Lantus (Insulin Glargine) Dosing and Administration for Diabetes Management
The recommended starting dosage of Lantus (insulin glargine) is 0.2 units/kg or up to 10 units once daily for insulin-naive patients with type 2 diabetes, and approximately one-third of the total daily insulin requirements for patients with type 1 diabetes. 1
Initial Dosing Recommendations
- For type 2 diabetes patients not currently on insulin therapy, start with 10 units or 0.1-0.2 units/kg of body weight once daily 2, 1
- For type 1 diabetes patients, total daily insulin requirements typically range from 0.4 to 1.0 units/kg/day, with 0.5 units/kg/day being typical for metabolically stable patients, with approximately 50% as basal insulin (Lantus) 3, 2
- For patients transitioning from NPH insulin once daily to Lantus, the recommended starting Lantus dosage is the same as the dosage of NPH that is being discontinued 1
- For patients transitioning from twice-daily NPH insulin to once-daily Lantus, the recommended starting Lantus dosage is 80% of the total NPH dosage that is being discontinued 1, 4
Administration Guidelines
- Administer Lantus subcutaneously once daily at any time of day, but at the same time every day to maintain stable blood glucose levels 5, 1
- Inject into the abdominal area, thigh, or deltoid, and rotate injection sites within the same region to reduce the risk of lipodystrophy 1
- Do not administer intravenously or via an insulin pump 1
- Do not dilute or mix Lantus with any other insulin or solution 1, 6
Dose Titration
- Increase the dose by 2-4 units every 3-4 days until fasting blood glucose reaches target range (80-130 mg/dL) 2, 7
- If fasting glucose is ≥180 mg/dL, consider increasing the dose by 4 units 2
- More aggressive titration can be used: increase by 0-2,4, or 6-8 units if mean fasting plasma glucose over the previous 3 days is ≥100-<120, ≥120-<140, ≥140-<180, or ≥180 mg/dL, respectively 7
- Patient self-titration (increasing insulin dose by 2 units every 3 days) has shown greater reductions in HbA1c compared to clinic-managed titration in some studies 7
Special Populations and Considerations
- For patients on enteral/parenteral feeding requiring insulin, a reasonable starting point is 10 units of insulin glargine every 24 hours 2
- For patients with higher risk of hypoglycemia, use the lower end of the dosing range (0.1 units/kg/day) 2
- In hospitalized elderly patients with diabetes, the starting insulin total daily dose should be reduced to 0.1–0.15 units/kg/day, given mainly as basal insulin 3
- For patients requiring high doses of insulin (>0.5 units/kg/day) with A1C remaining above target, consider advancing to combination injectable therapy with GLP-1 receptor agonists or multiple insulin doses 5
Important Clinical Considerations
- In patients with type 1 diabetes, Lantus must be used concomitantly with short-acting insulin to control postprandial glucose 1, 6
- Lantus provides a peakless profile with duration of action up to 24 hours, resulting in more stable glycemic control and fewer episodes of nocturnal hypoglycemia compared to NPH insulin 8, 6
- For patients experiencing hypoglycemia despite titration of once-daily Lantus, consider splitting the dose into a twice-daily regimen 9
- Increase the frequency of blood glucose monitoring during changes to insulin regimen to reduce the risk of hypoglycemia or hyperglycemia 1
- Concentrated formulations (U-300 glargine) are available for patients requiring larger doses, offering longer duration of action than U-100 formulations 5
Common Pitfalls to Avoid
- Delaying insulin therapy in patients not achieving glycemic goals can be harmful 2
- Not adjusting doses based on self-monitoring of blood glucose levels can lead to poor glycemic control 2
- Overbasalization (using higher than necessary basal insulin doses) can mask insufficient mealtime insulin coverage 5
- Failing to recognize that insulin requirements may change with weight changes, illness, or changes in physical activity 2
- Mixing Lantus with other insulins in the same syringe, which can alter its pharmacokinetic profile 1, 6