Garewal H S, Corrigan J J, Durie B G, Jeter M A, Damiano M L
JAMA. 1985 Feb 22;253(8):1154-6.
Danazol was given orally at a dose of 600 mg/day to six hemophiliacs for eight to 14 weeks. All patients showed a significant decrease in activated partial thromboplastin time (APTT) beginning with the first measurement (two weeks) and persisting until use of the drug was discontinued. However, a corresponding increase in the deficient factor activity could not be consistently demonstrated. Despite the shortened APTT, bleeding episodes continued in the severe hemophiliacs and the patient with Christmas disease. In four patients, bleeding appeared to increase in severity or change in pattern, and in two cases the bleeding manifestations did not respond to usual factor infusions but responded to discontinuation of the drug therapy and further factor replacement. Euglobulin lysis times were measured in five patients (one hemophiliac and four with nonhemophilic conditions) who were receiving danazol. The lysis times were markedly shortened. Increased fibrinolytic activity may be responsible for the increased bleeding manifestations in danazol-treated hemophiliacs.
给6名血友病患者口服达那唑,剂量为600毫克/天,持续8至14周。所有患者从首次测量(两周)开始活化部分凝血活酶时间(APTT)就显著降低,并一直持续到停药。然而,未能始终如一地证明缺乏因子活性相应增加。尽管APTT缩短,但重度血友病患者和患克里斯马斯病的患者仍有出血发作。在4名患者中,出血似乎在严重程度上增加或模式发生改变,在2例中,出血表现对常规因子输注无反应,但对停止药物治疗和进一步的因子替代有反应。对5名接受达那唑治疗的患者(1名血友病患者和4名非血友病患者)测量了优球蛋白溶解时间。溶解时间明显缩短。纤维蛋白溶解活性增加可能是达那唑治疗的血友病患者出血表现增加的原因。