MKSAP quiz: Management of new type 1 diabetes
This month's quiz asks readers to manage recent hypoglycemia in a 21-year-old woman diagnosed 3 months ago with type 1 diabetes after presenting to the emergency department with diabetic ketoacidosis.
A 21-year-old woman is evaluated for management of type 1 diabetes. She was diagnosed 3 months ago after presenting to the emergency department with diabetic ketoacidosis. Her HbA1c level at the time of diagnosis was 15.2%. She was discharged from the hospital on a basal and prandial insulin regimen with minor adjustments required as an outpatient. Her blood glucose log demonstrates a recent change manifesting as frequent symptomatic episodes of both fasting and postprandial hypoglycemia with blood glucose levels ranging from 50 to 65 mg/dL (2.8 to 3.6 mmol/L). Medications are insulin glargine and insulin aspart.
On physical examination, blood pressure is 110/70 mm Hg and pulse rate is 70/min. BMI is 19. The remainder of the examination is unremarkable. HbA1c level is 6.2%.
Which of the following is the most appropriate management for this patient's hypoglycemia?
A. Decrease insulin glargine, decrease insulin aspart
B. Decrease insulin glargine, decrease insulin aspart, add pramlintide
C. Discontinue insulin glargine, change insulin aspart to a sliding-scale regimen
D. Discontinue insulin glargine, discontinue insulin aspart
MKSAP Answer and Critique
The correct answer is A. Decrease insulin glargine, decrease insulin aspart. This item is available to MKSAP 17 subscribers as item 83 in the Endocrinology & Metabolism section. More information about MKSAP 17 is available online.
The most appropriate management for this patient's hypoglycemia is to decrease insulin glargine and insulin aspart. The glucose toxicity present at the time of diabetic ketoacidosis has diminished with an intensive insulin regimen. Her remaining functional pancreatic beta cells have regained the ability to produce some insulin in the “honeymoon” phase, which explains the hypoglycemia on previously well-tolerated doses of insulin. The decreased need for insulin will not be long term as pancreatic beta cells continue to be destroyed over the course of type 1 diabetes. Continuing insulin, even at low doses, is recommended during the “honeymoon” phase in order to preserve beta cell function as long as possible by reducing the metabolic stress on these cells. The low-dose insulin regimen can consist of a basal and prandial insulin combination or a basal insulin regimen. She is experiencing symptomatic postprandial and fasting hypoglycemia. Decreasing the insulin aspart and insulin glargine doses would address the prandial and fasting hypoglycemia, while also still providing low-dose insulin to protect the functioning beta cells. She will require close monitoring of her blood glucose levels to determine when insulin doses should be increased as she nears the end of the “honeymoon” phase. The “honeymoon” period may persist for several weeks to months.
Meal-time insulin doses are generally reduced by 50% when pramlintide is initiated due to the risk of hypoglycemia. The addition of pramlintide would likely exacerbate the current issue of hypoglycemia even with reduction of meal-time insulin.
The use of sliding-scale insulin without basal insulin is discouraged. When sliding-scale insulin is used without basal insulin, the likelihood of wide swings from hyperglycemia to hypoglycemia increases. Without a basal insulin regimen, she may not consistently receive daily insulin to decrease the metabolic stress on her functioning pancreatic beta cells.
Discontinuation of both insulin glargine and insulin aspart increases metabolic stress on the pancreatic beta cells and accelerates the loss of functional cells producing insulin. As pancreatic beta cell function declines toward the end of the “honeymoon” phase, the risk of diabetic ketoacidosis increases without any exogenous insulin.
Key Point
- Continuing insulin, even at low doses, is recommended during the “honeymoon phase” of type 1 diabetes mellitus to reduce metabolic stress on functioning beta cells and preserve any residual function for as long as possible.