Skip to main content
main-content

01.12.2018 | Viewpoint | Ausgabe 1/2018 Open Access

Critical Care 1/2018

High protein intake during the early phase of critical illness: yes or no?

Zeitschrift:
Critical Care > Ausgabe 1/2018
Autor:
Jean-Charles Preiser
Abbreviations
EAT-ICU
Early Goal-directed Nutrition in ICU Patients
ICU
Intensive care unit
ICU-AW
ICU-acquired muscle weakness
PEPaNIC
Early versus late parenteral nutrition in the pediatric intensive care unit

Introduction

A large consensus supports the provision of high protein intakes during the late phase of critical illness, e.g., during recovery when the ability to increase the synthesis of muscle proteins from the pool of circulating amino acids increases [ 1, 2]. However, controversial views are expressed regarding the amount of proteins to be given during the early phase of critical illness, when muscle protein breakdown outweighs muscle synthesis as a result of the resistance to anabolic stimuli [ 3, 4]. The proportion of nitrogen losses to be compensated by protein intake in the critically ill is a matter of debate, as reflected by recommendations cited in the most recently published guidelines: 1.2–2.5 g/kg of protein per day [ 5, 6] and the provision of an amount of protein lower than nitrogen losses [ 1, 4], in agreement with the “Baby stomach” concept [ 7]. These discrepant views based on experts’ opinions reflect the paucity of data from adequately powered clinical studies assessing the effects of different amounts of proteins on relevant endpoints [ 8].
Meanwhile, industrial companies recently started to market nutritional formulas containing high amounts of proteins or amino acids and promoted their use early during the course of critical illness, following experts’ opinions mainly based on associations between high nitrogen intakes and better outcomes and on biochemical arguments. The marketing of these solutions is possible as the legal standards do not require the same sequence of testing as for a new drug, i.e., phase I clinical trials to check the safety, phase II clinical trials to assess the efficacy, and phase III clinical trials to compare the new treatment with the current standard of care. In the field of nutrition, this sequence is usually not followed; as a result the issue of safety may have been overlooked [ 9]. Nonetheless, the issues raised by the three phases of clinical testing are relevant for nutritional solutions as well as for any new therapeutic modality.
The community of clinicians is then left with conflicting arguments either supporting the use of high protein solutions or cautioning against this practice (Fig.  1). This manuscript intends to summarize the arguments supporting both sides and the current clinical research.

High nitrogen intake during the early phase of critical illness: the pros

The renewed enthusiasm for high protein intake results mainly from attention paid to ICU-acquired muscle weakness (ICU-AW). Indeed, the importance of ICU-AW in the outcome of critically ill patients has been underlined by the description of long-term physical impairments and disabilities impairing the quality of life of survivors and increasing healthcare-related costs. The time course of muscle wasting is characterized by an initial abrupt drop in muscle mass and function followed by a slow, progressive recovery [ 1013]. Recently, decreased mitochondrial biogenesis and dysregulated lipid oxidation have been reported as contributors to compromised skeletal muscle bioenergetic status [ 14]. Clinically, in addition to a decrease in functional autonomy and quality of life, this prolonged muscle weakness represents a huge burden for society as a high proportion of patients who required an ICU stay lasting several days are unable to return to work or even to home [ 15].
The prevention of ICU-AW requires a multi-modal “bundle” approach, including the avoidance of sedation, early mobilization, and ambulation. The inclusion of high protein intakes in this bundle of measures appears logical as an adjunctive measure to limit the loss of muscle mass and function by boosting the synthesis of muscle proteins. High protein intake is expected to stimulate new protein synthesis, thereby preserving muscle mass [ 6]. The combination of physical activity, including active and passive mobilization, with high protein nutritional formulas or supplemental intravenous amino acids was suggested as a “must” for physical rehabilitation. Research in this area was even ranked as the number one priority by a group of experts [ 16]. Compelling retrospective data on large cohorts of patients support these expectations, as improved survival was observed in patients who received the highest amounts of protein, regardless of their physical activity [ 1720].
The results of a recent clinical prospective study confirm that it is possible to increase the circulating pool of amino acids with an enteral solution containing high amounts of proteins [ 21], in spite of high splanchnic extraction of some amino acids [ 22]. In other interventional studies, intravenous infusion of amino acids was found to be safe in patients at risk of acute renal failure [ 23] and transiently improved muscle function [ 24]. Improved 90-day survival was even found in a post-hoc analysis in the subset of patients with normal renal function [ 25].
Parallel to this quantitative approach, the qualitative aspects of proteins can also represent a promising area of clinical research. For instance, whey proteins could increase muscle synthesis more efficiently than soy or casein-based solutions as a result of their higher digestibility, their higher content in leucine, and their insulinotropic properties [ 26, 27]. Likewise, the effects of semi-elemental or elemental solutions should be re-considered as a means to improve digestibility and protein availability during enteral nutrition [ 28].

High nitrogen intake during the early phase of critical illness: the cons

On the “con” side of high protein intake, no clinical benefit has been reported from interventional studies comparing solutions containing high amounts of nutrients, including proteins, with standard amounts [ 2932]. However, in contrast to a potential benefit on muscle protein synthesis, the issue of the safety of high nitrogen intake during the acute phase of critical illness is an emerging concern. Indeed, a preplanned post-hoc analysis of the PEPaNIC study [ 33] that evaluated the effects of withholding parenteral nutrition in critically ill children suggests a linear positive correlation between the amount of amino acids provided and poorer outcome in the children randomized to the early parenteral nutrition group, until day 4 after admission [ 34] . The underlying mechanisms are not fully understood and are currently being investigated. Besides increased urea generation reported in the EAT-ICU (Early Goal-Directed Nutrition in ICU Patients) trial [ 35], increased production of glucagon leading to further oxidation of amino acids has also been reported [ 36].
Teleologically, muscle wasting could be considered a desirable consequence of adaptive anabolic resistance and lasts a few hours or days after injury [ 37]. The inability to respond to anabolic stimuli during the acute phase can be considered as a component of an adaptive response designed to provide substrates for gluconeogenesis in order to meet the requirements of vital organs and systems, an event known as auto-cannibalization or auto-cannibalism [ 3]. In this scenario, the loss of muscle would serve to supply gluconeogenetic organs. Likewise, the ability of muscles to build myofibrils will be limited and the provision of high amounts of amino acids will not attenuate the muscle wasting and could even amplify the degradation of amino acids.

Conclusions

The risk-to-benefit ratio of the provision of high amounts of proteins or amino acids during the early phase of critical illness is largely unknown. Some aspects have been investigated, while others are still unexplored.
Importantly, the optimal combination of proteins and physical activity is unknown [ 38]. This is a key issue when early physical activity is feasible and probably beneficial. Of note, the needs and protein metabolism of elderly and/or obese patients can differ from those of the overall ICU population [ 6, 39, 40].
Hopefully, some of the pending issues could be answered by some of the ongoing trials registered on clinicaltrials.​gov (Table  1). Most of the currently recruiting studies are prospective randomized controlled trials. The inclusion criteria studies are highly variable, even though an anticipated long stay and the requirement for mechanical ventilation are mandatory in most trials. The primary outcomes tend to focus on physical function in several studies, while all-cause mortality is less commonly used as a primary outcome. A wide range of interventions are being tested and compared to the standards of care, from supplemental proteins (1.5–3.0 g/kg/day) alone to combination with standardized physical activity.
Table 1
Ongoing studies currently recruiting adult patients (source: Clinicaltrials.​gov – Jul 23, 2018)
NCT number
Design
Region
Inclusion criteria
Primary outcome
Secondary outcomes
Intervention
Comparator
Planned sample size
01833624
Open-label PRCT
France
• Traumatic brain injury
• Non-traumatic brain injury: stroke, intracranial and/or subarachnoid hemorrhage, subdural and/or extradural hematoma
• Expected duration of mechanical ventilation > 48 h
Nutritional efficacy
Morbidity and mortality
Small-peptide enteral feeding formula
Whole-protein formula
206
02509520
PRCT
USA
• Age ≥ 45 years
• Respiratory insufficiency requiring mechanical ventilation
• ICU presentation < 6 days
• All four limbs intact and mobile
• Eligible for and able to participate in physical therapy
• Pre-admission Barthel Index > 70
-Muscle mass
-Global body strength
-Mobility status
-Short physical performance battery
-Time to weaning
-ICU/hospital length of stay
-Discharge disposition
-Weaning success
Functional strength and cardiopulmonary endurance training
MPR and high protein supplement goal of 1.6 g/kg/day protein
“No intervention”: MPR
“Active comparator”: MPR and high protein supplement
60
02106624
PRCT
China
• Need mechanical ventilation for more than 2 days
• Mean blood pressure more than 60 mmHg
• Predicted ICU stay more than 7 days
• Tolerance of parenteral or enteral nutrition
28-day and 90-day all cause mortality
-Duration on ventilators
-ICU stay
-Infection incidence rate
-Liver function and renal function
-Diameter of midpoint of musculus rectus femoris
-Serum concentration of albumin, pre-albumin, retinaldehyde binding protein, transferrin
-Change of body composition
Nitrogen supply is as much as 2.5–3.0 g per kilogram (lean mass weight; EN/PN)
1.2–1.5 g per kilogram (lean mass weight; EN/PN)
80
02678325
PRCT
Switzerland
• Adult patients (age 18 years or older)
• Expected stay at the ICU of 4 days upon admittance or longer
• Expected enteral feeding during at least 4 days
-Amount of protein
-Total amount of calories
-Nitrogen balance
-Gastric residual
-Number of diarrhea events
-Occurence of constipation as measured in time without defecation
High protein enteral nutrition formula (caloric density of 1.2 kcal/ml and protein percentage 33% of the total caloric intake)
Standardized normal protein enteral nutrition formula (caloric density of 1.2 kcal/ml and protein 20% of the total caloric intake)
90
02865408
Open-label PRCT
Canada
• Mechanically ventilated adult patients (> 18 years old) admitted to ICU with an expected ICU dependency (alive and need for mechanical ventilation)
• Vasopressor therapy, or mechanical circulatory support, at the point of screening of an additional 3 days, as estimated by the treating physician
Whole body protein balance
-Synthesis rates of hepatic secretory proteins
-Biomarker of amino acid restriction or repletion
-Metabolic substrates
-Resting energy expenditure
1.75 g/kg/day of protein (enteral supplemented with IV amino acids)
1.0 g/kg/day of protein (enteral)
30
03021902
Phase II RCT
USA
Requiring mechanical ventilation with actual or expected total duration of mechanical ventilation ≥ 48 h
Expected ICU stay ≥ 4 days after enrollment (to permit adequate exposure to the proposed intervention)
-Physical functioning
-Overall strength-upper and lower extremity
-Quadriceps force-lower extremity strength
-Hand held dynamometry
-Distal strength-hand grip strength
-Overall physical functional status
-Mortality
-Length of ventilation
-ICU and hospital
-ICU readmission
-Re-intubation
-Hospital-acquired infections
-Discharge location (e.g., home vs rehab)
-Body composition (ultrasound)
-Health-related quality of life
-Physical functioning (Katz Index of Independence in Activities of Daily Living)
-Physical functioning (mental and cognitive functioning)
-Health care resource utilization
IV amino acid (2.0–2.5 g/kg/day) + in-bed cycle ergometry
Usual care
142
03060668
Open-label PRCT
Brazil
•Critically ill patients
Mechanically ventilated
Expected length in the ICU > 3 days
Physical component of the SF-36
-Handgrip strength
-ICU and hospital mortality
Caloric intakes determined by indirect calorimetry + 2.0–2.2 g/kg/day of protein
25 kcal/kg/day and 1.4 to 1.5 g/kg/day of protein
294
03160547
Multi-center
pragmatic volunteer-driven
registry-based
randomized
Canada (over 100 international sites)
Nutritional high-risk
Mechanical ventilation
60-day mortality
-Nutritional adequacy
-Hospital mortality
-Readmission to ICU and hospital
-Duration of mechanical ventilation
-ICU length of stay
-Hospital length of stay
Higher prescription (≥ 2.2 g/kg/day) of protein (EN and/or PN)
A lower prescription (≤ 1.2 g/kg/day) of protein (EN and/or PN)
4000
03170401
PRCT
USA
Trauma/surgery
Enteral nutrition expected ≥ 1 week
Serum transthyretin at 3 weeks after injury
-Ventilator-free days
-Hospital-acquired pneumonia
Enteral protein supplementation
Standard enteral formula
500
03231540
PRC
Netherlands
• Admitted to intensive care
• Mechanically ventilated
• Expected duration of ventilation of 72 h
• Expected to tolerate and require enteral nutrition for more than 72 h
• SOFA score > 6 on admission day
In vitro loss of skeletal muscle function
-Loss of muscle function
-Medical research council sum score
-Changes in body composition (bioelectrical impedance analysis)
-Loss of muscle mass (ultrasound of the quadriceps femoris muscle and diaphragm, questionnaires)
-Quality of life
Whey protein supplement enriched enteral nutrition, with protein intake of 1.5 g/kg/day
Standard enteral nutrition, with protein intake of 1 g/kg/day
50
03319836
Retrospective
Canada
ICU patients
Daily total protein intake
-Caloric intake
-Feeding interruptions ( tolerance)
-Use of inotropes (pressors)
Very high protein enteral nutrition
Standard formula
40
Abbreviations: PRCT prospective randomized controlled trial, ICU intensive care unit, MPR mobility-based physical rehab, EN enteral nutrition, PN parenteral nutrition, SOFA Sequential Organ Failure Assessment
Meanwhile, owing to the potential risks of high amounts of proteins, the principle of precaution should prevail, i.e., the provision of 0.3–0.8 g proteins/kg/day during the early phase of critical illness. We definitely need to appraise more precisely the risk-to-benefit ratio by characterizing the relevant risks and measuring muscle function at the bedside as a proxy for the benefit of high protein intake.

Ethics approval and consent to participate

Not applicable.

Consent for publication

Not applicable.

Competing interests

The author declares that he has no competing interests.

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://​creativecommons.​org/​licenses/​by/​4.​0/​), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( http://​creativecommons.​org/​publicdomain/​zero/​1.​0/​) applies to the data made available in this article, unless otherwise stated.
Literatur
Über diesen Artikel

Weitere Artikel der Ausgabe 1/2018

Critical Care 1/2018 Zur Ausgabe

Neu im Fachgebiet AINS

Mail Icon II Newsletter

Bestellen Sie unseren kostenlosen Newsletter Update AINS und bleiben Sie gut informiert – ganz bequem per eMail.

Bildnachweise