coagulation automation joanna ellis, mls (ascp) keri brophy-martinez, mha/ed (ache), mt(ascp)
TRANSCRIPT
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Coagulation AutomationCoagulation Automation
Joanna Ellis, MLS (ASCP)
Keri Brophy-Martinez, MHA/ED (ACHE), MT(ASCP)
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Screening TestsScreening Tests Bleeding Time
◦ Manual method that evaluates primary hemostasis (being replaced by PFAs)
Prothrombin time (PT) ◦ Extrinsic and Common Pathways
Activated Partial Thromboplastin Time (aPTT)◦ Intrinsic and Common Pathways
Thrombin Time (TT or TCT)◦ Conversion of Fibrinogen to Fibrin
Quantitative Fibrinogen◦ Determines amount of fibrinogen
D-Dimer◦ Detects fragments from plasmin
degradation of the fibrin clot
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Specialized TestsSpecialized Tests Platelet Aggregation studies
◦ Measures ability of VWF to support agglutination of normal platelets by ristocetin
Platelet Function Assay (PFA)◦ Tests platelet adhesion and aggregation
Thrombelastography (TEG)/RoTEM◦ Real-time view of all stages of hemostasis
Mixing Studies◦ Identifies specific factor deficiencies or inhibitors
Specific Coagulation Factors◦ Determines actual activity of a factor such as Factor VIII
or IX Antithrombin (AT or ATIII)
◦ In the presence of heparin, low levels of AT indicate poor clinical response to heparin
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Current InstrumentationCurrent Instrumentation
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To See or To FeelTo See or To Feel
Automation approaches to clot detection:◦SEE Turbidometric Nephelometric
◦FEEL Mechanical/Viscosity based
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Instrument Instrument MetholodologiesMetholodologiesOptical/TurbidometricNephelometricMechanicalChromogenicImmunologic
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Optical Clot Detection Optical Clot Detection (Turbidimetry)(Turbidimetry)
Sample is added to a cuvetteA light source is directed through the
cuvette Initial absorbance of transmitted
light is measuredClot initiating reagents are added by
the automated instrumentationThe plasma becomes more opaque
when clotting is initiated, decreasing the light transmitted through the cuvette
The change in transmitted light is used to calculate the result
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Cascade M-4Cascade M-4(Instruments at RRC)(Instruments at RRC)Four cuvettes can be analyzed
at one timeSemi-automated Optical Clot
Detection◦The technician delivers the
sample and reagents into the cuvette
◦The changes in optical density are monitored
◦Clot times determined by instrument
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Nephelometric Clot Nephelometric Clot DetectionDetection
Sample is added to a sample cuvetteThe optically clear cuvette passes in
front of light sourceThe clot initiating reagents are
addedLight is scattered as the fibrin
strands formThe light scatters at different angles
and is measured by detectorsA clot curve is generated by
consecutive readings until clot completion.
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Mechanical Clot Mechanical Clot DetectionDetection
The sample is introduced to a cuvette that has a small steel ball inside
The cuvette continuously moves when testing begins
The clot initiating reagents are added to the sample
The fibrin strands begin to form and attach to the moving ball
An electrical circuit is either opened or closed when the ball moves away from the magnet because of the fibrin strands
Clot time is recorded.
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KC1 KC1 (Instruments at EVC)(Instruments at EVC)
•Semi-Automated Mechanical Clot Detection:
•The Ball Method uses a steel ball at the bottom of a cuvette that is held in place by a magnetic source. •While the cuvette continuously rotates, the technician adds the sample and reagents, which starts the timer. T•When true clot formation has occurred, the clot will incorporate the steel ball and pull it away from the magnetic source, stopping the timer.
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Chromogenic DetectionChromogenic DetectionUses a colorless substrate and a
chromophoreProtease activity of the factor allows the
substrate-chromophore complex to be cutColor change results and the OD is measured
at 405 nm.
Allows for specific coagulation factor activity to be measured.
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Immunologic Light Immunologic Light AbsorbanceAbsorbanceUses latex particles coated with antibodies
against select antigensOnce latex particles and antigens
agglutinate, more light is absorbed by the forming clot.
An increase in light absorbance is proportional to the antigen level.
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Tests that use a Clot Tests that use a Clot Detection MethodDetection Method
PTAPTTTTFibrinogenMixing StudiesSpecific Coagulation Factor
Assays◦FVIII◦FIX
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Aggregating ReagentsAggregating Reagents(Agonist)(Agonist)
CollagenADPEpinephrineRistocetinArachidonic Acid
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Platelet Function AnalyzerPlatelet Function Analyzer(PFA-100)(PFA-100)
Uses stimulators of platelet adhesion and aggregation in an environment that stimulates an injured blood vessel wall.
More sensitive screening test than the bleeding time method
Offers increased sensitivity for platelet dysfunction and von Willebrand’s disease
Nonspecific test- not diagnostic for any single disorder
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Platelet Function Platelet Function AnalyzerAnalyzer(PFA-100)(PFA-100)The instrument adds citrated blood to
a reservoir with either collagen/epinephrine (EPI) or collagen/adenosine diphosphate (ADP) on a bioactive membrane
A pressure sensor detects the formation of a platelet plug on the membrane
The time it takes to close the aperture in the membrane with the platelet plug is recorded.
The result is a function of platelet count, platelet activity, VWF activity, and hematocrit.
http://www.platelet-research.org/3/pfa.htm
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Platelet Platelet AggregometryAggregometry
Performed in specialized labs by experienced laboratory professionals
Performed on Aggregometer utilizing photometry
Measures light transmittance over a period of time
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Platelet aggregation patterns Platelet aggregation patterns in various disordersin various disorders
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VWF:Ristocetin VWF:Ristocetin CofactorCofactorVWF:RCoVWF:RCo Slowly centrifuged citrate sample yields
platelet-rich plasma (PRP). The PRP must be adjusted with the
patients PPP to reach a standard number of 200,000/µL
The sample is stirred, warmed to 37°C in a photometric aggregometer
The aggregating reagent (agonist) is added◦ In this case, Ristocetin
The platelets begin to aggregate which leads to a change in optical density (OD) of the PRP as measured by a absorbance detector.
The aggregometer records the changes in OD in a graphic curve.
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Thrombelastography Thrombelastography (TEG(TEG®®))Citrated Whole Blood based
analysisMonitors hemostasis in its entirety
◦Clot initiation through clot lysis◦Measures the net effect of all
hemostatic components interacting together during the clotting process
◦Demonstrates the hemostatic potential of a blood sample at a given point in time.
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Thrombelastography Thrombelastography (TEG(TEG®®))
•Sample of citrated whole blood is placed in a cup which has a pin carefully connected to a torsion wire.
•As the cup rotates in a back and forth movement, the aggregates formed within the cup cause the wire to become more rigidly placed and reflects the strength of the aggregates formed within the cup.
•The movement or lack of movement is reflected via either an optical or magnetic detector
•A graphic presentation is produced
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TEG Graphic ResultTEG Graphic Result
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Typical TEG Graph Typical TEG Graph PatternsPatterns
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Uses of TEGUses of TEG®®
Illustrates function and dysfunction in the Hemostatic system
Allows physicians to give appropriate amounts of FFP, Cryo, and platelets to control hemorrhage◦Reduces unnecessary use of blood
productsAllows effective management of
hypercoaguabilityDifferentiates surgical from
pathological bleeding
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RoTEMRoTEMRotational Rotational thromboelastometrythromboelastometry
Similar to TEGUses a heated cup that remains
stationary, while pin oscillates as the clot forms◦Uses automated pipetting
Provides data on clot kineticsUses optical detectionAdvantage- less sensitive to agitation
(compared to TEG)
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ReferencesReferences "Cascade M M4 Hemostasis Coagulation Analyzers
Clotting Assays PTs APTTs Thrombins Fibrinogens Factor Assays - Discovery Diagnostics Canadian Distributor Helena Laboratories." Hematology Stainers Microbiology Stainers Cytocentrifuges Osmometers Sweat Collection Blood Temperature Indicators Fecal Occult Blood Platelet Aggregation. Discovery Diagnostics and JLS Web Designs, 8 Sept. 2008. Web. 14 Nov. 2010. <http://www.discovery-diagnostics.com/Cascade_M4.asp>.
"Fiche Produit - Stago." Homepage Stago Corporate - Stago. Web. 14 Nov. 2010. <http://www.stago.com/nc/products-services/catalogue/analyzers/fiche-produit/selection/type-analyzers/reference/58609/group/sta-compact/>.
"KC1 DELTA COAG ANALYZER 1/EA - Trinity Biotech # G05000." LabSource.com - Your Source for Science and Safety! 2009. Web. 14 Nov. 2010. <http://www.labsource.com/Catalog/Item.aspx?ItemID=1392043>.
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ReferencesReferences McGlinchey, Kevin. "» More on Trinity’s KC1 and KC4
Educational Promotion." The Fritsma Factor: Your Interactive Hemostasis Resource. 5 Nov. 2009. Web. 14 Nov. 2010. <http://www.fritsmafactor.com/newfritsmafactor/?p=2044>.
McGlinchey, Kevin. "Coagulation Automation." Advance 19.6 (2010): 26-27. Print.
McKenzie, Shirlyn B. "Chapter 40." Clinical Laboratory Hematology. 2nd ed. Boston: Pearson, 2010. Web.
"PFA-100® System." Siemens Healthcare Worldwide. 2007. Web. 14 Nov. 2010. <http://www.medical.siemens.com/webapp/wcs/stores/servlet/ProductDisplay~q_catalogId~e_-111~a_catTree~e_100001,1023065,1028378,1015818~a_langId~e_-111~a_productId~e_182047~a_storeId~e_10001.htm>.