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表面活性剂治疗在患有急性呼吸窘迫综合征的早产儿和足月儿中的作用。

The role of surfactant treatment in preterm infants and term newborns with acute respiratory distress syndrome.

作者信息

Wirbelauer J, Speer C P

机构信息

University Children's Hospital, Würzburg, Germany.

出版信息

J Perinatol. 2009 May;29 Suppl 2:S18-22. doi: 10.1038/jp.2009.30.

Abstract

Surfactant treatment in preterm infants and term newborns with (acute respiratory distress syndrome) ARDS-like severe respiratory failure has become part of an individualized treatment strategy in many intensive care units around the world. These babies constitute heterogeneous groups of gestational ages, lung maturity, as well as of the underlying disease processes and postnatal interventions. The pathophysiology of respiratory failure in preterm infants is characterized by a combination of primary surfactant deficiency and surfactant inactivation as a result of plasma proteins leaking into the airways from areas of epithelial disruption and injury. Various pre- and postnatal factors, such as exposure to chorioamnionitis, pneumonia, sepsis and asphyxia, induce an injurious inflammatory response in the lungs of preterm infants, which may subsequently affect surfactant function, synthesis and alveolar stability. Surfactant inactivation--and dysfunction--is also a hallmark in newborns with meconium aspiration syndrome (MAS), pneumonia and other disorders affecting the pulmonary function. Although for the majority of suggested indications no data from randomized controlled trials exist, a surfactant replacement that counterbalances surfactant inactivation seems to improve oxygenation and lung function in many babies with ARDS without any apparent negative side effects. Newborns with MAS will definitely benefit from a reduced need for extracorporeal membrane oxygenation (ECMO). Clinical experience seems to justify surfactant treatment in neonates with ARDS.

摘要

在患有急性呼吸窘迫综合征(ARDS)样严重呼吸衰竭的早产儿和足月儿中,表面活性剂治疗已成为全球许多重症监护病房个体化治疗策略的一部分。这些婴儿在胎龄、肺成熟度以及潜在疾病过程和产后干预方面构成了异质性群体。早产儿呼吸衰竭的病理生理学特征是原发性表面活性剂缺乏与由于血浆蛋白从上皮破坏和损伤区域漏入气道而导致的表面活性剂失活相结合。各种产前和产后因素,如暴露于绒毛膜羊膜炎、肺炎、败血症和窒息,会在早产儿肺部引发有害的炎症反应,这随后可能影响表面活性剂功能、合成和肺泡稳定性。表面活性剂失活及功能障碍也是患有胎粪吸入综合征(MAS)、肺炎和其他影响肺功能疾病的新生儿的一个标志。尽管对于大多数建议的适应症,尚无来自随机对照试验的数据,但一种能抵消表面活性剂失活的表面活性剂替代疗法似乎能改善许多患有ARDS婴儿的氧合和肺功能,且无任何明显的负面副作用。患有MAS的新生儿肯定会因体外膜肺氧合(ECMO)需求的减少而受益。临床经验似乎证明了对患有ARDS的新生儿进行表面活性剂治疗的合理性。

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