A new hemophilia carrier nomenclature to define hemophilia in women and girls: Communication from the SSC of the ISTH.
Karin P M van GalenRoseline d'OironPaula JamesRezan Abdul-KadirPeter A KouidesRoshni KulkarniJohnny N MahlanguMaha OthmanFlora PeyvandiDawn RotelliniRochelle WinikoffRobert F SidonioPublished in: Journal of thrombosis and haemostasis : JTH (2021)
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.
Keyphrases
- healthcare
- end stage renal disease
- polycystic ovary syndrome
- chronic kidney disease
- newly diagnosed
- ejection fraction
- pregnancy outcomes
- magnetic resonance imaging
- palliative care
- prognostic factors
- preterm infants
- mental health
- type diabetes
- early onset
- pregnant women
- gene expression
- quality improvement
- dna methylation
- pain management
- cervical cancer screening
- skeletal muscle
- health insurance
- chronic pain
- electronic health record
- patient reported outcomes
- genome wide
- drug induced
- dual energy
- contrast enhanced