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作 者:宋甜蜜 谢瑶 漆洪波[2] 罗欣[1] Song Tianmi;Xie Yao;Qi Hongbo;Luo Xin(Department of Obstetrics and Gynecology,The First Affiliated Hospital of Chongqing Medical University;Department of Obstetrics and Gynecology,Women and Children’s Hospital of Chongqing Medical University)
机构地区:[1]重庆医科大学附属第一医院妇产科,重庆400016 [2]重庆医科大学附属妇女儿童医院妇产科,重庆401147
出 处:《重庆医科大学学报》2022年第12期1381-1384,共4页Journal of Chongqing Medical University
基 金:国家自然科学基金资助项目(编号:81771614、82171662);国家自然科学基金区域创新发展联合基金重点资助项目(编号:U21A20346)。
摘 要:抗磷脂综合征(antiphospholipid syndrome,APS)是一种自身免疫性疾病,可累及多器官及多系统。在妊娠期间由于孕妇血流动力学的改变,一旦合并APS可使机体处于高凝状态,因此极易发生胎盘血栓形成。同时抗磷脂抗体(antiphospholipid antibody,aPL)可通过破坏滋养细胞功能等多种机制造成子痫前期、胎儿生长受限、胎儿宫内死亡及其他不良结局。APS患者一旦发生产科合并症则被称为产科抗磷脂综合征(obstetric APS,OAPS)。本文就OAPS的诊断及分型、与不良妊娠结局的相关性、诊治现状及远期随访进行文献综述,以期为临床工作提供指导。Antiphospholipid syndrome(APS)is an autoimmune disease affecting multiple organs and systems.The combination of APS with maternal hemodynamic changes during pregnancy can put the body in a hypercoagulable state,making it highly susceptible to placental thrombosis.In addition,the effect of antiphospholipid antibody(aPL)on trophoblast cell function can cause preeclampsia,fetal growth restriction,intrauterine fetal death,and other adverse outcomes.It is called obstetric antiphospholipid syndrome(OAPS)when patients with APS develop obstetric complications.This article provides a literature review on the diagnosis and staging of OAPS,the correlation with adverse pregnancy outcomes,the current status of diagnosis and treatment,and long-term follow-up,with the aim of providing guidance for clinical work.
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