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Natural history study of factor IX deficiency with focus on treatment and complications (B-Natural)

Shapiro, Amy D. (författare)
Indiana Hemophilia and Thrombosis Center
Ragni, Margaret V. (författare)
University of Pittsburgh
Borhany, Munira (författare)
National Institute of Blood Disease and Bone Marrow Transplantation
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Abajas, Yasmina L. (författare)
University of North Carolina
Tarantino, Michael D. (författare)
Bleeding and Clotting Disorders Institute, Peoria
Holstein, Katharina (författare)
University Medical Center Hamburg-Eppendorf
Croteau, Stacy E. (författare)
Boston Children's Hospital
Liesner, Riana (författare)
Great Ormond Street Hospital
Tarango, Cristina (författare)
University of Cincinnati College of Medicine
Carvalho, Manuela (författare)
Sao Joao Hospital
McGuinn, Catherine (författare)
Weill Cornell Medical College
Funding, Eva (författare)
Copenhagen University Hospital
Kempton, Christine L. (författare)
Emory University
Bidlingmaier, Christoph (författare)
University Hospital Munich
Cohen, Alice (författare)
Newark Beth Israel Medical Center
Oldenburg, Johannes (författare)
University Hospital Bonn
Kearney, Susan (författare)
Children's Minnesota Center for Bleeding and Clotting Disorders
Knoll, Christine (författare)
Phoenix Children’s Hospital
Kuriakose, Philip (författare)
Henry Ford Health System
Acharya, Suchitra (författare)
Northwell Haemostasis and Thrombosis Centre
Reiss, Ulrike M. (författare)
St Jude Children´s Research Hospital, Memphis
Kulkarni, Roshni (författare)
Michigan State University
Witkop, Michelle (författare)
Munson Medical Center
Lethagen, Stefan (författare)
Swedish Orphan Biovitrum
Donfield, Sharyne (författare)
Rho, Inc.
LeBeau, Petra (författare)
Rho, Inc.
Berntorp, Erik (författare)
Lund University,Lunds universitet,Klinisk koagulationsmedicin, Malmö,Forskargrupper vid Lunds universitet,Clinical Coagulation, Malmö,Lund University Research Groups
Astermark, Jan (författare)
Lund University,Lunds universitet,Klinisk koagulationsmedicin, Malmö,Forskargrupper vid Lunds universitet,Clinical Coagulation, Malmö,Lund University Research Groups,Skåne University Hospital
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 (creator_code:org_t)
2020-12-05
2021
Engelska 11 s.
Ingår i: Haemophilia. - : Wiley. - 1351-8216 .- 1365-2516. ; 27:1, s. 49-59
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • Introduction: Haemophilia B (HB) is less well studied than haemophilia A (HA); despite similarities between the two inherited bleeding disorders, important differences remain that require further research. Aim: B-Natural is a multi-centre, prospective, observational study of HB, designed to increase understanding of clinical manifestations, treatment, quality-of-life (QoL), inhibitor development, immune tolerance induction (ITI) outcome, renal function and create a biorepository for future investigations. Methods: Participants include sibling pairs/groups without a current/history of inhibitors and singletons or siblings with a current/history of inhibitors followed for six months. Demographics, medical, social history and treatment were recorded. A physical examination including joint range of motion (ROM) was performed; QoL was assessed. Samples were collected for F9 gene mutation, HLA typing, non-inhibitory antibodies and renal function testing. Results: Twenty-four centres enrolled 224 individuals from 107 families including 29 with current/history of inhibitors. Of these, 68, 30.4%, had severe (<1% FIX level of normal); 114, 50.9%, moderate (1%-5%); and 42, 18.8%, mild (>5-<40%) disease. At enrolment, 53.1% had 50 + exposure days to exogenous FIX. Comparison of joint scores showed significant (P <.05) differences between those with severe (with/without inhibitors), and those with moderate/mild disease. The majority with severe disease, 80.0% with current/history of inhibitors and 64.3% of those without, were treated with prophylaxis. Conclusion: B-Natural provides data supporting an increased understanding of HB and its impact throughout life. The need for optimal disease control to normalize physical and psychosocial outcomes is underscored, and further analyses will contribute to an increased understanding of critical issues in HB.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Hematologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Hematology (hsv//eng)

Nyckelord

factor IX deficiency
FIX inhibitors
haemophilia B
joint range-of-motion
quality-of-life
treatment

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