狼疮活动与接受辅助生殖疗法的系统性红斑狼疮患者的妊娠结局:系统回顾和荟萃分析。

IF 2.9 3区 医学 Q2 RHEUMATOLOGY
Fatemeh Zahra Seyed-Kolbadi, Alireza Malektojari, Mohammad Hossein Zarei, Mina Keshavarz, Kosar Gorgin, Marzieh Bonyadi, Mohammad Hamed Ersi, Reza Farrokhseresht
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引用次数: 0

摘要

系统性红斑狼疮(SLE)是一种慢性自身免疫性疾病,主要影响育龄妇女。虽然怀孕和荷尔蒙应激可诱发系统性红斑狼疮复发,但辅助生殖疗法(ART)对系统性红斑狼疮患者的影响尚不明确。我们对 PubMed/Medline、Embase 和 CENTRAL 进行了检索,直至 2024 年 3 月 20 日,以寻找评估辅助生殖疗法后系统性红斑狼疮复发率和妊娠结局的观察性研究。我们的分析采用了随机效应荟萃分析和建议分级评估、发展和评价(GRADE)方法来评价证据质量。共有五项研究符合条件,涉及 237 名接受抗逆转录病毒疗法的系统性红斑狼疮女性患者。荟萃分析表明,系统性红斑狼疮复发率为 17%(95% CI:10-25%),证据质量为中等。关节炎复发的汇总患病率为 7%(95% CI:0-25%),证据质量较低。成功怀孕率为58%(95% CI:43-72%),活产率为96%(95% CI:83-100%),均为低质量证据。中度质量证据显示了妊娠并发症,包括胎膜早破(PPROM)8%(95% CI:3-16%)、流产 2%(95% CI:0-9%)、宫内胎儿死亡(IUFD)4%(95% CI:0-11%)和子痫前期 7%(95% CI:1-17%)。低质量证据显示,早产率为 10%(95% CI:0-32%),卵巢过度刺激综合征(OHSS)为 2%(95% CI:0-11%)。抗逆转录病毒疗法受孕者的系统性红斑狼疮复发以及妊娠并发症,如子宫内膜异位症、流产、先兆流产和子痫前期,与自然受孕的情况相当。这表明,系统性红斑狼疮患者在进行缜密的妊娠计划时,抗逆转录病毒疗法是相对安全的。要点 - 系统性红斑狼疮(SLE)是一种慢性自身免疫性疾病,主要影响育龄妇女。- 与健康妇女相比,患有系统性红斑狼疮的妇女怀孕会给母体和胎儿带来更高的风险。- 在接受抗逆转录病毒疗法时,系统性红斑狼疮的复发和妊娠并发症与自然受孕时的并发症相当,因此抗逆转录病毒疗法对系统性红斑狼疮患者相对安全。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Lupus activity and pregnancy outcomes in systemic lupus erythematosus patients undergoing assisted reproductive therapy: A systematic review and meta-analysis.

Systemic lupus erythematosus (SLE) is a chronic autoimmune disease primarily impacting women of childbearing age. While pregnancy and hormonal stress can trigger SLE flare-ups, the effects of assisted reproductive therapies (ARTs) on SLE patients are not well defined. We conducted a search of PubMed/Medline, Embase, and CENTRAL until March 20, 2024, to find observational studies assessing the prevalence of SLE flares and pregnancy outcomes following ARTs. Our analysis included random-effects meta-analysis and the Grading of Recommendations Assessment, Development, and Evaluation (GRADE) approach for evaluating evidence quality. Five studies involving 237 SLE women who underwent ARTs were eligible. The meta-analysis indicated a prevalence of SLE flares at 17% (95% CI: 10-25%) with moderate-quality evidence. The pooled prevalence of arthritis flares was 7% (95% CI: 0-25%) with low-quality evidence. Successful pregnancy rates were 58% (95% CI: 43-72%), and live birth rates were 96% (95% CI: 83-100%), both with low-quality evidence. Moderate-quality evidence showed pregnancy complications, including preterm premature rupture of membranes (PPROM) at 8% (95% CI: 3-16%), miscarriages at 2% (95% CI: 0-9%), intrauterine fetal demise (IUFD) at 4% (95% CI: 0-11%), and preeclampsia at 7% (95% CI: 1-17%). Low-quality evidence showed preterm labor at 10% (95% CI: 0-32%) and ovarian hyperstimulation syndrome (OHSS) at 2% (95% CI: 0-11%). SLE flares, as well as pregnancy complications such as IUFD, miscarriage, PPROM, and preeclampsia in ART recipients, are equivalent to those in spontaneous conception. This indicates that ART is relatively safe for SLE patients with meticulous pregnancy planning. Key Points • Systemic lupus erythematosus (SLE) is a chronic autoimmune disease primarily impacting women of childbearing age. • Pregnancy in women with SLE poses elevated maternal and fetal risks compared to healthy women. • SLE flares and pregnancy complications while receiving ART are equivalent to those in spontaneous conception and ART is relatively safe for SLE patients.

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来源期刊
Clinical Rheumatology
Clinical Rheumatology 医学-风湿病学
CiteScore
6.90
自引率
2.90%
发文量
441
审稿时长
3 months
期刊介绍: Clinical Rheumatology is an international English-language journal devoted to publishing original clinical investigation and research in the general field of rheumatology with accent on clinical aspects at postgraduate level. The journal succeeds Acta Rheumatologica Belgica, originally founded in 1945 as the official journal of the Belgian Rheumatology Society. Clinical Rheumatology aims to cover all modern trends in clinical and experimental research as well as the management and evaluation of diagnostic and treatment procedures connected with the inflammatory, immunologic, metabolic, genetic and degenerative soft and hard connective tissue diseases.
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