(1) The Blood
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THE BLOOD
Oxygen transport
Chemical nutrients for and wasteproducts from metabolic activities
Homeostatic governors: Hormones
Coagulation factors
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Blood Components
Formed Elements: Cells
Red cellsO2 carrying capacity
White cells--- Body defenses Platelets--Haemostasis
Plasma : Coagulation factors
Proteins Hormones
Antibodies etc
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Blood Transfusion
History:1667 : Sheep to human { Emerez }
1900 : Blood grouping A,B,O {Landesteiner}
1914 : First successful blood transfusion
1937 : First blood bank
1940 : Rhesus system
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Blood Loss
Loss of 10-20% of blood volume can becompensated immediately by shift ofinterstitial fluid
30-40 hours :blood volume replacement
5-6 weeks :Red cells and HB
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Blood preservation
Solutions
Acid citrate dextrose ACD
Citrate phosphate dextrose CPD
Citrate phosphate double dextrose
adenine CP2D
Cooling
Freezing
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Distribution of ABO groups in Britain
B.Group RBC Ag Serum AbFrequency
A A AntiB 42%
B B Anti A 8%
AB A&B Nil 3%
O Neither AntiA&B 47%
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Rhesus antibody Rh (D)
Positive in 85%
Negative in 15%
No antigen present against it but it can formlater
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Effects of banking on blood 1. Red cells:
Anaerobic metabolism
DecreaseATP& 23D
Results: Alters O2 dissociation curve Increase affinity of RBC to O2
Decrease O2 transport function
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Effects ofBanking on blood Platelates..Lysis
Clotting factors: ..II,VII, IX, XI are Stable
. V,VIII, are Unstable.
Plasma changes:
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Fresh whole blood Within 24 hours :
Good source of factor V & VII
Platelates ? 6 hours to lyse
Indications : RARE
Hazards Transmitting infective agents
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Packed Red Cells Reduced risk of hepatitis
Improved RBC viability Maintained ATP% 23DPG
Less danger of circulatory overload
Less reactions secondary to allergens
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Fresh Frozen Plasma Main indications:
Factors V&VIII deficiency
Hypovolemia ??
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Leucocyte and platelets washed RBC
After washing with normal saline
Only used for patients sensitive toWBCs or platelets
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Platelets Rich Plasma
(Platelets Concentrate)
Massive blood loss
Massive blood transfusion Inadequate destruction
Qualitative disorders The development of iso-immunity is an
important factor limiting its use aftermultiple transfusions
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CONCENTRATESAntihemophilic factor VIII
Cryoprecipitate Fibrinogen
Albumin
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Indication of transfusion of
blood and it
s products 1.Volume replacement:
Difficult to evaluate accurately How much can we loose before showing
significant symptoms and signs.
Operative estimation
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Indication for transfusion of
blood and its products2.Improvement of oxygenation
Chronic anaemiaAcute anaemia
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Indication for transfusion of
blood and its products3 . Replacement of clotting factors:
Dilutional coagulopathy Specific factors VIII,IX etc..
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Indications for Transfusion Traumatic accidents and hemorrhage.
During major operative procedures. Sever burns.
Post operative.
Preoperative. To arrest hemorrhage in hemolytic
anemias
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In case of multiple donors Cross-match between donors
Major and minor cross-match Cold agglutinin titer estimation
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Methods of administration Intravenous route
Rate: 5ml per minute
Then 10-20 per minute
When fast administration is needed:
USEBLOODWARMER
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Massive Transfusion 2500 ml Single transfusion
5000 ml within 24 hours
Effects : Delusionalthrombocytopenia
Decrease factors V,VIII IX
Acidosis
Hemolytic transfusion reactions due to crossincompatability
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Complications I..Hemolytic Reactions Major incompatibility
Sequences:
Hemoglobinemia
Hemoglobinuria
Disseminated intravascularcoagulopathy
Decreased Hb
Incr
eas
e biliru
bin
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CLINICAL MANIFESTATIONS
OF INCOMPATABILITY
Heatsensation Pains
Chills Respiratorydistress
Fever Hypotension
Tachycardia
#Hypotensionandexcessive bleedinginanesthetizedpatientsduringsurgery
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Management
Stop transfusion
Bloodsample for:
Cross-matching
Bilirubin
Others
MonitoringvitalsignsandUrinaryoutput
Alkalinazationofurine
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Complications II Allergic reactions
Causedmostlyby: minorantibodies
preservativesManifestations: Urticaria
fever
Anaphylactic reactions
Treatment: AntihistaminsAdrenalin
Steroids
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Complications III Transmission of infectious diseases
Malaria Brucella Syphilis
Viral Hepatitis B & C
HIV { AIDS}
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Fate ofBanked whole blood
after transfusion
Fresh blood 70% viable in 24hours
Banked 14 days 50% viable in 60days
Banked 28 days 25% viable in 60days