Back to Search
Start Over
Hemolysis related to intravenous immunoglobulins is dependent on the presence of anti-blood group A and B antibodies and individual susceptibility.
- Source :
- Transfusion; Nov2017, Vol. 57 Issue 11, p2629-2638, 10p, 1 Diagram, 3 Charts, 3 Graphs
- Publication Year :
- 2017
-
Abstract
- <bold>Background: </bold>Patients treated with intravenous immunoglobulins (IVIG) rarely experience symptomatic hemolysis. Although anti-A and anti-B isoagglutinins from the product are involved in most cases, the actual mechanisms triggering hemolysis are unclear.<bold>Study Design and Methods: </bold>A prospective, open-label, multicenter, single-arm clinical trial in 57 patients with immune thrombocytopenia treated with IVIG (Privigen, CSL Behring) was conducted.<bold>Results: </bold>Twenty-one patients received one infusion (1 g/kg) and 36 received two infusions (2 × 1 g/kg) of IVIG. After a study duration of more than 2 years, no cases of clinically significant hemolysis as defined in the protocol were identified. Data of patients with mild hematologic and biochemical changes were analyzed in more detail. Twelve cases (10/23 patients with blood group A1 and 2/11 patients with blood group B, all having received 2 g/kg IVIG) were adjudicated as mild hemolysis (median hemoglobin [Hb] decrease, -3.0 g/dL); Hb decreases were transient, with partial or full recovery achieved by last visit. Eighteen patients (31.6%), all with non-O blood group, of whom 16 (88.9%) received 2 g/kg IVIG, fulfilled post hoc criteria for hemolytic laboratory reactions. Red blood cell (RBC) eluates of all direct antiglobulin test-positive samples were negative for non-ABO blood group antibodies. Blood groups A and B antigen density on RBCs appeared to be a risk factor for hemolytic laboratory reactions. Platelet response to treatment was observed in 42 patients (74%); eight of 12 patients with complete response had blood group A1.<bold>Conclusion: </bold>Isoagglutinins are involved in clinically nonsignificant hemolysis after treatment with IVIG, but individual susceptibility varies greatly. [ABSTRACT FROM AUTHOR]
- Subjects :
- HEMOLYSIS & hemolysins
INTRAVENOUS immunoglobulins
IDIOPATHIC thrombocytopenic purpura
BLOOD groups
ERYTHROCYTES
THERAPEUTICS
ABO blood group system
CLINICAL trials
COMPARATIVE studies
DISEASE susceptibility
IMMUNITY
IMMUNOGLOBULINS
RESEARCH methodology
MEDICAL cooperation
RESEARCH
THROMBOPENIC purpura
EVALUATION research
DISEASE complications
Subjects
Details
- Language :
- English
- ISSN :
- 00411132
- Volume :
- 57
- Issue :
- 11
- Database :
- Complementary Index
- Journal :
- Transfusion
- Publication Type :
- Academic Journal
- Accession number :
- 126068497
- Full Text :
- https://doi.org/10.1111/trf.14289