For critically ill patients who require nutritional support, Q-NRG+ offers quick and accurate resting energy expenditure (REE) measurement through indirect calorimetry (IC). International guidelines recommend use of indirect calorimetry to guide energy prescription to avoid under- and over- feeding.1,2
“The accuracy of predictive equations is very low.
And this could lead to overfeeding or underfeeding
the patient leading to increased mortality or morbidity.”Dr. Pierre Singer
Inaccuracy of predictive equations4
Fast and reliable measurements
Accurate measurement of resting energy expenditure in around 10-15 minutes up to 70% FiO2.
Portable and easy to use
User-friendly touch screen and battery-powered for easy transport in the hospital.
Seamless integration
Compatible with current nutrition therapy workflows and all ventilators, patient canopies or masks.
Minimal maintenance
Automatic daily and monthly calibrations for simple maintenance and operation.
The Clinical Value of Q-NRG+
“I think we are now in a new period. With [Q-NRG+] we are going
to be able to tailor the level of energy administration to our patient,
thereby optimize the nutrition prescription.”Dr. Claude Pichard
Clinical Protocol
Comparison Sheet
Tech Spec Sheet
Learn more about Q-NRG+
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Important safety information
Q-NRG+ Indications for Use: This device is intended for the measurement of REE for spontaneously breathing and ventilated patients, with some limitations in accordance with labeling, within the following population: spontaneously breathing subjects >15 Kg (33 lb), when tested with the Canopy dilution technique, ventilated subjects >age 10 and >10 Kg (22 lb), and spontaneously breathing subjects > age 6 and >10 Kg (22 lb), when tested with Face Mask. This device is not suitable for operating in presence of flammable anesthetic gases or gases other than O2, CO2, N2 and water vapor. The device is to be used by physicians or by trained personnel under the responsibility of a physician. The device is not intended as a continuous monitoring device for surveillance of vital physiological processes.
Warnings: This device measures clinical parameters used to aid diagnosis and it is intended only as an adjunct device in patient assessment. In case of disturbing conditions, the shutdown is allowed because the safety of the device towards patients and operators is not affected, since the final evaluation is performed on the outcome data measured during a complete test. No modification of this device is allowed.
For the safe and proper use of the devices mentioned herein refer to the User Manual.