Pregnancy outcomes in patients with systemic vasculitis in the USA from 2007 to 2022: an administrative claims-based study

IF 29.5 1区 医学 Q1 RHEUMATOLOGY
Lancet Rheumatology Pub Date : 2026-02-01 Epub Date: 2025-10-17 DOI:10.1016/S2665-9913(25)00218-8
Audra Horomanski MD , Amadeia Rector MPH , Prof Gary M Shaw DrPH , Julia F Simard ScD
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引用次数: 0

Abstract

Background

Systemic vasculitides are rare, heterogeneous, inflammatory disorders associated with high morbidity and mortality. Recent therapeutic advancements have improved life expectancy and reproductive opportunities for patients with vasculitis, but research on preterm delivery, maternal pregnancy complications, and medication use is limited. We aimed to investigate pregnancy outcomes in patients with systemic vasculitis using administrative claims data.

Methods

In this administrative claims-based study, we identified pregnancies in patients aged 15–44 years at the time of delivery with and without (referent population) systemic vasculitis in the Merative MarketScan Commercial Databases from Jan 1, 2007, to Dec 31, 2022. The database includes de-identified inpatient and outpatient health encounters (of mostly privately insured patients) with employment-sponsored health insurance claims in the USA. For patients with vasculitis, at least two outpatient or one inpatient ICD ninth revision clinical modification or ICD tenth revision clinical modification vasculitis-coded visits occurring before or on the last menstrual period of the index pregnancy were required for inclusion in the study. Systemic vasculitis was categorised by vessel size; large, medium, small, and variable. We established the rate of adverse pregnancy outcomes, including hypertensive disorders of pregnancy, placental disorders, and preterm delivery phenotypes in both groups. We also described pregnancy characteristics, medication use, and complications in patients with systemic vasculitis stratified by parity. Outcomes were compared using minimally adjusted and propensity score-adjusted regression models. People with lived experience of vasculitis were not included in this study.

Findings

We included 729 pregnancies in 568 patients with vasculitis. 61 (8·4%) were in pregnancies of patients with large vessel vasculitis, 171 (23·5%) with medium vessel vasculitis, 247 (33·9%) with small vessel vasculitis, and 274 (37·6%) with variable vessel vasculitis. 8243 pregnancies in 5680 obstetric patients without vasculitis were included in the referent population. The median age at delivery was higher in the patients with vasculitis than in those in the referent population (33 years [IQR 29–36] vs 31 years [28–35]). Glucocorticoids were the most common treatment during pregnancy in patients with systemic vasculitis, with 159 (21·8%) receiving other immunosuppressive medications. Preterm delivery (before 37 weeks completed gestation) risk was higher in patients with vasculitis than in the referent population, with increased risk in both the minimally adjusted model (adjusted risk ratio [RR] 1·76 [95% CI 1·33–2·33]) and propensity score-adjusted model (propensity score-adjusted RR 1·52 [1·13–2·03]). Pre-eclampsia or eclampsia also occurred at a higher frequency in the population with systemic vasculitis than in the referent population in both models (minimally adjusted RR 1·91 [1·45–2·52] and propensity score-adjusted RR 1·51 [1·11–2·07]). For both preterm delivery and pre-eclampsia or eclampsia, the risk varied by parity and vessel size.

Interpretation

Pregnancies in patients with vasculitis had higher risks of preterm delivery and pre-eclampsia or eclampsia than pregnancies in the referent obstetric population. Although the contribution of disease-specific factors and comorbidities on these outcomes requires further investigation, these findings affirm the importance of pre-conception counselling and regular monitoring during pregnancy.

Funding

Stanford Maternal Child Health Research Institute; Stanford Institute for Immunity, Transplantation, and Infection; and Stanford Autoimmune and Allergy Supergroup.
2007年至2022年美国系统性血管炎患者的妊娠结局:一项基于行政索赔的研究
背景:全身性血管血管炎是一种罕见的、异质性的炎症性疾病,具有高发病率和死亡率。最近的治疗进展改善了血管炎患者的预期寿命和生殖机会,但关于早产、孕产妇妊娠并发症和药物使用的研究有限。我们的目的是利用行政索赔数据调查全身性血管炎患者的妊娠结局。方法:在这项基于行政索赔的研究中,我们在2007年1月1日至2022年12月31日的Merative MarketScan商业数据库中确定了分娩时年龄在15-44岁的怀孕患者,伴有和不伴有(参照人群)全身性血管炎。该数据库包括去识别的住院和门诊健康遭遇(主要是私人保险患者)与就业赞助的健康保险索赔在美国。对于血管炎患者,至少有两次门诊或一次住院的ICD第九版临床修改或ICD第十版临床修改的血管炎编码就诊,发生在指标妊娠的最后一个月经期之前或之后。系统性血管炎按血管大小分类;大,中,小,可变。我们确定了两组不良妊娠结局的发生率,包括妊娠高血压疾病、胎盘疾病和早产表型。我们还描述了按胎次分层的全身性血管炎患者的妊娠特征、药物使用和并发症。采用最小校正和倾向评分校正回归模型对结果进行比较。有血管炎生活经历的人不包括在这项研究中。结果:我们纳入了568例血管炎患者中的729例妊娠。大血管炎61例(8.4%),中血管炎171例(23.5%),小血管炎247例(33.9%),变异性血管炎274例(37.6%)。参考人群包括5680例无血管炎的产科患者中的8243例妊娠。血管炎患者的中位分娩年龄高于对照组(33岁[IQR 29-36] vs 31岁[28-35])。糖皮质激素是妊娠期全身性血管炎患者最常用的治疗方法,其中159例(21.8%)接受了其他免疫抑制药物。血管炎患者的早产(妊娠37周前)风险高于对照人群,最低校正模型(校正风险比[RR] 1.76 [95% CI 1.33 -2·33])和倾向评分校正模型(校正倾向评分RR为1.52[1.13 - 2.03])的风险均增加。在两种模型中,伴有全身性血管炎的人群发生先兆子痫或子痫的频率也高于对照人群(最低校正RR为1.91[1.45 - 2.52],倾向评分校正RR为1.51[1.11 - 2.07])。对于早产和先兆子痫或子痫,风险因胎次和血管大小而异。解释:与参考产科人群相比,血管炎患者妊娠有更高的早产和先兆子痫或子痫风险。虽然疾病特异性因素和合并症对这些结果的影响需要进一步调查,但这些发现肯定了孕前咨询和怀孕期间定期监测的重要性。资助:斯坦福妇幼保健研究所;斯坦福免疫、移植和感染研究所;斯坦福自身免疫和过敏超级小组
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来源期刊
Lancet Rheumatology
Lancet Rheumatology RHEUMATOLOGY-
CiteScore
34.70
自引率
3.10%
发文量
279
期刊介绍: The Lancet Rheumatology, an independent journal, is dedicated to publishing content relevant to rheumatology specialists worldwide. It focuses on studies that advance clinical practice, challenge existing norms, and advocate for changes in health policy. The journal covers clinical research, particularly clinical trials, expert reviews, and thought-provoking commentary on the diagnosis, classification, management, and prevention of rheumatic diseases, including arthritis, musculoskeletal disorders, connective tissue diseases, and immune system disorders. Additionally, it publishes high-quality translational studies supported by robust clinical data, prioritizing those that identify potential new therapeutic targets, advance precision medicine efforts, or directly contribute to future clinical trials. With its strong clinical orientation, The Lancet Rheumatology serves as an independent voice for the rheumatology community, advocating strongly for the enhancement of patients' lives affected by rheumatic diseases worldwide.
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