TY - JOUR
T1 - A new hemophilia carrier nomenclature to define hemophilia in women and girls
T2 - Communication from the SSC of the ISTH
AU - van Galen, Karin P.M.
AU - d’Oiron, Roseline
AU - James, Paula
AU - Abdul-Kadir, Rezan
AU - Kouides, Peter A.
AU - Kulkarni, Roshni
AU - Mahlangu, Johnny N.
AU - Othman, Maha
AU - Peyvandi, Flora
AU - Rotellini, Dawn
AU - Winikoff, Rochelle
AU - Sidonio, Robert F.
N1 - 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’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’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 Française des Hémophiles); and Dutch Society for Hemophilia Patients for their contribution and support.
Publisher Copyright:
© 2021 The Authors. Journal of Thrombosis and Haemostasis published by Wiley Periodicals LLC on behalf of International Society on Thrombosis and Haemostasis
PY - 2021/8
Y1 - 2021/8
N2 - 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.
AB - 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.
KW - bleeding
KW - hemophilia
KW - phenotype
KW - women’s health
UR - https://www.scopus.com/pages/publications/85111540679
U2 - 10.1111/jth.15397
DO - 10.1111/jth.15397
M3 - Article
C2 - 34327828
AN - SCOPUS:85111540679
SN - 1538-7933
VL - 19
SP - 1883
EP - 1887
JO - Journal of Thrombosis and Haemostasis
JF - Journal of Thrombosis and Haemostasis
IS - 8
ER -