R 333.5411 X-ray equipment.

Rule 411. (1) All x-ray tube housings in fixed fluoroscopic installations shall be of the diagnostic type. (2) The aluminum equivalent of the total filtration permanently in the useful beam shall not be less than 2.5 millimeters aluminum. (3) The source-patient distance on fluoroscopic machines should not be less than 45 centimeters (18 inches) and shall not be less than 30 centimeters (12 inches). (4) Provision shall be made to intercept the scattered x-rays from the undersurface of the table top and other structures under the fluoroscopic table if the tube is mounted under the table. A cone or shield shall provide the same degree of attenuation as is required of the tube housing. (5) A shielding device of at least 0.25 millimeter lead equivalence for covering the bucky slot during fluoroscopy shall be provided. (6) A shielding device of at least 0.25 millimeter lead equivalence, such as overlapping protective drapes or hinged or sliding panels, shall be used to intercept scattered radiation that would otherwise reach the fluoroscopist and others near the machine. (7) A fluoroscopic machine shall comply with both of the following: (a) The entire cross section of the useful beam shall be intercepted by the primary protective barrier of the fluoroscopic image assembly at any SID. The fluoroscopic tube shall not produce x-rays unless the barrier is in position to intercept the entire useful beam. The exposure rate due to transmission through the barrier with the attenuation block in the useful beam combined with radiation from the image intensifier, if provided, shall not exceed 2 milliroentgens per hour at 10 centimeters from an accessible surface of the fluoroscopic imaging assembly beyond the plane of the image receptor for each roentgen per minute of entrance exposure rate. (b) The entrance exposure rate shall be measured as described in subrule (15) of this rule. The exposure rate due to transmission through the primary barrier combined with radiation from the image intensifier shall be determined by measurements averaged over an area of 100 square centimeters with no linear dimension greater than 20 centimeters. If the source is below the tabletop, the measurement shall be made with the input surface of the fluoroscopic imaging assembly positioned 30 centimeters above the tabletop. If the source is above the tabletop and the SID is variable, the measurement shall be made with the end of the beam-limiting device or spacer as close to the tabletop as it can be placed, if it is not closer than 30 centimeters. Movable grids and compression devices shall be removed from the useful beam during the measurement. For all measurements, the attenuation block shall be positioned in the useful beam 10 centimeters from the point of measurement of the entrance exposure rate and between this point and the input surface of the fluoroscopic imaging assembly. (8) The lead equivalence of the barrier of conventional fluoroscopes shall be not less than 1.5 millimeters at 100 kVp, 1.8 millimeters at 125 kVp, and 2.0 millimeters at potentials greater than 125 kVp. (9) A beam-limiting device shall be provided to restrict the size of the useful beam to less than the area of the barrier. The x-ray tube and beam-limiting system shall be linked with the fluorescent screen assembly so that the useful beam at the fluorescent screen is confined within the barrier irrespective of the panel-screen distance. For image intensifiers, the useful beam shall be centered on the input phosphor. It should not exceed the diameter of the input phosphor during fluoroscopy or cine-recording. For spot film radiography with image intensifier equipment, the shutters should automatically open to the required field size before the exposure. (10) Beam-limiting devices, such as collimators, adjustable diaphragms, or shutters, shall provide the same degree of attenuation as is required of the tube housing. (11) A fluoroscopic machine shall comply with either of the following: (a) The x-ray field produced by nonimage-intensified fluoroscopic equipment shall not extend beyond the entire visible area of the image receptor. Means shall be provided to permit further limitation of the field. The minimum field size at the greatest SID shall be equal to or less than 5 by 5 centimeters. (b) For image-intensified fluoroscopic equipment, the total misalignment of the edges of the x-ray field with the respective edges of the visible area of the image receptor along any dimension of the visually defined field in the plane of the image receptor shall not exceed 3% of the SID. The sum, without regard to sign, of the misalignment along any 2 orthogonal dimensions intersecting at the center of the visible area of the image receptor shall not exceed 4% of the SID. For rectangular x-ray fields used with circular image receptors, the error in alignment shall be determined along the length and width dimensions of the x-ray field which pass through the center of the visible area of the image receptor. Means shall be provided to permit further limitation of the field. The minimum field size, at the greatest SID, shall be equal to or less than 5 by 5 centimeters. (12) X-ray production in the fluoroscopic mode shall be controlled by a device that requires continuous pressure by the operator for the entire time of an exposure. When recording serial fluoroscopic images, the operator shall be able to terminate the x-ray exposures at any time, but means may be provided to permit completion of any single exposure of the series in progress. (13) When the fluoroscope is operated at 80 kVp, the exposure rate at the position where the beam enters the patient shall not exceed 3.2 R/mA-min and should not exceed 2.1 R/mA-min. (14) Entrance exposure rate limits for fluoroscopic machines shall be as follows: (a) Machines with automatic exposure rate control shall not be operable at a combination of tube potential and current which results in an exposure rate in excess of 10 roentgens per minute at the point where the center of the useful beam enters the patient, except during recording of fluoroscopic images or when an optional high level control is provided. Special means of activation of high level controls, such as additional pressure applied continuously by the operator, shall be required to avoid accidental use. A continuous signal audible to the fluoroscopist shall indicate that the high level control is being employed. (b) Machines without automatic exposure rate control shall not be operable at a combination of tube potential and current which results in an exposure rate in excess of 5 roentgens per minute at the point where the center of the useful beam enters the patient, except during recording of fluoroscopic images or when an optional high level control is activated. Special means of activation of high level controls, such as additional pressure applied continuously by the operator, shall be provided to avoid accidental use. A continuous signal audible to the fluoroscopist shall indicate that the high level control is being employed. (15) Compliance with subrule (14) of this rule shall be determined as follows: (a) If the source is below the table, the exposure rate shall be measured 1 centimeter above the tabletop or cradle. (b) If the source is above the table, the exposure rate shall be measured at 30 centimeters above the tabletop with the end of the beam-limiting device or spacer positioned as closely as possible to the point of measurement. (c) In a C-arm type of fluoroscope, the exposure rate shall be measured 30 centimeters from the input surface of the fluoroscopic imaging assembly. (16) Means shall be provided to preset the cumulative on-time of the fluoroscopic tube. The maximum cumulative time of the timing device shall not exceed 5 minutes without resetting. A signal audible to the fluoroscopist shall indicate the completion of the preset cumulative on-time. This signal shall continue to sound while x-rays are produced until the timing device is reset. (17) Devices which indicate the x-ray tube potential and current shall be provided. On image intensified fluoroscopic equipment, these devices should be located in such a manner that the operator may monitor the tube potential and current during fluoroscopy. Editor's Note: An obvious error in R 325.5411 was corrected at the request of the promulgating agency, pursuant to Section 56 of 1969 PA 306, as amended by 2000 PA 262, MCL 24.256. The rule containing the error was published in Michigan Register, 2016 MR 10. The memorandum requesting the correction was published in Michigan Register, 2016 MR 16.