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Platelet Function in Cardiothoracic Surgery. Mike Poullis. Overview. Basic science What are they? How do they work? Methods of assessing platelet function Full blood count Microaggregation Macroaggregation Thromboelastography (TEG) Platelet function analyser Bleeding time
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Platelet Function in Cardiothoracic Surgery Mike Poullis
Overview • Basic science • What are they? • How do they work? • Methods of assessing platelet function • Full blood count • Microaggregation • Macroaggregation • Thromboelastography (TEG) • Platelet function analyser • Bleeding time • Clinical scenarios • Drugs • Medical conditions • Congenital disorders • Cardiopulmonary bypass • Aprotinin • HIT • On the ward
Basic science • What are they? • How do they work?
Coagulation System • Platelets • Soluble Factors • Red Cells • Soluble factors interact with platelets to form a mesh that RBCs stick to
How Do Platelets Work ? • Afferent pathway • Inside platelet pathway • Efferent pathway Inside platelet pathway Efferent pathway Afferent pathway
Platelet Agonists (Afferent) Agonist Receptor Adrenaline alpha Collagen VLA ADP ADP Thrombin PAR I and IV
The platelet Microaggregation and Macroaggregation
Mechanism of G protein receptor activation by soluble ligand eg ADP Soluble ligand (Reversible) Cell Membrane G protein
Mechanism of G protein receptor activation by protease eg Thrombin Protease eg thrombin (Irreversible) Cell Membrane G protein
(cont) Tethered ligand (Irreversible) Peptide Cell Membrane G protein Activation
PAR activating peptides PAR activating peptide (reversible) Cell Membrane G protein Activation
Actions proteolytic inhibitors eg Aprotinin Protease eg thrombin Aprotinin Cell Membrane G protein
PAR deactivation Protease eg thrombin Deactivator eg elastase aa 43/44 & 55/56 aa 41/42 (Irreversible) NH2 Cell Membrane G protein
Platelet Thrombin desensitisation 1 Neutrophil elastase cleaves PAR-1 Specific cleavage inhibits activation 2 Thrombin fragment deactivation theory
Efferent Agonist Receptor GP IIb/IIIa Fibrinogen GP Ib Von Willebrand Factor
Techniques to Understand • Microaggregation • Macroaggregation • Platelet function analysers • Thrombelastography • Calcium fluxes
Microaggregation and How to Count Platelets No No Size Size
Macroaggregation Increasing aggregation Time
What the Numbers/letters Mean • R: Time from initiation to initial fibrin formation • k: Time of clot formation until amplitude of 20 mm • Alpha angle: Acceleration (kinetics) of fibrin build up and cross-linking • MA - Maximum amplitude strength of clot (number function platelets, fibrin) • MA60: The rate of amplitude reduction 60 min. after MA (stability) of the clot
Tips and Tricks • Heparinase • Adding c7E3 Fab (ReoPro) to the TEG sample will eliminate platelet function from the thromboelastogram. • Antifibrinolytic agents such as Epsilon-Aminocaproic Acid, Tranexamic acid and Aprotinin
Normal Coagulation Profile Heparinase No Heparinase
Heparin Effect Heparinase No Heparinase
Calcium Flux Measurements 1 Thrombin 2 Adrenaline A control B Aprotinin
Tests of Platelet Function • Full blood count • Whole Blood tests • Microaggregation • Thrombelastography • Purified Platelet tests • Microaggregation • Macroaggregation • Platelet function analysers • Calcium flux • Skin bleeding time
Advantages of Techniques • Full blood count • Quick, easy, reproducible, understandable • Whole Blood tests • Microaggregation, Thrombelastography Easy MAJOR ADVANTAGE IS NO SAMPLE PREPERATION • Purified Platelet tests • Microaggregation Easy • Macroaggregation PRECISE DEFECT • Platelet function analysers PRECISE DEFECT • Calcium flux PRECISE DEFECT • Skin bleeding time • Whole body answer
Limitations of Techniques • Full blood count • Number not function • Whole Blood tests • Microaggregation No commercial kit • Thrombelastography?sensitivity • Purified Platelet tests YOU HAVE TO PREPARE THE PLATELETS • Microaggregation No commercial kit • Macroaggregation Experienced technician • Platelet function analysers No enzymes available • Calcium flux Expensive and experience needed • Skin bleeding time • Invasive, not specific
Clinical Scenarios • Drugs • Medical conditions • Congenital disorders • Cardiopulmonary bypass • Aprotinin • HIT • On the ward
Effect of Drugs on Platelet Function • Aspirin (Non steroidal anti inflammatory drugs) • Clopidogrel, Ticlopidine • ReoPro, Tirofiban • Prostacyclin • Hirudin • Ancrod
Aspirin (Non steroidal anti inflammatory drugs) TxA2 Platelet PgI2 Endothelium
ReoPro / Tirofiban / Integrilin Platelet Platelet GP 11b/111a Fibrin GP 11b/111a
Effect of Drugs on Platelet Function - Cont • Prostacyclin • Hirudin • Ancrod
Medical Conditions • Hyperglobulinaemia • Multiple myeloma and • Waldestrons macroglobulinaemia • Renal failure Uraemia • Liver disease • Myeloproliferative disorders • Essential thrombocythaemia • Polycytheamia • Myelodysplasias
Congenital Platelet disorders • All rare • VonWillibrands (commonest) • Glanzmann Thrombasthenia (Acquired common) • Bernard-Soulier • Platelet storage disorders
Von Willebrands Platelet Factor V111 vWF Endothelium Stabilisation and adhesion
Glanzmann Thrombasthenia • Genetic platelet disorder • Gp IIb/IIIa deficient or dysfunctional • FACS analysis
Bernard-Soulier • Large platelets • Phospholipid not made available • GP 1b deficiency Platelet Storage Disorders • ADP or 5-HT release deficiency • Defect in dense or alpha granules
How are platelets protected during CPB? • Heparin only works on soluble factors!