Drug Guide
Insulin degludec
Classification
Therapeutic: Antidiabetic agent
Pharmacological: Long-acting insulin
FDA Approved Indications
- Management of blood glucose in adults and children with diabetes mellitus
Mechanism of Action
Insulin degludec is an ultra-long-acting basal insulin that lowers blood glucose by facilitating cellular glucose uptake and inhibiting hepatic glucose production. It forms multi-hexamers upon injection, creating a depot that releases insulin slowly and steadily over time.
Dosage and Administration
Adult: Dosage varies based on individual needs; typically once daily by subcutaneous injection at the same time each day.
Pediatric: Dosage must be individualized based on patient response and blood glucose monitoring.
Geriatric: Use with caution in elderly patients; adjust dose based on renal function and risk of hypoglycemia.
Renal Impairment: Adjust dose as needed; closely monitor blood glucose levels.
Hepatic Impairment: Use with caution; hepatic impairment can alter insulin requirements.
Pharmacokinetics
Absorption: Absorbed slowly with a duration of action exceeding 24 hours.
Distribution: Distributed throughout the body; insulin binds to insulin receptors.
Metabolism: Metabolized locally at the site of injection and by hepatic enzymes.
Excretion: Primarily metabolized to inactive compounds, excreted via urine.
Half Life: Approximately 25 hours, providing a steady basal level.
Contraindications
- Hypoglycemia
- Allergy to insulin degludec or excipients
Precautions
- Use with caution in patients with hypoglycemia unawareness, hepatic or renal impairment, or during illness or stress. Monitor blood glucose frequently.
Adverse Reactions - Common
- Hypoglycemia (Common)
- Injection site reactions (Less common)
Adverse Reactions - Serious
- Severe hypoglycemia (Serious and requires immediate attention)
- Anaphylaxis (Rare)
Drug-Drug Interactions
- Other antidiabetic agents, corticosteroids,beta-blockers, diuretics
Drug-Food Interactions
- Alcohol may enhance hypoglycemia
Drug-Herb Interactions
N/ANursing Implications
Assessment: Monitor blood glucose levels regularly; assess for signs and symptoms of hypoglycemia and hyperglycemia.
Diagnoses:
- Risk for unstable blood glucose levels.
- Ineffective tissue perfusion (related to hypoglycemia or hyperglycemia)
Implementation: Administer subcutaneously at scheduled times; educate patient on injection technique.
Evaluation: Assess blood glucose and HbA1c levels periodically to evaluate treatment efficacy.
Patient/Family Teaching
- Administer insulin as prescribed, understanding the importance of consistent timing.
- Recognize symptoms of hypoglycemia and hyperglycemia.
- Carry quick-acting carbohydrate sources for hypoglycemia episodes.
- Maintain regular follow-up appointments.
Special Considerations
Black Box Warnings:
- Severe hypoglycemia can occur; patients should be closely monitored, especially during initiation or dose changes.
Genetic Factors: Pharmacogenomics may influence insulin sensitivity.
Lab Test Interference: None known.
Overdose Management
Signs/Symptoms: Severe hypoglycemia with rapid onset, potentially leading to loss of consciousness or seizures.
Treatment: Administer immediate carbohydrate intake; in severe cases, administer IV glucose or glucagon as per protocol.
Storage and Handling
Storage: Store unopened vials or pens in the refrigerator (2°C to 8°C). Once in use, can be kept at room temperature (up to 25°C) for up to 8 weeks.
Stability: Stable under recommended storage conditions; avoid freezing and direct sunlight.