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Fibrinolysis
Enzymatic breakdown of fibrin in blood clots.
Plasmin
Key enzyme responsible for degradation of fibrin.
Alpha-2 antiplasmin
Plasma inhibitor that inactivates plasmin.
Whole blood clot lysis time
Test that evaluates clot dissolution due to plasmin activity.
Normal whole blood clot lysis time
Clot lysis occurs after 24 hours.
Excessive plasmin activity in whole blood clot lysis
Clot lysis occurs in less than 24 hours.
Deficient plasmin activity
Clot remains beyond 72 hours in whole blood clot lysis.
Diluted blood clot lysis time
Test used to screen excessive fibrinolysis and monitor activity in MI and stroke.
Principle of diluted blood clot lysis time
Plasmin inhibitors lose activity upon dilution.
Plasma clot lysis time
Test using recalcified plasma clot incubated at 37°C and observed for lysis over 48 hours.
Normal plasma clot lysis time
Clot lysis in 6–10 hours.
Prolonged plasma clot lysis time
Lysis beyond the normal interval; lecture associates this with high plasmin inhibitors.
Shortened plasma clot lysis time
Clot lysis in less than 6 hours.
Euglobulin lysis time (ECLT)
Screening procedure measuring overall fibrinolytic activity.
Euglobulin fraction
Fraction containing fibrinogen, plasminogen, and plasminogen activators, with only traces of antiplasmins.
ECLT principle
Lysis of a fibrin clot formed by adding thrombin measures fibrinolytic activity.
1% acetic acid in ECLT
Precipitates the euglobulin fraction from diluted plasma.
Shortened ECLT
Less than 2 hours; indicates excessive fibrinolysis.
Prolonged ECLT
Beyond 2 hours; indicates deficient plasminogen activator.
Fibrinogen level affecting ECLT
Below 80 mg/dL makes fibrinolytic activity difficult to measure.
Reference fibrinogen level in lecture
200–400 mg/dL.
ECLT specimen handling
Set up immediately after collection and keep plasma on ice.
Protamine sulfate turbidity test
Test detecting fibrin monomers and fibrin degradation products.
Protamine sulfate test procedure
Mix patient/control plasma with varying protamine dilutions; incubate at room temperature for 30 minutes.
Positive protamine sulfate test
Turbid; indicates presence of fibrin monomers.
Negative protamine sulfate test
Non-turbid; indicates absence of fibrin monomers.
D-dimer
Specific fragment from degradation of cross-linked fibrin.
D-dimer clinical significance
Indicates ongoing fibrin formation and breakdown.
D-dimer negative cutoff in lecture
Less than 0.5 µg/mL.
Elevated D-dimer in lecture
Greater than 0.5 µg/mL; may occur in DIC, DVT, PE, or stroke.
Very high D-dimer in lecture
Greater than 2 µg/mL; associated with severe DIC and sepsis.
Preferred D-dimer specimen
Fresh citrated plasma.
Serum D-dimer compared with plasma
Serum has lower D-dimer levels than plasma.
Enzyme immunoassay for D-dimer
Quantitative, sensitive assay that is time-consuming.
Latex bead D-dimer assay
Rapid, simple, semiquantitative method useful for point-of-care testing.
Fibrin degradation product (FDP) assay
Uses antibodies against FDP; increased FDP signifies active fibrinolysis.
Tissue plasminogen activator (tPA) antigen
Plasma concentration can be estimated by enzyme immunoassay.
Low tPA levels
Impaired fibrinolysis and association with thrombotic disorders.
Plasminogen activator inhibitor-1 (PAI-1) assay
Assesses PAI-1 antigen or activity using available methods.
Prothrombin fragment 1.2 (F1.2)
Sensitive biological marker of thrombin generation and factor Xa activity.
Plasma antithrombin
Inactivates thrombin and other serine proteases, including activated factors XII, XI, X, and IX.
Effect of heparin on antithrombin
Accelerates antithrombin-mediated inactivation of thrombin.
Plasma thrombin time
Measures functional fibrinogen availability and is sensitive to heparin inhibition.
Prolonged thrombin time
May result from low fibrinogen, abnormal fibrinogen function, DIC, or abnormal fibrinolysis.
Lupus anticoagulant
Autoantibody associated with excess clot formation despite its name.
Heparin monitoring
PTT, as stated in the lecture.
Warfarin monitoring
PT, as stated in the lecture.