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Home » Baxter, Cosmed win FDA clearance for portable metabolism monitor

Baxter, Cosmed win FDA clearance for portable metabolism monitor

February 12, 2020 By Sean Whooley

Baxter Cosmed Q-NRG+ Indirect Calorimetry Device metabolism monitor
The Q-NRG+ indirect calorimetry device [Image courtesy of Cosmed]
Baxter (NYSE:BAX) announced that it won FDA 510(k) clearance for the Q-NRG+ metabolic monitoring device developed by its partner Cosmed for helping with nutrition therapy.

Q-NRG+ uses indirect calorimetry (IC) technology to measure a patient’s calorie needs or resting energy expenditure (REE). Together, those readings can be used to inform prescription and administration of nutrition therapy, including parenteral nutrition (PN), which is the intravenous administration of nutrients.

Through the partnership between the two companies, Baxter has the rights to bring Q-NRG+ to at least 18 markets around the world, with more expansion potentially on the horizon. The device is already available in 12 countries in Europe, along with Canada, Australia and New Zealand. According to a news release, Baxter intends to make Q-NRG+ available in the U.S. at the Aspen 2020 Nutrition Science & Practice Conference between March 28 and March 31.

Q-NRG+ is designed in a compact, portable fashion to move easily between patient rooms, enabling flexibility and hospital efficiency. It can test adult and pediatric patients, along with spontaneously breathing or mechanically ventilated patients, plus it calibrates between uses and doesn’t take long to warm up.

The device is indicated for measuring REE in spontaneously breathing patients who weigh more than 33 pounds when using a canopy and spontaneously breathing patients older than six who weigh more than 22 pounds when using a face mask. It is also indicated for use with ventilated subjects older than 10 and weighing more than 22 pounds.

“It can be challenging to prescribe clinical nutrition without knowing the exact caloric needs of a patient,” Baxter GM of U.S. hospital products Heather Knight said in the news release. “With Q-NRG+, clinicians will have access to the latest technology to accurately measure energy requirements and won’t have to rely on predictive equations or dated technology — which can be cumbersome and time-consuming.”

Filed Under: 510(k), Diagnostics, Featured, Food & Drug Administration (FDA), Patient Monitoring, Regulatory/Compliance, Weight loss Tagged With: Baxter, Cosmed

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About Sean Whooley

Sean Whooley is a senior editor who mainly produces work for MassDevice, Medical Design & Outsourcing and Drug Delivery Business News. He received a bachelor's degree in multiplatform journalism from the University of Maryland, College Park. You can connect with him on LinkedIn or email him at [email protected].

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