Coagulation Profile
Protocols
Intrinsic pathway
The intrinsic pathway is activated by contact with a damaged surface and goes as follows:
Factor XII → Factor XI → Factor IX (+ Factor VIII + vWF) → Common pathway
Extrinsic pathway
The extrinsic pathway is activated by the release of tissue factors and goes as follows:
Factor VII → Common pathway
Combined pathway
The combined pathway then proceeds the intrinsic/extrinsic pathways and goes as follows:
Factor X (+ Factor V) → Factor II → Factor I (+ Factor XIII → Fibrin mesh)
The diagram below should help put all of this into context.
NORMAL Level;
26-36 sec
CAUSES Increase APTT
- Lupus anti-coagulant (antiphospholipid syndrome)
- Heparin exposure
- Haemophilia A and B (Factor VIII and IX deficiency respectively)
- Factor XII deficiency
- Factor XI deficiency
- Contact factor deficiency e.g. prekallikrein (not clinically important)
- Artefact (incorrect amount of blood in the tube)
Normal Level: 12-16 sec
cause of increase PT:
- Deficiencies of factor 2,5,6 or 10
- Severe fibrinogen deficiency
Normal Level :
1.5-4 g/L
cause of decrease Fibrinogen:
- Liver failure
- DIC
Bleeding time normal: 2 to 7 minute
BT Increase: > 9 min
- Blood vessel defect.
- Platelet count may be decreased, or there is a defect in their function.
- Thrombocytopenia.
- Disseminated intravascular coagulation (D I C) where the platelets are consumed.
- Acute Leukemia.
- Coagulation factor deficiencies like Factor I, II, V, VIII, IX, and XI may show some increase.
- Hodgkin’s disease.
- Severe hepatic disease.
- Hemolytic disease of the newborn.
- Patients with uremia where there are a decrease and dysfunction of platelets.
- Patients with anti-inflammatory drugs like aspirin and indomethacin.
- In Von Willebrand disease.
Normal Clotting Time (CT)
- The expected range is 4 to 10 minutes.
- The glass tube method clotting time is 5 to 15 minutes.
- Siliconized tube’s clotting time is 19 to 60 minutes
Causes Of Prolonged Clotting Time:
- Coagulation factors deficiencies may be:
- Congenital.
- Acquired.
- Severe deficiency of any known plasma clotting factors except XIII (fibrin-stabilizing factor) and VII.
- Drugs like heparin and thrombin inhibitors.
- Marked hyperheparinemia.
- Afibrinogenemia.