Drug Guide
Diatrizoate meglumine and diatrizoate sodium
Classification
Therapeutic: Diagnostic radiocontrast agent
Pharmacological: Iodinated contrast media
FDA Approved Indications
- X-ray and CT imaging of the gastrointestinal tract, urinary tract, blood vessels, and other diagnostic procedures where iodine contrast enhancement is necessary
Mechanism of Action
Increases radiopacity of bodily structures by blocking X-rays, allowing detailed imaging. It contains iodine, which absorbs X-ray photons, enhancing contrast on radiologic images.
Dosage and Administration
Adult: Dose varies depending on the procedure, typically 30-100 mL via IV or oral routes; consult specific protocols.
Pediatric: Doses are weight and age-dependent; consult pediatric dosing guidelines.
Geriatric: Use with caution; start with lower doses due to risk of renal impairment.
Renal Impairment: Adjust doses and ensure adequate hydration; avoid in severe impairment.
Hepatic Impairment: No specific adjustments generally needed.
Pharmacokinetics
Absorption: Minimal systemic absorption when used intra-luminally; rapid absorption when administered intravenously.
Distribution: Distributes in blood and tissues subject to extracellular fluid volume.
Metabolism: Not metabolized; excreted unchanged.
Excretion: Primarily via kidneys in urine.
Half Life: Approximately 2 hours, but varies with renal function.
Contraindications
- Known hypersensitivity to iodine or contrast media.
- Thyroid dysfunction.
Precautions
- Use with caution in patients with asthma, renal impairment, or dehydration. Pre-procedure hydration recommended. Monitor thyroid function in susceptible patients.
Adverse Reactions - Common
- Taste disturbance, nausea, vomiting (Common)
- Warm sensation during injection (Common)
Adverse Reactions - Serious
- Anaphylactic shock (Rare)
- Nephrotoxicity (Uncommon in high doses or in renal impairment)
- Thyroid dysfunction, including hypothyroidism or hyperthyroidism (Rare)
Drug-Drug Interactions
- Medications that are nephrotoxic (e.g., aminoglycosides, NSAIDs)
- Medications affecting thyroid function
Drug-Food Interactions
N/ADrug-Herb Interactions
N/ANursing Implications
Assessment: Assess for allergies, renal function, thyroid status, and hydration.
Diagnoses:
- Risk for renal impairment
- Allergy risk
Implementation: Ensure proper hydration, monitor vital signs and renal function post-procedure, and observe for adverse reactions.
Evaluation: Monitor for adverse reactions, renal function, and patient's response to imaging.
Patient/Family Teaching
- Inform about possible warm sensation or taste changes during administration.
- Report any allergic reactions, chest pain, difficulty breathing.
- Maintain hydration before and after the procedure.
Special Considerations
Black Box Warnings:
- Risk of allergic reactions including anaphylaxis.
Genetic Factors: Thyroid disease may influence response.
Lab Test Interference: Can cause interference with thyroid function tests.
Overdose Management
Signs/Symptoms: Signs of overdose may include significant renal impairment, allergy, or adverse cardiovascular effects.
Treatment: Manage symptoms supportively; ensure hydration; provide emergency treatment for allergic reactions.
Storage and Handling
Storage: Store at room temperature, protect from light.
Stability: Stable under recommended storage conditions.