Spahn H, Kirch W, Mutschler E, Ohnhaus E E, Kitteringham N R, Lögering H J, Paar D
Br J Clin Pharmacol. 1984;17 Suppl 1(Suppl 1):97S-102S. doi: 10.1111/j.1365-2125.1984.tb02439.x.
Pharmacological interactions in both directions between phenprocoumon and atenolol and metoprolol were investigated using a crossover trial. Co-administration of phenprocoumon did not significantly affect Cmax, tmax, t1/2,22, AUC for atenolol or metoprolol. Co-administration of metoprolol, but not atenolol, increased mean plasma phenprocoumon concentrations 4 and 6 h after dosing and was caused by a decrease in the apparent volume of distribution. This increase in plasma phenprocoumon was not associated with an increase in prothrombin time or in the total area under the concentration-time curve. Although the transient increase of phenprocoumon plasma levels caused by metoprolol may be of little clinical significance after a single dose of phenprocoumon, a more important alteration in phenprocoumon disposition and effect should be considered in individual patients on long-term therapy.
采用交叉试验研究了苯丙香豆素与阿替洛尔和美托洛尔之间双向的药物相互作用。苯丙香豆素与阿替洛尔或美托洛尔合用时,对阿替洛尔或美托洛尔的Cmax、tmax、t1/2、22、AUC均无显著影响。美托洛尔(而非阿替洛尔)与苯丙香豆素合用时,给药后4小时和6小时的苯丙香豆素平均血浆浓度升高,这是由表观分布容积减小所致。血浆苯丙香豆素的这种升高与凝血酶原时间或浓度-时间曲线下总面积的增加无关。尽管单剂量苯丙香豆素后美托洛尔引起的苯丙香豆素血浆水平短暂升高可能临床意义不大,但对于长期治疗的个体患者,应考虑苯丙香豆素处置和效应的更重要改变。