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重症监护病房(ICU)患者肠内营养期间的胃肠功能障碍:风险因素、自然病程和临床意义。能量给予增强与常规方法的比较试验(TARGET)的事后分析。

Gastrointestinal dysfunction during enteral nutrition delivery in intensive care unit (ICU) patients: Risk factors, natural history, and clinical implications. A post-hoc analysis of The Augmented versus Routine approach to Giving Energy Trial (TARGET).

机构信息

Adelaide Medicine School, University of Adelaide, Adelaide, Australia.

Intensive Care Unit, Royal Adelaide Hospital, Adelaide, Australia.

出版信息

Am J Clin Nutr. 2022 Aug 4;116(2):589-598. doi: 10.1093/ajcn/nqac113.

DOI:10.1093/ajcn/nqac113
PMID:35472097
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9348974/
Abstract

BACKGROUND

Slow gastric emptying occurs frequently during critical illness and is roughly quantified at bedside by large gastric residual volumes (GRVs). A previously published trial (The Augmented versus Routine approach to Giving Energy Trial; TARGET) reported larger GRVs with energy-dense (1.5 kcal/mL) compared with standard (1.0 kcal/mL) enteral nutrition (EN), warranting further exploration.

OBJECTIVE

To assess the incidence, risk factors, duration, and timing of large GRVs (≥250 mL) and its relation to clinical outcomes in mechanically ventilated adults.

METHODS

A post-hoc analysis of TARGET data in patients with ≥1 GRV recorded. Data are n (%) or median [IQR].

RESULTS

Of 3876 included patients, 1777 (46%) had ≥1 GRV ≥250 mL, which was more common in males (50 compared with 39%; P < 0.001) and in patients receiving energy-dense compared with standard EN (52 compared with 40%; RR = 1.27 (95% CI: 1.19, 1.36); P < 0.001) in whom it also lasted longer (1 [0-2] compared with 0 [0-1] d; P < 0.001), with no difference in time of onset after EN initiation (day 1 [0-2] compared with 1 [0-2]; P = 0.970). Patients with GRV ≥250 mL were more likely to have the following: vasopressor administration (88 compared with 76%; RR = 1.15 [1.12, 1.19]; P < 0.001), positive blood cultures (16 compared with 8%; RR = 1.92 [1.60, 2.31]; P < 0.001), intravenous antimicrobials (88 compared with 81%; RR = 1.09 [1.06, 1.12]; P < 0.001), and prolonged intensive care unit (ICU) stay (ICU-free days to day 28; 12.9 [0.0-21.0] compared with 20.0 [3.9-24.0]; P < 0.001), hospital stay (hospital-free days to day 28: 0.0 [0.0-12.0] compared with 7.0 [0.0-17.6] d; P < 0.001), ventilatory support (ventilator-free days to day 28: 16.0 [0.0-23.0] compared with 22.0 [8.0-25.0]; P < 0.001), and a higher 90-d mortality (29 compared with 23%; adjusted: RR = 1.17 [1.05, 1.30]; P = 0.003).

CONCLUSION

Large GRVs were more common in males and those receiving energy-dense formulae, occurred early and were short-lived, and were associated with a number of negative clinical sequelae, including increased mortality, even when adjusted for illness severity. This trial was registered at clinicaltrials.gov as NCT02306746.

摘要

背景

危重病患者常出现胃排空缓慢,通过大量胃残留量(GRV)在床边粗略量化。先前发表的一项试验(能量增强与常规方法给予能量试验;TARGET)报告了与标准(1.0 kcal/mL)肠内营养(EN)相比,能量密集型(1.5 kcal/mL)的 GRV 更大,这需要进一步探索。

目的

评估机械通气成人中大量 GRV(≥250 mL)的发生率、危险因素、持续时间和时间,并评估其与临床结局的关系。

方法

对 TARGET 数据进行了一项基于患者的事后分析,记录了≥1 次 GRV≥250 mL 的患者。数据为 n(%)或中位数[IQR]。

结果

在纳入的 3876 例患者中,有 1777 例(46%)有≥1 次 GRV≥250 mL,男性(50%比 39%;P < 0.001)和接受能量密集型配方的患者更常见,与接受标准 EN 的患者相比,GRV≥250 mL 的患者也更常见(52%比 40%;RR=1.27(95%CI:1.19,1.36);P < 0.001),且持续时间更长(1[0-2]比 0[0-1] d;P < 0.001),在开始 EN 后,GRV 的发病时间无差异(第 1[0-2]天比第 1[0-2]天;P=0.970)。GRV≥250 mL 的患者更有可能出现以下情况:血管加压药的使用(88%比 76%;RR=1.15(1.12,1.19);P < 0.001),阳性血培养(16%比 8%;RR=1.92(1.60,2.31);P < 0.001),静脉用抗生素(88%比 81%;RR=1.09(1.06,1.12);P < 0.001),以及 ICU 住院时间延长(无 ICU 天数至第 28 天;12.9[0.0-21.0]比 20.0[3.9-24.0];P < 0.001),住院时间延长(无住院天数至第 28 天:0.0[0.0-12.0]比 7.0[0.0-17.6] d;P < 0.001),通气支持时间延长(无通气天数至第 28 天:16.0[0.0-23.0]比 22.0[8.0-25.0];P < 0.001),以及 90 天死亡率更高(29%比 23%;调整后:RR=1.17(1.05,1.30);P=0.003)。

结论

男性和接受能量密集型配方的患者更常见大量 GRV,GRV 发生早且持续时间短,与许多不良临床后果相关,包括死亡率增加,即使在调整了疾病严重程度后也是如此。该试验在 clinicaltrials.gov 上注册为 NCT02306746。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bd1f/9348974/08fc5abdc9a0/nqac113fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bd1f/9348974/08fc5abdc9a0/nqac113fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bd1f/9348974/08fc5abdc9a0/nqac113fig1.jpg

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