Current through Register Vol. 24-18, September 15, 2024
(1) No person shall make, sell, lease,
transfer, lend, or install X-ray equipment or the accessories used in
connection with such equipment unless such accessories and equipment, when
properly placed in operation and properly used, shall meet the requirements of
this chapter.
(2) The registrant in
control of the X-ray machines shall be responsible for directing the operation
of the X-ray machines. The registrant or registrant's agent shall assure the
following provisions are met in the operation of the X-ray machine or machines:
(a) The registrant shall not operate an X-ray
machine for diagnostic or therapeutic purposes when the X-ray machine:
(i) Does not meet the provisions of this
chapter; or
(ii) Is malfunctioning
and threatens the health or safety of the patient, operator, or general
public.
(b) X-ray
machine operator requirements.
(i)
Individuals operating the X-ray equipment shall be adequately instructed in
safe operating procedures and shall be able to demonstrate competence, upon
request from the department, in the correct use of the equipment. Required
areas of competence are listed in Appendix II. The department may determine
compliance with subsection (2)(b) of this section by observation, interview, or
testing;
(ii) A medical X-ray
machine operator shall be licensed, certified or registered by the department
as either:
(A) A health care practitioner,
licensed under
Title
18 RCW; or
(B) A diagnostic or therapeutic radiologic
technologist certified in accordance with
chapter
18.84 RCW; or
(C) An X-ray technician registered in
accordance with
chapter
18.84 RCW.
(c) At each X-ray
system's control panel, a chart shall be provided which specifies for the
examinations performed by that system the following information:
(i) Patient's anatomical size versus
technique factors utilized;
(ii)
Source to image receptor distance used;
(iii) Type and placement of patient shielding
used, for example, gonad, thyroid, lap apron;
(iv) If applicable, settings for automatic
exposure devices; and
(v) Type and
size of film or screen-film combination to be used.
(d) When required by the department, a
registrant shall create and provide to operators of the X-ray system, radiation
safety procedures which address patient and occupationally exposed personnel
safety. These procedures shall define restrictions of the operating technique
required for safe operation of the particular X-ray system;
(e) Except for patients who cannot be moved
out of the room and the patient being examined, only the staff and ancillary
personnel required for the medical procedure or training shall be present in
the room during the radiographic exposure. Other than the patient being
examined:
(i) All individuals shall be
positioned such that no part of the body including the extremities not
protected by 0.5 mm lead equivalent will be struck by the useful
beam;
(ii) The X-ray operator,
other staff and ancillary personnel shall be protected from the direct scatter
radiation by protective aprons or whole body protective barriers of not less
than 0.25 mm lead equivalent;
(iii)
Patients who cannot be removed from the room shall be:
(A) Protected from the direct scatter
radiation by whole body protective barriers of not less than 0.25 mm lead
equivalent; or
(B) Positioned so
the nearest portion of the body is at least 2 meters from both the tube head
and the nearest edge of the image receptor.
(iv) The department may require additional
protective devices when a portion of the body of staff or ancillary personnel
is potentially subjected to stray radiation which may result in that individual
receiving one quarter of the maximum permissible dose defined under WAC
246-221-010.
(f) Gonad shielding of not less than 0.5 mm
lead equivalent shall be used for patients of reproductive age during
radiographic procedures in which the gonads are in the direct (useful) beam,
except for cases when gonad shielding may interfere with the diagnostic
procedure;
(g) Persons shall not be
exposed to the useful beam except for healing arts purposes. Only a licensed
practitioner of the healing arts shall authorize an exposure to the useful
beam. This requirement prohibits deliberate exposure for the following
purposes:
(i) Exposure of an individual for
training, demonstration, or other purposes unless there are also healing arts
requirements and proper prescription is provided;
(ii) Except for mammography performed by
registered facilities on self-referred patients, the exposure of an individual
for the purpose of healing arts screening without prior written approval of the
state health officer; and
(iii)
Exposure of an individual for the sole purpose of satisfying a third party's
prerequisite for reimbursement under any health care plan, except for exposure
required under medicare provisions.
(h) When a patient or film must be provided
with auxiliary support during a radiation exposure:
(i) Mechanical holding devices shall be used
when the technique permits. The safety rules, when required under subdivision
(d) of this subsection, shall list individual projections where holding devices
cannot be utilized;
(ii) Written
safety procedures, when required under subdivision (d) of this subsection,
shall indicate the requirements for selecting a human holder and the procedure
the holder shall follow;
(iii) The
human holder shall be protected as required under subdivision (e)(i) of this
subsection;
(iv) No person shall be
used routinely to hold film or patients;
(v) When the patient must hold the film, the
portion of the body other than the area of clinical interest struck by the
useful beam shall be protected by not less than 0.5 mm lead equivalent
material;
(vi) Holding the film or
the patient shall be permitted only in very unusual and rare
situations.
(i)
Personnel dosimetry. All persons associated with the operation of an X-ray
system are subject to both the occupational exposure limits and the
requirements for the determination of the doses stated under WAC
246-221-020. In addition, when
protective clothing or devices are worn on portions of the body and a dosimeter
is required, at least one such dosimeter shall be utilized as follows:
(i) When an apron is worn, the monitoring
device shall be worn at the collar outside of the apron; and
(ii) The dose to the whole body based on the
maximum dose attributed to the most critical organ shall be recorded on the
reports required under WAC
246-221-230. If more than one
device is used or a record is made of the data, each dose shall be identified
with the area where the device was worn on the body.
(iii) Personnel monitoring of an operator
shall be required where:
(A) Exposure switch
cords are utilized that allow the operator to stand in an unprotected area
during exposures; and
(B)
Measurements by the department show ten percent of the exposure limits as
specified under WAC
246-221-010 may be
exceeded.
(iv) All
persons involved in the operation of a fluoroscope and working within the
fluoroscopy room during its operation shall wear a personnel dosimeter required
under WAC
246-221-090 and subsection
(2)(i)(i) of this section. If extremities are in or near the primary beam,
extremity dosimeters are also required;
(j) Healing arts screening utilizing
radiation. Any person proposing to conduct a healing arts screening program,
with the exception of a mammography program, shall not initiate such a program
without prior approval of the state health officer. When requesting such
approval, that person shall submit the information outlined under Appendix III
of this part. If information submitted becomes invalid or outdated, the state
health officer shall be notified immediately;
(k) When using scatter suppressing grids, the
grids shall be:
(i) Clearly labelled with the
focal distance for which they are designed to be used; and
(ii) Of the proper focal distance for the
source-to-image distances used.
(l) Procedures and auxiliary equipment
designed to minimize patient and personnel exposure commensurate with the
needed diagnostic information shall be utilized.
(i) Film cassettes without intensifying
screens shall not be used for any routine diagnostic radiological
imaging.
(ii) Portable or mobile
X-ray equipment shall be used only for examinations where it is impractical to
transfer the patient(s) to a stationary X-ray installation.
(m) Patient log. A medical X-ray
facility (chiropractors, allopathic and osteopathic physicians and hospitals
only) shall record for each X-ray diagnosis or treatment the patient's name,
type of X-ray procedures performed, and the date. A separate log is not
necessary if the required information is retrievable by reference to other
records.
Statutory Authority:
RCW
70.98.050. 94-06-017, § 246-225-020,
filed 2/22/94, effective 3/25/94. Statutory Authority:
RCW
70.98.050 and
70.98.080. 91-15-083 (Order 183),
§ 246-225-020, filed 7/23/91, effective 8/23/91. Statutory Authority:
RCW
43.70.040. 91-02-049 (Order 121), recodified
as § 246-225-020, filed 12/27/90, effective 1/31/91. Statutory Authority:
RCW
70.98.080. 87-01-031 (Order 2450), §
402-28-031, filed 12/11/86; 83-19-050 (Order 2026), § 402-28-031, filed
9/16/83. Statutory Authority:
RCW
70.98.050. 81-01-011 (Order 1570), §
402-28-031, filed 12/8/80; Order 1084, § 402-28-031, filed 1/14/76.
Formerly WAC 402-28-030 (part).