Evidence map›Paper›PMID 41676357›Full record

ArticleResearch and practice in thrombosis and haemostasis2026

Health-related quality of life in adults with von Willebrand disease: results of the French real-life Willebrand study on health-related quality of life.

Annie Borel-Derlon, Agnès Veyradier, Yohann Repessé, Nathalie Itzhar-Baïkan, Dominique Desprez, Fabienne Genre-Volot, Hervé Chambost, Laurent Ardillon, Brigitte Pan-Petesch, Sophie Bayart and 6 more

Abstract read
In one paragraph

Article in Research and practice in thrombosis and haemostasis, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

16 authors.

Annie Borel-DerlonHematology and Hemostasis Department, French Reference centre for von Willebrand disease, Haemophilia Treatment Centre, Caen, France.
Agnès VeyradierHematology Department, French Reference centre for von Willebrand disease, Haematology Unit, Lariboisière Hospital, Paris, France.
Yohann RepesséHematology and Hemostasis Department, French Reference centre for von Willebrand disease, Haemophilia Treatment Centre, Caen, France.
Nathalie Itzhar-BaïkanHematology Department, French Reference centre for von Willebrand disease, Haematology Unit, Lariboisière Hospital, Paris, France.
Dominique DesprezHematology Department, Haemophilia Treatment Centre, Strasbourg, France.
Fabienne Genre-VolotHematology Department, Haemophilia Treatment Centre, Dijon, France.
Hervé ChambostPediatric Hematology and Oncology Department, Haemophilia Treatment Centre, Marseille, France.
Laurent ArdillonHematology Department, Haemophilia Treatment Centre, Tours, France.
Brigitte Pan-PeteschHematology Department, Haemophilia Treatment Centre, Brest, France.
Sophie BayartPediatric Hematology Department, Haemophilia Treatment Centre, Rennes, France.
Malika Barthez-ToullecDepartment of Clinical Development and Medical Affairs, Laboratoire français du Fractionnement et des Biotechnologies (LFB), Les Ulis, France.
Grégory MarinDepartment of Statistics, Aixial, Boulogne-Billancourt, France.
Marie Hélène André-BonnetDepartment of Clinical Development and Medical Affairs, Laboratoire français du Fractionnement et des Biotechnologies (LFB), Les Ulis, France.
Sophie SusenHematology and Transfusion Department, French Reference centre for von Willebrand disease, Haemophilia Treatment Centre, Lille, France.
Sylvia von MackensenDepartment of Medical Psychology, University Medical Centre, Hamburg-Eppendorf, Germany.
Jenny GoudemandHematology and Transfusion Department, French Reference centre for von Willebrand disease, Haemophilia Treatment Centre, Lille, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Hemorrhagic events in von Willebrand disease (VWD) impair patients' physical health, daily functioning, and psychological/emotional well-being. While few studies have assessed health-related quality of life (HRQoL) in VWD, no prospective evaluation had been conducted in France. Objectives: The Willebrand study on HRQoL (WiSH-QoL) is an observational and prospective study that addressed this gap. Conducted in 27 French VWD treatment centers, it employed both generic and VWD-specific patient-reported outcome measures (PROs). Methods: Eligible patients included all ages and VWD types (type 1 restricted to basal von Willebrand factor antigen < 30 IU/dL). PROs (SF-36, VWD-QoL, and VWD-SAT) were assessed at baseline and 24 months. Results: In total, 224 adult patients were enrolled. Compared with the French general population, participants showed significantly reduced mental/emotional health and social/physical functioning. The VWD-specific PROs confirmed substantial physical impact in severe disease, including limitations in sports, leisure, and work. They also identified social impacts related to self-perception and relationships (family, others, and professionals). Physical and emotional well-being was particularly affected in women. Regardless of VWD type, patients reported mental health impacts, notably concerning future outlook. Social health deteriorated over time. Conclusion: The Willebrand study on HRQoL, using disease-specific PROs, reveals the real-life physical, emotional, and social burden of VWD, notably in severe forms and among women. By selecting key questions from these tools, clinicians can better assess these impacts across all patients and provide more comprehensive, long-term support for their well-being.

Indexed as

adultobservational studyquality of lifevon Willebrand Diseasewomen

Identifiers

PMID41676357
PMCPMC12887095

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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.