Protein Delivery in Intermittent and Continuous Enteral Nutrition in ICU Patients

Muscle Wasting in Critically Ill Clinical Trial

— ProBoNo  

Official title:

Protein Delivery in Intermittent and Continuous Enteral Nutrition in ICU Patients A Prospective, Randomised Controlled Pilot Study in Critical Ill Patients With a Protein-rich Formula

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT03587870
• Other study ID #: EKNZ 2018-00259
• Status: Recruiting
• Phase: N/A
• Start date: March 25, 2019
• Est. completion date: March 31, 2026

Study information

• Verified date: May 2024
• Source: University Hospital, Basel, Switzerland
• Contact: Alexa Hollinger, MD
• Phone: +41786747130
• Email: alexa.hollinger[@]usb.ch
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Acute skeletal muscle wasting in ICU patients is associated with functional impairment and with increased risk of death. Of what we know today, physical disability can persist up to 5 years. Adequate nutrition is the basis for an optimal recovery for ICU patients and for prevention of muscle wasting. Today, continuous feeding is still the standard enteral nutrition form for patients in the ICU to limit the incidence of aspiration. A study of Serpa et al. and Georgia et al. compared the continuous feeding versus a bolus nutrition with a feeding time of 30 - 60 minutes every 4 hours. They showed no statistical differences in complications between both groups.

ProBoNo is a prospective, randomized, controlled pilot study of critically ill patients with a protein- rich formula to explore the impact of continuous or intermittent bolus nutrition on muscle breakdown in ICU patients. The investigators would like to recruit 68 patients during the first 24 hours after surgical intensive care unit admission. Prior beginning of nutrition administration, and on the 7th day thereafter the investigators will perform a muscle biopsy and an ultrasound from the vastus lateralis muscle in both groups.

The primary outcome is the time from 6.00 am of the following day after admission until the patient reaches his daily protein's target quantity. Secondary outcomes include the diameter and densitiy of the hamstrings assessed by ultrasound and histology, the process of gastric residual volume, number of diarrhoea events and laboratory findings like glucose, urea and insulin like growth factor (IGF)-1, all compared between the two time points.

Intermittent feeding is not only more natural and could help to limit the muscle wasting in ICU patients, it is also easier to handle for the ICU caring medical team. A trial from Georgia et al. in 2007 compared continuous to intermittent enteral nutrition. They found that the intermittently fed patients reached their nutrition goal faster than those being continuously nourished. This might in part be explained by feeding interruptions in the continuous feeding regimen. Presumably, preoperative holding of tube feedings in the continuous nutrition group most commonly caused interruptions. Thus, independently from prevention of muscle breakdown, a bolus nutrition would be more attractive.

Description:

The relevance of early continuous or intermittent enteral feeding of critically ill patients has been discussed controversially in the last years. Today, continuous feeding is still the standard for enteral nutrition in the ICU. The continuous nutrition can prevent abdominal intolerance like vomiting, diarrhoea and aspiration. Pulmonary aspiration is the most dramatic consequence of enteral nutrition and can be limited by a continuous feeding as shown by a study in 2003. However, nutrition was started with a bolus of 125ml as baseline by force of gravity over 15 minutes. Compared to the continuous nutrition, this is considered much volume in a short time. Naturally, risk of gastric intolerance in this scenario is very high.

In other studies, a similar amount of nutrition was given over a longer period of time (30 - 60 minutes) every 4 hours. In each cohort (continuous and bolus), only one case of pulmonary aspiration or tube obstruction was detected. After this study, other trials with a similar result followed. In 2007 a trial of Georgia et al. showed no statistical differences in complications regarding tube feeding, no differences of diarrhoea, emesis or pneumonias between continuous and bolus nutrition. The feeding time for bolus nutrition is also a critical influential factor. When an intermittent feeding is given over a longer period of time (20-40 minutes), the incidence of nausea and vomiting has not increased.

Intermittent feeding is not only a good alternative to continuous feeding, but also more natural, as long-term intake of nutrition over 20 hours is not common in any mammal. The alimentary tract and metabolic pathways of humans seem designed for intermittent ingestion of essential nutrients reduced to a few times a day. Different hormones of the endocrine cells affect complex roles of gastrointestinal motility, gall bladder contraction and nutrient absorption. The level of these hormones depends on the amount of nutrient ingestion. This response of the hormones is almost completely abolished in continuous feeding. But in intermittent nutrition, hormones like incretin, glucose-dependent insulinotropic polypeptide (GLP-1) and glucose-dependent insulinotropic polypeptide (GIP) boost the level of insulin and the resulting carbohydrate load and therefore influence the muscle protein synthesis and breakdown.

In healthy individuals, the anabolic effects of feeding occur due to an increase on the synthetic rate of muscle protein synthesis of approximately 300% with a simultaneous 50% decrease in the rate of protein breakdown. Two studies of 2009 and 2011 compared the intermittent bolus and continuous feeding and the effect of protein synthesis in skeletal muscle in neonatal pigs. They analysed the fractional rates of protein synthesis in muscle samples of continuous and intermittent bolus feeding groups. They could show that although both groups, continuous and intermittent bolus feeding, stimulate muscle protein synthesis, but in the bolus-fed, in the fractional rates of protein synthesis called K's was greater after a meal.

An ongoing study wants to show the effect of bolus vs. continuous feeding in ICU patients related to muscle wasting by measurements of ultrasound and blood samples. In this trial, the investigators would like to have a similar approach but with different measurements. Using ultrasound and muscle biopsies, the investigators aim to determine whether intermittent enteral feeding could preserve muscle mass better or more than standard continuous enteral feeding in the critically ill patients. In addition, the investigators would like to assess if intermittent bolus feeding optimizes protein intake in the first 7 days of critical illness since the intermittent route is less affected by interruptions following treatment and diagnostic procedures.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 68
• Est. completion date: March 31, 2026
• Est. primary completion date: December 31, 2025
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Informed Consent as documented by signature

• Adult patients (age 18 years or older)

• Expected ICU stay of five days or longer

• Expected enteral feeding during at least five days

Exclusion Criteria:

• Pregnancy or breast feeding (women of childbearing age are tested for high beta-human chorionic gonadotropin (hCG) in urine or serum upon ICU admission)

• Clinically significant chronic or acute kidney insufficiency with a glomerular filtration rate (GFR) <15.

• BMI = 18 and = 35.

• Intestinal perforation, peritonitis, intestinal fistula, necrosis or other contraindication to enteral diet

• Death or discharge before 48 hours of observation

• Noradrenaline = 0.5 µg/kg bodyweight /min

• Inherited and chronic skeletal muscle disease (e.g. Morbus Duchenne or other motoneuron disease)

• Paralysis (e.g. hemiplegia, tetraplegia and paraplegia)

• Immunosuppression

• Haematologic malignancy

Related Conditions & MeSH terms

• Cachexia
• Critical Illness
• Muscle Wasting in Critically Ill
• Muscular Atrophy

Intervention

Other:
• Enteral nutrition with Fresubin Intensive
Comparison of intermittent (experimental) vs continuous (standard, active comparator) enteral nutrition on muscle wasting in critically ill patients

Locations

Country	Name	City	State
Switzerland	University Hospital Basel, operative ICU	Basel	Basel-Stadt

Sponsors (1)

Lead Sponsor	Collaborator
University Hospital, Basel, Switzerland

Country where clinical trial is conducted

Switzerland, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Daily protein target quantity	Is the time from 6.00 am of the following day after admission until the patient reaches his daily protein target quantity (1.2 g/ kg Biologische Wertigkeit (BW)/ biological value protein in the control group, to 1.5 g/kg BW protein in the experimental group).	During ICU stay for the duration of 7 days after study inclusion
Secondary	Diameter of the hamstrings	Diameter of the hamstrings assessed by ultrasound and histology	During ICU stay, exactly 7 days after study inclusion
Secondary	Gastric residual content	Amount of gastric residual volume (ml)	Every day during ICU stay for the duration of 7 days after study inclusion
Secondary	Diarrhoea	Number of diarrhoea events	Every day during ICU stay for the duration of 7 days after study inclusion
Secondary	Glucose (mmol/l) measurement	Laboratory parameters relevant to assess under enteral Nutrition (Glucose (mmol/l))	Every day during ICU stay for the duration of 7 days after study inclusion
Secondary	BUN (mg/dl) measurement	Laboratory parameters relevant to assess under enteral Nutrition (BUN (mg/dl))	Every day during ICU stay for the duration of 7 days after study inclusion
Secondary	IGF-1 (mmol/l) measurement	Laboratory parameters relevant to assess under enteral Nutrition (IGF-1 (mmol/l))	Every day during ICU stay for the duration of 7 days after study inclusion