Converting Insulin Infusion to Divided Subcutaneous Doses
To convert from IV insulin infusion to subcutaneous insulin, calculate the total 24-hour IV insulin dose, then give 50% as long-acting basal insulin (glargine or detemir) once daily in the evening, and divide the remaining 50% equally among three meals as rapid-acting insulin (aspart, lispro, or glulisine). 1
Step-by-Step Conversion Algorithm
Step 1: Calculate Total Daily Insulin Requirement
- Determine the total amount of IV insulin infused over the past 24 hours 1
- Use the infusion rate from the final 6-8 hours of the IV infusion for the most accurate calculation 2
- Example: If infusing 2 units/hour × 24 hours = 48 units total daily dose
Step 2: Divide Into Basal and Bolus Components
Basal insulin (long-acting):
- Give 50% of the 24-hour IV insulin total as basal insulin (glargine/Lantus or detemir/Levemir) 1
- Administer as a single dose in the evening 1
- Example: 48 units ÷ 2 = 24 units of glargine once daily
Bolus insulin (rapid-acting):
- Give the remaining 50% of the 24-hour IV insulin total, divided by 3, as rapid-acting insulin before each meal 1
- Use aspart (Novolog), lispro (Humalog), or glulisine before breakfast, lunch, and dinner 1
- Example: 48 units ÷ 2 = 24 units ÷ 3 = 8 units before each meal
Step 3: Timing of Transition
- Administer the first dose of basal insulin 2 hours before discontinuing the IV insulin infusion 2
- Continue IV insulin until the basal insulin has time to begin working 2
- Give the first rapid-acting insulin dose with the next meal after transition 1
Step 4: Adjust for Nutritional Status
- If the patient has insufficient caloric intake or is NPO, reduce both basal and bolus doses by 50% 1
- Resume full doses when normal oral intake resumes 1
Alternative Dosing Strategies Based on Evidence
Higher Conversion Ratios
Research suggests that using 80% of the total daily IV insulin requirement as basal insulin may achieve better glycemic control in the first 24 hours compared to 40-60% conversion 2. However, the guideline-recommended 50% split remains the standard approach 1.
Weight-Based Approach
- An alternative is 0.5 units/kg of basal insulin for patients transitioning from IV insulin 3
- This approach may result in higher basal doses but has shown similar safety profiles 3
- The percentage-based method (50% of TDI) remains more widely validated 1, 2
Monitoring and Titration
Initial Monitoring
- Check capillary blood glucose before each meal and at bedtime 1, 2
- Monitor for hypoglycemia, especially in the first 24-48 hours 2, 3
Dose Adjustments
- For fasting hyperglycemia: Increase basal insulin by 2 units every 3 days until fasting glucose reaches target 1
- For post-prandial hyperglycemia: Increase the corresponding meal's rapid-acting insulin by 1-2 units or 10-15% 1
- For hypoglycemia: Reduce the corresponding insulin dose by 10-20% if no clear precipitating cause is identified 1, 4
Common Pitfalls and How to Avoid Them
Pitfall 1: Using Unstable Infusion Rates
- Avoid calculating from periods of rapidly changing insulin requirements 2
- Use the most recent 6-8 hours of stable infusion rates for calculation 2
Pitfall 2: Inadequate Overlap Time
- Failure to overlap IV and subcutaneous insulin leads to hyperglycemic gaps 2
- Always give basal insulin 2 hours before stopping IV insulin 2
Pitfall 3: Not Adjusting for NPO Status
- Continuing full doses in NPO patients causes severe hypoglycemia 1
- Reduce both basal and bolus by 50% when caloric intake is insufficient 1
Pitfall 4: Overlooking Insulin Resistance
- Patients with high BMI or on medications like steroids may need higher doses 4, 5
- Consider starting at 0.3 units/kg for basal insulin in insulin-resistant patients 5
Special Populations
Type 1 Diabetes
- Always maintain basal insulin coverage to prevent diabetic ketoacidosis 1, 4
- Resume the patient's usual basal-bolus regimen at hospital doses 1
Type 2 Diabetes on Oral Agents
- Continue metformin if renal function permits (eGFR >30 mL/min for most agents, >60 mL/min for metformin) 1
- Consider gradually reducing rapid-acting insulin as oral agents resume effect 1