Relationship Between Protein Intake and ICU Skeletal Muscle Weakness

August 24, 2023 updated by: Tufts Medical Center
Muscle wasting is a common finding in critically ill patients and is associated with adverse outcomes. A good strategy for avoiding or decreasing muscle loss is adding adequate quantities of protein to the nutritional therapy administered during the acute phase of the disease during the ICU stay. The aim of this prospective study is to compare the effect of different levels of protein enteral feeding on Rectus Femoris Muscle mass in mechanically ventilated patients.

Study Overview

Status

Not yet recruiting

Detailed Description

Muscle wasting is a common finding in critically ill patients and is associated with adverse outcomes. Loss of mass and function of skeletal muscles start early in the first 24 h after admission and may persist for years (post-ICU syndrome).

It is a major cause of ICU-acquired muscle weakness and is associated with delayed weaning, prolonged ICU and hospital stay, and is an independent predictor of 1-year mortality.

Long-term muscle impairment affects the quality of life of ICU survivors as it is responsible for physical, mental, and cognitive dysfunction and increases the costs of health care services.

Trauma is always associated with stress leading to multisystem alterations, changes in macronutrient metabolism, as well as endocrine-metabolic activities, and immunological responses.

The stress response increases energy expenditure (EE) and the use of protein reserves. The mobilization of these reserves is not a unidirectional catabolic process but it results in an imbalance between protein synthesis and degradation depending on the magnitude of the trauma.

The resulting negative protein balance may be associated with immunosuppression; poor wound healing, muscle weakness, reduced survival, increasing length of hospitalization, and the accompanying costs.

Some authors consumed that a good strategy for avoidance or decreasing muscle loss is by adding adequate quantities of protein to the nutritional therapy administered during the acute phase of the disease during ICU stay.

In this regard, the evaluation of skeletal muscles by B- mode Ultra-Sonography is an emerging and reliable tool to assess muscle changes over time. It is a bedside technique, easy to use, and inexpensive.

Patients and methods:

Patients will be randomly classified into 2 groups 1:1 according to their protein intake:

Group I (low normal protein intake group):

Patients in this group will receive protein at (0.8 -1.5 gm/kg/day).

Group II (High normal protein intake group):

Patients in this group will receive protein (1.6 - 2.2 gm/kg/day).

For each patient on 1st day of admission, the following demographics and clinical data will be recorded: age, weight, body mass index (BMI), Glasgow Coma Scale (GCS), blood levels of albumin, total protein, and creatinine, then complete nutritional assessment is done for every patient by modified NUTRIC risk assessment tool.

Nutritional support This study will be carried out on you in the intensive care unit of tufts medical center. Enteral feeding will be started as soon as the condition will be stable, usually within 24 hours. The caloric requirement for you will be detected by indirect calorimetry or calculation (30/35 Kcal/Kg/day) and will be supplied in the form of high caloric Entral formula (1.5kcal/ml, 237ml contains 15.1 g protein) and the protein supplementation will be completed by the addition of enteral supplemental protein (beneprotein) as required to reach the target level of protein to reach at least minimum protein requirement 0.8 grams per kilogram of body weight Tube feeding will be started at a very low rate (10-20 ml/h) and the rate will be increased 25 ml every 6 hours until standard requirements of caloric and protein intake is achieved. The patient's intolerance to feeding is defined based on clinical signs (abdominal distention, vomiting, high gastric residual volume ≥ 500 cc) and will be excluded from the final analysis.

On 1st day of admission to the ICU, you will be intubated, ventilated, and sedated. Imaging by ultrasound on subsequent days will be performed in patients who will be still intubated and ventilated. An ultrasound (US) evaluation of the Rectus Femoris (RF) muscle will be performed on day 0 (within 24 h from admission),1st, and 5th day.

Assessment of Rectus Femoris muscle:

On 1st day of admission, all patients will be intubated, ventilated, and sedated. Imaging on subsequent days will be performed in patients who will be still intubated and ventilated. Skeletal muscles will be evaluated by US scan, collecting both quantitative and qualitative data.

An ultrasound (US) evaluation of the Rectus Femoris(RF) muscle will be performed in all patients on day 0 (within 24 h from trauma),1 st, and 5th day. We will use a US device with a 2- to 5-MHz linear probe. US settings (depth, gain, and focus) will be standardized for RF examination. Excess contact gel will be applied so to minimize underlying soft tissue distortion. The transducer will be placed perpendicular to the long axis of the muscle (i.e., perpendicular to the major axis of the limb), at 3/5 of the distance between the anterior superior iliac spine and the superior border of patella (i.e., about 15 cm from the patella) for the RF. The measurement points will be marked with indelible ink to ensure day-to-day consistency and facilitate subsequent measurements. After freezing the US image, quantitative parameters will be recorded for cross-sectional area (CSA) (computed from the perimetral contour of the muscle section). The value of CSA is considered to be proportional to the total mass of the skeletal muscle. We also will measure the Pennation angle of Rectus femoris (The pennation angle is defined as the angle between muscle fibers and the deep fascia of the muscle). Pennation angles will therefore be measured in the longitudinal ultrasound image as the orientation of the fibers of the rectus femoris was almost parallel to their fascia.

We also will record one qualitative parameter-echogenicity-that is expressed according to the Heckmatt Scale. Increased echogenicity is usually regarded as an index of myofibers depletion.

Measurements and monitoring

  1. Demographic data e.g. age, sex, weight body mass index (BMI), Modified Nutric score.
  2. Quantitative parameters:

    Pennation angle, the cross-sectional area of rectus femoris muscle: at baseline then at day 1 st, 5th after initiation of nutritional therapy.

  3. Qualitative parameter:

    Echogenicity by Heckmatt scale: at baseline then at baseline then at day 1 st, 5th after initiation of nutritional therapy.

  4. Serum albumin and total protein at baseline then at day 1 st, and 5th after initiation of nutritional therapy.
  5. Blood urea nitrogen, nitrogen balance at baseline then at day 1 st, 5th after initiation of nutritional therapy.
  6. The length of mechanical ventilation and ICU stay will be estimated and compared in the two groups.

Study Type

Observational

Enrollment (Estimated)

60

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult

Accepts Healthy Volunteers

No

Sampling Method

Non-Probability Sample

Study Population

all mechanically ventilated patients with a Glasgow Coma Scale ≤ 8 within 24 hours after the injury. only well-nourished ( Modified Nutric -Score for Risk Screening = 0- 4), previously healthy subjects

Description

Inclusion Criteria:

  • Adult patients of both sexes, 18-50 years old with a Glasgow Coma Scale ≤ 8 and an injury severity score (ISS>15) were admitted to our ICU within 24 hours after the injury. only well-nourished ( Modified Nutric -Score for Risk Screening = 0- 4), previously healthy subjects will be recruited.

Exclusion Criteria:

  1. Pregnancy, Patients with BMI ≥ 35,
  2. Vascular insufficiency or trauma to the lower limbs,
  3. History of neuromuscular diseases, Prolonged immobility prior to ICU admission,
  4. Comorbidities (renal, hepatic, cardiac disorders, chronic obstructive pulmonary disease, and diabetic patient),
  5. Patients with malignant diseases or immune disorders,
  6. Prolonged corticosteroids (CS) or neuromuscular blocking agents (NMBA) use,
  7. ARDS patient (P/F ratio ≤ 200), Sepsis, Multiorgan failure.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
low normal protein intake
the patient in this group will intake enteral protein feeding from 0.8- 1.5 gm /kg/day
high normal protein intake
the patient in this group will intake enteral protein feeding from 1.6 - 2.2 gm /kg/day

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
the percentage of reduction in the muscle mass measured by US.
Time Frame: day 0 , 1, and 5 days of ICU admission
the percentage of muscle mass change compared to the other group
day 0 , 1, and 5 days of ICU admission

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Pennation angle of rectus femoris muscle in degrees
Time Frame: day 0 , 1, and 5 days of ICU admission
calculate the Pennation angle of rectus femoris compared to the other group
day 0 , 1, and 5 days of ICU admission
Length of mechanical ventilation and ICU stay in days
Time Frame: until discharge or died
calculate the duration spent on the ventilator and days spent in the ICU reduced in both groups
until discharge or died
age in years
Time Frame: at the baseline day (0) of study
average age of each group in years and compared to each other
at the baseline day (0) of study
weight in kilograms
Time Frame: at the baseline day (0) of study
weight of each patient in kilograms and compared to each other
at the baseline day (0) of study
Body Mass index in Kilogram/meter square
Time Frame: at the baseline day (0) of study
weight and height will be combined to report BMI in kg/m^2
at the baseline day (0) of study
sex predominance in each group
Time Frame: at the baseline day (0) of study
sex predominance in each group and compare to each other
at the baseline day (0) of study
modified nutric score
Time Frame: at the baseline day (0) of study
International score for evaluation of nutritional status of the each patient in each group
at the baseline day (0) of study
cross- sectional area in centimeter
Time Frame: day 0 , 1, and 5 days of ICU admission
calculate the cross sectional area of rectus femoris compared to the other group
day 0 , 1, and 5 days of ICU admission
Echogenicity by Heckmatt scale
Time Frame: day 0 , 1, and 5 days of ICU admission
it is a international scale to detect the echogenecity
day 0 , 1, and 5 days of ICU admission
Serum albumin and total protein in grams per deciliter
Time Frame: day 0 , 1, and 5 days of ICU admission
measures Serum albumin and total protein for each patient in each group and compare between the two groups
day 0 , 1, and 5 days of ICU admission
Blood urea nitrogen in mg/dL
Time Frame: at baseline day (0) then at day 1 st, 5th after initiation of nutritional therapy..
measures Blood urea nitrogen each patient in each group and compare between the two groups
at baseline day (0) then at day 1 st, 5th after initiation of nutritional therapy..
nitrogen balance in gram per day
Time Frame: at baseline day (0) then at day 1 st, 5th after initiation of nutritional therapy.
measures nitrogen balance for each patient in each group and compare between the two groups
at baseline day (0) then at day 1 st, 5th after initiation of nutritional therapy.

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: PAVAN SEKHAR, MD, Tufts Medical Center

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Estimated)

September 1, 2023

Primary Completion (Estimated)

November 1, 2023

Study Completion (Estimated)

December 1, 2023

Study Registration Dates

First Submitted

January 11, 2023

First Submitted That Met QC Criteria

August 24, 2023

First Posted (Actual)

August 25, 2023

Study Record Updates

Last Update Posted (Actual)

August 25, 2023

Last Update Submitted That Met QC Criteria

August 24, 2023

Last Verified

August 1, 2023

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

IPD Plan Description

We measure the rectus femoris muscle thickness,pennation angle, cross-sectional area, and echogenicity.

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

Clinical Trials on Atrophy of Rectus Femoris Muscle (Physical Finding)

Subscribe