Switching From Standard to Extended Half-Life Coagulation Factor Replacement in Haemophilia: Clinical Outcomes and Costs of Care in Finland.

IF 3 2区 医学 Q2 HEMATOLOGY
Haemophilia Pub Date : 2025-06-21 DOI:10.1111/hae.70067
Mirkka Koivusalo, Timea Szanto, Tuomas Kovalainen, Aino Vesikansa, Outi Laine, Anu Partanen, Timo Siitonen, Marko Vesanen, Juha Mehtälä, Nina Sarnesto, Johanna Haapkylä, Anna-Elina Lehtinen, Riitta Lassila
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引用次数: 0

Abstract

Introduction: Real-world data are needed to evaluate treatment implementation, outcomes and costs of care in haemophilia patients switching prophylaxis from standard half-life (SHL) to extended half-life (EHL) clotting factor concentrates (CFCs).

Aim: We characterised treatment regimens, annual bleeding rate (ABR), adherence and costs in a nationwide Finnish haemophilia A (HA) and B (HB) cohort on prophylaxis, including non-switchers and switchers from SHL to EHL CFC.

Methods: This retrospective register study of adult patients with HA and HB was performed in University Hospitals during 2016-2021. Clinical and healthcare data were captured from electronic health records and national healthcare registers.

Results: Majority, 74% of HA and 71% of HB patients, switched from SHL to EHL. Thereafter, weekly mean infusions of CFC decreased (FVIII SHL 2.8, EHL 2.2; FIX SHL 1.6, EHL 0.9; p < 0.001). The mean annual consumption (international units, IU) increased by 18% from 219,534 per HA patient during SHL to 258,317 during EHL (p < 0.05) and declined per HB patient by 28% from 221,685 to 160,209 (p < 0.01). ABR appeared to decline after the switch in HA (mean SHL 2.8, EHL 0.9) and HB (SHL 1.6, EHL 0.8), while treatment adherence improved in HA from 81% to 95% (p < 0.01). The mean annual total costs of care in HA were €176,979 for SHL and €195,760 for EHL. In HB, the costs increased from €180,930 to €236,208 (p < 0.01).

Conclusions: Majority of patients on prophylaxis switched to EHL. The switch alleviated the infusion regimen, tended to lower bleeding rates and improved adherence with somewhat increased costs.

血友病从标准到延长半衰期凝血因子替代的转换:芬兰的临床结果和护理成本。
需要真实世界的数据来评估血友病患者从标准半衰期(SHL)转向延长半衰期(EHL)凝血因子浓缩物(CFCs)预防的治疗实施、结果和护理成本。目的:我们对芬兰全国性血友病a (HA)和B (HB)预防队列的治疗方案、年出血率(ABR)、依从性和成本进行了表征,包括未转换和从SHL切换到EHL CFC。方法:2016-2021年在大学医院对HA和HB成年患者进行回顾性登记研究。从电子健康记录和国家医疗保健登记册中获取临床和医疗保健数据。结果:大多数HA患者(74%)和HB患者(71%)从SHL转为EHL。此后,CFC每周平均输注量下降(FVIII SHL 2.8, EHL 2.2;修复SHL 1.6, ehl 0.9;结论:大多数接受预防治疗的患者改用EHL。这种转变减轻了输液方案,倾向于降低出血率,并在一定程度上增加了成本的情况下提高了依从性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Haemophilia
Haemophilia 医学-血液学
CiteScore
6.50
自引率
28.20%
发文量
226
审稿时长
3-6 weeks
期刊介绍: Haemophilia is an international journal dedicated to the exchange of information regarding the comprehensive care of haemophilia. The Journal contains review articles, original scientific papers and case reports related to haemophilia care, with frequent supplements. Subjects covered include: clotting factor deficiencies, both inherited and acquired: haemophilia A, B, von Willebrand''s disease, deficiencies of factor V, VII, X and XI replacement therapy for clotting factor deficiencies component therapy in the developing world transfusion transmitted disease haemophilia care and paediatrics, orthopaedics, gynaecology and obstetrics nursing laboratory diagnosis carrier detection psycho-social concerns economic issues audit inherited platelet disorders.
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