Stanford University School of Medicine, Stanford, California.
Kaiser Permanente Northern California, Oakland.
Arthritis Care Res (Hoboken). 2024 Apr;76(4):526-530. doi: 10.1002/acr.25279. Epub 2024 Feb 6.
Although the population of patients with systemic lupus erythematosus (SLE) is racially and ethnically diverse, many study populations are homogeneous. Further, data are often lacking on critical factors, such as antiphospholipid antibodies (aPLs). We investigated live birth rates in patients with SLE at Kaiser Permanente Northern California, including race and ethnicity and aPL data.
Electronic health records of pregnancies with outcomes observed from 2011 to 2020 were identified among patients with SLE. Prevalent SLE was defined as two or more International Classification of Diseases-coded visits seven or more days apart before the last menstrual period. We summarized patient characteristics, medication orders, health care use, and medication use. Pregnancy outcomes (live birth, stillbirth, spontaneous abortion, ectopic pregnancy, and molar pregnancy) were presented overall and stratified by race and ethnicity, aPL status, and nephritis history.
We identified 657 pregnancies among 453 patients with SLE. The cohort was diverse, reflecting the Northern California population (27% Asian, 26% Hispanic, 26% Non-Hispanic White, 13% Non-Hispanic Black, 5% multiracial, and approximately 2% Pacific Islander and Native American). Approximately 74% of observed pregnancies ended in live birth, 23% resulted in spontaneous abortion, 2% were ectopic or molar pregnancies, and <1% were stillbirths. There was limited variability in live births by race and ethnic group (72%-79%), aPL status (69.5%-77%), and nephritis history (71%-75%).
Our findings are consistent with previous studies; however, some methodologic differences may yield a range of live birth rates. We found that approximately 74% of pregnancies in patients with SLE ended in live birth, with modest variability in spontaneous abortion by race and ethnicity, nephritis history, and aPL status.
尽管系统性红斑狼疮(SLE)患者的人口在种族和民族上存在多样性,但许多研究人群是同质的。此外,通常缺乏抗磷脂抗体(aPL)等关键因素的数据。我们调查了 Kaiser Permanente 北加利福尼亚的 SLE 患者的活产率,包括种族和民族以及 aPL 数据。
从 2011 年至 2020 年观察到结局的妊娠电子健康记录中确定了患有 SLE 的患者。先前存在的 SLE 定义为两次或更多次国际疾病分类编码就诊,两次就诊间隔至少 7 天,且均发生在末次月经前。我们总结了患者特征、药物医嘱、医疗保健使用和药物使用情况。妊娠结局(活产、死产、自然流产、异位妊娠和葡萄胎)总体呈现,并按种族和民族、aPL 状态和肾炎病史进行分层。
我们在 453 名 SLE 患者中确定了 657 次妊娠。该队列具有多样性,反映了北加利福尼亚的人口(27%的亚洲人、26%的西班牙裔、26%的非西班牙裔白人、13%的非西班牙裔黑人、5%的多种族和大约 2%的太平洋岛民和美洲原住民)。约 74%的观察到的妊娠以活产结束,23%导致自然流产,2%为异位或葡萄胎妊娠,<1%为死产。种族和民族群体(72%-79%)、aPL 状态(69.5%-77%)和肾炎病史(71%-75%)之间的活产率差异不大。
我们的发现与之前的研究一致;然而,一些方法学差异可能会导致活产率的范围有所不同。我们发现,SLE 患者的妊娠中约有 74%以活产结束,种族和民族、肾炎病史和 aPL 状态对自然流产的影响差异不大。