Department of Health Services Research, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
Department of Clinical Epidemiology and Health Economics, School of Public Health, The University of Tokyo, Tokyo, Japan.
Int J Gynaecol Obstet. 2022 Dec;159(3):865-869. doi: 10.1002/ijgo.14237. Epub 2022 May 26.
To clarify the fetal safety of herbal Kampo medicines, including Hange-koboku-to, Koso-san, Nyoshin-san, Yokukansan, Yokukansan-kachinpi-hange, Saiko-keishikankyo-to, Keishi-karyukotu-borei-to, and Kanbaku-taisou-to, when administered to pregnant women with depression using a large healthcare administrative database.
We extracted data from the JMDC Claims Database (2005-2018) for this retrospective cohort study of pregnant women aged 19 years or older admitted to obstetric clinics or hospitals for delivery. Participants were classified into four groups: those without depression, those diagnosed with depression without medication, those given Kampo medicines for depression, and those given western medicines for depression. Neonatal outcomes (congenital anomalies, low birth weight, and preterm birth) were considered as the safety outcome measures.
We identified 179 707 eligible mothers. The adverse outcomes did not differ significantly between participants receiving Kampo medicine and those not diagnosed with depression during pregnancy. The proportion of low-birth-weight neonates did not differ significantly between the Kampo medicine and non-depression groups (adjusted odds ratio [aOR] 1.28; 95% confidence interval [CI] 0.86-1.91), but was significantly higher in the unmedicated depression group (aOR 1.31; 95% CI 1.07-1.61) and western medicine group (aOR 1.47; 95% CI 1.18-1.83).
Kampo medicines are safe for treating depression during pregnancy without increasing the incidence of congenital anomalies, low birth weight, or preterm birth.
利用大型医疗保健管理数据库,明确在患有抑郁症的孕妇中使用汉方草药(包括汉防己甲素、小柴胡汤、宁神灵、六君子汤、六君子汤加桂皮、柴芍六君子汤、加味一贯煎、完带汤)的胎儿安全性。
本回顾性队列研究从 JMDC 理赔数据库(2005-2018 年)中提取数据,纳入年龄在 19 岁及以上因分娩而入住妇产科诊所或医院的孕妇。参与者分为四组:无抑郁组、无抑郁但未用药组、汉方草药治疗抑郁组、西药治疗抑郁组。新生儿结局(先天性异常、低出生体重和早产)被视为安全性结局指标。
共纳入 179707 名符合条件的母亲。与未被诊断为孕期抑郁的参与者相比,接受汉方药物治疗的参与者的不良结局无显著差异。汉方药物组与非抑郁组的低出生体重儿比例无显著差异(调整后比值比[aOR]1.28;95%置信区间[CI]0.86-1.91),但在未用药抑郁组(aOR 1.31;95% CI 1.07-1.61)和西药组(aOR 1.47;95% CI 1.18-1.83)中显著更高。
汉方药物治疗孕期抑郁症安全,不会增加先天性异常、低出生体重或早产的发生率。