Leukoagglutinins are antibodies that react with white blood cells and sometimes cause febrile transfusion reactions. Patients who exhibit this type of transfusion reaction should receive leukocyte-poor blood for any subsequent transfusions.
This study is done when a transfusion reaction occurs even though compatible blood has been given. The donor plasma contains an antibody that reacts with recipient white cells to produce an acute clinical syndrome of fever, dyspnea, cough, pulmonary infiltrates, and, in more severe cases, cyanosis and hypertension. Patients immunized by previous transfusions, by pregnancy, or during allografts often experience these febrile, non-HTRs because of incompatible transfused leukocytes. This type of reaction must be confirmed (as compared with hemolytic reactions) before additional transfusions can be safely administered.
Obtain a 10-mL venous blood sample. Observe standard precautions.
Label the specimen with the patients name, date, and test(s) ordered and place in a biohazard bag for transport to the laboratory.
Agglutinating antibodies may appear in the donors plasma.
When the agglutinating antibody appears in the recipients plasma, febrile reactions are common; however, pulmonary manifestations do not occur.
Febrile reactions are more common in pregnant women and in individuals with a history of multiple transfusions.
Clinical Alert
Febrile reactions can be prevented by separating out white cells from the donor blood before transfusion.
Patients whose blood contains leukoagglutinins should be instructed that they generally need to be transfused with leukocyte-reduced blood to minimize these reactions.
Pretest Patient Care
Explain test purpose and procedure.
Follow guidelines in Chapter 1 for safe, effective, informed pretest care.
Posttest Patient Care
Review test results; report and record findings. Modify the nursing care plan as needed. Counsel the patient regarding future transfusion precautions.
Follow guidelines in Chapter 1 for safe, effective, informed posttest care.