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肠内营养支持方案(ASNET)在非危重症患者中的疗效和安全性增加:一项随机对照试验。

Increased Efficacy and Safety of Enteral Nutrition Support with a Protocol (ASNET) in Noncritical Patients: A Randomized Controlled Trial.

出版信息

J Acad Nutr Diet. 2018 Jan;118(1):52-61. doi: 10.1016/j.jand.2017.09.020.

Abstract

BACKGROUND

Unintentional underfeeding is common in patients receiving enteral nutrition (EN), and is associated with increased risk of malnutrition complications. Protocols for EN in critically ill patients have been shown to enhance adequacy, resulting in better clinical outcomes; however, outside of intensive care unit (ICU) settings, the influence of a protocol for EN is unknown.

OBJECTIVE

To evaluate the efficacy and safety of implementing an EN protocol in a noncritical setting.

DESIGN

Randomized controlled clinical trial.

PARTICIPANTS AND SETTINGS

This trial was conducted from 2014 to 2016 in 90 adult hospitalized patients (non-ICU) receiving exclusively EN. Patients with carcinomatosis, ICU admission, or <72 hours of EN were excluded.

INTERVENTION

The intervention group received EN according to a protocol, whereas the control group was fed according to standard practice.

MAIN OUTCOME MEASURES

The proportion of patients receiving ≥80% of their caloric target at Day 4 after EN initiation.

STATISTICAL ANALYSES PERFORMED

Student t test or Wilcoxon rank-sum test were used for continuous variables and the difference between the groups in the time to receipt of the optimal amount of nutrition was analyzed using Kaplan-Meier curves.

RESULTS

Forty-five patients were randomized to each group. At Day 4 after EN initiation, 61% of patients in the intervention arm had achieved the primary end point compared with 23% in the control group (P=0.001). In malnourished patients, 63% achieved the primary end point in the intervention group compared with 16% in the control group (P=0.003). The cumulative deficit on Day 4 was lower in the intervention arm compared with the control arm: 2,507 kcal (interquartile range [IQR]=1,262 to 2,908 kcal) vs 3,844 kcal (IQR=2,620 to 4,808 kcal) (P<0.001) and 116 g (IQR=69 to 151 g) vs 191 g (IQR=147 to 244 g) protein (P<0.001), respectively. The rates of gastrointestinal complications were not significantly different between groups.

CONCLUSIONS

Implementation of an EN protocol outside the ICU significantly improved the delivery of calories and protein when compared with current standard practice without increasing gastrointestinal complications.

摘要

背景

在接受肠内营养(EN)的患者中,非故意喂养不足很常见,并且与营养不良并发症的风险增加有关。已证明,危重症患者的 EN 方案可提高充分性,从而改善临床结局;然而,在重症监护病房(ICU)环境之外,EN 方案的影响尚不清楚。

目的

评估在非重症环境中实施 EN 方案的疗效和安全性。

设计

随机对照临床试验。

参与者和设置

这项试验于 2014 年至 2016 年在 90 名接受纯 EN 的成年住院患者(非 ICU)中进行。排除癌性转移、入住 ICU 或接受 EN<72 小时的患者。

干预

干预组根据方案接受 EN,而对照组则根据标准实践进行喂养。

主要观察指标

EN 开始后第 4 天接受≥80%热量目标的患者比例。

进行的统计分析

连续变量采用学生 t 检验或 Wilcoxon 秩和检验,采用 Kaplan-Meier 曲线分析两组达到最佳营养量的时间差异。

结果

45 名患者被随机分配到每组。在 EN 开始后第 4 天,干预组有 61%的患者达到了主要终点,而对照组为 23%(P=0.001)。在营养不良的患者中,干预组有 63%的患者达到了主要终点,而对照组为 16%(P=0.003)。与对照组相比,干预组第 4 天的累积不足量较低:2507 千卡(四分位距[IQR]=1262 至 2908 千卡)比 3844 千卡(IQR=2620 至 4808 千卡)(P<0.001)和 116 克(IQR=69 至 151 克)比 191 克(IQR=147 至 244 克)蛋白质(P<0.001)。两组胃肠道并发症发生率无显著差异。

结论

与当前标准实践相比,在 ICU 之外实施 EN 方案可显著提高热量和蛋白质的输送,而不会增加胃肠道并发症。

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