Rohilla Minakshi, Bhardwaj Mahak, Jain Vanita
Department of Obstetrics and Gynaecology, PGIMER Chandigarh, 160012, India.
Eur J Obstet Gynecol Reprod Biol X. 2024 Aug 30;24:100340. doi: 10.1016/j.eurox.2024.100340. eCollection 2024 Dec.
Antiphospholipid Syndrome (APS) is a systemic autoimmune thrombophilic condition characterized by obstetric manifestations, including pregnancy loss, preeclampsia and fetal growth restriction. Early diagnosis and management are key to improve maternal and neonatal outcomes.
The aim of this study is to assess the perinatal outcomes in APS, the development of various adverse pregnancy outcomes (APO), and their association with specific antibody profiles.
This observational study was carried out on booked cases of singleton pregnancy and diagnosed cases of primary APS in our High-Risk Pregnancy (HRP) clinic from January 2018 to December 2022 after approval from institutional ethics committee. Forty-three confirmed cases of primary APS were enrolled and started on low-dose aspirin and low-molecular-weight heparin (LMWH) as per the patient's body weight after confirmation of fetal heart activity radiologically until 36 weeks of gestation as a standard of care.
Forty patients (93 %) had obstetric APS, and three patients (7 %) had thrombotic APS. During the course of the current pregnancy, adverse pregnancy outcomes (APO) developed in 12 (30 %) out of 40 cases of obstetric APS and in all 3 patients with thrombotic APS. Preeclampsia was seen in 11 (25.5 %), FGR in 12 (27.9 %), and preterm birth in 7 (16.2 %) cases. Patients with an antibody profile showing the presence of Anti-β2 GP-I positivity and ACL positivity had fewer APOs (20 % and 29 %) in comparison to patients with a LA and triple positive antibody profile (55 % and 50 %).
Treatment of pregnant women with APS causes significant improvement in the live birth rate. The late pregnancy complications like preeclampsia, FGR, and premature birth, occurring despite treatment still remains a challenge and emphasizes the need for stringent antepartum surveillance and timely delivery.
抗磷脂综合征(APS)是一种全身性自身免疫性血栓形成倾向疾病,其特征为产科表现,包括妊娠丢失、先兆子痫和胎儿生长受限。早期诊断和管理是改善孕产妇和新生儿结局的关键。
本研究旨在评估APS的围产期结局、各种不良妊娠结局(APO)的发生情况及其与特定抗体谱的关联。
本观察性研究在获得机构伦理委员会批准后,于2018年1月至2022年12月在我们的高危妊娠(HRP)诊所对单胎妊娠的预约病例和原发性APS的确诊病例进行。纳入43例确诊的原发性APS病例,在经影像学确认胎儿心脏活动后,根据患者体重开始使用低剂量阿司匹林和低分子肝素(LMWH),直至妊娠36周作为标准治疗。
40例(93%)为产科APS,3例(7%)为血栓形成性APS。在本次妊娠过程中,40例产科APS病例中有12例(30%)出现不良妊娠结局(APO),3例血栓形成性APS患者均出现不良妊娠结局。先兆子痫见于11例(25.5%),胎儿生长受限见于12例(27.9%),早产见于7例(16.2%)。与狼疮抗凝物(LA)和三联抗体阳性的患者相比,抗体谱显示抗β2糖蛋白I(Anti-β2 GP-I)阳性和抗心磷脂抗体(ACL)阳性的患者不良妊娠结局较少(分别为20%和29%,而LA和三联抗体阳性的患者分别为55%和50%)。
对患有APS的孕妇进行治疗可显著提高活产率。尽管进行了治疗,但子痫前期、胎儿生长受限和早产等晚期妊娠并发症仍然是一个挑战,并强调需要进行严格的产前监测和适时分娩。