Lisichkov T
Vutr Boles. 1989;28(2):81-4.
The action of platelet aggregation and release reaction on the tendency toward bleeding in patients with hemophilia was studied. Were examined 43 patients with hemophilia A, 14 of them with hemorrhages, 5 patients with hemophilia B, 5 patients with hemophilia A and factor VIII inhibitor and 2 patients with congenital factor VII deficit. Disturbed aggregation with ADP was found in 2 patients and with adrenalin also in 2 patients with hemophilia A without hemorrhages, in 1 patient with hemophilia A with hemorrhages and in 1 patient with hemophilia B. In the remaining patients the examined indices were normal. No data for spontaneous aggregation were found. The results of the study indicate that no connection was established between the tendency toward bleeding in the hemophiliac patients and the platelet aggregation and release reaction. No data for platelet hyperactivation by the hemorrhages were found.
研究了血小板聚集和释放反应对血友病患者出血倾向的作用。检查了43例甲型血友病患者,其中14例有出血症状;5例乙型血友病患者;5例甲型血友病伴Ⅷ因子抑制剂患者;2例先天性Ⅶ因子缺乏患者。在2例无出血症状的甲型血友病患者、1例有出血症状的甲型血友病患者和1例乙型血友病患者中发现ADP诱导的聚集异常,另有2例无出血症状的甲型血友病患者肾上腺素诱导的聚集异常。其余患者的检测指标正常。未发现自发聚集的数据。研究结果表明,血友病患者的出血倾向与血小板聚集和释放反应之间未建立联系。未发现出血导致血小板过度活化的数据。