Literature DB >> 30419589

Epidemiology and Treatment of Patients with Haemophilia in Austria-Update from the Austrian Haemophilia Registry.

Judit Rejtő1, Sylvia Reitter-Pfoertner1, Sylvia Kepa1, Clemens Feistritzer2, Michael Grundbichler3, Alexander Hörbst4, Neil Jones5, Wolfgang Muntean6, Peter Neumeister7, Stefan Oberbichler4, Gerhard Schuster8, Rudolf Schwarz9, Katharina Thom10, Karl Zwiauer11, Werner Streif12, Christoph Male10, Ingrid Pabinger1.   

Abstract

The Austrian Haemophilia Registry collects epidemiological data on patients with haemophilia, on treatment modalities and potential side effects. The Registry covers more than 85% of the assumed total number of haemophilia patients in Austria. This report summarizes data on 753 patients: 84.3% (635) have haemophilia A and 15.7% (118) have haemophilia B. Patients' median age is 34 years (range: 1-93 years). Of the total cohort, 39.0% (294) patients have severe haemophilia, 11.3% (85) moderate haemophilia, and 49.4% (372) mild haemophilia. Of the patients with severe haemophilia, 38.4% (113) have been infected with hepatitis C virus (HCV) and 12.6% (37) are human immunodeficiency virus (HIV) positive. Overall, 10.6% (67) of patients with haemophilia A and 1.7% (2) of those with haemophilia B have had an inhibitor in their history. Among patients with severe haemophilia, 68.4% (201) receive prophylaxis and 28.6% (84) receive on-demand therapy. There are 65.0% (191) patients with severe haemophilia who are treated with recombinant products. In conclusion, most patients with severe haemophilia receive prophylactic treatment. HCV and HIV infections are still important issues in the Austrian haemophilia population. Georg Thieme Verlag KG Stuttgart · New York.

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Year:  2018        PMID: 30419589     DOI: 10.1055/s-0038-1675354

Source DB:  PubMed          Journal:  Hamostaseologie        ISSN: 0720-9355            Impact factor:   1.778


  2 in total

1.  Influence of blood group, von Willebrand factor levels, and age on factor VIII levels in non-severe haemophilia A.

Authors:  Judit Rejtő; Oliver Königsbrügge; Ella Grilz; Stefanie Hofer; Lisa-Marie Mauracher; Cornelia Gabler; Gerhard Schuster; Clemens Feistritzer; Raute Sunder-Plaßmann; Peter Quehenberger; Johanna Gebhart; Cihan Ay; Ingrid Pabinger
Journal:  J Thromb Haemost       Date:  2020-03-20       Impact factor: 5.824

2.  Establishing an online physical exercise program for people with hemophilia.

Authors:  Barbara Wagner; Axel Seuser; Steffen Krüger; Marie Luca Herzig; Thomas Hilberg; Cihan Ay; Timothy Hasenöhrl; Richard Crevenna
Journal:  Wien Klin Wochenschr       Date:  2019-09-18       Impact factor: 1.704

  2 in total

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