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what are some of the general causes?
antibodies to red cell antigens
antibodies to leukocyte or platelet antigens or plasma proteins
unavoidable reactions
technical errors
clerical errors/human error/ management system errors
extravascular hemolysis
IgG antibodies
doesn’t usually bind complement
slower destruction
RBCs are phagocytosed and destroyed by RE cells
signs of extravascular hemolysis
fever
decreasing hemoglobin
mild jaundice
hemoglobin doesnt rise as expected
possible to be asymptomatic
lab signs of extravascular hemolysis
a positive DAT
increased serum bilirubin
unexpected antibody now detected
intravascular hemolysis
red cell destroyed in the blood stream
caused by antigen-antibody complexes that bind complement
hemoglobin is released
usually seen with hemoglobinuria
can also cause coagulation cascade or neuroendocrine response
symptoms of acute hemolytic reactions
fever
chills
pain at site of infusion, chest, or back
hypotension/shock
nausea
facial flushing
shock
feeling of impending doom
hemoglobinuria
DIC
oliguria
anuria
lab signs of an acute hemolytic reaction
hemoglobinemia
hemoglobuniuria
serm bilirubin
positive DAT or weakly positive or negative (donor cells could be lysed)
treatment of acute hemolytic reactions
stop transfusion immediately but keep IV open
maintain blood pressure
maintain urine flow
causes of acute hemolytic reactions
clerical and human error leading to ABO mismatches
delayed hemolytic reactions
due to a secondary immune response
extravascular hemolysis
usually happens 3-14 days after transfusion
Febrile Nonhemolytic reaction (FNH)
rise in 1 degree celsius during or after a transfusion with no other apparent cause
cause:
cytokines from WBCs in the donor unit
antibody to WBCs, platelet antigens, or people who have been transfused multiple times
symptoms of FNH
fever
chills
patient discomfort
anxiety
treatment for FNH
rule out HTR or bacterial contamination
stop transfusion
antipyretics to bring down fever
can be prevented with leukoreduction
allergic reactions treatment
treat with antihistamines (mild)
can restart transfusion if symptoms resolve
for anaplyaxis have to rule out hemolysis and use epinephrine and fluids
allergic reactions
receiving plasma
cause: antibodies to plasma proteins in donor blood
usually mild
some occur in minutes and rash/hive/itching
can affect respiratory tract, GI tract, and the circulatory system
can also cause anaphylaxis
prevent: don’t give plasma to IgA deficient and wash red cells
cause of TRALI
antibodies to HLA, granulocyte antigens
passive transfer of donor antibodies
can lead to pulmonary edema
cytokines are released
neutrophils mediate endothelial damage
usually comes from female donors with multiple pregnancies or donors with multiple transfusions
treatment of TRALI
rule out hemolysis
stop transfusion
give O2
prevention of TRALI
test plasma for HLA antibodies
screenings
stop collection from female donors (not really)
cause of TACO
sudden increase in blood volume not tolerated well by compromised cardiac/pulmonary patients
treatment for TACO
stop transfusions
diuretics
give O2
therapeutic phlebotomy
prevention of TACO
dont give blood too fast
cause of GVHD
donor lymphs react and immune respond to recipient
immunocompetent lymphs engraft and multiply
greatest risks are for immunocompromised, intrauterine transfusions, and blood relatives
prevention for GVHD
leukoreduction
irradiate to stop lymph proliferation
3 steps that need to be taken if a HTR is suspected
clerical check (ID errors)
check for hemolysis (examine post reaction sample and compare to pre sample)
check for incompatibility (DAT on post specimen and compare to pre sample)
additional testing if HTR is suspected
ABO/Rh on pre and post
repeat crossmatches for pre and post
repeat ab screen on pre, post, and donor
culture on donor
check for non-immune hemolysis
post urine hemoglobin
post serum bilirubin
complications with massive transfusions
citrate toxicity from anticoagulant (give calcium)
hypothermia (reduce rate and use blood warmer)
hypokalemia/hyperkalemia (use fresher units for infants)
coagulopathy
iron overlaod (especially for chronic transfusion recipients; use iron chelators)
alloimmunization risks
RBC: 1%/unit; try identical phenotypic match
WBC: 10%/unit
development of antibodies to HLA, granulocyte, and platelet antigens
non-immune hemolysis
rare
overheat
seen with a negative DAT and no immune response
hung something with the IV
contaminated blood (yersinia)
stop transfusion and rule out causes
symptoms of TRALI
acute respiratory distress
bilateral pulmonary edema
severe hypoxemia