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Restricting and avoiding Blood Transfusions: What Options do we have?

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Restricting and avoiding Blood Transfusions: What Options do we have? Rajeshwari Subramaniam Deptt. Of Anaesthesiology A.I.I.M.S. www.anaesthesia.co.in anaesthesia.co ... – PowerPoint PPT presentation

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Title: Restricting and avoiding Blood Transfusions: What Options do we have?


1
Restricting and avoiding Blood Transfusions What
Options do we have?
  • Rajeshwari Subramaniam
  • Deptt. Of Anaesthesiology
  • A.I.I.M.S.

www.anaesthesia.co.in anaesthesia.co.in_at_gmail.c
om
2
Questions to be answered
  • What are the implications of anemia?
  • What are the benefits of a normal hematocrit?
  • How do we decide when to transfuse?
  • What are the risks of transfusion?
  • What are the alternatives to homologous
    transfusion?

3
What are the implications of Peri operative
Anemia?
  • DO2 CO x CaO2 (sat x 1.39 x Hb) PaO2 x0.003
  • Peri operative anemia usually co-exists with
    hypovolemia
  • Ability to tolerate reduction in DO2 depends on
    the ability to increase cardiac output
  • Myocardial contractility, HR, vascular tone
    with lossgt15

4
Problems of Peri operative Anemia
  • These responses are modified by
  • -age
  • -co morbid illness (CAD,CNS)
  • -pre existing Hb and plasma volume
  • -ß blockers, ACE inhibitors
  • -rapidity of loss
  • THE PROBLEM IS TO IDENTIFY THE PATIENT AT RISK

5
Problems of coronary circulation and myocardium
  • Myocardium has high O2 extraction ratio
  • O2 delivery can be increased only by increasing
    flow
  • Tachycardia compromises diastolic flow
  • With normal coronary circulation Hb up to 7g
    tolerated
  • ECG changes of ischemia at Hb 5g
  • Lactate production, death at Hb 3g

6
What is the urgency of replacing volume Hb?
  • Diversion of blood from skeletal, splanchnic beds
    to coronary and cerebral circulation
  • Mucosal ischemia-starting point of MODS, sepsis
  • Peri operative myocardial ischemia-high mortality
  • Un replaced blood loss ? coagulation problems,
    DIC

7
Beneficial effects of normalisation of Hct
  • in RBC volume, restoration of plasma volume
  • Restoration of blood flow to GIT
  • Restoration of viscosity? in shear stress, ADP
    production, platelet aggregation
  • Dispersal of platelets towards vessel wall

8
Anemia and NO
  • viscosity in anemia ? flow, shear stress,? NO
    production
  • Vasodilation at bleeding sites
  • in cyclic GMP in platelets, inhibition of
    platelet function, bleeding time
  • Hb best NO scavenger oxidizes NO
  • Minimum shear stress seen at Hct 30-35

9
Indications and Guidelines for intra-operative
RBC Transfusion
  • Based on Acute blood loss
  • -15 loss in an adult(500-750 ml)-no need to
    transfuse
  • -15-30loss-crystalloids/synthetic colloids
  • -30-40(1500-2000ml)-rapid IV resuscitation
    blood
  • -gt40-rapid volume replacement blood

10
Guidelines for Transfusion-continued
  • Based on Hb concentration
  • Actual and anticipated Hbgt10g
  • Indicated when Hb7g,at the rate of ongoing
    blood loss
  • Patients at risk trigger 8g(consensus)
  • Consider if patient will bleed due to coagulation
    abnormalities
  • Give appropriate coagulation factor/s

11
Patients at Risk
  • Coronary artery disease
  • Valvular heart disease (AS)
  • CHF
  • H/O transient ischemic attacks
  • Previous thrombotic stroke
  • However, still no consensus for transfusion
    trigger

12
Transfusion Strategy for Acute Blood Loss
13
Signs and symptoms Requiring Transfusion
  • Syncope
  • Dyspnea
  • Postural Hypotension
  • Tachycardia unresponsive to crystalloids
  • Angina/ECG changes
  • Transient ischemic attack

14
Patients under Anesthesia
  • If stable
  • -assess risk of myocardial/cerebral ischemia
  • -in the absence of risks,transfusion NOT
    indicated,regardless of Hb
  • -intravascular volume to be replaced
  • If unstable
  • -if at risk, transfuse
  • -if not at risk,crystalloidcolloid initially
  • -TRANSFUSE UNIT BY UNIT
  • -autologous blood if available

15
Guidelines for Transfusion(contd)
  • Transfusion in the ICU
  • -Overtransfusion may increase mortality
  • -Attention to volume, inotropic support
  • -Maintenance of BP and CO
  • -Crystalloids preferable

16
Guidelines for peri operative transfusion
  • Patient to be managed to avoid transfusion
  • Treat anemia before elective surgery
  • Discontinue anti platelet drugs
  • Reverse anticoagulation
  • Use pharmacologic agents to control bleeding
  • Strategies of autologous transfusion

17
Chronic Anemia
  • Do not transfuse if effective alternatives exist
  • Preferably transfuse at intervals to maintain Hb
    at lowest level not associated with symptoms
  • Consider recombinant erythropoietin
  • -zidovudine-induced anemia,CRF
  • -improves functional status

18
Risks associated with Transfusion
  • VIRAL INFECTIONS
  • Hepatitis A- 11,000,000
  • Hepatitis B- 150,000-1150,000
  • Hepatitis C- 11,900,000
  • Whats new Nucleic Acid Testing (NAT)
  • CMV-Up to 60 transmission from blood
  • Parvovirus B 19-Hydrops, Aplastic crisis

19
Risks of Transfusioncontd
  • Bacterial Contamination mortality
  • Red cells 2/106 (yersinia sp) 60
  • Platelets 83/106
    21
  • Hemolytic Reaction
  • Acute 1-4/106
    0.67
  • Delayed 1000/106 0-4
  • TRALI 200/106 60
  • Transfusion-mediated immuno modulation
  • -good for renal transplant, recurrent abortions
  • -increased mortality in CV, colorectal Ca

20
Other Hazards
  • Mismatched transfusion-114,000-118,000
  • Fatality-1800,000 units
  • West Nile Virus-Meningitis,encephalitis
  • Creutzfeldt-Jakob disease

21
Alternatives to Allogeneic (Homologous) Blood
  • Techniques
  • -Deliberate Hypotension
  • -Bloodless Surgery
  • -Tourniquet where appropriate
  • Drugs affecting coagulation
  • -Aprotinin(1.4mg?70mg/hr)
  • -e amino caproic acid(5-10g?1g/hr)
  • -Tranexamic acid(10mg/kg?1mg/kg/hr)
  • Erythropoietin pre treatment
  • Re combinant factor VIIa

22
Autologous Blood Use
  • Pre operative Autologous Donation (PAD)
  • Acute Normovolemic Hemodilution (ANH)
  • Intra operative Cell Salvage and Re- infusion
  • Post operative collection and Re infusion

23
What are the Advantages of PAD?
  • Avoids complications of allogeneic blood
  • Prevents red cell alloimmunization
  • Useful for patients with rare blood phenotypes or
    allo antibodies
  • Supplements blood supply
  • Provides reassurance to patients concerned about
    blood risks

24
Patient Selection for PAD
  • Hb 11.0g/dl
  • No age or weight limits
  • Volume 10.5 ml/kg per donation
  • Usually once a week
  • Last donation gt 72 hours before surgery
  • Patients with positive viral markers
  • Selected pediatric patients

25
Contra indications to PAD
  • Surgery unlikely to require transfusion
  • Evidence of infection/bacteremia
  • Scheduled surgery for AS
  • Unstable angina
  • MI /CVA lt 6 months
  • Active seizure disorder
  • Unstable angina, left main coronary block
  • Cyanotic CHD
  • Uncontrolled HT/ Pulmonary/ other medical dis.
  • Pregnancy

26
Potential Problems with PAD
  • Risk of misidentification
  • Infection/contamination of stored units
  • Volume overload
  • Increased cost of collection storage
  • Risk of patient becoming anemic
  • Aggressive Phlebotomy and iron, Erythropoietin
    3 weeks prior to surgery

27
Acute Normovolemic Hemodilution (ANH)
  • Blood removed shortly before surgery
  • Volume replacement with crystalloid/colloid
  • Blood stored in OT at room temperature
  • Volume EBV (Hi-Hf) Hav
  • Decrease in DO2, viscosity
  • Cardiac output, systemic vascular
    resistance, venous return
  • Oxygen extraction enhanced

28
Precautions
  • Hypovolemia, hypocapnia to be avoided
  • Oxygen supplementation
  • Reversible cognitive dysfunction in cerebral
    vascular disease
  • Coronary vasodilatation important to increase O2
    delivery to myocardium
  • Store close to patient and label appropriately

29
Precautionscontd
  • Establish 2 IV lines
  • Routine monitoring
  • Contraindications
  • Transfused in reverse order of collection
  • Room temperature storage not gt 8 hours
  • Increased HR be warned
  • Advantages all drawbacks of homologous blood
    eliminated low cost fresh whole blood

30
Red Cell Recovery and Re infusion
  • Blood from surgical field is collected into
    centrifuge bowl
  • Suction should be low, broad tipped
  • Large sponges rinsed in saline/RL
  • Heparin /ACD to be added (Ca reduces
    deformability)
  • Centrifuged to separate red cells from debris and
    WBCs
  • Washed with saline/glycine
  • Collected in reservoir with 40µm filter

31
The Cell Salvage System
32
Calculation of blood loss
  • (Hs/Hp x Vb xNb)/SE
  • E.g. THR 5 bowls(125 ml) used
  • HCT(bowls) 66,70,68,65,71(av68)
  • HCT(patient)32,30,34,30,28(av30.8)
  • Salvage efficiency 40
  • Blood Loss68 x 125 x5/ 30.8 x 40 3450 ml

33
What are the potential Complications of Cell
Salvage?
  • Poor wash quality-cell salvage syndrome (DIC,
    ARF)
  • Poor salvage rate due to non-dedicated personnel
  • Air embolism
  • Wrong wash solution

34
Current Status of Artificial O2 Carriers
  • Necessary steps
  • Stabilization to prevent dissociation into dimers
    (intravascular retention nephrotoxicity)
  • Decrease O2 affinity
  • Polymerization to increase Hb concentration at
    physiologic colloid oncotic pressure
  • Emulsification of PFCs to make them
    water-miscible

35
Hemoglobin-based O2 Carriers
  • Exhibit a sigmoidal O2 dissociation curve
  • Provide O2 and CO2 transport
  • Sourced from outdated banked blood, bovine blood
    or genetically engineered
  • Undergo virus inactivation and removal
  • Protection against prion contamination
  • Stabilised,polymerised

36
Difficulties and Side effects of Hb solutions
  • Nephrotoxicity-eliminated
  • Vasoconstriction-systemic and pulmonary
    hypertension causes-NO scavenging/increased O2
    supply to arteriolar wall
  • Abdominal pain, esophageal dysmotility due to NO
    modulation of smooth muscle relaxation
  • Interference with mixed venous O2 saturation

37
Kinds of Artificial Hbs
  • Diaspirin-linked Hb (DCLHb) stopped due to
    jaundice,pancreatitis,mortality
  • Human recombinant Hb (rHb 1.1,rHb 2.0)
    genetically expressed in E.Coli in 1990.Stopped
    in 2003
  • Polymerised bovine Hb based O2 carrier(HBOC-201)
    used in orthopedic cardiac trials
  • Maleimide activated polyethylene glycol modified
    Hb(MP4)high mol. Wt.,oncotic pressure,Hb conc
    28g/dl. Under trial.

38
Human Polymerised Hemoglobin (PolyHeme)
  • From outdated banked blood
  • Pyridoxylated and polymerized with glutaraldehyde
  • Has been tried in trauma and urgent surgery
    situations
  • 1u50g in 500ml171 patients with Hblt1g survived
    after 20u(10l)

39
Per Fluoro Carbon (PFC) Emulsion (OxyGent)
  • Carbon fluorine compounds with high gas
    dissolving capacity and low viscosity
  • Chemically and biologically inert
  • Dose 1.8g/kg
  • Taken up by RESemulsion broken down,re absorbed
    into blood and circulatesexcreted from lungs
  • Effective transport of dissolved O2
  • Submicron size enhances microcirculatory O2
    delivery

40
Nano-dimension artificial RBCs, Hb containing
liposomes
  • Purified Hb phospholipids cholesterol a
    tocopherol
  • Lead to rapid restoration of BP,microvascular
    blood flow and tissue oxygenation
  • Augmented ANH A technique of ANH combined with
    administration of O2 carriers and crystalloids

www.anaesthesia.co.in anaesthesia.co.in_at_gmail.c
om
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