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=== Symptomatic patients ===
=== Symptomatic patients ===
The goal is to maintain plasma glucose concentrations >70 mg/dL.<ref name="pmid23730298">{{cite journal| author=Avatapalle HB, Banerjee I, Shah S, Pryce M, Nicholson J, Rigby L et al.| title=Abnormal Neurodevelopmental Outcomes are Common in Children with Transient Congenital Hyperinsulinism. | journal=Front Endocrinol (Lausanne) | year= 2013 | volume= 4 | issue=  | pages= 60 | pmid=23730298 | doi=10.3389/fendo.2013.00060 | pmc=3657691 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=23730298  }}</ref>
The goal is to maintain plasma glucose concentrations >70 mg/dL.<ref name="pmid23730298">{{cite journal| author=Avatapalle HB, Banerjee I, Shah S, Pryce M, Nicholson J, Rigby L et al.| title=Abnormal Neurodevelopmental Outcomes are Common in Children with Transient Congenital Hyperinsulinism. | journal=Front Endocrinol (Lausanne) | year= 2013 | volume= 4 | issue=  | pages= 60 | pmid=23730298 | doi=10.3389/fendo.2013.00060 | pmc=3657691 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=23730298  }}</ref>
 
*Guidelines developed by the American Academy of Pediatrics suggest aggresive treatment in these patients because of the neurodevelopmental impairment associated:<ref name="pmid25819173">{{cite journal| author=Stanley CA, Rozance PJ, Thornton PS, De Leon DD, Harris D, Haymond MW et al.| title=Re-evaluating "transitional neonatal hypoglycemia": mechanism and implications for management. | journal=J Pediatr | year= 2015 | volume= 166 | issue= 6 | pages= 1520-5.e1 | pmid=25819173 | doi=10.1016/j.jpeds.2015.02.045 | pmc=4659381 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=25819173  }}</ref>
Guidelines developed by the American Academy of Pediatrics suggest aggresive treatment in these patients because of the neurodevelopmental impairment associated:<ref name="pmid25819173">{{cite journal| author=Stanley CA, Rozance PJ, Thornton PS, De Leon DD, Harris D, Haymond MW et al.| title=Re-evaluating "transitional neonatal hypoglycemia": mechanism and implications for management. | journal=J Pediatr | year= 2015 | volume= 166 | issue= 6 | pages= 1520-5.e1 | pmid=25819173 | doi=10.1016/j.jpeds.2015.02.045 | pmc=4659381 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=25819173  }}</ref>
**Who are less than 48 hours of life with plasma glucose levels <50 mg/dL 
**Who are less than 48 hours of life with plasma glucose levels <50 mg/dL 
**Who are greater than 48 hours of life with plasma glucose levels <60 mg/dL
**Who are greater than 48 hours of life with plasma glucose levels <60 mg/dL

Revision as of 15:14, 25 August 2017

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Mohammed Abdelwahed M.D[2]

Overview

Medical treatment of hypoglycemia depends on the severity of symptoms and the cause. If asymptomatic, repeating the measurement in short time and avoiding critical tasks. Twenty grams is usually sufficient to raise the blood glucose Severe in symptomatic patients. Subcutaneous or intramuscular injection or 25% dextrose intravenously. If postprandial hypoglycemia, patient should have frequent small meals or snacks and foods should be high in fiber, avoiding foods high in sugar. Surgery is the best treatment for insulinoma.

Medical Therapy

Asymptomatic:[1] 

Asymptomatic patients have blood glucose of ≤70 mg/dL with regular monitoring without any symptoms. Protective measurements should be done to prevent prgression such as:

  • Repeating the measurement in short time
  • Avoiding critical tasks
  • Ingestion of carbohydrates
  • Adjusting the regimen to avoid other attacks

Symptomatic:[2]

Severe: 

  • A subcutaneous or intramuscular injection of 0.5 to 1.0 mg of glucagon will correct hypoglycemia within 15 minutes.
  • If failed this attempt or in severe cases, 25% or 50% dextrose intravenously (IV) followed by subcutaneous glucose.
  • If these measures aren't available:
  • Squeezing a glucose gel in the space between the teeth and buccal mucosa with patient head tilted on side to prevent aspiration.
  • If glucose gel isn't available, putting table sugar under the tongue may save patient.[3]
  • Hypoglycemia due to hormone deficiencies such as hypopituitarism or adrenal insufficiency usually ceases when the appropriate hormone is replaced.
  • Patients with diabetes history who has loss of consciousness and there is no method to determine nature of coma; hypoglycemia or hyperglycemia,then glucose should be given empirically. This will correct hypoglycemia and will not be particularly dangerous if blood glucose concentration is high.
  • Intranasal glucagon was effective in treating insulin-induced hypoglycemia in adults with type 1 diabetes in some studies but it is still under investigation.[4]

Postprandial hypoglycemia

  • Frequent (every three hours) small meals or snacks.
  • Patient should use foods high in fiber, avoiding foods high in sugar.
  • Regular exercise regimen have been recommended.

Insulinoma

Surgery is the best treatment for insulinoma and other pancreatic masses but if multiple metastases or bad general condition medical therapy is accepted:

Neonatal hypoglycemia

Goal is to prevent neurologic complications of neonatal hypoglycemia.

Manangement differs between symptomatic and asymptomatic patients:

Symptomatic patients

The goal is to maintain plasma glucose concentrations >70 mg/dL.[7]

  • Guidelines developed by the American Academy of Pediatrics suggest aggresive treatment in these patients because of the neurodevelopmental impairment associated:[8]
    • Who are less than 48 hours of life with plasma glucose levels <50 mg/dL 
    • Who are greater than 48 hours of life with plasma glucose levels <60 mg/dL
    • Asymptomatic patients at risk for hypoglycemia or in patients in whom a low glucose concentration was identified as an incidental laboratory finding:
    • Who are less than 4 hours of life with plasma glucose levels <25 to 40 mg/dl.[9]
    • Who are between 4 and 24 hours of life with plasma glucose <35 to 45 mg/dl.
    • Who are between 24 and 48 hours of life with plasma glucose levels <45 to 50 mg/dl.[10]
    • Who are greater than 48 hours of life with plasma glucose levels <60 mg/dl.
    • In newborns with a suspected or confirmed genetic hypoglycemia disorder (such as a family history of a hypoglycemia disorder or physical exam features consistent with Beckwith-Wiedemann syndrome)
  • Intravenous bolus of 200 mg/kg dextrose is given over 5 m followed by the continuous administration of parenteral dextrose infusion at a rate of 6 to 8 mg/kg of dextrose per minute. [11]
  • Therapy should be initiated while awaiting laboratory confirmation of low blood glucose levels.[12]
  • The maximum rate of infusion for treatment is the maximum amount of fluids that neonate can deal with.
  • Dextrose at a concentration of 12.5 percent or less can be infused through an umbilical arterial catheter.
  • Patient's fluid should be monitored for volume overload or hyponatremia, diuretics may be indicated if volume overload ocurred.
  • Other interventions should be considered if the glucose infusion rate is 12 mg/kg per minute with non-responsive patients:
  • When the glucose concentration is stabilized, oral glucose is used by tapering for 4 days but the blood glucose level should be monitored.

Asymptomatic patients

The goal of management is to normalize patients blood glucose levels and prevent them from becoming symptomatic

Oral feeds

Guidelines from the American Association of Pediatrics recommend that oral feeding should be given as quickly as possible for asymptomatic patients: [15]

  • Blood glucose concentrations should be measured frequently starting 20 to 30 minutes after the initial and subsequent feedings
  • Plasma glucose levels should be greater than 50 to 60 mg/dL to prevent neurological sequales[16]
  • Infants less than 4 hours of age with plasma glucose <25 mg/dL
  • If plasma glucose concentration fails to increase, parenteral glucose is administered. If the plasma glucose increases to above 25 mg/dL, oral feedings should continue every two to three hours with preprandial measurements of plasma glucose concentration
  • Infants between 4 and 24 hours of age and with plasma glucose <35 mg/dL
  • If plasma glucose level fails to increase, parenteral glucose is administered. If the plasma glucose increases to above 35 mg/dL, oral feedings should continue every two to three hours with preprandial measurements of plasma glucose concentration.
  • If a patient becomes symptomatic or if plasma glucose fails to increase above 45 mg/dL after three oral feedings, then parenteral glucose should be given.

References

  1. Cryer PE (2009). "Preventing hypoglycaemia: what is the appropriate glucose alert value?". Diabetologia. 52 (1): 35–7. doi:10.1007/s00125-008-1205-7. PMID 19018509.
  2. Seaquist ER, Anderson J, Childs B, Cryer P, Dagogo-Jack S, Fish L; et al. (2013). "Hypoglycemia and diabetes: a report of a workgroup of the American Diabetes Association and the Endocrine Society". Diabetes Care. 36 (5): 1384–95. doi:10.2337/dc12-2480. PMC 3631867. PMID 23589542.
  3. Graz B, Dicko M, Willcox ML, Lambert B, Falquet J, Forster M; et al. (2008). "Sublingual sugar for hypoglycaemia in children with severe malaria: a pilot clinical study". Malar J. 7: 242. doi:10.1186/1475-2875-7-242. PMC 2605470. PMID 19025610.
  4. Rickels MR, Ruedy KJ, Foster NC, Piché CA, Dulude H, Sherr JL; et al. (2016). "Intranasal Glucagon for Treatment of Insulin-Induced Hypoglycemia in Adults With Type 1 Diabetes: A Randomized Crossover Noninferiority Study". Diabetes Care. 39 (2): 264–70. doi:10.2337/dc15-1498. PMC 4722945. PMID 26681725.
  5. Hirshberg B, Cochran C, Skarulis MC, Libutti SK, Alexander HR, Wood BJ; et al. (2005). "Malignant insulinoma: spectrum of unusual clinical features". Cancer. 104 (2): 264–72. doi:10.1002/cncr.21179. PMC 4136659. PMID 15937909.
  6. Aparicio T, Ducreux M, Baudin E, Sabourin JC, De Baere T, Mitry E; et al. (2001). "Antitumour activity of somatostatin analogues in progressive metastatic neuroendocrine tumours". Eur J Cancer. 37 (8): 1014–9. PMID 11334727.
  7. Avatapalle HB, Banerjee I, Shah S, Pryce M, Nicholson J, Rigby L; et al. (2013). "Abnormal Neurodevelopmental Outcomes are Common in Children with Transient Congenital Hyperinsulinism". Front Endocrinol (Lausanne). 4: 60. doi:10.3389/fendo.2013.00060. PMC 3657691. PMID 23730298.
  8. Stanley CA, Rozance PJ, Thornton PS, De Leon DD, Harris D, Haymond MW; et al. (2015). "Re-evaluating "transitional neonatal hypoglycemia": mechanism and implications for management". J Pediatr. 166 (6): 1520–5.e1. doi:10.1016/j.jpeds.2015.02.045. PMC 4659381. PMID 25819173.
  9. Committee on Fetus and Newborn. Adamkin DH (2011). "Postnatal glucose homeostasis in late-preterm and term infants". Pediatrics. 127 (3): 575–9. doi:10.1542/peds.2010-3851. PMID 21357346.
  10. Adamkin DH, Polin RA (2016). "Imperfect Advice: Neonatal Hypoglycemia". J Pediatr. 176: 195–6. doi:10.1016/j.jpeds.2016.05.051. PMID 27297210.
  11. Stanley CA, Rozance PJ, Thornton PS, De Leon DD, Harris D, Haymond MW; et al. (2015). "Re-evaluating "transitional neonatal hypoglycemia": mechanism and implications for management". J Pediatr. 166 (6): 1520–5.e1. doi:10.1016/j.jpeds.2015.02.045. PMC 4659381. PMID 25819173.
  12. Cornblath M, Schwartz R (1999). "Outcome of neonatal hypoglycaemia. Complete data are needed". BMJ. 318 (7177): 194–5. PMC 1114678. PMID 9888932.
  13. Hawdon JM, Aynsley-Green A, Ward Platt MP (1993). "Neonatal blood glucose concentrations: metabolic effects of intravenous glucagon and intragastric medium chain triglyceride". Arch Dis Child. 68 (3 Spec No): 255–61. PMC 1590376. PMID 8466259.
  14. Miralles RE, Lodha A, Perlman M, Moore AM (2002). "Experience with intravenous glucagon infusions as a treatment for resistant neonatal hypoglycemia". Arch Pediatr Adolesc Med. 156 (10): 999–1004. PMID 12361445.
  15. Committee on Fetus and Newborn. Adamkin DH (2011). "Postnatal glucose homeostasis in late-preterm and term infants". Pediatrics. 127 (3): 575–9. doi:10.1542/peds.2010-3851. PMID 21357346.
  16. Rozance PJ, Hay WW (2006). "Hypoglycemia in newborn infants: Features associated with adverse outcomes". Biol Neonate. 90 (2): 74–86. doi:10.1159/000091948. PMID 16534190.