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The PASTDUe Nutrition Ecosystem Project (PASTDUe) (PASTDUe)

Primary Purpose

Diet, Healthy, Food, Nutrition

Status
Recruiting
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Nutrition Ecosystem pathway
Comparator
Sponsored by
Duke University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Diet, Healthy

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Age >= 18 years
  2. ICU admission with major abdominal trauma, intra-abdominal sepsis, ischemic bowel/vascular emergencies, or penetrating trauma
  3. Not expected to receive oral or enteral nutrition for > 72 hours
  4. Primary team approval of PN

4. < 72 hours post-operative intervention

Exclusion Criteria:

  1. Expected death or withdrawal of life-sustaining treatment within the first 72 hours of ICU admission
  2. Patients admitted with

    • Diabetic ketoacidosis or non-ketotic hyperosmolar coma
    • MELD > 20 or acute fulminant hepatic failure
  3. Patients allergic to any component of parenteral nutrition or lipid solution
  4. Pregnant or breastfeeding patients
  5. Incarcerated or prisoner prior to admission

Sites / Locations

  • Duke University Medical CenterRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Other

Arm Label

Nutrition Ecosystem pathway

Comparator

Arm Description

parenteral nutrition initiated within 72 hours of operative intervention metabolic cart assessments to determine resting energy expenditure (REE) and guide registered dietitians (RDs) expedited delivery of oral nutrition supplements and a team-based approach on proper documentation of nutrition delivery and intake.

300 historical matched control subjects not having received TPN in the first 7 hospital days will be enrolled from Duke Electronic Health Record between January 2018 and June 2020.

Outcomes

Primary Outcome Measures

Number of nosocomial infection complications as measured by medical record review
ICU length of stay in days measured by medical record review

Secondary Outcome Measures

Incidence of protein-calorie malnutrition measured using AND/ASPEN-defined malnutrition criteria
Number of days patient is on ventilator measured by medical record review
Number of patients discharged home measured by medical record review/patient report
Number of patients discharged to rehabilitation center measured by medical record review/patient report
Number of patients discharged to nursing home measured by medical record review/patient report
ICU length of stay in days measured by medical record review
Length of hospital stay in days as measured by medical record review
Incidence of ED/hospital utilization as measured by medical record review/patient report
Number of TPN-related complications as measured by medical record review/patient report
Number of the different types of TPN-related complications as measured by medical record review/patient report
Number of deaths in 1-year as measured by medical record review/Legally Authorized Representative report

Full Information

First Posted
November 9, 2021
Last Updated
April 17, 2023
Sponsor
Duke University
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1. Study Identification

Unique Protocol Identification Number
NCT05127109
Brief Title
The PASTDUe Nutrition Ecosystem Project (PASTDUe)
Acronym
PASTDUe
Official Title
The PASTDUe Nutrition EcoSystem Pathway In Acute Care Abdominal Surgery and Trauma to Decrease Underfeeding and Complications
Study Type
Interventional

2. Study Status

Record Verification Date
April 2023
Overall Recruitment Status
Recruiting
Study Start Date
April 25, 2022 (Actual)
Primary Completion Date
January 1, 2025 (Anticipated)
Study Completion Date
January 1, 2026 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Duke University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
Yes
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
This is a research study to determine if a particular method of providing nutrition improves the clinical outcomes of patients in the intensive care unit (ICU) who have undergone abdominal surgery and would require nutrition delivered via the bloodstream (called total parenteral nutrition or TPN). The nutrition method we are testing is a structured nutrition delivery plan that involves tube feeding, oral nutrition supplements, and the use of a device (called an indirect calorimeter or IC) to measure calorie needs. This study will also use two devices to measure fat and muscle mass to examine changes during hospitalization. Subjects will be followed throughout hospitalization where nutrition status and fat and muscle mass will be closely monitored. Study activities will begin within 72 hours of a patient's abdominal surgery. TPN (total parenteral nutrition, a method of feeding that bypasses the usual process of eating and digestion) will be started, a non-invasive method of assessing calorie needs (indirect calorimetry (IC)) will be started, a urine sample will be collected to help assist in protein needs, and fat/muscle mass will be measured using bioelectrical impedance analysis (BIA), and an ultrasound. This is a minimal risk study and all products/devices used are non-invasive and FDA-approved. Indirect calorimetry and urine sample collection will be conducted every 3 days during the stay in the Intensive Care Unit - ICU, then every 5 days until hospital discharge. BIA and muscle ultrasound will be conducted every 7 days during ICU stay, then every 14 days until hospital discharge.
Detailed Description
The purpose of this prospective trial is to study the impact of the utilization of structured nutrition delivery pathway on 300 adult abdominal trauma and surgery patients admitted to a Duke University Medical Center (DUMC) intensive care unit (ICU) through a structured nutrition delivery pathway from surgical intervention to hospital discharge. Objectives include evaluating the impact of a structured nutrition delivery pathway on 1) nosocomial infectious complications as defined by CDC guidelines after 7 days of ICU admission and 2) protein-calorie malnutrition, ventilator use, hospital disposition, hospital and ICU length of stay, ED/hospital utilization, total parenteral nutrition (TPN)-related complications, 1-year mortality, and hospital charges. Patient outcomes will be compared to a retrospective cohort of 300 historical matched control subjects. The study intervention, a structured nutrition delivery pathway called the Nutrition Ecosystem pathway consists of the following collaborative parts to optimize nutrition intake and delivery within this patient population: 1) parenteral nutrition initiated within 72 hours of operative intervention 2) metabolic cart assessments to determine resting energy expenditure (REE) and guide registered dietitians (RDs) 3) expedited delivery of oral nutrition supplements and 4) a team-based approach on proper documentation of nutrition delivery and intake. The population group will consist of 300 surgical patients admitted to a DUMC ICU following emergent/urgent major abdominal surgery secondary to abdominal trauma, intra-abdominal sepsis, ischemic bowel/vascular emergencies, or penetrating trauma and are not expected to receive enteral or oral nutrition for at least 72 hours. 300 historical matched control subjects not having received TPN in the first 7 hospital days will be enrolled from Duke Electronic Health Record between January 2018 and June 2020. This study poses minimal risks to patients as the study activities match the current standard of care medical treatment such as nutrition delivery via TPN. Patients will benefit from metabolic and physiologic assessments, closer monitoring, and interdisciplinary support for nutrition optimization from nurses, dietitians, and providers throughout their hospitalization. Given patients' energy expenditure will be routinely measured by indirect calorimetry via a metabolic cart, a greater accuracy in caloric requirements will help achieve precision and goal nutrition for all participants.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diet, Healthy, Food, Nutrition, Intensive Care, Abdominal Trauma, Surgery, Intra-abdominal Infection, Sepsis, Ischemic Bowel, Vascular, Penetrating Abdominal Trauma, Enteral Feeding, Oral

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Model Description
Utilization of structured nutrition delivery pathway on 300 adult abdominal trauma and surgery patients admitted to a Duke University Medical Center (DUMC) intensive care unit (ICU) from surgical intervention to hospital discharge.
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
300 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Nutrition Ecosystem pathway
Arm Type
Experimental
Arm Description
parenteral nutrition initiated within 72 hours of operative intervention metabolic cart assessments to determine resting energy expenditure (REE) and guide registered dietitians (RDs) expedited delivery of oral nutrition supplements and a team-based approach on proper documentation of nutrition delivery and intake.
Arm Title
Comparator
Arm Type
Other
Arm Description
300 historical matched control subjects not having received TPN in the first 7 hospital days will be enrolled from Duke Electronic Health Record between January 2018 and June 2020.
Intervention Type
Combination Product
Intervention Name(s)
Nutrition Ecosystem pathway
Intervention Description
parenteral nutrition initiated within 72 hours of operative intervention Provided as clinically appropriate: Ensure Enlive, Ensure High-Protein, Nepro with Carb-Steady/ProSource Gelatein Plus, and/or ProSource Gelatein Plus metabolic cart assessments to determine resting energy expenditure (REE) and guide registered dietitians (RDs) Q-NRG Metabolic Cart (Indirect Calorimeter) and Quark RMR Metabolic Cart (Indirect Calorimeter) BWA 2.0 Advanced Bioelectric Impedance Spectroscopy (BIS) Philips Lumify L12-4 broadband linear array transducer ultrasound expedited delivery of oral nutrition supplements and a team-based approach on proper documentation of nutrition delivery and intake
Intervention Type
Other
Intervention Name(s)
Comparator
Intervention Description
retrospective cohort of 300 historical matched control subjects
Primary Outcome Measure Information:
Title
Number of nosocomial infection complications as measured by medical record review
Time Frame
From TPN initiation, daily until hospital discharge (up to 8 months)
Title
ICU length of stay in days measured by medical record review
Time Frame
From TPN initiation, daily until hospital discharge (up to 8 months)
Secondary Outcome Measure Information:
Title
Incidence of protein-calorie malnutrition measured using AND/ASPEN-defined malnutrition criteria
Time Frame
Measured daily from hospital admission to hospital discharge (up to 8 months)
Title
Number of days patient is on ventilator measured by medical record review
Time Frame
Measured daily from hospital admission up to hospital discharge (up to 8 months)
Title
Number of patients discharged home measured by medical record review/patient report
Time Frame
Recorded at hospital discharge (up to 8 months)]
Title
Number of patients discharged to rehabilitation center measured by medical record review/patient report
Time Frame
Recorded at hospital discharge (up to 8 months)]
Title
Number of patients discharged to nursing home measured by medical record review/patient report
Time Frame
Recorded at hospital discharge (up to 8 months)]
Title
ICU length of stay in days measured by medical record review
Time Frame
Measured from ICU admission to ICU discharge (up to 8 months)
Title
Length of hospital stay in days as measured by medical record review
Time Frame
Measured from hospital admission to hospital discharge (up to 8 months)
Title
Incidence of ED/hospital utilization as measured by medical record review/patient report
Time Frame
Measured from hospital discharge to 1-year post-hospital discharge]
Title
Number of TPN-related complications as measured by medical record review/patient report
Time Frame
Measured from TPN initiation until completion of TPN course/treatment (up to 8 months)
Title
Number of the different types of TPN-related complications as measured by medical record review/patient report
Time Frame
Measured from TPN initiation until completion of TPN course/treatment(up to 8 months)
Title
Number of deaths in 1-year as measured by medical record review/Legally Authorized Representative report
Time Frame
Measured from hospital discharge to 1-year post-hospital discharge]

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age >= 18 years ICU admission with major abdominal trauma, intra-abdominal sepsis, ischemic bowel/vascular emergencies, or penetrating trauma Not expected to receive oral or enteral nutrition for > 72 hours Primary team approval of PN 4. < 72 hours post-operative intervention Exclusion Criteria: Expected death or withdrawal of life-sustaining treatment within the first 72 hours of ICU admission Patients admitted with Diabetic ketoacidosis or non-ketotic hyperosmolar coma MELD > 20 or acute fulminant hepatic failure Patients allergic to any component of parenteral nutrition or lipid solution Pregnant or breastfeeding patients Incarcerated or prisoner prior to admission
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Paul E. Wischmeyer, MD
Phone
919-681-6437
Email
paul.wischmeyer@duke.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Jeroen Molinger
Phone
919-681-6437
Email
jeroen.molinger@duke.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Paul Wischmeyer
Organizational Affiliation
Duke University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Duke University Medical Center
City
Durham
State/Province
North Carolina
ZIP/Postal Code
27710
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Alicja Szydlowska, MBA
Phone
919-681-4377
Email
alicja.szydlowska@duke.edu

12. IPD Sharing Statement

Plan to Share IPD
No

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The PASTDUe Nutrition Ecosystem Project (PASTDUe)

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