Pediatric Hypoglycemia Medication

  • Author: Robert P Hoffman, MD; Chief Editor: Stephen Kemp, MD, PhD   more...
 
Updated: Aug 25, 2011
 

Medication Summary

Most medications used to treat hypoglycemia are hormonal and either replace a hormonal deficiency (ie, a cortisol or growth hormone deficiency) or suppress excess hormone production (octreotide). Diazoxide is an antihypertensive agent that also suppresses insulin secretion.

As previously mentioned, in infants with one of several disorders (eg, ketotic hypoglycemia, glycogen-storage disorder, free fatty acid metabolism defect, mild hyperinsulinism), hypoglycemia can be prevented with frequent feedings using a specifically designed diet, but when feeding is inadequate because of GI problems or other illnesses, parenteral dextrose can be used to obtain a rapid response. Fructose must be avoided in children with fructose diphosphatase deficiency.

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Insulin secretion inhibiting agents

Class Summary

Various mechanisms may alter insulin secretion. Diazoxide inhibits pancreatic secretion of insulin, stimulates glucose release from the liver, and stimulates catecholamine release, which elevates blood glucose levels. Octreotide is a peptide with pharmacologic action similar to that of somatostatin, which inhibits insulin secretion.

ATP-sensitive potassium channels (composed of the sulfonylurea receptor [SUR] and the potassium channel pore protein [Kir6.2]) function abnormally in persistent hyperinsulinemic hypoglycemia of infancy. These channels initiate depolarization of the beta-cell membrane and opening of calcium channels. The resultant increase in intracellular calcium triggers insulin secretion. Calcium channel blockers block the action of these calcium channels, decreasing insulin secretion. Nifedipine is the only calcium channel blocker for which data have been reported in clinical trials in humans.

Diazoxide (Proglycem)

 

Diazoxide is a first-line medical treatment for hyperinsulinism. This agent inhibits insulin release from the pancreas.

Octreotide (Sandostatin)

 

Octreotide, a synthetic polypeptide, is usually the second-line therapy for hyperinsulinism. It inhibits the release of many biologically active substances, including insulin.

Nifedipine (Adalat, Procardia, Afeditab)

 

Nifedipine acts to block calcium influx, which stimulates insulin secretion.

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Dextrose and glucose stimulators

Class Summary

Promptly activation of gluconeogenesis is achieved with glucagon. Emergent elevation of blood glucose levels requires IV dextrose.

Glucagon (GlucaGen)

 

This is the first-line home treatment for severe hypoglycemic reactions in patients with diabetes. Glucagon promotes glycogenolysis and gluconeogenesis, resulting in elevation of blood glucose levels. Glucagon may cause vomiting for 4-6 hours after administration.

Dextrose (D-glucose)

 

Dextrose is used to promptly elevate serum glucose levels. It is a monosaccharide that is absorbed from the intestine and is then distributed, stored, and used by the tissues.

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Contributor Information and Disclosures
Author

Robert P Hoffman, MD  Associate Professor of Pediatrics, Department of Pediatrics, Ohio State University College of Medicine

Robert P Hoffman, MD is a member of the following medical societies: American Diabetes Association, American Pediatric Society, Christian Medical & Dental Society, Endocrine Society, and Pediatric Endocrine Society

Disclosure: Nothing to disclose.

Specialty Editor Board

Karl S Roth, MD  Professor and Chair, Department of Pediatrics, Creighton University School of Medicine

Karl S Roth, MD is a member of the following medical societies: Alpha Omega Alpha, American Academy of Pediatrics, American College of Nutrition, American Pediatric Society, American Society for Clinical Nutrition, American Society of Nephrology, Association of American Medical Colleges, Medical Society of Virginia, New York Academy of Sciences, Sigma Xi, Society for Pediatric Research, and Southern Society for Pediatric Research

Disclosure: Nothing to disclose.

Mary L Windle, PharmD  Adjunct Associate Professor, University of Nebraska Medical Center College of Pharmacy; Editor-in-Chief, Medscape Drug Reference

Disclosure: Nothing to disclose.

George P Chrousos, MD, FAAP, MACP, MACE, FRCP(London)  Professor and Chair, First Department of Pediatrics, Athens University Medical School, Aghia Sophia Children's Hospital, Greece; UNESCO Chair on Adolescent Health Care, University of Athens, Greece

George P Chrousos, MD, FAAP, MACP, MACE, FRCP(London) is a member of the following medical societies: American Academy of Pediatrics, American College of Endocrinology, American College of Physicians, American Pediatric Society, American Society for Clinical Investigation, Association of American Physicians, Endocrine Society, Pediatric Endocrine Society, and Society for Pediatric Research

Disclosure: Nothing to disclose.

Chief Editor

Stephen Kemp, MD, PhD  Professor, Department of Pediatrics, Section of Pediatric Endocrinology, University of Arkansas for Medical Sciences College of Medicine, Arkansas Children's Hospital

Stephen Kemp, MD, PhD is a member of the following medical societies: American Academy of Pediatrics, American Association of Clinical Endocrinologists, American Pediatric Society, Endocrine Society, Phi Beta Kappa, Southern Medical Association, and Southern Society for Pediatric Research

Disclosure: Nothing to disclose.

References
  1. de Lonlay P, Giurgea I, Sempoux C, Touati G, Jaubert F, Rahier J, et al. Dominantly inherited hyperinsulinaemic hypoglycaemia. J Inherit Metab Dis. 2005;28(3):267-76. [Medline].

  2. Di Candia S, Gessi A, Pepe G, et al. Identification of a diffuse form of hyperinsulinemic hypoglycemia by 18-fluoro-L-3,4 dihydroxyphenylalanine positron emission tomography/CT in a patient carrying a novel mutation of the HADH gene. Eur J Endocrinol. Jun 2009;160(6):1019-23. [Medline].

  3. DePuy AM, Coassolo KM, Som DA, Smulian JC. Neonatal hypoglycemia in term, nondiabetic pregnancies. Am J Obstet Gynecol. May 2009;200(5):e45-51. [Medline].

  4. Tita AT, Landon MB, Spong CY, et al. Timing of elective repeat cesarean delivery at term and neonatal outcomes. N Engl J Med. Jan 8 2009;360(2):111-20. [Medline].

  5. Daly LP, Osterhoudt KC, Weinzimer SA. Presenting features of idiopathic ketotic hypoglycemia. J Emerg Med. Jul 2003;25(1):39-43. [Medline].

  6. [Guideline] Wight N, Marinelli KA. ABM clinical protocol #1: guidelines for glucose monitoring and treatment of hypoglycemia in breastfed neonates. Breastfeed Med. Autumn 2006;1(3):178-84. [Medline].

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Normal hypoglycemic counterregulation.
Interpretation of the critical sample.
 
 
 
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