Current through September 24, 2024
INFORMATION ON RADIATION SHIELDING REQUIRED FOR PLAN
REVIEWS
I. ALL THERAPEUTIC RADIATION
MACHINES
A. Basic facility information
including: name, telephone number and Agency registration number of the
individual responsible for preparation of the shielding plan; name and
telephone number of the facility supervisor; and the street address [including
room number] of the external beam radiation therapy facility. The plan should
also indicate whether this is a new structure or a modification to existing
structure(s).
B. All wall, floor,
and ceiling areas struck by the useful beam shall have primary
barriers.
C. Secondary barriers
shall be provided in all wall, floor, and ceiling areas not having primary
barriers.
II.
THERAPEUTIC RADIATION MACHINES UP TO 150 kV (PHOTONS ONLY)
In addition to the requirements listed in Section I.
above, therapeutic radiation machine facilities which produce only photons with
a maximum energy less than or equal to 150 kV shall submit shielding plans
which contain, as a minimum, the following additional information:
A. Equipment specifications, including the
make, model and serial number of the therapeutic radiation machine, as well as
the maximum technique factors.
B.
The maximum design workload for the facility, including the total anticipated
number of exposures/films per day and/or week, as well as the type of
treatment(s) or examination(s) which will be performed with the therapeutic
radiation machine.
C. A facility
blueprint/drawing indicating: scale [0.25 inch = 1 foot is typical]; direction
of North; normal location of the therapeutic radiation machine's radiation
port(s); the port's travel and traverse limits; general direction(s) of the
useful beam; locations of any windows and doors; and the location of the
therapeutic radiation machine control panel. If the control panel is located
inside the external beam radiation therapy treatment room, the location of the
operator's booth shall be noted on the plan and the operator's station at the
control panel shall be behind a protective barrier sufficient to ensure
compliance with 400.06 of these regulations.
D. The structural composition and thickness
or lead/concrete equivalent of all walls, doors, partitions, floor, and ceiling
of the room(s) concerned.
E. The
type of occupancy of all adjacent areas inclusive of space above and be low the
room(s) concerned. If there is an exterior wall, show distance to the closest
area(s) where it is likely that individuals may be present.
F. At least one example calculation which
shows the methodology used to determine the amount of shielding required for
each physical condition [i.e., primary and secondary/leakage barriers,
restricted and unrestricted areas, entry door(s) and shielding material in the
facility.]
(1) If commercial software is used
to generate shielding requirements, identify the software used and the
version/revision date.
(2) If the
software used to generate shielding requir. ements is not in the open
literature, submit quality control sample calculations to verify the result
obtained with the software.
III. THERAPEUTIC RADIATION MACHINES OVER 150
kV
In addition to the requirements listed in Section I.
above, therapeutic radiation machine facilities which produce photons with a
maximum energy in excess of 150 kV and/or electrons and/or protons or other
subatomic particles shall submit shielding plans which contain, as a minimum,
the following additional information:
A. Equipment specifications including
manufacturer, model number, and serial number of the therapeutic radiation
machine, rad/gray or rem/sievert per minute at the isocenter and the energy(s)
and type(s) of radiation produced [i.e., photon, electron]. The source to
isocenter distance shall be specified.
B. Maximum design workload for the facility
including total weekly radiation output, [expressed in rad/gray or rem/sievert
per minute at 1 meter], total beam-on time per day or week, the average
treatment time per patient, along with the anticipated number of patients to be
treated per day or week.
C.
Facility blueprint/drawing [including both floor plan and elevation views]
indicating relative orientation of the therapeutic radiation machine, scale
[0.25 inch = 1 foot is typical], type(s) and thickness of shielding
material(s), direction of North, the locations and size of all penetrations
through each shielding barrier [ceiling, walls and floor], as well as details
of the door(s) and maze.
D. The
structural composition and thickness or concrete equivalent of all walls,
doors, partitions, floor, and ceiling of the room(s) concerned
E. The type of occupancy of all adjacent
areas inclusive of space above and below the room(s) concerned. If there is an
exterior wall, show distance to the closest area(s) where it is likely that
individuals may be present.
F.
Description of all assumptions that were in shielding calculations including,
but not limited to, design energy [i.e., room may be designed for 6 MV unit
although only a 4 MV unit is currently proposed], workload, presence of
integral beam-stop in unit, occupancy and use(s) of adjacent areas, fraction of
time that primary beam will intercept each permanent barrier [walls, floor and
ceiling] and "allowed" radiation exposure in both restricted and unrestricted
areas.
G. At least one example
calculation which shows the methodology used to determine the amount of
shielding required for each physical condition [i.e., primary and
secondary/leakage barriers, restricted and unrestricted areas, small angle
scatter, entry door(s) and maze] and shielding material in the facility.
(1) If commercial software is used to
generate shielding requirements, identify the software used and the
version/revision date.
(2) If the
software used to generate shielding requirements is not in the open literature,
submit quality control sample calculations to verify the result obtained with
the software.
IV. NEUTRON SHIELDING
In addition to the requirements listed in Section III
above, therapeutic radiation machine facilities which are capable of operating
above 10 MV shall submit shielding plans which contain, as a minimum, the
following additional information:
A.
The structural composition, thickness and location of all neutron shielding
material.
B. Description of all
assumptions that were used in neutron shielding calculations including, but not
limited to, neutron spectra as a function of energy, neutron fluence rate,
absorbed dose and dose equivalent (due to neutrons) in both restricted and
unrestricted areas.
C. At least one
example calculation which shows the methodology used to determine the amount of
neutron shielding required for each physical condition [i.e. restricted and
unrestricted areas, entry door(s) and maze] and neutron shielding material
utilized in the facility.
(1) If commercial
software is used to generate shielding requirements, identify the software used
and the version/revision date.
(2)
If the software used to generate shielding requirements is not in the open
literature, submit quality control sample calculations to verify the result
obtained with the software.
D. The method(s) and instrumentation which
will be used to verify the adequacy of all neutron shielding installed in the
facility.
V. REFERENCES
A. NCRP Report 49, " Structural Shielding
Design and Evaluation for Medical Use of X-Rays and Gamma Rays of Energies Up
to 10 MeV" (1976).
B. NCRP Report
51, "Radiation Protection Design Guidelines for 0.1-100 MeV Particle
Accelerator Facilities" (1977).
C.
NCRP Report 79, "Neutron Contamination from Medical Electron Accelerators"
(1984).