Insulin Pump During Exercise

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Introduction[edit | edit source]

Insulin pump therapy, also known as continuous subcutaneous insulin infusion (CSII), is one of the most significant advances in diabetes technology in the last 50 years. Although the first commercial insulin pumps were available in the 1970s, rapid adoption of insulin pump technology did not occur until the early 2000s, following the completion of the landmark Diabetes Control and Complications Trial (DCCT) in the early 1990s. The DCCT established the value of intensive insulin therapy in maintaining tight glycemic control and preventing diabetic complications such as retinopathy, neuropathy, nephropathy, and cardiovascular disease. [1]

Pump use carries many pros for individuals with diabetes who are physically active. However, it may come with a few disadvantages.[2]

How insulin pump works[edit | edit source]

An insulin pump is a small, computerised device that constantly delivers rapid-acting insulin via a small catheter placed into the subcutaneous tissue and adhered to the skin (referred to as an "infusion set" or "infusion cannula"). The infusion set is connected to the pump via plastic tubing in most insulin pumps, and insulin is infused from the pump through the tubing to the infusion set cannula and into the subcutaneous tissue. Some pumps, known as "patch pumps," do not use tubes and instead stick to the skin directly. Patch pumps, which are programmed from a remote device, use wireless technology to deliver insulin through the infusion cannula. Insulin pumps often use insulin formulations that are rapid acting (i.e., insulin lispro, aspart, or glulisine). The FDA has cleared lispro and aspart for use in a pump insulin reservoir for up to 144 hours, but glulisine should be replaced every 48 hours due to the risk of crystallisation. Regular insulin is also FDA-approved for use in pumps and, due to its lower cost, is occasionally used instead of rapid-acting versions. Concentrated insulins (e.g., U200 or U500), dilute insulins (e.g., U50 or U10), and ultra-rapid-acting insulin analogues (e.g., Fiasp) are being researched but have not yet been approved by the FDA for use in pumps.Insulin pumps deliver insulin in two ways: continuously infusing rapid-acting insulin throughout the day and night (basal) and discrete, one-time doses of rapid-acting insulin administered by the user for meals or high blood glucose correction (bolus). hysiology, developmental life stage (i.e., puberty or growth), activity level, time of day, and sleep schedule are all factors that influence basal insulin requirements. Insulin pumps administer basal insulin in 0.01 unit/hour increments and allow for different rates of basal infusion throughout the day and night to improve glycemic control and individualise therapy, emulating nondiabetes physiology.

Pros for using insulin pump[edit | edit source]

  • Insulin pump therapy allows for more precise and flexible insulin dosing with fewer injections. Many individuals with type 1 diabetes mellitus report using insulin pump because they want improved glycemic control and a more flexible lifestyle.
  • Many studies and systemic reviews have demonstrated improved glycemic control and a reduction in hypoglycemia with insulin pump therapy in pediatric and adult populations with type 1 diabetes.
  • Parental satisfaction with insulin therapy is high.
  • Many advantages to managing unpredictable eating habits and low insulin requirements in the youngest children suggesting that insulin pump therapy may be an ideal option for many young children with type 1 diabetes and their families.

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References[edit | edit source]

  1. Berget C, Messer LH, Forlenza GP. A clinical overview of insulin pump therapy for the management of diabetes: past, present, and future of intensive therapy. Diabetes Spectrum. 2019 Aug 1;32(3):194-204.
  2. Colberg SR, Sigal RJ, Yardley JE, Riddell MC, Dunstan DW, Dempsey PC, Horton ES, Castorino K, Tate DF. Physical activity/exercise and diabetes: a position statement of the American Diabetes Association. Diabetes care. 2016 Nov 1;39(11):2065-79.