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首页> 外文期刊>Haemophilia: the official journal of the World Federation of Hemophilia >Presurgical pharmacokinetic analysis of a von Willebrand factor/factor VIII (VWF/FVIII) concentrate in patients with von Willebrand's disease (VWD) has limited value in dosing for surgery.
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Presurgical pharmacokinetic analysis of a von Willebrand factor/factor VIII (VWF/FVIII) concentrate in patients with von Willebrand's disease (VWD) has limited value in dosing for surgery.

机译:von Willebrand病(VWD)患者中浓缩的von Willebrand因子/ VIII因子(VWF / FVIII)的术前药代动力学分析在手术用药中价值有限。

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Optimal doses of von Willebrand Factor/Factor VIII (VWF/FVIII) concentrates for surgical procedures in patients with VWD need to be determined. A prospective, multicenter study was performed that included an initial pharmacokinetic (PK) assessment following a standard dose of VWF/FVIII concentrate (Humate-P(R)) to determine individual PK parameters and guide therapeutic dosing during surgery. Forty one subjects received 60 IU kg(1) VWF: RCo. Median plasma levels, half-life, mean change from baseline and in vivo recovery (IVR) values were determined for VWF:RCo, VWF:Ag, and FVIII: C, and area under the plasma time-concentration curve (AUC), mean residence time (MRT), clearance, volume of distribution and dose linearity were also assessed for VWF:RCo at various time points. Median baseline VWF:RCo level was 13 IU dL(1) (range, 6-124); with a mean change from baseline >100 IU dL(1) immediately after the infusion, decreasing to 10 IU dL(1) at 48 h postinfusion. The group median incremental in vivo recovery (IVR) for VWF:RCo was 2.4 IU dL(1) per IU kg(1), for VWF:Ag 2.3 IU dL(1) kg(1) and for FVIII:C was 2.7 IU dL(1) per IU kg(1). When analysing individual recovery values on repeated infusions, a very weak correlation was observed between presurgery IVR and IVR for both VWF:RCo and FVIII, measured at various times just prior to and after the surgical procedure. Although group median values were fairly consistent among repeated IVR measurements, the intra-individual IVR values for FVIII and VWF:RCo with repeated infusions showed a large degree of variability. IVR values obtained from pharmacokinetic analyses performed in advance of anticipated surgery do not reliably predict postinfusion circulating levels of VWF:RCo or FVIII attained preoperatively or with subsequent peri-operative infusions.
机译:需要确定VWD患者手术中的von Willebrand因子/因子VIII(VWF / FVIII)浓缩物的最佳剂量。进行了一项前瞻性,多中心研究,其中包括在标准剂量的VWF / FVIII浓缩物(Humate-P®)之后进行初始药代动力学(PK)评估,以确定各个PK参数并指导手术期间的治疗剂量。 41名受试者接受了60 IU kg(1)VWF:RCo。确定VWF:RCo,VWF:Ag和FVIII:C的血浆中值水平,半衰期,相对于基线的平均变化和体内恢复(IVR)值以及血浆时间浓度曲线(AUC)下的面积,平均值还在不同时间点对VWF:RCo评估了停留时间(MRT),清除率,分布体积和剂量线性。基线VWF:RCo中位数为13 IU dL(1)(范围6-124);输注后立即从基线> 100 IU dL(1)的平均变化,到输注后48 h降至10 IU dL(1)。 VWF:RCo的组体内平均增量恢复(IVR)为每IU kg(1)2.4 IU dL(1),VWF:Ag 2.3 IU dL(1)kg(1)和FVIII:C为2.7 IU每IU kg(1)dL(1)。当分析重复输注的个体恢复值时,对于VWF:RCo和FVIII,在术前IVR和IVR之间观察到非常弱的相关性,在手术前后分别在不同时间进行了测量。尽管重复IVR测量之间的组中值相当一致,但重复输注的FVIII和VWF:RCo的个体内IVR值显示出很大的可变性。从预期手术之前进行的药代动力学分析获得的IVR值不能可靠地预测术前或术后围手术期达到的VWF:RCo或FVIII的输注后循环水平。

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