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补充脂肪以促进早产儿生长。

Fat supplementation of human milk for promoting growth in preterm infants.

作者信息

Amissah Emma A, Brown Julie, Harding Jane E

机构信息

Liggins Institute, University of Auckland, Auckland, New Zealand.

出版信息

Cochrane Database Syst Rev. 2018 Jun 19;6(6):CD000341. doi: 10.1002/14651858.CD000341.pub2.

Abstract

BACKGROUND

As preterm infants do not experience the nutrient accretion and rapid growth phase of the third trimester of pregnancy, they are vulnerable to postnatal nutritional deficits, including of fat. Consequently, they require higher fat intakes compared to their full term counterparts to achieve adequate growth and development. Human milk fat provides the major energy needs of the preterm infant and also contributes to several metabolic and physiological functions. Although human milk has many benefits for this population, its fat content is highly variable and may be inadequate for their optimum growth and development. This is a 2018 update of a Cochrane Review last published in 2000.

OBJECTIVES

To determine whether supplementation of human milk with fat compared with unsupplemented human milk fed to preterm infants improves growth, body composition, cardio-metabolic, and neurodevelopmental outcomes without significant adverse effects.

SEARCH METHODS

We used the standard search strategy of Cochrane Neonatal to search the Cochrane Central Register of Controlled Trials (CENTRAL 2018, Issue 1), MEDLINE via PubMed (1966 to 08 February 2018), Embase (1980 to 08 February 2018), and CINAHL (1982 to 08 February 2018). We also searched clinical trials databases, conference proceedings, and the reference lists of retrieved articles for randomised controlled trials and quasi-randomised trials.

SELECTION CRITERIA

Published and unpublished randomised controlled trials were eligible if they used random or quasi-random methods to allocate preterm infants fed human milk in hospital to supplementation or no supplementation with additional fat.

DATA COLLECTION AND ANALYSIS

No new randomised controlled trials matching the selection criteria were found but we extracted data from the previously included trial due to changes in review outcomes from when the protocol was first published. Two reviewers independently abstracted data, assessed trial quality, and the quality of evidence at the outcome level using the Grading of Recommendations Assessment, Development and Evaluation (GRADE) criteria. We planned to perform meta-analyses using risk ratio (RR) for dichotomous data and mean difference (MD) for continuous data, with their respective 95% confidence intervals (CIs). We planned to use a fixed-effect model and to explore potential causes of heterogeneity via sensitivity analyses.

MAIN RESULTS

One randomised trial involving 14 preterm infants was included. There was no evidence of a clear difference between the fat-supplemented and unsupplemented groups in in-hospital rates of growth in weight (MD 0.6 g/kg/day, 95% CI -2.4 to 3.6; 1 RCT, n = 14 infants, very low-quality evidence), length (MD 0.1 cm/week, 95% CI -0.08 to 0.3; 1 RCT, n = 14 infants, very low-quality evidence) and head circumference (MD 0.2 cm/week, 95% CI -0.07 to 0.4; 1 RCT n = 14 infants, very low-quality evidence). There was no clear evidence that fat supplementation increased the risk of feeding intolerance (RR 3.0, 95% CI 0.1 to 64.3; 1 RCT, n = 16 infants, very low-quality evidence). No data were available regarding the effects of fat supplementation on long-term growth, body mass index, body composition, neurodevelopmental, or cardio-metabolic outcomes.

AUTHORS' CONCLUSIONS: The one included trial suggests no evidence of an effect of fat supplementation of human milk on short-term growth and feeding intolerance in preterm infants. However, the very low-quality evidence, small sample size, few events, and low precision diminishes our confidence that these results reflect the true effect of fat supplementation of human milk in preterm infants, and no long-term outcomes were reported. Further high-quality research should evaluate the effect on short and long-term growth, neurodevelopmental and cardio-metabolic outcomes in the context of the development of multicomponent fortifiers. Optimal dosage, adverse effects, and delivery practices should also be evaluated.

摘要

背景

由于早产儿未经历妊娠晚期的营养积累和快速生长阶段,他们易出现出生后的营养缺乏,包括脂肪缺乏。因此,与足月儿相比,他们需要更高的脂肪摄入量以实现充分的生长发育。人乳脂肪满足了早产儿的主要能量需求,并且对多种代谢和生理功能也有贡献。尽管人乳对这一群体有诸多益处,但其脂肪含量高度可变,可能不足以满足他们的最佳生长发育需求。这是Cochrane系统评价2000年首次发表后的2018年更新版。

目的

确定与未添加脂肪的人乳喂养相比,添加脂肪的人乳喂养早产儿是否能改善生长、身体成分、心脏代谢和神经发育结局且无显著不良反应。

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(CENTRAL 2018年第1期)、通过PubMed检索MEDLINE(1966年至2018年2月8日)、Embase(1980年至2018年2月8日)以及CINAHL(1982年至2018年2月8日)。我们还检索了临床试验数据库、会议论文集以及检索到的文章的参考文献列表,以查找随机对照试验和半随机试验。

入选标准

已发表和未发表的随机对照试验符合条件,若它们使用随机或半随机方法将住院期间接受人乳喂养的早产儿分配至添加或不添加额外脂肪的组。

数据收集与分析

未找到符合入选标准的新随机对照试验,但由于自方案首次发表以来评价结局有所变化,我们从之前纳入的试验中提取了数据。两名评价员独立提取数据,评估试验质量,并使用推荐分级的评估、制定与评价(GRADE)标准在结局层面评估证据质量。我们计划对二分类数据使用风险比(RR)、对连续性数据使用均数差(MD)及其各自的95%置信区间(CI)进行Meta分析。我们计划使用固定效应模型,并通过敏感性分析探索异质性的潜在原因。

主要结果

纳入了一项涉及14名早产儿的随机试验。在住院期间的体重增长(MD 0.6 g/kg/天,95% CI -2.4至3.6;1项RCT,n = 14名婴儿,极低质量证据)、身长(MD 0.1 cm/周,95% CI -0.08至0.3;1项RCT,n = 14名婴儿,极低质量证据)和头围(MD 0.2 cm/周,95% CI -0.07至0.4;1项RCT,n = 14名婴儿,极低质量证据)方面,添加脂肪组和未添加脂肪组之间没有明显差异的证据。没有明确证据表明添加脂肪会增加喂养不耐受的风险(RR 3.0,95% CI 0.1至64.3;1项RCT,n = 16名婴儿,极低质量证据)。关于添加脂肪对长期生长、体重指数、身体成分、神经发育或心脏代谢结局的影响,没有可用数据。

作者结论

纳入的一项试验表明,没有证据显示添加脂肪的人乳对早产儿的短期生长和喂养不耐受有影响。然而,极低质量的证据、小样本量、少量事件和低精确度降低了我们对这些结果反映添加脂肪的人乳在早产儿中真实效果的信心,并且没有报告长期结局情况。应在多成分强化剂研发的背景下,开展进一步的高质量研究以评估对短期和长期生长、神经发育和心脏代谢结局的影响。还应评估最佳剂量、不良反应和给药方式。

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本文引用的文献

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Longchain polyunsaturated fatty acid supplementation in preterm infants.早产儿补充长链多不饱和脂肪酸
Cochrane Database Syst Rev. 2016 Dec 20;12(12):CD000375. doi: 10.1002/14651858.CD000375.pub5.
3
Fatty acid requirements for the preterm infant.早产儿对脂肪酸的需求
Semin Fetal Neonatal Med. 2017 Feb;22(1):8-14. doi: 10.1016/j.siny.2016.08.009. Epub 2016 Sep 3.
5
Human Milk for Preterm Infants and Fortification.早产儿的母乳及强化
Nestle Nutr Inst Workshop Ser. 2016;86:109-19. doi: 10.1159/000442730. Epub 2016 Jun 27.
6
Multi-nutrient fortification of human milk for preterm infants.早产儿母乳的多种营养素强化
Cochrane Database Syst Rev. 2016 May 8(5):CD000343. doi: 10.1002/14651858.CD000343.pub3.
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Carnitine transport and fatty acid oxidation.肉碱转运与脂肪酸氧化。
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