Drug Guide
Iodixanol
Classification
Therapeutic: Diagnostic radiocontrast agent
Pharmacological: Iso-osmolar nonionic radiocontrast medium
FDA Approved Indications
- X-ray imaging of blood vessels and the urinary tract
- Computed tomography (CT) imaging
Mechanism of Action
Iodixanol enhances the contrast of blood vessels and organs during imaging procedures by increasing the attenuation of X-rays in the contrast-filled areas, providing better visualization.
Dosage and Administration
Adult: Dosing based on the type of procedure and patient weight; administered intravenously. Administer as prescribed by the physician.
Pediatric: Dosing customized based on weight and age, by protocol and physician discretion.
Geriatric: Use with caution, considering renal function and cardiovascular status.
Renal Impairment: Adjust dose or consider alternative imaging if renal impairment is present.
Hepatic Impairment: No specific dose adjustments established.
Pharmacokinetics
Absorption: Not absorbed orally; administered intravenously for imaging.
Distribution: Distributes within the extracellular fluid compartments.
Metabolism: Not metabolized; remains unchanged.
Excretion: Primarily excreted unchanged via the kidneys.
Half Life: Approximately 2 hours in patients with normal renal function.
Contraindications
- Known hypersensitivity to iodixanol or other contrast media.
- Previous allergic reactions to contrast agents.
Precautions
- Use with caution in patients with renal impairment, asthma, multiple myeloma, or allergies to iodine.
- Monitor renal function before and after administration.
- Premedicate in patients with known contrast hypersensitivity if indicated.
Adverse Reactions - Common
- Nausea (Common)
- Warm flushing sensation (Common)
- Headache (Common)
Adverse Reactions - Serious
- Anaphylactic reactions (Rare)
- Contrast-induced nephropathy (Moderate to high risk in susceptible patients)
Drug-Drug Interactions
- Other nephrotoxic drugs (e.g., aminoglycosides, NSAIDs)
- Beta-blockers and other drugs affecting renal function
Drug-Food Interactions
N/ADrug-Herb Interactions
N/ANursing Implications
Assessment: Evaluate allergy history, renal function, and hydration status before administration.
Diagnoses:
- Risk for allergic reaction
- Risk for renal impairment
Implementation: Administer as ordered, monitor for adverse reactions, ensure hydration.
Evaluation: Assess for adverse reactions and changes in renal function post-administration.
Patient/Family Teaching
- Report any allergic reactions such as rash, itching, or difficulty breathing.
- Inform about the importance of remaining well-hydrated before and after the procedure.
- Notify healthcare providers of any previous reactions to contrast media.
Special Considerations
Black Box Warnings:
- Risk of allergic reactions, including anaphylaxis.
- Risk of contrast-induced nephropathy, especially in patients with pre-existing renal impairment.
Genetic Factors: No specific genetic factors known.
Lab Test Interference: May interfere with thyroid function tests shortly after administration.
Overdose Management
Signs/Symptoms: Symptoms of overdose may include persistent nausea, vomiting, or allergic reactions.
Treatment: Supportive care; discontinue contrast, treat allergic reactions if present, ensure renal function is supported.
Storage and Handling
Storage: Store at room temperature, away from light and moisture.
Stability: Stable under recommended storage conditions.