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Effect of initial calorie intake via enteral nutrition in critical illness: a meta-analysis of randomised controlled trials

INTRODUCTION: Guidelines support the use of enteral nutrition to improve clinical outcomes in critical illness; however, the optimal calorie and protein intake remains unclear. The purpose of this meta-analysis was to quantitatively analyze randomised controlled trials with regard to clinical outcom...

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Autores principales: Tian, Feng, Wang, Xinying, Gao, Xuejin, Wan, Xiao, Wu, Chao, Zhang, Li, Li, Ning, Li, Jieshou
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4434568/
https://www.ncbi.nlm.nih.gov/pubmed/25927829
http://dx.doi.org/10.1186/s13054-015-0902-0
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author Tian, Feng
Wang, Xinying
Gao, Xuejin
Wan, Xiao
Wu, Chao
Zhang, Li
Li, Ning
Li, Jieshou
author_facet Tian, Feng
Wang, Xinying
Gao, Xuejin
Wan, Xiao
Wu, Chao
Zhang, Li
Li, Ning
Li, Jieshou
author_sort Tian, Feng
collection PubMed
description INTRODUCTION: Guidelines support the use of enteral nutrition to improve clinical outcomes in critical illness; however, the optimal calorie and protein intake remains unclear. The purpose of this meta-analysis was to quantitatively analyze randomised controlled trials with regard to clinical outcomes related to varying calorie and protein administration in critically ill adult patients. METHOD: We searched Medline, EMBASE, and Cochrane databases to identify randomised controlled trials that compared the effects of initially different calorie and protein intake in critical illness. The risk ratio (RR) and weighted mean difference with 95% confidence intervals (CI) were calculated using random-effects models. The primary endpoint was mortality; secondary endpoints included infection, pneumonia, gastrointestinal intolerance, hospital and intensive care unit lengths of stay, and mechanical ventilation days. RESULTS: In the eight randomised controlled trials that enrolled 1,895 patients there was no statistical difference between the low-energy and high-energy groups in mortality (RR, 0.90; 95% CI, 0.71 to 1.15; P = 0.40), infection (RR, 1.09; 95% CI, 0.92 to 1.29; P = 0.32), or the risk of gastrointestinal intolerance (RR, 0.84; 95% CI, 0.59 to 1.19; P = 0.33). In subgroup analysis, the low-energy subgroup, fed 33.3 to 66.6% of goal energy, showed a lower mortality than the high-energy group (RR, 0.68; 95% CI, 0.51 to 0.92; P = 0.01). The improvements in mortality and gastrointestinal intolerance were absent when calorie intake was >66.6% of goal energy in the low-energy group. High-energy intake combined with high-protein intake reduced the infections (RR, 1.25; 95% CI, 1.04 to 1.52; P = 0.02); however, when the daily protein intake was similar in both groups, a high-energy intake did not decrease the infections. No statistical differences were observed in other secondary outcomes. CONCLUSION: This meta-analysis indicates that high-energy intake does not improve outcomes and may increase complications in critically ill patients who are not malnourished. Initial moderate nutrient intake (33.3 to 66.6% of goal energy), compared to high energy, may reduce mortality, and a higher protein intake combined with high energy (≥0.85 g/kg per day) may decrease the infection rate. However, the contribution of energy versus protein intake to outcomes remains unknown. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13054-015-0902-0) contains supplementary material, which is available to authorized users.
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spelling pubmed-44345682015-05-19 Effect of initial calorie intake via enteral nutrition in critical illness: a meta-analysis of randomised controlled trials Tian, Feng Wang, Xinying Gao, Xuejin Wan, Xiao Wu, Chao Zhang, Li Li, Ning Li, Jieshou Crit Care Research INTRODUCTION: Guidelines support the use of enteral nutrition to improve clinical outcomes in critical illness; however, the optimal calorie and protein intake remains unclear. The purpose of this meta-analysis was to quantitatively analyze randomised controlled trials with regard to clinical outcomes related to varying calorie and protein administration in critically ill adult patients. METHOD: We searched Medline, EMBASE, and Cochrane databases to identify randomised controlled trials that compared the effects of initially different calorie and protein intake in critical illness. The risk ratio (RR) and weighted mean difference with 95% confidence intervals (CI) were calculated using random-effects models. The primary endpoint was mortality; secondary endpoints included infection, pneumonia, gastrointestinal intolerance, hospital and intensive care unit lengths of stay, and mechanical ventilation days. RESULTS: In the eight randomised controlled trials that enrolled 1,895 patients there was no statistical difference between the low-energy and high-energy groups in mortality (RR, 0.90; 95% CI, 0.71 to 1.15; P = 0.40), infection (RR, 1.09; 95% CI, 0.92 to 1.29; P = 0.32), or the risk of gastrointestinal intolerance (RR, 0.84; 95% CI, 0.59 to 1.19; P = 0.33). In subgroup analysis, the low-energy subgroup, fed 33.3 to 66.6% of goal energy, showed a lower mortality than the high-energy group (RR, 0.68; 95% CI, 0.51 to 0.92; P = 0.01). The improvements in mortality and gastrointestinal intolerance were absent when calorie intake was >66.6% of goal energy in the low-energy group. High-energy intake combined with high-protein intake reduced the infections (RR, 1.25; 95% CI, 1.04 to 1.52; P = 0.02); however, when the daily protein intake was similar in both groups, a high-energy intake did not decrease the infections. No statistical differences were observed in other secondary outcomes. CONCLUSION: This meta-analysis indicates that high-energy intake does not improve outcomes and may increase complications in critically ill patients who are not malnourished. Initial moderate nutrient intake (33.3 to 66.6% of goal energy), compared to high energy, may reduce mortality, and a higher protein intake combined with high energy (≥0.85 g/kg per day) may decrease the infection rate. However, the contribution of energy versus protein intake to outcomes remains unknown. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13054-015-0902-0) contains supplementary material, which is available to authorized users. BioMed Central 2015-04-20 2015 /pmc/articles/PMC4434568/ /pubmed/25927829 http://dx.doi.org/10.1186/s13054-015-0902-0 Text en © Tian et al.; licensee BioMed Central. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. 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.
spellingShingle Research
Tian, Feng
Wang, Xinying
Gao, Xuejin
Wan, Xiao
Wu, Chao
Zhang, Li
Li, Ning
Li, Jieshou
Effect of initial calorie intake via enteral nutrition in critical illness: a meta-analysis of randomised controlled trials
title Effect of initial calorie intake via enteral nutrition in critical illness: a meta-analysis of randomised controlled trials
title_full Effect of initial calorie intake via enteral nutrition in critical illness: a meta-analysis of randomised controlled trials
title_fullStr Effect of initial calorie intake via enteral nutrition in critical illness: a meta-analysis of randomised controlled trials
title_full_unstemmed Effect of initial calorie intake via enteral nutrition in critical illness: a meta-analysis of randomised controlled trials
title_short Effect of initial calorie intake via enteral nutrition in critical illness: a meta-analysis of randomised controlled trials
title_sort effect of initial calorie intake via enteral nutrition in critical illness: a meta-analysis of randomised controlled trials
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4434568/
https://www.ncbi.nlm.nih.gov/pubmed/25927829
http://dx.doi.org/10.1186/s13054-015-0902-0
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