Experts believe the method could be easily integrated into clinical settings and improve screening for PAD.

Many experts believe that artifcial intelligence could help address issues with reader variability on prostate MRIs. 

The Varipulse PFA platform originally gained FDA approval in 2024. According to Johnson & Johnson MedTech, this update was put in place to help the technology provide better patient outcomes going forward.

The first FDA-cleared AI model of its kind was found to be an accurate screening tool for cardiac amyloidosis.

Finerenone, sold by Bayer under the brand name Kerendia, is now approved in the United States for the treatment of HFmrEF and HFpEF. The drug has already been used for years to treat patients with chronic kidney disease and type 2 diabetes.

Edwards Lifesciences has recalled more than 61,000 medical devices due to the risk of a small piece of wire becoming exposed. No patient injuries have been reported at this time.

“Leaders in radiology must prioritize embedding a culture of feedback within their institutions, recognizing its crucial role in continuous improvement," experts charge. 

Findings are from a survey of 18,000 physicians across 43 states and working at over 100 healthcare organizations, who participated in the AMA Organizational Biopsy.

Selected through a national search, Achala Vagal, MD, will take on the title Aug. 1, bringing more than 20 years of experience serving the same school. 

Founded in 1969 and based in St. Louis, West County Radiological Group offers the full range of services including diagnostic and interventional radiology.