Calculating the Insulin Infusion Rate
The prescribed insulin dose is weight-based at
0.1 units/kg/h. For a patient weighing
58 kg, the required hourly dose is calculated as:
0.1 units/kg/h × 58 kg = 5.8 units/h
The pharmacy-prepared solution contains
50 units of regular insulin diluted in
100 mL of 0.9% sodium chloride. This yields a concentration of:
50 units ÷ 100 mL = 0.5 units/mL
To deliver
5.8 units/h using a solution with
0.5 units/mL, the infusion pump rate is:
5.8 units/h ÷ 0.5 units/mL = 11.6 mL/h
Key point! Always confirm the concentration on the pharmacy label before programming the pump. A common error is using the total volume (100 mL) as the hourly rate, which would deliver the entire 50 units in one hour — a massive overdose. The correct rate reflects only the dose needed per hour.
Watch out! In DKA, regular insulin is given as a continuous intravenous infusion because its short half-life allows rapid titration. The infusion is typically continued until the anion gap closes and blood glucose stabilizes, not simply until glucose normalizes. Frequent blood glucose monitoring (usually hourly) guides rate adjustments.
| Calculation Step | Formula | Result |
|---|
| Hourly insulin dose | 0.1 units/kg/h × 58 kg | 5.8 units/h |
| Solution concentration | 50 units ÷ 100 mL | 0.5 units/mL |
| Infusion pump rate | 5.8 units/h ÷ 0.5 units/mL | 11.6 mL/h |
The 2024 ADA/EASD consensus report on hyperglycemic crises emphasizes that intravenous regular insulin should be administered as a continuous infusion, with the initial rate based on weight and adjusted according to serial glucose and ketone measurements
[1]. The dosing approach in this question —
0.1 units/kg/h — aligns with the guideline-recommended starting range for adult DKA management. Accurate pump programming is a direct nursing responsibility that prevents both under-treatment (persistent ketosis) and over-treatment (hypoglycemia, hypokalemia).
References (research sources)
- [1]
Hyperglycemic Crises in Adults With Diabetes: A Consensus Report.GuidelineUmpierrez GE, Davis GM, ElSayed NA, Fadini GP, Galindo RJ, Hirsch IB, Klonoff DC, McCoy RG, Misra S, Gabbay RA, Bannuru RR, Dhatariya KK. (2024) · DOI: 10.2337/dci24-0032