Cheng Vienna, Amiri Neda, Cheng Vicki, Ellis Ursula, Cragg Jacquelyn J, Harrison Mark, Proulx Laurie, De Vera Mary A
University of British Columbia, Collaboration for Outcomes Research and Evaluation, and Arthritis Research Canada, Vancouver, British Columbia, Canada.
University of British Columbia, Arthritis Research Canada, and Mary Pack Arthritis Centre, Vancouver, British Columbia, Canada.
Arthritis Care Res (Hoboken). 2025 Jul;77(7):916-927. doi: 10.1002/acr.25502. Epub 2025 Feb 24.
Targeted synthetic disease-modifying antirheumatic drugs (tsDMARDs) have expanded the management of autoimmune diseases, including rheumatic diseases. As the use of these drugs grows, it is important to understand their effects on pregnancy. We conducted a scoping review to synthesize the current evidence on the impacts of tsDMARDs on pregnancy outcomes.
We searched the Embase, MEDLINE, and CENTRAL databases in November 2023. We included studies that examined tsDMARD exposure for chronic autoimmune disease(s), particularly in mothers during pregnancy, fathers before conception, and/or fetuses/neonates in utero. We extracted data on sample size, study design, tsDMARD exposure (dose and duration), and reproductive health outcomes.
Of 6,712 studies screened, eight were included, namely nine case reports, one case series, four cross-sectional studies, and one cohort study among patients with ulcerative colitis, rheumatoid arthritis, and psoriasis. Sample sizes ranged from 1 to 116 pregnancies or offspring, with six studies on tofacitinib, one on baricitinib, one on upadacitinib, and no studies on apremilast. Overall, 19 fetal/neonatal outcomes, six fetal/neonatal-maternal outcomes, and three maternal outcomes were extracted. The most frequently reported fetal/neonatal outcomes were congenital anomaly (n = 4), preterm birth (n = 4), and the fetal/neonatal-maternal outcome of spontaneous abortion (n = 4). Only one study reported on the maternal outcome of delivery via Cesarean section.
Our scoping review of evidence to date on the perinatal use of tsDMARDs reveal small sample sizes and a limited number of studies, all largely descriptive in nature. Findings highlight evidence gaps that preclude providers and patients from making informed decisions when considering the perinatal use of tsDMARDs.
靶向合成改善病情抗风湿药物(tsDMARDs)拓展了自身免疫性疾病(包括风湿性疾病)的治疗手段。随着这些药物的使用增加,了解它们对妊娠的影响至关重要。我们进行了一项范围综述,以综合目前关于tsDMARDs对妊娠结局影响的证据。
我们于2023年11月检索了Embase、MEDLINE和CENTRAL数据库。我们纳入了研究tsDMARDs用于慢性自身免疫性疾病暴露情况的研究,特别是孕期母亲、受孕前父亲以及子宫内胎儿/新生儿的暴露情况。我们提取了样本量、研究设计、tsDMARDs暴露(剂量和持续时间)以及生殖健康结局的数据。
在筛选的6712项研究中,纳入了8项,即9篇病例报告、1篇病例系列、4项横断面研究以及1项关于溃疡性结肠炎、类风湿关节炎和银屑病患者的队列研究。样本量从1至116例妊娠或后代不等,其中6项研究涉及托法替布,1项涉及巴瑞替尼,1项涉及乌帕替尼,没有关于阿普司特的研究。总体而言,提取了19项胎儿/新生儿结局、6项胎儿/新生儿 - 母亲结局以及3项母亲结局。最常报告的胎儿/新生儿结局是先天性异常(n = 4)、早产(n = 4)以及胎儿/新生儿 - 母亲结局中的自然流产(n = 4)。只有1项研究报告了剖宫产的母亲结局。
我们对tsDMARDs围产期使用证据的范围综述显示样本量小且研究数量有限,所有研究在很大程度上都是描述性的。研究结果突出了证据空白,这使得医疗服务提供者和患者在考虑tsDMARDs围产期使用时无法做出明智的决策。