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Cost-utility analysis of immune tolerance induction therapy versus on-demand treatment with recombinant factor VII for hemophilia A with high titer inhibitors in Iran

机译:伊朗对具有高滴度抑制剂的血友病A的免疫耐受诱导疗法与重组因子VII按需治疗的成本-效用分析

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Background: In developing countries, the treatment of hemophilia patients with inhibitors is presently the most challenging and serious issue in hemophilia management, direct costs of clotting factor concentrates accounting for >98% of the highest economic burden absorbed for the health care of patients in this setting. In the setting of chronic diseases, cost-utility analysis, which takes into account the beneficial effects of a given treatment/health care intervention in terms of health-related quality of life, is likely to be the most appropriate approach. Objective: The aim of this study was to assess the incremental cost-effectiveness ratios of immune tolerance induction (ITI) therapy with plasma-derived factor VIII concentrates versus on-demand treatment with recombinant-activated FVIIa (rFVIIa) in hemophilia A with high titer inhibitors from an Iranian Ministry of Health perspective. Methods: This study was based on the study of Knight et al, which evaluated the cost-effectiveness ratios of different treatments for hemophilia A with high-responding inhibitors. To adapt Knight et al's results to the Iranian context, a few clinical parameters were varied, and cost data were replaced with the corresponding Iranian estimates of resource use. The time horizon of the analysis was 10 years. One-way sensitivity analyses were performed, varying the cost of the clotting factor, the drug dose, and the administration frequency, to test the robustness of the analysis. Results: Comparison of the incremental cost-effectiveness ratios between the three ITI protocols and the on-demand regimen with rFVIIa shows that all three ITI protocols dominate the on-demand regimen with rFVIIa. Between the ITI protocols the low-dose ITI protocol dominates both the Bonn ITI protocol and the Malm? ITI protocol and would be the preferred ITI protocol. All of the three ITI protocols dominate the on-demand strategy, as they have both a lower average lifetime cost and higher quality-adjusted life-years (QALYs) gained. The cost per QALY gained for the Bonn ITI protocol compared with the Malm? ITI protocol was $249,391.84. The cost per QALY gained for the Bonn ITI protocol compared with the low-dose ITI protocol was $842,307.69. Conclusion: The results of data derived from our study suggest that the low-dose ITI protocol may be a less expensive and/or more cost-effective option compared with on-demand first-line treatment with rFVIIa.
机译:背景:在发展中国家,用抑制剂治疗血友病患者目前是血友病管理中最具挑战性和最严重的问题,凝血因子浓缩液的直接成本占该患者医疗保健所吸收的最高经济负担的98%以上设置。在慢性疾病的发生中,考虑到给定治疗/保健干预措施对健康相关的生活质量的有益影响的成本-效用分析可能是最合适的方法。目的:本研究旨在评估在高滴度的血友病患者中,血浆衍生的因子VIII浓缩物进行免疫耐受诱导(ITI)治疗与重组激活的FVIIa(rFVIIa)按需治疗的增量成本-效果比。从伊朗卫生部的角度来看抑制物。方法:本研究基于Knight等人的研究,该研究评估了高反应抑制剂对A型血友病的不同治疗方法的成本效益比。为了使Knight等人的结果适应伊朗的情况,改变了一些临床参数,并将成本数据替换为相应的伊朗对资源使用的估计。分析的时间范围为10年。进行单向敏感性分析,改变凝血因子的成本,药物剂量和给药频率,以测试分析的稳健性。结果:比较三种ITI方案和使用rFVIIa的按需方案之间的增量成本效益比,结果表明,所有三种ITI方案都主导了使用rFVIIa的按需方案。在ITI协议之间,低剂量ITI协议在Bonn ITI协议和Malm?协议中均占主导地位。 ITI协议,它将是首选的ITI协议。所有这三种ITI协议都主导了按需策略,因为它们具有较低的平均生命周期成本和较高的质量调整生命年(QALY)。与Malm?相比,Bonn ITI协议获得的每QALY成本? ITI协议价格为$ 249,391.84。波恩ITI协议与低剂量ITI协议相比,每个QALY的费用为842,307.69美元。结论:我们研究的数据结果表明,与按需一线治疗rFVIIa相比,低剂量ITI方案可能是一种更便宜和/或更具有成本效益的选择。

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