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A new hemophilia carrier nomenclature to define hemophilia in women and girls: Communication from the SSC of the ISTH

Hemophilia A and B predominantly attracts clinical attention in males due to X‐linked inheritance, introducing a bias toward female carriers to be asymptomatic. This common misconception is contradicted by an increasing body of evidence with consistent reporting on an increased bleeding tendency in...

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Autores principales: van Galen, Karin P. M., d’Oiron, Roseline, James, Paula, Abdul‐Kadir, Rezan, Kouides, Peter A., Kulkarni, Roshni, Mahlangu, Johnny N., Othman, Maha, Peyvandi, Flora, Rotellini, Dawn, Winikoff, Rochelle, Sidonio, Robert F.
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/PMC8361713/
https://www.ncbi.nlm.nih.gov/pubmed/34327828
http://dx.doi.org/10.1111/jth.15397
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author van Galen, Karin P. M.
d’Oiron, Roseline
James, Paula
Abdul‐Kadir, Rezan
Kouides, Peter A.
Kulkarni, Roshni
Mahlangu, Johnny N.
Othman, Maha
Peyvandi, Flora
Rotellini, Dawn
Winikoff, Rochelle
Sidonio, Robert F.
author_facet van Galen, Karin P. M.
d’Oiron, Roseline
James, Paula
Abdul‐Kadir, Rezan
Kouides, Peter A.
Kulkarni, Roshni
Mahlangu, Johnny N.
Othman, Maha
Peyvandi, Flora
Rotellini, Dawn
Winikoff, Rochelle
Sidonio, Robert F.
author_sort van Galen, Karin P. M.
collection PubMed
description Hemophilia A and B predominantly attracts clinical attention in males due to X‐linked inheritance, introducing a bias toward female carriers to be asymptomatic. This common misconception is contradicted by an increasing body of evidence with consistent reporting on an increased bleeding tendency in hemophilia carriers (HCs), including those with normal factor VIII/IX (FVIII/IX) levels. The term HC can hamper diagnosis, clinical care, and research. Therefore, a new nomenclature has been defined based on an open iterative process involving hemophilia experts, patients, and the International Society on Thrombosis and Haemostasis (ISTH) community. The resulting nomenclature accounts for personal bleeding history and baseline plasma FVIII/IX level. It distinguishes five clinically relevant HC categories: women/girls with mild, moderate, or severe hemophilia (FVIII/IX >0.05 and <0.40 IU/ml, 0.01–0.05 IU/ml, and <0.01 IU/ml, respectively), symptomatic and asymptomatic HC (FVIII/IX ≥0.40 IU/ml with and without a bleeding phenotype, respectively). This new nomenclature is aimed at improving diagnosis and management and applying uniform terminologies for clinical research.
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spelling pubmed-83617132021-08-17 A new hemophilia carrier nomenclature to define hemophilia in women and girls: Communication from the SSC of the ISTH van Galen, Karin P. M. d’Oiron, Roseline James, Paula Abdul‐Kadir, Rezan Kouides, Peter A. Kulkarni, Roshni Mahlangu, Johnny N. Othman, Maha Peyvandi, Flora Rotellini, Dawn Winikoff, Rochelle Sidonio, Robert F. J Thromb Haemost Isth Guidance and Guidelines Hemophilia A and B predominantly attracts clinical attention in males due to X‐linked inheritance, introducing a bias toward female carriers to be asymptomatic. This common misconception is contradicted by an increasing body of evidence with consistent reporting on an increased bleeding tendency in hemophilia carriers (HCs), including those with normal factor VIII/IX (FVIII/IX) levels. The term HC can hamper diagnosis, clinical care, and research. Therefore, a new nomenclature has been defined based on an open iterative process involving hemophilia experts, patients, and the International Society on Thrombosis and Haemostasis (ISTH) community. The resulting nomenclature accounts for personal bleeding history and baseline plasma FVIII/IX level. It distinguishes five clinically relevant HC categories: women/girls with mild, moderate, or severe hemophilia (FVIII/IX >0.05 and <0.40 IU/ml, 0.01–0.05 IU/ml, and <0.01 IU/ml, respectively), symptomatic and asymptomatic HC (FVIII/IX ≥0.40 IU/ml with and without a bleeding phenotype, respectively). This new nomenclature is aimed at improving diagnosis and management and applying uniform terminologies for clinical research. John Wiley and Sons Inc. 2021-07-29 2021-08 /pmc/articles/PMC8361713/ /pubmed/34327828 http://dx.doi.org/10.1111/jth.15397 Text en © 2021 The Authors. Journal of Thrombosis and Haemostasis published by Wiley Periodicals LLC on behalf of International Society on Thrombosis and Haemostasis https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Isth Guidance and Guidelines
van Galen, Karin P. M.
d’Oiron, Roseline
James, Paula
Abdul‐Kadir, Rezan
Kouides, Peter A.
Kulkarni, Roshni
Mahlangu, Johnny N.
Othman, Maha
Peyvandi, Flora
Rotellini, Dawn
Winikoff, Rochelle
Sidonio, Robert F.
A new hemophilia carrier nomenclature to define hemophilia in women and girls: Communication from the SSC of the ISTH
title A new hemophilia carrier nomenclature to define hemophilia in women and girls: Communication from the SSC of the ISTH
title_full A new hemophilia carrier nomenclature to define hemophilia in women and girls: Communication from the SSC of the ISTH
title_fullStr A new hemophilia carrier nomenclature to define hemophilia in women and girls: Communication from the SSC of the ISTH
title_full_unstemmed A new hemophilia carrier nomenclature to define hemophilia in women and girls: Communication from the SSC of the ISTH
title_short A new hemophilia carrier nomenclature to define hemophilia in women and girls: Communication from the SSC of the ISTH
title_sort new hemophilia carrier nomenclature to define hemophilia in women and girls: communication from the ssc of the isth
topic Isth Guidance and Guidelines
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8361713/
https://www.ncbi.nlm.nih.gov/pubmed/34327828
http://dx.doi.org/10.1111/jth.15397
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