How does the laboratory determine which direction the investigation
should take?
Each laboratory has standard operating
procedures that define the extent of the preliminary laboratory investiga-tion.
The first step in any investigation is a clerical check. This check involves
comparing identifying information on the transfusion request, blood product
label, compatibility label, pre- and post-transfusion blood samples, and blood
bank product release record. The purpose of the clerical check is to determine
whether the product implicated in the investigation was transfused to the
individual for whom it was intended.
The next step is a hemolysis check. The color
of plasma/serum from pre- and post-transfusion samples is compared for
hemolysis and direct antiglobulin testing is performed on the pre- and
post-transfusion samples.
The ABO and Rh type are also repeated on the
pre- and post-transfusion samples when the product implicated in the reaction
is a red cell product. This testing is not rou-tinely performed for non-red-cell
products, such as plasma or platelets, unless there is evidence of red cell
destruction. If there is evidence of a hemolytic reaction, the type and screen
and compatibility tests are completed on the pre- and post-transfusion samples.
In summary, the preliminary laboratory
investigation determines whether the implicated product was transfused to the
appropriate patient and classifies the reaction as hemolytic or non-hemolytic.
Additional testing is based on the patient’s signs and symptoms, the differential
diagnosis that this information suggests, and the specific product involved in
the investigation.
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