Drug Guide

Generic Name

Technetium Tc-99m Sulfur Colloid

Brand Names Tesuloid, Technecoll, Technetium Tc 99m Tsc, An-sulfur Colloid

Classification

Therapeutic: Diagnostic imaging agent

Pharmacological: Radioisotope

FDA Approved Indications

  • Liver/spleen imaging to evaluate organ size, shape, and function
  • Gastric emptying studies
  • Lymphoscintigraphy

Mechanism of Action

Technetium-99m emits gamma radiation detectable by a gamma camera. When bound to sulfur colloid, it localizes in the reticuloendothelial system, particularly in the liver, spleen, and lymph nodes, allowing imaging of these structures.

Dosage and Administration

Adult: Typically 2-10 mCi administered intravenously, depending on the study and patient size.

Pediatric: Dosing varies based on age and weight; consult specific protocols.

Geriatric: Adjust dose as needed based on renal or hepatic function, similar to adult dosing.

Renal Impairment: Use with caution; may require dose adjustment depending on severity.

Hepatic Impairment: Use with caution; hepatic function may influence distribution.

Pharmacokinetics

Absorption: Not applicable (administration is intravenous).

Distribution: Localizes in liver, spleen, lymph nodes via reticuloendothelial system.

Metabolism: Metabolized by the reticuloendothelial system; radioactive decay is by physical half-life.

Excretion: Excreted via biliary and/or renal pathways, depending on organ uptake.

Half Life: Approximate physical half-life of 6 hours for Tc-99m.

Contraindications

  • Allergy to sulfur colloid or technetium-99m

Precautions

  • Use caution in pregnancy unless benefits outweigh risks, as radiation exposure may harm fetal development.
  • Ensure proper patient identification and radiation safety procedures.

Adverse Reactions - Common

  • Local injection site pain or swelling (Rare)
  • Transient nausea or allergic reaction (Rare)

Adverse Reactions - Serious

  • Radiation-induced tissue damage or allergic reactions (Very rare)

Drug-Drug Interactions

  • None specifically noted; however, interactions with other radiopharmaceuticals should be considered.

Drug-Food Interactions

  • No significant interactions

Drug-Herb Interactions

  • No known interactions

Nursing Implications

Assessment: Confirm patient identity, allergy status, and pregnancy status.

Diagnoses:

  • Risk for radiation injury
  • Impaired tissue perfusion

Implementation: Ensure proper preparation and administration per protocol, observe for immediate adverse reactions.

Evaluation: Monitor for adverse reactions post-administration; verify quality of imaging results.

Patient/Family Teaching

  • Explain that the procedure involves a small amount of radioactive material, which is generally safe but requires safety precautions.
  • Advise on minimal contact and handling of bodily fluids for a specified period after the procedure.
  • Inform about possible temporary side effects, such as mild discomfort at injection site.

Special Considerations

Black Box Warnings:

  • Radiation risk to fetus; pregnancy should be avoided in women of childbearing age unless absolutely necessary.

Genetic Factors: No specific genetic considerations reported.

Lab Test Interference: May interfere with certain lab tests measuring radiation-sensitive substances.

Overdose Management

Signs/Symptoms: Radiation sickness symptoms such as nausea, vomiting, or skin tingling may occur with overdose.

Treatment: Supportive care, symptomatic treatment, and possibly chelation if indicated; consult radiation safety protocols.

Storage and Handling

Storage: Store at room temperature away from light and moisture; radioactive material must comply with institutional and regulatory requirements.

Stability: Stable for use within shelf life; check expiration date and storage conditions before use.

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