Division of Obstetrics and Gynaecology, The University of Western Australia, Perth, Western Australia, Australia; Centre for Perinatal and Neonatal Medicine, Tohoku University Hospital, Sendai, Japan; School of Veterinary and Life Sciences, Murdoch University, Perth, Western Australia, Australia.
Division of Pulmonary Biology, Cincinnati Children's Hospital Medical Center, 3333 Burnet Avenue | MLC 7029, Cincinnati, OH, 45229, USA.
Semin Fetal Neonatal Med. 2019 Jun;24(3):176-181. doi: 10.1016/j.siny.2019.05.003. Epub 2019 May 8.
Treatment with antenatal corticosteroids (ACS) is standard of care for women at risk of preterm birth between 24 and 34 weeks' gestation. ACS are increasingly used for other indications, including threated or indicated late preterm birth, elective cesarean, and in at-risk pregnancies for periviable gestations. However, the various drugs and doses being used worldwide have not been rigorously evaluated to optimize clinical responses and to minimize potential risks. Translational research in animal models indicate that a constant, low concentration fetal exposure to ACS is sufficient for lung maturation, resulting in lower fetal exposures. Clinical trials to develop dosing strategies with inexpensive and widely available drugs could promote greater use in low resource environments.
产前使用皮质类固醇(ACS)是 24 至 34 周妊娠早产风险妇女的标准治疗方法。ACS 越来越多地用于其他适应症,包括威胁或提示晚期早产、选择性剖宫产,以及在极早产儿风险的妊娠中。然而,世界各地使用的各种药物和剂量尚未经过严格评估,以优化临床反应并最小化潜在风险。动物模型中的转化研究表明,ACS 的恒定低浓度胎儿暴露足以促进肺成熟,从而降低胎儿暴露。开发具有成本效益和广泛可用药物的剂量策略的临床试验可以促进在资源匮乏环境中的更广泛应用。