My Bloody Talk. Dr Ben Turner MBBS, FANZCA, FCICM The Royal Children s Hospital, Melbourne

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Transcription:

My Bloody Talk Dr Ben Turner MBBS, FANZCA, FCICM The Royal Children s Hospital, Melbourne

Disclosures No conflicts of interest Interest in conflict

Blood transfusion Massive transfusion definitions Transfusion triggers Massive blood loss complications Massive transfusion protocols Complications of transfusion

Massive Transfusion Trauma Major surgery GI bleeding Birth trauma Bleeding diatheses Vascular malformations Feto-maternal haemorrhage

Signs that you may need to Transfuse How s it going up your end? Has this patient got a crossmatch? If you can no longer hear the music over the suckers Shit shit shit..

Transfusion Triggers Lower limit of Hb at which D02 becomes critical is not defined Theoretical level in adults is 2.5g/dL Validated in animals Healthy volunteers diluted to 4-5g/dL In Jehovah s Witness adults morbidity and mortality increase with anaemia but patients can survive with Hb 3g/dL. (Carson, 2002) Odds of death increase 2.5 times for every 1g/dL Hb is <8g/dL (Carson, 2002)

Massive Transfusion definition Paediatrics is different from adult medicine Both absolute and relative blood volumes differ in different sized and aged children 90-100ml/kg in preterm infant 60 ml/kg in female adolescent

Massive Transfusion definition Yaser et al, 2013 >50% TBV in <3hrs >100% TBV in 24hrs Transfusion for ongoing bleeding of >10% TBV in 10min

Massive Transfusion definition Does it matter? When you have to give enough blood that the transfusion may have physiologic consequences. STOP, LOOK, LISTEN, THINK

Physiologic complications of massive haemorrhage CVS Neurological Renal

Critical Triad Hypothermia Acidosis Coagulopathy

Assessment Temperature Haemoglobin Platelet count Coagulation screen INR/PT APTT Fibrinogen Acid-base status Ionised Ca++

Assessment Values indicative of critical physiological derangement T<35 C ph<7.2, base excess>-6, lactate >4mmol/l Ionised Ca++ <1.1mmol/l INR>1.5 APTT>1.5 x normal Fibrinogen <1.0g/l

Hypothermia Aetiology is multifactorial Trauma patients are frequently hypothermic on arrival at hospital and are exposed during assessment Surgical patients suffer exposure and effects of anaesthesia Most blood products are stored between 1-6 C Room temperature fluids are hypothermic

Hypothermia For each 1 C drop in temperature coagulation factor activity decreases by 10% Patients <34 C will be clinically coagulopathic Hypothermia causes platelet pooling in spleen <34 C platelet adhesion and aggregation is impaired

Acidosis Tissue hypoperfusion Decreased haemoglobin and O2 carriage Reduced cardiac output due to reduced pre-load Prolongs clotting time by impairing enzyme activity Reduces fibrinogen levels Reduces platelet count

Acidosis Treat the cause unless ph<7.2 NaHCO3 1ml/kg

Coagulopathy 25% of trauma patients are coagulopathic on arrival to hospital Systemic hypoperfusion has a dose dependent association with coagulopathy as measured by PT/APTT

Coagulopathy Shock increases thrombomodulin results in reduced thrombin, factors Va and VIIIa deactivates PAI-1, promoting fibrinolysis Complement cascade activation affects coagulation ñ tissue plasminogen activator and ò thrombin activatable fibrinolysis inhibitor lead to an increase in fibrinolysis

Management Most information comes from adult trauma studies Trauma differs in paediatrics Less penetrating trauma and more crush injuries

Guidelines 2012 National Blood Authority released: Patient Blood Guidelines:Module 1 Critical Bleeding/Massive Transfusion Endorsed by all major medical colleges in Australia Evidence based review of the literature using NHMRC grades A-D

Patient Blood Guidelines:Module 1 Critical Bleeding/Massive Transfusion http://www.blood.gov.au/pbm-module-1 Recommendations 2 Practice points 10 MTP protocol template

Recommendations Recommendation 1 Institutions develop an MTP that includes the dose, timing, and ratio of blood component therapy for use in trauma patients with, or at risk of, critical bleeding requiring massive transfusion (Grade C) Grade C body of evidence provides some support

Recommendations Recommendation 2 The routine use of rfviia in trauma patients with critical bleeding requiring massive transfusion is not recommended because of its lack of effect on mortality (grade B) and variable effect on morbidity (grade C) Grade B body of evidence can be trusted to guide practice in most situations

Massive Transfusion Protocol A system to streamline the availability and limit complications of massive transfusion in a critically bleeding child Provides clear guidelines for Trauma doctors Trauma nurses Haemotologist Laboratory staff Distribution orderlies

Massive Transfusion Protocol Activates a response in the blood bank Increase staff numbers Commence thawing frozen components Order urgent blood from the Blood Service

Massive Transfusion Protocol - template Local adaptation Multidisciplinary Incorporate recommendations and practice points Take into account local resources Provide details on how components will be delivered to the correct patient and location

Special circumstances Warfarin Add vit K, prothrombinex/ffp Head injury Platelet count >100 x 10 9 /L

Practice Point 4 In patients with critical bleeding requiring massive transfusion insufficient evidence was identified to support or refute the use of specific ratios of RBCs to blood components

Practice Point 10 Suggested doses of blood components are: FFP15ml/kg Platelets 1 adult therapeutic dose Cryoprecipitate 3-4g

Practice Point 8&9 rfviia MTP should include advice on the administration of rfviia May be considered if: Patient is salvagable Failed surgical or radiological measures Adequate blood component replacement ph>7.2, Temperature > 34 o C Initial dose 90mcg/kg is reasonable

Tranexamic acid CRASH II The Lancet, 2010 20,000 trauma patients with significant haemorrhage 274 hospitals, 40 countries Treated within 8 hrs of injury Tranexamic acid 1g over 10min, 1g over 8hrs

Tranexamic acid Significant reduction in all cause mortality RR 0.91 95% CI 0.85 0.97 Lower risk of death secondary to bleeding RR 0.85 95% CI 0.76-0.96 No increase in vaso occlusive disease in TXA group More effective if given within 3 hours

Transfusion Associated Complications Transfusion reactions AHTR, FNHTR (allergic) Immunological complications TRALI, TRIM, TA-GVHD, PTP

Transfusion Associated Complications Metabolic complications ê Ca ++, ê Mg ++, é K +, ê K +, metabolic alkalosis, impaired glucose homeostasis, Acidosis, Hypothermia Coagulopathy Infections TACO TANEC Air embolism

Conclusion Patients requiring massive transfusion may have significant metabolic derangement Prevent and treat the triad Acidosis Hypothermia Coagulopathy Develop MTP Remember blood transfusion has its own complications