孕期每日口服铁质补充剂。

IF 8.8 2区 医学 Q1 MEDICINE, GENERAL & INTERNAL
Julia L Finkelstein, Anna Cuthbert, Jo Weeks, Sudha Venkatramanan, Doreen Y Larvie, Luz Maria De-Regil, Maria Nieves Garcia-Casal
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The evidence is very uncertain for adverse effects (21.6% versus 18.0%; RR 1.29, 95% CI 0.83 to 2.02; 12 trials, 2423 women; very low-certainty evidence) and severe anaemia (Hb < 70 g/L) in the second/third trimester (< 1% versus 3.6%; RR 0.22, 95% CI 0.01 to 3.20; 8 trials, 1398 women; very low-certainty evidence). No trials reported clinical malaria or infection during pregnancy. Infant outcomes: Women taking iron supplements are probably less likely to have infants with low birthweight (5.2% versus 6.1%; RR 0.84, 95% CI 0.72 to 0.99; 12 trials, 18,290 infants; moderate-certainty evidence), compared to placebo or no iron supplementation. However, the evidence is very uncertain for infant birthweight (MD 24.9 g, 95% CI -125.81 to 175.60; 16 trials, 18,554 infants; very low-certainty evidence). There is probably little to no difference in preterm birth (7.6% versus 8.2%; RR 0.93, 95% CI 0.84 to 1.02; 11 trials, 18,827 infants; moderate-certainty evidence) and there may be little to no difference in neonatal death (1.4% versus 1.5%, RR 0.98, 95% CI 0.77 to 1.24; 4 trials, 17,243 infants; low-certainty evidence) or congenital anomalies, including neural tube defects (41 versus 48 events; RR 0.88, 95% CI 0.58 to 1.33; 4 trials, 14,377 infants; low-certainty evidence). Iron + folic supplementation compared to placebo or no iron + folic acid Maternal outcomes: Daily oral supplementation with iron + folic acid probably reduces maternal anaemia at term (12.1% versus 25.5%; RR 0.44, 95% CI 0.30 to 0.64; 4 trials, 1962 women; moderate-certainty evidence), and may reduce maternal iron deficiency at term (3.6% versus 15%; RR 0.24, 95% CI 0.06 to 0.99; 1 trial, 131 women; low-certainty evidence), compared to placebo or no iron + folic acid. 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引用次数: 0

摘要

背景:建议在孕期补充铁和叶酸以预防贫血,并可改善孕产妇、妊娠和婴儿的其他预后:研究孕期每日口服铁补充剂(单独或与叶酸或其他维生素和矿物质联合使用)作为产前护理干预措施的效果:我们检索了 2024 年 1 月 18 日的 Cochrane 妊娠和分娩试验注册中心(包括 CENTRAL、MEDLINE、Embase、CINAHL、ClinicalTrials.gov、WHO 国际临床试验注册平台、会议论文集),并检索了检索到的研究的参考文献列表:数据收集与分析:综述作者独立评估试验资格,根据预先设定的标准确定可信度,评估偏倚风险,提取数据并检查准确性。我们采用 GRADE 方法评估主要结果证据的确定性。我们预计试验之间的异质性很高;因此我们使用随机效应模型(平均治疗效果)对试验结果进行了汇总:我们纳入了 57 项试验,涉及 48971 名女性。共有 40 项试验比较了每日口服铁质补充剂与安慰剂或无铁质补充剂的效果;8 项试验评估了铁质+叶酸与安慰剂或无铁质+叶酸的效果。铁质补充剂与安慰剂或无铁质补充剂的比较 产妇结局:孕期补充铁剂可减少孕产妇贫血(4.0% 对 7.4%;风险比 (RR) 0.30,95% 置信区间 (CI) 0.20 至 0.47;14 项试验,13,543 名妇女;低确定性证据)和临产时缺铁(44.0% 对 66.0%;RR 0.51,95% CI 0.与安慰剂或不补充铁剂相比,可能会减少临产时产妇缺铁性贫血(5.0% 对 18.4%;RR 0.41,95% CI 0.26 对 0.63;7 项试验,2704 名妇女;中等确定性证据)。在孕产妇死亡方面可能几乎没有差异(2 对 4 例,RR 0.57,95% CI 0.12 至 2.69;3 项试验,14,060 名妇女;中度确定性证据)。在不良反应(21.6% 对 18.0%;RR 1.29,95% CI 0.83 至 2.02;12 项试验,2423 名妇女;极低确定性证据)和孕期第二/第三季度严重贫血(Hb < 70 g/L)(< 1%对 3.6%;RR 0.22,95% CI 0.01 至 3.20;8 项试验,1398 名妇女;极低确定性证据)方面,证据非常不确定。没有试验报告了临床疟疾或孕期感染情况。婴儿结局与安慰剂或不补充铁质相比,服用铁质补充剂的妇女所生的婴儿出生体重偏低的可能性较小(5.2% 对 6.1%;RR 0.84,95% CI 0.72 至 0.99;12 项试验,18290 名婴儿;中等确定性证据)。然而,婴儿出生体重方面的证据非常不确定(MD 24.9 g,95% CI -125.81 至 175.60;16 项试验,18554 名婴儿;极低确定性证据)。早产率可能几乎没有差异(7.6% 对 8.2%;RR 0.93,95% CI 0.84 至 1.02;11 项试验,18,827 名婴儿;中等确定性证据),新生儿死亡率可能几乎没有差异(1.4% 对 1.5%,RR 0.98,95% CI 0.77 至 1.24;4 项试验,17243 名婴儿;低度确定性证据)或先天性畸形,包括神经管缺陷(41 对 48 例;RR 0.88,95% CI 0.58 至 1.33;4 项试验,14377 名婴儿;低度确定性证据)。铁+叶酸补充剂与安慰剂或不含铁+叶酸补充剂的比较 孕产妇结局:与安慰剂或不补充铁+叶酸相比,每日口服铁+叶酸补充剂可能会减少临产时产妇贫血(12.1% 对 25.5%;RR 0.44,95% CI 0.30 至 0.64;4 项试验,1962 名妇女;中等确定性证据),并可能减少临产时产妇缺铁(3.6% 对 15%;RR 0.24,95% CI 0.06 至 0.99;1 项试验,131 名妇女;低确定性证据)。铁+叶酸对孕产妇缺铁性贫血(10.8% 对 25%;RR 0.43,95% CI 0.17 至 1.09;1 项试验,131 名妇女;极低确定性证据)或孕产妇死亡(无事件;1 项试验;极低确定性证据)的影响方面,证据非常不确定。与安慰剂或不含铁+叶酸相比,不良反应的证据不确定(21.0% 对 0.0%;RR 44.32,95% CI 2.77 至 709.09;1 项试验,456 名妇女;低确定性证据),第二或第三孕期严重贫血的证据非常不确定(< 1% 对 5.6%;RR 0.12,95% CI 0.02 至 0.63;4 项试验,506 名妇女;极低确定性证据)。婴儿结局:婴儿出生体重不足的情况可能几乎没有差异(33.4% 对 40.2%;RR 1.07,95% CI 0.31 至 3.0;4 项试验,506 名妇女;极低确定性证据)。
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Daily oral iron supplementation during pregnancy.

Background: Iron and folic acid supplementation have been recommended in pregnancy for anaemia prevention, and may improve other maternal, pregnancy, and infant outcomes.

Objectives: To examine the effects of daily oral iron supplementation during pregnancy, either alone or in combination with folic acid or with other vitamins and minerals, as an intervention in antenatal care.

Search methods: We searched the Cochrane Pregnancy and Childbirth Trials Registry on 18 January 2024 (including CENTRAL, MEDLINE, Embase, CINAHL, ClinicalTrials.gov, WHO's International Clinical Trials Registry Platform, conference proceedings), and searched reference lists of retrieved studies.

Selection criteria: Randomised or quasi-randomised trials that evaluated the effects of oral supplementation with daily iron, iron + folic acid, or iron + other vitamins and minerals during pregnancy were included.

Data collection and analysis: Review authors independently assessed trial eligibility, ascertained trustworthiness based on pre-defined criteria, assessed risk of bias, extracted data, and conducted checks for accuracy. We used the GRADE approach to assess the certainty of the evidence for primary outcomes. We anticipated high heterogeneity amongst trials; we pooled trial results using a random-effects model (average treatment effect).

Main results: We included 57 trials involving 48,971 women. A total of 40 trials compared the effects of daily oral supplements with iron to placebo or no iron; eight trials evaluated the effects of iron + folic acid compared to placebo or no iron + folic acid. Iron supplementation compared to placebo or no iron Maternal outcomes: Iron supplementation during pregnancy may reduce maternal anaemia (4.0% versus 7.4%; risk ratio (RR) 0.30, 95% confidence interval (CI) 0.20 to 0.47; 14 trials, 13,543 women; low-certainty evidence) and iron deficiency at term (44.0% versus 66.0%; RR 0.51, 95% CI 0.38 to 0.68; 8 trials, 2873 women; low-certainty evidence), and probably reduces maternal iron-deficiency anaemia at term (5.0% versus 18.4%; RR 0.41, 95% CI 0.26 to 0.63; 7 trials, 2704 women; moderate-certainty evidence), compared to placebo or no iron supplementation. There is probably little to no difference in maternal death (2 versus 4 events, RR 0.57, 95% CI 0.12 to 2.69; 3 trials, 14,060 women; moderate-certainty evidence). The evidence is very uncertain for adverse effects (21.6% versus 18.0%; RR 1.29, 95% CI 0.83 to 2.02; 12 trials, 2423 women; very low-certainty evidence) and severe anaemia (Hb < 70 g/L) in the second/third trimester (< 1% versus 3.6%; RR 0.22, 95% CI 0.01 to 3.20; 8 trials, 1398 women; very low-certainty evidence). No trials reported clinical malaria or infection during pregnancy. Infant outcomes: Women taking iron supplements are probably less likely to have infants with low birthweight (5.2% versus 6.1%; RR 0.84, 95% CI 0.72 to 0.99; 12 trials, 18,290 infants; moderate-certainty evidence), compared to placebo or no iron supplementation. However, the evidence is very uncertain for infant birthweight (MD 24.9 g, 95% CI -125.81 to 175.60; 16 trials, 18,554 infants; very low-certainty evidence). There is probably little to no difference in preterm birth (7.6% versus 8.2%; RR 0.93, 95% CI 0.84 to 1.02; 11 trials, 18,827 infants; moderate-certainty evidence) and there may be little to no difference in neonatal death (1.4% versus 1.5%, RR 0.98, 95% CI 0.77 to 1.24; 4 trials, 17,243 infants; low-certainty evidence) or congenital anomalies, including neural tube defects (41 versus 48 events; RR 0.88, 95% CI 0.58 to 1.33; 4 trials, 14,377 infants; low-certainty evidence). Iron + folic supplementation compared to placebo or no iron + folic acid Maternal outcomes: Daily oral supplementation with iron + folic acid probably reduces maternal anaemia at term (12.1% versus 25.5%; RR 0.44, 95% CI 0.30 to 0.64; 4 trials, 1962 women; moderate-certainty evidence), and may reduce maternal iron deficiency at term (3.6% versus 15%; RR 0.24, 95% CI 0.06 to 0.99; 1 trial, 131 women; low-certainty evidence), compared to placebo or no iron + folic acid. The evidence is very uncertain about the effects of iron + folic acid on maternal iron-deficiency anaemia (10.8% versus 25%; RR 0.43, 95% CI 0.17 to 1.09; 1 trial, 131 women; very low-certainty evidence), or maternal deaths (no events; 1 trial; very low-certainty evidence). The evidence is uncertain for adverse effects (21.0% versus 0.0%; RR 44.32, 95% CI 2.77 to 709.09; 1 trial, 456 women; low-certainty evidence), and the evidence is very uncertain for severe anaemia in the second or third trimester (< 1% versus 5.6%; RR 0.12, 95% CI 0.02 to 0.63; 4 trials, 506 women; very low-certainty evidence), compared to placebo or no iron + folic acid. Infant outcomes: There may be little to no difference in infant low birthweight (33.4% versus 40.2%; RR 1.07, 95% CI 0.31 to 3.74; 2 trials, 1311 infants; low-certainty evidence), comparing iron + folic acid supplementation to placebo or no iron + folic acid. Infants born to women who received iron + folic acid during pregnancy probably had higher birthweight (MD 57.73 g, 95% CI 7.66 to 107.79; 2 trials, 1365 infants; moderate-certainty evidence), compared to placebo or no iron + folic acid. There may be little to no difference in other infant outcomes, including preterm birth (19.4% versus 19.2%; RR 1.55, 95% CI 0.40 to 6.00; 3 trials, 1497 infants; low-certainty evidence), neonatal death (3.4% versus 4.2%; RR 0.81, 95% CI 0.51 to 1.30; 1 trial, 1793 infants; low-certainty evidence), or congenital anomalies (1.7% versus 2.4; RR 0.70, 95% CI 0.35 to 1.40; 1 trial, 1652 infants; low-certainty evidence), comparing iron + folic acid supplementation to placebo or no iron + folic acid. A total of 19 trials were conducted in malaria-endemic countries, or in settings with some malaria risk. No studies reported maternal clinical malaria; one study reported data on placental malaria.

Authors' conclusions: Daily oral iron supplementation during pregnancy may reduce maternal anaemia and iron deficiency at term. For other maternal and infant outcomes, there was little to no difference between groups or the evidence was uncertain. Future research is needed to examine the effects of iron supplementation on other maternal and infant health outcomes, including infant iron status, growth, and development.

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来源期刊
CiteScore
10.60
自引率
2.40%
发文量
173
审稿时长
1-2 weeks
期刊介绍: The Cochrane Database of Systematic Reviews (CDSR) stands as the premier database for systematic reviews in healthcare. It comprises Cochrane Reviews, along with protocols for these reviews, editorials, and supplements. Owned and operated by Cochrane, a worldwide independent network of healthcare stakeholders, the CDSR (ISSN 1469-493X) encompasses a broad spectrum of health-related topics, including health services.
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