Literature DB >> 6430366

The treatment of haemophilia A inhibitor with high dose intravenous immunoglobulin.

E Seifried, G Gaedicke, G Pindur, H Rasche.   

Abstract

In patients with Haemophilia A, the development of inhibitor is a life-threatening complication of treatment. These patients are at high risk for dangerous bleeding as a result of this acquired resistance to human Factor VIII concentrate. Although treatment of bleeding complications has been improved with the introduction of an activated prothrombin complex preparation, therapy remains unsatisfactory. Two patients with Haemophilia A inhibitor were treated with high dose intravenous immunoglobulin in the expectation of an immunosuppressive effect. A rise in the antibody titre at the same time as the administration of factor VIII concentrate showed that this treatment was ineffective in patients with Haemophilia A inhibitor.

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Year:  1984        PMID: 6430366     DOI: 10.1007/bf00319971

Source DB:  PubMed          Journal:  Blut        ISSN: 0006-5242


  14 in total

1.  Letter: A more uniform measurement of factor VIII inhibitors.

Authors: 
Journal:  Thromb Diath Haemorrh       Date:  1975-12-15

2.  Suppression of factor VIII antibody by combined factor VIII and cyclophosphamide.

Authors:  I M Nilsson; U Hedner; L Holmberg
Journal:  Acta Med Scand       Date:  1974 Jan-Feb

3.  Incidence and course of inhibitors among patients with classic hemophilia.

Authors:  C K Kasper
Journal:  Thromb Diath Haemorrh       Date:  1973-11

4.  Impaired cell-mediated immunity in patients with classic hemophilia.

Authors:  M M Lederman; O D Ratnoff; J J Scillian; P K Jones; B Schacter
Journal:  N Engl J Med       Date:  1983-01-13       Impact factor: 91.245

5.  Characterization of factor VIII antibodies.

Authors:  S S Shapiro
Journal:  Ann N Y Acad Sci       Date:  1975-01-20       Impact factor: 5.691

Review 6.  Chronic idiopathic thrombocytopenic purpura.

Authors:  R McMillan
Journal:  N Engl J Med       Date:  1981-05-07       Impact factor: 91.245

7.  Treatment of anti-factor VIII antibodies.

Authors:  P M Blatt; G C White; C W McMillan; H R Roberts
Journal:  Thromb Haemost       Date:  1977-08-31       Impact factor: 5.249

8.  High-dose intravenous gammaglobulin for idiopathic thrombocytopenic purpura in childhood.

Authors:  P Imbach; S Barandun; V d'Apuzzo; C Baumgartner; A Hirt; A Morell; E Rossi; M Schöni; M Vest; H P Wagner
Journal:  Lancet       Date:  1981-06-06       Impact factor: 79.321

9.  Heterogeneity of human circulating anticoagulants against antihemophilic factor (factor VIII).

Authors:  M C Poon; A C Wine; O D Ratnoff; G M Bernier
Journal:  Blood       Date:  1975-09       Impact factor: 22.113

10.  Antihemophilic factor inhibitors. Management with prothrombin complex concentrates.

Authors:  P Kelly; J A Penner
Journal:  JAMA       Date:  1976-11-01       Impact factor: 56.272

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  7 in total

Review 1.  Intravenous immunoglobulin therapy for acquired coagulation inhibitors: a critical review.

Authors:  Koji Yamamoto; Junki Takamatsu; Hidehiko Saito
Journal:  Int J Hematol       Date:  2007-05       Impact factor: 2.490

Review 2.  Intravenous immunoglobulin (IVIG) for the therapy of autoimmune disorders.

Authors:  S A Schwartz
Journal:  J Clin Immunol       Date:  1990-03       Impact factor: 8.317

3.  Successful treatment with high-dose intravenous immunoglobulin in a patient with spontaneous inhibitor to factor VIII.

Authors:  E Hiller; E Holler; R G Geursen; H Riess
Journal:  Blut       Date:  1986-02

4.  Experimental allergic neuritis: effect of plasma infusions.

Authors:  G K Harvey; J D Pollard; K Schindhelm; J G McLeod
Journal:  Clin Exp Immunol       Date:  1989-06       Impact factor: 4.330

5.  Immediate effects of intravenous IgG administration on peripheral blood B and T cells and polymorphonuclear cells in patients with myasthenia gravis.

Authors:  L Cook; J F Howard; J D Folds
Journal:  J Clin Immunol       Date:  1988-01       Impact factor: 8.317

6.  Treatment of refractory chronic idiopathic thrombocytopenic purpura with high dose intravenous immunoglobulin.

Authors:  E Seifried; G Pindur; H Stötter; M Wiesneth; H Rasche; H Heimpel
Journal:  Blut       Date:  1984-06

7.  Induction of split tolerance and clinical cure in high-responding hemophiliacs with factor IX antibodies.

Authors:  I M Nilsson; E Berntorp; O Zettervall
Journal:  Proc Natl Acad Sci U S A       Date:  1986-12       Impact factor: 11.205

  7 in total

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