Bech R M
Novo Nordisk, Gentofte, Denmark.
Haemostasis. 1996;26 Suppl 1:135-8. doi: 10.1159/000217255.
Recombinant factor VIIa (rFVIIa) improves haemostasis and eliminates the risk of transmission of blood-borne infection in haemophilia patients with inhibitors, acquired inhibitors to factor VIII or IX or FVII deficiency. rFVIIa has been available on a compassionate use basis since 1988 and has been administered to 111 patients for a total of 494 joint and muscle bleeding episodes. Seventy-nine percent of joint and 65% of muscle bleeding episodes were evaluated by the investigator as having an excellent/effective response. rFVIIa is also an effective treatment for joint and muscle bleeding episodes in patients undergoing immune tolerance regimens and does not affect the inhibitor titre level.
重组凝血因子VIIa(rFVIIa)可改善止血功能,并消除患有抑制剂、获得性VIII或IX因子抑制剂或FVII缺乏症的血友病患者血源性感染传播的风险。自1988年以来,rFVIIa一直在同情用药的基础上提供,已用于111名患者,共发生494次关节和肌肉出血事件。研究人员评估,79%的关节出血事件和65%的肌肉出血事件反应极佳/有效。rFVIIa也是接受免疫耐受方案患者关节和肌肉出血事件的有效治疗方法,且不影响抑制剂滴度水平。