(1) A licensee
authorized to use a gamma stereotactic radiosurgery unit for medical use shall
perform the following spot-checks:
(a)
Monthly:
(b) Before the first use
of the unit on a given day; and
(c)
After each source installation.
(2) To satisfy the requirements of paragraph
64E-5.6422(1)(a),
F.A.C., spot checks shall include the determination of:
(a) Assure the proper operation of the:
1. Treatment table retraction mechanism,
using backup battery power or hydraulic backups with the unit off;
2. Helmet microswitches;
3. Emergency timing circuits; and
4. Stereotactic frames and localizing devices
(trunnions).
(b)
Determine the following elements:
1. The
output for one typical set of operating conditions measured with the dosimetry
system described in subsection
64E-5.640(2),
F.A.C.;
2. The difference between
the measurement made in subparagraph
64E-5.6422(2)(b)
1., F.A.C., and the anticipated output, expressed as a percentage of the
anticipated output value obtained at last full calibration corrected
mathematically for physical decay;
3. Source output against computer
calculation;
4. Timer accuracy and
linearity over the range of use;
5.
On-off error; and
6. Trunnion
centricity.
(3)
A licensee shall perform spot-checks required by subsection
64E-5.6422(1),
F.A.C., following procedures established by the authorized medical
physicist.
(4) A licensee shall
have the authorized medical physicist review the results of each spot-check
within 15 days and promptly notify the licensee in writing of the results of
each spot-check. The licensee shall keep a copy of each written notification
for 3 years.
(5) To satisfy the
requirements of paragraphs
64E-5.6422(1)(b) and
(c), F.A.C., the licensee's spot-checks must
assure proper operation of the following:
(a)
Electrical interlocks at each gamma stereotactic radiosurgery room
entrance;
(b) Source exposure
indicator lights on the gamma stereotactic radiosurgery unit, on the control
console, and in the facility;
(c)
Viewing and intercom systems;
(d)
Timer termination;
(e) Radiation
monitors used to indicate room exposures; and
(f) Emergency off
buttons.
(6) If the
results of the checks required in subsection
64E-5.6422(5),
F.A.C., of this section indicate the malfunction of any system, a licensee
shall lock the control console in the off position and not use the unit except
as may be necessary to repair, replace, or check the malfunctioning
system.
(7) A licensee shall
arrange for the repair of any system identified in subsection
64E-5.6422(2),
F.A.C., that is not operating properly as soon as possible.
(8) A licensee shall maintain a record of
each spot-check required by subsections
64E-5.6422(2) and
(5), F.A.C., for 3 years and a copy of the
procedures required in subsections
64E-5.6422(2) and
(3), F.A.C., until the licensee no longer
possesses the gamma stereotactic radiosurgery unit. The record shall include:
(a) The date of the spot-check;
(b) The manufacturer's name, model number,
and serial number for the gamma stereotactic radiosurgery unit;
(c) The manufacturer's name, model number and
serial number of the instrument used to measure the output of the gamma
stereotactic radiosurgery unit;
(d)
The timer linearity and constancy;
(e) The calculated on-off error;
(f) A determination of trunnion
centricity;
(g) The difference
between the anticipated output and the measured output;
(h) An assessment of source output against
computer calculations;
(i)
Notations indicating the operability of radiation monitors, helmet
microswitches, emergency timing circuits, emergency off buttons, electrical
interlocks, source exposure indicator lights, viewing and intercom systems,
timer termination, treatment table retraction mechanism, and stereotactic
frames and localizing devices (trunnions); and
(j) The name of the individual who performed
the periodic spot-check and the signature of the authorized medical physicist
who reviewed the record of the spot-check.