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Clinical Trial
. 2015 Aug;100(8):2934-41.
doi: 10.1210/jc.2015-1682. Epub 2015 Jun 5.

Radiation Safety Precautions in (131)I Therapy of Graves' Disease Based on Actual Biokinetic Measurements

Affiliations
Clinical Trial

Radiation Safety Precautions in (131)I Therapy of Graves' Disease Based on Actual Biokinetic Measurements

Bin Liu et al. J Clin Endocrinol Metab. 2015 Aug.

Abstract

Context: Radiation protection is an integral part of targeted radionuclide therapy. How to offer rational radiation precautions to patients with Graves' disease (GD) undergoing (131)I therapy is still a matter of ongoing discussions.

Objective: The objective of the study was to formulate radiation precautions for GD patients undergoing (131)I therapy through actual biokinetic measurements for a particular population of patients.

Design: This was a prospective study.

Setting: The study was conducted at a university hospital.

Patients: From January 2009 through January 2012, consecutive GD patients prepared for (131)I therapy were prospectively recruited.

Main outcome measures: Pretherapy thyroid radioiodine uptake and uptake ratio (4 to 24 h radioiodine uptake) were measured. Serial whole-body dose-rate measurements after therapy were performed to deduce (131)I whole-body retention. Calculations based on deduced whole-body retention and measured thyroid radioiodine biokinetics were derived to determine the thyroidal and extrathyroidal compartment uptake fractions and effective half-lives. Precaution times necessary to avoid close contact with family members and the general public were derived from these parameters and regulatory dose limits.

Results: A total of 72 patients were eligible for the analysis. A high interpatient variability in (131)I biokinetics was observed: the mean peaking (131)I uptake (±1 SD) in the thyroid was 68% (±19%), and the range was 18%-89%; the mean effective (131)I half-life (±1 SD) in the remainder of the body was 5.1 (±0.9) hours (range 3.5-7.2 h). The mean measured initial dose rate (±1 SD) at 1.0 m after (131)I administration was 0.039 (±0.003) μSv·h(-1) · MBq(-1) (range 0.017-0.055 μSv·h(-1) · MBq(-1)). The 0.3:1.0 m initial dose rate ranged from 2.9 to 7.1, which was greatly lower than the projected ratio of 11.1 by the inverse square law approximation. On the basis of the measured radioiodine biokinetics and dose rates, detailed instructions were provided to limit nearby individuals' exposure.

Conclusion: The use of actual biokinetic measurements may remove the effect of variability errors associated with general default assumptions about the (131)I biokinetics in GD patients. The marked variability in (131)I biokinetics among GD patients reinforces the need for patient-specific iodine biokinetic measurements for radiation safety precautions.

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