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缓慢增加肠内喂养量以预防极低出生体重儿坏死性小肠结肠炎

Slow advancement of enteral feed volumes to prevent necrotising enterocolitis in very low birth weight infants.

作者信息

Oddie Sam J, Young Lauren, McGuire William

机构信息

Bradford Royal Infirmary, Duckworth Lane, Bradford, UK, BD9 6RJ.

出版信息

Cochrane Database Syst Rev. 2017 Aug 30;8(8):CD001241. doi: 10.1002/14651858.CD001241.pub7.

Abstract

BACKGROUND

Early enteral feeding practices are potentially modifiable risk factors for necrotising enterocolitis (NEC) in very preterm or very low birth weight (VLBW) infants. Observational studies suggest that conservative feeding regimens, including slowly advancing enteral feed volumes, reduce the risk of NEC. However, slow feed advancement may delay establishment of full enteral feeding and may be associated with metabolic and infectious morbidities secondary to prolonged exposure to parenteral nutrition.

OBJECTIVES

To determine effects of slow rates of enteral feed advancement on the incidence of NEC, mortality, and other morbidities in very preterm or VLBW infants.

SEARCH METHODS

We used the standard Cochrane Neonatal search strategy to search the Cochrane Central Register of Controlled Trials (CENTRAL; 2017, Issue 5), MEDLINE via PubMed (1966 to June 2017), Embase (1980 to June 2017), and the Cumulative Index to Nursing and Allied Health Literature (CINAHL; 1982 to June 2017). We searched clinical trials databases, conference proceedings, previous reviews, and reference lists of retrieved articles for randomised controlled trials (RCTs) and quasi-randomised trials.

SELECTION CRITERIA

Randomised or quasi-randomised controlled trials that assessed effects of slow (up to 24 mL/kg/d) versus faster rates of advancement of enteral feed volumes upon the incidence of NEC in very preterm or VLBW infants.

DATA COLLECTION AND ANALYSIS

Two review authors assessed trial eligibility and risk of bias and independently extracted data. We analysed treatment effects in individual trials and reported risk ratio (RR) and risk difference (RD) for dichotomous data, and mean difference (MD) for continuous data, with respective 95% confidence intervals (CIs). We used a fixed-effect model for meta-analyses and explored potential causes of heterogeneity via sensitivity analyses. We assessed the quality of evidence at the outcome level using the Grading of Recommendations Assessment, Development and Evaluation (GRADE) approach.

MAIN RESULTS

We identified 10 RCTs in which a total of 3753 infants participated (2804 infants participated in one large trial). Most participants were stable very preterm infants of birth weight appropriate for gestation. About one-third of all participants were extremely preterm or extremely low birth weight (ELBW), and about one-fifth were small for gestational age (SGA), growth-restricted, or compromised in utero, as indicated by absent or reversed end-diastolic flow velocity (AREDFV) in the fetal umbilical artery. Trials typically defined slow advancement as daily increments of 15 to 20 mL/kg, and faster advancement as daily increments of 30 to 40 mL/kg. Trials generally were of good methodological quality, although none was blinded.Meta-analyses did not show effects on risk of NEC (typical RR 1.07, 95% CI 0.83 to 1.39; RD 0.0, 95% CI -0.01 to 0.02) or all-cause mortality (typical RR 1.15, 95% CI 0.93 to 1.42; typical RD 0.01, 95% CI -0.01 to 0.03). Subgroup analyses of extremely preterm or ELBW infants, or of SGA or growth-restricted or growth-compromised infants, showed no evidence of an effect on risk of NEC or death. Slow feed advancement delayed establishment of full enteral nutrition by between about one and five days. Meta-analysis showed borderline increased risk of invasive infection (typical RR 1.15, 95% CI 1.00 to 1.32; typical RD 0.03, 95% CI 0.00 to 0.05). The GRADE quality of evidence for primary outcomes was "moderate", downgraded from "high" because of lack of blinding in the included trials.

AUTHORS' CONCLUSIONS: Available trial data do not provide evidence that advancing enteral feed volumes at daily increments of 15 to 20 mL/kg (compared with 30 to 40 mL/kg) reduces the risk of NEC or death in very preterm or VLBW infants, extremely preterm or ELBW infants, SGA or growth-restricted infants, or infants with antenatal AREDFV. Advancing the volume of enteral feeds at a slow rate results in several days of delay in establishing full enteral feeds and may increase the risk of invasive infection.

摘要

背景

早期肠内喂养方式可能是极早产儿或极低出生体重(VLBW)儿坏死性小肠结肠炎(NEC)的潜在可改变风险因素。观察性研究表明,保守的喂养方案,包括缓慢增加肠内喂养量,可降低NEC的风险。然而,缓慢增加喂养量可能会延迟完全肠内喂养的建立,并且可能与因长期接受肠外营养而继发的代谢和感染性疾病相关。

目的

确定缓慢增加肠内喂养量对极早产儿或VLBW儿NEC发病率、死亡率及其他疾病的影响。

检索方法

我们采用Cochrane新生儿标准检索策略,检索Cochrane对照试验中央注册库(CENTRAL;2017年第5期)、通过PubMed检索MEDLINE(1966年至2017年6月)、Embase(1980年至2017年6月)以及护理及相关健康文献累积索引(CINAHL;1982年至2017年6月)。我们检索了临床试验数据库、会议论文集、以往的综述以及检索到的文章的参考文献列表,以查找随机对照试验(RCT)和半随机试验。

入选标准

随机或半随机对照试验,评估缓慢(每日增加量达24 mL/kg/d)与较快增加肠内喂养量对极早产儿或VLBW儿NEC发病率的影响。

数据收集与分析

两位综述作者评估试验的合格性和偏倚风险,并独立提取数据。我们分析了各个试验的治疗效果,并报告了二分数据的风险比(RR)和风险差(RD),以及连续数据的均值差(MD),并分别给出95%置信区间(CI)。我们使用固定效应模型进行荟萃分析,并通过敏感性分析探索异质性的潜在原因。我们采用推荐分级评估、制定与评价(GRADE)方法在结局层面评估证据质量。

主要结果

我们识别出10项RCT,共有3753名婴儿参与(2804名婴儿参与了一项大型试验)。大多数参与者是出生体重与孕周相符的稳定极早产儿。所有参与者中约三分之一为极早产儿或超低出生体重(ELBW)儿,约五分之一为小于胎龄儿(SGA)、生长受限儿或宫内情况不佳的婴儿,胎儿脐动脉舒张末期血流速度缺失或反向(AREDFV)表明了这一点。试验通常将缓慢增加定义为每日增加15至20 mL/kg,较快增加定义为每日增加30至40 mL/kg。试验的方法学质量总体良好,尽管均未设盲。荟萃分析未显示对NEC风险(典型RR 1.07,95%CI 0.83至1.39;RD 0.0,95%CI -0.01至0.02)或全因死亡率(典型RR 1.15,95%CI 0.93至1.42;典型RD 0.01,95%CI -0.01至0.03)有影响。对极早产儿或ELBW儿,或SGA或生长受限或生长情况不佳的婴儿进行亚组分析,未显示对NEC风险或死亡有影响的证据。缓慢增加喂养量使完全肠内营养的建立延迟约1至5天。荟萃分析显示侵袭性感染风险有临界增加(典型RR 1.15,95%CI 1.00至1.32;典型RD 0.03,95%CI 0.00至0.05)。主要结局的GRADE证据质量为“中等”,因纳入试验未设盲而从“高”级别下调。

作者结论

现有试验数据未提供证据表明,每日以15至20 mL/kg(与30至40 mL/kg相比)的增量增加肠内喂养量可降低极早产儿或VLBW儿、极早产儿或ELBW儿、SGA或生长受限儿或产前有AREDFV的婴儿发生NEC或死亡的风险。缓慢增加肠内喂养量会导致完全肠内喂养的建立延迟数天,并可能增加侵袭性感染的风险。

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