Patient-reported data on the severity of Von Willebrand disease.

Von Willebrand disease classification disease severity patient reported outcome measures quality of life

Journal

Haemophilia : the official journal of the World Federation of Hemophilia
ISSN: 1365-2516
Titre abrégé: Haemophilia
Pays: England
ID NLM: 9442916

Informations de publication

Date de publication:
15 Oct 2024
Historique:
revised: 28 08 2024
received: 20 06 2024
accepted: 08 09 2024
medline: 15 10 2024
pubmed: 15 10 2024
entrez: 15 10 2024
Statut: aheadofprint

Résumé

The severity of Von Willebrand disease (VWD) is currently based on laboratory phenotype. However, little is known about the severity of the patient's experience with the disease. The most recent VWD guidelines highlight the need for patient-reported outcomes (PROs) in VWD. The study aimed to investigate the patient-perspective on VWD severity and to identify key factors that determine the severity of disease experienced by patients. Patients participated in a nationwide cross-sectional study on VWD in the Netherlands (WiN-study). Patients filled in a questionnaire containing questions on the experienced severity of VWD (4-point scale), bleeding score (BS) and quality of life (QoL). We included 736 patients, median age of 41.0 years (IQR 23.0-55.0) and 59.5% were women. A total of 443 had type 1, 269 type 2 and 24 type 3 VWD. Self-reported severity of VWD was categorized as severe (n = 52), moderate (n = 171), mild (n = 393) or negligible (n = 120). Classification by historically lowest FVIII:C levels < 0.20 IU/mL as a proxy for severe VWD aligned with patient-reported severity classification with a 72% accuracy. Type 3 VWD (OR = 4.02, 95%CI: 1.72-9.45), higher BS (OR = 1.09, 95%CI: 1.06-1.11), female sex (OR = 1.36, 95%CI: 1.01-1.83), haemostatic treatment in the year preceding study inclusion (OR = 1.53, 95%CI: 1.10-2.13) and historically lowest VWF:Act levels (OR = 0.26, 95%CI: 0.07-1.00) were independent determinants of patient-reported severity. This study shows that patient-reported data provide novel insights into the determinants of experienced disease severity. Our findings highlight the need for studies on PROs with validated questionnaires to assess the burden of VWD.

Identifiants

pubmed: 39403864
doi: 10.1111/hae.15103
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Stichting Haemophilia
Organisme : CSL Behring

Informations de copyright

© 2024 The Author(s). Haemophilia published by John Wiley & Sons Ltd.

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Auteurs

Calvin B van Kwawegen (CB)

Department of Hematology, Erasmus MC, University Medical Center Rotterdam, Rotterdam, The Netherlands.

Karin Fijnvandraat (K)

Amsterdam UMC, University of Amsterdam, Emma Children's Hospital, Pediatric Hematology, Amsterdam, The Netherlands.
Department of Molecular Cellular Hemostasis, Sanquin Research, Amsterdam, The Netherlands.

Marieke J H A Kruip (MJHA)

Department of Hematology, Erasmus MC, University Medical Center Rotterdam, Rotterdam, The Netherlands.

Joke de Meris (J)

Netherlands Hemophilia Society, Leiden, The Netherlands.

Saskia E M Schols (SEM)

Department of Hematology, Radboud University Medical Center, Hemophilia Treatment Centre Nijmegen-Eindhoven-Maastricht, Nijmegen, The Netherlands.

Karina Meijer (K)

Department of Hematology, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.

Johanna G van der Bom (JG)

Department of Clinical Epidemiology, Leiden University Medical Center, Leiden, The Netherlands.
Jon J. van Rood Center for Clinical Transfusion Medicine, Sanquin Research, Leiden, The Netherlands.

Marjon H Cnossen (MH)

Department of Pediatric Hematology, Erasmus MC-Sophia Children's Hospital, University Medical Center Rotterdam, Rotterdam, The Netherlands.

Karin P M van Galen (KPM)

Department van Creveldkliniek, University Medical Center Utrecht, Utrecht University, Utrecht, The Netherlands.

Ferdows Atiq (F)

Department of Hematology, Erasmus MC, University Medical Center Rotterdam, Rotterdam, The Netherlands.

Jeroen Eikenboom (J)

Department of Internal Medicine, Division of Thrombosis and Hemostasis, Leiden University Medical Center, Leiden, The Netherlands.
Einthoven Laboratory for Vascular and Regenerative Medicine, Leiden University Medical Center, Leiden, The Netherlands.

Frank W G Leebeek (FWG)

Department of Hematology, Erasmus MC, University Medical Center Rotterdam, Rotterdam, The Netherlands.

Classifications MeSH