Spellacy W N, Cruz A C, Buhi W C, Birk S A
Am J Obstet Gynecol. 1978 Jul 15;131(6):637-42. doi: 10.1016/0002-9378(78)90823-2.
Twenty-nine women in premature labor were randomly assigned to a ritodrine (N = 14) or placebo (N = 15) treatment group. Thirteen serial blood samples were drawn during the first 12 hours of therapy by intravenous drug infusion and they were analyzed for a variety of metabolic substances. There was a significant increase in the blood glucose level in the ritodrine group after one hour and this persisted for the 12 hours of intravenous drug treatment. Plasma insulin levels similarly did not increase in the placebo but significantly rose in the ritodrine group by 30 minutes, peaked at 2 1/2 hours, and remained elevated throughout the infusion. There were no significant differences between levels of plasma glucagon, cholesterol triglyceride, human placental lactogen, or human chorionic gonadotropin in the two treatment groups. Ritodrine caused significant maternal and fetal tachycardia. Its use in women with carbohydrate abnormalities should be monitored carefully. The increased glucose levels may lead to an increased fetal weight.
29名早产女性被随机分配到利托君治疗组(N = 14)或安慰剂组(N = 15)。在治疗的前12小时内,通过静脉输注药物抽取了13份系列血样,并对各种代谢物质进行了分析。利托君组在1小时后血糖水平显著升高,并在静脉药物治疗的12小时内持续升高。安慰剂组血浆胰岛素水平同样没有升高,但利托君组在30分钟时显著升高,在2.5小时达到峰值,并在整个输注过程中保持升高。两个治疗组之间血浆胰高血糖素、胆固醇甘油三酯、人胎盘催乳素或人绒毛膜促性腺激素水平没有显著差异。利托君导致母体和胎儿显著心动过速。在碳水化合物异常的女性中使用时应仔细监测。血糖水平升高可能导致胎儿体重增加。