What should be the starting dose of insulin glargine (Lantus), the insulin‑to‑carbohydrate ratio, and the correction factor for a 23‑year‑old woman with type 2 diabetes, weight 122 kg (BMI 41 kg/m²) receiving an intravenous insulin infusion of 6.5 U per hour?

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Transition from IV Insulin Infusion to Subcutaneous Basal‑Bolus Therapy

For a 23‑year‑old woman (122 kg, BMI 41) receiving 6.5 U/h IV insulin, initiate subcutaneous insulin with approximately 78 U insulin glargine (Lantus) once daily plus 26 U rapid‑acting insulin before each of three meals, administered 2–4 hours before stopping the IV infusion. 1, 2

Calculating the Total Daily Subcutaneous Dose

  • Base the subcutaneous total daily dose (TDD) on the IV insulin infusion rate during the prior 6–8 hours when stable glycemic control was achieved. 1
  • For an infusion rate of 6.5 U/h over 24 hours, the total IV insulin delivered is 156 U/day (6.5 U/h × 24 h). 1
  • Use 100 % of the 24‑hour IV insulin amount as the initial subcutaneous TDD (156 U/day), because this patient demonstrates severe insulin resistance requiring higher doses. 1, 2

Basal Insulin (Lantus) Dosing

  • Allocate 50 % of the TDD to basal insulin: 156 U ÷ 2 = 78 U insulin glargine once daily. 1, 2
  • Administer the basal dose 2–4 hours before discontinuing the IV insulin infusion to prevent rebound hyperglycemia and recurrent ketoacidosis. 1, 3
  • Continue the IV insulin for 1–2 hours after the subcutaneous basal injection to ensure adequate absorption. 1, 3
  • Give Lantus at 20:00 h (8 PM) as the preferred daily injection time to align with transition protocols. 2

Prandial (Rapid‑Acting) Insulin Dosing

  • Allocate the remaining 50 % of the TDD to prandial insulin: 156 U ÷ 2 = 78 U total prandial, divided equally among three meals = 26 U before each meal. 1, 2
  • Use a rapid‑acting analog (lispro, aspart, or glulisine) administered 0–15 minutes before meals. 1, 2

Carbohydrate‑to‑Insulin Ratio (Carb Ratio)

  • Calculate the insulin‑to‑carbohydrate ratio (ICR) using the formula: 450 ÷ TDD. 2
  • For a TDD of 156 U: 450 ÷ 156 = ≈ 2.9 g carbohydrate per 1 U insulin (round to 1 U per 3 g carbohydrate). 2
  • This ratio means the patient requires 1 U of rapid‑acting insulin for every 3 g of carbohydrate consumed. 2
  • Adjust the ICR if post‑prandial glucose consistently misses the target of <180 mg/dL. 2

Correction Factor (Insulin Sensitivity Factor)

  • Calculate the insulin sensitivity factor (ISF) using the formula: 1500 ÷ TDD for regular insulin or 1700 ÷ TDD for rapid‑acting analogs. 2
  • For rapid‑acting insulin with TDD of 156 U: 1700 ÷ 156 = ≈ 11 mg/dL per 1 U insulin. 2
  • This means 1 U of rapid‑acting insulin will lower blood glucose by approximately 11 mg/dL. 2
  • Correction dose = (Current glucose – Target glucose) ÷ ISF. 2
  • For example, if pre‑meal glucose is 250 mg/dL and target is 125 mg/dL: (250 – 125) ÷ 11 = ≈ 11 U correction dose, added to the scheduled prandial dose. 2

Simplified Correction Scale (Alternative)

  • Add 2 U rapid‑acting insulin for pre‑meal glucose >250 mg/dL. 1, 2
  • Add 4 U rapid‑acting insulin for pre‑meal glucose >350 mg/dL. 1, 2
  • These correction doses are in addition to the scheduled 26 U prandial dose, not a replacement. 1, 2

Monitoring Requirements During Transition

  • Check capillary glucose before each meal and at bedtime (minimum four times daily). 1, 2
  • Measure fasting glucose daily to guide basal insulin titration. 1, 2
  • Obtain 2‑hour post‑prandial glucose after each meal to assess prandial adequacy and guide carb ratio adjustments. 2
  • Monitor serum potassium every 2–4 hours during the transition, as insulin drives potassium intracellularly. 1, 3

Basal Insulin Titration Protocol

  • Increase Lantus by 2 U every 3 days if fasting glucose is 140–179 mg/dL. 1, 2
  • Increase Lantus by 4 U every 3 days if fasting glucose is ≥180 mg/dL. 1, 2
  • Target fasting glucose: 80–130 mg/dL. 1, 2
  • If unexplained hypoglycemia occurs (glucose <70 mg/dL), reduce the basal dose by 10–20 % immediately. 1, 2

Prandial Insulin Titration Protocol

  • Adjust each meal dose by 1–2 U (or 10–15 %) every 3 days based on the 2‑hour post‑prandial glucose reading. 1, 2
  • Target post‑prandial glucose: <180 mg/dL. 1, 2

Critical Threshold for Basal Insulin Escalation

  • When basal insulin approaches 0.5–1.0 U/kg/day (61–122 U for this patient), stop further basal escalation and intensify prandial insulin instead to avoid "over‑basalization" with increased hypoglycemia risk. 1, 2
  • Clinical signals of over‑basalization include basal dose >0.5 U/kg/day, bedtime‑to‑morning glucose drop ≥50 mg/dL, hypoglycemia episodes, and high glucose variability. 2

Hypoglycemia Management

  • Treat any glucose <70 mg/dL immediately with 15 g fast‑acting carbohydrate, recheck in 15 minutes, and repeat if needed. 1, 2
  • Never administer rapid‑acting insulin at bedtime as a sole correction dose, as this markedly raises nocturnal hypoglycemia risk. 1, 2

Adjunctive Therapy Considerations

  • Continue metformin at maximum tolerated dose (up to 2,000–2,550 mg/day) unless contraindicated, as this combination reduces total insulin requirements by 20–30 %. 2
  • Discontinue sulfonylureas when initiating basal‑bolus insulin to avoid additive hypoglycemia risk. 2

Common Pitfalls to Avoid

  • Do not stop the IV insulin infusion without first overlapping with subcutaneous basal insulin administered 2–4 hours earlier—this is the most common cause of recurrent diabetic ketoacidosis. 1, 3
  • Do not use sliding‑scale insulin as monotherapy; correction doses must supplement a scheduled basal‑bolus regimen. 1, 2
  • Do not continue escalating basal insulin beyond 0.5–1.0 U/kg/day without addressing post‑prandial hyperglycemia, as this leads to over‑basalization with increased hypoglycemia and suboptimal control. 1, 2

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Initial Dosing for Lantus (Insulin Glargine) in Patients Requiring Insulin Therapy

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2026

Guideline

Diabetic Ketoacidosis Treatment Guidelines

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2026

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This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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