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What factors are in the Intrinsic Path?
Factor XII
Factor XI
Factor IX
Factor VIII
HMWK
What test is used for the intrinsic pathway?
What drug does it monitor?
aPTT
Heparin
What factors are in the extrinsic path?
F VII
What test is for the extrinsic path?
What does it monitor?
PT
Monitors Coumadin
What factors are in the common path?
F X
F V
Prothrombin
Fibrinogen
F XIII
What factors are Vit. K Dependent?
F XI
F VII
F X
Prothrombin
What are the contact factors
F XII
F XI
HMWK
F XII Def.
Prolonged PTT
F XI def.
Hemophilia C
Normal: Plt. count/Bleeding Time/PT
Prolonged PTT
F IX Def.
Hemophilia B
Normal: Plt Count/Bleeding Time/PT
Prolonged PTT
F VIII Def.
Hemophilia A
Normal: Plt count/Bleeding time/PTT
Prolonged: PT
F VII Def.
Vit. K def.
Normal: Plt count/Bleeding time/ PTT
Prolonged: PT
F X Def.
Vit. K Def.
Normal: Plt count/PFA
Prolonged: PT/PTT
F V Def.
Normal:" Plt count/PFA/TT
Prolonged PT/PTT
Prothrombin Def.
Normal: Plt count/PFA
Prolonged: PT/PTT
Fibrinogen Def.
Normal: Plt count/PFA
Prolonged: PT/PTT/TT
F XII Def.
Screening test= Pt. plasma + 0.025M CaCl—> 5M Urea
if dissolves in 24hrs=def.
Plt anatomy and main points
peripheral zone- contains GPIb-IX, GPIIb/IIa, PF3
Structural zone- made of contractile proteins for shape and release of granules
Organelles Zone- Alpha granules (PF4, b- thromboglobulin, and PDGF) and Dense bodies (Storage pool for ADP/ATP)
Membranous zone- helps release chemicals, dense tubular system for storing iCal
ACT
Activated Clotting Time
Used to measure high levels of Heparin
Bleeding time
Obsolete
Prolonged= Plt function disorders, uremia, thrombocytopenia
Plt Function Analyzer/Assay
Uses Collagen/Epi and Collagen/ADP to stimulate Plt aggregation
If both are normal= No problems
If Col/Epi is abnormal and Col/ADP is normal=Aspirin Usage or True Plt defect`
VerifyNow
Cartridge test with fibrinogen, tests for aspirin, P2Y12 and GPIIb/IIa inhibitors
Whole blood Plt Aggregation
Measures Plt. aggregation and ADP release
Ristocetin Cofactor Assay
Also known as vWF activity assay
Ristocetin + Plts measures aggregation
Mixing Studies
Done after prolonged PT/PTT
Pt. plasma is mixed 1:1 with Pooled plasma
If it corrects= Factor def.
If it doesn’t correct= Factor inhibitor
Factor Assay
Used when suspected Factor Def.
Pt. plasma is mixed with pooled plasma that has all factors except suspected missing one
If PT/PTT corrects= Factor def.
If it doesn’t correct= Factor inhibitor
Thrombin Time
Tests for presence of Heparin
Thrombin + Pt. Plasma, time= how long fibrinogen takes to convert to fibrin
Quantitative Fibrinogen/Clauss Assay
Long time=Low fibrinogen= DIC/Fibrinolysis/Liver disease
Short time= High fibrinogen= Inflammation/pregnancy
Reptilase Time
Used with TT to detect Heparin contamination
Increased= dys/hypo/a- fibrinogenemia
D-Dimer
Measures Cross-linked fibrin degradation
pos= Maybe DIC
Neg= Patient doesn’t have DIC
Russell’s Vipper Venom
Directly activates F X
Confirmatory test for Lupus Ab
DRVVT- diluted= increased sensitivity
Anit Plt Drugs
Glycoprotein inhibitors- prevent plt adhesion via binding to GPIIb/IIIa
Plavix- blocks P2Y12 ADP receptor site on Plts
Aspirin- Irreversibly inhibits cyclooxygenase
Heparin
Inhibits Xa/IIa
Unfractionated- binds PF4, requires monitoring
LMWH- Only inactivates Xa, doesn’t require monitoring
Synthetic LMWH- binds antithrombin and Xa, very expensive
Primary Hemostasis Steps
Endothelial damgage (exposes collagen, releases PAF, serotonin, thromboxane A2, TF, vWF, PAI)
Plts attach to collagen, change shape due to agonists
Strong stimulus: Dense bodies release ADP, Ca, Serotonin
Weak Stimulus: Alpha granules release PF4 and Plt Derived GF
GPIIb/IIa sites are exposed and become receptors for fibrinogen
Fibrinogen cross-links IIb/IIIa sites, creates plt-to-plt aggregation
PF3 is released, which becomes action site for coag. factors
Plt agonists
ADP
Epi
Thrombin
Collagen
Ristocetin
Arachidonic acid