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Initial energy supplementation in critically ill patients receiving enteral nutrition: a systematic review and meta-analysis of randomized controlled trials

机译:接受肠内营养的重症患者的初始能量补充:随机对照试验的系统审查和荟萃分析

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Background and Objectives: Here we systematically reviewed and quantitatively analyzed randomized controlled trials (RCTs) to compare the important initial outcomes of critically ill adults receiving low- and highenergy enteral nutrition. Methods and Study Design: RCTs comparing low- and high-energy supplementation in critically ill adults receiving enteral nutrition admitted to the intensive care unit for an expected stay of >48 h were included. Abstracts submitted to major scientific meetings were included and the primary endpoint was mortality. The risk ratio (RR) and weighted mean difference (WMD) with 95% confidence intervals (CIs) were the effect measures. Results: Eleven RCTs (3,212 patients) were included. The groups did not differ significantly in mortality (RE, 0.94; 95% CI, 0.80-1.11; p=0.47), infections morbidity (RR 1.09; 95% CI 0.95-1.26; p=0.23), pneumonia morbidity (RR 1.04; 95% CI 0.88-1.23; p=0.68), hospital length of stay (WMD-0.27; 95% CI-3.21 to 3.76;p=0.88), intensive care unit length of stay (WMD-0.32; 95% CI,-1.81 to 1.16;p=0.46), mechanical ventilation days (WMD-0.30; 95% CI-1.42 to 0.82; p=0.60). The incidence of gastrointestinal intolerance was significantly lower in the low-energy group (RR 0.79; 95% CI 0.65-0.97; p<0.05). Conclusions: The initial administration of low- versus high-energy supplements did not impact clinical outcomes except for gastrointestinal intolerance in non-malnourished critically ill patients receiving enteral nutrition. The initial administration of high rather than low-energy may benefit these patients by reducing infections, but this effect might actually be attributable to the concomitant high protein intake.
机译:背景和目标:在这里,我们系统地审查和定量地分析了随机对照试验(RCT),以比较批评性成人的重要初始结果,接受低中活性肠内营养。方法和研究设计:RCT比较高能量补充在接受肠内营养的危险性成年人中,包括预期住院的预期保健单位> 48小时。包括提交给主要科学会议的摘要,主要终点是死亡率。具有95%置信区间(CIS)的风险比(RR)和加权平均差异(WMD)是效应措施。结果:包括11个RCT(3,212名患者)。该组在死亡率下显着差异(Re,0.94; 95%CI,0.8-1.11; p = 0.47),感染发病率(RR 1.09; 95%CI 0.95-1.26; p = 0.23),肺炎发病率(RR 1.04; 95%CI 0.88-1.23; p = 0.68),医院住院时间(WMD-0.27; 95%CI-3.21至3.76; P = 0.88),重症监护单位住院时间(WMD-0.32; 95%CI, - 1.81至1.16; p = 0.46),机械通气天(WMD-0.30; 95%CI-1.42至0.82; P = 0.60)。低能量基团(RR 0.79; 95%CI 0.65-0.97; P <0.05),胃肠道不耐受的发生率显着较低。结论:低与高能补充的初始施用并未影响临床结果,除非患有肠内营养的非营养不良患者的胃肠内不耐受性。初始施用高而不是低能量可以通过减少感染来使这些患者受益,但这种效果实际上可能归因于伴随的高蛋白摄入量。

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