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BLOOD & BLOOD
PRODUCTS
 BLOOD
1. Whole Blood
2. Packed Cell
3. Granulocytes
 BLOOD
PRODUCTS
1. F.F.P.
2. Cryoprecipitate
3. Platelete
Blood Components
Preparation
 Based on different specific gravities
 RBC : 1.08-1.09
 Platelet : 1.03-1.04
 By using differential centrifugation,blood
components separated into layers
 From a unit of
whole blood,the
centrifuged
product settle
out into
RBC,WBC &
platelet-rich
plasma(PRP).
 After separating
PRP fr the
bag,PRP again
being centrifuge
for a longer time
& harder spin.
 Plt is heavier
than plasma &
will settled at the
bottom of the
bag.
WHOLE BLOOD
 Source of product for all blood components
 400-500 ml
 Storage temperature :1-6 C
 Ind.:to maintain blood volume & O2 carrying
capacity in acute,massive blood loss.
 Actively bleeding pt>20% of body blood volume.
PACKED CELL
 Prepared by removing 200-250ml of plasma
from a unit of W.B.
 200-250 ml
 Do not contain functional platelets or
granulocytes
 Have the same O2 carrying capacity with
W.B
 Ind.:to increase the O2 carrying capacity in
anaemic pt who require an increase in their
red cell mass w/out increase in their blood
volume.
 1 unit: increase Hb level about 1g/dL
(10g/L)& Hct by 3%.
GRANULOCYTES
 Prepared by leukoparesis tech.
 Contain of
1. Large number of granulocytes
2. Other leucocytes
3. 20-50ml of RBC
 Ind.:
1. Supportive tx for pt with severe neutropenia
with documented sepsis unresponsive to
a/biotic tx.
2. Neonatal sepsis.
PLATELET
 Prepared by cytapheresis/by seperating
PRP fr a unit of W.B w/in 8H of
collection & recentrifuge to remove
plasma.
 Stored at 20-24C.
 Each unit of plt expected to increase
5000-10000 plt.
 Indications:
1. Prophylaxis.
2. Dilutional thrombocytopenia
3. Active bleeding d/t
thrombocytopenia/thrombocytopathy.
FRESH FROZEN PLASMA
 Prepared by removing plasma fr W.B w/in
8H of collection.
 Stored at –18C or below.
 Contains of:
1. Water,carbohydrates,fats,minerals
2. Proteins(all labile & stable clotting fx).
 200-225ml
 Each unit of FFP=increase the level of each
clotting fx by 2-3% in adults.
 Therapeutic dose : 10-15ml/kg.
 Indications:
1. As a replacement for isolated coagulation fx
def.
2. The reversal of warfarin Tx.
3. In the case of massive blood transfusion.
4. Antithrombin III def.Tx.
5. Correction of coagulopathy a/w liver
disease.
6. Thrombotic thrombocytopenic purpura.
CRYOPRECIPITATE
 The cold-insoluble portion of plasma that
remains after FFP has been thawed at 1-
6C.
 Contains of:
1. Factor VIII:C
2. Factor VIII:vWF
3. Factor XIII
4. Fibrinogen
5. About 10-15ml of plasma
 Stored at –18C & below.
 Indications:
1. von Willebrand’s disease
2. Hemophillia A
3. Factor XIII def.
4. Cong./acquired fibrinogen def.
COMPLICATIONS OF
BLOOD TRANSFUSION
COMPLICATIONS OF
BLOOD TRANSFUSION
ACUTE IMMUNOLOGIC
EFFECTS
1}Hemolytic transfusion reactions
 Mediators:IgM A/b (usuallyABO),
complement.
 Sx/sn:fever,chill,hemoglobinemia,
hemoglobinuria,hypotension,dyspne
a.
 Mx/px:decrease opportunities for
error,treat ARF & DIC.
2}Nonhemolytic febrile transfusion
reactions
 Mediators:A/b to HLA Class I Ag.
 Sx/sn:fever,chill.
 Mx/px:antipyretics,leukocyte depletion.
3}Allergic transfusion reactions.
 Mediators:plasma proteins(mild
reactions), A/b to IgA(anaphylactic
reactions).
 Sx/sn:urticaria,erythema,itching,
anaphylaxis.
 Mx/px:antihistamines;treat sx,transfuse
IgA-deficient components.
4}Noncardiogenic pulmonary transfusion
reactions
 Mediators:donor/recipient WBC A/b.
 Sx/sn:ARD,fever,chill,cyanosis,hypotens
ion,noncardiogenic pulmonary edema.
 Mx/px: vigorous respiratory support,
steroids.
ACUTE NONIMMUNOLOGIC
EFFECTS
1}Bacterial contamination
 Md :endotoxins produced by GN bact.
 Sx/sn:fever,shock,hemoglobinuria.
 Mx/px:IV a/biotics;treat hypotension &
DIC.
2}Circulatory overload
 Md: fluid volume.
 Sx/sn:coughing,cyanosis,orthopnea,sev
ere headache,peripheral edema,diff
breathing.
 Mx/px:administer subsequent Tx slowly
& in a small volume.
3}Hemolysis d/t physical/chemical means
 Md:exogenous destruction of RBC.
 Sx/sn:hemoglobinuria.
 Mx/px:document & rule out hemolysis
d/t other causes;treat DIC.
DELAYED IMMUNOLOGIC
EFFECTS
1}Hemolytic transfusion reactions.
 Md:IgG A/b.
 Sx/sn:shortened RBC
survival,decreased
Hb,fever,jaundice,hemoglobinuria.
 Mx/px:Ag-negative blood for further
transfusions.
2}Transfusion associated Graft-versus-host
disease
 Md:viable donor lymphocytes.
 Sx/sn:fever,skin
rash,desquamation,anorexia,nausea,
vomiting,diarrhea,hepatitis,pancytopenia
 Mx/px:gamma irradiation of cellular
components.
3}Post-transfusion purpura
 Md:platelet specific A/b.
 Sx/sn:thrombocytopenia,clinical
bleeding.
 Mx/px:IV Ig,plasma exchange,
corticosteroids.
DELAYED
NONIMMUNOLOGIC
EFFECTS
Transfusion-Induced Hemosiderosis.
 Md:Iron overload.
 Sx/sn: subclinical to death.
 Mx/px:decrease fq of
transfusion,neocytes, iron chelation
therapy.
STEPS TO BE FOLLOWED
1. Discontinue the transfusion.
2. Keep the IV line open with N/saline.
3. Check all labels,forms & pt
identification.
4. Report to Blood Bank personnel.
5. Send requested blood samples.
THANK
YOU

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blood_products.ppt

  • 2.  BLOOD 1. Whole Blood 2. Packed Cell 3. Granulocytes  BLOOD PRODUCTS 1. F.F.P. 2. Cryoprecipitate 3. Platelete
  • 3. Blood Components Preparation  Based on different specific gravities  RBC : 1.08-1.09  Platelet : 1.03-1.04  By using differential centrifugation,blood components separated into layers
  • 4.  From a unit of whole blood,the centrifuged product settle out into RBC,WBC & platelet-rich plasma(PRP).  After separating PRP fr the bag,PRP again being centrifuge for a longer time & harder spin.  Plt is heavier than plasma & will settled at the bottom of the bag.
  • 5. WHOLE BLOOD  Source of product for all blood components  400-500 ml  Storage temperature :1-6 C  Ind.:to maintain blood volume & O2 carrying capacity in acute,massive blood loss.  Actively bleeding pt>20% of body blood volume.
  • 6. PACKED CELL  Prepared by removing 200-250ml of plasma from a unit of W.B.  200-250 ml  Do not contain functional platelets or granulocytes  Have the same O2 carrying capacity with W.B  Ind.:to increase the O2 carrying capacity in anaemic pt who require an increase in their red cell mass w/out increase in their blood volume.  1 unit: increase Hb level about 1g/dL (10g/L)& Hct by 3%.
  • 7. GRANULOCYTES  Prepared by leukoparesis tech.  Contain of 1. Large number of granulocytes 2. Other leucocytes 3. 20-50ml of RBC  Ind.: 1. Supportive tx for pt with severe neutropenia with documented sepsis unresponsive to a/biotic tx. 2. Neonatal sepsis.
  • 8. PLATELET  Prepared by cytapheresis/by seperating PRP fr a unit of W.B w/in 8H of collection & recentrifuge to remove plasma.  Stored at 20-24C.  Each unit of plt expected to increase 5000-10000 plt.
  • 9.  Indications: 1. Prophylaxis. 2. Dilutional thrombocytopenia 3. Active bleeding d/t thrombocytopenia/thrombocytopathy.
  • 10. FRESH FROZEN PLASMA  Prepared by removing plasma fr W.B w/in 8H of collection.  Stored at –18C or below.  Contains of: 1. Water,carbohydrates,fats,minerals 2. Proteins(all labile & stable clotting fx).  200-225ml  Each unit of FFP=increase the level of each clotting fx by 2-3% in adults.  Therapeutic dose : 10-15ml/kg.
  • 11.  Indications: 1. As a replacement for isolated coagulation fx def. 2. The reversal of warfarin Tx. 3. In the case of massive blood transfusion. 4. Antithrombin III def.Tx. 5. Correction of coagulopathy a/w liver disease. 6. Thrombotic thrombocytopenic purpura.
  • 12. CRYOPRECIPITATE  The cold-insoluble portion of plasma that remains after FFP has been thawed at 1- 6C.  Contains of: 1. Factor VIII:C 2. Factor VIII:vWF 3. Factor XIII 4. Fibrinogen 5. About 10-15ml of plasma  Stored at –18C & below.
  • 13.  Indications: 1. von Willebrand’s disease 2. Hemophillia A 3. Factor XIII def. 4. Cong./acquired fibrinogen def.
  • 16. ACUTE IMMUNOLOGIC EFFECTS 1}Hemolytic transfusion reactions  Mediators:IgM A/b (usuallyABO), complement.  Sx/sn:fever,chill,hemoglobinemia, hemoglobinuria,hypotension,dyspne a.  Mx/px:decrease opportunities for error,treat ARF & DIC.
  • 17. 2}Nonhemolytic febrile transfusion reactions  Mediators:A/b to HLA Class I Ag.  Sx/sn:fever,chill.  Mx/px:antipyretics,leukocyte depletion.
  • 18. 3}Allergic transfusion reactions.  Mediators:plasma proteins(mild reactions), A/b to IgA(anaphylactic reactions).  Sx/sn:urticaria,erythema,itching, anaphylaxis.  Mx/px:antihistamines;treat sx,transfuse IgA-deficient components.
  • 19. 4}Noncardiogenic pulmonary transfusion reactions  Mediators:donor/recipient WBC A/b.  Sx/sn:ARD,fever,chill,cyanosis,hypotens ion,noncardiogenic pulmonary edema.  Mx/px: vigorous respiratory support, steroids.
  • 20. ACUTE NONIMMUNOLOGIC EFFECTS 1}Bacterial contamination  Md :endotoxins produced by GN bact.  Sx/sn:fever,shock,hemoglobinuria.  Mx/px:IV a/biotics;treat hypotension & DIC.
  • 21. 2}Circulatory overload  Md: fluid volume.  Sx/sn:coughing,cyanosis,orthopnea,sev ere headache,peripheral edema,diff breathing.  Mx/px:administer subsequent Tx slowly & in a small volume.
  • 22. 3}Hemolysis d/t physical/chemical means  Md:exogenous destruction of RBC.  Sx/sn:hemoglobinuria.  Mx/px:document & rule out hemolysis d/t other causes;treat DIC.
  • 23. DELAYED IMMUNOLOGIC EFFECTS 1}Hemolytic transfusion reactions.  Md:IgG A/b.  Sx/sn:shortened RBC survival,decreased Hb,fever,jaundice,hemoglobinuria.  Mx/px:Ag-negative blood for further transfusions.
  • 24. 2}Transfusion associated Graft-versus-host disease  Md:viable donor lymphocytes.  Sx/sn:fever,skin rash,desquamation,anorexia,nausea, vomiting,diarrhea,hepatitis,pancytopenia  Mx/px:gamma irradiation of cellular components.
  • 25. 3}Post-transfusion purpura  Md:platelet specific A/b.  Sx/sn:thrombocytopenia,clinical bleeding.  Mx/px:IV Ig,plasma exchange, corticosteroids.
  • 26. DELAYED NONIMMUNOLOGIC EFFECTS Transfusion-Induced Hemosiderosis.  Md:Iron overload.  Sx/sn: subclinical to death.  Mx/px:decrease fq of transfusion,neocytes, iron chelation therapy.
  • 27. STEPS TO BE FOLLOWED 1. Discontinue the transfusion. 2. Keep the IV line open with N/saline. 3. Check all labels,forms & pt identification. 4. Report to Blood Bank personnel. 5. Send requested blood samples.