Low-Protein, Hypocaloric Nutrition with Glutamine versus Full-Feeding in the Acute Phase in ICU Patients with Severe Traumatic Brain Injury
Authors Xiong W, Qian K
Received 8 December 2020
Accepted for publication 8 February 2021
Published 2 March 2021 Volume 2021:17 Pages 703—710
Checked for plagiarism Yes
Review by Single anonymous peer review
Peer reviewer comments 2
Editor who approved publication: Dr Yuping Ning
Weichuan Xiong,1,2 KeJian Qian2
1Department of Critical Care Medicine, The Third Affiliated Hospital of Nanchang University, Nanchang, 330006, People’s Republic of China; 2Department of Critical Care Medicine, The First Affiliated Hospital of Nanchang University, Nanchang, 330006, People’s Republic of China
Correspondence: KeJian Qian Email [email protected]
Objective: To investigate the 28-day mortality, the length of ICU stay, days in the hospital, days of ventilator use, adverse events, and nosocomial infection events of low-protein, hypocaloric nutrition with glutamine in the first 7 days of the intensive care unit (ICU) patients with severe traumatic brain injury (STBI).
Patients and Methods: A total of 53 patients diagnosed with STBI enrolled from the third affiliated hospital of Nanchang University (Nanchang, China), from January 2019 to July 2020, were divided into two groups. We performed a randomized prospective controlled trial. The intervention group (n=27) was nutritional supported (intestinal or parenteral) with a caloric capacity of 20– 40% of European Conference on Clinical Nutrition and Metabolism (ESPEN) recommendations; specifically, low-protein intake was 0.5– 0.7g/kg per day (containing the amount of alanyl-glutamine), glutamine was 0.3 g/kg per day, and the intervention treatment lasted for 7 days. The control group (n=26) was nutritionally supported with a caloric capacity of 70– 100% of ESPEN recommendations, and the protein intake was 1.2– 1.7 g/kg per day. The primary endpoint was 28-day mortality. Secondary endpoints were the length of ICU stay, days in the hospital, days of ventilator use, adverse events and nosocomial infection events.
Results: There were no differences in baseline characteristics between groups. Survival curve analysis using the Kaplan-Meier method revealed no significant difference in 28-day mortality between the two groups (P=0.31) while adverse events (χ2= 5.853, P=0.016), nosocomial infection rate (χ2 = 4.316, P=0.038), the length of ICU stay (t=− 2.617, P=0.012), hospitalization time (t=− 2.169, P=0.036), and days of ventilator use (t=− 2.144,P=0.037) of patients in the intervention group were significantly lower than those in the control group.
Conclusion: Low-protein, hypocaloric nutrition with glutamine did not show different outcomes in 28-day mortality compared to full-feeding nutritional support in the ICU patients with STBI. However, low-protein, hypocaloric nutrition with glutamine could provide a lower need for ICU time, hospitalization time, and ventilator time in the ICU patients with STBI.
Keywords: acute phase, severe traumatic brain injury, nutrition, low-protein, hypocaloric, glutamine
Brain injury indicates a severe trauma caused by violence on the head. Its mortality rate has dropped by 50% in the past 20 years. One of the reasons for the gradual decrease in brain injury mortality is the continuous improvement of intensive care technology.1 In the treatment of patients with severe brain injury, nutritional support plays a vital role in improving the prognosis of patients with severe brain injury. Now everyone’s consensus is that proper nutritional support is of great significance for the functional recovery of patients with severe brain injury. However, whether early nutrition can help reduce the abnormalities in the acute phase and improve the prognosis of patients is controversial, and has not been supported by the latest experiments in this field.
ICU clinicians often ask questions at this stage: Should patients with severe brain injury start nutritional support treatment in the early stage of the disease? Does adding glutamine help improve the prognosis? These questions have not been clearly answered by the latest ESPEN2 and the American Neurosurgery Guidelines.3
Therefore, these problems prompted us to explore whether the low-protein and low-calorie nutritional with glutamine in the acute phase is beneficial to improve the clinical outcome of patients with severe brain injury or not.
Patients and Methods
The study sample including 53 STBI patients was enrolled at the Department of intensive care unit (ICU) and Emergency intensive care unit (EICU) of the third affiliated hospital of Nanchang University (Nanchang, China), from January 2019 to July 2020. Patients meeting the inclusion criteria were randomly divided into an intervention group and a control group according to the random number. The randomization list is generated by a computer. We used opaque, sealed, and sequentially numbered envelopes to seal the random number. The feeding strategy cannot be designed in a double-blind manner due to the need to provide corresponding nutritional support. Only patients who completed 7 days of treatment were considered for analysis, and patients who did not end the follow-up period were excluded. The random number was returned to the sequence of patient replacement until the sample size was completed.
Inclusion criteria: ① patients with non-surgical treatment with a GCS score of 4 to 8; ② patients with no previous serious diseases of the blood system, respiratory system, endocrine system, cardiovascular system, and central nervous system, and no severe combined injury and skull base fracture; ③ all the selected cases were admitted to the hospital within 8 hours after the injury.
Exclusion criteria: ① hemorrhagic shock, severe cardiopulmonary disease, children under 18 and elderly over 70 years old; ② patients who had undergone surgery or died during the observation and treatment process (7 days).
The study was approved by the Ethics Committee of China Clinical Trial Center. This study was conducted in accordance with the Declaration of Helsinki. Written informed consent before enrollment in the study was provided by relatives. This trial has been registered in the Chinese Clinical Trial Registry, with the identifier of ChiCTR1800020106.
All patients were routinely provided with corresponding treatments such as sedation, hypothermia, muscle relaxants, dehydration, and anti-infection. According to ESPEN2 2018, the full feeding group (control group) and the permissive underfeeding group (intervention group) were determined.
The intervention group were nutritional supported (intestinal or parenteral) with a caloric capacity of 20–40% of European Conference on Clinical Nutrition and Metabolism (ESPEN) recommendations; specifically, low-protein intake was 0.5–0.7g/kg per day (containing the amount of glutamine), glutamine was 0.3 g/kg per day, and the intervention treatment lasted for 7 days.
The control group was nutritionally supported with a caloric capacity of 70–100% of ESPEN recommendations, and the protein intake was 1.2–1.7 g/kg per day, without glutamine.
The calorie and protein intake of the intervention group and the control group gradually returned to normal after the 8th day. The nutritional route of the two groups of patients was first enteral nutrition, and the enteral nutrition given was full-fledged. In the control group, two bottles of amino acids were supplemented parenterally to achieve the protein required for the test.
The primary endpoint was 28-day mortality. Secondary endpoints were adverse events (diarrhea, gastric retention, refeeding syndrome), the length of ICU stay, days in the hospital, days of ventilator use, and nosocomial infection events.
Sample size was calculated using PASS 15.0.5 software (NCSS, LLC. Kaysville, Utah, USA),The calculation of the sample size is based on the ability to change between groups (at least 80% of the power) during the 1 day of ICU hospitalization, and the power to simultaneously detect the 5% change in mortality during ICU hospitalization.
R open-source software (version 3.6.0) was used for statistical analysis. The Kaplan-Meier method was used for survival curve analysis. When the two groups of data are normally distributed data, t-test were used; Contingency Table 2 × 2 in size were analyzed with chi-square, Contingency Table 2 × 5 in size were analyzed with Fisher exact test when sparse data (b<5 observations) were present. The Kaplan-Meier method was used to analyze the survival curve. P-value <0.05 is considered statistically significant.
A total of 53 patients (male 37, female 16, age 22–69) with STBI were enrolled in this study and randomly divided into two groups. As presented in Table 1, there was no significant difference in gender, age, BMI score, APACHEⅡ score, and GCS score between the two groups.
Table 1 Baseline Characteristics of the Study Cohort
Changes in Secondary Endpoints After Treatment in Both Groups
Patients in the intervention group exhibited lower adverse events (P=0.038, Table 2), lower probability of nosocomial infection (P = 0.016, Table 2), shorter ICU time (P=0.012, Figure 1), shorter hospital stay (P=0.036, Figure 1), and longer time non-ventilator (P= 0.037, Figure 1) compared to the control group.
Table 2 Comparison of Nosocomial Infection and Adverse Events Between the Two Groups
Figure 1 Comparison of total hospital stay, ICU stay, and mechanical ventilation time. Duration in the ICU or hospital or on a ventilator greater than 12 hours per day is counted as one day. at-test performed. P value <0.05 is significant.
Comparison of the 28-Day Mortality Between the Two Groups
The Kaplan-Meier method was used to analyze the survival curve, revealing that the ICU survival rate of the intervention group was slightly higher than that of the control group while there was no statistically significant difference (P=0.31, Figure 2).
Figure 2 Comparison of 28-day mortality between the two groups.
Subgroup Analysis Based on GCS Score
According to the GCS score, patients with 4 points and 5 points were combined into group I, and patients with 6 points,7 points and 8 points were combined into group II. The survival rates of the intervention group and the control group on the 28th day were compared in group I and group II, respectively. As indicated by the GCS score in group II, the 28th-day survival rate of the intervention group was significantly higher than that of the control group, (Figure 3).
Figure 3 Subgroup analysis 28-day mortality between the two groups based on GCS score.
Traditionally, it is recommended to provide adequate nutritional support in the acute phase of critical illness to reduce catabolism and prevent malnutrition. This is considered to be a window period. Early nutritional support can reduce the severity of the disease and accelerate the recovery from inflammatory syndrome (SIRS). The nutritional treatment provided by clinicians during this time is a non-nutritional benefit.4 In the past ten years, experts in critical care medicine believed that complete starvation is essential for preserving autophagy. If feeding is provided in the early stage of critical illness, the stress response to injury will be disrupted.5 Patients during this period of time presents severe inflammation, insulin resistance, and intolerance to enteral feeding.6 Therefore, they believe that permissive underfeeding may be more beneficial in the acute phase of severe brain injury patients.7
In the 1980s, researchers revealed that the physiological characteristics of severe TBI patients in the acute phase were large amounts of catabolism, increased energy expenditure, severe pro-inflammatory reactions, insulin resistance, and increased AGI (acute gastrointestinal injury) risk. Some studies have unilaterally emphasized the need to provide enough calories for patients with severe TBI8 while the appearance of insulin resistance, gastrointestinal dysfunction, hyperglycemia on the nervous system, and other sequelae was caused by the lack of evaluation.9 After entering the ICU, patients with severe brain injury will be given corresponding treatments such as hypothermia, sedation, and mechanical ventilation. These treatment measures reduce the patient’s resting energy expenditure by 10–30%.10 Moreover, the use of tranquilizers and muscle relaxants further aggravates severe gastrointestinal dysfunction. This clinical study presented that patients in the intervention group experienced less gastrointestinal disorders, electrolyte imbalances, and high blood sugar compared to patients in the control group (Table 2). Therefore, blindly emphasizing adequate nutritional support in the acute phase of severe brain injury will only cause more complications, adversely affecting the prognosis of patients.
In the well-known PermiT test, Arabi et al11 compared permissive feeding (providing 40–60% of the target energy) with full feeding (70–100% of the target energy) for the impact of critically ill patients. The results of the study demonstrated that there was no difference in infection, ICU hospitalization, ICU mortality, or 90-day mortality between the two groups. However, these early low-calorie nutritional supports can be observed by reviewing recent clinical trials of nutritional support. There are more or fewer deficiencies in the design of the treatment in clinical research. The PermiT test only limits calories, not the intake of protein (the protein intake of both groups was 1.2–1.5 g/kg per day). In contrast, there is no special selection for severe brain injury patients to undergo intervention studies, though the EDEN trial12 (Early and Delayed Feeding Treatment of Acute Lung Injury or Acute Respiratory Distress Syndrome) studies have restricted calorie and protein intake. Therefore, the results of those clinical studies are worthy of further discussion.
During the development of severe TBI, the relationship between the body and nutrition becomes extremely complicated. In this clinical trial, the patients we enrolled suffered from a severe brain injury. The total amount of protein given to the observation group in the acute phase was 0.5–0.7g/(kg·d), and the intake of glutamine was 0.3 g/(kg·d). Someone will definitely ask, why do we design the experimental program in this way? The answer is that glutamine is an indispensable nutrient in the human body.13 When a severe brain injury occurs, Glutamine in the body gradually decreases, and endogenous glutamine cannot meet the needs of the body under stress, aggravating metabolic disorders and making many severe patients have very poor clinical outcomes.14 Therefore, some researchers suggest that patients with severe brain injury should be given supplementary glutamine at an early stage.15–17
Studies have discovered that both glutamine and low-dose amino acids have the potential to activate autophagy.18 Besides, the effect of autophagy explains that preserving (or minimizing) early nutrition may be more beneficial to critically ill patients.19 Recent observational studies have revealed20,21 that providing nutritional support rich in glutamine, either alone22 or combined with probiotics23 or alanine,24 can reduce hospitalization time and infection of moderate to severe traumatic brain injury. In the CALORIES25 and NUTRIREA-26 trials, lower calories and protein intake during the first week of ICU stay exhibited better clinical outcomes. Stroud26 compared the effects of different protein intakes in the treatment of protein-energy malnutrition, concluding that high-protein intakes are dangerous.
The National Institute of Health and Clinical Optimization (NICE) once recommended that nutritional support for patients with severe illness or injury start with an estimated 50% of the target energy and protein requirements.26 In clinical trials, we discovered that time in ICU, hospital stay, and ventilator time of the patients in the intervention group were significantly reduced (Figure 1). Therefore, we recommend that patients with severe brain injury should be given low-protein, hypocaloric nutrition supplemental glutamine at an early stage.
Since glutamine is administered parenterally, only single-blind experiments can be performed. The included critically ill patients were given enteral + parenteral nutrition support within 24 hours after admission. After nutritional support was provided, patients in the intervention group had a slight improvement in the primary endpoint (28-day mortality), though there was no statistical difference (Figure 2). However, the 28-day mortality of the two groups could not be simply compared. If we extend the use time of glutamine to 14 days according the ESPEN guideline, maybe there will be a statistical difference between the two groups.Regarding secondary endpoint,this clinical trial provided a reliable and accurate estimate of the infection rate, including catheter-related infections. The results showed that there were significant differences in nosocomial infection events between the two groups.Perhaps due to the reduction of nosocomial infections, patients in the intervention group also significantly reduced the time spent on ICU and mechanical ventilation (Table 2). From another perspective, the use of glutamine-enhanced low-protein low-calorie nutritional support in this clinical trial did not cause harm to critically ill patients with high nutritional risk. The patient’s mechanical ventilation time was significantly reduced compared to the control group; the results were similar to the results of Arabi.27 It was observed that the increase in calorie intake was independently related to the significant extension of mechanical ventilation time. The clinical studies of EPaNIC28 and PEPaNIC29 indicated that the early extraintestinal damage was caused by the increase in the dose of amino acids instead of other macronutrients in the recent secondary statistical analysis. The possible reason was that the high dose of amino acids strongly inhibited autophagy. In critical illness, the interaction between autophagy and immune response and inflammation is complex and has not been fully elucidated.
We performed a subgroup survival analysis and comparison of the included patients according to the GCS score, revealing that the patients with higher GCS scores received inadequate permissive feeding of low protein with glutamine compared to the control group; the 28-day mortality was significantly different (Figure 3). The possible reasons for this phenomenon need to be further explored.
Although the subgroup analysis is conducted according to the GCS score, the sample size between the two groups is still small, and the statistical power is poor. The clinical trial is a single-blind trial. It is safe. Meanwhile, it is inevitable that we will have some biases when implementing the treatment plan and evaluating the efficacy. This is the shortcoming of this clinical trial.
Although in this clinical trial, low-protein, hypocaloric nutritional support with appropriate supplemental glutamine given to critically ill patients with STBS in the acute phase did not decrease the patient’s 28-day mortality, the subgroup analysis exhibited some good effects on the results, and the secondary endpoints were significantly improved. Therefore, whether the low-protein and hypocaloric nutritional support treatment with glutamine in the acute phase has a relatively good effect on the outcome of critically ill patients with STBS deserves further investigation.
Data Sharing Statement
All necessary information about this study was presented in the manuscript. Owing to the respect and protection of our patients’ privacy, the raw data regarding our patients are not publicly available, but it is available from the corresponding authors upon reasonable request.
The authors declare no conflicts of interest.
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