Jones D C, Sanchez-Ramos L
Department of Obstetrics and Gynecology, University of Florida Health Science Center, Jacksonville.
Obstet Gynecol. 1990 Dec;76(6):1093-6.
Women destined to develop preeclampsia show an increased systemic pressor response to infused angiotensin II, and the angiotensin sensitivity test has been accepted as an appropriate means of identifying these women. However, the effect of angiotensin II infusion on uteroplacental blood flow is unknown and may be deleterious. Patients undergoing angiotensin sensitivity tests as part of a protocol examining the effect of aspirin on the incidence of preeclampsia were studied with Doppler velocimetry performed before and during the angiotensin II infusion. Fetal well-being was documented with biophysical profiles performed before and after the infusions. Neither the systolic-diastolic ratios in the uterine and umbilical arteries nor the biophysical profile scores were altered significantly (P = .43, P = .23, Wilcoxon signed-rank median test, and P = .35, Fisher exact test, respectively). These findings suggest that the angiotensin sensitivity test does not increase resistance to flow in the uterine or umbilical circulation, and therefore may be used safely in screening for preeclampsia.
注定会发生先兆子痫的女性对输注血管紧张素II的全身升压反应增强,血管紧张素敏感性试验已被公认为识别这些女性的合适方法。然而,输注血管紧张素II对子宫胎盘血流的影响尚不清楚,且可能有害。对作为研究阿司匹林对先兆子痫发病率影响方案一部分而接受血管紧张素敏感性试验的患者,在输注血管紧张素II之前和期间进行多普勒测速研究。在输注前后进行生物物理评分以记录胎儿健康状况。子宫和脐动脉的收缩期与舒张期比值以及生物物理评分均无显著改变(分别为P = 0.43、P = 0.23,采用Wilcoxon符号秩中位数检验,以及P = 0.35,采用Fisher精确检验)。这些发现表明,血管紧张素敏感性试验不会增加子宫或脐循环中的血流阻力,因此可安全用于先兆子痫的筛查。