Transfusion-associated graft-versus-host disease: Difference between revisions
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** Recipients of HLA-matched platelets |
** Recipients of HLA-matched platelets |
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** Patients treated with [[purine analogues]] (e.g. [[fludarabine]]), [[purine antagonists]] (e.g. [[bendamustine]]), [[alemtuzumab]], or [[anti-thymocyte globulin]] |
** Patients treated with [[purine analogues]] (e.g. [[fludarabine]]), [[purine antagonists]] (e.g. [[bendamustine]]), [[alemtuzumab]], or [[anti-thymocyte globulin]] |
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[[Category:Hematology]] |
Latest revision as of 21:22, 11 February 2022
Background
- Caused by transfusion of immune cells that mount an immune response against the recipient's tissue
- Usually in immunocompromised patients or patients who receive haploidentical blood products
- Rare
- Mortality over 90%, most mediated by severe sepsis
Clinical Manifestations
- Usually starts 1 to 2 weeks after transfusion
- Fever, rash, liver dysfunction, and diarrhea, followed by pancytopenia
Management
- Supportive care (including antibiotics)
Prevention
- Use irradiated blood components for recipients at high risk
- High risk patients include:
- Patients with severe congenital T-cell immunodeficiency
- Intrauterine transfusions (IUT)
- Neonatal exchange transfusions for infants with prior IUT
- Neonatal top-up transfusions for infants with prior IUT
- Patients with Hodgkin lymphoma
- Patients undergoing stem cell transplant
- Recipients of direct transfusions from family members
- Recipients of HLA-matched platelets
- Patients treated with purine analogues (e.g. fludarabine), purine antagonists (e.g. bendamustine), alemtuzumab, or anti-thymocyte globulin