglycaemia requires a thorough diagnostic workup to identify the underlying cause.
- Tailored treatment strategies, encompassing medical, surgical, and dietary approaches, are essential for preventing complications and ensuring optimal outcomes in affected children.
Abstract:
Hypoglycaemia is frequent in children and prompt management is required to prevent brain injury. In this article we will consider hypoglycaemia in children after the neonatal period. The most common causes are diabetes mellitus and idiopathic ketotic hypoglycaemia (IKH) but a number of endocrine disorders and inborn errors of metabolism (IEMs) need to be excluded. Elucidation of the diagnosis relies primarily on investigations during a hypoglycaemic episode but may also involve biochemical tests between episodes, dynamic endocrine tests and molecular genetics. Specific treatment such as cortisol replacement and pancreatic surgery may be required for endocrine causes of hypoglycaemia, such as adrenal insufficiency and congenital hyperinsulinism. In contrast, in IKH and most IEMs, hypoglycaemia is prevented by limiting the duration of fasting and maintaining a high glucose intake during illnesses.
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