Exam 3: Disorders of Hemostasis Flashcards

1
Q

How is plasmin formed from plasminogen?

A

plasminogen along with factor XII and tPA (tissue plasminogen activator - also uses epithelial plasminogen activator)

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2
Q

What is one way to determine if clotting has happened?

A

measuring dimers

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3
Q

Which factors are dependent upon Vitamin K?

A

II, VII, IX, and X

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4
Q

A dog has low platelets, what is this called?

A

thrombocytopenia

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5
Q

Which pathway does APTT test?

A

The intrinsic coagulation pathway

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6
Q

Whyaren’t you worried about testing for factor III in the extrinsic coagulation cascade?

A

without FIII, you’re dead. only need to test for VII.

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7
Q

Bleeding disorders 1

What are three factors that deter coagulation?

think simply

A

a physical barrier
a non wettable surface (is thromboresistant)
and anticoagulant proteins

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8
Q

Bleeding disorder 1

What are three factors that encourage coagulation?

A

contraction of damaged vessel
exposure of collagen factors (reduced blood flow and reducsed shear stresss…clot stability)
production of von willebrand factor

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9
Q

bleding disorder 1

Which is more effective, primary or secondary hemostasis? why?

A

secondary is stronger. primary hemostasis only results in a platelet plug

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10
Q

Bleeding disorder 1

What steps are the involved in primary hemostasis - and what proteins and what is their role?

A

Adhesion: GP1b and vWF allow platelets to adhere
Release reaction: platelets release their granules (proteins talke about below)
Aggregation: aggregation of platelets and platelet plug (upregulation of ADP and vWF bridges)
Platelets faciliatate the coagulation reaction via scramblase

fibrinogen binds platelets to platelets
vWF binds platelets to collagen
Ca2+ is a cofactor in coagulation
ADP+++ helps platelets express a receptor to bind to other platelets

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11
Q

Bleeding disorder 1

What are the vitamin K dependent factors? What commonly used household item could interfere with this?

A

2,7,9,10
rodenticide

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12
Q

bleeding disorder 1

What one main enzyme is needed for the coagulation cascade?

A

thrombin

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13
Q

bleeding disorder 1

What are coagulation factors activated by?

A

exposed TF on endothelial cells, microparticles or extravascular fibroblasts.

also negatively charges surfaces like collagen

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14
Q

bleeding disorder 1

what factors are involved in the intrinsic, extrinsic, and common pathways?

A

intrinsic (inside walmart): 12,11,9,8
extrinsic: (3) and 7
common: 10,5,2,1

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15
Q

bleeding disorder 1

How does the common pathway go from factor 10 to a stable clot?

A

10 to 10a
(Ca, PF3, Va) - prothrombinase
2 to 2a
Fibrinogen to fibrin
(13a)
stable fibrin clot

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16
Q

bleeding disorder 1

What clotting factors does the liver make and which ones do macrophages also make?

A

1,8,9,11,12,13
2,5,7,10

17
Q

bleeding disorder 1

can you run our of TFIII?

A

Not unless you’re dead

18
Q

bleeding disorder 1

what is involved in the break down of clots?

A

antithrombin makes up 70% of the anticoagulant proteins, it inactivates thrombin and active factors 12,11,10,9

19
Q

bleeding disorder 1

what can be mesured for evidence of clotting? What is this a process of?

A

D-dimers and Fibrin(ogen) degradation products

fibrinolysis - plasminogen to plasmin

20
Q

bleeding disorder 1

What would make you weary in thrombosis?

A

peeing out antithrombin due to a damaged glomerulus.

21
Q

what bleeding disorder is known as “clotting to death and bleeding to death at the same time?”

A

DIC, you’re clotting and running out of clotting factors. DIC can lead to liver failure.

22
Q

Why is vitmanin K important for coagulation and what does it have to do with bile obstruction?

A

Vitamin K is responsible for creating the activation site on coagulation factors.

vitamin K is fat soluble. The bile emulsifies fats. without fat, there can exist a vitamin K deficiency.

23
Q

What happens during thromboembolic disease?

A

pro-coagulant mechanisms overwhlem anticoagulant mechanisms and can cause vessel obstruction, poor or no perfusion and limb or organ dysfunction

24
Q

What are some primary and secondary ways to evaluate hemostasis?

A

primary: platelet count on a blood slide and bleeding time

Secondary: checking APTT and PT time, quantifying fibrinogen and vWF.

not mentioned is ACT (Activated clotting time) that is an old test that is no longer used.

25
Q

What are some clinical signs of a hemostasis disorder?

A

petechial (vascular and platelet abnormalities) and large hemorrahages (coagulation)

hemarthrosis is blood in the joints

26
Q

What are some acquired causes for vascular disease? what would lab results look like?

A

vasculitis, cushings, scurvy

mainly normal. prolonged bleeding and normal to decreased platelet count

coag tests would be normal

27
Q

You are looking at lab results for a hemostasis disorder. all coagulation tests are normal. there is prolonged bleeding and the ACT is slightly prolonged (can be normal to prolonged in current example). What may be the problem?

A

thrombocytopenia. these test don’t test for platelets, just the coagulation cascade. things are normal but something is not functioning.

28
Q

What breeds are susceptible to type I vWF?

A

doberman pinscher
welsh corgi
german sheperd
golden retriever
poodle

29
Q

What breeds are susceptible to type II vWF?

A

german shorthair pointer

30
Q

What breeds are susceptible to type III vWF?

A

scottish terrier, shetland sheepdog, chesapeake bay retriever

31
Q

What tests are normal for a vitamin k antagonism/ deficiency?

A

bleeding time, quantitative fibrinogen, and vWF

coagulation tests are prolonged

32
Q

DIC is a nonspecific response to many things like…? How does DIC present on lab results?

A

extensive tissue damage: heat stroke, pancreatitis, sever hypoxia
endotoxemia/septicemia
IMHA
Neolpasia (progoagulant proteins)
vascular disease
& more!

everything prolonged… every time.