Patient Care

This page includes news coverage of various aspects of patient healthcare, including new technology innovations, what is working, what is not, personalized medicine and remote and telemedicine delivery. Find specific news in the areas of Care DeliveryDigital TransformationPrecision MedicineRemote Monitoring and Telehealth.

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Report: Medicaid cuts could force hundreds of rural hospitals to close their doors

A report from the Chartis Center for Rural Health warns that many hospitals in rural communities are at risk of closure if Medicaid cuts pass through Congress and are enacted by President Donald Trump. According to the analysis, women and newborns will disproportionately lose access to care. 

FDA issues Class I recall on GE Carestations due to ventilation issue

The issue stems from a mode on the ventilation systems malfunctioning. Although no devices need to be removed from care settings, some will require repair.

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FDA issues emergency recall on resuscitation systems due to failure code

A specific model of AutoPulse resuscitation system manufactured by Zoll is prone to a failure code that could result in inadequate chest compressions being administered to patients. The affected kits must be removed from the supply chain immediately.

Suman Tandon, MD, FASNC, a cardiac imager at St. Francis Hospital and Heart Center, in Rosyln, New York, and an American Society of Nuclear Cardiology (ASNC) representative to the American Medical Association (AMA) House of Delegates (HOD), explains ASNC's concerns about artificial intelligence being used to automatically deny prior authorizations and prevent patients from accessing care.

ASNC and AMA push back against AI prior authorization denials

Suman Tandon, MD, a representative of the American Society of Nuclear Cardiology, explains her organization's concerns about artificial intelligence being used to automatically deny prior authorizations and prevent patients from accessing care.

the words "FDA recall" on a board

FDA declares Class I recall on heart surgery procedure kits from Medline

The news is related to an earlier recall of more than 316,000 Medtronic devices.

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]

American College of Cardiology now supports early use of medication to treat obesity

The group highlighted the proven effectiveness of these drugs, especially semaglutide and tirzepatide, while noting that eligibility, affordability and availability will still play key roles in any treatment decisions. 

black woman breast cancer pink ribbon

Eliminating extra fee for 3D mammography bolsters utilization, though disparities persist

Experts believe this new research offers important insights as practices adopt artificial intelligence in breast imaging, often with an extra out-of-pocket fee. 

artificial intelligence AI in healthcare

Healthcare AI today: Senate arguments, aging infrastructure, ‘elastic’ jobs, more

States’ rights or federal power? Senate Republicans are of two minds on AI regulation in the One Big Beautiful Bill.