Imaz Maria Luisa, Torra Mercè, Soy Dolors, García-Esteve Lluïsa, Martin-Santos Rocio
Department of Medicine, Institute of Neuroscience, University of Barcelona (UB), Barcelona, Spain.
Unit of Perinatal Mental Health, Department of Psychiatry and Psychology, Hospital Clínic, Institut d´Investigació Mèdica August Pi i Sunyer (IDIBAPS), Barcelona, Spain.
Front Pharmacol. 2019 Sep 10;10:1005. doi: 10.3389/fphar.2019.01005. eCollection 2019.
There is substantial evidence that postpartum prophylaxis with lithium lowers the rate of relapse in bipolar disorder. However, it is contraindicated during breastfeeding due to the high variability of the transfer into breast milk. We conducted a systematic review of the current evidence of studies assessing the transfer of lithium to lactating infants and short-term infant outcomes. An protocol was designed based on PRISMA guidelines. Searches in PubMed and LactMed were conducted until September 2018. Studies assessing lithium pharmacokinetic parameters and short-term infant outcomes were included. Quality was assessed using a checklist based on international guidelines (i.e., FDA). From 344 initial studies, 13 case reports/series with 39 mother-child dyads were included. Only 15% of studies complied with ≥50% of the items on the quality assessment checklist. Infants breastfeed a mean (SD) of 58.9 (83.3) days. Mean maternal lithium dose was 904 (293) mg/day, corresponding lithium plasma/serum concentration was 0.73(0.26) mEq/L, and breast milk concentration was 0.84(0.14) mEq/L. Mean infant lithium plasma/serum concentration was 0.23(0.26) mEq/L. Twenty-six (80%) infants had concentrations ≤0.30 mEq/L without adverse effects. Eight (20%) showed a transient adverse event (i.e., acute toxicity or thyroid alterations). All of them were also prenatally exposed to lithium monotherapy or polytherapy. The current evidence comes from studies with a degree of heterogeneity and of low-moderate quality. However, it identifies areas of improvement for future clinical lactation studies of lithium and provides support for some clinical recommendations.
有大量证据表明,产后使用锂盐进行预防可降低双相情感障碍的复发率。然而,由于锂盐转入母乳的情况差异很大,母乳喂养期间禁用。我们对评估锂盐向哺乳婴儿的转移情况及婴儿短期结局的现有研究证据进行了系统综述。根据PRISMA指南设计了一项方案。检索了PubMed和LactMed,检索截止至2018年9月。纳入了评估锂盐药代动力学参数及婴儿短期结局的研究。使用基于国际指南(即美国食品药品监督管理局)的清单评估质量。从344项初始研究中,纳入了13篇病例报告/系列,涉及39对母婴。只有15%的研究符合质量评估清单中≥50%的条目。婴儿平均(标准差)母乳喂养58.9(83.3)天。母亲锂盐平均剂量为904(293)mg/天,相应的锂血浆/血清浓度为0.73(0.26)mEq/L,母乳浓度为0.84(0.14)mEq/L。婴儿锂血浆/血清平均浓度为0.23(0.26)mEq/L。26名(80%)婴儿的浓度≤0.30 mEq/L,无不良影响。8名(20%)出现短暂不良事件(即急性毒性或甲状腺改变)。他们均在产前接受过锂盐单药治疗或联合治疗。目前的证据来自异质性程度较高且质量为低-中度的研究。然而,它确定了未来锂盐临床泌乳研究的改进领域,并为一些临床建议提供了支持。