Clinical syndrome developing from donor lymphocytes after transfusion characterized by skin rash, diarrhea, fever, enlarged liver, elevated liver enzymes, marrow aplasia, and/or pancytopenia
TA-GVHD
Caused by an immunologic attack by viable donor lymphocytes contained in the transfused blood component against the transfusion recipient
Treatment for TA-GVHD
Immunosuppressive medication e.g. corticosteroids
Post-transfusion purpura (PTP)
Rare transfusion reaction with severe and sudden drop in platelet count, usually occurring 5 to 10 days after transfusion due to alloimmunization to platelet-specific antibodies from prior transfusion or pregnancy
Implicated alloantibodies in PTP
Human platelet antigens HPA-1a or HPA-3a
Platelet count in PTP
Usually less than 10,000
Symptoms of PTP
Purpura, bleeding from mucous membranes, GI bleeding, hematuria
First line treatment for PTP
Intravenous immunoglobulin (IVIG)
Next option for PTP if IVIG doesn't work
Plasma exchange with FFP
Transfusion-associated hepatitis can be caused by HAV, HBV, HCV, HDV, or HEV