Prophylactic versus on-demand treatment strategies for severe haemophilia: a comparison of costs and long-term outcome

被引:168
作者
Fischer, K
Van der Bom, JG
Molho, P
Negrier, C
Mauser-Bunschoten, EP
Roosendaal, G
De Kleijn, P
Grobbee, DE
Van den Berg, HM
机构
[1] Univ Utrecht, Dept Paediat, Med Ctr, NL-3508 AB Utrecht, Netherlands
[2] Univ Utrecht, Van Creveldklin, Med Ctr, NL-3508 AB Utrecht, Netherlands
[3] Univ Utrecht, Julius Ctr Hlth Sci Ctr & Primary Care, Med Ctr, NL-3508 AB Utrecht, Netherlands
[4] Univ Utrecht, Dept Rehabil & Nutr Sci, Med Ctr, NL-3508 AB Utrecht, Netherlands
[5] Cochin Hosp Grp, Paris, France
[6] Hop Edouard Herriot, Lyon, France
关键词
arthropathy; clotting factor consumption; haemarthrosis; health-related quality of life; Pettersson score;
D O I
10.1046/j.1365-2516.2002.00695.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
A multicentre study was performed to compare clotting factor use and outcome between on-demand and prophylactic treatment strategies for patients with severe haemophilia. Data on treatment and outcome of 49 Dutch patients with severe haemophilia, born 1970-80, primarily treated with prophylaxis, were compared with those of 106 French patients, who were primarily treated on demand. Dutch patients received intermediate dose prophylaxis, for a median duration of 12.7 years. Patients primarily treated with prophylaxis had fewer joint bleeds per year (median 2.8 vs. 11.5), a higher proportion of patients without joint bleeds (29% vs. 9%), lower clinical scores (median 2.0 vs. 8.0), and less arthropathy as measured by the Pettersson score (median 7 points vs. 16 points). Mean annual clotting factor use was equal at 1488 +/- 783 IU kg(-1) year(-1) (mean +/- standard deviation) for patients primarily treated with prophylaxis and 1612 +/- 1442 IU kg(-1) year(-1) for patients primarily treated on demand. These findings suggest that, compared with a primarily on-demand treatment strategy, a primarily prophylactic treatment strategy leads to better outcome at equal treatment costs in young adults with severe haemophilia.
引用
收藏
页码:745 / 752
页数:8
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