Hypoglycemia in Infants and Children

作者: Francis M. Hoe

DOI: 10.1016/J.YAPD.2008.07.008

关键词:

摘要: Hypoglycemia is an important problem in infants and children. It can cause seizures, coma, permanent brain damage, death. Several metabolic systems are activated during fasting to prevent hypoglycemia. Thus, hypoglycemia be viewed as a failure of one these or abnormality the hormones that controls systems. This review supplements ‘‘Hypoglycemia Newborns Infants’’ by Dekelbab Sperling [1], which appeared earlier volume this series. The previous article discussed signs symptoms its effect on central nervous system. also etiology, evaluation, management hypoglycemia, with particular focus neonatal hyperinsulinism. expands upon discussing other causes children context abnormal adaptation fasting. FASTING ADAPTATION body stores energy form glycogen, triglycerides, protein liver, fat, muscle. During fasting, several convert into fuels tissues use (Fig. 1). Glycogenolysis converts glycogen liver glucose. Lipolysis triglycerides fat fatty acids glycerol. Proteolysis muscle amino acids. Gluconeogenesis glycerol gluconeogenic glucose liver. Fatty undergo oxidation produce acetyl coenzyme A (acetyl-CoA). Acetyl-CoA undergoes ketogenesis ketones, such b-hydroxybutyrate.

参考文章(56)
David N. Finegold, Charles A. Stanley, Lester Baker, Glycemic response to glucagon during fasting hypoglycemia: An aid in the diagnosis of hyperinsulinism The Journal of Pediatrics. ,vol. 96, pp. 257- 259 ,(1980) , 10.1016/S0022-3476(80)80817-1
Hector Chavez, Drew Ozolins, Joseph D. Losek, Hypoglycemia and propranolol in pediatric behavioral disorders Pediatrics. ,vol. 103, pp. 1290- 1292 ,(1999) , 10.1542/PEDS.103.6.1290
Amy A. Ernst, Kathleen Jones, Todd G. Nick, Julie Sanchez, Ethanol ingestion and related hypoglycemia in a pediatric and adolescent emergency department population Academic Emergency Medicine. ,vol. 3, pp. 46- 49 ,(1996) , 10.1111/J.1553-2712.1996.TB03302.X
Angels García-Cazorla, Daniel Rabier, Guy Touati, Bernadette Chadefaux-Vekemans, Cécile Marsac, Pascale de Lonlay, Jean-Marie Saudubray, Pyruvate carboxylase deficiency: metabolic characteristics and new neurological aspects. Annals of Neurology. ,vol. 59, pp. 121- 127 ,(2006) , 10.1002/ANA.20709
G. Srinivasan, R.S. Pildes, G. Cattamanchi, S. Voora, L.D. Lilien, Plasma glucose values in normal neonates: a new look. The Journal of Pediatrics. ,vol. 109, pp. 114- 117 ,(1986) , 10.1016/S0022-3476(86)80588-1
F. A. HOMMES, K. BENDIEN, J. D. ELEMA, H. J. BREMER, I. LOMBECK, Two cases of phosphoenolpyruvate carboxykinase deficiency. Acta Paediatrica. ,vol. 65, pp. 233- 240 ,(1976) , 10.1111/J.1651-2227.1976.TB16543.X
Diva D. Ng, Robert J. Ferry, Andrea Kelly, Stuart A. Weinzimer, Charles A. Stanley, Lorraine E.Levitt Katz, Acarbose treatment of postprandial hypoglycemia in children after Nissen fundoplication. The Journal of Pediatrics. ,vol. 139, pp. 877- 879 ,(2001) , 10.1067/MPD.2001.119169
Vincent Marks, J. Derrick Teale, Drug-induced hypoglycemia. Endocrinology and Metabolism Clinics of North America. ,vol. 28, pp. 555- 577 ,(1999) , 10.1016/S0889-8529(05)70088-8
Charles A. Stanley, Hyperinsulinism in infants and children Pediatric Clinics of North America. ,vol. 44, pp. 363- 374 ,(1997) , 10.1016/S0031-3955(05)70481-8
Francis M. Hoe, Paul S. Thornton, Laura A. Wanner, Linda Steinkrauss, Rebecca A. Simmons, Charles A. Stanley, Clinical features and insulin regulation in infants with a syndrome of prolonged neonatal hyperinsulinism The Journal of Pediatrics. ,vol. 148, pp. 207- 212 ,(2006) , 10.1016/J.JPEDS.2005.10.002