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短期相对禁忌早期肠内营养的危重症患者早期肠外营养:一项随机对照试验。

Early parenteral nutrition in critically ill patients with short-term relative contraindications to early enteral nutrition: a randomized controlled trial.

机构信息

Northern Clinical School Intensive Care Research Unit, University of Sydney, Sydney, Australia.

出版信息

JAMA. 2013 May 22;309(20):2130-8. doi: 10.1001/jama.2013.5124.

Abstract

IMPORTANCE

Systematic reviews suggest adult patients in intensive care units (ICUs) with relative contraindications to early enteral nutrition (EN) may benefit from parenteral nutrition (PN) provided within 24 hours of ICU admission.

OBJECTIVE

To determine whether providing early PN to critically ill adults with relative contraindications to early EN alters outcomes.

DESIGN, SETTING, AND PARTICIPANTS: Multicenter, randomized, single-blind clinical trial conducted between October 2006 and June 2011 in ICUs of 31 community and tertiary hospitals in Australia and New Zealand. Participants were critically ill adults with relative contraindications to early EN who were expected to remain in the ICU longer than 2 days.

INTERVENTIONS

Random allocation to pragmatic standard care or early PN.

MAIN OUTCOMES AND MEASURES

Day-60 mortality; quality of life, infections, and body composition.

RESULTS

A total of 1372 patients were randomized (686 to standard care, 686 to early PN). Of 682 patients receiving standard care, 199 patients (29.2%) initially commenced EN, 186 patients (27.3%) initially commenced PN, and 278 patients (40.8%) remained unfed. Time to EN or PN in patients receiving standard care was 2.8 days (95% CI, 2.3 to 3.4). Patients receiving early PN commenced PN a mean of 44 minutes after enrollment (95% CI, 36 to 55). Day-60 mortality did not differ significantly (22.8% for standard care vs 21.5% for early PN; risk difference, -1.26%; 95% CI, -6.6 to 4.1; P = .60). Early PN patients rated day-60 quality of life (RAND-36 General Health Status) statistically, but not clinically meaningfully, higher (45.5 for standard care vs 49.8 for early PN; mean difference, 4.3; 95% CI, 0.95 to 7.58; P = .01). Early PN patients required fewer days of invasive ventilation (7.73 vs 7.26 days per 10 patient × ICU days, risk difference, -0.47; 95% CI, -0.82 to -0.11; P = .01) and, based on Subjective Global Assessment, experienced less muscle wasting (0.43 vs 0.27 score increase per week; mean difference, -0.16; 95% CI, -0.28 to -0.038; P = .01) and fat loss (0.44 vs 0.31 score increase per week; mean difference, -0.13; 95% CI, -0.25 to -0.01; P = .04).

CONCLUSIONS AND RELEVANCE

The provision of early PN to critically ill adults with relative contraindications to early EN, compared with standard care, did not result in a difference in day-60 mortality. The early PN strategy resulted in significantly fewer days of invasive ventilation but not significantly shorter ICU or hospital stays.

TRIAL REGISTRATION

anzctr.org.au Identifier: ACTRN012605000704695.

摘要

重要性

系统评价表明,对于 ICU 中存在早期肠内营养相对禁忌证的成年患者,在 ICU 入住后 24 小时内给予肠外营养(PN)可能有益。

目的

确定对存在早期 EN 相对禁忌证的危重症成人给予早期 PN 是否会改变结局。

设计、地点和参与者:2006 年 10 月至 2011 年 6 月在澳大利亚和新西兰 31 家社区和三级医院的 ICU 中进行的多中心、随机、单盲临床试验。参与者为预计 ICU 入住时间超过 2 天的存在早期 EN 相对禁忌证的危重症成人。

干预措施

随机分配到实用标准护理或早期 PN。

主要结局和测量指标

第 60 天死亡率;生活质量、感染和身体成分。

结果

共随机分配 1372 名患者(标准护理组 686 名,早期 PN 组 686 名)。在接受标准护理的 682 名患者中,199 名患者(29.2%)最初开始接受 EN,186 名患者(27.3%)最初开始接受 PN,278 名患者(40.8%)仍未进食。接受标准护理的患者接受 EN 或 PN 的时间为 2.8 天(95%CI,2.3 至 3.4)。接受早期 PN 的患者在入组后平均 44 分钟开始接受 PN(95%CI,36 至 55)。第 60 天死亡率无显著差异(标准护理组为 22.8%,早期 PN 组为 21.5%;风险差异,-1.26%;95%CI,-6.6 至 4.1;P =.60)。早期 PN 患者在第 60 天的生活质量(RAND-36 一般健康状况)评分上具有统计学意义,但无临床意义上的更高(标准护理组为 45.5,早期 PN 组为 49.8;平均差异,4.3;95%CI,0.95 至 7.58;P =.01)。早期 PN 患者需要更少的有创通气天数(每 10 名患者 ICU 天数的侵袭性通气天数,标准护理组为 7.73 天,早期 PN 组为 7.26 天,风险差异,-0.47;95%CI,-0.82 至 -0.11;P =.01),并且根据主观综合评估,肌肉萎缩(每周评分增加 0.43 与 0.27,平均差异,-0.16;95%CI,-0.28 至 -0.038;P =.01)和脂肪损失(每周评分增加 0.44 与 0.31,平均差异,-0.13;95%CI,-0.25 至 -0.01;P =.04)的发生率较低。

结论和相关性

与标准护理相比,对存在早期 EN 相对禁忌证的危重症成人给予早期 PN 并不会导致第 60 天死亡率的差异。早期 PN 策略可显著减少有创通气天数,但不会显著缩短 ICU 或住院时间。

试验注册

anzctr.org.au 标识符:ACTRN012605000704695。

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