11. Hypoglycemia
Published Online: 23 FEB 2012
DOI: 10.1002/9781119968153.ch11
Copyright © 2012 John Wiley & Sons, Ltd.
Book Title

Handbook of Clinical Pediatric Endocrinology, Second Edition
Additional Information
How to Cite
Brook, C. G. D. and Dattani, M. T. (2012) Hypoglycemia, in Handbook of Clinical Pediatric Endocrinology, Second Edition, Wiley-Blackwell, Oxford, UK. doi: 10.1002/9781119968153.ch11
Publication History
- Published Online: 23 FEB 2012
- Published Print: 13 APR 2012
ISBN Information
Print ISBN: 9780470657881
Online ISBN: 9781119968153
- Summary
- Chapter
Keywords:
- Beckwith–Wiedemann syndrome;
- consequences of hypoglycemia;
- disorders of glycosylation;
- hyperinsulinism;
- hypoglycemia;
- metabolic causes of hypoglycemia;
- nesidioblastosis;
- pancreatic development
Summary
This chapter elucidates hypoglycemia, which carries serious short- and long-term consequences from incorrect management. Maintenance of a normal blood glucose concentration is critical to brain development and function so hypoglycemia is a medical emergency. The best time to make the diagnosis is by taking the correct blood and urine samples at the point of crisis. Delay in management may precipitate complications but intervention without the diagnostic samples delays the diagnosis until either another similar event takes place or hypoglycemia can be reproduced during a planned elective fasting study. The most practical course is to take samples at the first opportunity and institute treatment without delay. The risk of harm as a result of hypoglycemia is greater in infants and children because brain size is relatively greater to body size than later in life. Glucose is the prime source of energy for the brain but ketones can provide an alternative source in chronic hypoglycemia.
