Js. Dzieczkowski et al., CHARACTERIZATION OF REACTIONS AFTER EXCLUSIVE TRANSFUSION OF WHITE CELL-REDUCED CELLULAR BLOOD COMPONENTS, Transfusion, 35(1), 1995, pp. 20-25
Background: Potential adverse effects of white cells (WBCs) within tra
nsfused cellular blood components include febrile nonhemolytic transfu
sion reactions (FNHTRs), alloimmunization, transmission of infectious
diseases, transfusion-related acute lung injury, and immunomodulation.
Although exclusive use of WBC-reduced components to prevent alloimmun
ization and cytomegalovirus transmission has been studied, the use of
these components to avert FNHTR has not been examined. Study Design an
d Methods: Transfusion reactions (FNHTRs allergic reactions, and other
s) were characterized in recipients of 12,277 WBC-reduced single-donor
apheresis platelets (SDAPs) and/or red cells (RBCs). Medical and labo
ratory evaluations for possible infectious and immunologic (alloimmuni
zation) causes of each reaction were undertaken, and the benefit of fu
rther modification of components for the prevention of subsequent reac
tions was also evaluated. Results: Transfusion reactions occurred afte
r 481 (3.92%) of 12,277 transfusions. Allergic reactions occurred more
commonly after transfusion of SDAPs (3.69%) than of RBCs (0.51%). Con
versely FNHTRs occurred more commonly after transfusion of RBCs (2.15%
) than of SDAPs (1.58%). HLA antibodies were present in a posttransfus
ion sample from 27 (10.6%) of 255 patients; bacterial contamination wa
s a possible cause of only 2 (0.42%) of 481 reactions. In patients wit
h recurrent FNHTRs, further WBC reduction in components did not wholly
prevent further FNHTRs. Conclusion: The incidence of FNHTRs and alloi
mmunization after exclusive transfusion of WBC-reduced RBCs and SDAPs
was low. Further WBC reduction in components transfused to patients wi
th a history of recurrent FNHTRs does not completely prevent subsequen
t reactions.