Alaska Administrative Code
Title 7 - Health and Social Services
Part 2 - Public Health
Chapter 18 - Radiation Sources and Radiation Protection
Article 4 - Use of Radiation Sources in the Healing Arts
7 AAC 18.450 - Medical radiographic installation
Current through August 30, 2024
(a) A medical radiographic installation must use a diagnostic type protective x-ray tube housing and must meet the requirements of this section.
(b) Medical radiographic equipment must define the useful beam with a diaphragm, cone, or adjustable collimator capable of restricting the beam to the area of clinical interest, providing the same degree of attenuation as is required of the protective tube housing. These devices must be calibrated in terms of the size of the projected useful beam at specified source-film distances and must limit the target-to-skin distance to not less than 12 inches (30 centimeters).
(c) Radiographic equipment must be equipped with adjustable collimators and light localizers to define the entire field and produce a visible indication of adequate collimation and alignment on the x-ray film. Field size indication on adjustable collimators must be accurately aligned with the x-ray field to within two percent of the source-image receptor-distance (SID) at all possible positions of the x-ray tube, except when positive beam limitation is functional, in use, and a health physics survey confirms that the positive beam limitation confines the beam to within two percent of the SID.
(d) Except when contraindicated for a particular medical purpose, the aluminum equivalent of the total filtration in the useful beam may not be less than 0.5 millimeters for equipment operating below 50 kVp; may not be less than 1.5 millimeters for equipment operating from 50 kVp to 70 kVp; and may not be less than 2.5 millimeters for equipment operating above 70 kVp. If the filter in the machine is not accessible for examination or the total filtration is unknown, the requirements of this section are met if the half-value layer of the useful beam is not less than that listed for "Other X-Ray Systems" in Table I of 21 C.F.R. 1020.30(m), as revised as of April 1, 2008, and adopted by reference.
(e) A device must automatically terminate the exposure after a preset time or exposure.
(f) The exposure switch must be of a dead-man type switch and must be arranged in a manner that the switch cannot be operated outside a shielded area, except that exposure switches for spot film devices used in conjunction with fluoroscopic tables and for mobile diagnostic radiographic equipment are exempt from this shielding requirement.
(g) The exposure switch for mobile equipment must be arranged in a manner that the operator can stand at least six feet from the patient and well away from the useful beam.
(h) The control panel must include
(i) All wall, floor, and ceiling areas that may intercept the useful beam must have primary barriers.
(j) A primary barrier in a wall must extend to a height of at least 84 inches or 210 centimeters above the floor.
(k) A secondary barrier must be provided in all wall, floor, and ceiling areas not having a primary barrier or where the primary barrier requirements are lower than the secondary barrier requirements. In a radiographic installation where the average radiographic workload is comparatively low, the conventional structural material in ordinary walls, floors, and ceilings may suffice as a primary barrier and secondary barrier without adding special shielding materials, particularly if the useful beam cannot be directed at occupied areas.
(l) The operator's station must be behind a protective barrier that will intercept the entire useful beam and any radiation that has been scattered only once. An operator must be unable to energize the tube while outside the protective barrier, except that spot film devices used in conjunction with fluoroscopic tables are exempted from this requirement.
(m) A window of lead equivalent glass, equal to that required by the adjacent barrier, mirror system, or closed circuit television monitor, must be provided and it must be large enough and placed in a manner that the operator can see the patient during the exposure without having to leave the protective area.
(n) If a patient must be held in position for radiography, a mechanical supporting, or restraining device must be used unless the device will interfere with the diagnosis.
(o) If a patient must be held by an individual, that individual must be protected with appropriate shielding devices, such as protective gloves and apron, and that individual must be positioned in a manner that no part of that individual's body will be struck by the useful beam.
(p) An individual occupationally exposed to radiation may not hold a patient during an exposure, except during an emergency. An individual may not be regularly used for this service.
(q) Only an individual required for the radiographic procedure may be in the radiographic room during exposure and, except for the patient, no unprotected parts of the individual's body may be in the useful beam.
(r) The useful beam must be restricted to the area of the image receptor, and evidence of beam edges must show up on at least three sides of each radiographic image, except where a properly functioning positive beam limiting device is in place.
(s) A patient must be provided with a shield to protect the gonadal area of the body, unless the use of a shield prohibits a proper diagnosis.
(t) A protective apron and gloves must be tested at least annually to verify the continued integrity of radiation shielding properties sufficient to meet the standards of 7 AAC 18.440(l).
(u) A chest photofluorographic installation does not meet radiation safety requirements and may not be used.
(v) Mobile diagnostic radiographic equipment must meet the requirements of this section, except for the
(w) A registrant who uses film imaging and processing of the images shall establish processing quality control procedures at regular intervals that at least include
(x) A registrant who uses electronic, digital, or computerized imaging methods shall establish quality control procedures that include at least
Authority:AS 18.60.475
AS 18.60.485