insulin aspart(redirected from Novomix 30)
Also found in: Dictionary.
insulin aspart(in-su-lin as-spart) ,
insulin aspart protamine suspension/insulin aspart injection mixture,
NovoLOG Mix 70/30(trade name),
Novomix 30(trade name)
Pregnancy Category: B (insulin aspart)
Pregnancy Category: C (insulin aspart protamine suspension/insulin aspart injection mixtures)
Control of hyperglycemia in patients with type 1 or type 2 diabetes mellitus.
Lowers blood glucose by :
- stimulating glucose uptake in skeletal muscle and fat,
- inhibiting hepatic glucose production.
Other actions of insulin:
- inhibition of lipolysis and proteolysis,
- enhanced protein synthesis.
A rapid-acting insulin with more rapid onset and shorter duration than human regular insulin; should be used with an intermediate- or long-acting insulin.
Control of hyperglycemia in diabetic patients.
Absorption: Rapid acting.
Distribution: Identical to endogenous insulin.
Metabolism and Excretion: Metabolized by liver, spleen, kidney, and muscle.
Half-life: Approximately 60–90 min.
Time/action profile (hypoglycemic effect)
|Subcut||within 15 min||1–2 hr||3–4 hr|
Contraindicated in: Hypoglycemia; Allergy or hypersensitivity to insulin aspart.
Use Cautiously in: Stress and infection, which may temporarily ↑ insulin requirements; Renal/hepatic impairment (may ↓ insulin requirements); Must be used with a longer-acting insulin in patients with type 1 diabetes; Concomitant use with pioglitazone or rosiglitazone (↑ risk of fluid retention and worsening HF) Obstetric: May temporarily ↑ insulin requirements; Pediatric: Children <6 yr (safety not established).
Adverse Reactions/Side Effects
- hypoglycemia (life-threatening)
- allergic reactions including anaphylaxis (life-threatening)
Drug-Drug interactionBeta blockers and clonidine may mask some of the signs and symptoms of hypoglycemia.Corticosteroids, thyroid supplements, estrogens, isoniazid, niacin,phenothiazines, and rifampin may ↑ insulin requirements.Alcohol, ACE inhibitors, MAO inhibitors, octreotide, oral hypoglycemic agents, and salicylates, may ↓ insulin requirements.Concurrent use with pioglitazone or rosiglitazone may ↑ risk of fluid retention and worsening HFGlucosamine may worsen blood glucose control.Fenugreek, chromium, and coenzyme Q-10 may produce additive hypoglycemic effects.
Subcutaneous (Adults and Children) Determined by needs of the patients; generally 0.5–1 units/kg/day total. 50–70% may be given as insulin aspart, and the remainder as intermediate- or long-acting insulin. May also be given via subcutaneous infusion pump; initial programming based on total daily dose of insulin given in previous regimen with 50% of total daily dose given as premeal boluses and 50% of total daily dose given as basal infusion; dose can then be adjusted based on response.
Insulin aspart: 100 units/mL in 10-mL vials and 3-mL PenFill cartidges for use with NovoPen 4 Insulin Delivery Devices and NovoFine disposable needles
Insulin aspart protamine suspension/insulin aspart injection mixture: 70% insulin aspart protamine suspension and 30% insulin aspart injection—NovoLog Mix 70/30 100 units/mL in 10-mL vials and 3-mL disposable delivery devices
- Assess for symptoms of hypoglycemia (anxiety; restlessness; tingling in hands, feet, lips, or tongue; chills; cold sweats; confusion; cool, pale skin; difficulty in concentration; drowsiness; nightmares or trouble sleeping; excessive hunger; headache; irritability; nausea; nervousness; tachycardia; tremor; weakness; unsteady gait)and hyperglycemia (confusion, drowsiness; flushed, dry skin; fruit-like breath odor; rapid, deep breathing, polyuria; loss of appetite; nausea; vomiting; unusual thirst) during therapy.
- Monitor body weight periodically. Changes in weight may necessitate changes in insulin dose.
- Lab Test Considerations: Monitor blood glucose every 6 hr during therapy, more frequently in ketoacidosis and times of stress. A1C may be monitored every 3–6 mo to determine effectiveness. Overdose is manifested by symptoms of hypoglycemia. Mild hypoglycemia may be treated by ingestion of oral glucose. Severe hypoglycemia is a life-threatening emergency; treatment consists of IV glucose, glucagon, or epinephrine.
Potential Nursing DiagnosesNoncompliance (Patient/Family Teaching)
- high alert: Medication errors involving insulins have resulted in serious patient harm and death. Clarify all ambiguous orders and do not accept orders using the abbreviation “u” for units, which can be misread as a zero or the numeral 4 and has resulted in tenfold overdoses. Insulins are available in different types and strengths. Check type, dose, and expiration date with another licensed nurse. Do not interchange insulins without consulting physician or other health care professional.
- Do not confuse Novolog with Novolin.
- Due to the short duration of action, insulin aspart must be used with a longer-acting insulin or insulin infusion pump therapy.
- Check type, species source, dose, and expiration date with another licensed nurse. Do not interchange insulins without consulting physician or other health care professional.
- Use only insulin syringes to draw up dose. The unit markings on the insulin syringe must match the insulin's units/mL.
- When mixing insulins, draw insulin aspart into syringe first to avoid contamination of regular insulin vial. Administer immediately after mixing. Do not mix with crystalline zinc insulin preparations.
- Insulin aspart should be refrigerated, but do not freeze or administer solution if it has been frozen. Cartridges or vials may be kept at room temperature for up to 28 days if kept from excessive heat and sunlight. Do not use if cloudy, discolored, or unusually viscous. Never use the PenFill cartridge after the expiration date on the PenFill cartridge or on the box.
- Because of the short duration of insulin aspart, supplementation with longer-acting insulin is usually necessary to control blood glucose levels.
- Subcutaneous: Administer insulin aspart subcut in the abdominal wall, thigh, or upper arm within 5–10 min before a meal. Rotate injection sites.
- When used in pumps: Change the solution in the reservoir at least every 6 days, change the infusion set, and the infusion set insertion site at least every 3 days. Do not mix with other insulins or with a diluent when used in the pump.
- pH: 7.2–7.6.
- Intravenous: May be given IV in selected clinical situations under appropriate medical supervision. Diluent: Dilute with 0.9% NaCl or D5W in infusion systems using polypropylene infusion bags. Concentration: 0.05–1 unit/mL.
- May be administered via disposable external insulin pump. Do not administer solution that appears thickened, cloudy, discolored, or contains particles. Store cartridges for pump in refrigerator. Do not mix with other insulins or solutions when used with pump. Choose a new infusion site every 48 hr. Discard cartridges after 7 days, even if solution remains.
- Instruct patient on proper technique for administration. Include type of insulin, equipment (syringe, cartridge pens, external pumps, alcohol swabs), storage, and place to discard syringes. Discuss the importance of not changing brands of insulin or syringes, selection and rotation of injection sites, and compliance with therapeutic regimen. Caution patient that insulin pens should not be shared with others, even if clean needles are used.
- Demonstrate technique for mixing insulins by drawing up insulin aspart first and rolling intermediate-acting insulin vial between palms to mix, rather than shaking (may cause inaccurate dose).
- Explain to patient that this medication controls hyperglycemia but does not cure diabetes. Therapy is long term.
- Instruct patient in proper testing of serum glucose and ketones. These tests should be closely monitored during periods of stress or illness and health care professional notified of significant changes.
- Emphasize the importance of compliance with nutritional guidelines and regular exercise as directed by health care professional.
- Advise patient to notify health care professional of all Rx or OTC medications, vitamins, or herbal products being taken and to consult with health care professional before taking other medications.
- Advise patient to notify health care professional of medication regimen prior to treatment or surgery.
- Advise patient to notify health care professional if nausea, vomiting, or fever develops, if unable to eat regular diet, or if blood sugar levels are not controlled.
- Instruct patient on signs and symptoms of hypoglycemia and hyperglycemia and what to do if they occur.
- Advise patient to notify health care professional if pregnancy is planned or suspected or if breastfeeding or planning to breastfeed.
- Patients with diabetes mellitus should carry a source of sugar (candy, glucose gel) and identification describing their disease and treatment regimen at all times.
- Emphasize the importance of regular follow-up, especially during first few weeks of therapy.
- Control of blood glucose levels in diabetic patients without hypoglycemic or hyperglycemic episodes.
A rapid-acting insulin analog whose amino acid sequence differs from that of human insulin by the substitution of aspartic acid for proline in the B chain, used in the treatment of type 1 and type 2 diabetes.
a rapid-acting analog of human insulin created by recombinant DNA technology, in which an aspartate residue has been substituted for the usual proline at position 28 on the insulin B chain. It is administered subcutaneously for the treatment of diabetes mellitus.
A rapidly acting insulin administered subcutaneously, with action similar to that of insulin lispro. Aspartic acid replaces proline at a crucial position in the insulin molecule.
See also: insulin