Department of Haematology, Royal Devon and Exeter Hospital, Exeter, UK.
Haemophilia. 2010 Jul 1;16(4):569-83. doi: 10.1111/j.1365-2516.2009.02118.x. Epub 2009 Nov 11.
The rare inherited coagulation factor deficiencies (deficiencies of factors I, II, V, VII, XI, XIII, combined FV + FVII deficiency, combined deficiency of the vitamin K dependent factors and von Willebrand disease type 3) have an aggregate prevalence of approximately 1:100,000. They may cause recurrent life or function threatening haemorrhage. In this article we review the available literature on long-term prophylaxis and, where possible, make recommendations on this important area.
罕见的遗传性凝血因子缺乏症(因子 I、II、V、VII、XI、XIII 缺乏症,FV+VII 联合缺乏症,维生素 K 依赖性因子联合缺乏症和 von Willebrand 病 3 型)的总患病率约为 1:100000。它们可能导致反复发作的危及生命或功能的出血。本文回顾了关于长期预防的现有文献,并在可能的情况下就这一重要领域提出了建议。