让选择发出声音:世界血友病联合会共享决策工具的发展评论。

IF 3 2区 医学 Q2 HEMATOLOGY Haemophilia Pub Date : 2024-12-04 DOI:10.1111/hae.15133
Leonard A. Valentino, Kate Khair
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引用次数: 0

摘要

由世界血友病联合会(WFH)开发的共同决策(SDM)工具提供了血友病患者(PwH)与其医疗保健专业人员(HCPs)合作参与并达成治疗决策的过程的清晰简明概述。这个工具将适用于所有出血性疾病患者,而不仅仅是PwH患者。
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Giving Choice a Voice: Commentary on Development of the World Federation of Hemophilia Shared Decision-Making Tool

The shared decision-making (SDM) tool developed by the World Federation of Hemophilia (WFH) provides a clear and concise overview of the process by which people with haemophilia (PwH) can collaborate with their healthcare professionals (HCPs) to engage and arrive at a therapeutic decision. This tool will be useful for all people with all bleeding disorders, not just PwH.

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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.
期刊最新文献
Fracture Risk in People With Haemophilia A and B: A Systematic Review and Meta-Analysis. On the Price of Valoctogene Roxaparvovec in Germany and Italy. Pathogenic Mechanisms in Congenital Afibrinogenemia: A Systematic Review of Genetic Variants. Perioperative Management With Efanesoctocog Alfa in Patients With Haemophilia A in the Phase 3 XTEND-1 and XTEND-Kids Studies. Real-World Treatment Patterns and Long-Term Clinical Outcomes in Thai Patients With Acquired Haemophilia A.
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