Moving towards Normalization of haemostasis and health equity: Evolving treatment goals for haemophilia A

IF 3 2区 医学 Q2 HEMATOLOGY
Haemophilia Pub Date : 2024-07-10 DOI:10.1111/hae.15031
Pål André Holme, Jan Blatný, Pratima Chowdary, Riitta Lassila, Niamh O'Connell, Cédric Hermans, María Teresa Álvarez Román, Claude Négrier, Antonio Coppola, Johannes Oldenburg
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Abstract

Background

Treatment options for people with haemophilia are evolving at a rapid pace and a range of prophylactic treatment options using various technologies are currently available, each with their own distinct safety and efficacy profile.

Treatment goals

The access to replacement therapy and prophylaxis has driven a dramatic reduction in mortality and resultant increase in life expectancy. Beyond this, the abolition of bleeds and preservation of joint health represent the expected, but rarely attained, goals of haemophilia treatment and care. These outcomes also do not address the complexity of health-related quality of life impacted by haemophilia and its treatment.

Conclusion

Capitalizing on the major potential of therapeutic innovations, ‘Normalization’ of haemostasis, as a concept, should include the aspiration of enabling individuals to live as normal a life as possible, free from haemophilia-imposed limitations. To achieve this—being supported by the data reviewed in this manuscript—the concept of haemostatic and life Normalization needs to be explored and debated within the wider multidisciplinary teams and haemophilia community.

Abstract Image

实现止血正常化和健康公平:不断发展的血友病 A 治疗目标。
背景:血友病患者的治疗方案发展迅速,目前有一系列采用不同技术的预防性治疗方案,每种方案都有其独特的安全性和有效性:治疗目标:替代疗法和预防性疗法的普及大大降低了死亡率,延长了预期寿命。除此之外,消除出血和保持关节健康是血友病治疗和护理的预期目标,但很少能实现。这些结果也没有解决血友病及其治疗所影响的与健康相关的生活质量的复杂性:结论:利用治疗创新的巨大潜力,止血 "正常化 "作为一个概念,应包括让患者尽可能过上正常生活的愿望,摆脱血友病带来的限制。为了实现这一目标--本手稿所回顾的数据支持了这一点--止血和生活正常化的概念需要在更广泛的多学科团队和血友病社区中进行探索和讨论。
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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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