血友病的新疗法:提高公平获得治疗的机会。

IF 2.1 Q3 HEMATOLOGY
Journal of Blood Medicine Pub Date : 2025-02-20 eCollection Date: 2025-01-01 DOI:10.2147/JBM.S490588
Magdalena Lewandowska, Sonia Nasr, Amy D Shapiro
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引用次数: 0

摘要

近年来,基因疗法和生物工程止血分子已经彻底改变了血友病患者的治疗方法。这些创新疗法旨在减轻治疗负担,提高患者的生活质量。其他新疗法,包括下一代模拟剂和重新平衡止血的药物,目前正在临床试验中进行评估。技术进步,如即时肌骨骼超声和人工智能,可能会改善患者的诊断和治疗结果。然而,对于世界上大多数血友病患者来说,无法获得诊断和有效治疗。实现所有血友病患者的健康公平需要更好地识别获得最佳护理的障碍,包括社会经济地位、种族/民族、性别、疾病严重程度、抑制剂状况、年龄和血友病治疗中心的使用情况。应确保所有患者获得新型血友病疗法。改善公平的方法包括患者和临床医生之间的决策伙伴关系、利益相关者的参与和制药行业的支持。新型血友病疗法的开发应与以患者为中心的护理方法相结合,以改善所有患者的卫生公平。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Emerging Therapies in Hemophilia: Improving Equitable Access to Care.

In recent years, gene therapy and bio-engineered hemostatic molecules have revolutionized treatment for people with hemophilia. These innovative therapies aim to decrease treatment burden and improve patient quality of life. Additional novel therapies, including next-generation mimetics and agents that rebalance hemostasis, are currently being evaluated in clinical trials. Technological advances such as point-of-care musculoskeletal ultrasound and artificial intelligence may improve patient diagnostic and treatment outcomes. However, for the majority of patients with hemophilia worldwide, diagnosis and effective treatment are inaccessible. Achieving health equity for all hemophilia patients requires improved identification of barriers to optimal care, including socioeconomic status, race/ethnicity, gender, disease severity, inhibitor status, age, and use of Hemophilia Treatment Centers. Access to novel hemophilia therapies should be ensured for all patients. Approaches to improving equity include a decision-making partnership between the patient and clinician, stakeholder engagement, and pharmaceutical industry support. The development of novel hemophilia therapies should be leveraged with a patient-centered care approach to improve health equity for all patients.

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来源期刊
CiteScore
3.50
自引率
0.00%
发文量
94
审稿时长
16 weeks
期刊介绍: The Journal of Blood Medicine is an international, peer-reviewed, open access, online journal publishing laboratory, experimental and clinical aspects of all topics pertaining to blood based medicine including but not limited to: Transfusion Medicine (blood components, stem cell transplantation, apheresis, gene based therapeutics), Blood collection, Donor issues, Transmittable diseases, and Blood banking logistics, Immunohematology, Artificial and alternative blood based therapeutics, Hematology including disorders/pathology related to leukocytes/immunology, red cells, platelets and hemostasis, Biotechnology/nanotechnology of blood related medicine, Legal aspects of blood medicine, Historical perspectives. Original research, short reports, reviews, case reports and commentaries are invited.
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