Surfactant therapy for respiratory distress syndrome in premature neonates: a comparative review.

Sean B Ainsworth, David W A Milligan
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引用次数: 35

Abstract

Exogenous surfactant therapy has been part of the routine care of preterm neonates with respiratory distress syndrome (RDS) since the beginning of the 1990s. Discoveries that led to its development as a therapeutic agent span the whole of the 20th century but it was not until 1980 that the first successful use of exogenous surfactant therapy in a human population was reported. Since then, randomized controlled studies demonstrated that surfactant therapy was not only well tolerated but that it significantly reduced both neonatal mortality and pulmonary air leaks; importantly, those surviving neonates were not at greater risk of subsequent neurological impairment. Surfactants may be of animal or synthetic origin. Both types of surfactants have been extensively studied in animal models and in clinical trials to determine the optimum timing, dose size and frequency, route and method of administration. The advantages of one type of surfactant over another are discussed in relation to biophysical properties, animal studies and results of randomized trials in neonatal populations. Animal-derived exogenous surfactants are the treatment of choice at the present time with relatively few adverse effects related largely to changes in oxygenation and heart rate during surfactant administration. The optimum dose of surfactant is usually 100 mg/kg. The use of surfactant with high frequency oscillation and continuous positive pressure modes of respiratory support presents different problems compared with its use with conventional ventilation. The different components of surfactant have important functions that influence its effectiveness both in the primary function of the reduction of surface tension and also in secondary, but nonetheless just as important, role of lung defense. With greater understanding of the individual surfactant components, particularly the surfactant-associated proteins, development of newer synthetic surfactants has been made possible. Despite being an effective therapy for RDS, surfactant has failed to have a significant impact on the incidence of chronic lung disease in survivors. Paradoxically the cost of care has increased as surviving neonates are more immature and consume a greater proportion of neonatal intensive care resources. Despite this, surfactant is considered a cost-effective therapy for RDS compared with other therapeutic interventions in premature infants.

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表面活性剂治疗早产儿呼吸窘迫综合征的比较综述。
自20世纪90年代初以来,外源性表面活性剂治疗已成为早产儿呼吸窘迫综合征(RDS)常规护理的一部分。导致其发展成为一种治疗剂的发现跨越了整个20世纪,但直到1980年才首次成功地在人群中使用外源性表面活性剂治疗。从那时起,随机对照研究表明,表面活性剂治疗不仅耐受性良好,而且显著降低新生儿死亡率和肺漏气;重要的是,那些存活下来的新生儿随后出现神经损伤的风险并不大。表面活性剂可能来源于动物或人工合成。这两种类型的表面活性剂已在动物模型和临床试验中进行了广泛的研究,以确定最佳的时间、剂量大小和频率、给药途径和方法。本文讨论了一种表面活性剂相对于另一种表面活性剂的生物物理特性、动物研究和新生儿随机试验的结果。动物源性外源性表面活性剂是目前的首选治疗方法,其副作用相对较少,主要与表面活性剂给药期间氧合和心率的变化有关。表面活性剂的最佳用量通常为100mg /kg。使用具有高频振荡和连续正压模式的表面活性剂进行呼吸支持与使用常规通气相比存在不同的问题。表面活性剂的不同成分具有重要的功能,影响其降低表面张力的主要功能和肺部防御的次要功能,但同样重要。随着对各个表面活性剂组分,特别是与表面活性剂相关的蛋白质的进一步了解,开发新的合成表面活性剂成为可能。尽管表面活性剂是一种有效的治疗RDS的方法,但它未能对幸存者慢性肺病的发病率产生显著影响。矛盾的是,随着存活下来的新生儿更加不成熟,并且消耗了新生儿重症监护资源的更大比例,护理成本也增加了。尽管如此,与其他早产儿治疗干预措施相比,表面活性剂被认为是一种具有成本效益的治疗RDS的方法。
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