Clinical Epidemiology Unit, Department of Medicine Solna, Karolinska University Hospital, Karolinska Institutet, Stockholm, Sweden.
Department of Global Public Health and Primary Care, University of Bergen, Bergen, Norway.
JAMA Neurol. 2024 Sep 1;81(9):985-995. doi: 10.1001/jamaneurol.2024.2375.
Maternal epilepsy is associated with adverse pregnancy and neonatal outcomes. A better understanding of this condition and the associated risk of mortality and morbidity at the time of delivery could help reduce adverse outcomes.
To determine the risk of severe maternal and perinatal morbidity and mortality among women with epilepsy.
DESIGN, SETTING, PARTICIPANTS: This prospective population-based register study in Denmark, Finland, Iceland, Norway, and Sweden took place between January 1, 1996, and December 31, 2017. Data analysis was performed from August 2022 to November 2023. Participants included all singleton births at 22 weeks' gestation or longer. Births with missing or invalid information on birth weight or gestational length were excluded. The study team identified 4 511 267 deliveries, of which 4 475 984 were to women without epilepsy and 35 283 to mothers with epilepsy.
Maternal epilepsy diagnosis recorded before childbirth. Prenatal exposure to antiseizure medication (ASM), defined as any maternal prescription fills from conception to childbirth, was also examined.
Composite severe maternal morbidity and mortality occurring in pregnancy or within 42 days postpartum and composite severe neonatal morbidity (eg, neonatal convulsions) and perinatal mortality (ie, stillbirths and deaths) during the first 28 days of life. Multivariable generalized estimating equations with logit-link were used to obtain adjusted odds ratios (aORs) and 95% CIs.
The mean (SD) age at delivery for women in the epilepsy cohort was 29.9 (5.3) years. The rate of composite severe maternal morbidity and mortality was also higher in women with epilepsy compared with those without epilepsy (36.9 vs 25.4 per 1000 deliveries). Women with epilepsy also had a significantly higher risk of death (0.23 deaths per 1000 deliveries) compared with women without epilepsy (0.05 deaths per 1000 deliveries) with an aOR of 3.86 (95% CI, 1.48-8.10). In particular, maternal epilepsy was associated with increased odds of severe preeclampsia, embolism, disseminated intravascular coagulation or shock, cerebrovascular events, and severe mental health conditions. Fetuses and infants of women with epilepsy were at elevated odds of mortality (aOR, 1.20; 95% CI, 1.05-1.38) and severe neonatal morbidity (aOR, 1.48; 95% CI, 1.40-1.56). In analyses restricted to women with epilepsy, women exposed to ASM compared with those unexposed had higher odds of severe maternal morbidity (aOR ,1.24; 95% CI, 1.10-1.48) and their neonates had an increased odd of mortality and severe morbidity (aOR, 1.37; 95% CI, 1.23-1.52).
This multinational study shows that women with epilepsy were at considerably higher risk of severe maternal and perinatal outcomes and increased risk of death during pregnancy and postpartum. Maternal epilepsy and maternal use of ASM were associated with increased maternal morbidity and perinatal mortality and morbidity.
母体癫痫与不良妊娠和新生儿结局有关。更好地了解这种情况以及分娩时的死亡率和发病率相关风险,有助于降低不良结局。
确定癫痫女性严重母体和围产发病率和死亡率的风险。
设计、地点、参与者:本研究为丹麦、芬兰、冰岛、挪威和瑞典的前瞻性基于人群的注册研究,于 1996 年 1 月 1 日至 2017 年 12 月 31 日进行。数据分析于 2022 年 8 月至 2023 年 11 月进行。参与者包括妊娠 22 周或以上的所有单胎分娩。排除出生体重或胎龄缺失或无效信息的分娩。研究小组确定了 4511267 次分娩,其中 4475984 次分娩为无癫痫的母亲,35283 次分娩为患有癫痫的母亲。
分娩前诊断为母体癫痫。产前接触抗癫痫药物(ASM),定义为从受孕到分娩的任何母亲处方用药,也进行了检查。
妊娠或产后 42 天内发生的复合严重母体发病率和死亡率,以及新生儿出生后 28 天内发生的复合严重新生儿发病率(如新生儿惊厥)和围产儿死亡率(即死产和死亡)。使用对数链接的多变量广义估计方程来获得调整后的优势比(aOR)和 95%置信区间(CI)。
癫痫队列中女性的平均(SD)分娩年龄为 29.9(5.3)岁。与无癫痫女性相比,癫痫女性的复合严重母体发病率和死亡率也更高(每 1000 次分娩中有 36.9 例与 25.4 例)。与无癫痫女性(每 1000 次分娩中有 0.05 例死亡)相比,癫痫女性的死亡风险也显著更高(每 1000 次分娩中有 0.23 例死亡),aOR 为 3.86(95%CI,1.48-8.10)。特别是,母体癫痫与严重子痫前期、栓塞、弥漫性血管内凝血或休克、脑血管事件和严重精神健康状况的发生风险增加有关。癫痫女性的胎儿和婴儿死亡率(aOR,1.20;95%CI,1.05-1.38)和严重新生儿发病率(aOR,1.48;95%CI,1.40-1.56)的几率也升高。在仅针对癫痫女性的分析中,与未暴露于 ASM 的女性相比,暴露于 ASM 的女性发生严重母体发病率的几率更高(aOR,1.24;95%CI,1.10-1.48),其新生儿的死亡率和严重发病率也增加(aOR,1.37;95%CI,1.23-1.52)。
这项多国研究表明,癫痫女性严重母体和围产期结局以及妊娠和产后死亡的风险显著更高。母体癫痫和母体使用 ASM 与母体发病率和围产儿死亡率和发病率增加有关。