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[用己丙肾上腺素和羟苄羟麻黄碱进行保胎治疗时的血流动力学变化]

[Hemodynamic changes during tocolysis with hexoprenaline and fenoterol].

作者信息

Heilmann L, Siekmann U, Ludwig H

出版信息

Z Geburtshilfe Perinatol. 1983 Jan-Feb;187(1):11-6.

PMID:6682592
Abstract

The authors examined two groups of 50 patients each who had been given an average dose of 0.24 microgram/min Hexoprenaline or respectively 1.8 micrograms/min Fenoterol as beta-mimetics for premature labor. The patients who received Fenoterol were also given Verapamil as additional medication in a ratio of 1 : 40. In addition to blood pressure, heart rate, urine elimination and serum or urine osmolarity, the hemodynamic parameters stroke volume, cardiac output and total peripheral resistance were investigated. Stroke volume was measured by means of impedance cardiography. Giving equipotent doses, Hexoprenaline/Fenoterol dose ratio of 1 : 8, there was a slower and smaller increase in heart rate over 24 hours with Hexoprenaline, with identical suppression of uterine contractility (external tocography). This was also reflected in the cardiac output, while there were no differences in the stroke volumes. Inhibition of diuresis was lower with Hexoprenaline. This might be due to the fact that since there is no organ specificity for beta-1 or respectively beta-2 receptors and the patterns of distribution differ, Hexoprenaline has a somewhat less pronounced action on beta-1 receptors than Fenoterol, though the same beta-2 action.

摘要

作者对两组各50名患者进行了研究,这些患者均接受了平均剂量为0.24微克/分钟的海索那林或分别为1.8微克/分钟的非诺特罗作为早产的β-拟交感神经药。接受非诺特罗的患者还按1:40的比例加用了维拉帕米。除了血压、心率、尿量及血清或尿液渗透压外,还研究了血流动力学参数每搏输出量、心输出量和总外周阻力。每搏输出量通过阻抗心动图测量。给予等效剂量,海索那林/非诺特罗剂量比为1:8时,海索那林在24小时内心率升高较慢且幅度较小,但子宫收缩抑制作用(外部宫缩图)相同。这也反映在心输出量上,而每搏输出量没有差异。海索那林对利尿的抑制作用较低。这可能是由于β-1或分别β-2受体没有器官特异性且分布模式不同,海索那林对β-1受体的作用比非诺特罗稍弱,但其β-2作用相同。

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