Literature DB >> 19432921

Haemophilia in Spain.

J A Aznar1, F Lucía, L Abad-Franch, V Jiménez-Yuste, R Pérez, J Batlle, I Balda, R Parra, V R Cortina.   

Abstract

To determine the prevalence of haemophilia A and B and their complications in Spain, and to characterize the health care network providing support to haemophiliac patients. The study examines clinical and genetic characteristics, treatment options, and complications observed during the course of the disease. Cross-sectional multi-centre study. The study population were patients with HA and HB in active follow-up at any Spanish hospital by December 2006. We studied 2400 haemophiliacs, 2081 (86.7%) HA and 319 (13.3%) HB patients. Illness was severe in 32.3% of patients, moderate in 16.4%, and mild in 51.3%. Genetic screening was carried out in 32.6% of the patients. Treatment administered in 2006 consisted of coagulation factor concentrates in 60% of patients. Until December 2006, 45.8% of severely ill patients were taking prophylaxis. The mean number of bleeding episodes in 2006 was four for patients not receiving primary prophylaxis and 1.3 for those taking primary prophylaxis. Thirty percent of patients had established haemophiliac arthropathy in at least one joint; 16.8% of patients were HIV-infected and 34.8% HCV-infected. Inhibitors were detected in 10% of severe HA patients and in 6.5% of severe HB patients. Immune tolerance induction therapy was started in 34 patients. This is the first comprehensive study on the epidemiology of haemophilia in Spain. It will enable us to draw comparisons with neighbouring countries, to assess the quality of care provided to haemophiliacs in Spain, and to provide evidence-based guidance for the even provision and improvement of such care.

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Year:  2009        PMID: 19432921     DOI: 10.1111/j.1365-2516.2009.02001.x

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


  19 in total

1.  Ultrashort echo time quantitative susceptibility mapping (UTE-QSM) for detection of hemosiderin deposition in hemophilic arthropathy: A feasibility study.

Authors:  Hyungseok Jang; Annette von Drygalski; Jonathan Wong; Jenny Y Zhou; Peter Aguero; Xing Lu; Xin Cheng; Scott T Ball; Yajun Ma; Eric Y Chang; Jiang Du
Journal:  Magn Reson Med       Date:  2020-07-14       Impact factor: 4.668

2.  Vascular Permeability and Remodelling Coincide with Inflammatory and Reparative Processes after Joint Bleeding in Factor VIII-Deficient Mice.

Authors:  Esther J Cooke; Jenny Y Zhou; Tine Wyseure; Shweta Joshi; Vikas Bhat; Donald L Durden; Laurent O Mosnier; Annette von Drygalski
Journal:  Thromb Haemost       Date:  2018-05-30       Impact factor: 5.249

3.  TAFI deficiency causes maladaptive vascular remodeling after hemophilic joint bleeding.

Authors:  Tine Wyseure; Tingyi Yang; Jenny Y Zhou; Esther J Cooke; Bettina Wanko; Merissa Olmer; Ruchi Agashe; Yosuke Morodomi; Niels Behrendt; Martin Lotz; John Morser; Annette von Drygalski; Laurent O Mosnier
Journal:  JCI Insight       Date:  2019-10-03

4.  Etranacogene dezaparvovec (AMT-061 phase 2b): normal/near normal FIX activity and bleed cessation in hemophilia B.

Authors:  Annette Von Drygalski; Adam Giermasz; Giancarlo Castaman; Nigel S Key; Susan Lattimore; Frank W G Leebeek; Wolfgang Miesbach; Michael Recht; Alison Long; Robert Gut; Eileen K Sawyer; Steven W Pipe
Journal:  Blood Adv       Date:  2019-11-12

5.  Mechanisms of vascular permeability and remodeling associated with hemarthrosis in factor VIII-deficient mice.

Authors:  Esther J Cooke; Tine Wyseure; Jenny Y Zhou; Srila Gopal; Chanond A Nasamran; Kathleen M Fisch; Tina Manon-Jensen; Morten A Karsdal; Laurent O Mosnier; Annette von Drygalski
Journal:  J Thromb Haemost       Date:  2019-08-09       Impact factor: 5.824

6.  FVIII regulates the molecular profile of endothelial cells: functional impact on the blood barrier and macrophage behavior.

Authors:  Marie Cadé; Javier Muñoz-Garcia; Antoine Babuty; Louis Paré; Denis Cochonneau; Karim Fekir; Mathias Chatelais; Marie-Françoise Heymann; Anna Lokajczyk; Catherine Boisson-Vidal; Dominique Heymann
Journal:  Cell Mol Life Sci       Date:  2022-02-21       Impact factor: 9.261

7.  Vascular remodeling underlies rebleeding in hemophilic arthropathy.

Authors:  Vikas Bhat; Merissa Olmer; Shweta Joshi; Donald L Durden; Thomas J Cramer; Richard Fw Barnes; Scott T Ball; Tudor H Hughes; Mauricio Silva; James V Luck; Randy E Moore; Laurent O Mosnier; Annette von Drygalski
Journal:  Am J Hematol       Date:  2015-10-08       Impact factor: 10.047

Review 8.  Advances and challenges in hemophilic arthropathy.

Authors:  Tine Wyseure; Laurent O Mosnier; Annette von Drygalski
Journal:  Semin Hematol       Date:  2015-10-26       Impact factor: 3.851

9.  Treatment of hemophilia B: focus on recombinant factor IX.

Authors:  Massimo Franchini; Francesco Frattini; Silvia Crestani; Cinzia Sissa; Carlo Bonfanti
Journal:  Biologics       Date:  2013-02-12

10.  Defective TAFI activation in hemophilia A mice is a major contributor to joint bleeding.

Authors:  Tine Wyseure; Esther J Cooke; Paul J Declerck; Niels Behrendt; Joost C M Meijers; Annette von Drygalski; Laurent O Mosnier
Journal:  Blood       Date:  2018-07-19       Impact factor: 25.476

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