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Medicare fraud

The years-long scheme involved sending kickbacks to physicians who ordered unnecessary transcranial doppler exams. Two conspirators have now been sentenced to prison and ordered to pay substantial fines.

simulation of the conduction pathway relative to various cardiac structures.

The newly cleared CARA System from Cara Medical was designed to help clinicians before and during a variety of cardiac procedures. It provides a personalized 3D map of the patient's cardiac conduction system and then overlays that map onto live fluoroscopic images.

money stocks

The government watchdog analyzed about 153 million radiology claims from a five-year period for its new report to Congress, with lawmakers now advocating for change. 

radiology clock alarm turnaround time efficiency

Oulu University Hospital lost one of its MRI after relocation and consolidation but was able to maintain output with the help of deep-learning technology. 

The money was meant for Minnesota, where criminals were indicted for abusing the Medicaid system to run bogus daycare centers. The Centers for Medicare & Medicaid Services did not specify how the state can rectify the situation to the Trump administration’s satisfaction. 

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The recall has been designated as the most serious, Class I, but the issue can be remedied with a software update. The affected devices are Ivenix Large Volume Pumps manufactured by Fresenius Kabi.

The treatment addresses cancers that express Nectin-4, a protein found in excess of 80% to 90% of urothelial cancer patients.

New research is sounding the alarm on the amount of radiation patients undergoing cardiac imaging are exposed to, prompting experts to call for updated protocols. 

The treatment addresses cancers that express Nectin-4, a protein found in excess of 80% to 90% of urothelial cancer patients.

New research is sounding the alarm on the amount of radiation patients undergoing cardiac imaging are exposed to, prompting experts to call for updated protocols. 

A majority of medical devices involved in Class I recalls were never required by the U.S. Food and Drug Administration (FDA) to undergo premarket or postmarket clinical testing, according to new research published in Annals of Internal Medicine.[1]

Recurrent strokes and TIAs were rare, though bleeding events among women did stand out as a trend to watch going forward.

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Identifying patients with alcohol use disorder prior to treatment may help care teams plan ahead and anticipate potential complications.

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The years-long scheme involved sending kickbacks to physicians who ordered unnecessary transcranial doppler exams. Two conspirators have now been sentenced to prison and ordered to pay substantial fines.