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孕期女性的多种微量营养素补充

Multiple-micronutrient supplementation for women during pregnancy.

作者信息

Haider Batool A, Bhutta Zulfiqar A

机构信息

Department of Global Health and Population, Harvard School of Public Health, 677 Huntington Avenue, Boston, MA, USA, 02115.

Centre for Global Child Health, Hospital for Sick Children, Toronto, ON, Canada, M5G A04.

出版信息

Cochrane Database Syst Rev. 2017 Apr 13;4(4):CD004905. doi: 10.1002/14651858.CD004905.pub5.


DOI:10.1002/14651858.CD004905.pub5
PMID:28407219
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6478115/
Abstract

BACKGROUND: Multiple-micronutrient (MMN) deficiencies often coexist among women of reproductive age in low- to middle-income countries. They are exacerbated in pregnancy due to the increased demands, leading to potentially adverse effects on the mother and developing fetus. Though supplementation with MMNs has been recommended earlier because of the evidence of impact on pregnancy outcomes, a consensus is yet to be reached regarding the replacement of iron and folic acid supplementation with MMNs. Since the last update of this Cochrane review, evidence from a few large trials has recently been made available, the inclusion of which is critical to inform policy. OBJECTIVES: To evaluate the benefits of oral multiple-micronutrient supplementation during pregnancy on maternal, fetal and infant health outcomes. SEARCH METHODS: We searched the Cochrane Pregnancy and Childbirth Group's Trials Register (11 March 2015) and reference lists of retrieved articles and key reviews. We also contacted experts in the field for additional and ongoing trials. SELECTION CRITERIA: All prospective randomised controlled trials evaluating MMN supplementation with iron and folic acid during pregnancy and its effects on the pregnancy outcome were eligible, irrespective of language or the publication status of the trials. We included cluster-randomised trials, but quasi-randomised trials were excluded. DATA COLLECTION AND ANALYSIS: Two review authors independently assessed trials for inclusion and risk of bias, extracted data and checked them for accuracy. The quality of the evidence was assessed using the GRADE approach. MAIN RESULTS: Nineteen trials (involving 138,538 women) were identified as eligible for inclusion in this review but only 17 trials (involving 137,791 women) contributed data to the review. Fifteen of these 17 trials were carried out in low and middle-income countries and compared MMN supplements with iron and folic acid versus iron with or without folic acid. Two trials carried out in the UK compared MMN with a placebo. MMN with iron and folic acid versus iron, with or without folic acid (15 trials): MMN resulted in a significant decrease in the number of newborn infants identified as low birthweight (LBW) (average risk ratio (RR) 0.88, 95% confidence interval (CI) 0.85 to 0.91; high-quality evidence) or small-for-gestational age (SGA) (average RR 0.92, 95% CI 0.86 to 0.98; moderate-quality evidence). No significant differences were shown for other maternal and pregnancy outcomes: preterm births (average RR 0.96, 95% CI 0.90 to 1.03; high-quality evidence), stillbirth (average RR 0.97, 95% CI 0.87, 1.09; high-quality evidence), maternal anaemia in the third trimester (average RR 1.03, 95% CI 0.85 to 1.24), miscarriage (average RR 0.91, 95% CI 0.80 to 1.03), maternal mortality (average RR 0.97, 95% CI 0.63 to 1.48), perinatal mortality (average RR 1.01, 95% CI 0.91 to 1.13; high-quality evidence), neonatal mortality (average RR 1.06, 95% CI 0.92 to 1.22; high-quality evidence), or risk of delivery via a caesarean section (average RR 1.04; 95% CI 0.74 to 1.46).A number of prespecified, clinically important outcomes could not be assessed due to insufficient or non-available data. Single trials reported results for: very preterm birth < 34 weeks, macrosomia, side-effects of supplements, nutritional status of children, and congenital anomalies including neural tube defects and neurodevelopmental outcome: Bayley Scales of Infant Development (BSID) scores. None of these trials reported pre-eclampsia, placental abruption, premature rupture of membranes, cost of supplementation, and maternal well-being or satisfaction.When assessed according to GRADE criteria, the quality of evidence for the review's primary outcomes overall was good. Pooled results for primary outcomes were based on multiple trials with large sample sizes and precise estimates. The following outcomes were graded to be as of high quality: preterm birth, LBW, perinatal mortality, stillbirth and neonatal mortality. The outcome of SGA was graded to be of moderate quality, with evidence downgraded by one for funnel plot asymmetry and potential publication bias.We carried out sensitivity analysis excluding trials with high levels of sample attrition (> 20%); results were consistent with the main analysis except for the findings for SGA (average RR 0.91, 95% CI 0.84 to 1.00). We explored heterogeneity through subgroup analyses by maternal height and body mass index (BMI), timing of supplementation and dose of iron. Subgroup differences were observed for maternal BMI for the outcome preterm birth, with significant findings among women with low BMI. Subgroup differences were also observed for maternal BMI and maternal height for the outcome SGA, indicating a significant impact among women with higher maternal BMI and height. The overall analysis of perinatal mortality, although showed a non-significant effect of MMN supplements versus iron with or without folic acid, was found to have substantial statistical heterogeneity. Subgroup differences were observed for timing of supplementation for this outcome, indicating a significantly higher impact with late initiation of supplementation. The findings between subgroups for other primary outcomes were inconclusive. MMN versus placebo (two trials): A single trial in the UK found no clear differences between groups for preterm birth, SGA, LBW or maternal anaemia in the third trimester. A second trial reported the number of women with pre-eclampsia; there was no evidence of a difference between groups. Other outcomes were not reported. AUTHORS' CONCLUSIONS: Our findings support the effect of MMN supplements with iron and folic acid in improving some birth outcomes. Overall, pregnant women who received MMN supplementation had fewer low birthweight babies and small-for-gestational-age babies. The findings, consistently observed in several systematic evaluations of evidence, provide a basis to guide the replacement of iron and folic acid with MMN supplements containing iron and folic acid for pregnant women in low and middle-income countries where MMN deficiencies are common among women of reproductive age. Efforts could focus on the integration of this intervention in maternal nutrition and antenatal care programs in low and middle-income countries.

摘要

背景:在低收入和中等收入国家,育龄妇女中多种微量营养素(MMN)缺乏往往并存。由于需求增加,孕期这些缺乏情况会加剧,从而对母亲和发育中的胎儿产生潜在不利影响。尽管早期因有证据表明MMN对妊娠结局有影响而推荐补充MMN,但对于用MMN替代铁和叶酸补充剂尚未达成共识。自本Cochrane综述上次更新以来,最近有一些大型试验的证据可供使用,纳入这些证据对为政策提供信息至关重要。 目的:评估孕期口服多种微量营养素补充剂对孕产妇、胎儿和婴儿健康结局的益处。 检索方法:我们检索了Cochrane妊娠与分娩组试验注册库(截至2015年3月11日)以及检索到的文章和关键综述的参考文献列表。我们还联系了该领域的专家以获取更多和正在进行的试验信息。 选择标准:所有评估孕期补充MMN联合铁和叶酸及其对妊娠结局影响的前瞻性随机对照试验均符合条件,无论试验的语言或发表状态如何。我们纳入整群随机试验,但排除半随机试验。 数据收集与分析:两位综述作者独立评估试验是否纳入及偏倚风险,提取数据并检查其准确性。使用GRADE方法评估证据质量。 主要结果:19项试验(涉及138,538名妇女)被确定符合纳入本综述的条件,但只有17项试验(涉及137,791名妇女)为综述提供了数据。这17项试验中有15项在低收入和中等收入国家进行,比较了MMN补充剂联合铁和叶酸与铁(含或不含叶酸)的效果。在英国进行的两项试验将MMN与安慰剂进行了比较。MMN联合铁和叶酸与铁(含或不含叶酸)(15项试验):MMN导致低出生体重(LBW)新生儿数量显著减少(平均风险比(RR)0.88,95%置信区间(CI)0.85至0.91;高质量证据)或小于胎龄儿(SGA)数量显著减少(平均RR 0.92,95%CI 0.86至0.98;中等质量证据)。在其他孕产妇和妊娠结局方面未显示出显著差异:早产(平均RR 0.96,95%CI 0.90至1.03;高质量证据)、死产(平均RR 0.97,95%CI 0.87至1.09;高质量证据)、孕晚期孕产妇贫血(平均RR 1.03,95%CI 0.85至1.24)、流产(平均RR 0.91,95%CI 0.80至1.03)、孕产妇死亡率(平均RR 0.97,95%CI 0.63至1.48)、围产期死亡率(平均RR 1.01,95%CI 0.91至1.13;高质量证据)、新生儿死亡率(平均RR 1.06,95%CI 0.92至1.22;高质量证据)或剖宫产风险(平均RR 1.04;95%CI 0.74至1.46)。由于数据不足或无法获取,一些预先设定的、具有临床重要性的结局无法评估。单项试验报告了以下结果:孕周<34周的极早产、巨大儿、补充剂的副作用、儿童营养状况以及先天性异常,包括神经管缺陷和神经发育结局:贝利婴儿发育量表(BSID)评分。这些试验均未报告子痫前期、胎盘早剥、胎膜早破、补充剂成本以及孕产妇幸福感或满意度。根据GRADE标准评估时,本综述主要结局的证据质量总体良好。主要结局的汇总结果基于多个大样本量且估计精确的试验。以下结局被评为高质量:早产、LBW、围产期死亡率、死产和新生儿死亡率。SGA结局被评为中等质量,证据因漏斗图不对称和潜在发表偏倚而降级一级。我们进行了敏感性分析,排除样本流失率高(>20%)的试验;结果与主要分析一致,但SGA的结果除外(平均RR 0.91,95%CI 0.84至1.00)。我们通过按孕产妇身高和体重指数(BMI)、补充时间和铁剂量进行亚组分析来探索异质性。在早产结局方面,观察到孕产妇BMI的亚组差异,在BMI低的妇女中有显著发现。在SGA结局方面,也观察到孕产妇BMI和身高的亚组差异,表明在孕产妇BMI和身高较高的妇女中有显著影响。围产期死亡率的总体分析虽然显示MMN补充剂与含或不含叶酸的铁相比无显著效果,但发现存在大量统计异质性。在该结局的补充时间方面观察到亚组差异,表明补充开始时间晚时影响显著更高。其他主要结局亚组间的结果尚无定论。MMN与安慰剂(两项试验):英国的一项单项试验发现,两组在早产、SGA、LBW或孕晚期孕产妇贫血方面无明显差异。第二项试验报告了子痫前期妇女的数量;两组之间没有差异的证据。未报告其他结局。 作者结论:我们的研究结果支持补充含MMN联合铁和叶酸对改善某些出生结局的作用。总体而言,接受MMN补充剂的孕妇所生低出生体重儿和小于胎龄儿较少。在多项系统证据评估中一致观察到的这些结果,为指导在育龄妇女中MMN缺乏常见的低收入和中等收入国家用含MMN联合铁和叶酸的补充剂替代铁和叶酸补充剂提供了依据。工作重点可放在将此干预措施纳入低收入和中等收入国家的孕产妇营养和产前保健计划中。

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