@article{95ff196f0b604407880188724d79db18,
title = "A new hemophilia carrier nomenclature to define hemophilia in women and girls: Communication from the SSC of the ISTH",
abstract = "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.",
keywords = "bleeding, hemophilia, phenotype, women{\textquoteright}s health",
author = "{van Galen}, {Karin P.M.} and Roseline d{\textquoteright}Oiron and Paula James and Rezan Abdul-Kadir and Kouides, {Peter A.} and Roshni Kulkarni and Mahlangu, {Johnny N.} and Maha Othman and Flora Peyvandi and Dawn Rotellini and Rochelle Winikoff and Sidonio, {Robert F.}",
note = "Funding Information: The project was supported intellectually by the International Society on Thrombosis and Haemostasis Scientific and Standardization Committees on FVIII/IX & Rare Coagulation Disorders and Women{\textquoteright}s Health Issues in Thrombosis & Hemostasis. Specifically, we would like to thank Dr. Malinowski, Dr. Grandona, and Dr. Casais for their input and all other SSC co‐chairs for their support. There has been no commercial funding. Next to ISTH we{\textquoteright}d like to acknowledge the Coalition for Hemophilia B; National Hemophilia Foundation; Hemophilia Federation of America; European Association for Haemophilia and Allied Disorders Women and Bleeding Disorders Working group, specifically Michelle Lavin; the European Haemophilia Consortium; Association of Hemophilia Clinic Directors of Canada (AHCDC) and Canadian Hemophilia Society; women committee of the French Society for Hemophilia Patients (Association Fran{\c c}aise des H{\'e}mophiles); and Dutch Society for Hemophilia Patients for their contribution and support. Publisher Copyright: {\textcopyright} 2021 The Authors. Journal of Thrombosis and Haemostasis published by Wiley Periodicals LLC on behalf of International Society on Thrombosis and Haemostasis",
year = "2021",
month = aug,
doi = "10.1111/jth.15397",
language = "English",
volume = "19",
pages = "1883--1887",
journal = "Journal of Thrombosis and Haemostasis",
issn = "1538-7933",
publisher = "Wiley-Blackwell",
number = "8",
}