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Read or Download Quality Assurance for Diagnostic Imaging Equipment (Ncrp Report : No. 99) PDF
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Extra resources for Quality Assurance for Diagnostic Imaging Equipment (Ncrp Report : No. 99)
Example text
Comment: This is the primary objective of the entire image facility. It is the most important aspect of the facility operation. 1 MANAGEMENT OF PERSONNEL ACTIVITIES 1 41 and consultation with the referring physician. 2. There shall be a written report of every imaging study produced in the facility. Control: Pathology and surgery reports on patients who have had imaging studies done should be sent to the imaging facility and, when appropriate, these should be compared with the interpretations of imaging studies.
These control limits can apply, for instance, to the limits in acceptable density for a sensitometric strip or the limits on radiation emitted a t a certain mA and kVp setting of a machine. The upper and lower control limits should be established so that the diagnostic value of the image will not be significantly compromised before the limits are reached and corrective action is required. , for x-ray generators used over a limited range of kVp and mA, the control limits for kVp may be reduced. In setting the control limits, remember that limits that are set too close to the operating level will result in: (a) increased service calls, (b) increased downtime for service and quality control tests, (c) increased operating cost, and (d) decreased patient flow.
Open packages of photographic film should be stored in an area with humidity ranging between 40 and 60 percent. Photographic materials should not be stored in areas where they can be exposed to chemical fumes or radiation. Sources of ionizing radiation include radioisotopes,radioactive wastes, and direct or scattered x rays. 1 STORAGE, DARKROOM, AND PROCESSING 1 45 edge. Even two or three boxes stacked horizontally can cause pressure artifacts. Photographic chemicals should receive reasonable care in terms of storage conditions.