Literature DB >> 27354149

The evolution of comprehensive haemophilia care in the United States: perspectives from the frontline.

L M Aledort1.   

Abstract

The establishment of dedicated comprehensive treatment centres more than a half century ago transformed the management of haemophilia in the United States. Formerly, a disease associated with crippling disability and premature death, today, persons with haemophilia who are treated appropriately from infancy and do not develop inhibitors can expect a normal life expectancy and relatively few bleeding episodes. The evolution of the comprehensive haemophilia care, while chastened by the viral epidemics of the 1980s, has been marked by ongoing advances, including prophylaxis, immune tolerance induction, new drugs and gene therapy research. Current challenges include sustaining the comprehensive care model despite decreased funding and expanding the delivery and affordability of comprehensive haemophilia care.
© 2016 John Wiley & Sons Ltd.

Entities:  

Keywords:  clotting factor concentrate; comprehensive care; haemophilia; haemophilia treatment centres; inhibitors

Mesh:

Substances:

Year:  2016        PMID: 27354149     DOI: 10.1111/hae.12970

Source DB:  PubMed          Journal:  Haemophilia        ISSN: 1351-8216            Impact factor:   4.287


  2 in total

1.  Tailoring of medical treatment: hemostasis and thrombosis towards precision medicine.

Authors:  Giovanni Di Minno; Elena Tremoli
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2.  Building access to care in adult sickle cell disease: defining models of care, essential components, and economic aspects.

Authors:  Julie Kanter; Wally R Smith; Payal C Desai; Marsha Treadwell; Biree Andemariam; Jane Little; Diane Nugent; Susan Claster; Deepa G Manwani; Judith Baker; John J Strouse; Ifeyinwa Osunkwo; Rosalyn W Stewart; Allison King; Lisa M Shook; John D Roberts; Sophie Lanzkron
Journal:  Blood Adv       Date:  2020-08-25
  2 in total

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