首页> 美国卫生研究院文献>Journal of the National Medical Association >Modified bovine surfactant (Survanta) versus a protein-free surfactant (Exosurf) in the treatment of respiratory distress syndrome in preterm infants: a pilot study.
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Modified bovine surfactant (Survanta) versus a protein-free surfactant (Exosurf) in the treatment of respiratory distress syndrome in preterm infants: a pilot study.

机译:改良牛表面活性剂(Survanta)与无蛋白表面活性剂(Exosurf)在早产儿呼吸窘迫综合征的治疗中的初步研究。

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摘要

We undertook a prospective, randomized, non-blinded pilot study to determine whether infants with respiratory distress syndrome (RDS) who were treated with protein-containing bovine surfactant (Survanta, Ross/Abbott Laboratories, Columbus, Ohio) had earlier and larger responses in gas exchange when compared with similar infants treated with a synthetic surfactant (Exosurf, Burroughs Wellcome, Research Triangle Park, North Carolina). Forty-one infants weighing between 600 g and 1750 g at birth with RDS of sufficient severity to require assisted ventilation with an FiO2 > 0.39 were enrolled in the study and treated with surfactant from 1 to 8 hours after birth. Infants were randomly selected to receive treatment with either Exosurf or Survanta. Despite randomization, the Survanta group was overrepresented with factors associated with greater severity of RDS (lower birthweight, more males, and fewer African Americans). No statistically significant difference was found in the primary outcome measure (arterial/alveolar PaO2 > 0.3 at 24 hours) by univariate or multivariate analysis. The percentage of responders in the Survanta-treated group was significantly increased 24 hours after treatment in two of four secondary measures of oxygenation when analyzed by univariate tests using one-tailed P values. Based on these results, we anticipate that acute outcomes after Survanta or Exosurf will approximate those found in this trial and that differences in measures of oxygenation between treatment groups will approximate 30% to 50% 24 hours after initial treatment.
机译:我们进行了一项前瞻性,随机,无盲的前瞻性研究,以确定接受含蛋白质的牛表面活性剂(Survanta,Ross / Abbott Laboratories,俄亥俄州哥伦布)治疗的患有呼吸窘迫综合征(RDS)的婴儿在早期是否有较大的反应。与使用合成表面活性剂治疗的类似婴儿(Exosurf,Burroughs Wellcome,北卡罗来纳州三角研究园)进行气体交换时。研究入选了四十一名婴儿,其出生时体重在600克至1750克之间,其RDS的严重性足以要求FiO2> 0.39的辅助通气,并在出生后1至8小时内用表面活性剂进行治疗。随机选择婴儿接受Exosurf或Survanta的治疗。尽管有随机分组,但Survanta组中与RDS严重程度较高(出生体重较低,男性较多,非裔美国人较少)相关的因素过多。通过单变量或多变量分析,在主要结局指标(24小时的动脉/肺泡PaO2> 0.3)中未发现统计学上的显着差异。当通过单尾检验使用单尾检验P值进行单变量检验时,在接受苏万达治疗的组中,在治疗后24小时内,有四个次要的氧合作用措施中有两个是显着增加了应答者的百分比。根据这些结果,我们预计Survanta或Exosurf术后的急性预后将接近该试验中发现的预后,并且初始治疗后24小时,治疗组之间的充氧量差异将约为30%至50%。

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