Egberts J, de Winter J P, Sedin G, de Kleine M J, Broberger U, van Bel F, Curstedt T, Robertson B
Department of Obstetrics and Gynecology, University of Leiden, The Netherlands.
Pediatrics. 1993 Dec;92(6):768-74.
The aim of this randomized clinical trial was to evaluate the immediate effects of prophylactic administration of Curosurf and to compare outcomes after prophylactic or expectant management.
Porcine surfactant (Curosurf, 200 mg/kg body weight) was administered intratracheally within 10 minutes of birth to preterm neonates with a gestational age of 26 to 29 weeks (n = 75); rescue-eligible neonates (n = 72) were initially subjected to a sham maneuver. The primary end points of the trial, evaluated at the age of 6 hours, were to obtain (1) a 40% decrease in the ratio between transcutaneous oxygen tension (tcPO2) (kPa) and fraction of inspired oxygen (FIO2), and (2) a 50% decrease in the incidence of radiologically verified respiratory distress syndrome (RDS). After 6 to 24 hours, a similar dose of surfactant was given to the neonates of both the prophylaxis and the rescue-eligible group, if they needed mechanical ventilation with an FIO2 > or = 0.6.
At 6 hours the prophylaxis group had, in comparison with the rescue-eligible group, significantly higher tcPO2/FIO2 ratios (mean +/- SD: 39.7 +/- 15.3 vs 28.1 +/- 18.1; P < .001) and less severe RDS by radiological scoring (chi 2 = 14.9; P = .005). Severe RDS was present in 19% of the prophylactically treated neonates versus 32% in the rescue-eligible group (P < .05). The prophylaxis group needed shorter periods of FIO2 > 0.40 than the rescue-eligible neonates (P < .01), and eight neonates of the prophylaxis group (11%) versus 23 of the rescue-eligible group (32%) qualified for rescue treatment with surfactant in the interval 6 to 24 hours (P < .01). There were no differences in the incidence or severity of pneumothorax, pulmonary interstitial emphysema, cerebral hemorrhage, periventricular leukomalacia, patent ductus arteriosus, in the duration of mechanical ventilation or time in supplemental oxygen, or in mortality.
Subgroup analysis revealed (1) that administration of corticosteroids reduced the risk of developing neonatal RDS as effectively as did surfactant prophylaxis at birth, and (2) that prophylaxis was effective especially in neonates with gestational age < 28 weeks or birth weight < 1000 g, in male neonates, and in neonates who had received no antenatal treatment with corticosteroids. Our data indicate that prophylactic treatment with surfactant should be considered in high-risk neonates fulfilling these latter criteria.
本随机临床试验旨在评估预防性给予珂立苏的即刻效果,并比较预防性处理与期待性处理后的结局。
对胎龄26至29周的早产新生儿(n = 75)在出生后10分钟内气管内给予猪肺表面活性物质(珂立苏,200mg/kg体重);符合抢救条件的新生儿(n = 72)最初进行假操作。在6小时龄时评估的试验主要终点为:(1)经皮氧分压(tcPO2)(kPa)与吸入氧分数(FIO2)之比降低40%,(2)经放射学证实的呼吸窘迫综合征(RDS)发生率降低50%。6至24小时后,如果预防性处理组和符合抢救条件组的新生儿需要FIO2≥0.6的机械通气,则给予相似剂量的表面活性物质。
在6小时时,与符合抢救条件组相比,预防性处理组的tcPO2/FIO2比值显著更高(均值±标准差:39.7±15.3 vs 28.1±18.1;P <.001),且放射学评分显示RDS较轻(χ2 = 14.9;P =.005)。预防性处理的新生儿中19%发生严重RDS,符合抢救条件组为32%(P <.05)。预防性处理组需要FIO2>0.40的时间比符合抢救条件的新生儿短(P <.01),预防性处理组有8名新生儿(11%),符合抢救条件组有23名新生儿(32%)在6至24小时期间符合用表面活性物质进行抢救治疗的条件(P <.01)。气胸、肺间质肺气肿、脑出血、脑室周围白质软化、动脉导管未闭的发生率及严重程度、机械通气时间、吸氧时间或死亡率方面无差异。
亚组分析显示:(1)给予皮质类固醇降低新生儿RDS发生风险的效果与出生时表面活性物质预防效果相同;(2)预防尤其在胎龄<28周或出生体重<1000g的新生儿、男婴以及未接受产前皮质类固醇治疗的新生儿中有效。我们的数据表明,对于符合后述标准的高危新生儿应考虑进行表面活性物质预防性治疗。