New Activity
Play Matching Game
1. Delayed HTR
2. Alloimmunization to RBC Antigens
3. Alloimmunization to HLA Antigen
4. Transfusion-Associated Graft-Versus-Host Disease (TA-GVHD)
5. Post-Transfusion Purpura
6. Iron Overload/Transfusion Induced Hemosiderosis
7. Hematologic Events Associated with Transfusions

Prevention: irradiate blood products prior to transfusion

Cause: immune response to foreign RBC antigens

Prevention: Avoid unnecessary transfusio

Cause: immunologically competent donor WBCs form antibodies to recipient antigens, mounting an immune response against the patient 

Cause: massive transfusion leads to low levels of platelets and/or coagulation proteins that do not survive blood storage conditions

Cause: chronic transfusions leading to a build-up of excess iron in liver, heart, and endocrine glands

Treatment: corticosteroids, plasmapheresis

Cause: immune response to foreign antigens on WBCs and platelets

Prevention: check records, use fresh specimens for Ab screening and XM, use Ag-negative blood.

Cause: recipient antibody to platelets (usually anti-P1A1) 

Prevention: avoid unnecessary transfusion, give leuko-reduced or irradiated blood where indicated

Prevention: transfuse P1A1 negative platelets in the future

Cause: recipient antibody to antigen on donor RBCs causing (mostly extravascular) hemolysis

Treatment: iron chelation therapy

Treatment: treat as necessary based on Sx, evaluate renal function, pay close attention to differential diagnosis with sickle cell patients (may resemble sickle crisis).

Treatment: does not respond to most treatment regimens

Prevention: monitor platelets during and after transfusion 

Prevention: keep transfusions to a minimum, transfuse with neocytes

Treatment: administer platelets