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Bleeding Symptoms and von Willebrand Factor Levels: 30-Year Experience in a Tertiary Care Center

Correlations between bleeding symptoms and von Willebrand factor (VWF) levels may help to predict hemorrhagic severity in the Westerners with von Willebrand disease (VWD), but data in Asians are lacking. In this study, Thai patients with VWF levels <50 IU/dL without any secondary causes were enro...

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Autores principales: Moonla, Chatphatai, Akkawat, Benjaporn, Kittikalayawong, Yaowaree, Sukperm, Autcharaporn, Meesanun, Mukmanee, Uaprasert, Noppacharn, Sosothikul, Darintr, Rojnuckarin, Ponlapat
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6829631/
https://www.ncbi.nlm.nih.gov/pubmed/31359769
http://dx.doi.org/10.1177/1076029619866916
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author Moonla, Chatphatai
Akkawat, Benjaporn
Kittikalayawong, Yaowaree
Sukperm, Autcharaporn
Meesanun, Mukmanee
Uaprasert, Noppacharn
Sosothikul, Darintr
Rojnuckarin, Ponlapat
author_facet Moonla, Chatphatai
Akkawat, Benjaporn
Kittikalayawong, Yaowaree
Sukperm, Autcharaporn
Meesanun, Mukmanee
Uaprasert, Noppacharn
Sosothikul, Darintr
Rojnuckarin, Ponlapat
author_sort Moonla, Chatphatai
collection PubMed
description Correlations between bleeding symptoms and von Willebrand factor (VWF) levels may help to predict hemorrhagic severity in the Westerners with von Willebrand disease (VWD), but data in Asians are lacking. In this study, Thai patients with VWF levels <50 IU/dL without any secondary causes were enrolled from 1988 to 2018 to determine the relationship between VWF levels and hemorrhagic manifestations. According to the current concept, we reclassified VWD and low VWF by VWF levels ≤30 and 30 to 50 IU/dL, respectively. Type 2 VWD was diagnosed if VWF activity to antigen ratio was ≤0.6. Bleeding severity was determined by the condensed MCMDM-1VWD bleeding score (BS). Among 83 patients, VWF activities showed negative correlations with BS (P = .001), which were higher in type 2 (median: 7, interquartile range [IQR]: 5-11) compared with type 1 VWD (median: 3, IQR: 2-4) and low VWF (median: 4, IQR: 2-8). Bleeding symptoms were indistinguishable between type 1 VWD and low VWF using the 30 IU/dL cutoff point. However, VWF ristocetin cofactor activity or gain-of-function mutant glycoprotein Ib binding activity <36.5 IU/dL and VWF collagen binding activity <34.5 IU/dL could predict increased bleeding risk (BS ≥3) by 92.3% specificity and 70.0% sensitivity (P < .0001).
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spelling pubmed-68296312019-11-07 Bleeding Symptoms and von Willebrand Factor Levels: 30-Year Experience in a Tertiary Care Center Moonla, Chatphatai Akkawat, Benjaporn Kittikalayawong, Yaowaree Sukperm, Autcharaporn Meesanun, Mukmanee Uaprasert, Noppacharn Sosothikul, Darintr Rojnuckarin, Ponlapat Clin Appl Thromb Hemost Original Article Correlations between bleeding symptoms and von Willebrand factor (VWF) levels may help to predict hemorrhagic severity in the Westerners with von Willebrand disease (VWD), but data in Asians are lacking. In this study, Thai patients with VWF levels <50 IU/dL without any secondary causes were enrolled from 1988 to 2018 to determine the relationship between VWF levels and hemorrhagic manifestations. According to the current concept, we reclassified VWD and low VWF by VWF levels ≤30 and 30 to 50 IU/dL, respectively. Type 2 VWD was diagnosed if VWF activity to antigen ratio was ≤0.6. Bleeding severity was determined by the condensed MCMDM-1VWD bleeding score (BS). Among 83 patients, VWF activities showed negative correlations with BS (P = .001), which were higher in type 2 (median: 7, interquartile range [IQR]: 5-11) compared with type 1 VWD (median: 3, IQR: 2-4) and low VWF (median: 4, IQR: 2-8). Bleeding symptoms were indistinguishable between type 1 VWD and low VWF using the 30 IU/dL cutoff point. However, VWF ristocetin cofactor activity or gain-of-function mutant glycoprotein Ib binding activity <36.5 IU/dL and VWF collagen binding activity <34.5 IU/dL could predict increased bleeding risk (BS ≥3) by 92.3% specificity and 70.0% sensitivity (P < .0001). SAGE Publications 2019-07-30 /pmc/articles/PMC6829631/ /pubmed/31359769 http://dx.doi.org/10.1177/1076029619866916 Text en © The Author(s) 2019 http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Original Article
Moonla, Chatphatai
Akkawat, Benjaporn
Kittikalayawong, Yaowaree
Sukperm, Autcharaporn
Meesanun, Mukmanee
Uaprasert, Noppacharn
Sosothikul, Darintr
Rojnuckarin, Ponlapat
Bleeding Symptoms and von Willebrand Factor Levels: 30-Year Experience in a Tertiary Care Center
title Bleeding Symptoms and von Willebrand Factor Levels: 30-Year Experience in a Tertiary Care Center
title_full Bleeding Symptoms and von Willebrand Factor Levels: 30-Year Experience in a Tertiary Care Center
title_fullStr Bleeding Symptoms and von Willebrand Factor Levels: 30-Year Experience in a Tertiary Care Center
title_full_unstemmed Bleeding Symptoms and von Willebrand Factor Levels: 30-Year Experience in a Tertiary Care Center
title_short Bleeding Symptoms and von Willebrand Factor Levels: 30-Year Experience in a Tertiary Care Center
title_sort bleeding symptoms and von willebrand factor levels: 30-year experience in a tertiary care center
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6829631/
https://www.ncbi.nlm.nih.gov/pubmed/31359769
http://dx.doi.org/10.1177/1076029619866916
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