Emergency-use authorization granted for AI-based COVID management

The FDA has cleared an AI startup based in Israel to market its predictive-analytics product to ICUs during the present pandemic.

Clew Medical announced the emergency-use authorization June 16, saying its ICU-specific platform can identify patients at heightened risk of developing life-threatening COVID complications such as respiratory failure and hemodynamic instability.

The company says it trained its AI models on nearly 100,000 ICU patients.

The software, called ClewICU, works as a web application and is intended for use in tele-ICU settings as well as local ICUs.

The idea is to give COVID care teams advance warning on patients at greatest risk of serious symptoms, the company adds, which can increase time available for intervening early, planning ahead and allocating resources enterprise- or community-wide.

Dave Pearson

Dave P. has worked in journalism, marketing and public relations for more than 30 years, frequently concentrating on hospitals, healthcare technology and Catholic communications. He has also specialized in fundraising communications, ghostwriting for CEOs of local, national and global charities, nonprofits and foundations.

Around the web

The final list also included diabetes drugs sold by Boehringer Ingelheim and Merck. The first round of drug price negotiations reduced the Medicare prices for 10 popular drugs by up to 79%. 

HHS has thought through the ways AI can and should become an integral part of healthcare, human services and public health. Last Friday—possibly just days ahead of seating a new secretary—the agency released a detailed plan for getting there from here.

Philips is recalling the software associated with its Mobile Cardiac Outpatient Telemetry devices after certain high-risk ECG events were never routed to trained cardiology technicians as intended. The issue, which lasted for two years, has been linked to more than 100 injuries.