Uguz Faruk, Sharma Verinder
Department of Psychiatry, Meram Faculty of Medicine, Necmettin Erbakan University, Konya, Turkey.
Department of Psychiatry and Obstetrics and Gynecology, Western University, Parkwood Institute, London, ON, Canada.
Bipolar Disord. 2016 Jun;18(4):325-33. doi: 10.1111/bdi.12398. Epub 2016 Jun 14.
This review examined the safety of mood stabilizers in exposed breastfed infants.
PubMed was searched for English language reports between 1 January 1995 and 30 August 2015 by using combinations of key words breastfeeding, lactation, postpartum period, puerperium, mood stabilizers, lithium, lamotrigine, valproate, carbamazepine, and oxcarbazepine. Case reports, case series, and prospective or cross-sectional studies including relevant data such as relative infant dose, milk-to-plasma ratio, infant drug plasma levels, and adverse events were identified.
A total of 26 of 604 relevant reports in PubMed were included in the study. These reports included lamotrigine (122 cases in 12 reports), lithium (26 cases in five reports), carbamazepine (64 cases in five reports), valproate (nine cases in three reports), and oxcarbazepine (two cases in two reports). Of 26 reports, one report included both carbamazepine and valproate. The reports suggest that a considerable amount of lithium and lamotrigine are excreted into breast milk. There is a paucity of data on valproate and oxcarbazepine; however, the infant/maternal ratio of serum drug concentration seems to be lower in valproate exposure compared to other mood stabilizers. The incidence of adverse events in infants exposed to mood stabilizers is reported to be very low.
The current data suggest that mood stabilizers can be prescribed without any adverse events in most infants in lactating women. The available reports also suggest a low prevalence rate of laboratory abnormalities including hepatic, kidney, and thyroid functions in the infants. Additional studies examining short-term and especially long-term effects of mood stabilizers on breastfed infants are required.
本综述探讨了心境稳定剂对接受母乳喂养婴儿的安全性。
在PubMed数据库中检索1995年1月1日至2015年8月30日期间的英文报告,使用了“母乳喂养”“哺乳期”“产后期”“产褥期”“心境稳定剂”“锂盐”“拉莫三嗪”“丙戊酸盐”“卡马西平”和“奥卡西平”等关键词组合。确定了病例报告、病例系列以及前瞻性或横断面研究,包括相对婴儿剂量、乳汁与血浆比值、婴儿药物血浆水平和不良事件等相关数据。
PubMed中604篇相关报告中的26篇被纳入本研究。这些报告包括拉莫三嗪(12篇报告中的122例)、锂盐(5篇报告中的26例)、卡马西平(5篇报告中的64例)、丙戊酸盐(3篇报告中的9例)和奥卡西平(2篇报告中的2例)。26篇报告中,1篇报告同时涉及卡马西平和丙戊酸盐。报告表明,大量的锂盐和拉莫三嗪会排泄到母乳中。关于丙戊酸盐和奥卡西平的数据较少;然而,与其他心境稳定剂相比,丙戊酸盐暴露时血清药物浓度的婴儿/母体比值似乎较低。据报道,暴露于心境稳定剂的婴儿中不良事件的发生率非常低。
目前的数据表明,在大多数哺乳期妇女的婴儿中,开具心境稳定剂不会出现任何不良事件。现有报告还表明,婴儿中包括肝、肾和甲状腺功能在内的实验室异常发生率较低。需要进一步研究心境稳定剂对母乳喂养婴儿的短期尤其是长期影响。