Haemophilia A and haemophilia B - Are there relevant clinical differences?

被引:0
|
作者
Klamroth, R. [1 ]
Orlovic, M. [1 ]
Kubicek-Hofman, C. [1 ]
Gottstein, S. [1 ]
机构
[1] Vivantes Klinikum Friedrichshain, Klin Innere Med Angiol & Hamostaseol, Hamophiliezentrum Sprechstunde Gerinnungsstorunge, D-10249 Berlin, Germany
来源
HAMOSTASEOLOGIE | 2010年 / 30卷 / 4A期
关键词
Haemophilia B; DEFICIENCY; SEVERITY;
D O I
暂无
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Haemophilia B (HB) was described in 1952 as a single disease for the first time In comparison to haemophilia A (HA) the bleeding tendency seemed to be less severe The aim of this study wan. investigate this hypothesis in all patients with HA and HB treated in the haemophilia care center of the Vivantes Klinikum Patients, methods All patients with severe HA and H8 treated at the haemophilia care center were included We evaluated the regimen of replacement therapy and factor concentrate consumption within the last 5 years (1/2004 to 12/2008) Intracerebral bleeds were analysed over the Whole life span of the included patients Results 111/181 patients with HA had the severe-form and 12/34 patients severe HB 4/12 patients with severe HB had a history of intracerebral bleeding in comparison to 5/111 patients with severe HA 2/8 adult patient's With severe HB used a prophylactic treatment with factor concentrates (mean consumption 1289 IU factor IX/kg BW/year) in contrast to 60/95 adult patients with HA (mean consumption 2109 IU factor VIII/kg BW/year) Conclusion The data suggest a milder bleeding type of patients with severe HB in comparison to patients with severe HA but may be patients with severe HB are at higher-risk for intracerebral bleeds
引用
收藏
页码:S26 / S27
页数:2
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