1 / 40

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

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@gmail.com. Questions to be answered. What are the implications of anemia? What are the benefits of a normal hematocrit?

hop
Download Presentation

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

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript


  1. Restricting and avoiding Blood Transfusions: What Options do we have? Rajeshwari Subramaniam Deptt. Of Anaesthesiology A.I.I.M.S. www.anaesthesia.co.inanaesthesia.co.in@gmail.com

  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 loss>15%

  4. Problems of Peri operative Anemia • These responses are modified by: -age -co morbid illness (CAD,CNS) -pre existing Hb and plasma volume -β 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 -15-30%loss-crystalloids/synthetic colloids -30-40%(1500-2000ml)-rapid IV resuscitation± blood ->40%-rapid volume replacement+ blood

  10. Guidelines for Transfusion-continued • Based on Hb concentration: • Actual and anticipated Hb>10g% • Indicated when Hb≤7g%,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,crystalloid+colloid initially -TRANSFUSE UNIT BY UNIT -autologous blood if available

  15. Guidelines for Transfusion(cont’d) • 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- 1:1,000,000 • Hepatitis B- 1:50,000-1:150,000 • Hepatitis C- 1:1,900,000 • What’s new: Nucleic Acid Testing (NAT) • CMV-Up to 60% transmission from blood • Parvovirus B 19-Hydrops, Aplastic crisis

  19. Risks of Transfusion…cont’d • 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-1:14,000-1:18,000 • Fatality-1:800,000 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) -ε 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 > 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 < 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. Precautions…cont’d • Establish 2 IV lines • Routine monitoring • Contraindications • Transfused in reverse order of collection • Room temperature storage not > 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 Loss=68% 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 • 1u=50g in 500ml;171 patients with Hb<1g% 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 RES;emulsion broken down,re absorbed into blood and circulates;excreted 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 + α 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.inanaesthesia.co.in@gmail.com

More Related