Hay C R, Doughty H I, Savidge G F
University Department of Haematology, Manchester Royal Infirmary, UK.
Blood Coagul Fibrinolysis. 1996 Mar;7 Suppl 1:S15-9.
In a clinical trial, 24 patients with haemophilia A who needed surgery or had suffered severe bleeding were treated by continuous infusion of Monoclate P, a factor VIII concentrate that is immunopurified by monoclonal antibodies. Continuous infusion of Monoclate P began with a dose of 2 U/kg per h that was adjusted according to the results of factor VIII assays to achieve a factor VIII target level of 100 IU/dl for 2 days and then 80 IU/dl for 5 days. The safety, efficacy, and economics of this approach were assessed. No haemorrhagic episodes were observed. The continuous infusion was convenient and had the advantage of producing steady-state levels of factor VIII. With a single-compartment model, we found median factor VIII clearance values of 3.11 (range 1.79-7.78) x 10(3) litres/kg per h, elimination rates of 5.0-19.4 x 10(-2)/h and a median half-life of 9.9 h (range 4.8-20.0 h). Clearance and the elimination rate appeared to decline over the infusion period, as judged by the decreasing infusion rate required to maintain the target concentration of factor VIII. An economic comparison with bolus therapy, using theoretically derived bolus dosages, indicated that the potential saving was related inversely to the factor VIII half-life. Potential savings of 75% were predicted on the first postoperative day, averaging 35% over the full course of therapy.
在一项临床试验中,24名需要手术或曾发生严重出血的甲型血友病患者接受了Monoclate P持续输注治疗,Monoclate P是一种通过单克隆抗体免疫纯化的凝血因子VIII浓缩物。Monoclate P持续输注开始时的剂量为每小时2 U/kg,根据凝血因子VIII检测结果进行调整,以使凝血因子VIII目标水平在2天内达到100 IU/dl,然后在5天内达到80 IU/dl。对该方法的安全性、有效性和经济性进行了评估。未观察到出血事件。持续输注方便,具有产生稳定状态凝血因子VIII水平的优点。采用单室模型,我们发现凝血因子VIII清除率的中位数为3.11(范围1.79 - 7.78)×10³升/千克每小时,消除率为5.0 - 19.4×10⁻²/小时,半衰期中位数为9.9小时(范围4.8 - 20.0小时)。根据维持凝血因子VIII目标浓度所需输注速率的降低判断,清除率和消除率在输注期间似乎下降。与采用理论推导的推注剂量的推注疗法进行的经济学比较表明,潜在节省与凝血因子VIII半衰期成反比。预计术后第一天可节省75%,整个治疗过程平均节省35%。