Literature DB >> 1509398

Prevalence of inhibitors in a population of 3435 hemophilia patients in France. French Hemophilia Study Group.

Y Sultan1.   

Abstract

A cooperative study between the 37 centers of the French Hemophilia Study Group was undertaken to establish the prevalence of inhibitor patients in the French hemophilia population. The prevalence reported in the literature varies widely from 3.6% to 17.5%. Some of the studies are dealing with a small number of patients and inhibitor patients are reported either to the total number of hemophiliacs or to the severely affected ones. The French study provided information concerning 3,435 hemophiliacs and showed a prevalence of 6.2% for the overall population. Prevalence of inhibitors was found to be 7% in the population of hemophilia A patients and 12.8% in the population of severely affected ones. The prevalence of inhibitors in the population of hemophilia patients was 2% and 4% in the population of severely affected hemophilia B patients. The cooperative study also showed that 47.5% of inhibitors are detected before 10 years of age and that 82% of inhibitor patients are high responders. Analysis of inhibitor detection in patients under the age often showed that there was a peak in the population of 2 years old children. Although not comparable to the present study the high incidence of inhibitors with ultrapurified and recombinant FVIII reported in previously untransfused patient may be borne in mind.

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Year:  1992        PMID: 1509398

Source DB:  PubMed          Journal:  Thromb Haemost        ISSN: 0340-6245            Impact factor:   5.249


  24 in total

1.  Determinants of drug costs in hopitalised patients with haemophilia: impact of recombinant activated factor VII.

Authors:  Jean Philippe Galanaud; Nathalie Pelletier-Fleury; Hélène Logerot-Lebrun; Thierry Lambert
Journal:  Pharmacoeconomics       Date:  2003       Impact factor: 4.981

2.  Acquired inhibitors of clotting factors: AICE recommendations for diagnosis and management.

Authors:  Massimo Franchini; Giancarlo Castaman; Antonio Coppola; Cristina Santoro; Ezio Zanon; Giovanni Di Minno; Massimo Morfini; Elena Santagostino; Angiola Rocino
Journal:  Blood Transfus       Date:  2015-06-24       Impact factor: 3.443

3.  Plasma exchange and immunosuppressive therapy in a case of mild haemophilia A with inhibitors and a life-threatening lower limb haemorrhage.

Authors:  Chiara Ambaglio; Fabio Lodo; Alice Trinchero; Nicola Ghidelli; Cesare Perotti; Claudia Del Fante; Gabriella Gamba
Journal:  Blood Transfus       Date:  2013-01-02       Impact factor: 3.443

4.  A survey of the management of newborns with severe hemophilia in Canada.

Authors:  Paul C Moorehead; Jamie Ray; Nicholas J Barrowman; Brigitte Lemyre; Robert Klaassen
Journal:  Paediatr Child Health       Date:  2013-04       Impact factor: 2.253

5.  Inhibitor development in two patients with mild haemophilia A - spontaneous disappearance and no recurrence of the inhibitor after re-challenge.

Authors:  Sylvia Reitter-Pfoertner; Birgit Horvath; Klaus Lechner; Raute Sunder-Plassmann; Christine Mannhalter; Ingrid Pabinger
Journal:  Wien Klin Wochenschr       Date:  2012-01-18       Impact factor: 1.704

Review 6.  Alloantibodies in von Willebrand disease.

Authors:  Paula D James; David Lillicrap; Pier M Mannucci
Journal:  Blood       Date:  2013-01-07       Impact factor: 22.113

7.  The Epidemiology of FVIII Inhibitors in Indian Haemophilia A Patients.

Authors:  Patricia Pinto; Tejashree Shelar; Vidhya Nawadkar; Darshana Mirgal; Alfiya Mukaddam; Preethi Nair; Priyanka Kasatkar; Tejasvita Gaikwad; Shahnaz Ali; Anshul Jadli; Rucha Patil; Anita Parihar; Sharda Shanbhag; Bipin Kulkarni; Kanjaksha Ghosh; Shrimati Shetty
Journal:  Indian J Hematol Blood Transfus       Date:  2014-02-05       Impact factor: 0.900

Review 8.  Immune response to FVIII in hemophilia A: an overview of risk factors.

Authors:  Kanjaksha Ghosh; Shrimati Shetty
Journal:  Clin Rev Allergy Immunol       Date:  2009-10       Impact factor: 8.667

9.  Factor VIII inhibitors in hemophilia A: rationale and latest evidence.

Authors:  Char Witmer; Guy Young
Journal:  Ther Adv Hematol       Date:  2013-02

10.  Development of a transgenic mouse model with immune tolerance for human coagulation factor VIIa.

Authors:  Christine Lenk; Sabine Unterthurner; Maria Schuster; Markus Weiller; Gerhard Antoine; Mantas Malisauskas; Friedrich Scheiflinger; Hans-Peter Schwarz; Maurus de la Rosa; Birgit M Reipert
Journal:  Pharm Res       Date:  2013-06-18       Impact factor: 4.200

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