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Blood Transfusion Review

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Title: Hemat8-Tranfusion Medicine Last modified by: shindawi Created Date: 12/1/1996 7:20:54 PM Document presentation format: 35mm Slides Other titles – PowerPoint PPT presentation

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Title: Blood Transfusion Review


1
Blood Transfusion Review
  • Salwa Hindawi
  • Medical Director of Blood Transfusion Services
  • KAUH

2
Donor Patient
The risks associated with transfusion can be
reduced by - Effective blood donor
selection. - Screening for TTI in the blood
donor population. high quality blood
grouping, compatibility testing. - Component
separation and storage. -
Appropriate clinical use of blood and blood
products. - Quality assurance
3
Blood Donation
  • WB every 8 weeks, Hct gt 38
  • Plateletpheresis every 3 days or 24 times per
    year, Hct gt 38
  • Autologous Blood
  • WB every 3 days
  • up to 3 days prior to surgery
  • Hct gt 33

4
Steps in Blood Banking
  • Type and Screen (T S) (Done for low
    probability of transfusion)
  • ABO and Rh type
  • Antibody screen
  • Antibody identification
  • DAT
  • Type and Crossmatch (T C) (Done for high
    probability of transfusion)
  • above steps plus Crossmatch

5
Direct Antiglobulin Test (DAT)
  • also called the direct Coombs test
  • adding anti-IgG to detect IgG that is attached to
    the RBCs
  • also detects C3 complement fragments on the RBC
    surface
  • DAT is performed in the investigation of immune
    hemolytic anemia and transfusion reactions

6
Indirect Antiglobulin Test (IAT)
  • detects free antibodies in the serum
  • the IAT test is performed during the antibody
    screen and antibody identification

7
Type and Screen (T S)
  • an ABO and Rh type and an antibody screen and
    antibody identification are done when the patient
    is admitted
  • only testing necessary if low probability of
    transfusion

8
Antibody Screen (IAT)
  • recipients serum is added to 3 test RBCs (in test
    tubes 1 to 3 ) which have all of the important
    RBC antigens on them
  • therefore if one or more of the three screening
    cells is positive then a RBC antibody is present
    in the serum
  • then do an antibody panel to identify the
    antibody present

9
Antibody Identification (IAT)
  • after the screening RBCs are positive then do an
    antibody identification
  • recipients serum is added to 10 test RBCs in a
    panel (test tubes 1 to 10) which contain all of
    the important antigens
  • the antibody in the serum is identified

10
Major Crossmatch (Compatibility testing)
  • donor RBCs (unit of blood) are tested with
    recipient serum
  • to detect unexpected recipient antibodies
  • this checks to see if the transfusion is
    compatible

11
Type and Cross (T C)
  • includes an ABO and Rh type and antibody screen
    and antibody identification
  • in addition includes a crossmatch where specific
    units of blood are held back for up to three days
    for a particular patient
  • for a high probability of transfusion

12
Crossmatch to Transfusion ratio (CT ratio)
  • blood is used more efficiently when the number of
    units set aside for a particular patient
    (crossmatched) are actually transfused.
  • when a patient does not need blood, it is good
    practice to get a T S but not a T C
  • CT ratio is less than 21

13
Maximum Surgical Blood Order Schedule (MSBOS)
  • Is a guideline to order standard number of units
    of RBCs to be crossmatched for a specific
    surgical procedure, based on average use in the
    institution
  • examples
  • angioplasty TS
  • aortic dissection TC 6

14
Red cell Antigens ABO type
  • present on RBCs, GI tract and vascular
    endothelium
  • three alleles A, B, O, the A and B alleles code
    for glycosyltransferases
  • specificity of the antigen is in its terminal
    sugar
  • galactosamine for A
  • galactose for B

15
ABO type continued
  • Pt Cells Pt Serum
  • vs vs
  • anti -A anti-B A cells B cells
  • A 0 0 40
  • B 0 0 11
  • AB 0 0 4
  • 0 0 0 45

16
Rh Type
  • Five important antigens of the Rh system are D,
    C, E, c, and e
  • These antigens are product of two genes RHD and
    RHCE located on chromosome 1p36
  • These one set of three D/d C/c and E/e is
    inherited from each parent
  • example father CDe and mother cde then the
    genotype is CcDdee and the phenotype is CcDe

17
Rh type
  • Rh blood group antigens are present only on RBCs
  • Rh positive means that the D antigen is present
    (85 on the population)
  • Rh negative means that the D antigen is absent
    (15 of the population)
  • the D antigen is highly immunogenic
  • More than 80 of D negative persons receiving D
    positive blood are expected to develop anti-D

18
Hemolytic Disease of the Newborn(HDN)
  • D antigen is the most important cause of HDN
  • mother is D neg, father is D pos and fetus is D
    positive
  • fetus D positive RBCs enter mothers
    circulation and mother makes anti-D of IgG type
    which crosses the placenta
  • first pregnancy not affected
  • Maternal IgG crosses the placenta and affects the
    second D positive pregnancy
  • anti-D formation in mother prevented with Rhogam

19
Other Blood Group Systems
  • clinically significant blood group systems are
    Kell (K), Kidd (Jk), Duffy (Fy) and Rh (E,e,C,c)
    systems.
  • antibodies are made by people who lack the
    antigen on their RBCs
  • and have been exposed to RBCs containing the
    antigen

20
Other Blood Group Systems
  • The following are not clinically significant
  • I I
  • Le Lewis love
  • M my
  • N new
  • H honda
  • P prelude

21
Blood Used on Emergency Basis
  • Blood used on Emergency Basis
  • for a patient that is bleeding out
  • and the blood type is unknown
  • group O, Rh negative, uncrossmatched
  • recipient may have an unexpected antibody
  • after 5 min use ABO and Rh type specific blood

22
Whole Blood
  • 450 ml of whole blood with 63 ml of anticoagulant
  • need for oxygen carrying capacity and volume
    replacement
  • no viable platelets or WBC
  • decreased labile coagulation factors (Factor V
    and VIII)
  • Not available since it is not efficient
    utilization of blood

23
Packed Red Blood Cells (PRBCs)
  • 200-250 ml of RBCs and 50 ml of plasma
  • Hematocrit 55-70 depending on anticoagulant
  • shelf life 35 to 42 days depending on the
    anticoagulant
  • treatment of symptomatic anemia where oxygen
    carrying capacity is needed

24
Leukocyte Reduced RBCs
  • RBCs with 99.99 of WBCs removed by leukocyte
    reduction filter
  • prevents repeated nonhemolytic febrile
    transfusion reactions
  • reduces immunosuppression of recipient by donor
    WBC
  • decreases post-operative surgical infections due
    to reduced immunosuppression

25
Leukocyte Reduced RBCs continued
  • prevents or delays HLA alloimmunization
  • identical to CMV seronegative blood
  • does not prevent graft versus host disease, only
    gamma irradiation prevents graft versus host
    disease

26
Indications for Leukocyte Reduced RBC continued
  • after second nonhemolytic febrile transfusion
    reaction
  • newly diagnosed leukemics
  • long term multiple transfused patients
  • sickle cell disease
  • aplastic anemia
  • thalassemia

27
Frozen RBCs
  • store RBCs for up to 10 years at -70C in glycerol
  • glycerol is a cryopreservative solution
  • used for
  • rare blood types for patients with multiple
    antibodies
  • autologous blood for a postponed operation

28
(Gamma) Irradiated RBCs
  • RBCs and platelets are exposed to gamma
    irradiation at 2500 rads for 4.5 minutes
  • this inactivates the T lymphocytes in the donor
    unit and prevents graft versus host disease in an
    immunocompromised recipient

29
Indications for Gamma Irradiated RBCs
  • bone marrow transplant recipients
  • congenital immunodeficiency syndromes
  • intrauterine transfusions
  • transfusions from all blood relatives
  • Hodgkins disease
  • WBC products (to neutropenic patient)
  • (never Stem Cells)

30
Plateletpheresis
  • donated by a single donor
  • 3.0 x 10 E11 platelets plus 300 ml of plasma,
    expires after 5 days
  • raises the platelet count 30,000
  • used for all platelet transfusions until less
    than 10,000 platelet increase

31
Pooled Platelets
  • are prepared from the platelet portion of 6 whole
    blood units plus 300 ml of plasma (potential for
    6 infectious disease exposures) expires after 5
    days
  • 6 X 5 X 10 E10 3.0 x 10 E 11 platelets
  • 6 x 5000 rise /RD plt 30,000
  • transfuse the patient with platelets from many
    donors to see which platelets will raise the
    platelet count

32
Indications for Platelets
  • low platelet count or functional abnormality
  • major bleed, major surgery gt100,000
  • minor bleed, minor procedure gt50,000
  • prevent spontaneous bleed gt 10,000

33
Low Post-transfusion Increment to Platelets
  • 1 hour post (platelet recovery) poor
  • platelet alloantibodies
  • platelet autoantibodies
  • hepatosplenomegaly
  • 24 hour post (platelet survival) poor
  • infection bleeding
  • DIC fever

34
Fresh Frozen Plasma (FFP)
  • 200-250 ml of plasma frozen at -18C within 8
    hours of collection
  • no platelets are present
  • contains all coagulation factors
  • an unconcentrated source of fibrinogen
  • use Cryo to correct a low fibrinogen level
  • needs 20-30 min lead time to thaw prior to use

35
FFP Continued
  • used in patients with multiple coagulation factor
    deficiencies
  • liver disease
  • DIC
  • massive transfusion
  • indicated when PT/PTT are gt17/55 sec
  • not used if non bleeding or for volume replacement

36
Cryoprecipitate (Cryo)
  • a white precipitate that forms when FFP at -18C
    is thawed to 4C
  • volume is 10 to 15 ml
  • adult dose is 10 to 20 pooled units
  • 30 minutes is needed for thawing and pooling

37
Cryoprecipitate continued
  • Cryoprecipitate can be used for the replacement
    of all of the following
  • vWF vWD
  • Factor VIII Hemoplilia A
  • Factor XIII Factor XIII def
  • Fibrinogen dec. fibrinogen
  • head injury, massive bleed, trauma,

38
Complications of Blood Transfusion
  • Immediate Delayed
  • HTR GVHD
  • FNTR PTP
  • TRALI Iron
    overload
  • Bacterial
    Infectious
  • contamination diseases
  • Allergic, Anaphylaxis Alloimmunization

39
Transfusion Transmitted Disease (TTD)
  • HBV 1 in 63,000
  • HCV 1 in 103,000
  • HTLV-I 1 in 641,000
  • HTLV-II 1 in 641,000
  • HIV-1 1 in 587,000
  • HIV-2 lt 1 in 1,000,000

40
Acute Hemolytic Transfusion Reaction
  • a clerical error (wrong specimen, wrong patient)
  • 1 in 6,000 to 25,000 transfusions
  • back pain, chest pain, fever, red urine,
    oliguria, shock, DIC, death in 1 in 4
  • stop the transfusion

41
Work up of An AHTR
  • start normal saline
  • treat patient symptomatically
  • send blood bag and tubing to culture
  • send red top and purple top tubes
  • urine specimen for hemoglobinuria
  • DAT is positive

42
Non Hemolytic Febrile Transfusion Reaction
  • NHFTR (1100)
  • Recipient has WBC antibodies to Donor WBCs
    contained within RBCs and Plateletpheresis
    products
  • DAT is negative
  • rise in temperature by 2F or 1C
  • other causes for fever are eliminated

43
Allergic (Urticarial) Transfusion Reaction
  • Recipient has antibodies to the Donors plasma
    proteins (1 in 1000)
  • offending protein is not identified
  • urticaria, itching, flushing, wheezing
  • this is the only transfusion reaction where the
    blood that is hanging can be restarted after
    treatment with Benadryl
  • if symptoms continue then STOP

44
Anaphlyactic Transfusion Reaction
  • anaphylactic reaction (1 in 150,000)
  • 1 in 700-900 people never made IgA
  • occurs when exposed to normal blood products
    which contain IgA
  • bronchospasm, vomiting and diarrhea and vascular
    collapse
  • treat with Epinepherine, Solu-Medrol,

45
Circulatory Overload
  • marginal cardiovascular status
  • given blood components too rapidly
  • develops acute shortness of breath, heart
    failure, edema (1 10,000)
  • systolic BP increases 50 mm
  • infuse slowly, not to exceed 4 hours
  • split the unit of RBC and give half

46
Transfusion Related Acute Leukocyte Lung Injury
  • TRALI reaction (110,000)
  • Donor plasma contains WBC antibodies that when
    transfused to the recipient cause agglutination
    of recipients WBC in the pulmonary capillary
    beds
  • Chest X ray looks like ARDS
  • Donor removed from donating blood

47
Sepsis from Bacterial Comtamination
  • Platelets
  • skin contaminants most common cause
  • plateletpheresis 1 in 5000
  • pooled platelets 1 in 1000
  • RBC
  • Sepsis from RBC due to Yersinia, Enterics or
    Gram Positive 1 in 3,000,000

48
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