Drug Guide

Generic Name

Iodixanol

Brand Names Visipaque 270, Visipaque 320

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/A

Drug-Herb Interactions

N/A

Nursing 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.

This guide is for educational purposes only and is not intended for clinical use.