Coag screen interpretation Flashcards
Background knowledge
Natural anticoagulants: proteins C and S (inactivate factors V and VIII); antithrombin (inactivates many clotting factors)
Vitamin K dependent clotting factors: II, VII, IX, X (+ proteins C and S)
PT and INR = extrinsic
Only factor VII involved in extrinsic pathway
Isolated factor VII deficiencies are rare so PT / INR is only affected by globally reduced clotting factor synthesis or increased consumption:
Warfarin / vit K deficiency
Liver disease
DIC
APTT = intrinsic
Involves similar clotting factors to extrinsic pathway + VIII, IX and XI so is affected by:
Warfarin / vit K deficiency
Liver disease
DIC
Plus anything that affects factor VIII (haemophilia A, vWB), factor IX (haemophilia B) or factor XI (haemophilia C)
Bleeding time = platelet function
Measures platelet plug formation
Rarely used in practice
Fibrinogen
Clotting factor involved in final stages of coagulation
Reflects blood’s clotting ability (low = increased bleeding risk; high = may increase clotting)
Low levels due to increased consumption (DIC) or decreased production (liver disease, malnutrition)
Acute phase protein so may be high due to inflammation, malignancy, trauma, infection
Factor synthesis problems
Vitamin K deficiency - can be due to fat malabsorption or a simple dietary deficiency. Affects clotting factors 2,7,9 and 10 therefor both pathways.
Liver failure - global deficiency affecting both extrinsic and intrinsic pathways. Management is mainly supportive.
Consumption
DIC - in severe systemic illness dying cells release procoagulants resulting in fibrin generation which can occlude small vessels. This consumes platelets and clotting factors resulting in bleeding elsewhere. Thrombocytopaenia, increased PT and APTT, raised d-dimer and fibrin degredation products. TX CAUSE.
Drugs
Warfarin (vitamin K antagonist) - factors 2, 7, 9 and 10. Monitored using INR (extrinsic pathway).
Heparin (increases antithrombin activity):
SC LMWH (e.g. enoxaparin) - activity mediated by inhibition of factor Xa. Effects more predictable therefor monitoring not required. Anti-factor Xa assay.
Unfractionated heparin - use in renal failure. Only works for 4 hours. Monitor using APTT ratio.
Deficiencies
Haemophilia A (VIII), B (IX), C (XI) - haemarthroses and muscle haematomas
VWd - platelet disorder of bleeding (petechiae, menorrhagia, contact bleeding)
Autoimmune
Anti-phospholipid syndrome - arterial and venous thromboembolism. Prolonged APTT.