Insulin, Regular

Category:

  • Miscellaneous

Description:

  • Antidiabetic agent

Indications:

  • Diabetes mellitus

  • Diabetic ketoacidosis

  • Hyperkalemia

  • Nutritional supplementation

Contraindications:

  • Hypoglycemia, porcine hypersensitivity (if from pork)

Precautions:

  • Pregnancy category B

  • Hypoglycemia related to dose

  • Renal impairment/failure, hepatic disease

Adverse Reactions (Side Effects):

  • anaphylactoid reactions, hyperinulinism, hypoglycemia, hypokalemia

  • reaction at injection site, insulin resistance, lipodystrophy, nausea, vomiting

  • pruritus, sinus tachycardia, urticaria

 

Dosage:

Administered subcutaneously, intramuscularly, and intravenously

  • Diabetes mellitus type I or diabetes type II inadequately managed by diet and oral hypoglycemics: 

    • Adult and child: 

      • SC range 0.1-2.5 units/kg/day; 

      • most patients require 0.5-1.2 units/kg/day.

  • Diabetic ketoacidosis: 

    • Adult: Initially, 0.1 unit/kg/hr continuous IV INF in addition to adequate fluid therapy (usually 0.9% NaCl at 1 L/hour for 2-3 hours, then 0.45% NaCl).  

    • When blood glucose reaches 250 mg/dl, fluid therapy should be changed to 5% dextrose in 0.45% NaCl, while IV INF of insulin is continued at roughly half the initial rate until acidosis is also corrected.

  • Child: 

    • Initially, 0.1 unit/kg IV BOLUS, followed by 0.1 unit/kg/hour (range 0.05-0.2 units/kg/hour) continuous IV INF until blood glucose reaches 250 mg/dl, at which time IV dextrose may be added while IV INF of insulin is continued until acidosis is also corrected.

  • Nutiritional supplement in neonates to optimize caloric intake while on parenteral nutrition:  

    • 0.01-0.1 units/kg/hour via continuous IV INF. (start at lower end of dosage range)

  • Hyperkalemia: 

    • Adult: 5-10 units IV in 50ml D50W over 5 minutes

Subcutaneous Dosing:

  • Individualize dosage based on careful monitoring of blood glucose and other clinical parameters.

  • Administer 30 minutes prior to a meal

  • Inject into upper thighs, upper arms, buttocks, or abdomen.  Inject over 2-4 seconds.

 

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Approved for public release; Distribution is unlimited.

The information contained here is an abbreviated summary. For more detailed and complete information, consult the manufacturer's product information sheets or standard textbooks.

Source: Operational Medicine 2001, Health Care in Military Settings, NAVMED P-5139, May 1, 2001, Bureau of Medicine and Surgery, Department of the Navy, 2300 E Street NW, Washington, D.C., 20372-5300.

Bureau of Medicine and Surgery
Department of the Navy
2300 E Street NW
Washington, D.C
20372-5300

Operational Medicine
 Health Care in Military Settings
CAPT Michael John Hughey, MC, USNR
NAVMED P-5139
  January 1, 2001

United States Special Operations Command
7701 Tampa Point Blvd.
MacDill AFB, Florida
33621-5323

*This web version is provided by The Brookside Associates, LLC.  It contains original contents from the official US Navy NAVMED P-5139, but has been reformatted for web access and includes advertising and links that were not present in the original version. The medical information presented was reviewed and felt to be accurate in 2001. Medical knowledge and practice methods may have changed since that time. Some links may no longer be active. This web version has not been approved by the Department of the Navy or the Department of Defense. The presence of any advertising on these pages does not constitute an endorsement of that product or service by either the US Department of Defense or the Brookside Associates. The Brookside Associates is a private organization, not affiliated with the United States Department of Defense.

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