Management of Persons With Haemophilia Requiring Antithrombotic Therapy: A Canadian Modified Delphi Consensus Study

IF 3 2区 医学 Q2 HEMATOLOGY
Haemophilia Pub Date : 2025-04-17 DOI:10.1111/hae.70047
Kelsey Uminski, Tzu-Fei Wang, Lisa Duffett, Alan Tinmouth, Roy Khalife
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Abstract

Introduction

Advancements in haemophilia care have extended the life expectancy of persons with haemophilia (PWH), giving rise to new clinical challenges including the need for antithrombotic therapy (ATT) in mitigating arterial or venous thrombotic risk. However, evidence to support clinical decision-making in this context remains limited, despite its growing importance.

Aims

To develop Canadian consensus recommendations for managing PWH requiring ATT.

Methods

A modified Delphi technique was used. Initial statements were generated using information from a scoping literature review and focus groups with Canadian haemophilia experts. Key areas included risk assessment, tailored treatment planning, ATT selection and management of breakthrough bleeding. Expert panellists were recruited through the Association of Haemophilia Clinic Directors of Canada using convenience sampling. Participants independently reviewed and rated each statement using a 7-point agreement-based Likert scale, with consensus defined a priori as over 70% agreement among panellists. Statements that did not reach consensus in the first round were modified based on participants’ comments.

Results

Eight physicians (median experience in PWH care: 11.0 years) from five haemophilia treatment centres across four Canadian provinces participated. All panellists had experience managing thromboembolic complications and using ATTs in PWH. Consensus was attained for 32 statements on general aspects of care, risk assessment, treatment planning and management of bleeding complications. All statements attained consensus after two rounds with a 100% completion rate.

Conclusion

This Canadian study yielded 32 consensus-based recommendations for managing PWH requiring ATT, addressing an unmet need to guide clinical decision-making in this complex and evolving area.

血友病患者需要抗血栓治疗的管理:加拿大修改的德尔菲共识研究。
血友病治疗的进步延长了血友病患者(PWH)的预期寿命,带来了新的临床挑战,包括需要抗血栓治疗(ATT)来减轻动脉或静脉血栓形成的风险。然而,在这种情况下支持临床决策的证据仍然有限,尽管它越来越重要。目的:为管理需要at的PWH制定加拿大共识建议。方法:采用改进的德尔菲技术。最初的陈述是根据加拿大血友病专家的范围文献综述和焦点小组的信息生成的。关键领域包括风险评估、量身定制的治疗计划、ATT的选择和突破性出血的管理。专家小组成员是通过加拿大血友病诊所主任协会使用方便抽样招募的。参与者使用基于7分共识的李克特量表独立审查和评价每个陈述,共识被先验地定义为小组成员之间超过70%的共识。第一轮未达成共识的发言将根据与会者的意见进行修改。结果:来自加拿大四个省五个血友病治疗中心的八名医生(PWH护理的中位经验:11.0年)参与了研究。所有小组成员都有处理血栓栓塞并发症和在PWH中使用ats的经验。关于出血并发症的一般护理、风险评估、治疗计划和管理的32项声明达成了共识。两轮后,所有陈述均达成一致,完成率为100%。结论:加拿大的这项研究为管理需要ATT的PWH提供了32项基于共识的建议,解决了在这一复杂和不断发展的领域指导临床决策的未满足需求。
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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