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对当前关于妊娠和哺乳期系统性炎症性风湿病治疗建议的批判性评价。

Critical review of the current recommendations for the treatment of systemic inflammatory rheumatic diseases during pregnancy and lactation.

机构信息

Department of Rheumatology, Universidade do Estado do Rio de Janeiro, Rio de Janeiro, Brazil; Pós-graduação em Ciências Médicas (PGCM), Faculdade de Ciências, Médicas, Universidade do Estado do Rio de Janeiro, Rio de Janeiro, Brazil.

Department of Obstetrics, Universidade do Estado do Rio de Janeiro, Rio de Janeiro, Brazil; Department of Obstetrics, Instituto Fernandes Figueira, FIOCRUZ, Rio de Janeiro, Brazil; Pós-graduação em Ciências Médicas (PGCM), Faculdade de Ciências, Médicas, Universidade do Estado do Rio de Janeiro, Rio de Janeiro, Brazil.

出版信息

Autoimmun Rev. 2016 Oct;15(10):955-63. doi: 10.1016/j.autrev.2016.07.014. Epub 2016 Aug 1.

Abstract

The crucial issue for a better pregnancy outcome in women with autoimmune rheumatic diseases is appropriate planning, with counseling of the ideal timing and treatment adaptation. Drugs used to treat rheumatic diseases may interfere with fertility or increase the risk of miscarriages and congenital abnormalities. MTX use post-conception is clearly linked to abortions as well as major birth defects, so it should be stopped 3months before conception. Leflunomide causes abnormalities in animals even in low doses. Although in humans, it does not seem to be as harmful as MTX, when pregnancy is detected in a patient on leflunomide, cholestyramine is given for washout. Sulfasalazine can be used safely and is an option for those patients who were on MTX or leflunomide. Azathioprine is generally the immunosuppressive of choice in many high-risk pregnancy centers because of the safety profile and its steroid-sparing property. Cyclosporine and tacrolimus can also be used as steroid-sparing agents, but experience is smaller. Although prednisone and prednisolone are inactivated in the placenta, we try to limit the dose to the minimal effective one, to prevent side effects. Antimalarials have been broadly studied and are safe during pregnancy and breastfeeding. Among biologic disease modifying anti-rheumatic agents (bDMARD), the anti-TNFs that have been used for longer are the ones with greater experience. The large monoclonal antibodies do not cross the placenta in the first trimester, and after conception, the decision to continue medication should be taken individually. The experience is larger in women with inflammatory bowel diseases, where anti-TNF is generally maintained at least until 30weeks to reduce fetal exposure. Live vaccines should not be administrated to the infant in the first 6months of life. Pregnancy data for rituximab, abatacept, anakinra, tocilizumab, ustekinumab, belimumab, and tofacitinib are limited and their use in pregnancy cannot currently be recommended.

摘要

对于患有自身免疫性风湿病的女性来说,实现更好妊娠结局的关键问题是进行适当的规划,包括理想时机的咨询和治疗方案的调整。用于治疗风湿病的药物可能会干扰生育能力或增加流产和先天畸形的风险。孕后使用 MTX 显然与流产以及重大出生缺陷有关,因此应在受孕前 3 个月停止使用。来氟米特即使低剂量也会在动物中引起畸形。虽然在人类中,它似乎不像 MTX 那样有害,但当患者在使用来氟米特时发现怀孕,会给予考来烯胺进行冲洗。柳氮磺胺吡啶可以安全使用,并且是那些曾使用 MTX 或来氟米特的患者的选择。硫唑嘌呤由于其安全性和类固醇节约特性,通常是许多高危妊娠中心的首选免疫抑制剂。环孢素和他克莫司也可用作类固醇节约药物,但经验较少。虽然泼尼松和泼尼松龙在胎盘内失活,但我们尽量将剂量限制在最小有效剂量,以防止副作用。抗疟药已广泛研究,在妊娠和哺乳期是安全的。在生物制剂疾病修饰抗风湿药物(bDMARD)中,使用时间较长的抗 TNF 药物具有更多的经验。大型单克隆抗体在妊娠早期不会穿过胎盘,在受孕后,应单独决定是否继续用药。在炎症性肠病患者中,这种经验更大,通常至少要维持抗 TNF 治疗至 30 周,以减少胎儿暴露。在婴儿出生后的头 6 个月内,不应给其接种活疫苗。利妥昔单抗、阿巴西普、阿那白滞素、托珠单抗、乌司奴单抗、贝利尤单抗和托法替布的妊娠数据有限,目前不能推荐在妊娠期间使用。

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