Discuss the Indications and Complications of Blood Transfusion
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Transcript of Discuss the Indications and Complications of Blood Transfusion
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5/19/12
DISCUSS THE INDICATIONS ANDCOMPLICATIONS OF BLOODTRANSFUSION AND THEIRMANAGEMENT
BY
DR TELLA A.O.
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OUTLINE
INTRODUCTION
BRIEF HISTORICAL BACKGROUND
PRINCIPLES OF BLOOD TRANSFUSION
DONATION AND COLLECTION OF BLOOD
BLOOD PRODUCTS AND THEIR INDICATIONS
EFFECTS OF STORAGE OF BLOODCOMPLICATIONS/HAZARDS OF TRANSFUSION
PREVENTION & MANAGEMENT OFCOMPLICATIONS
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INTRODUCTION
Blood is a vehicular organ that perfuse allother organs.
Association of blood with life & vitality
known from time immemorial.BT is a form of organ transplantation that is
very invaluable esp. in surgical patients.
Has potential hazards which have increasedsensitivity to its use.
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HISTORICAL PERSPECTIVE
First man-to man BT in 1818 by J. Blundell
Landsteiner discovered ABO blood grps in1900 & later, Rh factor was recognized by
Levine & Stetson in 1939.Methods of collecting & storage of blood
became available thereafter.
First blood bank established in 1937 at CookCounty Hospital in Chicago.
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PRINCIPLES OF BLOODTRANSFUSIONAvoid BT if at all possible.
Proper testing of donated blood is ensured.
Only components needed should be given.
Anaemia should be corrected before electivesurgery.
If 1 unit is needed, then BT is not necessary.
However, single unit transfusions may bejustifiable in some settings.
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PRINCIPLES (contd)
Avoid automatic transfusion threshold.
Hb conc. Alone is not enough indicator forBT.
Informed consent.
Appropriate identification of the bloodcomponent selected for the patient.
Vital sign monitoring.
Blood should be administered slowly duringthe 1st 30 min.
No medications/drugs should be added to the
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BLOOD DONATION &COLLECTIONAppropriate donor selection.
Pre-donation screening.
Blood collection process manually or usingautomated collection devices. The vol.collected is standardized for the collectionbag used e.g. 450 ml + 63ml CPDA-1 bag.
Blood component separation.Post-donation observation & ADR to donation.
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BLOOD PRODUCTS
BLOOD COMPONENTS:(A)Oxygen carrying components-->
- RBC concentrate/Packed RBCs.
- Leucocyte poor RBCs.-RBC + additive solution.-Washed RBCs.
- Frozen red cells/Deglycerolized RBCs.(B)Platelet Products:
- Platelet rich plasma (PRP)
- Platelet concentrate
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Immune Serum Globulin
- Immune serum globulin(IgG)
- Hepatitis B immune globulin
- Varicella zoster immune globulin
- Rh immune Globulin
- Tetanus Immune globulin- Rabies
- Rubella
- Hepatitis A.
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INDICATIONS FOR BLOODTRANSFUSION
COMPONENTS
COMPOSITION
VOLUME INDICATIONSFOR USE
Whole Blood Allcomponents
450/500ml Hypovolaemic anaemia;Massive BT;EBT; DIC
Packed RBCs RBCs; WBCS;Plts; Plasma;
(Hct=75%)
250ml Symptomaticanaemia
WashedRBCS
RBCs; Noplasma;
reduced
180ml Symptomaticanaemia;
Allergic
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COMPONENTS COMPOSITION VOLUME INDICATIONSFOR USE
Plateletconcentrates
Plts 5.5X1010/unit;
WBCs; RBCs; Plasma50ml/unit Thrombocytop
enia;Chemotherapy-inducedanaemia
Granulocytes WBCs1.0X1010/unit; Lymphocytes;Platelets
220ml Neutropenia;Infectionsunresponsiveto antibiotics
FFP All coagulationfactors
220ml Def. of labile& stablefactors
Thawed
plasma
Reduced
factors V andVIII
220ml Def. of stable
factors
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BLOOD STORAGE &PRESERVATIONWhole blood is refrigerated after collection
ASAP at T of 2-6C.
The shelf-life of the blood depends on the
anticoagulant used:ACD {67.5ml} --- 21 daysCPD {63ml} --- 21 daysCPDA-1 {63ml} --- 1-35 days
SAGM --- 42 days
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STORAGE OF OTHER COMPONENTS:1) Platelet concentrate 22C for up to 7 days.2) Fresh Frozen plasma At -18C for up to 12 months.3) Cryoprecipitate Below -18C for up to 12 months.4) Frozen Deglycerolized RBCs
Preserved with glycerol or dimethyl-1-sulpoxide at -80C for years.
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EFFECTS OF STORAGE
RBCs: ATP; 2,3-DPG; K+ plasma.
Leucocytes: Not viable after 24 hrs.
Platelets: Not viable after 24 hrs but remainsfor 2 weeks.
Electrolytes--K+;Na+;Ca++.
Clotting factors.
pH: Continuing RC glycolysis generates lacticacid.
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COMPLICATIONS/HAZARDS OFBLOOD TRANSFUSION
(A) IMMEDIATE BTR IMMUNOLOGIC:
-Immediate Haemolytic
BTR.-Allergic & AnaphylacticBTR
NON-IMMUNOLOGIC:-Febrile TR
-Bact. Contamination-Circulatory overload-Cardiac arrest-Embolism(air/particles)-Acute lung injury
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DELAYED BTR
IMMUNOLOGIC:-Post-transfusion TP-Delayed Haemolytic BTR-Graft versus Host disease.-Tansfusion-related immunomodulation
NON-IMMUNOLOGIC-Thrombophlebitis-Transmission of diseases:HBV;HCV;HIV;CMV;EBV;Syphilis;Malaria;Chagas dx;Toxoplasmosis;-Iron overload-Citrate toxicity-Haemosiderosis
-Cxns of massive BT.
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TRANSFUSION REACTIONS MECHANISMS
Febrile NHTR Incomp. btw Ag on donorWBCs/plts & Ab in the
recipient plasma; Bactpyrogens
Immediate HTR Immune Ab of Rh system; Ab
of the IgM/IgG class whichactivates complemt
Allergic & AnaphylacticReactions
Hypersensitivity to donorplasma proteins (IgE-mediated)
Transfusion-related AcuteLung injury
Ab in donor plasma reactivewith recipients WBCs
(agglutination occurs in pulm.
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MASSIVE BLOOD TRANSFUSION
Transfusion of equivalent of TBV within 24hrs.
Transfusion of more than half of the TBV in 1
hr.TBV is 70ml/kg in adults and 80-90ml/kg in
children.
Indications include massive blood loss fromtrauma; ruptured aortic aneurysm; massiveGI bleeding; Liver transplantation etc.
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PROBLEMS OF MASSIVE BT
Haemolytic BTR: Usually due to error.
Circulatory overload.
Cardiac arrest:
-Hypothermia; -hyperkalaemia;-hypocalcaemia; -Acidosis.
Respiratory complications:
-ARDS; TR-ALI Impaired oxygen delivery.
Bleeding diasthesis.
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ACUTE TRANSFUSIONREACTIONS
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MANAGEMENT OFTRANSFUSION REACTIONSSTOP THE TRANSFUSION IMMEDIATELY.
Infusion of N/S.
Monitoring of V/S: T, Pulse,RR & BP.
O is given if pulm. symptoms areprominent.
Brief P/E is carried out to assess the patient.
Sample is taken & sent with the blood for re-crossmatching.
Freshly voided urine sample/catheter
specimen.
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PREVENTION OF TRANSFUSIONREACTIONAppropriate pre-testing & proper labelling.
Improved blood bank services.
Encouraging voluntary non-remunerated
blood donation.
Exploiting Autologous Transfusion:-Autologous pre-donation
-AISH-Intraoperative blood salvage
Use of pharmacologic agents:EP ;Haematinics
Good anaesthetic & surgical management.
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CHALLENGES OF BLOODTRANSFUSION
Limitations of our blood banks- storage &blood separation.
Religious objections to blood transfusion.
Blood procurement in emergencies.
Blood procurement in cases of candidatesfor massive blood transfusion.
Blood for patients with AIHD
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BLOOD SUBSTITUTES &ALTERNATIVES
PLASMA SUBSTITUTES: These are colloid and
crystalloid solutions used for maintaining the
circulation volume following acute haemorrhage,
shock, burns and septicaemias. Plasma substituteshave no 02 carrying capacity and also lack
haemostatic properties.
Crystalloids No oncotic activity
Colloids temporary oncotic activity (short half life)
Plasma substitutes are used in emergency prior to the
availability of compatible blood and appropriate
blood product.
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CRYSTALLOIDS:-0.9% saline solution.-Ringers Lactate.-Darrows solution.
-5% Dextrose.
COLLOIDS:-Dextrans.
-Hydroxylethyl starch.-Gelatin (Haemacel).
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CRYSTALLOIDS VS COLLOIDS
Solutions Advantages Disadvantages
Crystalloids Readily available Lackof oncotic
Easy storage pressure inplasma
Easy administration
Non-immunogenic
Non-toxic
Do not inhibit synthesis
of albumin
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ARTIFICIAL O CARRIERS
Synthetic O2 carrying agents are stillexperimental:
Two classes exist Perfluorochemicals
and,Chemically modified Hb
The perfluorochemicals are fluorinatedhydrocarbons. They readily dissolve
oxygen, but are poorly soluble in plasma.One of these compounds fluorosol DAhas been studied in animals and is currentlybeing studied in humans.
Side effects: hypotension and DIC,
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CONCLUSION
Blood transfusion is an essential componentof therapy for a wide variety of disorders.However, the hazards of allogeneic BT havealso been well documented over the years.
Thus while researches are on-going todiscover the perfect blood substitute, thereis always the need to weigh benefits against
risks so as to make the best use of this scarcehuman resource.
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THANK YOU.