Circulation · 2000 · 158 citations · 40 references
MedicineCardiologyHematologyCardiothoracic SurgeryClinical CardiologyHemostasisAortic StenosisPlatelet ActivationPlatelet AggregationPlatelet FunctionPlatelet PhysiologyPrimary HemostasisPlatelet Aggregation DefectsPlatelet ClearancePlatelet HemostasisPlatelet-von Willebrand Factor InteractionsShear-induced Platelet AggregationVon Willebrand Factor FunctionVon Willebrand Factor InteractionsVon Willebrand Factor-platelet Interaction
BACKGROUND: Excessive bleeding may complicate congenital cardiac defects. To explain the pathogenesis of this abnormality, we evaluated selected parameters of primary hemostasis in patients with aortic valve stenosis before and after corrective surgery. METHODS AND RESULTS: We examined shear-induced platelet aggregation with the filter aggregometer test and von Willebrand factor (vWF) structure by evaluating the multimeric distribution and extent of subunit proteolysis. The platelet count was reduced before corrective surgery, and shear-induced platelet aggregation was impaired. Moreover, vWF multimers of higher molecular mass were decreased, and proteolytic subunit fragments were increased. After correction of the cardiac defect, all of these parameters returned to normal. CONCLUSIONS: Alterations of vWF and platelet function may contribute to the bleeding diathesis in patients with aortic valve stenosis. Improvement after corrective surgery suggests that the passage of blood through a stenosed aortic valve may result in shear forces that induce vWF interaction with platelets in the circulation and, in turn, trigger platelet clearance, vWF degradation, and the impairment of primary hemostasis.
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Epidemiological investigation of the prevalence of von Willebrand's disease
F Rodeghiero, Giancarlo Castaman, E Dini · Blood · 1987 · 1K citations · Full text
Medicine, Health Sciences, Pathology +11
Joel L. Moake, NA Turner, NA Stathopoulos et al. · Journal of Clinical Investigation · 1986 · 610 citations · Full text
Medicine, Cell Biology, Hematology +17