Incidence of postpartum depression after treatment of postpartum anaemia with intravenous ferric carboxymaltose, intravenous ferric derisomaltose or oral ferrous sulphate: A randomized clinical trial

IF 1.5 Q3 OBSTETRICS & GYNECOLOGY
Lea Bombač Tavčar , Hana Hrobat , Lea Gornik , Vislava Globevnik Velikonja , Miha Lučovnik
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Abstract

Objectives

This study aimed to explore whether the type of iron preparation used to treat postpartum anaemia affects the incidence of postpartum depression and whether the risk of postpartum depression is higher in postpartum patients with anaemia who were adequately treated compared to the general postpartum population.

Study design

Single-center, open-label, randomized trial. Women were allocated to receive intravenous ferric carboxymaltose, intravenous ferric derisomaltose or oral ferrous sulphate. Intravenous iron was given in one or two doses, while ferrous sulphate as two 80 mg tablets once daily. Primary outcome was postpartum depression measured by Edinburgh Postnatal Depression Scale (EPDS) six weeks postpartum. Haematological parameters were analyzed as secondary outcomes. Kruskal-Wallis test was used for group comparison (p < 0.05 significant). The chi-square test was applied to compare categorical variables as well as the group of all subjects treated for anaemia in the study with the historical data for the Slovenian postpartum population.

Results

Three-hundred women with postpartum anemia (hemoglobin < 100 g/L within 48-hours postpartum) were included between September 2020 and March 2022 in tertiary perinatal center. Most characteristics were similar across groups. EPDS score at six weeks postpartum did not differ between groups. The treatment modality of postpartum anaemia did not have a statistically significant effect on the EPDS score six weeks after treatment (p = 0.10), nor did it have a statistically significant effect on the difference in EPDS scores before and after treatment (p = 0.68). The proportions of participants who scored 10 or more points on the EPDS scores at six weeks postpartum were not statistically different between the groups (p = 0.79). The proportion of participants with an EPDS score of 10 or more at six weeks postpartum in the total study population did not differ significantly from previously reported proportion of postpartum women with EPDS score of 10 or more in the general population (12 % vs. 21 %; p < 0.001).

Conclusions

Maternal depression at 6 weeks postpartum did not differ in women treated for postpartum anemia with intravenous ferric carboxymaltose, intravenous ferric derisomaltose or oral ferrous sulphate. Participants with postpartum anaemia who are adequately treated with either oral or intravenous iron preparations are not at a higher risk of postpartum depression than the general population at six weeks postpartum.

静脉注射羧麦芽糖铁、静脉注射脱体铁或口服硫酸亚铁治疗产后贫血后产后抑郁的发生率:一项随机临床试验
目的本研究旨在探讨用于治疗产后贫血的铁制剂类型是否会影响产后抑郁症的发生率,以及与一般产后人群相比,得到充分治疗的产后贫血患者患产后抑郁症的风险是否更高。研究设计单中心、开放标签、随机试验。女性被分配接受静脉注射羧麦芽糖铁、静脉注射脱体铁或口服硫酸亚铁。静脉注射铁的剂量为一到两次,硫酸亚铁的剂量为两片80mg,每天一次。主要结果是产后6周通过爱丁堡产后抑郁量表(EPDS)测量的产后抑郁。将血液学参数作为次要结果进行分析。Kruskal-Wallis检验用于组比较(p<0.05显著)。卡方检验用于比较分类变量以及研究中接受贫血治疗的所有受试者组与斯洛文尼亚产后人群的历史数据。结果2020年9月至2022年3月,300名产后贫血(产后48小时内血红蛋白<100g/L)妇女被纳入三级围产期中心。大多数特征在各组之间是相似的。产后6周的EPDS评分在各组之间没有差异。产后贫血的治疗方式对治疗后6周的EPDS评分没有统计学上的显著影响(p=0.10),它对治疗前后EPDS评分的差异也没有统计学意义(p=0.68)。产后六周EPDS评分达到10分或以上的参与者比例在两组之间没有统计学差异(p=0.79)研究人群与之前报道的EPDS评分为10或以上的产后妇女在普通人群中的比例没有显著差异(12%对21%;p<0.001)。产后贫血的参与者在产后六周时,如果口服或静脉注射铁制剂进行了充分治疗,患产后抑郁症的风险并不比普通人群高。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
2.20
自引率
0.00%
发文量
31
审稿时长
58 days
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