Long W, Corbet A, Cotton R, Courtney S, McGuiness G, Walter D, Watts J, Smyth J, Bard H, Chernick V
Clinical Research Division, Wellcome Research Laboratories, Research Triangle Park, NC 27709.
N Engl J Med. 1991 Dec 12;325(24):1696-703. doi: 10.1056/NEJM199112123252404.
Surfactant-replacement therapy is now recognized as a life-saving and safe intervention in small premature infants, but there is little evidence concerning its risks and benefits in larger premature infants.
We conducted a placebo-controlled, blinded trial in 1237 infants with respiratory distress who were enrolled at 23 hospitals in the United States and 13 hospitals in Canada. At entry all the infants weighed at least 1250 g, were receiving mechanical ventilation, and had a ratio of arterial to alveolar oxygen tension below 0.22. The initial dose of either the synthetic surfactant (Exosurf, 5 ml per kilogram of body weight) or air (the placebo) was administered less than 24 hours after birth, with a second dose given 12 hours later. A total of 614 infants were assigned to receive surfactant, and 623 to receive placebo.
Fewer infants in the surfactant group than in the placebo group died before 28 days of age or survived at 28 days with bronchopulmonary dysplasia (7 percent vs. 12 percent, P = 0.002). In the first 28 days of life, there were fewer deaths due to respiratory distress syndrome in the surfactant group (1 percent vs. 3 percent, P = 0.043), lower overall neonatal mortality (4 percent vs. 7 percent, P = 0.04), and a lower incidence of bronchopulmonary dysplasia (3 percent vs. 6 percent, P = 0.008). There was also a significantly lower incidence of pulmonary air leaks, intraventricular hemorrhage, patent ductus arteriosus, seizures, hypotension, and pulmonary hypertension in the surfactant group. The infants treated with surfactant were weaned from oxygen and mechanical ventilation significantly sooner than those given placebo, and they less often required high-frequency ventilation or extracorporeal membrane oxygenation. The primary side effect observed more frequently among the infants who received surfactant treatment was pulmonary hemorrhage (six infants vs. one infant, P = 0.055).
In infants weighing at least 1250 g at birth who have respiratory distress syndrome, treatment with two doses of synthetic surfactant improves survival and reduces perinatal morbidity.
表面活性剂替代疗法目前被认为是挽救小早产儿生命且安全的干预措施,但关于其在较大早产儿中的风险和益处的证据很少。
我们在美国的23家医院和加拿大的13家医院对1237例患有呼吸窘迫的婴儿进行了一项安慰剂对照、双盲试验。入组时所有婴儿体重至少1250克,正在接受机械通气,且动脉血氧分压与肺泡血氧分压之比低于0.22。合成表面活性剂(固尔苏,每千克体重5毫升)或空气(安慰剂)的初始剂量在出生后24小时内给予,12小时后给予第二剂。总共614例婴儿被分配接受表面活性剂治疗,623例接受安慰剂治疗。
表面活性剂组在28日龄前死亡或28日龄时存活但患有支气管肺发育不良的婴儿少于安慰剂组(7%对12%,P = 0.002)。在出生后的前28天,表面活性剂组因呼吸窘迫综合征导致的死亡较少(1%对3%,P = 0.043),总体新生儿死亡率较低(4%对7%,P = 0.04),支气管肺发育不良的发生率较低(3%对6%,P = 0.008)。表面活性剂组肺空气泄漏、脑室内出血、动脉导管未闭、惊厥、低血压和肺动脉高压的发生率也显著较低。接受表面活性剂治疗的婴儿比接受安慰剂的婴儿更快地撤掉氧气和机械通气,且他们较少需要高频通气或体外膜肺氧合。在接受表面活性剂治疗的婴儿中更频繁观察到的主要副作用是肺出血(6例婴儿对1例婴儿,P = 0.055)。
对于出生时体重至少1250克且患有呼吸窘迫综合征的婴儿,两剂合成表面活性剂治疗可提高生存率并降低围产期发病率。