Sziegoleit W, Förster W, Maier E, Assmann I, Fiehring H, Schulz H E, Crodel H W, Gutschker A
Z Gesamte Inn Med. 1976 Jul 1;31(13):501-3.
In experiments of treatment carried out on 39 patients with cardiac insufficiency with tachyarrhythmia for the partially synthetic, new heart glycoside 3',4'-dipropionyl helveticosol the following clinico-pharmacological data of efficacy were approximately established on an average: level of full efficacy 2.7 mg, daily coefficient of disappearing 40%, coefficient of enteral absorption 30%, daily maintenance dose intravenously 1.1 mg and orally 3.7 mg.
在对39例伴有快速性心律失常的心功能不全患者进行的治疗实验中,对于部分合成的新型强心苷3',4'-二丙酰羟基毛地黄毒苷,大致平均确定了以下疗效的临床药理学数据:完全疗效水平为2.7毫克,每日消除系数为40%,肠道吸收系数为30%,静脉注射每日维持剂量为1.1毫克,口服为3.7毫克。