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This document provides information for parents or family caregivers who are caring for children undergoing treatment for neuroblastoma with 131I-MIBG, including safety instructions and guidelines
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How to fill out 131i-mibg
How to fill out 131I-MIBG
01
Gather all required materials including 131I-MIBG vial, syringes, and safety equipment.
02
Ensure that the area is well-ventilated and that all safety protocols are in place.
03
Verify the patient's identity and confirm the doctor's order for the 131I-MIBG treatment.
04
Clean the injection site on the patient with an antiseptic wipe.
05
Draw the prescribed dose of 131I-MIBG into the syringe, ensuring not to touch the needle.
06
Check for air bubbles in the syringe and expel them carefully if present.
07
Administer the injection slowly into the specified site and apply gentle pressure afterward.
08
Dispose of all used materials in accordance with radioactive waste disposal guidelines.
09
Monitor the patient for any immediate reactions post-injection.
Who needs 131I-MIBG?
01
Patients with certain types of neuroendocrine tumors, such as pheochromocytomas or neuroblastomas.
02
Individuals who have overexpressed adrenergic receptors and require targeted radiotherapy.
03
Patients with metastatic disease that has not responded to other treatments.
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What is the I 131 MIBG treatment?
I-131 MIBG is administered to a child through an intravenous line and absorbed by tumor cells. This therapy destroys tumors while sparing normal, healthy tissue. I-131 MIBG is well tolerated. The major side effect of therapy is low blood counts.
What is a MIBG scan in English?
An MIBG scan is a nuclear imaging test that helps healthcare providers diagnose and assess neuroendocrine tumors. Your provider injects a radioactive tracer, called iodine meta-iodobenzylguanidine (MIBG), into your bloodstream. A special camera detects the tracer and takes images inside your body.
What is the I-131 MIBG treatment?
I-131 MIBG is administered to a child through an intravenous line and absorbed by tumor cells. This therapy destroys tumors while sparing normal, healthy tissue. I-131 MIBG is well tolerated. The major side effect of therapy is low blood counts.
What is the difference between MIBG 123 and 131?
Iodine-123 has 13 hours of half-life and allows imaging up to 48 hours. Iodine-131 is only used when iodine-123 is not available. The higher energy photons emitted by iodine-131 render it inferior to iodine-123 because of higher dose it gives to patients 9.
What is I-123 MIBG used for?
I-123 MIBG scintigraphy is an imaging test used to detect certain types of neuroendocrine tumors. Neuroendocrine tumors detected with this scan include neuroblastomas, paragangliomas and pheochromocytomas.
What is the difference between MIBG 131 and 123?
Iodine-123 has 13 hours of half-life and allows imaging up to 48 hours. Iodine-131 is only used when iodine-123 is not available. The higher energy photons emitted by iodine-131 render it inferior to iodine-123 because of higher dose it gives to patients 9.
What is the difference between I-123 and i-131?
The 2 most frequently used radiotracers for thyroid tissue scans are I-123 and I-131. The primary differences between the 2 radiotracers are: I-123 has a half-life of approximately 13 hours, decays by gamma emission, and delivers superior image quality.
What is 131i in the thyroid?
Radioiodine therapy is a nuclear medicine treatment. Doctors use it to treat an overactive thyroid, a condition called hyperthyroidism. They also may use it to treat thyroid cancer.
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What is 131I-MIBG?
131I-MIBG (Iodine-131 Metaiodobenzylguanidine) is a radioactive compound used primarily in the diagnosis and treatment of certain types of neuroendocrine tumors, particularly neuroblastoma and pheochromocytoma.
Who is required to file 131I-MIBG?
Healthcare facilities and professionals administering 131I-MIBG treatments or diagnostic procedures are required to file appropriate documentation related to the use of this radioactive substance.
How to fill out 131I-MIBG?
Filling out 131I-MIBG forms typically involves providing patient information, details about the procedure, dosage administered, and the administering physician's details. It's essential to follow specific guidelines provided by the regulatory body.
What is the purpose of 131I-MIBG?
The purpose of 131I-MIBG is to provide targeted radiation therapy for certain types of cancer, allowing for the destruction of tumor cells while minimizing damage to surrounding healthy tissue.
What information must be reported on 131I-MIBG?
The information that must be reported on 131I-MIBG includes the patient's medical history, indications for use, dose administered, route of administration, monitoring observations, and any adverse reactions.
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