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Platelet transfusion containing ABO-incompatible plasma and hepatic veno-occlusive disease after hematopoietic transplantation in young children.

AbstractBACKGROUND:
Hepatic veno-occlusive disease is a major limiting factor of high-dose chemotherapy in children. The cells lining the hepatic vascular endothelium express blood group A and/or B antigens according to the patient's blood group. We designed a study evaluating the impact of platelet concentrates containing ABO-incompatible plasma transfused to young children with a high risk of hepatic veno-occlusive disease.
METHODS:
In all, 186 consecutive children (median age: 4 years, range: 0.75-17 years), treated with high-dose chemotherapy containing busulfan followed by hematopoietic stem cell transplantation for neuroblastoma (n=112) or brain tumor (n=74) between 1988 and 1998, were investigated. The main endpoint was the occurrence of hepatic veno-occlusive disease. Multivariate analysis was performed using a Cox's regression model with transfusion of platelet concentrates containing ABO-incompatible plasma as a time-dependent covariate.
RESULTS:
We found that 73 out of 186 (39%) children developed hepatic veno-occlusive disease after transplantation. Multivariate analysis demonstrated that two factors significantly increased the risk of hepatic veno-occlusive disease occurrence: transfusion of platelet concentrates containing ABO-incompatible plasma (P=0.003) and use of melphalan in the conditioning regimen (P=0.006). Conversely, the number of platelet concentrates transfusions per week, child's age, weight, sex, and use of cyclophosphamide in the conditioning regimen had no effect.
CONCLUSIONS:
Transfusion of platelet concentrates containing ABO-incompatible plasma increases the risk of hepatic veno-occlusive disease in young children treated with a busulfan-containing regimen. Binding of A and/or B antigens expressed on the surface of hepatic endothelial cells may promote this complication. Transfusion of platelet concentrates containing ABO-incompatible plasma should be avoided in these children.
AuthorsValérie Lapierre, Cédric Mahé, Anne Aupérin, Férial Stambouli, Nadia Oubouzar, Dominique Tramalloni, Ellen Benhamou, Pierre Tiberghien, Olivier Hartmann
JournalTransplantation (Transplantation) Vol. 80 Issue 3 Pg. 314-9 (Aug 15 2005) ISSN: 0041-1337 [Print] United States
PMID16082325 (Publication Type: Journal Article)
Chemical References
  • ABO Blood-Group System
  • Antineoplastic Agents
  • Cyclophosphamide
  • Busulfan
Topics
  • ABO Blood-Group System
  • Adolescent
  • Antineoplastic Agents (adverse effects)
  • Brain Neoplasms (therapy)
  • Busulfan (pharmacology)
  • Chemical and Drug Induced Liver Injury
  • Child
  • Child, Preschool
  • Cyclophosphamide (pharmacology)
  • Female
  • Follow-Up Studies
  • Hematopoietic Stem Cell Transplantation
  • Hepatic Veno-Occlusive Disease (chemically induced, therapy)
  • Humans
  • Infant
  • Liver Diseases (therapy)
  • Male
  • Multivariate Analysis
  • Neuroblastoma (therapy)
  • Platelet Transfusion (methods)
  • Proportional Hazards Models
  • Risk Factors
  • Time Factors
  • Transplantation Conditioning

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