BLOOD GROUPS, TYPING & MATCHING - PowerPoint PPT Presentation

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BLOOD GROUPS, TYPING & MATCHING

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The ABO Blood Group System. There are four major blood groups determined by the presence or absence of two antigens – A and B – on the surface of red blood cells: Group A – has only the A antigen on red cells (and B antibody in the plasma) Group B – has only the B antigen on red cells (and A antibody in the plasma) – PowerPoint PPT presentation

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Title: BLOOD GROUPS, TYPING & MATCHING


1
Blood Groups, Blood Typing Blood
Transfusions
By Dr. K. Ambreesha Assit. Professor, Department
of Physiology MNR College Hospital Sangarddy
2
Contents
  • Blood Groups Various types
  • Agglutinins and agglutinogens
  • 3. Land Steiners law
  • 4. Cross matching
  • Erythroblastsis fetalis
  • 6. Blood transfusion and transfusion reactions
  • 7. Importance of blood Grouping

3
History
In the year of 1901 Karl Land Steiner discovered
the classical ABO system and was given Nobel
Prize in 1930.
4
1. The most important Blood
Group systems are
1. ABO system 2. Rh system 3. MNS system
Less important blood group systems
1. Lutheran 2. Kell 3. Lewis 4. Duffy 5. Bombay,
etc..
5
2. Land Steiners law
  • If an agglutinogen is present on red cells of
    blood, the corresponding agglutinin must be
    absent from the plasma.
  • If the particular antigen is absent, the
  • corresponding antibody must be present.
  • Note The 2nd law is a fact, but not must .
  • Ex. Absence of Rh antigen is
    not accompanied by
  • the presence of anti-Rh
    antibody.

6
A. Classical ABO System
7
Classical ABO System
8
Classical ABO System
9
Classical ABO System
Blood Type Antigens (Agglutinogens) on Red Blood Cells Antibodies (Agglutinins) in Plasma
A A Anti-B
B B Anti-A
AB A B None
O Neither Anti-A Anti-B
Note A has 2 sub units A1 and A2
10

Percentage of Distribution of ABO Blood Groups
11
Formation of the A antigen
B. Inheritance of ABO System
RBC
Glucose
Galactose
N-acetyl glucosamine
Galactose
N-acetylgalactosamine
Fucose
12
3. Basis of ABO Blood Group
ABO agglutinogens
  • The fructose containing H ag is the basic ag
    found
  • in all individuals
  • In case of ag A, N acetyl galactosamine as
    terminal
  • sugar on H ag
  • In ag B the terminal sugar is galactose
  • In AB persons both transferases are present
    while in
  • O group none of the enzymes present.

13
Formation of the B antigen
RBC
Glucose
Galactose
N-acetylglucosamine
Galactose
Galactose
Fucose
14
4. How an individual gets his/her Blood Group
Gene received from parents Group of of offspring Genotype
AA A AA
AO A AO
BB B BB
BO B BO
AB AB AB
OO O OO
15
ABO agglutinins
  • These are natural antibodies and belongs to Ig M
    and so do not cross the placental barrier.
  • These are called cold agglutinins because they
    react better between 5-20c
  • They appear after birth due to exposure to A and
    B antigens, which may enter the body along with
    food or bacteria

16
Blood Typing/grouping/matching
Note Typing is done on the basis of
agglutination
17
Major and Minor Cross matching of blood
Donors Blood
Patients blood
Minor Cross matching
Plasma
Major Cross matching
RBCs
Patients Plasma Donors RBCs Major
Cross-Match
Donors Plasma Patients RBCs Minor
Cross-Match
TASK Mix and place a drop of plasma or RBC onto
slide/test tube Observe for
Agglutination or Hemolysis.
18
Compatibility between the donors cells and
recipients serum
Anti- Body
Receive From
Donate To





Type
Antigen
A
A
A or O
A or AB
Anti - B
B
Anti - A
B
B or AB
B or O
UniversalReceiver
Neither
AB
A B
AB,A,B,O
AB
UniversalDonor
O
None
Both
O
O,A,B,AB
19
RBC Compatibility
20
6. Effects of ABO Incompatible blood transfusion
  1. Immediate effects Fever, chills nausea,
    vomiting, chest pain, back pain and rigor
  2. Delayed effects Jaundice, cardiac shock and
    renal shut down

21
II. Rh Blood group system
  • Landsteiner and Weiner discovered this group in
    1940.
  • 7. Rh factor
  • Rh factor is an ag present in RBC
  • First discovered in Rhesus monkey so
  • named as Rh factor
  • The person having D ag are called Rh ve and
    without D ag are called Rh- ve
  • Importance Erythroblastosisfetalis is the
    condition occur because of Rh incompatibility

22
Rh Blood group system Group
Rh Rh-
O 38.5 6.5
A 34.3 5.7
B 8.6 1.4
AB 4.3 0.7
23
Rh agglutinins
  • These are called warm abs as they react better at
    body temp 37c
  • 2. The Rh abs belongs to Ig G group and can
    enter the fetal circulation through placenta.

24
Rh
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Exercise-1
30
Rh group-applied aspect
  • Transfusion reactions

31
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Haemolytic disease of new born HDN
About 1 in 10 pregnancies involve an Rh-negative
mother and an Rh-positive father
33
Hemolytic Disease of Newborn
  • Rh antibodies attack fetal blood
  • causing severe anemia

34
3. The HDN is associated with the following
features
  • Haemolytic anaemia
  • b. Erythro blastosis fetalis
  • Due to excess destruction of RBSs there is an
    increased production of RBSs not only from the
    bone marrow but also from liver and spleen
  • Due to rapid destruction, blast cells are
    released into the circulation called EBF.

35
Blood film of a fetus affected by HDN showing
increased number of normaoblasts
36
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  • C. Kernicterus Due to haemolysis excess
    bilirubin is formed. This causes jaundice. The
    excess bilirubin enters the brain and causes
    permanent damage
  • D. Hydrops fetalis The fetus
  • may develop oedema of all the
  • organs leading to the intra uterine
  • death.

38
  • Prevention
  • By marriage counseling
  • Rh-ve mother with Rh ve fetus should be
    administered anti-D abs at 28th and 34th weeks of
    gestation
  • Rh-ve mother with Rh ve fetus-anti D abs are
    given immediately after 1st delivery within 48h.
    to neutralize the ags that would have entered the
    mothers blood

39
  • 8. Treatment of HDN
  • Erythroblastosisfetalis
  • Exchange transfusion
  • 1. Is replacement of newborn babys
  • blood with Rh- ve blood.
  • 2. Babys Rh ve blood is removed
  • slowly an about 400ml of Rh-ve is
  • infused is called exchange
  • transfusion

40
  • III. MNS System
  • In 1921,Landsteinerand Levine discovered this
    blood group
  • They are used in medico legal cases like parent
    dispute etc.,
  • 9. Medico-legal Importance
  • 1. Any red stain on a clotting may be claimed
    to be a supposed victim
  • 2. Therefore it is first confirmed that it is
    really a human blood
  • 3. Blood Group of extracted sample can be then
    prove or disprove the claim of the victim
  • 4. In doubtful cases DNA finger printing would
    help.

41
  • IV. Bombay Blood Group
  • This is the rare blood group in which H ag is
    absent, Since there is no H ag there is no ag A
    or ag B on RBC.
  • However, the plasma contains anti- A, anti-B and
    anti-H abs.
  • As a result , such a person can receive blood
    only from person having Bombay blood group

42
  • Importance of Blood Groups
  • To avoid transfusion reactions of blood
  • Medico legal cases like disputed parented age
    and to find out the criminals
  • Research purposes as some blood groups are
    associated with a high incidence of certain
    disease
  • For matching the tissues during organ
    transplantation
  • For preventing development of HDN

43
  • Blood Transfusion

44
  • Transfusion The 1st blood transfusion was made
    in 1667 by Dr. Jean Baptiste. Sheep blood was
    transfused to a 15 yr old boy.
  • Transfusion is done to restore blood volume
    when there is
  • a decrease in blood volume.
  • Ex. Hemorrhage, burns ,dehydration, severe
    anaemia and
  • surgery

45
Blood Substitutes
  • When the required blood group is not available
    we give blood substitutes
  • Ex Packed RBCs, Platelet conc., plasma,
    saline, volume expanders, Albumin and clotting
    factor concentrate
  • Collection of Blood About 350-500ml of blood
    depending on the Hb level

46
Effect of storage
  • Blood is stored in siliconized bottles in blood
    banks at 4c
  • An anticoagulant ACD / CPD is used for preventing
    clotting
  • 10. Blood undergoes the following changes
  • during storage
  • Increases in Na, decrease in Kwith net
    increase in water
  • As a result the cell swells and is susceptible
    to
  • haemolysis, after 20 days most of RBC get lysed.

47
Precautions of transfusion
  • Select healthy donor for transfusion
  • Matching and typing should be done
  • Before we use the blood, it should be warmed to
    the normal body temp.
  • Transfusion should be done at a slower rate
  • Whole blood transfusion
  • Autologous transfusion
  • Blood doping

48
Treatment
  • Stop transfusion immediately on signs of
    incompatibility
  • 2. To suppress reaction, corticosteroids and
    Antihistamines are also administered
  • 3. If anuria is present, dialysis is given till
    the kidney function is recovered
  • 4. Anaemia may be treated suitably
  • 5. Osmotic dieresis should be induced
  •  

49
Give Blood and Save lives !!
Thank you
50
BLANKS
  • A new born with blood group B ve is having
    Erythroblastosis fetalis, Which is the most
    appropriate line of treatment exchange
    transfusion with Bve
  • The person is known as universal donor if he/she
    belongs to blood group O
  • Major crossmatching is tested between donors
    cells and recipient plasma
  • The person is universal recipient if he or she
    belongs to blood groupAB
  • One of the most lethal effects of transfusion
    reaction is acute Kidney shutdown
  • Erythroblastosisfoetalis is the mother is Rh-ve
    and fetus is Rh ve

51
Essay
  • Name the various blood groups? Describe its
    importance? Add a note on transfusion reactions?
  • 2. What is the physiological basis of blood
    groups and how they determined? Give an account
    of the significance of Rh factor?

52
Short notes
  • Transfusion reactions
  • 2. Erythroblastosisfetalis
  • 3. ABO system
  • 4. Rh factor

53
Ultra short notes
  • Name the different blood groups and describe how
    an individual gets his/ her blood group?
  • 2. What is Rh factor? What is its importance?
  • 3. What are the effects of incompatible blood
    transfusion?
  • 4. Explain the basis of ABO blood grouping?
  • 5. Describe the medico legal importance of blood
    groups?

54
  • 6. What is cross matching and mis-matching?
  • 7. Mention the other types of blood grouping
    other than ABO system?
  • 8. What is treatment of Erythroblast sis fetalis?
  • 9. What are the changes that occur in stored
    blood? What is the significance of these changes?
  • 10. What are the disadvantages of prolonged
    storage of blood in blood banks?
  •  
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