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Longitudinal bleeding assessment in von Willebrand disease utilizing an interim bleeding score.
Lavin, Michelle; Christopherson, Pamela; Grabell, Julie; Abshire, Thomas; Flood, Veronica; Haberichter, Sandra L; Lillicrap, David; O'Donnell, James S; Montgomery, Robert R; James, Paula D.
Affiliation
  • Lavin M; National Coagulation Centre, St. James's Hospital, Dublin, Ireland.
  • Christopherson P; Irish Centre for Vascular Biology, Royal College of Surgeons in Ireland, Dublin, Ireland.
  • Grabell J; Blood Research Institute, Versiti, Milwaukee, Wisconsin, USA.
  • Abshire T; Department of Medicine, Queen's University, Kingston, Ontario, Canada.
  • Flood V; Blood Research Institute, Versiti, Milwaukee, Wisconsin, USA.
  • Haberichter SL; Blood Research Institute, Versiti, Milwaukee, Wisconsin, USA.
  • Lillicrap D; Blood Research Institute, Versiti, Milwaukee, Wisconsin, USA.
  • O'Donnell JS; Department of Pathology & Molecular Medicine, Queen's University, Kingston, Ontario, Canada.
  • Montgomery RR; National Coagulation Centre, St. James's Hospital, Dublin, Ireland.
  • James PD; Irish Centre for Vascular Biology, Royal College of Surgeons in Ireland, Dublin, Ireland.
J Thromb Haemost ; 20(10): 2246-2254, 2022 10.
Article in En | MEDLINE | ID: mdl-35780487
ABSTRACT

BACKGROUND:

Assessment of bleeding phenotype is critically important in the diagnosis of von Willebrand disease (VWD). Despite advances in bleeding assessment tools (BATs), standardized tools to evaluate bleeding following diagnosis (interim bleeding) are lacking.

OBJECTIVES:

We assessed the clinical utility of an interim bleeding protocol in a multicenter, international study involving patients with VWD.

METHODS:

The enrolment ISTH BAT formed the original bleeding score (0 BS). At follow-up, the International Society on Thrombosis and Haemostasis BAT was repeated but included only interval bleeding (Interim BS, 1 BS). Both scores were annualized (0 BS/yr, 1 BS/yr). BS were analyzed by VWD subtype, plasma VWF level, sex, and age.

RESULTS:

Interim BS discriminated by subtype, with significantly increased 0 BS and 1 BS in patients with type 3 VWD. In patients with type 1 VWD, a positive or negative 0 BS did not predict future bleeding, with similar 1 BS/yr (median 1.0 vs. 0.7, p = .2). Despite significantly higher 0 BS in females with type 1 VWD than males (median 7 vs. 5, p = .0012), 1 BS were not significantly different (median 4 vs. 4, p = .16). While 0 BS were lower in children than adults with type 1 VWD, interim BS were similar (median 5 vs. 3, p = .5; 1BS/yr, median 1 vs. 0.8, p = .7). Interestingly, in those with plasma von Willebrand factorristocetin cofactor levels >50 IU/dl, interim BS rates were similar to those 30-50 IU/dl (1 BS/yr 0.8 vs. 1.3, p = .5).

CONCLUSION:

This study provides both a new approach to longitudinal bleeding assessment and insights into the evolution of bleeding in VWD.
Subject(s)
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Full text: 1 Database: MEDLINE Main subject: Von Willebrand Diseases / Von Willebrand Disease, Type 1 / Von Willebrand Disease, Type 3 Type of study: Clinical_trials / Diagnostic_studies / Guideline / Prognostic_studies / Risk_factors_studies Limits: Female / Humans / Male Language: En Year: 2022 Type: Article

Full text: 1 Database: MEDLINE Main subject: Von Willebrand Diseases / Von Willebrand Disease, Type 1 / Von Willebrand Disease, Type 3 Type of study: Clinical_trials / Diagnostic_studies / Guideline / Prognostic_studies / Risk_factors_studies Limits: Female / Humans / Male Language: En Year: 2022 Type: Article