Gerris J, Thiery M, Bogaert M, De Schaepdryver A
Eur J Clin Pharmacol. 1980 Nov;18(6):443-8. doi: 10.1007/BF00874653.
The uterine inhibitory effect and potential maternal and fetal side effects of two beta-mimetic compounds, ritodrine hydrochloride and fenoterol hydrobromide, were compared in a randomized trial. The drugs were administered by intravenous infusion to 24 healthy term nulliparous women during effective first-stage labour; each of them received fenoterol (1, 2, or 4 microgram/min) or ritodrine (100, 200, or 400 microgram/min). There was no difference between the drugs in the intensity of the uterine inhibition. However, for a similar inhibitory effect, the duration of tocolysis was longer after ritodrine. During the intrapartum and neonatal periods, neither compound induced any change in the fetal parameters investigated, and their effects on maternal parameters were comparable.
在一项随机试验中,比较了两种β-拟交感神经化合物盐酸利托君和氢溴酸非诺特罗对子宫的抑制作用以及潜在的母婴副作用。在有效的第一产程中,通过静脉输注将药物给予24名健康足月未产妇;她们每人接受非诺特罗(1、2或4微克/分钟)或利托君(100、200或400微克/分钟)。两种药物在子宫抑制强度上没有差异。然而,对于相似的抑制效果,利托君用药后宫缩抑制持续时间更长。在产时和新生儿期,两种化合物均未引起所研究的胎儿参数发生任何变化,并且它们对母体参数的影响相当。