Shankaran S, Papile L A, Wright L L, Ehrenkranz R A, Mele L, Lemons J A, Korones S B, Stevenson D K, Donovan E F, Stoll B J, Fanaroff A A, Oh W
Wayne State University, Detroit, MI, USA.
N Engl J Med. 1997 Aug 14;337(7):466-71. doi: 10.1056/NEJM199708143370705.
The administration of phenobarbital to pregnant women before delivery has been thought to decrease the frequency of intracranial hemorrhage in preterm infants. To evaluate this potential neuroprotective therapy further, we determined the effect of antenatal administration of phenobarbital on the frequency of neonatal intracranial hemorrhage and early death.
We studied 610 women who were 24 to 33 weeks pregnant and who were expected to deliver their infants within 24 hours. The women were randomly assigned to receive either phenobarbital (10 mg per kilogram of body weight) or placebo intravenously, followed by maintenance doses until delivery or 34 weeks of gestation. The infants born to these women underwent cranial ultrasonography to detect the presence of intracranial hemorrhage.
There were 309 women in the phenobarbital group and 301 in the placebo group. A total of 247 women (80 percent) in the phenobarbital group and 235 (78 percent) in the placebo group delivered within 24 hours after infusion of the study drug or administration of the last maintenance dose. Intracranial hemorrhage or early death occurred in 83 of the 344 infants born to the women in the phenobarbital group (24 percent) and in 74 of the 324 born to the women in the placebo group (23 percent; risk ratio for the infants in the phenobarbital group, 1.1; 95 percent confidence interval, 0.8 to 1.4). Among infants born before 34 weeks' gestation in whom ultrasonographic studies were performed, intracranial hemorrhage was diagnosed in 70 of 311 infants in the phenobarbital group (23 percent) and 64 of 279 in the placebo group (23 percent; risk ratio, 1.0; 95 percent confidence interval, 0.8 to 1.4).
Antenatal administration of phenobarbital does not decrease the risk of intracranial hemorrhage or early death in preterm infants.
过去认为,在分娩前给孕妇使用苯巴比妥可降低早产儿颅内出血的发生率。为了进一步评估这种潜在的神经保护疗法,我们确定了产前使用苯巴比妥对新生儿颅内出血发生率和早期死亡的影响。
我们研究了610名怀孕24至33周且预计在24小时内分娩的妇女。这些妇女被随机分配静脉注射苯巴比妥(每公斤体重10毫克)或安慰剂,随后给予维持剂量直至分娩或妊娠34周。这些妇女所生的婴儿接受了头颅超声检查以检测颅内出血情况。
苯巴比妥组有309名妇女,安慰剂组有301名妇女。苯巴比妥组共有247名妇女(80%)和安慰剂组235名妇女(78%)在输注研究药物或给予最后一次维持剂量后24小时内分娩。苯巴比妥组妇女所生的344名婴儿中有83名(24%)发生颅内出血或早期死亡,安慰剂组妇女所生的324名婴儿中有74名(23%)发生颅内出血或早期死亡(苯巴比妥组婴儿的风险比为1.1;95%置信区间为0.8至1.4)。在妊娠34周前出生且进行了超声检查的婴儿中,苯巴比妥组311名婴儿中有70名(23%)被诊断为颅内出血,安慰剂组279名婴儿中有64名(23%)被诊断为颅内出血(风险比为1.0;95%置信区间为0.8至1.4)。
产前使用苯巴比妥并不能降低早产儿颅内出血或早期死亡的风险。