Key result
Von Willebrand factor testing remains an unproven adjunct and cannot replace echocardiography for prosthetic valve dysfunction.
Why the study?
Imaging for prosthetic valve surveillance has limitations, and the role of von Willebrand factor biomarkers as a biologic signal of abnormal flow in prosthetic valve dysfunction remains observational and unvalidated in randomized trials.
Does Von Willebrand factor biomarker testing reliably identify prosthetic valve dysfunction compared to standard imaging?
Does Von Willebrand factor biomarker testing reliably identify prosthetic valve dysfunction compared to standard imaging?
VWF biomarkers offer a biologic signal for prosthetic valve dysfunction but currently remain an investigational adjunct that should not replace guideline-directed echocardiographic surveillance.
Echocardiography remains standard for prosthetic valve assessment; leaves open hypothesis-generating adjunctive role for VWF pending prospective validation.
Imaging remains the foundation of prosthetic valve surveillance because it identifies valve morphology, lesion mechanism, and hemodynamic severity. However, acoustic shadowing, eccentric or multiple regurgitant jets, loading conditions, and reader variability can complicate assessment, particularly for paravalvular regurgitation after transcatheter aortic valve replacement. High shear stress unfolds von Willebrand factor (VWF), promotes proteolysis of its high-molecular-weight multimers, and produces a measurable defect in primary hemostasis. Multimer analysis, closure time with adenosine diphosphate (CT-ADP), and the VWF activity-to-antigen ratio therefore provide a biologic signal of abnormal flow rather than an anatomic image. Prospective studies show that VWF abnormalities track residual paravalvular regurgitation during transcatheter aortic valve replacement, occur with dysfunctional prostheses, change after mitral paravalvular-leak repair, and are associated with bleeding. The evidence nevertheless remains observational; most diagnostic cohorts are small and single-center, thresholds lack independent validation, assays are vulnerable to hematologic and preanalytic confounding, and no completed randomized trial has shown that VWF-guided management improves outcomes. VWF testing is best viewed as an investigational adjunct when imaging and the clinical picture are discordant or when prosthetic dysfunction coexists with otherwise unexplained bleeding. It should not replace guideline-directed echocardiography or be used for routine surveillance outside research protocols.
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Arshad et al. (2026) conducted a review in Prosthetic Valve Dysfunction. Von Willebrand factor biomarker testing was evaluated. Von Willebrand factor biomarker testing is an investigational adjunct for prosthetic valve dysfunction supported only by observational data and should not replace guideline-directed echocardiography.
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