News | Computed Tomography (CT) | November 10, 2015

CT operators will have to begin reporting scans on Medicare patients with non-complaint equipment starting Jan. 1, 2016

XR-29, CMS, Medicare, delay, low-dose CT, computed tomography

Image courtesy of Toshiba America Medical Systems


November 10, 2015 — This fall, imaging pundits discussed the possible delay of XR-29, a standard designed by the Centers for Medicare and Medicaid (CMS) to encourage computed tomography (CT) providers to upgrade their equipment to low-dose configurations. But it doesn’t look like that is going to happen.

The Centers for Medicare and Medicaid Services (CMS) has announced that, effective Jan. 1, 2016, CT operators will have to report scans performed on Medicare patients with equipment that does not comply with the “Smart Dose” standard. Additionally, those out of compliance will take a 5 percent hit in Medicare technical payments throughout 2015; this penalty will increase to 15 percent in 2017 and later. According to CMS, testing for compliance with XR-29 will be done as part of the periodic accreditation of the CT scanners.

The decision will likely catch more than a few American sites flat-footed. In August, an Association for Medical Imaging Management (AHRA) survey found that 36 percent of respondents would not be compliant with the standard, if it took effect as scheduled. The result could be a surge of interest at the Radiological Society of North America (RSNA) annual meeting in modern CTs, which are optimized for low-dose scanning.

For more information: www.medicalimaging.com


Related Content

News | X-Ray

April 29, 2026 — Results from a new study* presented at the American Roentgen Ray Society’s (ARRS) 2026 annual meeting ...

Time April 29, 2026
arrow
News | Imaging Software Development

April 28, 2026 — Avatar Medical has been granted FDA 510(k) clearance for Avatar Medical Vision, its software platform ...

Time April 28, 2026
arrow
News | Cardiac Imaging

April 28, 2026 — Abbott has received U.S. Food and Drug Administration (FDA) clearance and CE Mark for its next ...

Time April 28, 2026
arrow
News | FDA

April 16, 2026 — Royal Philips has received U.S. Food and Drug Administration 510(k) clearance for the Philips Spectral ...

Time April 20, 2026
arrow
News | Radiology Imaging

April 7, 2026 — Onvida Health and Siemens Healthineers have entered a 10-year Value Partnership¹ designed to bring the ...

Time April 09, 2026
arrow
News | Radiology Business

March 31, 2026 — Radon Medical Imaging, a medical imaging equipment maintenance and repair services company, has has ...

Time March 31, 2026
arrow
News | Radiology Imaging

March 26, 2026 — GE HealthCare has announced a renewed research collaboration with Stanford Medicine Department of ...

Time March 30, 2026
arrow
News | Cardiac Imaging

March 28, 2026 — When Ashley Perlow felt a sharp pain shoot across her chest and into both wrists, she didn't think it ...

Time March 30, 2026
arrow
News | FDA

March 24, 2026 — MARS Bioimaging, a New Zealand–headquartered medical device company, has received U.S. Food and Drug ...

Time March 25, 2026
arrow
News | Radiology Imaging

March 23, 2026 — Samsung Medison hsa announced that its U.S. medical imaging businesses, previously operating as ...

Time March 23, 2026
arrow
Subscribe Now