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The use of heat-treated Factor VIII-concentrates in von Willebrand's disease.

作者信息

Köhler M, Hellstern P, Wenzel E

出版信息

Blut. 1985 Jan;50(1):25-7. doi: 10.1007/BF00319766.

DOI:10.1007/BF00319766
PMID:3917697
Abstract

In vitro investigations have demonstrated a high F VIII:Rcof potency and a high F VIII:Rcof/F VIII R:Ag ratio of two heat-treated F VIII concentrates. We therefore studied the in vivo effectiveness of these preparations (F VIII HSR, Behringwerke Marburg and F VIII HTR, Travenol) in five patients with von Willebrand's disease (vWd). In the steady state in vivo recoveries of F VIII:Rcof ranged from 73-153% after transfusion of F VIII HSR and from 11.5-17% after F VIII HTR respectively. The gain of F VIII-complex after F VIII HS was comparable to cryopecipitate (KryobulinR SP, Immuno AG Wien). All three products shortened the bleeding-time. Three of our five patients underwent surgery (Billroth I, papillotomy, laparatomy, open heart surgery) under F VIII HS cover without bleeding complications. The dose applied ranged from 20 to 40 U/kg at 8 or 12 h intervals for a period of approx. 14 days. Serum-transaminase elevations were observed in two of four patients after F VIII HT treatment. Although the risk of hepatitis of heat-treated F VIII concentrates remains to be determined, these products proved to be effective in vWd. The major advantages of these preparations are stability, rapid solubility, a low content of contaminating proteins, and a rapid, general availability.

摘要

相似文献

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The use of heat-treated Factor VIII-concentrates in von Willebrand's disease.
Blut. 1985 Jan;50(1):25-7. doi: 10.1007/BF00319766.
2
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引用本文的文献

1
Hemostatic effect of a heat-treated factor VIII concentrate (Haemate P) in von Willebrand's disease.热处理的凝血因子VIII浓缩物(海莫特P)对血管性血友病的止血作用。
Blut. 1988 Apr;56(4):171-8. doi: 10.1007/BF00320748.

本文引用的文献

1
Factor VIII:C and VIII:CAg response in patients with haemophilia A and von Willebrand's disease after administration of different factor VIII concentrates or plasma.血友病A和血管性血友病患者在输注不同的凝血因子VIII浓缩物或血浆后,凝血因子VIII:C和VIII:CAg的反应
Br J Haematol. 1981 Apr;47(4):587-96. doi: 10.1111/j.1365-2141.1981.tb02688.x.
2
In vitro characterization of commercial Factor VIII concentrates: long-term follow-up.商业性凝血因子VIII浓缩物的体外特性:长期随访
Blut. 1984 Jul;49(1):53-9. doi: 10.1007/BF00320384.
3
The standardized normal Ivy bleeding time and its prolongation by aspirin.
标准化的常春藤出血时间及其因阿司匹林而延长的情况。
Blood. 1969 Aug;34(2):204-15.
4
Correction of the hemostatic defects in Von Willebrand's disease.血管性血友病止血缺陷的纠正。
Blood. 1967 Sep;30(3):375-80.
5
Letter: Relation of von Willebrand factor to bleeding time.信函:血管性血友病因子与出血时间的关系。
N Engl J Med. 1974 Aug 22;291(8):420. doi: 10.1056/NEJM197408222910817.
6
Antihemophilic factor concentrate therapy in von Willebrand disease. Dissociation of bleeding-time factor and ristocetin-cofactor activities.血管性血友病中的抗血友病因子浓缩物治疗。出血时间因子与瑞斯托霉素辅因子活性的分离。
JAMA. 1976 Dec 13;236(24):2770-2.
7
Failure of AHF concentration to control bleeding in von Willebrand's disease.
Am J Med. 1976 Mar;60(3):357-60. doi: 10.1016/0002-9343(76)90751-8.
8
Characteristics of various factor VIII concentrates used in treatment of haemophilia A.用于治疗甲型血友病的各种凝血因子VIII浓缩剂的特性。
Br J Haematol. 1977 Dec;37(4):543-57. doi: 10.1111/j.1365-2141.1977.tb01028.x.
9
Platelet function and immunologic parameters in von Willebrand's disease following cryoprecipitate and factor VIII concentrate infusion.
Am J Med. 1977 Mar;62(3):369-76. doi: 10.1016/0002-9343(77)90834-8.