Interpretation and Optimization of Nutrition in the Intensive Care Units

Last updated: August 9, 2024
Sponsor: Dim3
Overall Status: Active - Recruiting

Phase

N/A

Condition

Diet And Nutrition

Treatment

Usual care

Nutritional support prescription and delivery monitoring feedback

Clinical Study ID

NCT06342895
2020_1113
2022-A00103-40
  • Ages > 18
  • All Genders

Study Summary

Despite recommendations, inadequate nutritional intake in intensive care unit (ICU) patients remains frequent and can lead to complications such as infections, increased length of stay, prolonged weaning from ventilation, increased long-term mortality, and decreased quality of life after intensive care. Studies have shown that patients only receive up to 50-60% of prescribed calories and proteins due to many factors leading to nutritional support interruptions such as ICU procedures, physical therapy, transport for imaging or invasive procedures outside the ICU, and nutrition intolerance.

Furthermore, this discrepancy between prescribed and delivered nutrition may go largely unnoticed, due to issues concerning inadequate manual or automated monitoring of delivered nutrition. A joint "Call to Action" by ASPEN, the Academy of Nutrition and Dietetics, and the American Society of Health-System Pharmacists stated that parenteral nutrition errors and their contributing factors could be prevented by improving the functionality of in-house Clinical Decision Support Systems and the interfaces between electronic health records (EHRs), automated preparation devices and pharmacy systems.

Nutrow® is a software package designed to support nutritional management based on the calculation of recommended calorie and protein requirements, real-time calculation and monitoring of calorie and protein prescriptions, real-time calculation and monitoring of calories and protein truly delivered to patients, and information feedback to prescribers. Feedim® is a Medical Device Data System (MDDS), designed by Dim3, which transmits information from enteral feeding pumps to third-party software, such as Nutrow®.

The aim of the study is to assess whether the joint use of Nutrow-Feedim improves the achievement of nutritional objectives in ICU patients prior to oral intake by reducing the discrepancy between prescribed and delivered calories and protein.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Age 18 and over.

  • French Social Security system registration.

  • First stay in ICU

  • Admitted to the Lille University Hospital Surgical ICU for at least 3 days.

  • Active enteral and/or parenteral nutritional support prescription

  • Patient and/or next-of-kin informed about the study and having consented toparticipation in the study.

Exclusion

Exclusion Criteria:

  • Age under 18

  • Burn patient

  • Admitted to the ICU with a prior active enteral/parenteral nutritional supportbefore day 3, except trophic nutrition

  • Dying patient, not-to-be-resuscitated order, or other treatment limitation decisionat ICU admission

  • Adult under guardianship

  • Department of corrections inmate

Study Design

Total Participants: 144
Treatment Group(s): 2
Primary Treatment: Usual care
Phase:
Study Start date:
April 10, 2024
Estimated Completion Date:
September 30, 2025

Connect with a study center

  • University Hospital Lille

    Lille, 59037
    France

    Active - Recruiting

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