Canibaño Beatriz, Deleu Dirk, Mesraoua Boulenouar, Melikyan Gayane, Ibrahim Faiza, Hanssens Yolande
Department of Neurology, Neuroscience Institute, Hamad Medical Corporation, Doha, Qatar.
Clinical Services Unit, Pharmacy, Hamad Medical Corporation, Doha, Qatar.
J Drug Assess. 2020 Jan 23;9(1):20-36. doi: 10.1080/21556660.2020.1721507. eCollection 2020.
To review the current evidence regarding pregnancy-related issues in multiple sclerosis (MS) and to provide recommendations specific for each of them. A systematic review was performed based on a comprehensive literature search. MS has no effect on fertility, pregnancy or fetal outcomes, and pregnancies do not affect the long-term disease course and accumulation of disability. There is a potential risk for relapse after use of gonadotropin-releasing hormone agonists during assisted reproduction techniques. At short-term, pregnancy leads to a reduction of relapses during the third trimester, followed by an increased risk of relapses during the first three months postpartum. Pregnancies in MS are not high risk pregnancies, and MS does not influence the mode of delivery or anesthesia unless in the presence of significant disability. MRI is not contraindicated during pregnancy; however, gadolinium contrast media should be avoided whenever possible. It is safe to use pulse dose methylprednisolone infusions to manage acute disabling relapses during pregnancy and breastfeeding. However, its use during the first trimester of pregnancy is still controversial. Women with MS should be encouraged to breastfeed with a possible favorable effect of exclusive breastfeeding. Disease-modifying drugs can be classified according to their potential for pregnancy-associated risk and impact on fetal outcome. Interferon beta (IFNβ) and glatiramer acetate (GA) may be continued until pregnancy is confirmed and, after consideration of the individual risk-benefit if continued, during pregnancy. The benefit of continuing natalizumab during the entire pregnancy may outweigh the risk of recurring disease activity, particularly in women with highly active MS. GA and IFNβ are considered safe during breastfeeding. The use of natalizumab during pregnancy or lactation requires monitoring of the newborn. This review provides current evidence and recommendations for counseling and management of women with MS preconception, during pregnancy and postpartum.
回顾目前关于多发性硬化症(MS)中与妊娠相关问题的证据,并针对每个问题提供具体建议。基于全面的文献检索进行了系统综述。MS对生育力、妊娠或胎儿结局没有影响,妊娠也不会影响疾病的长期病程和残疾累积。在辅助生殖技术中使用促性腺激素释放激素激动剂后有复发的潜在风险。短期内,妊娠会导致孕晚期复发减少,随后产后前三个月复发风险增加。MS患者的妊娠并非高危妊娠,除非存在严重残疾,MS不会影响分娩方式或麻醉。孕期MRI并非禁忌;然而,应尽可能避免使用钆对比剂。在妊娠和哺乳期使用脉冲剂量甲泼尼龙输注来治疗急性致残性复发是安全的。然而,在妊娠早期使用仍存在争议。应鼓励MS女性进行母乳喂养,纯母乳喂养可能有有利影响。疾病修正药物可根据其与妊娠相关的风险及对胎儿结局的影响进行分类。干扰素β(IFNβ)和醋酸格拉替雷(GA)可持续使用至确认妊娠,在考虑继续使用的个体风险效益后,也可在孕期使用。在整个孕期继续使用那他珠单抗的益处可能超过疾病复发活动的风险,特别是对于高度活跃的MS女性。GA和IFNβ在母乳喂养期间被认为是安全的。在妊娠或哺乳期使用那他珠单抗需要对新生儿进行监测。本综述为MS女性孕前、孕期及产后的咨询和管理提供了当前的证据和建议。