Clinic of Obstetrics and Gynaecology, Institute of Clinical Medicine, Faculty of Medicine, Vilnius University, Vilnius, Lithuania.
Curr Opin Obstet Gynecol. 2021 Oct 1;33(5):378-383. doi: 10.1097/GCO.0000000000000731.
To provide the latest evidence and treatment advances of multiple sclerosis in women of childbearing age prior to conception, during pregnancy and postpartum.
Recent changes permitting interferon beta (IFN-β) use in pregnancy and breastfeeding has broadened the choices of disease modifying treatments (DMTs) for patients with high relapse rates. Natalizumab may also be continued until 34 weeks of pregnancy for patients requiring persisting treatment. Drugs with a known potential of teratogenicity such as fingolimod or teriflunomide should be avoided and recommended wash-out times for medications such as cladribine, alemtuzumab or ocrelizumab should be considered. Teriflunomide and fingolimod are not recommended during breastfeeding, however, glatiramer acetate and IFN-β are considered to be safe.
The evidence of potential fetotoxicities and adverse pregnancy outcomes associated with DMTs is increasing, although more research is needed to evaluate the safety of drugs and to track long-term health outcomes for the mother and the child.
在妊娠前、妊娠期间和产后,为育龄期女性提供多发性硬化症的最新证据和治疗进展。
最近允许干扰素-β(IFN-β)在妊娠和哺乳期使用的变化拓宽了高复发率患者的疾病修正治疗(DMT)选择。对于需要持续治疗的患者,那他珠单抗也可以持续使用至妊娠 34 周。应避免使用具有已知致畸潜力的药物,如芬戈莫德或特立氟胺,并应考虑如克拉屈滨、阿仑单抗或奥瑞珠单抗等药物的冲洗时间。特立氟胺和芬戈莫德不建议在哺乳期使用,但醋酸格拉替雷和 IFN-β被认为是安全的。
尽管需要更多的研究来评估药物的安全性,并跟踪母亲和孩子的长期健康结果,但与 DMT 相关的潜在胎儿毒性和不良妊娠结局的证据正在增加。