Jones P, Fearns M, Forbes C, Stuart J
Br Med J. 1978 Jun 3;1(6125):1447-50. doi: 10.1136/bmj.1.6125.1447.
Data on home treatment for patients with haemophilia A (factor VIII deficient haemophilia) were compiled for 1975 and 1976 from questionnaires answered by directors of haemophilia centres throughout the United Kingdom. There were 48 haemophilia centres in 1975 and 71 in 1976. The number of patients on or in training for home treatment increased from 267 to 488 in the two years, and a further 241 haemophiliacs were considered suitable for home therapy by the end of 1976. Apart from a small (but increasing) number of haemophiliacs on prophylactic treatment, most patients were on low-dose (250-500 units) on-demand regimens, using a mean of 20 000 factor VIII units per patient per year in 1976. An estimated 55% of the blood product used for home therapy in the UK in 1976 was imported from commercial sources. Despite the fact that the numbers of patients on home treatment have increased, so that about 60% of the potential population were receiving or being considered for home treatment in 1976, inadequacies in the service still remain. In some centres follow-up is clearly inadequate; about 15% of patients still rely on cryoprecipitate; and too little money has been invested in making the NHS self-sufficient in factor VIII production.
1975年和1976年,英国各地血友病中心的负责人通过问卷调查,收集了甲型血友病(VIII因子缺乏型血友病)患者在家治疗的数据。1975年有48个血友病中心,1976年有71个。接受或正在接受在家治疗培训的患者人数在这两年间从267人增加到488人,到1976年底,另有241名血友病患者被认为适合在家治疗。除了少数(但在增加)接受预防性治疗的血友病患者外,大多数患者采用低剂量(250 - 500单位)按需治疗方案,1976年每位患者每年平均使用20000单位VIII因子。1976年,英国用于在家治疗的血液制品估计有55%是从商业渠道进口的。尽管接受在家治疗的患者人数有所增加,以至于1976年约60%的潜在人群正在接受或被考虑接受在家治疗,但服务仍存在不足。在一些中心,随访明显不足;约15%的患者仍依赖冷沉淀;而且在使国民保健制度在VIII因子生产方面实现自给自足方面投入的资金太少。