Centre for Neonatal Research and Education, University of Western Australia, Perth, WA, Australia.
Neonatology. 2012;101(4):337-44. doi: 10.1159/000337354. Epub 2012 Jun 1.
Instilled bolus surfactant is the only approved surfactant treatment for neonatal respiratory distress syndrome. However, recent trends towards increased utilization of noninvasive respiratory support for preterm infants with surfactant deficiency have created a demand for a similarly noninvasive means of administering exogenous surfactant. Past approaches to surfactant nebulization met with varying success due to inefficient aerosol devices resulting in low intrapulmonary delivery doses of surfactant with variable clinical effectiveness. The recent development of vibrating membrane nebulizers, coupled with appropriate positioning of the interface device, indicates that efficient delivery of aerosolized surfactant is now a realistic goal in infants. Evidence of clinical effect despite low total administered dose in pilot studies, together with suggestions of enhanced homogeneity of pulmonary distribution indicate that this therapy may be applied in a cost-effective manner, with minimal patient handling and disruption. These studies need to be subjected to appropriately designed randomized controlled trials. Further work is also required to determine the optimum delivery route (mask, intranasal prong, nasopharyngeal or laryngeal), dosing amount and redosing interval.
滴注肺表面活性物质是治疗新生儿呼吸窘迫综合征的唯一批准的肺表面活性物质治疗方法。然而,最近早产儿肺表面活性物质缺乏时使用非侵入性呼吸支持的趋势有所增加,这就需要一种同样非侵入性的方法来给予外源性肺表面活性物质。过去的肺表面活性物质雾化方法由于气溶胶装置效率低下,导致肺内给予的肺表面活性物质剂量低,临床效果也各不相同,因此取得的成功也各不相同。最近振动膜雾化器的发展,加上接口装置的适当定位,表明在婴儿中高效输送雾化肺表面活性物质现在是一个现实的目标。尽管在试点研究中给予的总剂量较低,但仍有临床效果的证据,加上肺内分布均匀性增强的提示,表明这种治疗方法可以以具有成本效益的方式应用,患者的处理和干扰最小。这些研究需要经过适当设计的随机对照试验。还需要进一步研究确定最佳输送途径(面罩、鼻内叉、鼻咽或喉)、剂量和重复剂量间隔。