Louisiana Administrative Code
Title 33 - ENVIRONMENTAL QUALITY
Part XV - Radiation Protection
Chapter 7 - Use of Radionuclides in the Healing Arts
Section XV-744 - Brachytherapy Records
Universal Citation: LA Admin Code XV-744
Current through Register Vol. 50, No. 9, September 20, 2024
A. Brachytherapy Sources Inventory
1. A licensee
shall maintain accountability at all times for all brachytherapy sources in
storage or use.
2. As soon as
possible after removing sources from a patient or a human research subject, the
licensee shall return brachytherapy sources to an area of storage from the area
of use, and immediately count or otherwise verify the number returned to ensure
that all sources taken from the storage area have been returned.
3. A licensee shall maintain a record of
brachytherapy source accountability required by Paragraphs 1 and 2 of this
Section for three years.
a. For temporary
implants, the record shall include:
i. the
number and activity of sources removed from storage, the time and date they
were removed from storage, the name of the individual who removed them from
storage, and the location of use; and
ii. the number and activity of sources
returned to storage, the time and date they were returned to storage, and the
name of the individual who returned them to storage.
b. For permanent implants, the record shall
include:
i. the number and activity of sources
removed from storage, the date they were removed from storage, and the name of
the individual who removed them from storage;
ii. the number and activity of sources not
implanted, the date they were returned to storage, and the name of the
individual who returned them to storage; and
iii. the number and activity of sources
permanently implanted in the patient or human research subject.
B. Records of Calibration Measurements of Brachytherapy Sources
1. A licensee shall maintain a record of the
calibrations of brachytherapy sources required by LAC 33:XV.719 for three years
after the last use of the source.
2. The record shall include:
a. the date of the calibration;
b. the manufacturer's name, model number, and
serial number for the source and the instruments used to calibrate the
source;
c. the source output or
activity;
d. the source positioning
accuracy within the applicators; and
e. the signature of the authorized medical
physicist.
C. Records of Decay of Strontium-90 Sources for Ophthalmic Treatments
1. A licensee shall maintain a record of the
activity of a strontium-90 source required by LAC 33:XV.719 for the life of the
source.
2. The record shall
include:
a. the date and initial activity of
the source as determined in accordance with LAC 33:XV.719; and
b. for each decay calculation, the date and
the source activity as determined in accordance with LAC 33:XV.719.
AUTHORITY NOTE: Promulgated in accordance with R.S. 30:2001 et seq. and 2104.B.
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