Pathophysiology of Coagulopathy Flashcards

1
Q

What differences in solubility exist between fibrin and fibrinogen?

A

Fibrinogen - soluble

Fibin - not soluble

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

What products are created from fibrinogen cleavage by plasmin?

A

Fibrin monomer
Fibrinopeptide A
Fibrinopeptide B

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Why does a fibrin polymer by itself not last very long?

A

Fibrin polymers are only bound through hydrogen bonding and so are transient in the fast moving blood
**Typically only lasts about 24 hours

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

What clotting factor is primarily responsible for prolonging the life of a fibrin clot?
• how so?

A

XIII, it creates COVALENT crosslinks between fibrin polymers

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

What would happen if you cut someone who had a factor 13 deficiency?

A

They would clot then re-bleed

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

What does the prothrombolytic complex consist of?

A
Factor Xa (enzyme)
Factor V (cofactor) 
Ca2+
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

When you need to perform clotting assays should you use plasma or serum?

A

Plasma, serum lacks clotting factors because blood has been allowed to clot

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

If you have a prolonged PT only, what factors may be messed up?

A

PT - EXTRINSIC pathway measurement
• Factor VII

**Tissue Factor really isn’t measured because its part of the reagent that is added to perform the test

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

If you have a prolonged PT and PTT what factors may be messed up?

A

PTT and PT - INTRINSIC and EXTRINSIC measurement
• If both are messed up it must be in a pathway common to both - COMMON PATH

  • Factor II
  • Factor V
  • Factor X
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

If you have a prolonged PTT only, what factors may be messed up?

A

PTT - INTRINSIC pathway measured

  • Factor XII
  • Factor XI
  • Factor VIII
  • Factor IX
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Suppose you have a clotting factor that is severely mutated but PT and PTT are normal, what factor is this likely to be?

A

Factor XIII, is needed for crosslinking only but lack of XIII will not hinder initial clot formation

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Suppose you have a clot, then at 5M urea and it returns to blood. What is a likely cause?

A

Factor XIII deficiency, clot returns to blood because Urea disrupts normal hydrogen bonding in the clot

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

What are the proenzymes in the coagulation cascade?

• Cofactors?

A

Proenzyme:
• II, VII, IX, X, IX ***Note: 1st four are all vit. K dep.

Cofactor:
• Tissue Factor, Factor VIII, factor V

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

T or F: people who take warfarin have fewer clotting factors.

A

False, people who take Warfarin have the same amount of clotting factors, they just aren’t active because they aren’t gamma carboxylated

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Why is measurement of D-dimers important?

A

It is something that could ONLY show up in fibrin that has been previously polymerized

DON’T MAKE Dx. ON THE BASIS OF D-DIMERS

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

Where is thombomodulin found?

• What does it do?

A
  • Thrombomodulin - found on surface of normal epithelial cells
  • Activates protein C after combining with thrombin
17
Q

T or F: antithrombin acts on all serine proteases except for VIII.

A

False, VIII is not a serine protease.

• It acts on all serine proteases (II, IX, X) except VII.

18
Q

What should be the 1st and 2nd things in your differential diagnosis of thombocytopenia in adults?

A
  1. COULD IT BE LAB ARTIFACT?

2. Malignancies, Sequestration, Consumption

19
Q

What physical sign suggests sequestration of platelets?

A

• Big Spleen

20
Q

***What triad should make you think TTP?

A
  • Fluctuating Neurological Symtoms
  • Unexplained Fever
  • Thrombocytopenia

**These are all very random when separate but should stand out to you when you see them together

21
Q

What should you do if you see the TTP triad of:
• Fluctuating Neurological Symptoms
• Unexplained Fever
• Thrombocytopenia

A

Peripheral blood smear to check for Schistocytes

**If you see them, start treating for TTP and run tests to do a differential between TTP, HUS, and aHUS

22
Q

Look up ITP (immune thrombocytopenia purpura) if you don’t talk about it in class tomorrow

A

Look up ITP (immune thrombocytopenia purpura) if you don’t talk about it in class tomorrow