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The effect of glutamine therapy on outcomes in critically ill patients: a meta-analysis of randomized controlled trials
INTRODUCTION: Glutamine supplementation is supposed to reduce mortality and nosocomial infections in critically ill patients. However, the recently published reducing deaths due to oxidative stress (REDOX) trials did not provide evidence supporting this. This study investigated the impact of glutami...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4057299/ https://www.ncbi.nlm.nih.gov/pubmed/24401636 http://dx.doi.org/10.1186/cc13185 |
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author | Chen, Qi-Hong Yang, Yi He, Hong-Li Xie, Jian-Feng Cai, Shi-Xia Liu, Ai-Ran Wang, Hua-Ling Qiu, Hai-Bo |
author_facet | Chen, Qi-Hong Yang, Yi He, Hong-Li Xie, Jian-Feng Cai, Shi-Xia Liu, Ai-Ran Wang, Hua-Ling Qiu, Hai-Bo |
author_sort | Chen, Qi-Hong |
collection | PubMed |
description | INTRODUCTION: Glutamine supplementation is supposed to reduce mortality and nosocomial infections in critically ill patients. However, the recently published reducing deaths due to oxidative stress (REDOX) trials did not provide evidence supporting this. This study investigated the impact of glutamine-supplemented nutrition on the outcomes of critically ill patients using a meta-analysis. METHODS: We searched for and gathered data from the Cochrane Central Register of Controlled Trials, MEDLINE, Elsevier, Web of Science and ClinicalTrials.gov databases reporting the effects of glutamine supplementation on outcomes in critically ill patients. We produced subgroup analyses of the trials according to specific patient populations, modes of nutrition and glutamine dosages. RESULTS: Among 823 related articles, eighteen Randomized Controlled Trials (RCTs) met all inclusion criteria. Mortality events among 3,383 patients were reported in 17 RCTs. Mortality showed no significant difference between glutamine group and control group. In the high dosage subgroup (above 0.5 g/kg/d), the mortality rate in the glutamine group was significantly higher than that of the control group (relative risk (RR) 1.18; 95% confidence interval (CI), 1.02 to 1.38; P = 0.03). In 15 trials, which included a total of 2,862 patients, glutamine supplementation reportedly affected the incidence of nosocomial infections in the critically ill patients observed. The incidence of nosocomial infections in the glutamine group was significantly lower than that of the control group (RR 0.85; 95% CI, 0.74 to 0.97; P = 0.02). In the surgical ICU subgroup, glutamine supplementation statistically reduced the rate of nosocomial infections (RR 0.70; 95% CI, 0.52 to 0.94; P = 0.04). In the parental nutrition subgroup, glutamine supplementation statistically reduced the rate of nosocomial infections (RR 0.83; 95% CI, 0.70 to 0.98; P = 0.03). The length of hospital stay was reported in 14 trials, in which a total of 2,777 patients were enrolled; however, the patient length of stay was not affected by glutamine supplementation. CONCLUSIONS: Glutamine supplementation conferred no overall mortality and length of hospital stay benefit in critically ill patients. However, this therapy reduced nosocomial infections among critically ill patients, which differed according to patient populations, modes of nutrition and glutamine dosages. |
format | Online Article Text |
id | pubmed-4057299 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-40572992014-06-14 The effect of glutamine therapy on outcomes in critically ill patients: a meta-analysis of randomized controlled trials Chen, Qi-Hong Yang, Yi He, Hong-Li Xie, Jian-Feng Cai, Shi-Xia Liu, Ai-Ran Wang, Hua-Ling Qiu, Hai-Bo Crit Care Research INTRODUCTION: Glutamine supplementation is supposed to reduce mortality and nosocomial infections in critically ill patients. However, the recently published reducing deaths due to oxidative stress (REDOX) trials did not provide evidence supporting this. This study investigated the impact of glutamine-supplemented nutrition on the outcomes of critically ill patients using a meta-analysis. METHODS: We searched for and gathered data from the Cochrane Central Register of Controlled Trials, MEDLINE, Elsevier, Web of Science and ClinicalTrials.gov databases reporting the effects of glutamine supplementation on outcomes in critically ill patients. We produced subgroup analyses of the trials according to specific patient populations, modes of nutrition and glutamine dosages. RESULTS: Among 823 related articles, eighteen Randomized Controlled Trials (RCTs) met all inclusion criteria. Mortality events among 3,383 patients were reported in 17 RCTs. Mortality showed no significant difference between glutamine group and control group. In the high dosage subgroup (above 0.5 g/kg/d), the mortality rate in the glutamine group was significantly higher than that of the control group (relative risk (RR) 1.18; 95% confidence interval (CI), 1.02 to 1.38; P = 0.03). In 15 trials, which included a total of 2,862 patients, glutamine supplementation reportedly affected the incidence of nosocomial infections in the critically ill patients observed. The incidence of nosocomial infections in the glutamine group was significantly lower than that of the control group (RR 0.85; 95% CI, 0.74 to 0.97; P = 0.02). In the surgical ICU subgroup, glutamine supplementation statistically reduced the rate of nosocomial infections (RR 0.70; 95% CI, 0.52 to 0.94; P = 0.04). In the parental nutrition subgroup, glutamine supplementation statistically reduced the rate of nosocomial infections (RR 0.83; 95% CI, 0.70 to 0.98; P = 0.03). The length of hospital stay was reported in 14 trials, in which a total of 2,777 patients were enrolled; however, the patient length of stay was not affected by glutamine supplementation. CONCLUSIONS: Glutamine supplementation conferred no overall mortality and length of hospital stay benefit in critically ill patients. However, this therapy reduced nosocomial infections among critically ill patients, which differed according to patient populations, modes of nutrition and glutamine dosages. BioMed Central 2014 2014-01-09 /pmc/articles/PMC4057299/ /pubmed/24401636 http://dx.doi.org/10.1186/cc13185 Text en Copyright © 2014 Chen et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Chen, Qi-Hong Yang, Yi He, Hong-Li Xie, Jian-Feng Cai, Shi-Xia Liu, Ai-Ran Wang, Hua-Ling Qiu, Hai-Bo The effect of glutamine therapy on outcomes in critically ill patients: a meta-analysis of randomized controlled trials |
title | The effect of glutamine therapy on outcomes in critically ill patients: a meta-analysis of randomized controlled trials |
title_full | The effect of glutamine therapy on outcomes in critically ill patients: a meta-analysis of randomized controlled trials |
title_fullStr | The effect of glutamine therapy on outcomes in critically ill patients: a meta-analysis of randomized controlled trials |
title_full_unstemmed | The effect of glutamine therapy on outcomes in critically ill patients: a meta-analysis of randomized controlled trials |
title_short | The effect of glutamine therapy on outcomes in critically ill patients: a meta-analysis of randomized controlled trials |
title_sort | effect of glutamine therapy on outcomes in critically ill patients: a meta-analysis of randomized controlled trials |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4057299/ https://www.ncbi.nlm.nih.gov/pubmed/24401636 http://dx.doi.org/10.1186/cc13185 |
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