ABID / DAT / IMMUNE MEDIATED HEMOLYSIS Flashcards
True/ false - in serologic antibody detection involving complement, plasma should be used for testing.
False.
Only serum provides complement. Otherwise, the terms are interchangeable
Which of the ff antibodies to a blood group system does NOT show dosage? A. Kidd B. MNS C. Kell D. Rhesus
C. Kell
The rest of the choices, as well as Duffy show dosage
What might be the cause of a reactive (positive) autocontrol in the IAT phase, but non reactive (negative) with DAT?
A. Presence of WARM auto antibody
B. Presence of antibody against enhancement media
C. Presence of allo antibody coating donor red cells
D. Presence of anti -IH
B. Presence of antibody against enhancement media
What might be the cause of a reactive (positive) autocontrol in the IAT phase as well as with DAT?
A. Presence of WARM auto antibody
B. Presence of antibody against enhancement media
C. Presence of allo antibody coating donor red cells
D. Presence of anti -IH
C. Presence of allo antibody coating donor red cells
This occurs if recently transfused pt has formed allo antibody for which the donor red cells are positive for
True / false - In ABIDs of patients with partial / weak / altered Rh antigen, Rh antibodies should still be considered.
True
In antibody identification workups with negative auto control, which of the ff should be considered when some or all cells are reactive, in multiple strengths and phases?
A. Suspect the presence of a single antibody, perform rule outs, and test select red cells to rule in suspected antibody
B. Suspect multiple antibodies, consider dosage, perform extended phenotype to determine if the antibody is against common or high incidence antigen
C. Suspect weakly reactive antibody or antibody showing dosage, use enhancement techniques, select reagent cells that have double dose expression
D. Suspect antibody to low incidence antigen or antibody to HLA antigen, use reagents that are positive for low incidence antigens or known HLA antigens
B. Suspect multiple antibodies, consider dosage, perform extended phenotype to determine if the antibody is against common or high incidence antigen
In antibody identification workups with negative auto control, which of the ff should be considered when some red cells are weakly reactive and common antibodies appear to be ruled out?
A. Suspect the presence of a single antibody, perform rule outs, and test select red cells to rule in suspected antibody
B. Suspect multiple antibodies, consider dosage, perform extended phenotype to determine if the antibody is against common or high incidence antigen
C. Suspect weakly reactive antibody or antibody showing dosage, use enhancement techniques, select reagent cells that have double dose expression
D. Suspect antibody to low incidence antigen or antibody to HLA antigen, use reagents that are positive for low incidence antigens or known HLA antigens
C. Suspect weakly reactive antibody or antibody showing dosage, use enhancement techniques, select reagent cells that have double dose expression
In antibody identification workups with negative auto control, which of the ff should be considered when some red cells are reactive in same phases and showing similar strengths?
A. Suspect the presence of a single antibody, perform rule outs, and test select red cells to rule in suspected antibody
B. Suspect multiple antibodies, consider dosage, perform extended phenotype to determine if the antibody is against common or high incidence antigen
C. Suspect weakly reactive antibody or antibody showing dosage, use enhancement techniques, select reagent cells that have double dose expression
D. Suspect antibody to low incidence antigen or antibody to HLA antigen, use reagents that are positive for low incidence antigens or known HLA antigens
A. Suspect the presence of a single antibody, perform rule outs, and test select red cells to rule in suspected antibody
In antibody identification workups with negative auto control, which of the ff should be considered when only one red cell is reactive?
A. Suspect the presence of a single antibody, perform rule outs, and test select red cells to rule in suspected antibody
B. Suspect multiple antibodies, consider dosage, perform extended phenotype to determine if the antibody is against common or high incidence antigen
C. Suspect weakly reactive antibody or antibody showing dosage, use enhancement techniques, select reagent cells that have double dose expression
D. Suspect antibody to low incidence antigen or antibody to HLA antigen, use reagents that are positive for low incidence antigens or known HLA antigens
D. Suspect antibody to low incidence antigen or antibody to HLA antigen, use reagents that are positive for low incidence antigens or known HLA antigens
This occurs when the development of a new allo antibody in a patient following transfusion results in serologic or hemolytic evidence of destruction of incompatible transfused red cells that were compatible at the time of infusion.
Delayed transfusion reaction
What is the most likely cause of an autocontrol that is non reactive, but reactive with all reagent red cells with uniform strength an in the same phase?
A. Antibody to high prevalence antigen
B. Multiple allo antibodies
C. Presence of warm auto antibody
D. Presence of antibody against enhancement media
A. Antibody to high prevalence antigen
Which ancestry / ethnicity is anti-Kpb mostly found in? A. African american B. Native american C. European D. Arabs
C. European
Which ancestry / ethnicity is anti-Di(b) mostly found in? A. African american B. Native american C. European D. Arabs
B. Native american
An in Asians as well
Which ancestry / ethnicity is the phenotype for this high prevalence antigens mosty found in? S-, s-, U+ A. Blacks B. Arabs C. Whites D. Mexicans
A. Blacks
Which ancestry / ethnicity is the phenotype for this high prevalence antigens mosty found in?: Yt (a+) A. Blacks B. Arabs C. Whites D. Mexicans
B. Arabs
Which ancestry / ethnicity is the phenotype for this high prevalence antigens mosty found in? k(+) A. Blacks B. Arabs C. Whites D. Mexicans
C. Whites
Whites>any
A patient’s antibody screen cells came up reactive but when DAT on autologous red cells were done, results were non reactive. What might be the possible cause for this pattern of reactivity?
A. Patient may have antibody to high prevalence antigen
B. Patient may have antibody to low prevalence antigen
C. Patient may have an autoantibody
D. Patient may have an allo antibody
D. Patient may have an allo antibody
What is the best way to obtain a patient’s red cells for phenotyping if the patient has been recently transfused?
A. Treat red cells with 0.01M DTT then centrifuge the sample
B. Obtain a sample immediately after transfusion, subject the patient’s red cells to heat elution to separate it from donor cells
C. Separate patient’s red cells by centrifugation using a sample drawn 3 days or more after last transfusion
D. Obtain sample 3 days after last transfusion, wash cells with hypotonic saline then centrifuge sample
C. Separate patient’s red cells by centrifugation using a sample drawn 3 days or more after last transfusion
Young / new cells will be on top
A - done when cold auto is present
B - this technique removes IgG antibodies coating red cells
D - Washing cells in hypotonic solution is used to separate patient’s sickled cells (will not lyse)
Which of the ff enzymes / chemical modification treatment of red cells destroys or weakens CD38 in red cells? A. Chloroquine diphosphate B. Trypsin C. Glycine HCl / EDTA D. DTT
B. Trypsin
Which of the ff enzymes / chemical modification treatment of red cells destroys or weakens Class I HLA antigens in red cells? A. Chloroquine diphosphate B. Trypsin C. Glycine HCl / EDTA D. DTT
A. Chloroquine diphosphate