Secondary Hemostasis Flashcards

(34 cards)

1
Q

Expression of which cofactors initiates coagulation?

A

Tissue factor (III)

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2
Q

Which coagulation factor drives amplification?

A

Thrombin (IIa)

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3
Q

What are the 4 VitK dependent coagulation factors?

A

2, 7, 10, 9.. coagulation time!

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4
Q

What factor increases antithrombin activity?

A

Heparin

Increase activity by 1000x

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5
Q

Where is heparin found in the body?

A

Expressed on endothelial cells and circulates in the plasma

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6
Q

If you have a protein losing enteropathy, are you hypo or hyper -coagulable?

A

Hypercoaguable –> loss of antithrombin

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7
Q

What are the two major end products of fibrinolysis ?

A

Fibrin degradation products (FDP)

D-dimers

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8
Q

When are fibrin degradation products and D-dimers increased??

A

When there is increased clotting—> increased clot breakdown

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9
Q

What is responsible for clot degradation

A

Plasmin

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10
Q

To run coagulation tests, how should blood be collected?

A

“Clean stick”

Avoid taking blood from heparinized catheter

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11
Q

Blood for coagulation tests should be collected in ??

A

Sodium citrate tube (blue top) –> calcium chelator

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12
Q

What two tests can be used to measure the intrinsic pathway?

A

Activated partial prothrombin time (PPT)

Activated clotting time (ACT)

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13
Q

What test is more sensitive for measuring the intrinsic pathway of coagulation?

A

Activated prothrombin time (70% factor deficiency to produce result)

–>ACT requires a 95% deficiency to produce a result

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14
Q

What test can be used to measure the extrinsic pathway?

A

Prothrombin time (PT)

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15
Q

What test is good to detect a vitamin k deficiency due to the short half life of its coagulation factors

A

PT -> extrinsic pathway (factor VII)

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16
Q

If you have a prolonged PT, what are your two differentials?

A

Factor VII deficiency

Common pathway deficiency

17
Q

If you have a prolonged PTT, but a normal PT, what can you infer from these results?

A

Deficiency in factors 12, 11, 9, or 8 (intrinsic pathway)

18
Q

If you have a normal PPT and and prolonged PT, what can you infer from these results?

A

Deficiency in factor VII

19
Q

If PTT is prolonged and PT is prolonged, what can you infer?

A

Deficiency in factors of the common pathway

20
Q

If there is an increase in FDP or D-dimers, what is the cause?

A

Increased fibrinolysis
Severe internal hemorrhage
Decreased FDP clearance by the liver

21
Q

What toxin is commonly associated with vitK deficiency

22
Q

What bleeding pattern do you expect in an animal with vitK deficiency?

A

Increase bleeding

  • anemia, weakness
  • hypovolemia
  • dyspnea
  • lameness
  • neurological
23
Q
RBC: anemic (regenerative) 
PLT: normal 
MPV: normal 
PTT/ACT: prolonged 
PT: prolonged
A

Vitamin K coagulopathy

24
Q

What are common causes of DIC?

A

Induction of tissue factor -sepsis, tissue necrosis, neoplasia

Endothelial damage - exposed collagen

Proteolytic enzyme -snake venom or pancreatitis

25
What are the two phases of DIC?
Hypercoaguable phase (thrombosis and ischemic necrosis) Consumptive phase (bleed)
26
What phase of DIC results in bleeding?
Consumptive phase
27
What bleeding pattern is seen in DIC?
Mucosal due to PLT consumption | Hemorrhage due to factor consumption
28
What is the cardinal change seen in DIC?
Thrombocytopenia
29
Thrombocytopenia Prolonged PTT/PT Increased FDP and D-dimers Decreased antithrombin Hemorrhagic anemia Schistocytes What dis?
DIC
30
Why are coagulopathies associated with liver disease?
Decreased production of coagulation factors and/or Production of dysfunctional platelets
31
What is the classic presentation of an inherited factor deficiency?
Young animal with bleeding disorder
32
What are the three most common inherited factor deficiencies?
Hemophilia A Hemophilia B Factor XII (Hageman's disease )
33
What common inherited factor deficiencies are associated with bleeding
Hemophilia A: VII | Hemophilia B: IX
34
PLT: normal BMMT: normal PTT/ACT: prolonged PT: normal
Inherited factor deficiency