Presentation on theme: "Blood Transfusion Reactions (BTR) & the Blood Bank:Explaining the Link"— Presentation transcript:
1Blood Transfusion Reactions (BTR) & the Blood Bank:Explaining the Link
2Objectives Early identification of common transfusion reactions Differentiate life threatening reactions from benign transfusion reactionsManage common immunologic transfusion reactions.
3Immune mediated transfusion reactions Febrile non hemolytic tranx rxnsImmune mediated hemolysis---Acute and delayed hemolytic reactionsAnaphylactic transfusion rxnsUrticarial transfusion rxnsPost-transfusion purpuraGVHDTRALI –Transfusion Related Acute Lung Injury (pulm leuko-agglutinin reactions)
4Non immune mediated reactions Physical reactions: thermal i.e. heat or cold inducedInfectious; Hepatitis B/C, malaria, HIV, etc.Chemical; citrate toxicity, hypo/hyperkalemia, iron overloadAcute hypotensive reaction: mediated by bradykinins and occurs in patients with faulty bradykinin metabolism on ACE IOsmotic injuryCongenital and acquired hemolytic anemias
5What to DO ?Early recognition of signs/symptoms suggestive of a transfusion reaction and prompt reporting to the blood bank are essential.The most common symptoms are chills, rigors, fever, dyspnea, light-headedness, urticaria, itching, and flank pain. If any of these symptoms (other than localized urticaria and itching) (?) occur, the transfusion should be stopped immediately and the IV line kept open with normal saline.
6What to DO?The remainder of the blood product and clotted and anticoagulated samples of the patient's blood should be sent to the blood bank for investigation.
7Immunologic Reactions classic blood transfusion reaction are usually immunologic and occur to interactions of inherited/ acquired Ab with foreign Ag from transfused bloodIncidence of rxns-most common cause is transfused of non-matched blood mostly to clerical error-2x more common in infants than adults-more common in patients with hematological and oncological conditions
8Febrile Non Hemolytic Tranfusion Reactions(FNHTR) Most common, usually benign without sequelaA least rise of temp. of 1o C15% will have a reaction in the future with subsequent transfusionEtiologyClass 1 HLA Ab (HLA 5)directed against contaminating WBC in red cell concentrationCytokines IL-1, 6,8 and TNF alpha generated in stored blood/products
9ManagementDiscontinue transfusion, rule out hemolysis i.e. check labels, repeat type and cross, coombs testPreventionLeukoreduction
10Acute Hemolytic Reactions Rapid destruction of RBC immediately after within 24 hours of transfusion.Occurs due to rapid transfused RBC destruction by preformed recipients AbsIgM mediated complement fixation leading to rapid intra vascular hemolysisMost common causes are clerical or procedural errors
11Acute hemolytic rxns Clinical presentation Classic presenting triad of Fever, flank pain and reddish brown urine from hemoglobinuria.DIC may be presenting mode
12Conditions – destroy donor cells Naturally occuring or stimulated alloantibodies (anti-A, Kell, Jka , Fya)AutoantibodiesDrug-associated antibodiesBacterial Contamination
13Conditions –destroy recipient cells Incompatible (ABO)Infusion of large amount of hypotonic solutionsMechanical Trauma
14Actions ?If AHTR is suspected, one of the first steps is to recheck the sample and patient identifications. Diagnosis is confirmed by measuring urinary Hb, bilirubin, and haptoglobin.Intravascular hemolysis produces free Hb in the plasma and urine; haptoglobin levels are very low. Hyperbilirubinemia may follow.After the acute phase, the degree of acute renal failure determines the prognosis.Prolonged oliguria and shock are poor prognostic signs.
15Laboratory TestsPatient Samples -Reconfirmation of ABO, Rh type and Antibody screen and Direct Coombs Test, and Antibody identification- CBC-Urinalysis (to document hemoglubinuria)- Serum bilirubin- BUN, Creatinine and Quantitation of Urine Output-Coagulation screen- PT, PTT,TT,FDP, Fibrinogen levelsProduct Samples- Reconfirmation and ABO and Rh typing and antibody screen results
16Laboratory evaluation of suspected hemolytic reaction The work up of suspected transfusion reaction includes : 1.Check all the records to ensure that the correct unit of blood was transfused to the right patient. This includes : - Patient’s details - Blood requisition form - Compatibility report - Labels
17Laboratory evaluation of suspected hemolytic reaction Clerical errors a. Incorrect labeling - recipient’s sample - blood bag - pilot tubes - request form b. Misidentification of patient at time of collection of sample or transfusion of blood c. Mix-up of samples at time of collection.
18Laboratory evaluation of suspected hemolytic reaction Till the time a clerical error is not ruled out, stop issuing of all blood units from the blood bank, as it may lead to issue of another mismatched blood due to mix-up of samples or other clerical errors.
19Laboratory evaluation of suspected hemolytic reaction 2. Technical errors a. Error in blood grouping of donor and recipient samples b. Error in compatibility testing - faulty technique - weak antibodies not detected by routine tests 3. Destruction of recipient red cells by donor antibodies. This occurs due to indiscriminate use of group 0 blood which may contain potent anti-A and anti-B.
20Laboratory evaluation of suspected hemolytic reaction The following samples must be immediately sent to the laboratory and blood bank. - Post transfusion sample in plain vial (5m1) - Post transfusion sample in EDTA vial (3m1) - Blood bag along with transfusion set - Urine (post-transfusion) 1st sample - Coagulation profile-citrated blood sample - Blood cultures from the blood bag and the patient
21Laboratory evaluation of suspected hemolytic reaction The pre-transfusion sample should be preserved in the laboratory for 7 days. For evaluation of a patient with hemolytic reactions the investigation may be divided into three: 1. Investigation for evidence of increased red cell destruction 2. Investigation for identification of cause of hemolysis 3. Investigation to follow up of a patient with proven hemolysis
22Tests for evidence of increased red cell destruction 1. Centrifuge the post-transfusion blood sample and examine the supernatent plasma.Compare this with the pre-transfusion sample. A pink or red colour in the post-transfusion sample indicates hemolysis and presence of free hemoglobin Perform a Direct antiglobulin test (DAT) on the post-transfusion sample. A positive test indicate immune hemolysis. A negative DAT with hemoglobinemia suggests a non-immune hemolysis e.g. due to mechanical trauma or thermal damage.
23Tests for evidence of increased red cell destruction 3. Reticulocyte count is raised in patient with hemolysis Pre-and post hemoglobin value Serum unconjugated bilirubin estimation.
24Tests to establish the cause of hemolysis 1. Repeat ABO and Rh grouping on the pre-and post-transfusion samples and from the bag. If blood group of the pre-and post-transfusion sample do not agree, it may be due to error in patient identification, drawing or grouping of blood. Another patient’s sample may have been drawn at the same time and labeled incorrectly. If the donor sample is not of the same group as indicated on the bag, an error in labeling or grouping and also in the compatibility testing should be suspected
25Tests to establish the cause of hemolysis 2. Repeat the compatibility testing on pre-and post-transfusion samples with a sample of blood from the bag. The testing must be done using saline, enzyme/albumin and indirect antiglobulin techniques. If both the samples show incompatibility- an error in the pre-transfusion testing.The donor sample may have been incorrectly labelled or the crossmatch reaction was incorrectly read as negative. If the incompatibility is seen only with the postransfusion sample, an anamnestic response should be suspected.If both crossmatches are compatible and there is a strong suspicion of hemolysis, further tests are required.
26Tests to establish the cause of hemolysis 3. Perform an antibody screening on the pre-and post-transfusion samples. If an antibody is detected, it should be identified.An antibody in the post transfusion sample may be due to - Anamnestic response (e.g. anti-Kidd, anti-MNS and anti-Duffy antibodies) - Passively acquired antibody from donor plasma. Antibody screening must be done..
27Tests to establish the cause of hemolysis 4. Examine a stained peripheral blood film for spherocytes and crenated cells, presence of which favors a diagnosis of immune hemolysis.
28Tests done to follow up a patient with proven hemolysis 1. Test sample for serum unconjugated bilirubin levels2. Measure plasma hemoglobin levels.3. Serum haptoglobins are reduced.
29Tests done to follow up a patient with proven hemolysis 4. Examine the post-transfusion urine sample for free hemoglobin.Done in a freshly collected sample of urine. In the event of delay in evaluation of a hemolytic reaction, the urine may be tested for hemosiderin.The presence of intact red cells indicates hemorrhage and not hemolysis.
30Tests done to follow up a patient with proven hemolysis 5. Perform a coagulation screen (PT,PTT,TT) and platelet count to check for DIC. 6. Monitor blood urea & serum creatinine to assess renal function.
31Tests for non-immune hemolysis 1. Examine the bag for discoloration or clots, any abnormal mass, foul small or a fuzzy cell: plasma interface. Take specimens from the bag for culture at 4°C, 20°C and 37°C for bacterial and fungal cultures and also for gram’s staining.2. Examine the plasma in the bag for presence of free hemoglobin. If present, it indicates improper storage of the unit of blood over heating or over-cooling ,injection of drugs or hypotonic solutions. Presence of free hemoglobin in the administration tubing suggests that the same tube was used for administration of dextrose/other solutions.3. The possibility of mechanical/osmotic hemolysis should also be suspected
32Delayed hemolytic transfusion rxns Generally occurs within 3-10 days of tranxUsually due to senescent Ab response on re-exposure to a foreign red cell Ag . The Ab was not detected in pretransfusion testing.History of previous pregnancy, transfusion or transplantUsually extra vascular and is less severe than acuteOther Abs often Rh and KiddClinical presentationFalling HCT, low grade fever, slight increase in indirect bilirubin, spherocytes on blood smear
33Delayed hemolytic transfusion rxns Laboratory features 1. A fall in hemoglobin not attributed to any other cause.2. Appearance of a new alloantibody.3. Spherocytosis is observed in blood films which may be the only indicator.4. Direct antiglobulin test is positive. The test becomes positive a few days after transfusion and remains until all incompatible cells have been eliminated.
34Delayed hemolytic transfusion rxns 5. Antibody detection . The antibody is detected 4-7 days after transfusion and peaks after days Sensitive antibody detection techniques in pretransfusion testing may prevent DHTRs.