VEHS > resources > radiation safety > radiation safety manuals
| Vanderbilt University Online Radiation Safety Policies & Procedures Manual | ![]() |
| Table of Contents |
|
< Section 2: Obtaining Authorization to Use Radioactive Material |
Section 4: Policies and General Procedures for Radioactive Material Use > |
Section 3: Personnel Monitoring
The State of Tennessee requires monitoring of individuals' radiation exposure if it is expected that a person will receive a dose in excess of 10%. The annual occupational dose limits for an adult radiation worker are given in Table 1:
| Table 1: Occupational Dose Limits for Adults | |
| Description | Dose Limit |
| Whole Body | 5,000 mrem/yr (50 mSv/yr) |
| Skin | 50,000 mrem/yr (500 mSv/yr) |
| Extremity | 50,000 mrem/yr (500 mSv/yr) |
| Any organ other than the lens of the eye | 50,000 mrem/yr (500 mSv/yr) |
| Lens of the eye | 15,000 mrem/yr (150 mSv/yr) |
The annual occupational dose limits for minors are 10% of the limits for adult radiation workers. Therefore, minors have a whole body occupational dose limit of 500 mrem/yr (5 mSv/yr). Radiation badges are required if an individual is expected to receive 10% of the applicable limit, for minors this corresponds to 50 mrem/yr (0.5 mSv/yr). All minors who work with sources of ionizing radiation or in a laboratory using radioactive material are require to wear a dosimeter.
The dose limit for an embryo/fetus of a declared pregnant woman is 500 mrem (5 mSv) for the entire gestation period and the dose should not exceed 50 mrem/month (0.5 mSv/month). These limits can only be enforced if the pregnancy is declared. A declared pregnant woman is defined as a woman who has voluntarily informed her employer in writing of her pregnancy and the estimated date of conception. Declaration forms and counseling are available from VEHS, the VEHS web site www.safety.vanderbilt.edu, or Occupational Health Services. The pregnancy declaration form must be submitted to Occupational Health Services.
Permanent copies of personnel dosimetry records are maintained by VEHS. Copies are also distributed monthly to the various departmental badge representatives.
VEHS will issue radiation badges commensurate with the type of ionizing radiation being used. Radiation badges are issued to workers who are likely to exceed 10% of the occupational dose limits. Workers may work with radioactive material and not be issued a radiation badge. Radiation badges will be issue based on the following: 1) VEHS analysis of potential radiation exposure, 2) the type of radiation emitted from the radioactive material, 3) the quantity of radioactive material handled, and 4) the handling time. Badge applications may be obtained from VEHS, the VEHS web site www.safety.vanderbilt.edu, or the badge representative. Permanent records of personnel exposures are maintained by VEHS. Employees can review and discuss their radiation exposure records with VEHS staff.
C. Responsibilities for Personnel Dosimeter Users
1. Thyroid Monitoring Requirements for Unsealed Sources of Radioiodine
Before handling quantities of radioiodine exceeding 10% of the values given in Table 2 an individual must have a baseline thyroid bioassay. A thyroid bioassay is required when an individual handles unsealed quantities of radioiodine that exceed those shown in Table 2. The thyroid bioassay must be performed within ten days after handling the radioiodine.
| Table 2: Thyroid Bioassay Requirements | ||
| Type of Operations | Volatile Form | Bound to Nonvolatile Agent |
| Processes on open bench, with possible escape of iodine from process vessels | 1 mCi (37 MBq) | 10 mCi (370 MBq) |
| Processes carried out in adequate fume hood | 10 mCi (370 MBq) | 100 mCi (3.7 GBq) |
Note: Quantities are considered to be the cumulative amount in processes handled by a worker during a 3 month period. Capsules (such as gelatin capsules given to patients for diagnostic tests) may be considered to contain radioiodine in nonvolatile form.
Bioassay Requirements for Nuclear Medicine Personnel:
Nuclear Medicine personnel who handle (or administer) less than 30 mCi (1.11 GBq) of Na131I in capsule form are required to have a thyroid bioassay at least once per calendar quarter, or 30 mCi (1.11 GBq) or more of Na131I in capsule form are required to have a thyroid bioassay within ten days after handling the radioiodine.
Enforcement:
Failure to comply will result in a termination of ordering privileges for the PI.
Time and Location of Measurements:
Call VEHS (2-2057) to schedule a thyroid bioassay appointment.Thyroid Action Levels:
Thyroid activities in excess of 0.00012 mCi (4.44 kBq) of 125I or 0.000040 mCi (1.48 kBq) of 131I requires an investigation of the operations involved and the implementation of corrective action. Repeat thyroid bioassays will be required.
2. Tritium Bioassay Requirements
Individuals involved in operations that utilize, at any one time, more than 100 mCi (3.7 GBq) of 3H in a non-contained form, other than metallic foil, shall have urine bioassays performed within one week following a single operation and at weekly intervals for continuing operations. The assay frequency for continuing operations may be reduced to monthly after the first calendar quarter, dependent upon initial results.
3. Accidents
Bioassays may be required if a person has been involved in a spill or other incident in which there may have been a significant intake of radioactive material. Bioassays may include urinalysis, analysis of other excreta such as fecal samples and nose wipes, whole body or thyroid counts.