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Criteria for low von Willebrand factor diagnosis and risk score to predict future bleeding

BACKGROUND: Important diagnostic and clinical aspects of moderately reduced von Willebrand factor (VWF) levels are still unknown. There is no clear evidence which cutoff value (0.50 vs 0.60 IU/ml) should be used to diagnose “low VWF.” Also, the incidence of bleeding after the diagnosis has been made...

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Autores principales: Atiq, Ferdows, Wuijster, Esmee, de Maat, Moniek P.M., Kruip, Marieke J.H.A., Cnossen, Marjon H., Leebeek, Frank W.G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7986755/
https://www.ncbi.nlm.nih.gov/pubmed/33370487
http://dx.doi.org/10.1111/jth.15227
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author Atiq, Ferdows
Wuijster, Esmee
de Maat, Moniek P.M.
Kruip, Marieke J.H.A.
Cnossen, Marjon H.
Leebeek, Frank W.G.
author_facet Atiq, Ferdows
Wuijster, Esmee
de Maat, Moniek P.M.
Kruip, Marieke J.H.A.
Cnossen, Marjon H.
Leebeek, Frank W.G.
author_sort Atiq, Ferdows
collection PubMed
description BACKGROUND: Important diagnostic and clinical aspects of moderately reduced von Willebrand factor (VWF) levels are still unknown. There is no clear evidence which cutoff value (0.50 vs 0.60 IU/ml) should be used to diagnose “low VWF.” Also, the incidence of bleeding after the diagnosis has been made, and risk factors for bleeding are unknown yet. OBJECTIVES: To investigate the incidence of postsurgical bleeding, postpartum hemorrhage (PPH), and traumatic and spontaneous bleeding after low VWF diagnosis, and to develop a risk score to predict future bleeding. METHODS: We performed a cohort study in patients with historically lowest VWF levels of 0.31 to 0.60 IU/ml. Clinical data of patients were retrospectively collected. RESULTS: We included 439 patients with low VWF. During a follow‐up of 6.3 ± 3.7 years, 259 surgical procedures, 81 deliveries, and 109 spontaneous and traumatic bleeding episodes were reported. The incidence of postsurgical bleeding was 2.7%, whereas 10% of deliveries was complicated by PPH. Overall, 65 patients (14.8%) had bleeding requiring treatment, which was not different between patients with historically lowest VWF levels of 0.31–0.50 and 0.51–0.60 IU/ml (p = .154). Age <18 years, abnormal bleeding score at diagnosis, and being referred for bleeding symptoms at the time of diagnosis were independent risk factors for bleeding during follow‐up, and therefore included in the risk score. CONCLUSIONS: The cutoff value of low VWF diagnosis should be set at 0.60 IU/ml. Furthermore, a risk score is developed to identify individuals with a high risk for bleeding after low VWF diagnosis.
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spelling pubmed-79867552021-03-25 Criteria for low von Willebrand factor diagnosis and risk score to predict future bleeding Atiq, Ferdows Wuijster, Esmee de Maat, Moniek P.M. Kruip, Marieke J.H.A. Cnossen, Marjon H. Leebeek, Frank W.G. J Thromb Haemost HAEMOSTASIS BACKGROUND: Important diagnostic and clinical aspects of moderately reduced von Willebrand factor (VWF) levels are still unknown. There is no clear evidence which cutoff value (0.50 vs 0.60 IU/ml) should be used to diagnose “low VWF.” Also, the incidence of bleeding after the diagnosis has been made, and risk factors for bleeding are unknown yet. OBJECTIVES: To investigate the incidence of postsurgical bleeding, postpartum hemorrhage (PPH), and traumatic and spontaneous bleeding after low VWF diagnosis, and to develop a risk score to predict future bleeding. METHODS: We performed a cohort study in patients with historically lowest VWF levels of 0.31 to 0.60 IU/ml. Clinical data of patients were retrospectively collected. RESULTS: We included 439 patients with low VWF. During a follow‐up of 6.3 ± 3.7 years, 259 surgical procedures, 81 deliveries, and 109 spontaneous and traumatic bleeding episodes were reported. The incidence of postsurgical bleeding was 2.7%, whereas 10% of deliveries was complicated by PPH. Overall, 65 patients (14.8%) had bleeding requiring treatment, which was not different between patients with historically lowest VWF levels of 0.31–0.50 and 0.51–0.60 IU/ml (p = .154). Age <18 years, abnormal bleeding score at diagnosis, and being referred for bleeding symptoms at the time of diagnosis were independent risk factors for bleeding during follow‐up, and therefore included in the risk score. CONCLUSIONS: The cutoff value of low VWF diagnosis should be set at 0.60 IU/ml. Furthermore, a risk score is developed to identify individuals with a high risk for bleeding after low VWF diagnosis. John Wiley and Sons Inc. 2021-01-24 2021-03 /pmc/articles/PMC7986755/ /pubmed/33370487 http://dx.doi.org/10.1111/jth.15227 Text en © 2021 The Authors. Journal of Thrombosis and Haemostasis published by Wiley Periodicals LLC on behalf of International Society on Thrombosis and Haemostasis. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle HAEMOSTASIS
Atiq, Ferdows
Wuijster, Esmee
de Maat, Moniek P.M.
Kruip, Marieke J.H.A.
Cnossen, Marjon H.
Leebeek, Frank W.G.
Criteria for low von Willebrand factor diagnosis and risk score to predict future bleeding
title Criteria for low von Willebrand factor diagnosis and risk score to predict future bleeding
title_full Criteria for low von Willebrand factor diagnosis and risk score to predict future bleeding
title_fullStr Criteria for low von Willebrand factor diagnosis and risk score to predict future bleeding
title_full_unstemmed Criteria for low von Willebrand factor diagnosis and risk score to predict future bleeding
title_short Criteria for low von Willebrand factor diagnosis and risk score to predict future bleeding
title_sort criteria for low von willebrand factor diagnosis and risk score to predict future bleeding
topic HAEMOSTASIS
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7986755/
https://www.ncbi.nlm.nih.gov/pubmed/33370487
http://dx.doi.org/10.1111/jth.15227
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