Hoekstra R E, Jackson J C, Myers T F, Frantz I D, Stern M E, Powers W F, Maurer M, Raye J R, Carrier S T, Gunkel J H
Minneapolis Childrens Medical Center, Seattle, Washington.
Pediatrics. 1991 Jul;88(1):10-8.
To determine whether multiple doses of bovine surfactant would improve neonatal mortality in very premature neonates, we conducted two multicenter controlled trials under identical protocols; the results were combined for analysis. Four hundred and thirty neonates born between 23 and 29 weeks gestation and weighing 600 to 1250 g at birth were assigned randomly at birth to receive either 100 mg of phospholipids/kg of Survanta, a modified bovine surfactant (n = 210), or a sham air placebo (n = 220) within 15 minutes of birth. Neonates who developed respiratory distress syndrome and required mechanical ventilation with at least 30% oxygen could be given up to three more doses in the first 48 hours after birth. Dosing was performed by investigators not involved in the clinical care of the neonates; nursery staff were kept blinded as to the treatment assignment. Cause of death was determined by a panel of three independent, board-certified neonatologists after blindly reviewing case report forms and autopsy reports. Fewer Survanta-treated neonates died of any cause (11.4% vs 18.8%, P = .031), died of respiratory distress syndrome (1.9% vs 15.6%, P less than .001), and either died or developed bronchopulmonary dysplasia due to respiratory distress syndrome (39.5% vs 49.1%, P = .044). The incidence of respiratory distress syndrome was also lower in Survanta-treated neonates (28.0% vs 56.9%, P less than .001), and the Survanta-treated neonates' oxygenation and ventilatory status were improved significantly at 72 hours. Survanta-treated neonates were also at lowered risk of developing pulmonary interstitial emphysema (23.3% vs 36.9%, P = .002) and other forms of pulmonary air leaks (9.6% vs 20.8%, P .002).(ABSTRACT TRUNCATED AT 250 WORDS)
为了确定多次剂量的牛肺表面活性物质是否会改善极早产儿的新生儿死亡率,我们按照相同方案进行了两项多中心对照试验;将结果合并进行分析。430例孕23至29周出生、出生体重600至1250克的新生儿在出生时被随机分配,在出生后15分钟内接受100毫克磷脂/千克的固尔苏(一种改良的牛肺表面活性物质,n = 210)或假空气安慰剂(n = 220)。发生呼吸窘迫综合征且需要机械通气且至少使用30%氧气的新生儿,在出生后的头48小时内可再给予多达三剂。给药由不参与新生儿临床护理的研究人员进行;新生儿护理人员对治疗分配情况不知情。死因由三名独立的、具有委员会认证的新生儿科医生组成的小组在盲审病例报告表和尸检报告后确定。接受固尔苏治疗的新生儿因任何原因死亡的较少(11.4%对18.8%,P = 0.031),死于呼吸窘迫综合征的较少(1.9%对15.6%,P小于0.001),因呼吸窘迫综合征死亡或发生支气管肺发育不良的较少(39.5%对49.1%,P = 0.044)。接受固尔苏治疗的新生儿呼吸窘迫综合征的发生率也较低(28.0%对56.9%,P小于0.001),且在72小时时接受固尔苏治疗的新生儿的氧合和通气状态有显著改善。接受固尔苏治疗的新生儿发生肺间质肺气肿的风险也较低(23.3%对36.9%,P = 0.002)以及其他形式的肺漏气的风险较低(9.6%对20.8%,P = 0.002)。(摘要截短于250字)