Literature DB >> 34480812

Women and girls with haemophilia receiving care at specialized haemophilia treatment centres in the United States.

Connie H Miller1,2, J Michael Soucie1,2, Vanessa R Byams1, Amanda B Payne1, Robert F Sidonio3, Tyler W Buckner4, Christopher J Bean1.   

Abstract

INTRODUCTION: Females may have haemophilia with the same factor VIII (FVIII) or factor IX (FIX) levels as affected males. Characterization of females with haemophilia would be useful for health care planning to meet their unique needs. Federally-funded haemophilia treatment centres (HTCs) in the United States contribute data on all individuals with bleeding disorders receiving care to the Population Profile (HTC PP) component of the Community Counts Public Health Surveillance of Bleeding Disorders project. AIMS: To estimate the number of females with haemophilia receiving care at HTCs in the United States and compare their characteristics with those of males with haemophilia.
METHODS: HTC PP data collected on people receiving care at an HTC from January 2012 through September 2020 with haemophilia A and B were evaluated by sex for demographic and clinical characteristics.
RESULTS: A factor level < 40% was reported for 23,196 males (97.8%) and 1667 females (47.6%) attending HTCs; 51 (.48%) severe, 79 (1.4%) moderate, and 1537 (17.9%) mild haemophilia patients were female. Females were older, more often White, and less often non-Hispanic than males. Females were less likely to have history of HIV or HCV infection, even among those with severe disease, but twice as likely to have infection status unknown. Females with mild haemophilia were more often uninsured than males.
CONCLUSIONS: Females with severe or moderate haemophilia are uncommon, even in specialized care centres; however, almost one in five patients with mild haemophilia was female, indicating needs for specialized care based on factor level and history for affected females.
© 2021 John Wiley & Sons Ltd. This article has been contributed to by US Government employees and their work is in the public domain in the USA.

Entities:  

Keywords:  factor IX; factor VIII; haemophilia A; haemophilia B

Mesh:

Substances:

Year:  2021        PMID: 34480812      PMCID: PMC8663793          DOI: 10.1111/hae.14403

Source DB:  PubMed          Journal:  Haemophilia        ISSN: 1351-8216            Impact factor:   4.263


  21 in total

1.  Hemophilia B: characterization of genetic variants and detection of carriers.

Authors:  C K Kasper; B Osterud; J Y Minami; W Shonick; S I Rapaport
Journal:  Blood       Date:  1977-09       Impact factor: 22.113

2.  Functional characterization of the 5'-regulatory region of human factor IX gene.

Authors:  J P Salier; S Hirosawa; K Kurachi
Journal:  J Biol Chem       Date:  1990-04-25       Impact factor: 5.157

3.  Clotting factor level is not a good predictor of bleeding in carriers of haemophilia A and B.

Authors:  Anna Olsson; Margareta Hellgren; Erik Berntorp; Rolf Ljung; Fariba Baghaei
Journal:  Blood Coagul Fibrinolysis       Date:  2014-07       Impact factor: 1.276

4.  Definitions in hemophilia: communication from the SSC of the ISTH.

Authors:  V S Blanchette; N S Key; L R Ljung; M J Manco-Johnson; H M van den Berg; A Srivastava
Journal:  J Thromb Haemost       Date:  2014-09-03       Impact factor: 5.824

5.  Carrier detection in hemophilia A: a cooperative international study. I. The carrier phenotype.

Authors:  J B Graham; C R Rizza; J Chediak; P M Mannucci; E Briët; R Ljung; C K Kasper; E M Essien; P P Green
Journal:  Blood       Date:  1986-06       Impact factor: 22.113

6.  Murine coagulation factor VIII is synthesized in endothelial cells.

Authors:  Lesley A Everett; Audrey C A Cleuren; Rami N Khoriaty; David Ginsburg
Journal:  Blood       Date:  2014-04-09       Impact factor: 22.113

7.  Bleeding in carriers of hemophilia.

Authors:  Iris Plug; Eveline P Mauser-Bunschoten; Annette H J T Bröcker-Vriends; Hans Kristian Ploos van Amstel; Johanna G van der Bom; Joanna E M van Diemen-Homan; José Willemse; Frits R Rosendaal
Journal:  Blood       Date:  2006-03-21       Impact factor: 22.113

8.  Severe and moderate haemophilia A and B in US females.

Authors:  D M Di Michele; C Gibb; J M Lefkowitz; Q Ni; L M Gerber; A Ganguly
Journal:  Haemophilia       Date:  2014-03       Impact factor: 4.287

9.  A conditional knockout mouse model reveals endothelial cells as the principal and possibly exclusive source of plasma factor VIII.

Authors:  Scot A Fahs; Matthew T Hille; Qizhen Shi; Hartmut Weiler; Robert R Montgomery
Journal:  Blood       Date:  2014-04-04       Impact factor: 22.113

10.  Community counts: Evolution of a national surveillance system for bleeding disorders.

Authors:  Marilyn J Manco-Johnson; Vanessa R Byams; Michael Recht; Becky Dudley; Brandi Dupervil; Diane J Aschman; Meredith Oakley; Suzanne Kapica; Mariam Voutsis; Steven Humes; Roshni Kulkarni; Althea M Grant
Journal:  Am J Hematol       Date:  2018-04-28       Impact factor: 10.047

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  1 in total

1.  Occurrence rates of inherited bleeding disorders other than haemophilia and von Willebrand disease among people receiving care in specialized treatment centres in the United States.

Authors:  Connie H Miller; J Michael Soucie; Vanessa R Byams; Amanda B Payne; Karon Abe; Magdalena Lewandowska; Amy D Shapiro
Journal:  Haemophilia       Date:  2022-03-04       Impact factor: 4.263

  1 in total

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