Literature DB >> 23557438

Haemophilia care in Europe - a survey of 35 countries.

B O'Mahony1, D Noone, P L F Giangrande, L Prihodova.   

Abstract

A questionnaire was circulated in 2012 to national haemophilia patient organizations in Europe affiliated to the European Haemophilia Consortium (EHC) and the World Federation of Hemophilia (WFH) to seek information about the organization of haemophilia care and treatment available at a national level. The 35 responses received highlighted major differences in the availability of treatment and care. There was a wide range in factor VIII consumption with usage ranging from 0.20 IU per capita in Armenia to 8.56 IU per capita in Sweden (median: IU per capita). The decrease in health budgets in many countries was not matched by decreases in use of FVIII per capita. In the 19 countries that responded to the previous survey, there was a significant improvement in access to prophylaxis and home treatment.
© 2013 John Wiley & Sons Ltd.

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Year:  2013        PMID: 23557438     DOI: 10.1111/hae.12125

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


  20 in total

Review 1.  The demand for factor VIII and for factor IX and the toll fractionation product surplus management.

Authors:  Gabriele Calizzani; Samantha Profili; Fabio Candura; Monica Lanzoni; Stefania Vaglio; Livia Cannata; Giancarlo M Liumbruno; Massimo Franchini; Pier Mannuccio Mannucci; Giuliano Grazzini
Journal:  Blood Transfus       Date:  2013-09       Impact factor: 3.443

2.  Tailoring care to haemophilia patients' needs: which specialty and when?

Authors:  Massimo Morfini; Gary Benson; Victor Jiménez-Yuste; Rolf Ljung; Pier Mannuccio Mannucci; Gianluigi Pasta; Eduardo Remor; Silva Zupančić Šalek
Journal:  Blood Transfus       Date:  2015-05-20       Impact factor: 3.443

Review 3.  Haemophilia Centre certification system across Europe: the Belgian experience.

Authors:  Cedric Hermans
Journal:  Blood Transfus       Date:  2014-04       Impact factor: 3.443

Review 4.  The European Haemophilia Network (EUHANET).

Authors:  Michael Makris; Gabriele Calizzani; Kathelijn Fischer; Alexander Gatt; Estelle Gilman; Robert Hollingsworth; Thierry Lambert; Riitta Lassila; Pier Mannuccio Mannucci; Flora Peyvandi; Jerzy Windyga
Journal:  Blood Transfus       Date:  2014-04       Impact factor: 3.443

5.  The European standards of Haemophilia Centres.

Authors:  Paul Giangrande; Gabriele Calizzani; Ivana Menichini; Fabio Candura; Pier Mannuccio Mannucci; Michael Makris
Journal:  Blood Transfus       Date:  2014-04       Impact factor: 3.443

6.  Social/economic costs and quality of life in patients with haemophilia in Europe.

Authors:  Marianna Cavazza; Yllka Kodra; Patrizio Armeni; Marta De Santis; Julio López-Bastida; Renata Linertová; Juan Oliva-Moreno; Pedro Serrano-Aguilar; Manuel Posada-de-la-Paz; Domenica Taruscio; Arrigo Schieppati; Georgi Iskrov; László Gulácsi; Johann Matthias Graf von der Schulenburg; Panos Kanavos; Karine Chevreul; Ulf Persson; Giovanni Fattore
Journal:  Eur J Health Econ       Date:  2016-04-05

Review 7.  Standardizing terms, definitions and concepts for describing and interpreting unwanted immunogenicity of biopharmaceuticals: recommendations of the Innovative Medicines Initiative ABIRISK consortium.

Authors:  B Rup; M Pallardy; D Sikkema; T Albert; M Allez; P Broet; C Carini; P Creeke; J Davidson; N De Vries; D Finco; A Fogdell-Hahn; E Havrdova; A Hincelin-Mery; M C Holland; P E H Jensen; E C Jury; H Kirby; D Kramer; S Lacroix-Desmazes; J Legrand; E Maggi; B Maillère; X Mariette; C Mauri; V Mikol; D Mulleman; J Oldenburg; G Paintaud; C R Pedersen; N Ruperto; R Seitz; S Spindeldreher; F Deisenhammer
Journal:  Clin Exp Immunol       Date:  2015-07-02       Impact factor: 4.330

8.  Persons with Haemophilia in Sweden- Experiences and Strategies in Everyday Life. A Single Centre Study.

Authors:  Elisabeth Brodin; Katharina S Sunnerhagen; Fariba Baghaei; Marie Törnbom
Journal:  PLoS One       Date:  2015-10-02       Impact factor: 3.240

9.  The health and economic burden of haemophilia in Belgium: a rare, expensive and challenging disease.

Authors:  Séverine Henrard; Brecht Devleesschauwer; Philippe Beutels; Michael Callens; Frank De Smet; Cedric Hermans; Niko Speybroeck
Journal:  Orphanet J Rare Dis       Date:  2014-03-21       Impact factor: 4.123

Review 10.  Systematic review on the evaluation criteria of orphan medicines in Central and Eastern European countries.

Authors:  Tamás Zelei; Mária J Molnár; Márta Szegedi; Zoltán Kaló
Journal:  Orphanet J Rare Dis       Date:  2016-06-04       Impact factor: 4.123

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