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母体低血红蛋白浓度和高血红蛋白浓度与不良母婴健康结局的关系:一项更新的全球系统评价和荟萃分析。

Maternal low and high hemoglobin concentrations and associations with adverse maternal and infant health outcomes: an updated global systematic review and meta-analysis.

机构信息

Hubert Department of Global Health, Emory University, 1518 Clifton Road NE, 30322, Atlanta, GA, USA.

Department of Nutrition and Food Sciences, University of Rhode Island, 02881, Kingston, United States.

出版信息

BMC Pregnancy Childbirth. 2023 Apr 19;23(1):264. doi: 10.1186/s12884-023-05489-6.

Abstract

BACKGROUND

Growing evidence suggests low and high maternal hemoglobin (Hb) concentrations may have adverse consequences for maternal and child health. There remain questions on specific Hb thresholds to define anemia and high Hb as well as how cutoffs may vary by anemia etiology and timing of assessment.

METHODS

We conducted an updated systematic review (using PubMed and Cochrane Review) on low (< 110 g/L) and high (≥ 130 g/L) maternal Hb concentrations and associations with a range of maternal and infant health outcomes. We examined associations by timing of Hb assessment (preconception; first, second, and third trimesters, as well as at any time point in pregnancy), varying cutoffs used for defining low and high hemoglobin concentrations and performed stratified analyses by iron-deficiency anemia. We conducted meta-analyses to obtain odds ratios (OR) and 95% confidence intervals.

RESULTS

The updated systematic review included 148 studies. Low maternal Hb at any time point in pregnancy was associated with: low birthweight, LBW (OR (95% CI) 1.28 (1.22-1.35)), very low birthweight, VLBW (2.15 (1.47-3.13)), preterm birth, PTB (1.35 (1.29-1.42)), small-for-gestational age, SGA (1.11 (1.02-1.19)), stillbirth 1.43 (1.24-1.65)), perinatal mortality (1.75 (1.28-2.39)), neonatal mortality (1.25 (1.16-1.34), postpartum hemorrhage (1.69 (1.45-1.97)), transfusion (3.68 (2.58-5.26)), pre-eclampsia (1.57 (1.23-2.01)), and prenatal depression (1.44 (1.24-1.68)). For maternal mortality, the OR was higher for Hb < 90 (4.83 (2.17-10.74)) than for Hb < 100 (2.87 (1.08-7.67)). High maternal Hb was associated with: VLBW (1.35 (1.16-1.57)), PTB (1.12 (1.00-1.25)), SGA (1.17 (1.09-1.25)), stillbirth (1.32 (1.09-1.60)), maternal mortality (2.01 (1.12-3.61)), gestational diabetes (1.71 (1.19-2.46)), and pre-eclampsia (1.34 (1.16-1.56)). Stronger associations were noted earlier in pregnancy for low Hb and adverse birth outcomes while the role of timing of high Hb was inconsistent. Lower Hb cutoffs were associated with greater odds of poor outcomes; for high Hb, data were too limited to identify patterns. Information on anemia etiology was limited; relationships did not vary by iron-deficiency anemia.

CONCLUSION

Both low and high maternal Hb concentrations during pregnancy are strong predictors of adverse maternal and infant health outcomes. Additional research is needed to establish healthy reference ranges and design effective interventions to optimize maternal Hb during pregnancy.

摘要

背景

越来越多的证据表明,孕妇的低血红蛋白(Hb)和高血红蛋白浓度可能对母婴健康产生不良影响。目前仍存在一些问题,例如特定的 Hb 阈值来定义贫血和高血红蛋白,以及贫血病因和评估时间如何影响截断值。

方法

我们使用 PubMed 和 Cochrane Review 进行了一项更新的系统评价,研究了低(<110g/L)和高(≥130g/L)孕妇 Hb 浓度与一系列母婴健康结局的关系。我们通过 Hb 评估的时间(受孕前;第一、二、三孕期以及孕期的任何时间点)来检查关联,还研究了用于定义低和高血红蛋白浓度的不同截断值,并按缺铁性贫血进行分层分析。我们进行了荟萃分析以获得优势比(OR)和 95%置信区间。

结果

更新的系统评价包括 148 项研究。孕妇在孕期任何时间点的低 Hb 与以下情况有关:低出生体重(LBW)(OR(95%CI)1.28(1.22-1.35))、极低出生体重(VLBW)(2.15(1.47-3.13))、早产(PTB)(1.35(1.29-1.42))、小于胎龄儿(SGA)(1.11(1.02-1.19))、死胎(1.43(1.24-1.65))、围产儿死亡率(1.75(1.28-2.39))、新生儿死亡率(1.25(1.16-1.34))、产后出血(1.69(1.45-1.97))、输血(3.68(2.58-5.26))、子痫前期(1.57(1.23-2.01))和产前抑郁(1.44(1.24-1.68))。对于孕产妇死亡率,Hb<90 的 OR 高于 Hb<100(4.83(2.17-10.74))。高孕妇 Hb 与以下情况有关:VLBW(1.35(1.16-1.57))、PTB(1.12(1.00-1.25))、SGA(1.17(1.09-1.25))、死胎(1.32(1.09-1.60))、孕产妇死亡率(2.01(1.12-3.61))、妊娠期糖尿病(1.71(1.19-2.46))和子痫前期(1.34(1.16-1.56))。在妊娠早期,低 Hb 与不良的出生结局之间的关联更强,而高 Hb 的作用时间不一致。较低的 Hb 截断值与较差的结局发生几率更高相关;对于高 Hb,数据太有限,无法确定模式。有关贫血病因的信息有限;这些关系不因缺铁性贫血而有所不同。

结论

孕妇在怀孕期间的低血红蛋白和高血红蛋白浓度都是不良母婴健康结局的有力预测指标。需要进一步研究来确定健康的参考范围,并设计有效的干预措施来优化孕妇在怀孕期间的 Hb 水平。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cbed/10114461/48bcbb262a61/12884_2023_5489_Fig1_HTML.jpg

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