Literature DB >> 24762268

Haemophilia care - beyond the treatment guidelines.

A Srivastava1.   

Abstract

Care for people with haemophilia (PWH) has improved much over the last two decades leading to near normal lives for those receiving early regular prophylaxis with clotting factor concentrates (CFC). Yet, there are significant limitations of those practices. In the absence of a well-defined optimal prophylaxis protocol, there are wide variations in practices with a two to threefold difference in doses. In those parts of the world where there are constraints on the availability of CFC, episodic replacement remains the norm for most patients even though it is evident that this does not change the natural history of the disease over a wide range of doses. Suitable prophylactic protocols therefore need to be developed wherever possible at these doses. Finally, there are only limited data on long-term outcomes in haemophilia from anywhere in the world. The practice of documenting specific outcomes as part of the regular evaluation of PWH needs to be established and the appropriate instruments used to assess them. Definitions of clinical events and endpoints of interventions in clinical studies are being developed to help such data collection. The correlations between different replacement therapy protocols and specific outcomes will help define what is best at different dose levels. Such data will allow better health planning and treatment choices throughout the world.
© 2014 John Wiley & Sons Ltd.

Entities:  

Keywords:  assessment; doses; haemophilia; optimal; outcomes; prophylaxis

Mesh:

Substances:

Year:  2014        PMID: 24762268     DOI: 10.1111/hae.12429

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


  8 in total

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2.  "la synoviorthèse" can more than synovitis!

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Journal:  Int J Hematol       Date:  2018-05-08       Impact factor: 2.490

4.  Abnormal joint and bone wound healing in hemophilia mice is improved by extending factor IX activity after hemarthrosis.

Authors:  Junjiang Sun; Baolai Hua; Eric W Livingston; Sarah Taves; Peter B Johansen; Maureane Hoffman; Mirella Ezban; Dougald M Monroe; Ted A Bateman; Paul E Monahan
Journal:  Blood       Date:  2016-12-30       Impact factor: 22.113

Review 5.  Damoctocog Alfa Pegol: A Review in Haemophilia A.

Authors:  Julia Paik; Emma D Deeks
Journal:  Drugs       Date:  2019-07       Impact factor: 9.546

6.  Construct validity of patient-reported outcome instruments in US adults with hemophilia: results from the Pain, Functional Impairment, and Quality of life (P-FiQ) study.

Authors:  Katharine Batt; Michael Recht; David L Cooper; Neeraj N Iyer; Christine L Kempton
Journal:  Patient Prefer Adherence       Date:  2017-08-09       Impact factor: 2.711

Review 7.  Lonoctocog Alfa: A Review in Haemophilia A.

Authors:  Zaina T Al-Salama; Lesley J Scott
Journal:  Drugs       Date:  2017-10       Impact factor: 9.546

8.  Clot stability as a determinant of effective factor VIII replacement in hemophilia A.

Authors:  L Leong; I N Chernysh; Y Xu; D Sim; C Nagaswami; Z de Lange; S Kosolapova; A Cuker; K Kauser; J W Weisel
Journal:  Res Pract Thromb Haemost       Date:  2017-08-10
  8 in total

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