N Engl J Med. 1992 Jul 30;327(5):308-12. doi: 10.1056/NEJM199207303270503.
Beta-adrenergic agonists are commonly used to arrest premature labor. Although treatment of preterm labor with these agents can delay delivery by 24 to 48 hours, the potential risks and benefits to the mother and infant before and after delivery have not been adequately assessed.
We randomly assigned 708 women with preterm labor at six hospitals to receive an intravenous infusion of either the beta-adrenergic agonist ritodrine (n = 352) or placebo (n = 356). Assignment was made with stratification according to four categories of gestational age (20 to 23 weeks, 24 to 27 weeks, 28 to 31 weeks, and 32 to 35 weeks). The primary objective was to assess the effect of ritodrine on perinatal mortality. Secondary objectives were the evaluation of the causes of perinatal death, the extent to which delivery was delayed with ritodrine, and the effects on birth weight, maternal morbidity, neonatal morbidity, and infant morbidity at 18 months of postnatal age, corrected for preterm delivery.
Among the 771 infants born to the women in the study (including 63 pairs of twins), there were 23 deaths (6.1 percent) in the ritodrine group and 25 deaths (6.4 percent) in the placebo group (event-rate difference, -0.3 percent; 95 percent confidence interval, -3.7 percent to 3.1 percent). There was no difference between the groups in the extent of delay of delivery, the incidence of delivery before 37 weeks' gestation, the proportion of babies weighing less than 2500 g, or measures of neonatal morbidity. Maternal morbidity (such as chest pain and cardiac arrhythmias) occurred more frequently but not exclusively in the ritodrine group. One infant born to a woman in the ritodrine group and five infants born to women in the placebo group had cerebral palsy (P = 0.09). There was a slight but not significant trend toward an improved score on the Bayley Psychomotor Development Index at 18 months of age among the infants of the ritodrine-treated women.
We found that the use of ritodrine in the treatment of preterm labor had no significant beneficial effect on perinatal mortality, the frequency of prolongation of pregnancy to term, or birth weight.
β-肾上腺素能激动剂常用于抑制早产。尽管使用这些药物治疗早产可使分娩延迟24至48小时,但尚未充分评估其对母婴在分娩前后的潜在风险和益处。
我们将六家医院的708例早产妇女随机分为两组,分别接受静脉输注β-肾上腺素能激动剂利托君(n = 352)或安慰剂(n = 356)。根据四个孕周类别(20至23周、24至27周、28至31周和32至35周)进行分层随机分组。主要目的是评估利托君对围产期死亡率的影响。次要目的包括评估围产期死亡原因、利托君延迟分娩的程度,以及对出生体重、母亲发病率、新生儿发病率和18个月龄(校正早产因素)婴儿发病率的影响。
研究中的妇女共分娩771例婴儿(包括63对双胞胎),利托君组有23例死亡(6.1%),安慰剂组有25例死亡(6.4%)(事件发生率差异为-0.3%;95%置信区间为-3.7%至3.1%)。两组在分娩延迟程度、孕37周前分娩发生率、体重小于2500 g的婴儿比例或新生儿发病率指标方面无差异。母亲发病率(如胸痛和心律失常)在利托君组更常见,但并非仅见于该组。利托君组一名妇女所生婴儿和安慰剂组五名妇女所生婴儿患有脑瘫(P = 0.09)。接受利托君治疗的妇女所生婴儿在18个月龄时,贝利心理运动发育指数得分有轻微但不显著的改善趋势。
我们发现,使用利托君治疗早产对围产期死亡率、延长孕周至足月的频率或出生体重均无显著有益影响。