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Diagnostic Imaging Accreditation Standards version 4.1
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As discussed in further detail within Dr. Jeremy Beach’s Medical Matters article, CPSA’s version 4.1 (v4.1) Diagnostic Imaging (DI) Accreditation Standards were launched on July 11, detailing two specific amendments:
- Expansion and clarification of the medical director eligibility criteria, and
- Removal of 25km geographical distance criteria in reference to the provision of tele-ultrasound (tele-US)
The revisions were thoughtfully and carefully discussed by several CPSA committees and acknowledge the changing landscape of DI service provision. Feedback and draft revisions stemmed from various levels of input, standard exemption requests, and two commissioned and external third-party reports (on tele-US) from recognized bodies/institutions. After careful consideration, these amendments were made to follow evidence, align with best practices across jurisdictions and support health care accessibility for all. In particular, the impacts of the 25km amendment will be carefully monitored for future consideration.
When adding tele-US as a service to a facility, regardless of whether on-site US is already offered, all facilities must go through the process of receiving a formal approval in writing from CPSA. There are still limitations on tele-US, and musculoskeletal, hernia and diagnostic breast US exams may NOT be performed via tele-US.
New imaging facilities (or existing facilities adding a new modality) will be accredited to v4.1 standards. Facilities undergoing their four-year accreditation cycle between July 11 and Dec. 31, 2025, will be assessed against the v4 standards. These facilities will be expected to work towards v4.1 compliance, with the requirement for all imaging facilities to comply to v4.1 standards by Jan. 1, 2026.
For more information on v4.1, please visit our website.
Questions? Email accreditation@cpsa.ab.ca
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