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THE DOWNS VETERINARY PRACTICE
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Assessment of clotting, tests and interpretation Platelet count
Pathway
tested: Primary haemostasis
Method:
Automatic counter inaccurate
Manual count better
Assessment of blood smear can indicate if
platelet levels are
adequate.
11-25 platelets/oil immersion field is equivalent to an approximate count of >165x109/l
Normal values: Dog 150-400x109/l
Cat
150-400 x109/l
Abnormal values:
low
values (thrombocytopenia) may be due to excessive consumption eg bleeding, immune-mediated
destruction, sequestration, or reduced production eg bone marrow disease
High
values may be due to physiological causes eg splenic contraction, rebound thrombocytosis
post-thrombocytopenia, reactive thrombocytosis in non-specific inflammatory conditions and
primary thrombocytosis such as platelet leukaemia. Buccal mucosal bleeding time
Pathway
tested: Primary haemostasis (platelet function)
Method: The
upper lip is tied back and a shallow incision made in the non-vascular mucosa with a
spring0loaded cutting device such as a Simplate or Surgicutt). Filter or blotting paper is
used to absorb blood without touching the wound and disturbing the forming clot. The time
taken for bleeding to stop is measured.
Normal values:
Dog 1.7 to 4.2 minutes
Cat 1.0 to 2.4 minutes
Abnormal values:
Elevated
bleeding times are seen in problems of platelet number eg immune-mediated
thrombocytopenia, and problems of platelet function such as von Willebrands disease. Clot retraction
Pathway
tested: Primary haemostasis (platelet function)
Method: Add 1ml
of whole blood to a glass tube containing 1ml of 0.9% saline and allow to clot. Examine
the tube hourly for signs of clot retraction.
Normal values:
The clot should reduce to approximately 50% of its original volume within 2 hours.
Abnormal values:
Failure of clot retraction implies severe thrombocyte dysfunction. vWF antigen
Pathway
tested: Primary haemostastis (platelet function)
Method: Collect
blood into trisodium citrate, separate immediately and send to lab. Discuss sample and
shipping requirements with lab first.
Normal values:
see individual labs
Abnormal values:
vWF is decreased in von Willebrands disease. It may be increased in physiological
conditions such as exercise and parturition, and pathological conditions such as liver
disease and azotaemia. Activated clotting time
Pathway
tested: Secondary haemostasis (intrinsic and common pathways)
Method: Prewarm
a tube containing diatomaceous earth to 37C. Discard fist 0.5ml of blood. Draw up a
further 2ml and add to tube. Mix gently and incubate at 37C. Tilt every 10 seconds to
examine for the first signs of coagulation.
Normal values:
Dog 60 to 110 seconds, Cat 50 to 75 seconds
Abnormal values:
Increased ACT implies a severe abnormality of the intrinsic and/or common pathways, but
will also be increased in severe thrombocytopenia and hypofibrinogenaemia. Whole blood clotting time
Pathway
tested: Secondary haemostasis (intrinsic and common pathways)
Method: Discard
the first 0,5 ml of blood, then draw 4ml of blood and place 2ml into each of 2 glass
tubes. Record the time until coagulation has occurred, gently tilting the tube to 90
degrees every 30 seconds to observe clotting.
Normal values:
Dog and cat 6 to 7 minutes
Abnormal values:
Increased WBCT implies a severe abnormality of the intrinsic and/or common pathways, but
will also be increased in severe thrombocytopenia and hypofibrinogenaemia. Prothrombin time
Pathway
tested: Secondary haemostasis (extrinsic and common pathways)
Method: Take
blood into a sodium citrate to the exact fill level. Discuss shipping requirements with
lab.
Normal values:
See individual labs
Abnormal values:
Prolongation of PT occurs with acquired vitamin K deficiency, liver disease, specific
inherited factor deficiencies and DIC Activated partial thromboplastin time
Pathway
tested: Secondary haemostasis (intrinsic and common pathways)
Method: Take
blood into a sodium citrate to the exact fill level. Discuss shipping requirements with
lab.
Normal values:
See individual labs
Abnormal values:
Prolongation of APTT occurs in specific factor deficiencies eg Haemophilia A.
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