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美国母胎医学会声明:妊娠 12 周内自然或人工流产后应用 RhD 免疫球蛋白。

Society for Maternal-Fetal Medicine Statement: RhD immune globulin after spontaneous or induced abortion at less than 12 weeks of gestation.

出版信息

Am J Obstet Gynecol. 2024 May;230(5):B2-B5. doi: 10.1016/j.ajog.2024.02.288. Epub 2024 Feb 28.

Abstract

Guidelines for the management of first-trimester spontaneous and induced abortion vary in terms of rhesus factor D (RhD) testing and RhD immune globulin (RhIg) administration. These existing guidelines are based on limited data that do not convincingly demonstrate the safety of withholding RhIg for first-trimester abortions or pregnancy losses. Given the adverse fetal and neonatal outcomes associated with RhD alloimmunization, prevention of maternal sensitization is essential in RhD-negative patients who may experience subsequent pregnancies. In care settings in which RhD testing and RhIg administration are logistically and financially feasible and do not hinder access to abortion care, we recommend offering both RhD testing and RhIg administration for spontaneous and induced abortion at <12 weeks of gestation in unsensitized, RhD-negative individuals. Guidelines for RhD testing and RhIg administration in the first trimester must balance the prevention of alloimmunization with the individual- and population-level harms of restricted access to abortion.

摘要

关于早期自然流产和人工流产中 Rh 因子 D(RhD)检测和 RhD 免疫球蛋白(RhIg)应用的管理指南,在 RhD 检测和 RhIg 应用方面存在差异。这些现有的指南是基于有限的数据,这些数据并不能令人信服地证明在早期流产或妊娠丢失时不使用 RhIg 的安全性。鉴于 RhD 同种免疫与胎儿和新生儿不良结局相关,对于可能经历后续妊娠的 RhD 阴性患者,预防母体致敏至关重要。在 RhD 检测和 RhIg 应用在后勤和财务上可行且不会阻碍堕胎护理的获得的护理环境中,我们建议在未致敏的 RhD 阴性个体中,对妊娠<12 周的自然流产和人工流产提供 RhD 检测和 RhIg 应用。在第一个孕期中 RhD 检测和 RhIg 管理的指南必须在预防同种免疫与限制堕胎机会对个人和人群的危害之间取得平衡。

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