2012-09-01
Determinants of bleeding phenotype in adult patients with moderate or severe von Willebrand disease
Publication
Publication
Thrombosis and Haemostasis: international journal for vascular biology and medicine , Volume 108 - Issue 4 p. 683- 692
We performed a nation-wide cross-sectional study to evaluate determinants of bleeding symptoms in a large unselected cohort of adults with von Willebrand disease (VWD). VWD patients were included (n=664), based on lowest historically measured VWF:Ag and VWF:Act levels ≤30 U/dl. Menorrhagia (85%), cutaneous bleeding (77%), bleeding from minor wounds (77%) and oral-cavity bleeding (62%) occurred most frequently. Higher age was associated with a higher bleeding score (BS), determined according to Tosetto, in females. A 10 year increase in age was associated with 0.8 point (95% confidence interval [CI] 0.4-1.1) higher BS. Females had higher BS than males (median 12 vs. 10, p=0.012). BS differed significantly between VWD type 1, 2 and 3: median 9 (-2-31), 13 (-1-33) and 19.5 (1-35), respectively (p<0.001). BS was strongly associated with VWF and FVIII levels: individuals with VWF:Ag levels ≤10 IU/dl, VWF:Act ≤10 IU/dl and FVIII:C ≤10 IU/dl had, respectively, 5.3 point (95%CI 3.2-7.3), 4.3 point (95%CI 2.9-5.8) and 9.6 point (95%CI 6.5-12.7) higher BS, than those with levels >30 IU/dl. In type 3 patients 1 IU/dl FVIII:C decrease was associated with 0.6 point (95% CI 0.1-1.1) BS increase (p=0.021). In conclusion, in VWD patients the bleeding phenotype is strongly associated with type of VWD and VWF and FVIII levels.
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doi.org/10.1160/TH12-04-0244, hdl.handle.net/1765/75142 | |
Thrombosis and Haemostasis: international journal for vascular biology and medicine | |
Organisation | Department of Pediatrics |
de Wee, E., Sanders, Y., Mauser-Bunschoten, E., van der Bom, A., Degenaar-Dujardin, M. E. L., Eikenboom, J., … Leebeek, F. (2012). Determinants of bleeding phenotype in adult patients with moderate or severe von Willebrand disease. Thrombosis and Haemostasis: international journal for vascular biology and medicine, 108(4), 683–692. doi:10.1160/TH12-04-0244 |