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早产儿或低出生体重儿的早期完全肠内喂养。

Early full enteral feeding for preterm or low birth weight infants.

机构信息

Centre for Reviews and Dissemination, University of York, York, UK.

Mental Health and Addiction Research Group, Department of Health Sciences, University of York, York, UK.

出版信息

Cochrane Database Syst Rev. 2020 Dec 27;12(12):CD013542. doi: 10.1002/14651858.CD013542.pub2.

Abstract

BACKGROUND

The introduction and advancement of enteral feeds for preterm or low birth weight infants is often delayed because of concerns that early full enteral feeding will not be well tolerated or may increase the risk of necrotising enterocolitis. Early full enteral feeding, however, might increase nutrient intake and growth rates; accelerate intestinal physiological, metabolic, and microbiomic postnatal transition; and reduce the risk of complications associated with intravascular devices for fluid administration.  OBJECTIVES: To determine how early full enteral feeding, compared with delayed or progressive introduction of enteral feeds, affects growth and adverse events such as necrotising enterocolitis, in preterm or low birth weight infants.

SEARCH METHODS

We used the standard search strategy of Cochrane Neonatal to search Cochrane Central Register of Controlled Trials; MEDLINE Ovid, Embase Ovid, Maternity & Infant Care Database Ovid, the Cumulative Index to Nursing and Allied Health Literature, and clinical trials databases, conference proceedings, and the reference lists of retrieved articles for randomised controlled trials and quasi-randomised trials to October 2020.

SELECTION CRITERIA

Randomised controlled trials that compared early full enteral feeding with delayed or progressive introduction of enteral feeds in preterm or low birth weight infants.

DATA COLLECTION AND ANALYSIS

We used the standard methods of Cochrane Neonatal. Two review authors separately assessed trial eligibility, evaluated trial quality, extracted data, and synthesised effect estimates using risk ratios (RR), risk differences, and mean differences (MD) with 95% confidence intervals (CI). We used the GRADE approach to assess the certainty of evidence.

MAIN RESULTS

We included six trials. All were undertaken in the 2010s in neonatal care facilities in India. In total, 526 infants participated. Most were very preterm infants of birth weight between 1000 g and 1500 g. Trials were of good methodological quality, but a potential source of bias was that parents, clinicians, and investigators were not masked. The trials compared early full feeding (60 mL/kg to 80 mL/kg on day one after birth) with minimal enteral feeding (typically 20 mL/kg on day one) supplemented with intravenous fluids. Feed volumes were advanced daily as tolerated by 20 mL/kg to 30 mL/kg body weight to a target steady-state volume of 150 mL/kg to 180 mL/kg/day. All participating infants were fed preferentially with maternal expressed breast milk, with two trials supplementing insufficient volumes with donor breast milk and four supplementing with preterm formula.  Few data were available to assess growth parameters. One trial (64 participants) reported a slower rate of weight gain (median difference -3.0 g/kg/day), and another (180 participants) reported a faster rate of weight gain in the early full enteral feeding group (MD 1.2 g/kg/day). We did not meta-analyse these data (very low-certainty evidence). None of the trials reported rate of head circumference growth. One trial reported that the mean z-score for weight at hospital discharge was higher in the early full enteral feeding group (MD 0.24, 95% CI 0.06 to 0.42; low-certainty evidence). Meta-analyses showed no evidence of an effect on necrotising enterocolitis (RR 0.98, 95% CI 0.38 to 2.54; 6 trials, 522 participants; I² = 51%; very low-certainty evidence).

AUTHORS' CONCLUSIONS: Trials provided insufficient data to determine with any certainty how early full enteral feeding, compared with delayed or progressive introduction of enteral feeds, affects growth in preterm or low birth weight infants. We are uncertain whether early full enteral feeding affects the risk of necrotising enterocolitis because of the risk of bias in the trials (due to lack of masking), inconsistency, and imprecision.

摘要

背景

由于担心早期完全肠内喂养不能被很好地耐受或可能增加坏死性小肠结肠炎的风险,早产儿或低出生体重儿的肠内喂养的引入和进展往往会被延迟。然而,早期完全肠内喂养可能会增加营养摄入和生长速度;加速肠道生理、代谢和微生物组的产后过渡;并降低与静脉输液装置相关的并发症的风险。

目的

确定与延迟或逐步引入肠内喂养相比,早期完全肠内喂养如何影响早产儿或低出生体重儿的生长和坏死性小肠结肠炎等不良事件。

检索方法

我们使用 Cochrane 新生儿组的标准检索策略,检索 Cochrane 对照试验中心注册库;MEDLINE Ovid、Embase Ovid、Maternity & Infant Care Database Ovid、Cumulative Index to Nursing and Allied Health Literature,以及临床试验数据库、会议记录和检索文章的参考文献,以获取 2020 年 10 月前的随机对照试验和准随机试验。

选择标准

比较早产儿或低出生体重儿早期完全肠内喂养与延迟或逐步引入肠内喂养的随机对照试验。

数据收集和分析

我们使用 Cochrane 新生儿的标准方法。两名综述作者分别评估试验的纳入标准、评估试验质量、提取数据,并使用风险比(RR)、风险差异和均数差(MD)及其 95%置信区间(CI)来综合效应估计值。我们使用 GRADE 方法评估证据的确定性。

主要结果

我们纳入了六项试验。所有试验均在印度的新生儿护理机构进行,时间均在 2010 年代。共有 526 名婴儿参与。大多数是非常早产儿,出生体重在 1000 克至 1500 克之间。试验的方法学质量较高,但潜在的偏倚来源是父母、临床医生和研究人员没有被蒙蔽。这些试验将早期完全喂养(出生后第一天 60 毫升/公斤至 80 毫升/公斤)与最小的肠内喂养(通常是第一天 20 毫升/公斤)进行比较,并用静脉输液进行补充。根据耐受情况,每日将喂养量增加 20 毫升/公斤至 30 毫升/公斤体重,目标稳定喂养量为 150 毫升/公斤至 180 毫升/公斤/天。所有参与的婴儿都优先接受母亲的母乳,有两个试验用捐赠的母乳补充不足的量,四个试验用早产儿配方奶补充。几乎没有数据可用于评估生长参数。一项试验(64 名参与者)报告体重增长速度较慢(中位数差异-3.0 克/公斤/天),另一项试验(180 名参与者)报告早期完全肠内喂养组体重增长速度较快(MD 1.2 克/公斤/天)。我们没有对这些数据进行荟萃分析(极低确定性证据)。没有试验报告头围生长率。一项试验报告,早期完全肠内喂养组出院时体重的平均 z 评分较高(MD 0.24,95%CI 0.06 至 0.42;低确定性证据)。荟萃分析显示,早期完全肠内喂养对坏死性小肠结肠炎没有影响(RR 0.98,95%CI 0.38 至 2.54;6 项试验,522 名参与者;I²=51%;极低确定性证据)。

作者结论

试验提供的数据不足以确定与延迟或逐步引入肠内喂养相比,早期完全肠内喂养如何能更确定地影响早产儿或低出生体重儿的生长。由于试验存在偏倚(由于缺乏蒙蔽)、不一致性和不精确性,我们不确定早期完全肠内喂养是否会影响坏死性小肠结肠炎的风险。

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