HELPING
DELIVER OPTIMAL
INDIVIDUALISED
NUTRITION

Find out how Q-NRG+ can help to optimise nutrition therapy for your patients

 
 
 
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INTRODUCING Q-NRG+

Patient energy needs are dynamic throughout recovery and variable by condition8

Adapted from Rattanachaiwong S, and Singer P. Clin Nutr 2019;38:2531-2544

ESPEN and ASPEN guidelines recommend IC to accurately measure resting energy expenditure [REE] for critically ill, mechanically ventilated patients.1, 9

 
Adapted from Rattanachaiwong S, and Singer P. Clin Nutr 2019;38:2531-2544

Predictive equations, while often used, are inaccurate up to 50% of the time in critically ill patients which may lead to over or underfeeding or increased risk of infection.2-3

 

* Of prescribed nutritional needs

Despite clinical guidelines, most ICU patients receive only 58% of their prescribed nutritional needs7 and less than 50% of the recommended amount of protein during their first week in the ICU and beyond.6

*Of recommended protein

 

Point of care5

  • Portable and easily transported between rooms
  • Flexibility to use mechanically ventilated and spontaneou sly breathing patients

Accuracy5

  • REE range 0-7200 Kcal/day
  • Accuracy +/- 3% or 36 Kcal/day whichever is greater

Speed5

  • 10-15 mins to run test
  • Minimal warm-up time, minimal calibration time

Ease5

  • Real-time, user friendly dashboard
  • Metabolic assessment is available for download as PDF or CSV filet

Easy to use at point of care, the Q-NRG+ metabolic monitor is a fast and accurate standalone indirect calorimeter that determines dynamic energy needs over time, enabling REE measurement and effective nutrition prescriptions.4-5

References

Any medical device product quality complaints (including medical device adverse incidents) relating to Baxter products can be reported directly to the Baxter Country Quality Assurance Team on +44(0)1604 704603, or by email to UK_SHS_QA_Complaints@baxter.com. In Ireland on +353 (0)1 2065500 or by email to shs_complaints_dublin@baxter.com

Alternatively please report directly to your Baxter Representative, who will take the details and forward to the Baxter Country Quality Assurance Team.

Medical device adverse incidents should also be reported to the MHRA.

Reporting forms and information can be found at: www.mhra.gov.uk/safetyinformation/ reportingsafetyproblems/index.htm. In Ireland to the HPRA. Reporting forms and information can be found at: http://www.hpra.ie/homepage/about-us/report-an-issue.

For safe and proper use of the device, please refer to User’s Manual



About Us

Every day, millions of patients and caregivers rely on Baxter’s leading portfolio of critical, nutritional, renal, hospital and surgical care products and services. For more than 85 years, we’ve been operating at the critical intersection where innovations that save and sustain lives meet the healthcare providers that make it happen. Operating in the UK for over 60 years, Baxter is one of the largest suppliers to the NHS, producing more than 7,500 products and services.

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UKI-CN21-210030 October 2021