Pregnancy outcomes in ANCA-associated vasculitis patients: A systematic review and meta-analysis

医学 显微镜下多血管炎 肉芽肿伴多发性血管炎 怀孕 嗜酸性 血管炎 荟萃分析 抗中性粒细胞胞浆抗体 产科 疾病 儿科 宫内生长受限 内科学 妊娠期 病理 生物 遗传学
作者
Styliani Partalidou,Apostolos Mamopoulos,Despoina Dimopoulou,Pantelis Sarafidis,Theodoros Dimitroulas
出处
期刊:Joint Bone Spine [Elsevier]
卷期号:90 (6): 105609-105609 被引量:3
标识
DOI:10.1016/j.jbspin.2023.105609
摘要

Antineutrophil cytoplasmic antibody (ANCA) associated vasculitis (AAV), namely granulomatosis with polyangiitis, eosinophilic granulomatosis with polyangiitis and microscopic polyangiitis constitute a group of rare systemic vasculitides, affecting small vessels. Genders are equally affected, with symptoms most commonly presenting during and/or after the fifth decade of life, but AAV may also present in younger individuals. As advanced maternal age is becoming common and safe over the last decades, it is now more feasible for middle-aged women suffering from AAV to get pregnant. Although adverse pregnancy outcomes have been thoroughly investigated in other systemic diseases, the exact prevalence of pregnancy complications and unfavorable outcomes in pregnant women with AAV has not been systematically evaluated.We researched PubMed, Scopus, Cochrane Library and Cinahl databases until September, 2022. Three blinded investigators extracted data and assessed the risk of bias. A random effects model was used for the analysis. The outcomes studied were pre-term delivery, intrauterine growth restriction (IUGR) neonates and disease flare.We included six studies with 92 pregnancies in patients with AAV. The prevalence of pre-term delivery, IUGR neonates and disease flare were 18% (CI: 0.10-0.30, P=non-significant), 20% (CI: 0.11-0.33, P=non-significant) and 28% (CI: 0.09-0.59, P<0.01), respectively.The analysis demonstrated higher occurrence of adverse outcomes in pregnant women suffering from AAV accompanied by an increased risk of disease flare during pregnancy. These findings underline the importance of preconception counseling and the necessity of close monitoring in these patients similarly to other systemic inflammatory diseases.
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