2. BLOOD :
INTRODUCTION:
Blood is a specialized fluid which consist of liquid and cellular elements.
Liquid part is specialized protein rich fluid known as plasma
Cellular elements which are suspended in it are
o RBC
o WBC
o PLATELETS
Total circulatory blood volume is about 8% of body weight.
3. Functions :
• Deliver oxygen to tissues.
• Nutrients and constitutional elements such as A.A. to tissue.
• Remove waste products
• Acts as a highway for hormones to reach their destined target
tissue.
• Forms blood clots and prevent itself from being lost excessively.
4.
5. RED BLOOD CELLS :
Carry hemoglobin in circulation.
Biconcave disks in shape.
Life span of 120 days.
Average RBC count is approx.: 5.4 million/microliter in male
and 4.8 million/microliter in female.
Diameter is 7.5 micrometer.
Thickness is 2 micrometer.
6. Characteristics Of Red Blood Cells:
MALE FEMALE
HCT 47 42
RBC 5.4 4.8
HB 16 14
MCV 87 87
MCH 29 29
MCHC 34 34
MCD 7.5 7.5
7. WHITE BLOOD CELLS :
There are various types of white blood cells. These are
Polymorphonuclear leukocytes (most abundant cells)
o Neutrophils
o Eosinophils
o Basophilic.
Lymphocytes.
Monocytes.
Acts as powerful defense against tumor and infectious agent.
Range 4000-11000 per microliter.
8. PLATELETS :
Range 200000-500000 per microliter.
Small granulated bodies that lack nuclei and
aggregate at site of injury.
Diameter is 2-4 micrometer
Half life is 4 days.
9. PLASMA :
1. It’s a remarkable fluids which contains
o Ions.
o Inorganic molecules.
o Organic molecules.
Consist of 5% of body weight.
Few plasma proteins are mention below
o Albumin
o Globulin
o Fibrinogen
10. NORMAL VALUES FOR THE CELLULAR
ELEMENTS IN HUMAN BLOOD
CELLS Cells/μL Approximate Normal Percentage of Total White
Cells
Total White Blood Cells
Granulocytes
9000 4000–11,000
Neutrophils 5400 3000-6000 50-70
Eosinophils 275 150-300 1-4
Basophils 35 0-100 0.4
Lymphocytes 2750 1500-4000 20-40
Monocytes 540 300-600 2-8
Erythrocytes
Male 5.4 * 106
Female 4.8 * 106
Platelets 300000 200000-500000
11.
12.
13. History of blood transfusion :
1492 Pope innocent VIII suffers a stroke and receive a blood transfusion from 3 10 years old boy. All of them died later.
1665 Richard lower in oxford conducts the first successful canine transfusion.
1667 Jean-Baptiste denis reports successful sheep-human transfusions.
1678 Animal and human transfusion are banned in France because of poor result.
1818 James Blundell perform 1st successful/documented human transfusion in a woman suffering post-partum haemorrhage.
1901 Karl Landsteiner discovers ABO system.
1914 Belgian physician albert hustin performed first non-direct transfusion using sodium citrate as anti-coagulant
1926 British Red Cross instituted the first blood transfusion service in world.
1939 Rhesus system was identified and recognized as major cause of transfusion reactions.
14.
15. COMPONENTS OF BLOOD :
A constituent of blood, separated from whole blood.
few are listed below :
Packed red cells.
Fresh Frozen Plasma.
Cryoprecipitate.
Platelets
Granulocyte transfusion.
Prothrombin complex concentrates.
Factor 8 concentrate
Factor 9 concentrate
Other plasma fractions :
Albumin
Gamma globulin
16. COMPONENTS THERAPY AND THEIR
INDICATIONS:
1. Whole blood:
Although its ideal to replace the lost blood with whole
blood
Nowadays its rarely used.
17.
18. PACKED RED CELLS:
a. Main aim of transfusion here is to increase the oxygen-carrying capacity
of blood in anemic or bleeding patients.
b. Packed red blood cells are spun down and concentrated packs of red
blood cell s
c. Each unit is approx. 330ml and has hct of 50-70%
d. 1 unit increase Hb by .08-1 g/dl or Hct 3%
e. Stored at 2-6 Celsius.
19. PERIOPERATIVE RBC TRANSFUSION
CRITERIA :
Hb Level Indications
< 6 Probably will benefit for transfusion
6-8 Transfusion unlikely to be benefit in the absence of bleeding
or impending surgery
> 8 No indication for transfusion in the absence of other risk
factors
20. PLATELETS :
Prepared either from whole blood by centrifugation or by platelet
pheresis of single or multiple donors.
Supplied as a pooled platelet concentrate and contain about 250*109
/l
Stored for 5 days at 20-24 celsius.
1 unit of platelets increase the platelet count by approx.: 30-
50*109/l .
Indications:
Non-bleeding, stable inpatients : 10*109/l
Non-bleeding stable outpatients : 20*109/l
Major invasive procedures or bleeding : 50*109/l
Operation at critical sites such as brain and eyes : 100*109/l.
21. Contraindication for Platelet transfusion :
Autoimmune idiopathic thrombocytopenic purpura
Thrombotic thrombocytopenic purpura.
Heparin induced thrombocytopenia
Bleeding due to coagulopathy
22. FRESH FROZEN PLASMA :
Prepared by removing from fresh blood and freezing it at -30 celsius
to preserve liable clotting factors.
It contains normal levels of all coagulation factors.
Frozen with in 8 hours of collection
Stored at -40 - -50 celsiuS
Usual dose is 10-20ml/kg
Volume is approx.: 200-250ml.
23. Indication
PT or aPTT 1.5 Times normal in a bleeding patient.
Warfarin overdose with life threatening bleeding
Patients with multiple coagulation defects resulting from
hepatic insufficiency.
DIC
Factors def for which specific factors conc: are unavailable
Liable clotting factors have been depleted by transfusion of
very large volumes of old blood stored.
24. CRYOPRECIPITATE :
It’s a supernatant precipitate of FFP.
Contents : factor 8,13, VWF and fibrinogen
1 unit = 20 ml of volume
1 unit increases fibrinogen conc: by 7-8mg/dl
Usually administered in pool of 5 to 10 units
Stored at -30 celsius
Shelf life of 2 years.
Indications :
DIC
Low fibrinogen states
25. GRANULOCYTE CONCENTRATES :
Prepared from whole blood as buffy coats
Uses:
Patients with severe neutropenia with definitive evidence of
bacterial infections.
26. PROTHROBIN COMPLEX
CONCENTRATES :
These are highly purified concentrates prepared from pooled
plasma
Prepared with two formulations
3 factors: 2,9 and 10
4 factors: 2,7,9 and 10
Indications:
Emergency reversal of anticoagulant warfarin therapy in
uncontrolled hemorrhage.
Treatment or prophylaxis of bleeding in congenital deficiency
of vitamin k dependent factor
27. FACTOR 8 AND 9 CONCENTRATION:
Freeze dried preparations
Prepared from large pools of plasma
Indications:
Hemophilia
Von Willebrand's disease (where recombinant factors aren’t
available)
28. ALBUMIN :
Two preparations :
Human Albumin Solution 4.5%
Human Albumin Solution 20%
Indications:
Acute severe hypoalbuminemia
Replacement of fluid for plasma exchange
20% albumin solution is particularly useful for nephrotic syn and
liver disease who are fluid overloaded and resistant to diuretics
29. COMPLICATIONS:
IMMUNOLOGICAL NON-IMMUNOLOGICAL
Alloimmunization and incompatibility Transmission of infection:
Red Cells:
Immediate haemolytic transfusion reaction
Delayed haemolytic transfusion reaction
Viruses:
HAV,HBV,HCV,HI
V,HHV8
Parasites:
Malaria,
toxoplasmosis
Bacteria
Yersinia
enterocolitica
Staphylococcus
spp
Leukocytes and platelets :
Non haemolytic transfusion reaction
Post transfusion purpura
Poor survival of transfused platelets and granulocytes
Graft versus host disease
Lung injury (TRALI)
Iron overload due to multiple transfusion
Massive transfusion
Thrombophlebitis
Circulatory failure due volume overload
(TACO)
Plasma proteins:
Urticarial and anaphylactic reactions
each contains ap-proximately 29 pg of hemoglobin. There are thus about 3 ×1013 red blood cells and about 900 g of hemoglobin
in the circulating blood of an adult man
The red, oxygen-carrying pigment in the red blood cells of vertebrates is hemoglobin,a protein with a molecular weight
of 64,450. Hemoglobin is a globular molecule made up of four subunits Each subunit contains heme moiety conjugated to a polypeptide. Heme is an iron-containing porphyrin derivative The polypeptides are referred to collectively as the globin portion of the hemoglobin molecule.
Thus, hemoglobin A is designated α2β2 Not all the hemoglobin in the blood of normal adults is hemoglobin A. About 2.5% of the hemoglobin is hemoglobin A2 in which βchains are replaced by δchains (α2δ2).
hemoglobin A1c(HbA1c), has a glucose attached to the terminal valine in each βchain and is of special interest because it increases in the blood of patients with poorly controlled diabetes mellitus
Male Female
Hematocrit (Hct) (%) 47 42
Red blood cells (RBC)
(106/μL)5.4 4.8
MCD IS IN Micrometer is Mean diameter of 500 cells in smear
Young granulocytes have horse shoe shaped nuclei which becomes multilobed as they grow older
Among them only eosinophil are the one which are stained with acidic dyes
Lymphocytes have large round nuclei and scanty cytoplasm
Monocytes have abundant agranular cytoplasm and kidney shaped nuclei
Granulocytes – 4-8 hours in blood and 4-5 days in tissues
Monocytes – 10-20 hours in blood and becomes macrophages in tissue and can live upto months
Lymphocytes weeks or months moving from circulation into tissue and back again
Eosinophil cells are found most abundant in respiratory mucosa and gut mucosa
Platelets are small, granulated bodies that aggregate at sites of
vascular injury
they lack nuclei
The megakaryo-cytes,giant cells in the bone marrow, form platelets by pinching
off bits of cytoplasm and extruding them into the circulation
Between 60% and 75% of the platelets that have been extruded
from the bone marrow are in the circulating blood, and the re-mainder are mostly in the spleen
Cytoplasm of platelets contains actin myosin glycogen lysosomes and 2 types of granules
Alpha granules : contain clotting factors and PDGF
Dense granules : non protein substance : serotonin and ADP
Serum has same composition as plasma except that it’s fibrinogen and clotting factors 2,5 and 8 have been removed and have higher serotonin content due to breakdown of platelets during clotting.
Albumin exert osmotic force of about 25%.
Plasma albumin level 3.5-5.0g/dl .
Responsible for 15% of buffering capacity Total exchangeable albumin pool is 4.0 to 5.0 g/kg bodyweight..
6-8% of exchangeable pool is degraded per day and degraded albumin is replaced by hepatic synthesis of 200-400mg/kg/day.
38-45% of albumin in intravascular and among rest much of the rest of it is in the skin
Blood product : any therapeutic substance prepared from human blood
Whole blood : unseparated blood collected into an approved container containing an anticoagulant preservative solution
Platelet and plasma collected by apheresis
Few important indications for blood transfusion :
Following haemorrhage which may be due to
Trauma with severe blood loss
Bleeding from pathological lesion ( such as esophageal varices)
Major operative procedures with extensive dissection in which fair amount of blood is lost
After extensive burns where a good deal of blood is destroyed in burnt skin
Before operation: urgent surgery not sufficient time for iron therapy (cardiac output doesn’t rise until HB value < 7gm/dl)
Post operative: severe anemia has resulted from infections
WHOLE BLOOD
Unit consist of 450ml +- 10%
+63 ml of anticoagulant
Leukocyte depleted
Stored at 4 celsius
Shelf life of 5-6 weeks
All plasma is virtually removed and an additive solution. This solution of 100ml is used which is responsible for shelf life of PRC. These solutions are
SAG-M (Saline-adenine-glucose-mannitol) shelf life of 5 weeks
CPD (citrate-phosphate-dextrose) shelf life of 2-3 weeks
Patient of CAD or risk of ischemia are candidates of higher threshold ( no any significant advantage has been seen)
AUTOLOGOUS BLOOD:
Patients donate their own blood 3 weeks before surgery retransfusion during operation.
Blood can be collected in cell saver which washes and collects RBC which can then be returned to patient
Must never be placed in ice or refrigerated. Which can cause platelet activation.
Note : pt with myelodysplasia or aplastic anemia can tolerate continuously below 10000/microliter and 5000/microliter. In these pt there is no need for prophylactic transfusion due to risk of alloimmunization and platelet refractoriness.
Note: pts on clopidogrel who are actively bleeding and undergo major surgery may require continuous infusion of platelets during this process alternative nowadays with limited success are arginine vasopressor or it’s analogue.
DIFFERENT PALTELET CONTENT : SDP WBDP WBDPOOL
Also its not useful in patient who have splenomegaly.
ONLY REQUIRES ABO COMPATIBILITY
Prepared by removing from fresh blood and freezing it at -30 celsius to preserve liable clotting factors.
It contains normal levels of all coagulation factors.
Frozen with in 8 hours of collection
Stored at -40 - -50 celsiuS
Usual dose is 10-20ml/kg
Volume is approx.: 200-250ml.
Note : in case of warfarin overdose patients who are not bleeding and have raised abnormal PT should be treated with vit k instead.
Vit k 10mg iv slowly
No longer recommended for hemophilia A and VWF def due to greater risk of virus transmission compared to virus inactivated coagulation factor conc:
Note: the no: of granulocytes collected may be increased by treating donors with G.CSF and Steroids.
Notes: Albumin solution should not be used to treat patients with malnutrition or chronic renal disease or liver disease with low serum albumin levels.
Notes : inappropriate fluids for acute volume replacement or for treatment of shock
Normal immunoglobulins are used for hypogammaglobulinaemia.
Specific immunoglobulins which are obtained from donors of high titers of antibodies few such preparations are
Anti-d
Anti hepatitis B
Anti-varicella zoster
Human Albumin Solution 4.5%
4.5g/l albumin
160 mmol/l sodium
Available form 50,100,250 and 500
Human Albumin Solution 20%
200g/l albumin
130 mmol/l sodium
Available 50 and 100ml
VIRUSES : CMV,EBV
Red cells 1. immediate haemolytic transfusion reaction : occurs due to ABO incompatibility sym fever,rigors, lumbar pain ,chest pain, nausea,vomiting,dyspnea , hypotension, haemoglobinurea and RF. And bleeding due to DIC is a bad prognostic sign. Treatment according to shock protocols to maintain vitals and avoid renal failure. Confirmed by evidence of hemolysis such as haemoglobinurea. Urine output should be maintained at >100ml/hour with use of iv fluids diuretics or mannitol if necessary and excertion of free hb can be aided by alkalization of urine so sodium bicarbonate can be added to increase ph >7.5
In delayed pt usually develop jaundice and anaemia
Non haemolytic transfusion reaction: usual cause are the presence of alloimunized recipient acting against donor leukocytes results in release of pyrogens or cytokines sym: flushing tachycardia fever chills and rigors
TRALI: CAN OCCUR WITHIN 6 HOURS OF TRANSFUSION Characterized by dyspnea HYPOXEMIA HYPOTENSION fever cough and shadowing in perihilar and lower lung field on chest x ray needs respiratory support usually mechanical ventilation is frequently necessary resolve in 48-96 hours mortality is 16%
Usually associated with multiparous women donated blood
Post transfusion purpura: rare syndrome that starts with in 7 – 10 days after transfusion present with severe thrombocytopenia and purpura. Hpa-1a antigen……effective therapy is ivig or plasmapheresis
Graft vs host disease: thought to be due to immunocompetent donor t lymphocytes sym rash elevataed lft and severe pancytopenia prevention by irradiation because contains 80% mortality
Complications of massive transfusions: coagulopathy hypocalcaemia hyperkalaemia hypokalaemia hypothermia
Vascular air embolism : goal of treatment 1. prevent further air entry 2. reduction of air volume entered
3. Haemodynamic support
1.hyperberic oxygen therapy 2. partial left lateral decibutus position if air is trapped in rt side of heart
3. Tedelenberg position to optimize hemodynamics 4. aspiration of air from rt atrium by use of bunegin albin multiorifice catheter
5. Maintaining systemic arterial pressure with optimal fluids and ionotropic support to heart
Deferoxaime
Dosage
Acute episode : 1 ig im followed by 500mg 4hourly 2 further doses if not responded clinically than further doses can be givine in 4-12 hours interval upto max of 6g in a day if pt is in shocked than infusion rate of first dose will be approx.: 15/mg/kg/hr and for next subsequent dose is 125mg/hr
Chronic cases : sc 1-2g or 20-40mg/kg/day over 8-24 hours
Leukoreduction : performed by the use of filters to eliminate WBC contamination prestorage or at the bedside
Indicated : 1.nonhemolytic febrile transfusion reaction 2. transfusion transmitted CMV infection 3. formation of HLA alloantibodies
CMV seronegative: indicated for immunocompromised patients only to reduce the risk if CMV transmission
Gamma irradiation: eliminates immunologically competent lymphocytes inorder to prevent transfusion associated graft versus host disease indication: 1.immunocompromised pt 2. BM transplant recipients 3.pt who receive direct donations from HLA match donors or relatives
Washing : blood products is rarely indicated and considered only for
Recipient with IG A def
Hx of anaphylactic reactions