Beck O A, Abdulla S, Hochrein H
MMW Munch Med Wochenschr. 1975 Aug 29;117(35):1369-72.
After oral administration, and depending on dosage, propaphenone produces a uniform delay of the excitation conduction in the region of the atrium, ventricle and atrioventricular conduction. At a dosage of 5 or 10 mg/kg body-weight (1 or 2x 300 mg capsules) propaphenone causes an average delay of excitation conduction of + 11% or + 19% of the initial value, and of + 39% (capsule) or + 30% (sugar coated tablet) at 14 mg/kg body-weight. The maximum effect is attained 2.5 to 4 hours after administration. A prolongation of conduction times and consequently of the anti-arrhythmic efficacy, is still found eight hours after oral ingestion.
口服后,根据剂量不同,普罗帕酮会使心房、心室及房室传导区域的兴奋传导均匀延迟。当体重剂量为5或10mg/kg(1或2粒300mg胶囊)时,普罗帕酮会使兴奋传导平均延迟至初始值的+11%或+19%,而当体重剂量为14mg/kg时,延迟至+39%(胶囊)或+30%(糖衣片)。给药后2.5至4小时达到最大效果。口服八小时后仍可发现传导时间延长,从而抗心律失常疗效也得以延长。