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CHICAGO - USPSTF’s mammography screening guidelines to a decline in screening and may lead to a significant number of missed cancers, researchers found.

Two Studies Challenge Mammography Guideline Changes

CHICAGO - Radiation received by other organs during a mammogram is very low and does not present an increased cancer risk, researchers found.

Mammography Scatter Radiation Presents No Cancer Risk

CHICAGO - Breast cancer risk estimates increase with frequent CT scans, particularly among younger patients, researchers found.

Breast Cancer Risk Increase with Repeat Imaging

CHICAGO - Radiologists can more accurately diagnose abuse of elderly patients thanks to new research that points to a discernible pattern of radiological symptoms.

Radiologists Find Patterns Indicative of Elder Abuse

Emphasizing enhanced workflow efficiency for mammography exams, GE HealthCare will unveil the Pristina Via mammography platform at the Radiological Society of North America (RSNA) conference.

In addition to offering zero-click acquisition to facilitate streamlined workflow, the 

 incorporates prior image comparison, irrespective of mammography vendor, to aid in mammography assessments, according to GE HealthCare.

The company adds that the Pristina Via system offers image to image cycle time for digital breast tomosynthesis (DBT) that is up to twice as fast as other mammography platforms, as well as the lowest radiation dose for all breast thicknesses.

“Simplifying, automating, and streamlining the mammography exam to improve in-room workflows is critical to driving patient compliance and access to screening,” said John Simon, M.D., the CEO of SimonMed. “The enhancements offered by Pristina Via are part of our mission of making advanced technology accessible.”

The new mammography system reportedly offers features that promote workflow efficiency as well as patient comfort.

Topic

GE HealthCare Introduces Pristina Via Mammography System at RSNA

The use of artificial intelligence (AI) tools to provide quantitative coronary tomography (AI-QCT) and coronary plaque analysis (AI-CPA) based on coronary computed tomography angiography (CCTA) will soon be covered by four Medicare administrative contractors (MACs).

Starting on November 24, the MACs Palmetto GBA, National Government Services (NGS), CGS Administrators and WPS administrative groups will cover the use of AI-QCT and AI-CPA for Medicare beneficiaries with acute or stable chest pain, and no known coronary artery disease (CAD), according to a recently updated local coverage determination (LCD) issued by the Centers for Medicare and Medicaid Services (CMS).

The LCD noted coverage of AI tools will be provided for the testing of patients deemed to be at intermediate risk for CAD, or those classified by the Coronary Artery Disease Reporting and Data System (CAD-RADS) as having CAD-RADS 1, CAD-RADS 2 or CAD-RADS 3, based on CCTA findings. The coverage will also apply for those who have had negative or inconclusive evaluation for acute coronary syndrome (ACS), according to the LCD.

The use of the FDA-cleared AI modalities 

“Coronary artery disease is the underlying cause of about 50% of deaths,” noted Ron Blankstein, M.D., the director of cardiac computed tomography at Brigham and Women's Hospital and a professor of medicine at Harvard Medical School in Boston. “Medicare coverage of HeartFlow Plaque Analysis is a major step forward in improving coronary artery disease management. The earlier we can diagnose and use tools to provide accurate plaque quantification, the earlier we can provide tailored treatments, potentially improving outcomes for patients.”

“We are also extremely thankful to the many physicians and medical society partners who used their voices to advocate for this essential AI-QCT technology. Until Cleerly, health-care providers have not had a way to easily and completely assess the primary cause of heart attacks, atherosclerotic plaque burden and type in a non-invasive way, which is especially important for our senior population,” noted James L. Kim, M.D., the CEO and founder of Cleerly. “This decision by the MACs represents a significant step in advancing the field of cardiology and providing the best possible care for our seniors.”

(Editor’s note: For related content, see “

FDA Clears Software for Enhancing CCTA Assessment of Atherosclerosis

Coronary CT Angiography Study Shows Link Between Major Cardiovascular Events and High Lipid Core Burden

Meta-Analysis Shows Superiority of CT Angiography Over SPECT and Functional Testing for Obstructive CAD

1. Centers for Medicare and Medicaid Services (CMS). Artificial intelligence enabled CT based quantitative coronary topography (AI-QCT)/coronary plaque analysis (AI-CPA). Available at: 

https://www.cms.gov/medicare-coverage-database/view/lcd.aspx?lcdid=39851&ver=10

 . Published October 10, 2024. Accessed October 14, 2024.

2. Cleerly. Medicare administrative contractors approve coverage of Cleerly heart scans to Medicare recipients. Business Wire. Available at: 

https://www.businesswire.com/news/home/20241014694634/en/Medicare-Administrative-Contractors-Approve-Coverage-of-Cleerly-Heart-Scans-to-Medicare-Recipients

 . Published October 14, 2024. Accessed October 14, 2024.

3. HeartFlow. HeartFlow announces favorable coverage determination for plaque analysis by four Medicare administrative contractors. GlobeNewswire. Available at: 

https://www.globenewswire.com/news-release/2024/10/11/2962144/0/en/HeartFlow-Announces-Favorable-Coverage-Determination-for-Plaque-Analysis-by-Four-Medicare-Administrative-Contractors.html

4. Elucid. Elucid announces favorable Medicare coverage of AI coronary plaque analysis. Business Wire. Available at: 

https://www.businesswire.com/news/home/20241015489543/en/Elucid-Announces-Favorable-Medicare-Coverage-of-AI-Coronary-Plaque-Analysis

 . Published October 15, 2024. Accessed October 15, 2024.

Four Medicare administrative contractors (MACs) will provide coverage of AI-enabled coronary plaque analysis and quantitative coronary tomography assessment of coronary computed tomography angiography (CCTA) for Medicare beneficiaries starting in November 2024.

Medicare to Cover AI-Powered, CCTA-Based Coronary Plaque Analysis and Quantitative Coronary Topography 

The Food and Drug Administration (FDA) has granted 510(k) clearance for AngioFlow™, an artificial intelligence (AI)-enabled perfusion imaging software that may facilitate more timely assessments of perfusion status prior to endovascular procedures.

Offering color-coded perfusion mapping that identifies regions with reduced cerebral blood flow and blood volume, 

 provides results within minutes of a cone-beam computed tomography (CT) scan, according to RapidAI, the manufacturer of AngioFlow.

In addition to potential cost savings by reducing redundant imaging, RaidAI emphasized that AngioFlow’s timely assessments may reduce long-term disability risks and facilitate life-saving interventions for patients in need of acute stroke care.

“AngioFlow by RapidAI will allow physicians to assess the need for additional imaging immediately in the interventional suite. By avoiding unnecessary scans, stroke patients can receive the timely care that can be the difference between being able to walk out of a hospital to their homes versus being discharged to a skilled nursing facility,” said Abhishek Singh, MD, DABPN, DUCNS, who is affiliated with the Creighton University School of Medicine in Omaha, Nebraska.

The company added that AngioFlow has been validated in more than 10 clinical trials.

Reportedly validated in more than 10 clinical trials, the AngioFlow perfusion imaging software enables timely identification of brain regions with cerebral blood flow reduction and those with significant hypoperfusion.

FDA Clears AI-Powered Qualitative Perfusion Mapping for Cone-Beam CT

An emerging deep learning (DL) model, which assesses magnetic resonance imaging (MRI) and clinical data, demonstrated a nine percent higher C-index for predicting prostate cancer (PCa) progression than two established risk calculators drawn from the European Randomized Study of Screening for Prostate Cancer (ERSPC) and the Prostate Cancer Prevention Trial (PCPT).

For the multicenter retrospective study, recently published in 

, the researchers assessed the DL model in 1,143 patients (median age of 64) and 1,607 MRI scans. In addition to evaluation of baseline MRI exams, the DL model reviewed clinical parameters including patient age, prostate-specific antigen (PSA) level, PSA density and prostate volume, according to the study. The internal test set was comprised of 686 patients and a total of 829 MRI scan, and external validation testing was conducted in 457 patients (778 MRI scans).

The researchers found that internal testing showed a higher C-index for the DL model (68 percent) in contrast to 59 percent for the ERPC and PCPT risk calculator models for predicting the progression of low-risk PCa to clinically significant 

 (csPCa). The study authors noted no significant differences between the tools with respect to the C-index in external validation testing with the DL model being equivalent to the PCP risk calculator (56 percent) and lower than the ERSPC risk calculator model (61 percent).

However, the researchers also determined in external validation testing that the DL model was associated with a hazard ratio (HR) of 1.32 for predicting progression to csPCa in comparison to 1.24 for the ERSPC (1.24) and PCPT models (1.09).

Employing the DL scoring model, the study authors said external validation testing showed that not having follow-up imaging for two years in the DL risk group 

1 had less than 10 percent risk of missing csPCa development. The absence of follow-up imaging for three years in this patient population was associated with a 13 percent risk of having csPCa, according to the researchers.

“In our analysis, follow-up schedules based on DL risk scores would have allowed a substantial proportion of patients to forego follow-up for 3 years with 13% or lower risk of missing disease progression,” wrote lead study author Christian Roest, MSc, who is affiliated with the Department of Radiology at University Medical Center Groningen in Groningen, the Netherlands, and colleagues.

(Editor’s note: For addition content on prostate cancer imaging, click 

When assessing the DL risk scoring model to predict PCa progression to International Society of Urological Pathology (ISUP) grades of 

 3, the researchers noted the DL model had a 1.44 HR.

“This result is particularly relevant because some active surveillance protocols may allow patients who have PCa with an ISUP grade of 2 to enroll under specific conditions (eg, the absence of cribriform growth or use less strict criteria (eg, ISUP grade ≥ 3) to trigger active treatment,” added Roest and colleagues. “ … The model’s ability to estimate the risk of progression to PCa with ISUP grade 3 or higher suggests the utility of DL risk scores across diverse surveillance protocols.”

Study Emphasizes PSMA PET Staging of High-Risk, Hormone-Sensitive Prostate Cancer

AI Segmentation, Intraprostatic Tumor Volume and Metastases: What a New mpMRI Study Reveals

MRI-Based AI Radiomics Model Offers ‘Robust’ Prediction of Perineural Invasion in Prostate Cancer

In regard to study limitations, the authors acknowledged differences between the two institutions contributing to the cohort of reviewed cases with one facility opting to conduct prostate biopsies prior to initial MRI. They also conceded that the intended population for the PCPT risk indicator differed from that of the study cohort for the MRI-based deep learning tool for estimating risk for PCa progression.

Employing baseline MRI and clinical data, an emerging deep learning model was 32 percent more likely to predict the progression of low-risk prostate cancer (PCa) to clinically significant prostate cancer (csPCa), according to new research.

Clinical

Can MRI-Based AI Enhance Risk Stratification in Prostate Cancer?

A 12-year-old boy presents to the emergency department with acute pain in the medial aspect of his right elbow after pitching in a baseball game. He also complains of dull lateral elbow pain that has been present for weeks. AP, oblique, and lateral radiographs of the right elbow were obtained.

Medial and lateral epicondyle avulsion fractures

Medial epicondyle avulsion fracture and osteochondritis dissecans of the capitellum

A 12-year-old boy presents to the emergency department with acute pain in the medial aspect of his right elbow after pitching in a baseball game. 

Image IQ: 12-year-old Boy With Acute Medial Elbow Pain

In light of recent advances for the treatment of Alzheimer’s disease (AD) and new developments in reimbursement for the use of diagnostic radiopharmaceuticals, the Society of Nuclear Medicine and Molecular Imaging (SNMMI) and the Alzheimer’s Association have issued new appropriate use criteria (AUC) for the employment of positron emission tomography (PET) in patients with mild cognitive impairment (MCI).

new AUC reflects the first updates for amyloid PET since the original AUC from 2013 as well as new criteria for tau PET

Here are 11 takeaways from the newly released AUC.

1. For patients younger than 65 years of age who present with MCI or dementia syndrome with suspected AD, the AUC indicates a high confidence in appropriate use of amyloid PET. In an update to the AUC, there is also high confidence in amyloid PET for determining patient eligibility for approved amyloid-targeting therapy.

2. For the aforementioned clinical scenarios, there is moderate confidence in the use of tau PET, according to the AUC.

3. While there is moderate confidence for the use of amyloid PET in patients presenting with MCI or dementia consistent with AD pathology in those 

 65 years of age, the AUC suggests uncertainty about the use of tau PET in this patient population but notes the possibility of appropriate use.

4. When there are atypical features of AD pathology (ranging from non-amnestic clinical presentation to an etiologically mixed presentation) in patients presenting with MCI or dementia, the AUC is “somewhat confident” in tau PET tracer use with a moderate confidence level for amyloid PET.

5. For determining disease severity or monitoring the progression of disease in patients diagnosed with MCI or dementia due to AD, the AUC indicates uncertainty with tau PET with a possibility that it is rarely appropriate. The AUC maintains with a high degree of confidence that amyloid PET use is rarely appropriate in this patient population.

6. In one of the updates for amyloid PET, the AUC suggests moderate confidence in appropriate use of these tracers for monitoring patient response to amyloid-targeting therapy. The evidence is inconclusive or lacking for use of tau PET in this patient population, according to the AUC.

Ascertaining the Prognosis of Patients with Suspected Alzheimer’s Disease Pathology

7. To inform the prognosis of patients with MCI and clinical suspicion of AD, the AUC notes moderate confidence with amyloid PET and is “somewhat confident” with the use of tau PET for these patients.

8. To inform the prognosis of patients with dementia and suspected AD pathology, the AUC is somewhat confident in the use of tau PET, but expresses uncertainty with regard to amyloid PET tracers, noting a possibility that these tracers are rarely appropriate in this patient population.

Where the New AUC Stands on Imaging for Lewy Body Disease

9. While expressing uncertainty about tau PET for patients with prodromal Lewy body disease or dementia with Lewy bodies (DLB), the AUC acknowledges the possibility that it may be appropriate in rare situations. For these patients, the AUC indicates moderate confidence that amyloid PET is rarely appropriate.

How Cerebrospinal Fluid Biomarker Results Impact Appropriateness of Amyloid PET and Tau PET

10. When there are conclusive cerebrospinal fluid (CSF) biomarker results for patients presenting with MCI or dementia, the AUC is somewhat confident that amyloid PET is rarely appropriate. While noting uncertainty about tau PET in this patient population, the AUC indicates the possibility that tau PET tracer use is appropriate.

11. When there is inconclusive or equivocal CSF biomarker results for patients with MCI or dementia, the AUC expresses moderate confidence in amyloid PET and indicates the possibility that tau PET tracer use is appropriate albeit with a degree of uncertainty.

The appropriate use criteria (AUC) reflect updates to the 2013 AUC for amyloid PET and new criteria for tau PET in the diagnosis and monitoring of patients with mild cognitive impairment (MCI).

Jennifer Wholey

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