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. 2014 Jan 9;18(1):R8. doi: 10.1186/cc13185.
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.
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.
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.
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.
补充谷氨酰胺被认为可以降低重症患者的死亡率和医院感染率。然而,最近发表的氧化应激导致死亡减少(REDOX)试验并未提供支持这一观点的证据。本研究通过荟萃分析探讨了补充谷氨酰胺的营养支持对重症患者预后的影响。
我们在Cochrane对照试验中央注册库、MEDLINE、爱思唯尔、科学网和ClinicalTrials.gov数据库中检索并收集了报告补充谷氨酰胺对重症患者预后影响的数据。我们根据特定患者群体、营养方式和谷氨酰胺剂量对试验进行了亚组分析。
在823篇相关文章中,18项随机对照试验(RCT)符合所有纳入标准。17项RCT报告了3383例患者的死亡事件。谷氨酰胺组和对照组的死亡率无显著差异。在高剂量亚组(高于0.5 g/kg/d)中,谷氨酰胺组的死亡率显著高于对照组(相对风险(RR)1.18;95%置信区间(CI),1.02至1.38;P = 0.03)。在15项试验中,共纳入2862例患者,据报道补充谷氨酰胺影响了所观察的重症患者医院感染的发生率。谷氨酰胺组的医院感染发生率显著低于对照组(RR 0.85;95% CI,0.74至0.97;P = 0.02)。在外科重症监护病房亚组中,补充谷氨酰胺在统计学上降低了医院感染率(RR 0.70;95% CI,0.52至0.94;P = 0.04)。在肠外营养亚组中,补充谷氨酰胺在统计学上降低了医院感染率(RR 0.83;95% CI,0.70至0.98;P = 0.03)。14项试验报告了住院时间,共纳入2777例患者;然而,补充谷氨酰胺并未影响患者的住院时间。
补充谷氨酰胺对重症患者的总体死亡率和住院时间并无益处。然而,这种治疗方法降低了重症患者的医院感染率,且根据患者群体、营养方式和谷氨酰胺剂量的不同而有所差异。