Evidence map›Paper›PMID 39494972›Full record

ReviewHaemophilia : the official journal of the World Federation of Hemophilia2024

The haemophilia joint health score for the assessment of joint health in patients with haemophilia.

Cihan Ay, Maria Elisa Mancuso, Davide Matino, Karen Strike, Gianluigi Pasta

Abstract readReview
In one paragraph

Review in Haemophilia : the official journal of the World Federation of Hemophilia, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

13 citing papers in PubMed.

  1. Article
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  12. The haemophilia joint health score for the assessment of joint health in patients with haemophilia.Haemophilia : the official journal of the World Federation of Hemophilia · 2024
    Review
  13. Haemophilia Joint Health Score Ranges Across the Lifespan: Variation by Haemophilia Type and Severity.Haemophilia : the official journal of the World Federation of Hemophilia
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Cihan AyDivision of Haematology and Haemostaseology, Department of Medicine I, Medical University of Vienna, Vienna, Austria.ORCID https://orcid.org/0000-0003-2607-9717
Maria Elisa MancusoIRCCS Humanitas Research Hospital, Rozzano, Milan, Italy.
Davide MatinoMcMaster University in Hamilton, Hamilton, Canada.
Karen StrikeMcMaster Children's Hospital, Hamilton Health Sciences, McMaster University, Hamilton, Canada.ORCID https://orcid.org/0000-0002-5598-2051
Gianluigi PastaIRCCS Fondazione Policlinico San Matteo, Pavia, Italy.ORCID https://orcid.org/0000-0002-1919-5130

Funding

Novo Nordisk
6 · The paper itself

Abstract

introductionThe 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.

aimTo 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.

methodsWe 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.

resultsOur 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.

conclusionsHigh 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.

Indexed as

Hemophilia AJoint DiseasesHumansJointsSeverity of Illness Indexclinical relevancehaemophiliahealthjoint diseasejoints

Identifiers

PMID39494972
PMCPMC11659503

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.