Insulin

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Continuing Education Activity

Insulin is a medication used in the treatment and management of diabetes mellitus type-1 and sometimes diabetes mellitus type-2, both of which are significant risk factors for coronary artery disease, stroke, peripheral vascular disease, and a host of other vascular conditions. This activity reviews the indications, contraindications, activity, adverse events, and other key elements of Insulin therapy in the clinical setting related to the essential points needed by members of an interprofessional team managing the care of patients with diabetes and its related conditions and sequelae.

Objectives:

  • Outline the mechanism of action of insulin.

  • Review the adverse effects of insulin therapy.

  • Summarize the potential toxicity of insulin therapy.

  • Describe some interprofessional team strategies for improving care coordination and communication to decrease the complications of insulin therapy.

Indications

Insulin is a peptide hormone secreted in the body by beta cells of islets of Langerhans of the pancreas and regulates blood glucose levels. Medical treatment with insulin is indicated when there is inadequate production or increased insulin demands in the body.[1]

The FDA-approved indications for treatment with insulin are as follows.

Outpatient Indications for Insulin

Insulin is primarily used for the treatment of diabetes mellitus. According to the American Diabetes Association, in 2018, 34.2 million Americans, or 10.5% of the U.S. population, had diabetes. Approximately 90 to 95% of patients with diabetes have type 2 or insulin-resistant diabetes, 5 to 10% have type 1 diabetes, and 1 to 2% have maturity-onset of young diabetes (MODY).[2] 

  • In Type 1 or juvenile diabetes mellitus, pancreatic beta cells are destroyed by the body’s immune system or trauma or injury to the pancreas, leading to decreased or absent insulin production.[3] Patients with type-1 diabetes always require insulin.[4][5]
  • Type 2 diabetes mellitus is the most common type of diabetes and usually occurs after the age of 45 years. However, children and teens are also developing it more frequently, mainly due to childhood obesity. In type 2 diabetes, cells are resistant to the action of insulin. The exact cause of this is unknown, but factors such as genetics, obesity, metabolic syndrome, or sedentary lifestyle play a role. As the pancreas secretes more insulin to try to get glucose into the cells, they eventually burn out, and glucose starts building up in the blood. Treatment with insulin is necessary for the later stages of type 2 diabetes.[6][7]
  • Maturity onset diabetes of young (MODY) is an inherited condition in which beta cells of the pancreas cannot secrete insulin due to genetic mutation.[8] Patients are younger, healthy weight, without antibodies for islet cells of the pancreas, and have first-degree relatives with a similar type of diabetes. Insulin or sulfonylureas are treatment options.
  • Gestational diabetes mellitus (GDM): Approximately 4% of all pregnancies in the U.S. are complicated by GDM.[2] Screening for GDM is performed during 24 to 28 weeks of pregnancy, and initial treatment is with diet and exercise. Treatment is necessary to prevent complications of preeclampsia, macrosomia, and shoulder dystocia. When diet and exercise fail to control the blood sugar level, insulin is indicated.[9]

Inpatient Indications for Insulin

  • Management of diabetes mellitus patients in the hospital: Glycemic control in patients with type 1 and type 2 diabetes admitted to general wards for conditions other than diabetes is achievable with subcutaneous or intravenous insulin infusion. This therapeutic approach is to avoid hypoglycemia, hyperglycemia, volume depletion, or electrolyte abnormalities during hospitalization.[10]
  • Diabetic ketoacidosis (DKA) and hyperosmolar hyperglycemia (HHS) are complications of type 1 and type 2 diabetes, respectively, and both represent extremes in hyperglycemia. Insulin is indicated in both DKA and HHS to normalize blood glucose levels.[11][12]
  • Stress-related hyperglycemia: Hyperglycemia in non-diabetic critically ill patients, like ICU, surgical, or trauma patients, is managed by insulin. In stress, hormones like catecholamine, glucagon, growth hormones, cortisol, as well as glycogenolysis and gluconeogenesis, cause hyperglycemia related to poor outcomes in hospitalized patients. Therefore, insulin is used to maintain a blood glucose concentration of 140 to 180 mg/dl in these critically ill patients.[13]
  • Treatment of hyperkalemia: IV insulin is used to help manage hyperkalemia in hospitalized end-stage renal disease (ESRD) patients.[14][15]

Mechanism of Action

Insulin acts by directly binding to its receptors on the plasma membranes of the cells. These receptors are present on all the cells, but their density depends on the type of cells, with the maximum density being on the hepatic cells and adipocytes.

The insulin receptor is a heterotetrameric glycoprotein consisting of two subunits, the alpha and the beta subunits. The extracellular alpha subunits have insulin binding sites. The beta subunits, which are transmembranous, have tyrosine kinase activity.[16] When insulin binds to the alpha subunits, it activates the tyrosine kinase activity in the beta subunit, which causes the translocation of glucose transporters from the cytoplasm to the cell's surface.[17] These glucose transporters allow the influx of glucose from the blood into the cell, thus reducing blood glucose levels.[18]

Insulin causes the following effects in the cells[19]:

  • Hepatic cells: Promotes glycogenesis, inhibits gluconeogenesis
  • Adipocytes: Promotes lipogenesis, inhibits lipolysis
  • Muscle cells: Promotes glycogenesis and protein synthesis. Inhibits protein catabolism
  • Pancreatic beta cells: Inhibits glucagon release
  • Brain cells: Involved in appetite regulation

Depending on the duration of action, insulin is categorized as short-acting, intermediate-acting, and long-acting.

Rapid-acting insulins (lispro and aspart) start their action in 5 to 15 minutes and peak in 30 minutes. The duration of action is 3 to 5 hours. They are generally used before meals and are always used along with short-acting or long-acting insulins to control sugar levels throughout the day.

Short-acting (regular insulin) starts the action in 30 to 40 minutes and peaks in 90 to 120 minutes. The duration of action is 6 to 8 hours. Patients take these agents before meals, and food is necessary within 30 minutes after its administration to avoid hypoglycemia.

Intermediate-acting insulins (NPH) start the action in 1 to 4 hours and peak in 4 to 8 hours. Dosing is usually twice a day and helps maintain blood sugar levels throughout the day.

Long-acting insulins, such as glargine and detemir, start action in 1 to 2 hours. They provide a plateau effect over 12 to 24 hours. Dosing is usually during the night time after meals. Their long duration of action helps in reducing the frequency of dosing throughout the day.

Administration

Insulin administration can be via subcutaneous, intravenous, and intramuscular routes. The route of administration usually depends on the patient's condition and setting.

The subcutaneous route is the most widespread route of administration and is preferred by most patients due to its ease and convenience in administration. Patients use the subcutaneous route in the form of insulin syringes, pens, and pumps. It is an easy and convenient way for patients to self-administer.

Intravenous insulin is used in the hospital setting, especially when immediate and close monitoring of blood glucose levels is needed.[20] It is used in patients with diabetic ketoacidosis, hyperosmolar hyperglycemic state, severe hyperkalemia, beta-blocker toxicity, and calcium channel blocker toxicity. All of these cases require emergency treatment, and hence, intravenous insulin is used.

Intramuscular insulin use is rare and utilizes concentrated regular insulin. In 2014, the FDA approved an inhalable insulin formulation. It passes through the lungs and into the bloodstream and provides a rapid onset of action within 12 minutes. It can be taken by patients with diabetes type 1 and type 2 before meals. The insulin pump is a device that works like a natural pancreas. It replaces the need for long-acting insulin and continuously delivers small amounts of short-acting insulin to the body throughout the day.

Adverse Effects

Adverse effects of insulin are classified according to those caused by the drug itself and those caused by the specific route of administration. Hypoglycemia is, by far, the most common adverse effect of insulin therapy.[21] The other adverse effects of insulin therapy include weight gain and rarely electrolyte disturbances like hypokalemia, especially when used along with other drugs causing hypokalemia.

The subcutaneous route of administration also has adverse effects. Pain at the injection site and lipodystrophy at the injection site are the most common adverse effects of daily subcutaneous injections.[22] Other adverse effects like peripheral hyperinsulinemia and decreased compliance are also seen in the population using the subcutaneous route for insulin administration.

Somogyi effect: Some patients who take insulin before bed wake up with high blood sugar levels. This effect occurs when the insulin causes a hypoglycemic condition in the body, which activates hormones such as cortisol and adrenaline, resulting in rebound hyperglycemia; this can be corrected by reducing the dose of bedtime insulin or changing the time of insulin dosing.

Dawn phenomenon: It is the presence of high blood glucose levels in the body in the early hours of the day due to inadequate insulin in the body. To correct this phenomenon, the dose of bedtime insulin needs to increase to be able to keep the blood glucose levels under control throughout the night and the early hours of the morning.[23]

Contraindications

Though there are no absolute contraindications to insulin therapy, the dose of insulin needs to be adjusted and monitored in numerous settings.

  • Insulin dosing requires adjustment in patients with renal impairment and liver failure, as insulin metabolism occurs in the liver, excreted in the urine.
  • Insulin dose and blood glucose levels should be carefully monitored in patients with a history of hypoglycemic episodes.
  • Insulin should not be given with other drugs, which also cause hypokalemia, like diuretics.
  • Vomiting and diarrhea cause a hypokalemic state in the body, and clinicians and patients should exercise care when administering insulin as it also causes hypokalemia.
  • Insulin is also contraindicated in patients with cresol sensitivity, as insulin preparations contain cresol.

Monitoring

Insulin has a low therapeutic index, and blood glucose levels require regular monitoring to avoid adverse effects like hypoglycemia. Patient education should be provided about symptoms of hypoglycemia so that they can take immediate action when necessary. Monitoring for glucose levels is usually performed by fingerstick blood glucose test or glucose sensor device, both of which give instantaneous readings of blood glucose levels. Other tests, such as hemoglobin-A1c, can estimate glucose control over the past three months and enable insulin adjustment accordingly.

Toxicity

Insulin taken in large doses will cause symptoms of hypoglycemia in the patient. Some of these symptoms include headache, dizziness, palpitations, sweating, abdominal pain, and blurred vision. The immediate therapy for such patients is increasing the levels of glucose. In a conscious patient, this can be done by eating a high-energy bar or drinking a glass of glucose water. If the patient is unconscious, he needs to be hospitalized, given dextrose solution intravenously, and continuously monitors glucose levels.

Enhancing Healthcare Team Outcomes

Insulin is a widely used medicine in hospital settings for the management of hyperglycemia. Insulin is regarded as a high alert medication as its misuse is associated with significant risks such as hypoglycemia, and medical errors are common when using it in hospitals.[24][25] Deal et al. found that the most commonly reported errors were related to missed doses of insulin (25%), timing errors (22.7%), and missed documentation of doses (15.5% of patients).[26] These problems reveal several system errors that merit attention. Rousseau et al. identified various problems causing errors in the hospital use of insulin, such as frequent staff turnover, the involvement of various healthcare providers, none of which are specifically responsible for overall glycemic management, lack of perception of insulin as a “high alert medication,” rapidly evolving diabetes management and lack of education of staff on insulin management.[24] To minimize these errors following measures should be undertaken,

  • Availability of standardized protocols
  • Continuing education of providers
  • Communication between nurses on different shifts
  • Adequate communication between nurses, physicians, and pharmacists
  • Training professionals in insulin therapy of inpatients

Diabetes is a complex disease, and insulin is its most effective treatment. An interprofessional team approach is always essential for the management of diabetes in both outpatient as well as inpatient settings. When prescribing insulin in an outpatient setting, patient education is necessary regarding the disease, use, and side effects of insulin. A variety of healthcare professionals, such as dieticians, endocrinologists, exercise professionals, ophthalmologists, and podiatrists, should work with the patient under the coordination of the primary care providers to manage this disease. [Level 5]


Details

Editor:

Aelia Akbar

Updated:

7/10/2023 2:23:04 PM

References


[1]

Mathieu C, Gillard P, Benhalima K. Insulin analogues in type 1 diabetes mellitus: getting better all the time. Nature reviews. Endocrinology. 2017 Jul:13(7):385-399. doi: 10.1038/nrendo.2017.39. Epub 2017 Apr 21     [PubMed PMID: 28429780]


[2]

American Diabetes Association. Diagnosis and classification of diabetes mellitus. Diabetes care. 2009 Jan:32 Suppl 1(Suppl 1):S62-7. doi: 10.2337/dc09-S062. Epub     [PubMed PMID: 19118289]


[3]

Smith MJ, Simmons KM, Cambier JC. B cells in type 1 diabetes mellitus and diabetic kidney disease. Nature reviews. Nephrology. 2017 Oct 17:13(11):712-720. doi: 10.1038/nrneph.2017.138. Epub     [PubMed PMID: 29038537]


[4]

van Belle TL, Coppieters KT, von Herrath MG. Type 1 diabetes: etiology, immunology, and therapeutic strategies. Physiological reviews. 2011 Jan:91(1):79-118. doi: 10.1152/physrev.00003.2010. Epub     [PubMed PMID: 21248163]


[5]

DiMeglio LA, Evans-Molina C, Oram RA. Type 1 diabetes. Lancet (London, England). 2018 Jun 16:391(10138):2449-2462. doi: 10.1016/S0140-6736(18)31320-5. Epub     [PubMed PMID: 29916386]


[6]

Donner T, Muñoz M. Update on insulin therapy for type 2 diabetes. The Journal of clinical endocrinology and metabolism. 2012 May:97(5):1405-13. doi: 10.1210/jc.2011-2202. Epub 2012 Mar 22     [PubMed PMID: 22442275]


[7]

Howard-Thompson A, Khan M, Jones M, George CM. Type 2 Diabetes Mellitus: Outpatient Insulin Management. American family physician. 2018 Jan 1:97(1):29-37     [PubMed PMID: 29365240]


[8]

Anık A, Çatlı G, Abacı A, Böber E. Maturity-onset diabetes of the young (MODY): an update. Journal of pediatric endocrinology & metabolism : JPEM. 2015 Mar:28(3-4):251-63. doi: 10.1515/jpem-2014-0384. Epub     [PubMed PMID: 25581748]


[9]

Patti AM, Giglio RV, Pafili K, Rizzo M, Papanas N. Pharmacotherapy for gestational diabetes. Expert opinion on pharmacotherapy. 2018 Sep:19(13):1407-1414. doi: 10.1080/14656566.2018.1509955. Epub 2018 Aug 23     [PubMed PMID: 30136869]

Level 3 (low-level) evidence

[10]

American Diabetes Association. 15. Diabetes Care in the Hospital: Standards of Medical Care in Diabetes-2020. Diabetes care. 2020 Jan:43(Suppl 1):S193-S202. doi: 10.2337/dc20-S015. Epub     [PubMed PMID: 31862758]


[11]

Umpierrez G, Korytkowski M. Diabetic emergencies - ketoacidosis, hyperglycaemic hyperosmolar state and hypoglycaemia. Nature reviews. Endocrinology. 2016 Apr:12(4):222-32. doi: 10.1038/nrendo.2016.15. Epub 2016 Feb 19     [PubMed PMID: 26893262]


[12]

Thomovsky E. Fluid and Electrolyte Therapy in Diabetic Ketoacidosis. The Veterinary clinics of North America. Small animal practice. 2017 Mar:47(2):491-503. doi: 10.1016/j.cvsm.2016.09.012. Epub 2016 Dec 23     [PubMed PMID: 28017407]

Level 3 (low-level) evidence

[13]

Vanhorebeek I, Gunst J, Van den Berghe G. Critical Care Management of Stress-Induced Hyperglycemia. Current diabetes reports. 2018 Feb 26:18(4):17. doi: 10.1007/s11892-018-0988-2. Epub 2018 Feb 26     [PubMed PMID: 29479638]


[14]

Ahmed J, Weisberg LS. Hyperkalemia in dialysis patients. Seminars in dialysis. 2001 Sep-Oct:14(5):348-56     [PubMed PMID: 11679104]


[15]

Long B, Warix JR, Koyfman A. Controversies in Management of Hyperkalemia. The Journal of emergency medicine. 2018 Aug:55(2):192-205. doi: 10.1016/j.jemermed.2018.04.004. Epub 2018 May 3     [PubMed PMID: 29731287]


[16]

Kahn CR. The molecular mechanism of insulin action. Annual review of medicine. 1985:36():429-51     [PubMed PMID: 2986528]


[17]

Posner BI. Insulin Signalling: The Inside Story. Canadian journal of diabetes. 2017 Feb:41(1):108-113. doi: 10.1016/j.jcjd.2016.07.002. Epub 2016 Sep 7     [PubMed PMID: 27614806]


[18]

Jaldin-Fincati JR, Pavarotti M, Frendo-Cumbo S, Bilan PJ, Klip A. Update on GLUT4 Vesicle Traffic: A Cornerstone of Insulin Action. Trends in endocrinology and metabolism: TEM. 2017 Aug:28(8):597-611. doi: 10.1016/j.tem.2017.05.002. Epub 2017 Jun 8     [PubMed PMID: 28602209]


[19]

Wilcox G. Insulin and insulin resistance. The Clinical biochemist. Reviews. 2005 May:26(2):19-39     [PubMed PMID: 16278749]


[20]

Pérez A, Ramos A, Carreras G. Insulin Therapy in Hospitalized Patients. American journal of therapeutics. 2020 Jan/Feb:27(1):e71-e78. doi: 10.1097/MJT.0000000000001078. Epub     [PubMed PMID: 31833876]


[21]

Unger J, Parkin C. Hypoglycemia in insulin-treated diabetes: a case for increased vigilance. Postgraduate medicine. 2011 Jul:123(4):81-91. doi: 10.3810/pgm.2011.07.2307. Epub     [PubMed PMID: 21680992]

Level 3 (low-level) evidence

[22]

Radermecker RP, Piérard GE, Scheen AJ. Lipodystrophy reactions to insulin: effects of continuous insulin infusion and new insulin analogs. American journal of clinical dermatology. 2007:8(1):21-8     [PubMed PMID: 17298103]


[23]

Rybicka M, Krysiak R, Okopień B. The dawn phenomenon and the Somogyi effect - two phenomena of morning hyperglycaemia. Endokrynologia Polska. 2011:62(3):276-84     [PubMed PMID: 21717414]


[24]

Rousseau MP, Beauchesne MF, Naud AS, Leblond J, Cossette B, Lanthier L, Grondin F, Bernier F. An interprofessional qualitative study of barriers and potential solutions for the safe use of insulin in the hospital setting. Canadian journal of diabetes. 2014 Apr:38(2):85-9. doi: 10.1016/j.jcjd.2014.01.013. Epub     [PubMed PMID: 24690502]


[25]

Cohen MR. Pharmacists' role in ensuring safe and effective hospital use of insulin. American journal of health-system pharmacy : AJHP : official journal of the American Society of Health-System Pharmacists. 2010 Aug:67(16 Suppl 8):S17-21. doi: 10.2146/ajhp100173. Epub     [PubMed PMID: 20689148]


[26]

Deal EN, Liu A, Wise LL, Honick KA, Tobin GS. Inpatient insulin orders: are patients getting what is prescribed? Journal of hospital medicine. 2011 Nov:6(9):526-9. doi: 10.1002/jhm.938. Epub 2011 Oct 31     [PubMed PMID: 22042479]