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Factor VIII concentrate for hemophilia: comparison of two heat-treated products.用于血友病的凝血因子 VIII 浓缩剂:两种热处理产品的比较。
CMAJ. 1987 Jan 15;136(2):150-2.
2
[Clinical evaluation of a new factor VIII concentrate in hemophilic children].
Pediatr Med Chir. 1983 May-Jun;5(3):49-55.
3
Factor VIII: C (FVIII: C) recovery and half-life after infusion of steam-treated high purity factor VIII concentrate in severe hemophilia A--comparison of one-stage assay, two-stage assay and a chromogenic substrate assay.重度甲型血友病患者输注经蒸汽处理的高纯度凝血因子 VIII 浓缩物后凝血因子 VIII:C(FVIII:C)的回收率及半衰期——一期法检测、二期法检测与发色底物法检测的比较
Thromb Haemost. 1986 Dec 15;56(3):353-9.
4
Lyophilized cryoprecipitate for children with hemophilia A.
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A limited sampling strategy for estimating individual pharmacokinetic parameters of coagulation factor VIII in patients with hemophilia A.一种用于估计甲型血友病患者凝血因子 VIII 个体药代动力学参数的有限采样策略。
Ther Drug Monit. 2007 Feb;29(1):20-6. doi: 10.1097/FTD.0b013e3180311384.
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[Clinical testing of Premofil M SRK, a blood coagulation factor VIII concentrate purified from human plasma using monoclonal an antibodies].
Schweiz Med Wochenschr. 1991 Nov 2;121(44):1624-7.
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[Inhibitor hemophilia A--diagnostic and therapeutic significance of controlled substitutions with factor VIII].[抑制性血友病A——凝血因子VIII控制替代治疗的诊断和治疗意义]
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The half-life of infused factor VIII is shorter in hemophiliac patients with blood group O than in those with blood group A.
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In vitro factor VIII recovery during the delivery of ultrapure factor VIII concentrate by continuous infusion.通过持续输注递送超纯凝血因子VIII浓缩物期间的体外凝血因子VIII回收率。
Am J Hematol. 1996 Feb;51(2):99-103. doi: 10.1002/(SICI)1096-8652(199602)51:2<99::AID-AJH1>3.0.CO;2-1.
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Factor VIII half-life and clinical phenotype of severe hemophilia A.重度甲型血友病的凝血因子 VIII 半衰期及临床表型
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Some characteristics of aggregates of IgG and plasma proteins in heat-treated factor VIII concentrates.热处理的凝血因子 VIII 浓缩物中 IgG 与血浆蛋白聚集体的一些特性
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本文引用的文献

1
Calculations of factor VIII in vivo recovery and half-life.体内因子VIII回收率和半衰期的计算。
Scand J Haematol Suppl. 1984;40:165-74. doi: 10.1111/j.1600-0609.1984.tb02560.x.
2
The acquired immunodeficiency syndrome in patients with hemophilia.血友病患者的获得性免疫缺陷综合征
Ann Intern Med. 1984 Apr;100(4):499-504. doi: 10.7326/0003-4819-100-4-499.
3
Transmission of non-A, non-B hepatitis by heat-treated factor VIII concentrate.
Lancet. 1985 Jul 6;2(8445):1-4. doi: 10.1016/s0140-6736(85)90055-8.
4
Inactivation of lymphadenopathy-associated virus by heat, gamma rays, and ultraviolet light.通过加热、伽马射线和紫外线使淋巴结病相关病毒失活。
Lancet. 1985 Jan 26;1(8422):188-9. doi: 10.1016/s0140-6736(85)92026-4.

用于血友病的凝血因子 VIII 浓缩剂:两种热处理产品的比较。

Factor VIII concentrate for hemophilia: comparison of two heat-treated products.

作者信息

Walker I R, Pai M K, Blair B A, Johnston M A, Birkett N J, Ofosu F A, Naylor D H

出版信息

CMAJ. 1987 Jan 15;136(2):150-2.

PMID:3098401
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1492010/
Abstract

In a controlled trial of heat-treated factor VIII concentrate from Cutter Laboratories and from Connaught Laboratories Limited, 25 patients with hemophilia received Cutter factor VIII and 24 patients with hemophilia received Connaught factor VIII. The mean increase in factor VIII level was similar for the two products (1.88% and 1.98% per unit/kg of body weight respectively [p greater than 0.1], or 89% and 95% respectively of the expected increase [p greater than 0.1]). In-vivo survival (the duration of factor VIII in the circulation) was compared after seven infusions of each product. The mean half-disappearance times were 10.7 and 9.1 hours respectively (p = 0.1), and the mean biologic half-lives were 11.6 and 9.9 hours respectively (p = 0.04); the clinical significance of the latter difference is dubious. Both products could be reconstituted satisfactorily from the dried state. Two subjects experienced relatively minor side effects following infusion of one lot of Cutter factor VIII. Individual responses to both products showed considerable variation. Therefore, when it is critical to attain predetermined levels of factor VIII, such as before and after surgery, factor VIII assays should be performed to check the patient's response.

摘要

在一项针对卡特实验室(Cutter Laboratories)和康诺特实验室有限公司(Connaught Laboratories Limited)热处理VIII因子浓缩物的对照试验中,25名血友病患者接受了卡特VIII因子,24名血友病患者接受了康诺特VIII因子。两种产品的VIII因子水平平均升高情况相似(分别为每单位/千克体重1.88%和1.98%[p大于0.1],或分别为预期升高幅度的89%和95%[p大于0.1])。在对每种产品进行七次输注后,比较了体内存活情况(VIII因子在循环中的持续时间)。平均半衰期分别为10.7小时和9.1小时(p = 0.1),平均生物学半衰期分别为11.6小时和9.9小时(p = 0.04);后一差异的临床意义尚不确定。两种产品均能从干燥状态令人满意地复溶。两名受试者在输注一批卡特VIII因子后出现了相对轻微的副作用。个体对两种产品的反应差异很大。因此,当达到预定的VIII因子水平至关重要时,如手术前后,应进行VIII因子检测以检查患者的反应。