Literature DB >> 12828671

Prophylaxis for severe haemophilia: clinical and economical issues.

K Fischer1, M Van Den Berg.   

Abstract

Patients with severe haemophilia are treated either in case of bleeds only (on demand), or with regular infusions of clotting factor to prevent bleeds (prophylaxis). The introduction of prophylaxis has been hampered by issues of cost and viral safety. In order to compare results and treatment cost of different treatment strategies in adults, three cohorts of patients with severe haemophilia (born 1970-1980) were compared. 106 French patients were treated on demand, 49 Dutch patients were treated with intermediate dose prophylaxis, and 24 Swedish patients were treated with high dose prophylaxis. The annual number of joint bleeds, and the radiological Pettersson score were used to compare outcome, annual clotting factor consumption was used to compare costs. Prophylaxis reduced bleeds and arthropathy: patients treated on demand had a median of 11.5 joint bleeds/year and a median Pettersson score of 16 points, for intermediate dose prophylaxis median bleeds were 2.8 and Pettersson score was 7 points, and for high dose prophylaxis median bleeds were 0.5 joint bleeds and Pettersson score was 4 points. All differences were statistically significant, except the Pettersson scores in both prophylactic regimens. Treatment cost was only increased for high dose prophylaxis: mean clotting factor consumption was 1612 IU kg-1 yr-1 for on demand treatment, 1488 IU kg-1 yr-1 for intermediate dose prophylaxis, and 4012 IU kg-1 yr-1 for high dose prophylaxis. In young adults, the cost of intermediate dose prophylaxis is similar, but outcome is better than for on demand treatment. The cost of high dose prophylaxis is twofold higher, further improving outcome only slightly.

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Year:  2003        PMID: 12828671     DOI: 10.1046/j.1365-2516.2003.00764.x

Source DB:  PubMed          Journal:  Haemophilia        ISSN: 1351-8216            Impact factor:   4.287


  14 in total

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4.  Ectopic platelet-delivered factor (F) VIII for the treatment of Hemophilia A: Plasma and platelet FVIII, is it all the same?

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5.  [Breakthrough bleeding in adult patients with severe hemophilia A receiving low- and intermediate-dose FVIII for tertiary prophylaxis: characteristics and influencing factors].

Authors:  Shi-Qiu Qiu; Jin-Mu Zhuang; Xuan Zhou; Rui-Xue Yin; Zhu-Qin Liu; Fei Ma; Ying-Jia Li; Jing Sun
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6.  The IL-10 polarized cytokine pattern in innate and adaptive immunity cells contribute to the development of FVIII inhibitors.

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7.  Costs and utilization of treatment in patients with hemophilia.

Authors:  Patrícia Rocha; Manuela Carvalho; Manuela Lopes; Fernando Araújo
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8.  Economic burden of high-responding inhibitors in patients with hemophilia A in Taiwan.

Authors:  Tsu-Chiang Tu; Shin-Nan Cheng; Jye-Daa Chen; Thau-Ming Cham; Mei-Ing Chung
Journal:  Yonsei Med J       Date:  2013-03-01       Impact factor: 2.759

9.  Prevalence, incidence, and factor concentrate usage trends of hemophiliacs in Taiwan.

Authors:  Tsu-Chiang Tu; Wen-Shyong Liou; Tsui-Yun Chou; Tsung-Kun Lin; Chuan-Fang Lee; Jye-Daa Chen; Thau-Ming Cham; Mei-Ing Chung
Journal:  Yonsei Med J       Date:  2013-01-01       Impact factor: 2.759

10.  The Need for Gene Therapy for the Effective Treatment of Hemophilia.

Authors:  Tung Wynn; William B Slayton; Roland W Herzog
Journal:  J Genet Syndr Gene Ther       Date:  2012-08-20
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