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Lucinactant (Surfaxin~(TM)) for prevention and treatment of respiratory distress syndrome in newborns

机译:用于预防和治疗新生儿呼吸窘迫综合症的Lucinactant(Surfaxin〜(TM))

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Respiratory distress syndrome, resulting from the deficiency of endogenous surfactant, remains a leading cause of mortality and morbidity in preterm infants. Exogenous surfactant replacement therapy is one of the most widely researched areas in neonatal medicine and is now accepted as the standard of care for preventing and treating respiratory distress syndrome in these newborns. Exogenous surfactant replacement therapy has evolved in the past three decades, but controversies still exist as to the choice of preparation (i.e., is one better than the others?), dosing and volume of individual preparations, and cost. At present, animal-derived surfactants that contain proteins appear to be the choice of most clinicians; however, they may have the limitation of being derived from animal sources. This has prompted the development of newer synthetic surfactants such as lucinactant (Surfaxin?, Discovery Laboratories, PA, USA), which contains the protein B mimic synthetic peptide, sinapultide. Although it is not yet commercially available or approved for clinical use by regulatory authorities, recent Phase III clinical trials with lucinactant demonstrated promising results with similar efficacy to animal-derived surfactants whilst avoiding the disadvantage associated with animal products. The availability of such a surfactant in large amounts at a relatively lower production cost should also prompt further investigations regarding expanded use of surfactants in conditions other than neonatal respiratory distress syndrome, such as meconium aspiration syndromes and pneumonia, and as a vehicle for administering drugs directly to the lungs. There are also some developments towards making aerosolized forms of surfactant, which could be administered noninvasively, thus obviating the need for endotracheal intubation and its associated complications. The purpose of this article is to provide an appraisal of the recent advances in surfactant replacement therapy and its future developments.
机译:由内源性表面活性剂缺乏引起的呼吸窘迫综合征仍然是早产儿死亡和发病的主要原因。外源性表面活性剂替代疗法是新生儿医学中研究最广泛的领域之一,现已被接受为预防和治疗这些新生儿呼吸窘迫综合征的护理标准。在过去的三十年中,外源性表面活性剂替代疗法得到了发展,但是关于制剂的选择(即,一种制剂比其他制剂更好?),单个制剂的剂量和量以及成本方面仍存在争议。目前,包含蛋白质的动物源性表面活性剂似乎是大多数临床医生的选择。但是,它们可能有动物来源的限制。这促使开发了新的合成表面活性剂,例如光亮剂(Surfaxin?,Discovery Laboratories,PA,美国),其中包含蛋白质B模拟合成肽西那普利。尽管尚未上市或获得监管机构批准用于临床,但最近使用光敏剂进行的III期临床试验证明了令人鼓舞的结果,其功效与动物源性表面活性剂相似,同时避免了与动物产品相关的缺点。以相对较低的生产成本大量获得这种表面活性剂还应该促使人们进一步开展研究,以在除新生儿呼吸窘迫综合征(例如胎粪吸入综合征和肺炎)以外的其他条件下,以及作为直接给药的媒介物,扩大使用表面活性剂。到肺部。制备雾化形式的表面活性剂也有一些进展,可以无创地给药,从而消除了对气管插管及其相关并发症的需要。本文的目的是对表面活性剂替代疗法的最新进展及其未来发展进行评估。

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