Radiologists who use imaging-related electronic record-keeping could qualify for some of the $19 billion in economic recovery money set aside for electronic health record conversion if they meet the federal government’s definition of “meaningful use” for their records.
Radiologists who use imaging-related electronic record-keeping could qualify for some of the $19 billion in economic recovery money set aside for electronic health record conversion if they meet the federal government's definition of "meaningful use" for their records.
A federal advisory committee to the U.S. Department of Health and Human Services took a first stab June 16 at defining meaningful use as it pertains to EHRs.
"Today we outlined a vision for where we are heading with the concept of meaningful use," said David Blumenthal, chair of the HHS Health Information Technology Policy Committee. "That vision calls for the exchange of information on a wide range of items."
The HIT Policy Committee focused on recommendations from its Meaningful Use Workgroup. A general guide appearing in the preamble of its work noted that meaningful use should ultimately be linked to achieving measurable outcomes in patient engagement, care coordination, and population health.
A meaningful use matrix included several specifics that apply to medical imaging. One is an objective for 2011 governing the exchange of test results among care providers. A second 2011 goal involves a measure calling for reporting of the percentages of patients aged 50 and older who receive annual colorectal cancer screenings and of women over the same age who get annual mammograms. A metric potentially to be applied in 2013 calls for the measurement of inappropriate imaging procedures, such as the use of MRI for acute low back pain.
Agreement on a final definition is months away. Blumenthal emphasized that the committee's work is only advisory and that the Centers for Medicare and Medicaid Services, which is part of HHS, will write the final rules.
The public will have until June 26 to comment on today's recommendations.
FDA Grants Expanded 510(k) Clearance for Xenoview 3T MRI Chest Coil in GE HealthCare MRI Platforms
November 21st 2024Utilized in conjunction with hyperpolarized Xenon-129 for the assessment of lung ventilation, the chest coil can now be employed in the Signa Premier and Discovery MR750 3T MRI systems.
FDA Clears AI-Powered Ultrasound Software for Cardiac Amyloidosis Detection
November 20th 2024The AI-enabled EchoGo® Amyloidosis software for echocardiography has reportedly demonstrated an 84.5 percent sensitivity rate for diagnosing cardiac amyloidosis in heart failure patients 65 years of age and older.
New Study Examines Agreement Between Radiologists and Referring Clinicians on Follow-Up Imaging
November 18th 2024Agreement on follow-up imaging was 41 percent more likely with recommendations by thoracic radiologists and 36 percent less likely on recommendations for follow-up nuclear imaging, according to new research.