Insulin Detemir
Insulin Detemir
Generic Name
Insulin Detemir
Mechanism
- Insulin Detemir is a long‑acting basal insulin analogue that mimics endogenous basal insulin secretion.
- It contains a fatty‑acid (myristic acid) side‑chain that binds to albumin in the plasma, producing a slow, stable release of insulin over ≥24 h.
- By competing with glucagon and inhibiting hepatic gluconeogenesis, it lowers fasting glucose, while peripheral tissues (muscle, adipose) uptake glucose via the insulin receptor tyrosine‑kinase pathway.
- The albumin‑binding property gives Insulin Detemir a predictable, flat insulin curve with a lower peak‑to‑trough variability compared to older basal analogues.
Pharmacokinetics
| Parameter | Typical Value | Implications |
| Onset | 1–2 h | Useful for outpatient basal coverage. |
| Peak | Minimal (flat profile) | Reduces hypoglycemia risk. |
| Duration | ≥24 h (often 25–30 h) | Enables once‑daily dosing. |
| Half‑life | ~25 h | Allows dose adjustments without dramatic swings. |
| Metabolism | Hepatic de‑acylation → insulin & myristic acid | Minimal renal clearance. |
| Distribution | Albumin‑binding (≈95 %) | Contributes to flat action. |
• Food interaction: Large meals delay absorption by ~1 h; adjust carbohydrate counts accordingly.
Indications
- Type 1 diabetes mellitus requiring basal insulin to maintain fasting glycaemic control.
- Type 2 diabetes mellitus in patients needing basal insulin component of multiple daily injection (MDI) or basal‑bolus regimens.
- Gestational diabetes when long‑acting insulin is needed (use with caution; local guidelines preferred).
Contraindications
Contraindications
• Known hypersensitivity to insulin or detemir components.
Warnings
• Hypoglycaemia: Occasional asymptomatic episodes; caution in elderly, renal impairment, hepatic disease, or with concomitant sulfonylureas.
• Renal/Hepatic impairment: Use with caution; monitor for altered glucose homeostasis.
• Pregnancy: Use only if benefits outweigh risks; prefer human insulin analogues with more pregnancy data.
• Severe hepatic disease: May alter metabolism; start at low dose.
Dosing
- Initiation: 0.2 IU/kg/day (≈10 IU) once daily; dose adjusted to fasting capillary glucose 4–7 mmol/L (70–125 mg/dL).
- Adjustment: 2–4 IU increments every 2–3 days; aim for fasting glucose 5–7 mmol/L (90–125 mg/dL).
- Route: Subcutaneous injection; preferred sites: abdomen, thigh, or upper arm (avoid injection sites with lipohypertrophy).
- Timing: Administer at the same time each day; consistent with bedtime or waking routine.
- Special populations:
- *Elderly:* Titrate slower; watch for hypoglycemia.
- *Renal/hepatic impairment:* Start lower (≈0.1 IU/kg/day) and titrate cautiously.
Monitoring
- Self‑monitoring of blood glucose (SMBG): fasting, pre‑prandial, and bedtime.
- HbA1c: every 3–6 months or sooner if dose changes >10 %.
- Renal/hepatic panels: baseline and annually (or sooner if clinical concern).
- Weight: every visit (document changes >5 % as potential therapy issue).
- Electrolytes & serum insulin: if unexplained hypoglycaemia.
Clinical Pearls
- “Flat‑curve” advantage: Because Insulin Detemir has minimal peak action, it’s especially useful for patients prone to nocturnal hypoglycaemia; consider bedtime dosing.
- Albumin dependence: In hypoalbuminemia (e.g., nephrotic syndrome), the drug may dissociate more rapidly, shortening duration – monitor glucose closely.
- Combination with long‑acting GLP‑1 agonists: Can blunt weight gain; useful in obese type 2 patients when basal insulin alone is insufficient.
- Switching strategy: When transitioning from human basal insulin, maintain the same dose‑per‑day and titrate with a 1‑1 split between previous and detemir doses initially.
- Patient education: Encourage patients to note the exact time of injection; inconsistent timing can increase variability in glucose control.
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• *This drug card is intended for educational use by medical students and healthcare professionals and reflects current evidence-based practice as of 2026.*