A Longitudinal Investigation of Energy Expenditure and Substrate Utilization in Critically Ill Patients (EPIC)

  • STATUS
    Recruiting
  • End date
    Feb 19, 2024
  • participants needed
    1250
  • sponsor
    Karolinska University Hospital
Updated on 19 June 2022

Summary

The metabolic alterations associated with critical illness have significant implications for the nutritional management of ICU patients. Despite this, little is known about these changes in patients requiring prolonged organ support and nutritional therapy.

The overall aim of this study is to describe changes in metabolism over time in a large prospective cohort of patients requiring >10 days of ICU care. Our hypothesis is that there is a significant change in mean energy expenditure and respiratory quotient (RQ) between the early (day 1-3), intermediate (day 4-10) and late (>10 days) phase in ICU.

Description

Background

Critical illness has profound effects on human metabolism. The most prominent feature in the early phase is an upregulation of catabolic pathways, which promotes the production of endogenous energy substrates and net protein breakdown [1].

There is very little published data describing trends of energy expenditure and substrate utilization in patients with a prolonged ICU stay. While this group only constitutes a small fraction of ICU patients, it accounts for a large part of ICU resource allocation, morbidity and mortality [2]. Several studies have been conducted in recent years to better characterize patients with persistent critical illness, focusing on markers of catabolism and inflammation [3, 4]. It is not known if these changes are associated with alterations in energy metabolism and substrate utilization.

Bridging these knowledge gaps will improve our understanding of the nutritional needs and metabolism of patients beyond the early phase in ICU. We therefore plan to conduct a prospective observational multi-center study to address these questions.

Aim and hypothesis

The overall aim of this project is to describe longitudinal changes in energy expenditure and associated clinical characteristics in a large cohort of patients with a prolonged ICU stay. Our hypothesis is that there is a significant change in mean energy expenditure and respiratory quotient (RQ) between the early (day 1-3), intermediate (day 4-10) and late (>10 days) phase in ICU. Correlations between metabolic rate and other clinical characteristics will also be analysed for hypothesis-generating purposes.

Population

All adult ICU patients with at least one measurement of energy expenditure by indirect calorimetry at participating study sites will be included in the study. Study sites are encouraged to routinely perform indirect calorimetry every 3-4 days. Study subjects will be followed until ICU discharge or death, whichever comes first.

Data collection and reporting

Patient data will be reported pseudonymized through a secure online form.

On admission

  • Admission date
  • Admission diagnosis (ICD-10)
  • Surgery prior to admission (YES/NO), elective or emergent
  • Outcome prediction score (SAPS 3, APACHE III/IV, MPM, etc.) and risk of death on admission (%)
  • ICU source admission (ER/ward/OT/other ICU)
  • Days in hospital before ICU admission

Demographic and anthropometric data:

  • Sex (male/female)
  • Age (years)
  • Weight (kg)
  • Height (cm)

Chronic comorbidities registered in electronic health records (YES/NO):

  • Hypertension
  • Ischemic heart disease
  • Heart failure
  • Diabetes mellitus
  • COPD
  • Chronic kidney disease
  • End-stage renal disease
  • Liver cirrhosis
  • Active cancer (not in complete remission)
  • Haematological malignancy
  • Solid organ transplant

On the day of each indirect calorimetry

  • REE (kcal/24 h), RQ, VO2 (ml/min), VCO2 (ml/min) and date of investigation
  • Invasive mechanical ventilation (YES/NO) or renal replacement therapy (YES/NO)

If YES to invasive mechanical ventilation:

  • Fraction of inspired oxygen
  • Positive end-expiratory pressure (cmH2O)

Factors that may influence REE:

  • Sequential organ failure assessment (SOFA) score
  • Fever (≥38.5 ℃) within 2h of measurement (YES/NO/MISSING)
  • Richmond Agitation-Sedation Scale score

Results of daily blood tests if available from routine testing:

  • P-CRP (mg/L)
  • P-albumin (g/L)
  • P-urea (mmol/L)
  • P-creatinine (μmol/L)
  • Haemoglobin (g/L)

Medications, nutrition and other therapies:

  • Infusions of vasoactive medications (YES/NO, if YES → name of medication(s))
  • Infusions of sedatives or analgesics (YES/NO, if YES → name of medication(s), if propofol → infusion rate at time of measurement)
  • Infusions of parenteral and/or enteral nutrition (YES/NO, if YES → brand name, formulation and rate at time of measurement)

On discharge

  • Discharge date
  • Survival status (ALIVE/DEAD)
  • Sepsis during ICU stay (NO/SEPSIS/SEPTIC SHOCK)

Sample size considerations

The goal of this study is to include ≥200 patients with an ICU length of stay of >10 days. Based on data from the Swedish Intensive Care Registry between 2015-2019, these patients accounted for 5% of all ICU admissions [5]. This proportion is comparable to results from a registry study conducted in Australia and New Zealand of over one million ICU admissions [2]. Based on these figures we intend to screen 6000 unique patients for study participation, accounting for the possibility that multiple measurements of indirect calorimetry are not consistently performed. In total we expect to include around 1250 unique subjects with at least one measurement with indirect calorimetry.

Statistics

Descriptive data will be presented as mean +/- standard deviation or median (interquartile range) as appropriate. The primary and secondary outcome measures will be analysed using a generalized linear mixed-effects model. Exploratory outcomes and their association to other clinical variables will be analysed using generalized linear regression models. If values are found to be not missing at random, conditional logistic regression censoring will be used to calculate inverse probability weights for accounting for difference in drop-out probabilities.

Details
Condition Critical Illness
Treatment Indirect calorimetry
Clinical Study IdentifierNCT05124860
SponsorKarolinska University Hospital
Last Modified on19 June 2022

Eligibility

Yes No Not Sure

Inclusion Criteria

>/= 18 years old
Admitted to the ICU of a participating study site
At least one measurement of energy expenditure performed during ICU stay

Exclusion Criteria

Patients readmitted to the ICU of a participating study site >72 hours after ICU discharge and already included in the study (≥1 measurement of energy expenditure performed during prior admission). If a patient is readmitted within ≤72 hours of ICU discharge this is considered a continuation of the last ICU admission for the purposes of this study
Burns >20% of body surface area
Pregnancy
Clear my responses

How to participate?

Step 1 Connect with a study center
What happens next?
  • You can expect the study team to contact you via email or phone in the next few days.
  • Sign up as volunteer to help accelerate the development of new treatments and to get notified about similar trials.

You are contacting

Investigator Avatar

Primary Contact

site

0/250

Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

Learn more

If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

Learn more

Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

Learn more

Similar trials to consider

Loading...

Not finding what you're looking for?

Every year hundreds of thousands of volunteers step forward to participate in research. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.

Sign up as volunteer

user name

Added by • 

 • 

Private

Reply by • Private
Loading...

Lorem ipsum dolor sit amet consectetur, adipisicing elit. Ipsa vel nobis alias. Quae eveniet velit voluptate quo doloribus maxime et dicta in sequi, corporis quod. Ea, dolor eius? Dolore, vel!

  The passcode will expire in None.
Loading...

No annotations made yet

Add a private note
  • abc Select a piece of text from the left.
  • Add notes visible only to you.
  • Send it to people through a passcode protected link.
Add a private note