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Immune tolerance for haemophilia patients with inhibitors: analysis of the western United States experience. The Tri-Regional Nursing Group.
- Source :
-
Haemophilia : the official journal of the World Federation of Hemophilia [Haemophilia] 2000 Sep; Vol. 6 (5), pp. 526-32. - Publication Year :
- 2000
-
Abstract
- The experience with immune tolerance (IT) induction therapy for haemophilia patients with inhibitors, instituted during 1990-97 at 17 haemophilia treatment centres in the western United States, was reviewed. IT was instituted in 104 of 139 (75%) of all identified haemophilia A and haemophilia B patients with inhibitors. Doses and schedules for IT varied but most patients were treated with a daily administration of 25-200 units kg-1 day-1. Successful immune tolerance (defined as Bethesda Unit titres < 1.0) was achieved in 57 of 81 (78%) patients who completed therapy. IT success was significantly greater for those patients with historic titres < 100 BU (P < 0.0003) and those with titres of < 10 BU at initiation of IT (P < 0.0001). IT success was uniformly achieved in 16 patients with low to moderate responding inhibitors. IT in infants < 2 years of age was problematic due to the presence of high titre inhibitors and complications of venous access. Frequent complications of IT included increased bleeding during intravenous access device insertion (20%) and infections associated with venous access devices (64%). IT is widely accepted as a treatment modality for haemophilia patients with inhibitors. Patient participation in IT regimens and management during therapy is facilitated greatly by the efforts of treatment centre nurse coordinators who are knowledgeable about haemophilia and its complications. Additional clinical trials will be necessary to define better initial dose, schedule, dose adjustment and success/failure criteria for IT.
- Subjects :
- Adolescent
Adult
Aged
Anaphylaxis chemically induced
Catheterization, Peripheral adverse effects
Child
Child, Preschool
Factor VIII adverse effects
Factor VIII therapeutic use
Health Care Surveys
Hemophilia A complications
Hemophilia A epidemiology
Humans
Immunotherapy
Infant
Infant, Newborn
Infections etiology
Middle Aged
Prevalence
Recombinant Proteins adverse effects
Recombinant Proteins immunology
Recombinant Proteins therapeutic use
Retrospective Studies
Southwestern United States
Treatment Outcome
Factor VIII immunology
Hemophilia A immunology
Immune Tolerance
Isoantibodies blood
Subjects
Details
- Language :
- English
- ISSN :
- 1351-8216
- Volume :
- 6
- Issue :
- 5
- Database :
- MEDLINE
- Journal :
- Haemophilia : the official journal of the World Federation of Hemophilia
- Publication Type :
- Academic Journal
- Accession number :
- 11012697
- Full Text :
- https://doi.org/10.1046/j.1365-2516.2000.00412.x