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Congenital bleeding disorders. Rational treatment options.

作者信息

Seremetis S V, Aledort L M

机构信息

Division of Hematology, Mount Sinai Hospital, New York, New York.

出版信息

Drugs. 1993 Apr;45(4):541-7. doi: 10.2165/00003495-199345040-00006.

DOI:10.2165/00003495-199345040-00006
PMID:7684674
Abstract

There are rational, effective choices available for the treatment of common inherited bleeding disorders, according to assessment of safety, efficacy and cost. All currently available products for patients with haemophilia A (factor VIII deficiency) are comparable in terms of efficacy and viral safety. However, high purity products are recommended for those with coexisting human immunodeficiency virus (HIV) infection. Many patients with mild haemophilia A and most with von Willebrand's disease can be treated with desmopressin, which can be given as an intranasal spray in some countries. For the treatment of patients with factor XI deficiency, fresh frozen plasma remains the standard care, although solvent-detergent-treated fresh frozen plasma and factor XI concentrate are currently being investigated as alternatives. In the treatment of haemophilia B (factor IX deficiency), purified factor IX concentrates are particularly useful in clinical settings where large amounts of concentrate are to be used (e.g. surgical prophylaxis). Their usefulness in other contexts needs clarification. Treatment of inhibitors that may develop in response to administered coagulation factors is still limited to the use of prothrombin complex concentrates and porcine factor VIII. Active clinical trials are currently assessing the efficacy and safety of recombinant factor VIIa, Xa and tissue factor in this indication.

摘要

相似文献

1
Congenital bleeding disorders. Rational treatment options.
Drugs. 1993 Apr;45(4):541-7. doi: 10.2165/00003495-199345040-00006.
2
Hemophilia and von Willebrand's disease: 2. Management. Association of Hemophilia Clinic Directors of Canada.血友病和血管性血友病:2. 管理。加拿大血友病诊所主任协会
CMAJ. 1995 Jul 15;153(2):147-57.
3
Current therapy for rare factor deficiencies.罕见因子缺乏症的当前治疗方法。
Haemophilia. 2001 Jan;7 Suppl 1:16-22. doi: 10.1046/j.1365-2516.2001.00100.x.
4
Surgical care of patients with hereditary disorders of blood coagulation.遗传性凝血障碍患者的外科治疗
Mod Treat. 1968 Jan;5(1):61-83.
5
Non-thrombotic-, non-inhibitor-associated adverse reactions to coagulation factor concentrates for treatment of patients with hemophilia and von Willebrand's disease: a systematic review of prospective studies.非血栓形成、非抑制剂相关的凝血因子浓缩物治疗血友病和血管性血友病患者的不良反应:前瞻性研究的系统评价。
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6
Multiple congenital coagulopathies co-expressed with Von Willebrand's disease: the experience of Hemophilia Region III Treatment Centers over 25 years and review of the literature.与血管性血友病共同表达的多种先天性凝血病:血友病三区治疗中心25年的经验及文献综述
Haemophilia. 2007 Nov;13(6):685-96. doi: 10.1111/j.1365-2516.2007.01541.x.
7
Inherited bleeding disorders.遗传性出血性疾病。
Baillieres Clin Haematol. 1991 Apr;4(2):291-332. doi: 10.1016/s0950-3536(05)80162-3.
8
Peri-operative management of patients with coagulation disorders.凝血功能障碍患者的围手术期管理。
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Progress in the treatment of bleeding disorders.出血性疾病治疗的进展。
Thromb Res. 2011 Jan;127 Suppl 1:S3-5. doi: 10.1016/j.thromres.2010.10.007. Epub 2010 Oct 29.
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Prevention of hepatitis C virus infection in children with haemophilia A and B and von Willebrand's disease.甲型和乙型血友病及血管性血友病患儿丙型肝炎病毒感染的预防。
Thromb Haemost. 1992 Jan 23;67(1):184.

本文引用的文献

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The management of bleeding in hemophilia.
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Postoperative thromboses in hemophilia B.乙型血友病术后血栓形成
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Detection of factor X activation in humans.人类中凝血因子X激活的检测。
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7
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Molecular and cellular biology of blood coagulation.血液凝固的分子与细胞生物学
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9
Therapy with factor IX concentrate resulting in DIC and thromboembolic phenomena.使用凝血因子IX浓缩物治疗导致弥散性血管内凝血和血栓栓塞现象。
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1-Deamino-8-d-arginine vasopressin: a new pharmacological approach to the management of haemophilia and von Willebrands' diseases.1-去氨基-8-D-精氨酸加压素:治疗血友病和血管性血友病的一种新的药理学方法。
Lancet. 1977 Apr 23;1(8017):869-72. doi: 10.1016/s0140-6736(77)91197-7.