Abstract

This guideline was developed collaboratively by the American College of Radiology (ACR), the American Association of Physicists in Medicine (AAPM), and the Society for Imaging Informatics in Medicine (SIIM). Increasingly, medical imaging and patient information are being managed using digital data during acquisition, transmission, storage, display, interpretation, and consultation. The management of these data during each of these operations may have an impact on the quality of patient care. “CR” and “DR” are the commonly used terms for digital radiography detectors. CR is the acronym for computed radiography, and DR is an acronym for digital radiography. CR uses a photostimulable storage phosphor that stores the latent image, which is subsequently read out using a stimulating laser beam. It can be easily adapted to a cassette-based system analogous to that used in screen-film (SF) radiography. Historically, the acronym DR has been used to describe a flat-panel digital X-ray imaging system that reads the transmitted X-ray signal immediately after exposure with the detector in place. Generically, the term CR is applied to passive detector systems, while the term DR is applied to active detectors. This guideline is applicable to the practice of digital radiography. It defines motivations, qualifications of personnel, equipment guidelines, data manipulation and management, and quality control (QC) and quality improvement procedures for the use of digital radiography that should result in high-quality radiological patient care. In all cases for which an ACR practice guideline or technical standard exists for the modality being used or the specific examination being performed, that guideline or standard will continue to apply when digital image data management systems are used.

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