用于评估血友病患者关节健康状况的血友病关节健康评分。

IF 3 2区 医学 Q2 HEMATOLOGY Haemophilia Pub Date : 2024-11-04 DOI:10.1111/hae.15116
Cihan Ay, Maria Elisa Mancuso, Davide Matino, Karen Strike, Gianluigi Pasta
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引用次数: 0

摘要

简介血友病关节健康评分(HJHS)是一种用于评估血友病患者关节变化的工具。目的:评估报告血友病关节健康评分随时间变化的现有文献,并评估临床相关结果的可能临界值以及有意义的评分变化的理想随访时间:我们对 2011 年至 2023 年间发表的采用 HJHS 2.1 版检测血友病患者关节健康变化的研究进行了文献检索。我们重点关注那些评估 HJHS 变化的临床相关性、评估临界值的使用情况并报告随访情况的研究:我们的搜索发现了 213 篇出版物,其中 53 篇(25%)被认为与本综述相关。其中,33 篇(62%)出版物报告了 HJHS 总分,20 篇(38%)报告了单一的 HJHS 联合评分,而报告 HJHS 评分/变化的方式差异很大。10篇出版物(19%)对临床相关性进行了评估,但其计算方法各不相同(定义截断分数、测量标准化反应平均值或最小检测变化)。这10项研究的随访时间从2周到8年不等:结论:评估 HJHS 随时间推移而发生的变化存在很大差异,其主要原因是灵敏度较低,而且对该评分的解释和临床相关性缺乏共识。因此,在使用 HJHS 的同时,还应使用灵敏度更高的工具,以更好地确定血友病患者的关节健康状况。
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The haemophilia joint health score for the assessment of joint health in patients with haemophilia.

Introduction: The haemophilia joint health score (HJHS) is a tool used to assess joint changes in patients with haemophilia. There is lack of consensus on the interpretation of HJHS scores and their clinical relevance.

Aim: To evaluate available literature reporting HJHS changes over time and assess a possible cut-off value for clinically relevant outcomes and the ideal follow-up for a meaningful score change.

Methods: We conducted a literature search of studies published between 2011 and 2023 where the HJHS version 2.1 had been adopted to detect changes in joint health in patients with haemophilia. We focused on studies that assessed clinical relevance of HJHS changes, evaluated the use of cut-off values and reported a follow-up over time.

Results: Our search identified 213 publications of which 53 (25%) were deemed relevant for this review. Of these, 33 (62%) publications reported the total HJHS score and 20 (38%) reported a single joint HJHS score, while the way of reporting HJHS scores/change was highly variable. Ten publications (19%) assessed clinical relevance, but their methods of calculation differed (defining a cut-off score, measuring standardised response mean or minimal detectable change). The follow-up duration varied from 2 weeks to 8 years in these 10 studies.

Conclusions: High variability in assessing HJHS change over time is the primary consequence of its low sensitivity, and the lack of consensus on interpretation and clinical relevance of the score. Therefore, more sensitive tools should be used alongside HJHS to better define the joint health status of patients with haemophilia.

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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
The haemophilia joint health score for the assessment of joint health in patients with haemophilia. Performance of instrumental activities of daily living in patients with haemophilic arthropathy. A cross-sectional cohort study. A novel gene editing lexicon strategy for the haemophilia community: Research plan for development and preliminary results. Breaking barriers in haemophilia A care: One-year real-world experience with emicizumab prophylaxis at Civil Service Hospital, Kathmandu, Nepal. Moderate haemophilia A: Recommendations from a Spanish panel of experts.
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