Literature DB >> 3103425

Incidence of inhibitors in patients with severe and moderate hemophilia A treated with factor VIII concentrates.

I Schwarzinger, I Pabinger, C Korninger, F Haschke, M Kundi, H Niessner, K Lechner.   

Abstract

Recent data published on the prevalence of inhibitors to factor VIII in hemophiliacs on treatment show great variations, with prevalence rates ranging from 3.6 to 14.2%. We have studied the cumulative risk of inhibitor development in a cohort of 62 patients with hemophilia A. All patients were born after 1960, were natives of the Vienna area, had a factor VIII activity of less than 5%, and were treated at least once. Using the method of Cutler and Ederer, the cumulative risk of inhibitor development was found to be 24% at the age of 25 years. Most inhibitors developed between the ages of 3 and 7 years. The current prevalence of F VIII inhibitors in the group of patients studied is 17.5%. It is concluded that prevalence data underestimate the true risk of inhibitor development.

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Year:  1987        PMID: 3103425     DOI: 10.1002/ajh.2830240303

Source DB:  PubMed          Journal:  Am J Hematol        ISSN: 0361-8609            Impact factor:   10.047


  8 in total

Review 1.  Hemophilia treatment in historical perspective: a review of medical and social developments.

Authors:  F R Rosendaal; C Smit; E Briët
Journal:  Ann Hematol       Date:  1991-02       Impact factor: 3.673

2.  Healthy subjects produce both anti-factor VIII and specific anti-idiotypic antibodies.

Authors:  J G Gilles; J M Saint-Remy
Journal:  J Clin Invest       Date:  1994-10       Impact factor: 14.808

Review 3.  Inhibitor questions: plasma-derived factor VIII and recombinant factor VIII.

Authors:  G Bray
Journal:  Ann Hematol       Date:  1994       Impact factor: 3.673

4.  Tolerance to factor VIII inhibitors in hemophilia A patients: a French twist.

Authors:  V Pascual; J D Capra
Journal:  J Clin Invest       Date:  1996-03-15       Impact factor: 14.808

5.  The molecular genetic analysis of haemophilia A; characterization of six partial deletions in the factor VIII gene.

Authors:  D S Millar; R A Steinbrecher; K Wieland; C B Grundy; U Martinowitz; M Krawczak; B Zoll; D Whitmore; J Stephenson; R S Mibashan
Journal:  Hum Genet       Date:  1990-12       Impact factor: 4.132

6.  Clinical evaluation of a recombinant factor VIII preparation (Kogenate) in previously untreated patients with hemophilia A.

Authors:  A Yoshioka; K Fukutake; J Takamatsu; A Shirahata
Journal:  Int J Hematol       Date:  2003-12       Impact factor: 2.490

7.  Neutralizing antiidiotypic antibodies to factor VIII inhibitors after desensitization in patients with hemophilia A.

Authors:  J G Gilles; B Desqueper; H Lenk; J Vermylen; J M Saint-Remy
Journal:  J Clin Invest       Date:  1996-03-15       Impact factor: 14.808

8.  The prevalence of anti-factor VIII and anti-factor IX antibodies among patients with hemophilia in Rabat, Morocco: a single center experience.

Authors:  Meryem Bouyadmar; Mohamed El Khorassani; Maria El Kababri; Amina Kili; Laila Hessissen
Journal:  Pan Afr Med J       Date:  2022-02-14
  8 in total

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