Chapter 14: Clinical Disturbances of Blood Coagulation 2 Flashcards

1
Q

What does deficiencies of one or more coagulation factors often cause?

A

Hematomas

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2
Q

Large area of hemorrhage

A

hematoma

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3
Q

True or false: Deficiencies of phase I coagulation factors are relatively rare and are usually hereditary.

A

True

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4
Q

Coagulation factors of which phase are deficient in people with Hemophilia A, Hemophilia B, and von Willebrand’s disease?

A

Phase I

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5
Q

What coagulation factors are people with Hemophilia A and B deficient in? What causes this deficiency?

A

Phase 1; it is hereditary

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6
Q

What coagulation factors are people with von Willebrand’s disease deficient in?

A

Phase 1 (von Willebrand Factor)

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7
Q

What is the most common bleeding disorder? What causes it?

A

von Willebrand Disease; deficiency of von Willebrand Factor

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8
Q

Which conditions caused by deficiencies of Phase I coagulation factors are relatively common (exceptions to the rule that most coagulation factor deficiencies are rare):

A

1) Hemophilia A
2) Hemophilia B
3) von Willebrand Factor

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9
Q

Which phase of blood coagulation are Factors IX and X part of?

A

Phase I

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10
Q

What is the most common bleeding disorder?

A

von Willebrand’s Disease

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11
Q

What is the most common clotting disorder?

A

Thrombocytopenia

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12
Q

What type of hereditary disease is hemophilia?

A

X-linked recessive

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13
Q

What is the most common hereditary bleeding disease?

A

Hemophilia

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14
Q

What are the symptoms of hemophilia?

A

Episodic bleeding in joints and internal organs after minor injury; potentially intracranial bleeds.

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15
Q

True or false: Hemophilia affects only females.

A

False; it affects only males, unless an affected male and carrier female are parents.

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16
Q

A decrease in which coagulation factor causes Hemophilia A? Which phase of coagulation is this factor part of?

A

factor VIII (anti-hemophilic factor); Phase I

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17
Q

A decrease in which coagulation factor causes Hemophilia B? Which phase of coagulation is this factor part of?

A

factor IX (Christmas factor)

18
Q

A decrease in which coagulation factor causes von Willebrand’s Disease? Which role does this factor play?

A

vWF; required by platelets to adhere to the vessel wall at the injury site.

19
Q

How does vWF work?

A

Adheres to a damaged wall and forms a lattice framework, allowing platelets and coagulation factors to adhere, interact, and form a clot.

20
Q

Besides vWF, what other factor do von Willebrand Disease patients have low levels of in their circulation?

A

factor VIII (they make enough of it, but b/c of the low vWF, cannot bind and maintain normal levels in circulation).

21
Q

How can patients with Hemophilia or von Willebrand’s Disease be treated?

A

With factor concentrates

22
Q

True or false: Phase I coagulation disturbances are usually hereditary.

A

True

23
Q

True or false: Phase II hereditary disturbances are usually hereditary.

A

False; usually acquired.

24
Q

What are the two causes of Phase 2 coagulation disturbances?

A

1) Prothrombin deficiency

2) Deficiency of factors required to convert prothrombin to thrombin.

25
Q

Where are the factors required to convert prothrombin to thrombin located?

A

In the liver

26
Q

Which key vitamin is required for the synthesis of most phase II coagulation factors?

A

Vitamin K (fat soluble)

27
Q

What is required for vitamin K absorption?

A

Bile

28
Q

Where does most of our vitamin K come from?

A

Mostly made by intestinal bacteria; also from green, leafy veggies

29
Q

What can phase 2 disturbances be caused by?

A

1) Drugs that reduce vit K synthesis (e.g., anticoagulants)
2) Inadequate bacterial synthesis of vit K (e.g., b/c of prolonged antibiotic use)
3) Inadequate absorption of vit K (blockage of common bile duct)
4) Severe liver disease (impairs synthesis of coagulation factors)

30
Q

What are anticoagulant drugs that inhibit of vitamin K-dependent factors used for?

A

To decrease the risk of clotting in certain patients

31
Q

Why might prolonged antibiotic use cause a phase II clotting disorder?

A

It could eradicate the intestinal bacteria needed for the synthesis of vitamin K.

32
Q

True or false: Newborns lack gut bacteria.

A

True

33
Q

What does DIC stand for? What causes it?

A

Disseminated (widespread) Intravascular Coagulation; caused by products being released into the circulation that have thromboplastic activity (i.e., activate the coagulation mechanism)

34
Q

Activate the coagulation mechanism

A

thromboplastic

35
Q

When might you see DIC (disseminated intravascular coagulation)?

A

1) Disease associated with shock or tissue necrosis.
2) Sepsis (overwhelming bacterial infection)
3) Amniotic fluid entering circulation postpartum
4) Other causes of tissue necrosis.

36
Q

formation of a blood clot that obstructs blood flow in a vessel

A

thrombosis

37
Q

An abnormal bleeding state that leads to rapid and widespread activation of blood coagulation.

A

Disseminated Intravascular Coagulation Syndrome (Consumption Coagulopathy)

38
Q

What is the net result of DIC?

A

Widespread hemorrhaging

39
Q

Why does DIC result in hemorrhaging?

A

1) Platelets and plasma coagulation factors are consumed quickly, so their blood levels drop.
2) Body activates fibrinolysin system, leading to fibrin degradation products that further inhibit coagulation.

40
Q

What is the comparative frequency of occurrence of platelet problems, coagulation disturbances, or DIC (disseminated intravascular coagulation)?

A

Platelet problems > Coagulation disturbances > DIC