BLOOD AND BLOOD COMPONENTS COLLECTION.ppt
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BLOOD AND BLOOD COMPONENTS
COLLECTIONTRANSFUSION AND
PRESERVATION OF BLOOD
PRESENTED BY
DR ABAS RASHID BHATMVSC SCHOLAR IST YEAR
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REASONS OF BLOOD COLLECTIONBlood Tests
Transfusion
Blood Biochemistry
Pathogen identification
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METHODSBlood samples are collected by venal
puncture on live animal, as cleanly aspossible, using sterile equipment, and with
respect for the welfare of the animal.
Use new needle and syringe for each animal.
Dispose needles properly,
Clean the puncture area with 70% alcohol,Handle animals calmly and using appropriate
restraint,
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Cont Although most techniques do not
require large amount of blood it is
preferable to collect at least2.5mL of blood, but ideally 10mLin large animals, and 4-6mL in
small animals.
Identify the sample with a
permanent method and fill thesampling form at the time ofsampling.
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SITES OF BLOOD COLLECTION Jugular veins (large animals),
Brachial, brachiocephalic, femoral, tarsal veins,
Cranial Vena cava in pigs,
Mammary veins,
Ear veins in pigs: 20 gauge needle,
Saphenous veins, retro-orbital veins, intracardial
punction in rodents, small vertebrates, use a 23
gauge needle,
Wings (brachial) in chicken, use 20 to 23 gauge
needle.
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PRECAUTIONWhole blood is prone to hemolysis.
Preferentially use a vacutainer instead of asyringe
If you have to transfer the blood from a syringe
to a sample container, remove the needle firstand transfer slowly and smoothly
Do not shake the blood.
Do not freeze whole blood.
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TRANSFERRING OF BLOOD.BLOOD TRANSFER
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Whole blood samples preservation
WHOLE BLOOD means with allConstituents
the blood needs to be stored properly , withan anticoagulant. Different anticoagulants are
available in commercial tubes such as: EDTA(purple tubes) or Heparin (green tubes).However EDTA is often recommended.For virology antibiotics may be added. 200units of penicillin and 200 mg of streptomycinper ml of blood.
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Whole blood samples should be sent to the
laboratory in an insulated container with ice
at 4C.
.They should not be frozen.
->Blood samples for virology must be sent tothe laboratory within 24 to 72 hours
depending on virus survivability.
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PLASMA COLLECTION
Supernatent of
unclotted blood
Stored at -20 deg cel.
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SERUM
SERUM=PLASMA
CLOTTING
FACTORS
PRESERVED BY
REFRIGERATION
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Blood Transfusion InVeterinary practice
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Introduction
Significant increase in blood transfusionsfor over the past 20 years in small animal
medicin
Mostcommonly used products: whole
blood, packed red blood cells, plasma
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Whole blood PLASMA
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Blood Types
Canine:
Thirteen canine blood types
Designated by DEA (Dog Erythrocyte Antigen) & a
number (DEA 1, DEA 2, DEA 3, etc).
Important alleles of DEA 1: 1.1 and 1.2
DEA 1.1 positive (most common type) => universal
recipient DEA 1.1 and 1.2 negative => universal donor
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Blood Types
Feline
AB blood type system
Types: A, B, AB (very rare)
Naturally occurring alloantibodies to other blood
groups => no universal donor in cats
Type A cats: weak anti-B alloantibodies (weak
reaction if transfused w/ B blood) Type B cats: high anti-A alloantibodies (severe
reaction if transfused w/ A blood)
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Cross-matching Predicts a transfusion recipients response to a donors
RBCs and plasma Majorcross-match
detects antibodies in the recipients plasma that can cause ahemolytic reaction to donor RBCs
Minorcross-match detects antibodies in the donors plasma that might react to
recipients RBCs
RBC agglutination = Incompatibility
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Incubation for 15min at 37C,room temperature , and
4C
CROSSMATCH DONOR(ml) RECIPIENT(ml)
RED CELL SERUM RED CELL SERUM
MAJOR 0.1 --- --- 0.1
MINOR --- 0.1 0.1 ---
DONOR CONTROL 0.1 0.1 --- ---
RECIPIENT CONT. ---- --- 0.1 0.1
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Cross-matching - Canine
Dogs lack naturally occurring alloantibodies =>
a cross-match does not need to be performed
on a patient receiving a transfusion for the
first time
Sensitization takes about 3 days
No cross-match needed if transfused within the
previous 72 hours
Cross-match becomes necessary 72 hours after a
dog receives a transfusion
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Cross-matching - Feline
All cats should be cross-matchedif blood type is
unknown or typing card unavailable
D
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Donors
Canine
Good generalhealth
Between 1-8 years ofage
Minimum weightof 25 Kg (55 lb) - allows 450 mL ofblood to be collected
PCVshould be 40%
Currenton vaccinations (DALPP, Rabies)
Yearly exam and full CBC/Chemistry / heartwormantigen test
Infectious diseases screening:.>Donors should not have had any previoustransfusions because of risk to foreign RBC antigens
and the development of antibodies
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TRANSFUSION IN LARGE ANIMALS
OCCASIONAL
SHOULD BE Checked for compatibility
Done in babesiosis,anemia,blood loss etcBiological compatibility test(10 ml blood iv)
Isttransfusionno risk
2ndtransfusion-risk
C i Bl d C ll ti
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Canine Blood Collection
Donorin lateral recumbency
Fur over the jugular vein is clippedand aseptically prepped
A 16g needle is inserted into the jugular vein
The bag is gently rocked back and forth as it fills,
distributing the anti-coagulant(63ml CPDA)evenly; the sample is periodically weighed untilthe proper volume is achieved
Canine units are usually450 mL or 450 grams The hemostat is clamped back
Pressure is applied to jugular vein to preventhematoma
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Dosages
ACD@15ml per 100 ml bloodCPD and CPDA-1 @14ml per 100 ml
blood
at 2 to 6C, ACD whole blood and CPD
whole blood can be used within 21 days
after collection. (70% live rbc)In CPDA-135 DAYS
Heparin less used
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Administration
Blood products should be allowed tocome to room temperature beforeadministration
Plasma is thawed by placing theplasma in a protective plastic bag andsubmerging it in a warm water bathnot exceeding 98.6 F (37 C) - 30-60minutes is generally adequate forthawing.
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Administration
Several routes may be used for administeringblood products
Intravenous (via 22-18g IVC) is the most common
and effective, delivering blood products directlyinto circulation
Intraosseous is also effective when vascular
access is difficult or unsuccessful and often usedfor neonates
Intraperitoneal
Plasma transfusion: for clotting factors
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Plasma transfusion: for clotting factors
170-220 m in-line filter
Smaller doses may be given via a 17um Hemo-nate
filter Filters prevent protein debris, cellular debris, and
blood clots from passing to the patient
Blood products may be infused via free drip,
syringe pump and fluid pump
Amount of donor whole blood (ml) required:
= 90 x BW (kg) x Desired PCV-Actual PCVDonor PCV
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Administration Administration rates are variable
Patients with massive hemorrhagemayrequire a rapid transfusion
Patients with chronic anemia need a slower infusion
Blood components should always be infused slowly (1mL/kg) for the initial 15-30 minutes while observing fortransfusion reaction
Subsequently, the rate may be increased to 5-10
mL/kg/hr The blood product should be infused as quickly as the
patient can safely tolerate, while maintaining detailedmonitoring
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Reactions
Immune-mediated Hemolytic
Acute
Delayed Non-hemolytic
Non-immune-mediated
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ReactionSIGNS
Chills, Fever, Urticaria, Tachycardia,Dyspnea, Nausea and vomiting,Tightness in the chest, chest ,
HHypotension, Bronchospasm,Angioneurotic edema, Anaphylaxis,Shock, Pulmonary edema, and
Congestivefailure
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MANAGEMENT OF RXNS
Treatment depends on the severityDiscontinuing thtransfusion
+administering drugs to stop the
hypersensitivity reaction Like CPM,
coticosteriods,adrenaline.
Once medications have taken effect and the patientis stabilized, the transfusion may be continued
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COMPLICATIONS
Hypocalcemia
Fluid OVERLOAD
Disease transmission
COAGULOPATHIES(HEPARIN)
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THANKS
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