Yardumian D A, Mackie I J, Bull H, Goldstone A H, Machin S J
Br J Haematol. 1985 May;60(1):109-16. doi: 10.1111/j.1365-2141.1985.tb07391.x.
We describe two patients suffering from vascular problems refractory to conventional treatment, who received prolonged continuous infusion of ZK 36374, a stable prostacyclin analogue. During the infusion, the patients' platelets became progressively refractory to the in vitro inhibitory action of exogenous ZK 36374. During the early stages of the infusions, platelet aggregability studied ex vivo was inhibited, but this effect too diminished progressively as the infusions continued. The platelets of one patient become spontaneously aggregable and hyperaggregable to standard agonists during the last 2 d of his 9 d infusion. This effect was not seen during an initial 10 d infusion in our second patient, who was concurrently receiving indomethacin, a reversible cyclo-oxygenase inhibitor. However, such hyperaggregability became evident in the platelets of this patient during a second, shorter continuous infusion after cessation of the indomethacin. The hyperaggregability was accompanied in each case by a significant rise in serum thromboxane B2 levels.
我们描述了两名患有常规治疗难以治愈的血管问题的患者,他们接受了稳定的前列环素类似物ZK 36374的长时间持续输注。在输注过程中,患者的血小板对外源性ZK 36374的体外抑制作用逐渐产生耐药性。在输注早期,体外研究的血小板聚集性受到抑制,但随着输注持续,这种作用也逐渐减弱。一名患者在9天输注的最后2天,其血小板对标准激动剂出现自发聚集和高聚集性。在我们的第二名患者最初10天的输注过程中未观察到这种效应,该患者同时接受了可逆的环氧化酶抑制剂吲哚美辛。然而,在停用吲哚美辛后的第二次较短时间的连续输注期间,该患者的血小板出现了明显的高聚集性。在每种情况下,高聚集性都伴随着血清血栓素B2水平的显著升高。