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长期使用皮质类固醇预防或治疗支气管肺发育不良的远期影响:权衡利弊。

Long-term effects of postnatal corticosteroids to prevent or treat bronchopulmonary dysplasia: Balancing the risks and benefits.

机构信息

Level 7, Newborn Research, Royal Women's Hospital, 20 Flemington Road, Parkville, VIC, 3052, Australia.

Level 7, Dept of Obstetrics & Gynaecology, University of Melbourne, Royal Women's Hospital, 20 Flemington Road, Parkville, VIC, 3052, Australia.

出版信息

Semin Fetal Neonatal Med. 2019 Jun;24(3):197-201. doi: 10.1016/j.siny.2019.03.002. Epub 2019 Mar 28.

Abstract

Postnatal corticosteroids are effective in preventing or treating bronchopulmonary dysplasia (BPD) in preterm newborns, but their benefits need to exceed their risks. Several types of corticosteroids, and different timing and administration modes have been trialed. Systemic corticosteroids, given either early or late, have proven efficacy for reducing BPD and the combined outcome of death or BPD. Inhaled corticosteroids are less effective. However, systemic dexamethasone given early is associated with more neurosensory disability and cerebral palsy in survivors. The risk of adverse neurodevelopment is highest if dexamethasone is given to preterm infants at low risk of BPD. Current trials focus on corticosteroids, mixed with surfactant, delivered intratracheally directly to the lung, which may avoid some systemic adverse effects of corticosteroids. Early trials of intratracheal corticosteroids are encouraging, but more data are needed to determine whether this method of administration is preferable to systemic corticosteroids for preventing or treating BPD.

摘要

产后皮质类固醇可有效预防或治疗早产儿支气管肺发育不良(BPD),但其益处需超过风险。多种类型的皮质类固醇,以及不同的时机和给药方式已进行了试验。早期或晚期给予全身皮质类固醇,已被证明可降低 BPD 及死亡或 BPD 合并的发生率。吸入皮质类固醇的效果较差。但是,早期给予全身地塞米松与幸存者中更多的神经感觉障碍和脑瘫相关。如果将地塞米松用于 BPD 风险低的早产儿,那么不良神经发育的风险最高。目前的试验主要集中在皮质类固醇上,这些皮质类固醇与表面活性剂混合,通过气管内途径直接输送到肺部,这可能避免皮质类固醇的一些全身不良反应。气管内皮质类固醇的早期试验令人鼓舞,但需要更多的数据来确定这种给药方式是否优于全身皮质类固醇来预防或治疗 BPD。

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