Dodd N J, Gordge M P, Weston M J
Br J Clin Pharmacol. 1983;15 Suppl 1(Suppl 1):67S-70S. doi: 10.1111/j.1365-2125.1983.tb02110.x.
1 We have assessed the thromboxane synthetase inhibitor, dazoxiben (UK 37248), during dialysis in a double-blind, placebo-controlled crossover study. 2 Thromboxane generation was markedly inhibited, and there was an increase in serum 6-keto prostaglandin F1 alpha levels during active treatment studies. 3 We were unable to demonstrate any reduction of platelet activation, or dialyser fibrin deposition, nor were heparin requirements altered by the drug. 4 Dazoxiben had no adverse effects.
我们在一项双盲、安慰剂对照的交叉研究中评估了血栓素合成酶抑制剂达唑氧苯(UK 37248)在透析过程中的作用。
在积极治疗研究期间,血栓素的生成受到显著抑制,血清6-酮前列腺素F1α水平有所升高。
我们未能证明血小板活化或透析器纤维蛋白沉积有任何减少,该药物也未改变肝素的用量。
达唑氧苯没有不良反应。