Literature DB >> 24009969

Evaluation of inhibitor antibody in hemophiliaA population.

Hassan Mahmoodi Nesheli1, Amereh Hadizadeh, Ali Bijani.   

Abstract

BACKGROUND: Inhibitor antibody to exogenous Factor VIII (FVIII) is a major complication of hemophilia treatment. This study was conducted to determine the prevalence of inhibitor antibody directed against FVIII.
METHODS: From May 2010 to May 2011, 52 patients with severe hemophilia A admitted in Amirkola Children's Hospital were evaluated. Those who had abnormal mixing study, antibody against FVIII were measured. Data were collected and analyzed.
RESULTS: The age range of the patients was 4-60 years. The inhibitor antibody was seen in 9 (17.3%) patients. The mean age of patients with inhibitor at the time of diagnosis was 10.22 years (ranged 4-31 years). Old patients had more hemarthrosis than young patients. The mean level of inhibitor antibody was 8.47 Bethesda unit (ranged 2.3-29). Six patients had inhibitor antibody level ≥5 Bethesda unit and three patients had inhibitor antibody level <5 Bethesda unit.
CONCLUSION: This study showed that the prevalence of inhibitor antibodies in young patients is more than the old patients.

Entities:  

Keywords:  Hemarthrosis; Inhibitory antibody; concentrated FVIII; hemophilia A

Year:  2013        PMID: 24009969      PMCID: PMC3755836     

Source DB:  PubMed          Journal:  Caspian J Intern Med        ISSN: 2008-6164


  21 in total

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Authors:  F Rosner
Journal:  Ann Intern Med       Date:  1969-04       Impact factor: 25.391

2.  Production of factor VIII deficient plasma by immunodepletion using three monoclonal antibodies.

Authors:  T Takase; F Rotblat; A H Goodall; P B Kernoff; S Middleton; S Chand; K W Denson; D E Austen; E G Tuddenham
Journal:  Br J Haematol       Date:  1987-08       Impact factor: 6.998

3.  An analysis of factors affecting the incidence of inhibitor formation in patients with congenital haemophilia in Japan.

Authors:  A Shirahata; K Fukutake; S Higasa; J Mimaya; T Oka; M Shima; J Takamatsu; M Taki; M Taneichi; A Yoshioka
Journal:  Haemophilia       Date:  2011-06-20       Impact factor: 4.287

4.  Risk of inhibitor development in mild haemophilia A increases with age.

Authors:  E P Mauser-Bunschoten; I E M Den Uijl; R E G Schutgens; G Roosendaal; K Fischer
Journal:  Haemophilia       Date:  2011-08-19       Impact factor: 4.287

5.  Low incidence of factor VIII inhibitors in previously untreated patients during prophylaxis, on-demand treatment and surgical procedures, with Octanate®: interim report from an ongoing prospective clinical study.

Authors:  A Klukowska; V Komrska; M Jansen; P Laguna
Journal:  Haemophilia       Date:  2010-12-01       Impact factor: 4.287

6.  Influence of the type of factor VIII concentrate on the incidence of factor VIII inhibitors in previously untreated patients with severe hemophilia A.

Authors:  Jenny Goudemand; Chantal Rothschild; Virginie Demiguel; Christine Vinciguerrat; Thierry Lambert; Hervé Chambost; Annie Borel-Derlon; Ségolène Claeyssens; Yves Laurian; Thierry Calvez
Journal:  Blood       Date:  2005-09-15       Impact factor: 22.113

7.  Alloantibodies to factor VIII in haemophilia.

Authors:  A Zakarija; S Harris; A W Rademaker; J Brewer; J Krudysz-Amblo; S Butenas; K G Mann; D Green
Journal:  Haemophilia       Date:  2011-02-07       Impact factor: 4.287

8.  Home treatment of haemarthroses using a single dose regimen of recombinant activated factor VII in patients with haemophilia and inhibitors. A multi-centre, randomised, double-blind, cross-over trial.

Authors:  Khan Kavakli; Mike Makris; Bulent Zulfikar; Elizabeth Erhardtsen; Zvi S Abrams; Gili Kenet
Journal:  Thromb Haemost       Date:  2006-04       Impact factor: 5.249

Review 9.  Italian guidelines for the diagnosis and treatment of patients with haemophilia and inhibitors.

Authors:  A Gringeri; P M Mannucci
Journal:  Haemophilia       Date:  2005-11       Impact factor: 4.287

10.  Severe and moderate hemophilia A: identification of 38 new genetic alterations.

Authors:  Pilar Casaña; Noelia Cabrera; Ana Rosa Cid; Saturnino Haya; Magdalena Beneyto; Carmen Espinós; Vicente Cortina; Maria Angeles Dasí; Josè Antonio Aznar
Journal:  Haematologica       Date:  2008-04-09       Impact factor: 9.941

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