Equipment Quality Control
Ionizing Radiation
Each imaging facility should have documented policies and procedures for monitoring and evaluating the effective management, safety, and operation of equipment involved in the use of ionizing radiation for therapy, diagnosis and imaging. The quality control program should be designed to minimize patient, personnel, and public radiation risks and to maximize the quality of the diagnostic information or therapeutic benefit.
Equipment performance should be monitored and typical patient dose estimates should be made by a qualified medical physicist as described in the appropriate ACR-AAPM Technical Standard for Physics Equipment Performance Monitoring. Typical patient dose estimates should be compared against national benchmarks or diagnostic reference levels (DRLs), if available, and protocols should be reviewed if doses exceed DRLs. Routine quality control testing should be conducted by properly trained individuals with review at least annually by the supervising physician and qualified medical physicist as described in the appropriate ACR-AAPM Technical Standard for Physics Equipment Performance Monitoring.
Magnetic Resonance Imaging
Each facility should have documented policies and procedures for monitoring and evaluating the effective management, safety, and proper performance of magnetic resonance imaging equipment. Equipment performance should be monitored by a qualified medical physicist or a qualified MR Scientist as described in the ACR–AAPM Technical Standard for Diagnostic Medical Physics Performance Monitoring of Magnetic Resonance Imaging (MRI) Equipment. A documented quality control program shall be maintained at the MR site. Routine quality control testing should be conducted by properly trained individuals with review at least annually by the supervising physician and qualified medical physicist as described in the ACR–AAPM Technical Standard for Diagnostic Medical Physics Monitoring of Magnetic Resonance Imaging (MRI) Equipment."
Ultrasound
Each facility should have documented policies and procedures for monitoring and evaluating the effective management, safety, and proper performance of ultrasound imaging equipment. Equipment performance should be monitored by properly trained individuals under the supervision of a qualified medical physicist as described in the ACR–AAPM Technical Standard for Diagnostic Medical Physics Performance Monitoring of Real Time Ultrasound Equipment. The quality control program should be designed to maximize the quality of the diagnostic information. Routine quality control testing should be conducted by properly trained individuals with review at least annually by the supervising physician and qualified medical physicist as described in the ACR–AAPM Technical Standard for Diagnostic Medical Physics Monitoring of Real Time Ultrasound Equipment.
Infection Control
Each facility should have policies and procedures in place to control the spread of infection among patients and personnel. These should include adherence to universal precautions and the use of clean or aseptic techniques as warranted by the procedure or intervention being performed.
Safety
Each facility should have in place policies and procedures to provide for the safety of patients and personnel. These should include attention to the physical environment, the proper use, storage, and disposal of medications and hazardous materials and their attendant equipment, and methods for addressing medical and other emergencies.
Patient Education
Each facility should have in place policies and procedures for educating and informing patients about procedures and/or interventions to be performed and facility processes for the same. This should include appropriate instructions for patient preparation and aftercare, if any. This information should be provided in an appropriate form to the patient and family, such as that provided on the ACR-RSNA website, www.RadiologyInfo.org.
Quality Improvement
Examinations should be systematically reviewed and evaluated as part of the overall quality improvement program at the facility. Monitoring should include evaluation of the accuracy of interpretation as well as the appropriateness of the examination. Complications and adverse events should be recorded and periodically reviewed in order to identify opportunities to improve patient care. These data should be collected in a manner that complies with statutory and regulatory peer-review procedures in order to ensure the confidentiality of the peer-review process; 1998, amended 2008 (Res. 1-e), revised 2018 (Res. 33-c).