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BLOOD TRANSFUSION
By_Arindam Mondal.
Blood transfusion
 Blood is an amazing fluid
 Keeps us warm
 Provides nutrients for cells, tissues and organs
 Removes waste products from various sites .
Blood transfusion
Theoritical Yield of components
 1 unit of blood theoritically gives
- 1 unit FFP
- 1 unit PRBC’s
- 1 random donor unit platelet
Blood transfusion
Blood components
 Packed red blood cells (PRBC)
 Platelets (PRP)
 Fresh Frozen Plasma (FFP)
 Cryoprecipate (CP)
 Cryo poor plasma (CPP)
Blood transfusion
Rational Use of Blood
Rational
- Right product
- Right dose
- Right time
- Right reasons
Blood transfusion
 Rationale behind Rational use of blood
- Economy – Scarcity of source
4 get blood component in 1 unit
- Safety – inherent risk involved in blood
transfusion
1 in 2 million gets HIV
- Scientifically appropriate
Haematinic in nutritional anaemia
BLOOD TRANSFUSION
 History :
 In 1667 Jean Baptiste Denis 1st transfusied – 3 units
Sheep blood in human successfully. his second try failed
& young man died.
 In 1825 1st human blood was transfused by
Dr. Philip Syng Physic of Philadelphia.
 In 1828 Blundell transfused blood to a pt. of postpartum
hemorrhage.
BLOOD TRANSFUSION
 In 1900 Landsteiner discovers A,B & O type
 Blood
 In 1902 Von De Castello and Sturil discovered
AB type blood - the era of modern
blood transfusion
 In 1940 cross matching, anticoagulation and storage of
blood and blood bank started and these developments
made routine blood transfusion possible
 In 1937 1st Blood bank in U.S.
BLOOD TRANSFUSION
 Blood groups –
 Major Blood groups:- based on presence of antigen on
RBCs surface.
 20 antigens identified in human , only three are important
being strongly antigenic.
A B and D ( Rh antigen).
 A & B antigens have natural corresponding Antibodies in
serum.
BLOOD TRANSFUSION
 No natural antibody D in serum , but formation can be
stimulated by giving
Rh +ve blood to Rh-ve
or
Acquired during delivery of a Rh +ve baby
Acquired antibody can cross placental barrier
Rh +ve in 85%
BLOOD TRANSFUSION
 Major Blood Groups are
 GROUP Antigen Antibody
A A B
B B A
AB AB Nil
O Nil AB
BLOOD TRANSFUSION
 Indication of blood transfusion :
A. Severe blood loss –
Traumatic
Pathological conditions
During operation
Severe burn
B. Anaemia Hb. < 8 Gms%
Post op. - pt. became anaemic
Pre-op. - In anaemia, packed cell
BLOOD TRANSFUSION
C. Prophylactic :
Prior to surgery –
Hemophilia
Thrombocytopenia
Liver disease
D. Septicemia
BLOOD TRANSFUSION
 Types of transfusion ( Blood fractions)
A. Packed cells :
Chr.anaemia, old age, Children.
B. Plasma
Burn, Hypo-albuminaemia, Severe
protein loss
BLOOD TRANSFUSION
C. Human albumin 4.5%
D. Fresh frozen plasma :
Contains all coagulation factor
E. Cryoprecipitate : haemophilia
( Rich in factor VIII & fibrinogen.)
F. Fibrinigen: DIC, Afibrinogenaemia
G. Platelet rich plasma - Thrombocytopenia
H. Platelet Concentrate. -----// -----//----//
BLOOD TRANSFUSION
 Collection of blood :
75ml of CPD ( Citrate phosphate Dextrose)
solution
Storage: 4⁰ C. ± 2⁰ C , in higher temp. >2hrs blood infected
In Stored Blood :
- RBCs. Lost in three weeks
- WBCs destroyed rapidly
- Platelets reduced in 24 hrs.
- Clotting factors are labile and level falls
quickly.
BLOOD TRANSFUSION
 Transfusion reaction :
A. Hemolytic transfusion reaction:
Causes –
- Incompitible blood.
- Out dated blood
- Hemolysed blood
Heating, Shacking, over
freezing, Infection
BLOOD TRANSFUSION
Clinical feature
Fever with chills & rigor
Flushing of face
Tightness of chest
Loin pain
Haemoglobinuria
oliguria
Bleeding
BLOOD TRANSFUSION
- Hypotension, Jaundice, DIC, Hyperkalemia
T/T
- Stop Blood & send sample for rechecking
- I/V Fluid
- Antihistaminic –
- Inj. Chlorphenaramine - 10mg.
- Steroids
- Dialysis
Monitor : pulse, BP, Urine output,
BLOOD TRANSFUSION
B. Non hemolitic reaction
i) Simple pyrexial reaction-
. Pyrogens
. Infected blood
. Rapid transfusion
BLOOD TRANSFUSION
ii) Allergic Reaction –
C/f - Appears within few hours
. Urticarial rashes & oedema
. Anaphylactic shock
iii) Bleeding diathesis :
. DIC
BLOOD TRANSFUSION
 Complication of blood transfusion;
A. Infections-
Serum hepatitis
HIV Infection
Bacterial infection
Malaria
Suphilis
B. Air embolism
BLOOD TRANSFUSION
C. Thrombocytopenia
D. Coagulation Failure -
. Dilution of coagulation
factor / platelet
. DIC
T/T Replace co- agulation factor
E. Citrate intoxication.
BLOOD TRANSFUSION
 Treatment ;
- Stop Blood & send sample for rechecking
- I/V Fluid
- Antihistaminic – Inj.Avil
- Inj. Hydrocartisone 100mg. I/V
- I/V Manitol
- 7.5% Naco3
- hemodialysis
BLOOD TRANSFUSION
Blood Substitute:
1) Human albumin 4.5% - no risk of hepatitis
2) Dextrans – to improve plasma volume
i) Low molecular Wt. ( 40)
- very effective to restore volume
immediately
- transitory effect
- Prevent sludging in kidney
BLOOD TRANSFUSION
 Ii) high molecular wt. ( 110, 70 )
- Less effective.
- Long acting
Precautions :
Take blood sample for X-match & grouping
Before
- Precipitate abnormal bleeding
- Not more then 1000ml Dextrans
Hemophilia
Hemophilia
 It is most common X- linked recessive congenital
coagulation disorder.
 Males are symptomatic ,
 females are carrier.
BLOOD TRANSFUSION
 Types :
Hemophilia A – Factor VIII deficiency
Hemophilia B – Factor IX deficiency
 Incidence ; 1 in 10,000 Males , 80% to 85% are HemophiliaA
BLOOD TRANSFUSION
 Classification :
Depends on Functional level of Factor VIII c .
Mild – Factor level 5% to 30% of normel
Moderate- ,, ,, 2% to 5%
Severe ,, ,, < 2%
BLOOD TRANSFUSION
 Presentation on severity:
Severe – Spontaneous bleeding in Muscle, Joints
Mild & Moderate – Bleed after Trauma
Diag. – History & investigation
Investigation _ BT, PT, aPTT, Fact. VIII & IX l…
Hem. A Hem. B
BT, N N
PT, N N
aPTT prolonged Abnormal
VIII:C / factor IX VIII:C decreased Fact. IX decreased
TT N N
vWF: Ag N N
BLOOD TRANSFUSION
- Factor IX is Vit. K dependent hence in deficiency of Vit K
factor IX is decreased.
- But In Vit. K.deficiency PT is prolonged and returns to Normal
after Inj. Vit. K.
BLOOD TRANSFUSION
 Treatment :
. Factor replacement
. Tab. Trenaximic acid 500 mg , tds
. Tab metrozyle 400 mg tds
. Controle bleeding Direct pressure
BLOOD TRANSFUSION
Preparation of pt. for Dental Procedure :
- Polishing / Scaling – No factor replacement
- Extraction –
- Good oral hygiene, to avoid need of
tooth extraction
- Factor replacement depending on
severity of disease
BLOOD TRANSFUSION
 Preparation of hemophilicpt. for tooth extraction :
Desired % Factor VIII Factor IX Days
30 -50 15 -25 Unt/ Kg 30-50 unit /kg 0-2
20-30 10-15 Unt / Kg 20-30 unit./ kg 2-4
 Calculation of factor dose :
- Hemo A - % of dose needed * body wt.Kg / 2
- Hemo B - % of dose needed * body wt. Kg
BLOOD TRANSFUSION
- Antifibrinolytic – Tranexamic acid 500 mg, from previous night
of surg and continue for 7-8 days after extration
- Metroniadazol – 400mg tds. For 7 days
- Mouth washes with 8.5% tranexamic acid .
- cavity to be packed with fibrin glue.
- Vicryl suture to be used.
Thank U

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Blood transfusion & Hemophilia...

  • 2. Blood transfusion  Blood is an amazing fluid  Keeps us warm  Provides nutrients for cells, tissues and organs  Removes waste products from various sites .
  • 3. Blood transfusion Theoritical Yield of components  1 unit of blood theoritically gives - 1 unit FFP - 1 unit PRBC’s - 1 random donor unit platelet
  • 4. Blood transfusion Blood components  Packed red blood cells (PRBC)  Platelets (PRP)  Fresh Frozen Plasma (FFP)  Cryoprecipate (CP)  Cryo poor plasma (CPP)
  • 5. Blood transfusion Rational Use of Blood Rational - Right product - Right dose - Right time - Right reasons
  • 6. Blood transfusion  Rationale behind Rational use of blood - Economy – Scarcity of source 4 get blood component in 1 unit - Safety – inherent risk involved in blood transfusion 1 in 2 million gets HIV - Scientifically appropriate Haematinic in nutritional anaemia
  • 7. BLOOD TRANSFUSION  History :  In 1667 Jean Baptiste Denis 1st transfusied – 3 units Sheep blood in human successfully. his second try failed & young man died.  In 1825 1st human blood was transfused by Dr. Philip Syng Physic of Philadelphia.  In 1828 Blundell transfused blood to a pt. of postpartum hemorrhage.
  • 8. BLOOD TRANSFUSION  In 1900 Landsteiner discovers A,B & O type  Blood  In 1902 Von De Castello and Sturil discovered AB type blood - the era of modern blood transfusion  In 1940 cross matching, anticoagulation and storage of blood and blood bank started and these developments made routine blood transfusion possible  In 1937 1st Blood bank in U.S.
  • 9. BLOOD TRANSFUSION  Blood groups –  Major Blood groups:- based on presence of antigen on RBCs surface.  20 antigens identified in human , only three are important being strongly antigenic. A B and D ( Rh antigen).  A & B antigens have natural corresponding Antibodies in serum.
  • 10. BLOOD TRANSFUSION  No natural antibody D in serum , but formation can be stimulated by giving Rh +ve blood to Rh-ve or Acquired during delivery of a Rh +ve baby Acquired antibody can cross placental barrier Rh +ve in 85%
  • 11. BLOOD TRANSFUSION  Major Blood Groups are  GROUP Antigen Antibody A A B B B A AB AB Nil O Nil AB
  • 12. BLOOD TRANSFUSION  Indication of blood transfusion : A. Severe blood loss – Traumatic Pathological conditions During operation Severe burn B. Anaemia Hb. < 8 Gms% Post op. - pt. became anaemic Pre-op. - In anaemia, packed cell
  • 13. BLOOD TRANSFUSION C. Prophylactic : Prior to surgery – Hemophilia Thrombocytopenia Liver disease D. Septicemia
  • 14. BLOOD TRANSFUSION  Types of transfusion ( Blood fractions) A. Packed cells : Chr.anaemia, old age, Children. B. Plasma Burn, Hypo-albuminaemia, Severe protein loss
  • 15. BLOOD TRANSFUSION C. Human albumin 4.5% D. Fresh frozen plasma : Contains all coagulation factor E. Cryoprecipitate : haemophilia ( Rich in factor VIII & fibrinogen.) F. Fibrinigen: DIC, Afibrinogenaemia G. Platelet rich plasma - Thrombocytopenia H. Platelet Concentrate. -----// -----//----//
  • 16. BLOOD TRANSFUSION  Collection of blood : 75ml of CPD ( Citrate phosphate Dextrose) solution Storage: 4⁰ C. ± 2⁰ C , in higher temp. >2hrs blood infected In Stored Blood : - RBCs. Lost in three weeks - WBCs destroyed rapidly - Platelets reduced in 24 hrs. - Clotting factors are labile and level falls quickly.
  • 17. BLOOD TRANSFUSION  Transfusion reaction : A. Hemolytic transfusion reaction: Causes – - Incompitible blood. - Out dated blood - Hemolysed blood Heating, Shacking, over freezing, Infection
  • 18. BLOOD TRANSFUSION Clinical feature Fever with chills & rigor Flushing of face Tightness of chest Loin pain Haemoglobinuria oliguria Bleeding
  • 19. BLOOD TRANSFUSION - Hypotension, Jaundice, DIC, Hyperkalemia T/T - Stop Blood & send sample for rechecking - I/V Fluid - Antihistaminic – - Inj. Chlorphenaramine - 10mg. - Steroids - Dialysis Monitor : pulse, BP, Urine output,
  • 20. BLOOD TRANSFUSION B. Non hemolitic reaction i) Simple pyrexial reaction- . Pyrogens . Infected blood . Rapid transfusion
  • 21. BLOOD TRANSFUSION ii) Allergic Reaction – C/f - Appears within few hours . Urticarial rashes & oedema . Anaphylactic shock iii) Bleeding diathesis : . DIC
  • 22. BLOOD TRANSFUSION  Complication of blood transfusion; A. Infections- Serum hepatitis HIV Infection Bacterial infection Malaria Suphilis B. Air embolism
  • 23. BLOOD TRANSFUSION C. Thrombocytopenia D. Coagulation Failure - . Dilution of coagulation factor / platelet . DIC T/T Replace co- agulation factor E. Citrate intoxication.
  • 24. BLOOD TRANSFUSION  Treatment ; - Stop Blood & send sample for rechecking - I/V Fluid - Antihistaminic – Inj.Avil - Inj. Hydrocartisone 100mg. I/V - I/V Manitol - 7.5% Naco3 - hemodialysis
  • 25. BLOOD TRANSFUSION Blood Substitute: 1) Human albumin 4.5% - no risk of hepatitis 2) Dextrans – to improve plasma volume i) Low molecular Wt. ( 40) - very effective to restore volume immediately - transitory effect - Prevent sludging in kidney
  • 26. BLOOD TRANSFUSION  Ii) high molecular wt. ( 110, 70 ) - Less effective. - Long acting Precautions : Take blood sample for X-match & grouping Before - Precipitate abnormal bleeding - Not more then 1000ml Dextrans
  • 28. Hemophilia  It is most common X- linked recessive congenital coagulation disorder.  Males are symptomatic ,  females are carrier.
  • 29. BLOOD TRANSFUSION  Types : Hemophilia A – Factor VIII deficiency Hemophilia B – Factor IX deficiency  Incidence ; 1 in 10,000 Males , 80% to 85% are HemophiliaA
  • 30. BLOOD TRANSFUSION  Classification : Depends on Functional level of Factor VIII c . Mild – Factor level 5% to 30% of normel Moderate- ,, ,, 2% to 5% Severe ,, ,, < 2%
  • 31. BLOOD TRANSFUSION  Presentation on severity: Severe – Spontaneous bleeding in Muscle, Joints Mild & Moderate – Bleed after Trauma Diag. – History & investigation Investigation _ BT, PT, aPTT, Fact. VIII & IX l… Hem. A Hem. B BT, N N PT, N N aPTT prolonged Abnormal VIII:C / factor IX VIII:C decreased Fact. IX decreased TT N N vWF: Ag N N
  • 32. BLOOD TRANSFUSION - Factor IX is Vit. K dependent hence in deficiency of Vit K factor IX is decreased. - But In Vit. K.deficiency PT is prolonged and returns to Normal after Inj. Vit. K.
  • 33. BLOOD TRANSFUSION  Treatment : . Factor replacement . Tab. Trenaximic acid 500 mg , tds . Tab metrozyle 400 mg tds . Controle bleeding Direct pressure
  • 34. BLOOD TRANSFUSION Preparation of pt. for Dental Procedure : - Polishing / Scaling – No factor replacement - Extraction – - Good oral hygiene, to avoid need of tooth extraction - Factor replacement depending on severity of disease
  • 35. BLOOD TRANSFUSION  Preparation of hemophilicpt. for tooth extraction : Desired % Factor VIII Factor IX Days 30 -50 15 -25 Unt/ Kg 30-50 unit /kg 0-2 20-30 10-15 Unt / Kg 20-30 unit./ kg 2-4  Calculation of factor dose : - Hemo A - % of dose needed * body wt.Kg / 2 - Hemo B - % of dose needed * body wt. Kg
  • 36. BLOOD TRANSFUSION - Antifibrinolytic – Tranexamic acid 500 mg, from previous night of surg and continue for 7-8 days after extration - Metroniadazol – 400mg tds. For 7 days - Mouth washes with 8.5% tranexamic acid . - cavity to be packed with fibrin glue. - Vicryl suture to be used.