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Indirect Calorimetry Usage and Effect in Ventilator-free Days and Muscle Thickness in Septic Ventilated Patients

Primary Purpose

Sepsis, Critical Illness, Respiratory Failure

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Caloric delivery will target results of IC measurement.
Sponsored by
Baylor Research Institute
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Sepsis focused on measuring sepsis, nutrition, indirect calorimetry, muscle thickness

Eligibility Criteria

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

Inclusion Criteria:

  • New Medical ICU admits
  • Mechanically ventilated for one day and less than 3 days upon enrollment
  • Adults 18 years or older
  • Expected length of ICU stay greater than 3 days
  • Initiated on nutrition support (parenteral/or enteral nutrition)
  • Sepsis diagnosis documented by physician within one day of ICU admit
  • Signed informed consent

Exclusion Criteria:

  • Does not meet all criteria of valid indirect calorimetry test for baseline -measurement
  • Receiving pulmonary inhaled vasodilator
  • Extracorporeal Membrane, Oxygenation (ECMO)
  • Pregnancy
  • Patients required to be in prone position
  • Reintubation
  • DNR/AND
  • Prisoner
  • Employee of BSWH
  • Students in contractual agreement with BSWH entity

Sites / Locations

  • Baylor University Medical Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Measured Arm

Estimated Arm

Arm Description

Patients allocated to the measured energy expenditure (group M) will receive the intervention. Caloric delivery will target results of IC measurement.

Patients allocated to the estimated energy expenditure (group E) will receive nutrition with caloric intake calculated based on the Penn State equation.

Outcomes

Primary Outcome Measures

Ventilator free days (VFD)
The number of days from day 1 to day 28 (of hospital admission) on which the patient was not on the mechanical ventilator. If the patient expired or requires more than 28 days of mechanical ventilation, the value is zero.

Secondary Outcome Measures

Calorie and protein adequacy
Nutritional adequacy of caloric and protein delivery is measured as a ratio of the calories and protein received by the patient compared to the calories and protein prescribed during mechanical ventilation. The ratios are determined individually for calories and protein.
Change in quadricep muscle thickness
Evaluation of the change in muscle thickness during study enrollment in correlation with the adequacy of nutrition delivery.
Change in diaphragm muscle thickness
Evaluation of the change in muscle thickness during study enrollment in correlation with the adequacy of nutrition delivery.

Full Information

First Posted
January 17, 2018
Last Updated
October 21, 2020
Sponsor
Baylor Research Institute
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1. Study Identification

Unique Protocol Identification Number
NCT03440593
Brief Title
Indirect Calorimetry Usage and Effect in Ventilator-free Days and Muscle Thickness in Septic Ventilated Patients
Official Title
Utilization of Indirect Calorimetry for Calculation of Nutritional Goals and Its Effect in Ventilator-free Days and Muscle Thickness in Septic Mechanically Ventilated Patients
Study Type
Interventional

2. Study Status

Record Verification Date
January 2019
Overall Recruitment Status
Completed
Study Start Date
September 10, 2018 (Actual)
Primary Completion Date
May 31, 2019 (Actual)
Study Completion Date
October 3, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Baylor Research Institute

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Patients admitted to the ICU with diagnosis of sepsis and requiring mechanical ventilation for at least 24-hours and receiving enteral or parenteral nutrition will be prospectively randomized to one of two arms. Patients allocated to the estimated energy expenditure group will receive nutrition with caloric intake calculated based on the Penn State equation. Patients randomized to the measured group will receive nutrition with caloric intake calculated based on IC measurement present in the GE ventilator. Patients in the estimated group will have IC performed, but these data will not be used for prescription of nutrition. An equal number of beds within the ICU will be allocated to the measured group and the estimated group. The primary objective is to assess whether the utilization of indirect calorimetry for caloric goal calculation results in improvement in muscular structure, and consequent reduction of mechanical ventilation duration in patients with sepsis in comparison to utilizing the Penn State estimation equation for caloric goal calculation. The secondary objective is to assess whether the utilization of indirect calorimetry for caloric goal calculation results in improved adequacy of nutritional delivery in comparison to the adequacy of nutritional delivered when utilizing the Penn State estimation equation. Adult patients (> 18 years of age) admitted to the hospital with diagnosis of sepsis, and who require mechanical ventilation during hospitalization will be considered. Patients newly ventilated for at least one day but less than three days will be included in the study. Informed consent will be obtained from the legal authorized representative (LAR).
Detailed Description
Mechanically ventilated septic patients admitted to the ICU receiving enteral and or parenteral nutrition will be randomly allocated to one of the aforementioned groups. Demographic information, parameters obtained from the ventilator, muscle measurements through ultrasonography, and clinical information, such as time spent on the mechanical ventilation, time spent in ICU and in the hospital will be collected. Participants will enroll in the study upon admission to the ICU until one of the following occurs-patient is extubated, discharged from the ICU, or death with a maximum of 14 days of ICU admission. Upon inclusion, IC will be assessed at baseline in all patients and then twice weekly. Bedside ultrasonography of the diaphragm and quadricep muscle thickness will be performed upon enrollment of the study (within 3 days of MV and within 1 day of study enrollment) and repeated every 3-5 days with a minimum of twice weekly while on the MV. Severity of illness score (APACHE IV), cause of sepsis, ventilator data, such as average tidal volumes and plateau pressures, cumulative and equivalent doses of sedatives (propofol, midazolam, lorazepam) and analgesics (fentanyl, hydromorphone) will be collected. Presence of delirium during ventilation, based on ICU-CAM scores will be included, as well.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Sepsis, Critical Illness, Respiratory Failure, Nutrition Disorders, Calorie Deficiency, Diaphragm Injury, Quadriceps Muscle Atrophy
Keywords
sepsis, nutrition, indirect calorimetry, muscle thickness

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
25 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Measured Arm
Arm Type
Experimental
Arm Description
Patients allocated to the measured energy expenditure (group M) will receive the intervention. Caloric delivery will target results of IC measurement.
Arm Title
Estimated Arm
Arm Type
No Intervention
Arm Description
Patients allocated to the estimated energy expenditure (group E) will receive nutrition with caloric intake calculated based on the Penn State equation.
Intervention Type
Other
Intervention Name(s)
Caloric delivery will target results of IC measurement.
Intervention Description
The prescribed calories to be delivered will be set to target the measurement obtained from performing indirect calorimetry (IC). IC measures the gas exchange of oxygen consumption and carbon dioxide production to determine the true metabolic needs for cellular respiration. The expenditure of calories will be measured utilizing the gas module incorporated within the General Electric Carescape R860 ventilators.
Primary Outcome Measure Information:
Title
Ventilator free days (VFD)
Description
The number of days from day 1 to day 28 (of hospital admission) on which the patient was not on the mechanical ventilator. If the patient expired or requires more than 28 days of mechanical ventilation, the value is zero.
Time Frame
From current hospital admission date until the date of hospital discharge, date of death from any cause, whichever came first, assessed up to 28 days.
Secondary Outcome Measure Information:
Title
Calorie and protein adequacy
Description
Nutritional adequacy of caloric and protein delivery is measured as a ratio of the calories and protein received by the patient compared to the calories and protein prescribed during mechanical ventilation. The ratios are determined individually for calories and protein.
Time Frame
Nutritional adequacy will be assessed from day one of ventilation in all patients until extubation from the MV or date of death, whichever came first, assessed up to 14 days.
Title
Change in quadricep muscle thickness
Description
Evaluation of the change in muscle thickness during study enrollment in correlation with the adequacy of nutrition delivery.
Time Frame
Quadricep muscle thickness will be measured upon enrollment to the study (within 72 hours of MV) and every 3-5 days with a minimum of two times per 7 days until extubation from the MV or date of death, whichever came first, assessed up to 14 days.
Title
Change in diaphragm muscle thickness
Description
Evaluation of the change in muscle thickness during study enrollment in correlation with the adequacy of nutrition delivery.
Time Frame
Diaphragm muscle thickness will be measured upon enrollment to the study (within 72 hours of MV) and then every 3-5 days with a minimum of two times per 7 days until extubation from the MV or date of death, whichever came first, assessed up to 14 days.
Other Pre-specified Outcome Measures:
Title
Hospital Mortality
Description
Expiration of the participant will be classified as "yes" if patient expired during the current hospital admission.
Time Frame
From current hospital admission date until the date of hospital discharge or date of death from any cause, whichever came first, assessed up to 24 months.
Title
Hospital length of stay
Description
Total number of days patient was admitted to the hospital for the current admission.
Time Frame
From current hospital admission date until the date of hospital discharge or date of death from any cause, whichever came first, assessed up to 24 months.
Title
Intensive care unit length of stay
Description
Total number of days patient was admitted in the intensive care unit for the current hospital admission.
Time Frame
From current hospital admission date until the date of hospital discharge or date of death from any cause, whichever came first, assessed up to 24 months.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: New Medical ICU admits Mechanically ventilated for one day and less than 3 days upon enrollment Adults 18 years or older Expected length of ICU stay greater than 3 days Initiated on nutrition support (parenteral/or enteral nutrition) Sepsis diagnosis documented by physician within one day of ICU admit Signed informed consent Exclusion Criteria: Does not meet all criteria of valid indirect calorimetry test for baseline -measurement Receiving pulmonary inhaled vasodilator Extracorporeal Membrane, Oxygenation (ECMO) Pregnancy Patients required to be in prone position Reintubation DNR/AND Prisoner Employee of BSWH Students in contractual agreement with BSWH entity
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ashley Mullins, MS
Organizational Affiliation
Baylor Health Care System
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Ariel Modrykamien, MD
Organizational Affiliation
Baylor Health Care System
Official's Role
Principal Investigator
Facility Information:
Facility Name
Baylor University Medical Center
City
Dallas
State/Province
Texas
ZIP/Postal Code
75246
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No

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Indirect Calorimetry Usage and Effect in Ventilator-free Days and Muscle Thickness in Septic Ventilated Patients

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