HCP 3 Flashcards

1
Q

What are the progenitor cells to platelets?

A

Giant Megakaryocytes

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2
Q

How long do platelets last in circulation?

A

7-10 days

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3
Q

List the different platelet binding proteins that platelets have and what they bind to

A
  • GpIc/IIa: laminin and fibronectin
  • GpIb: vWF
  • GpIa/IIa: collagen exposed on subendothelium
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4
Q

Contents of alpha granule?

A

Factor V, Fibronectin, vWF, Fibrinogen, PDGF, PF4, TGF

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5
Q

Contents of delta (dense) granule?

A

Serotonin, ADP, ATP, Ca2+, Epinephrine

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6
Q

Where is vWF made and where is it found?

A

Made by endothelial cells and megakaryocytes

Found in Weibel-Palade bodies, circulation, and alpha granules

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7
Q

What do endothelial cells express to prevent platelet activation/aggregation?

A

PGI2 (prostacyclin), Nitric oxide, ADPase

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8
Q

What 2 events are referred to as “platelet activation”?

A
  • Shape change of platelet from discoid to spikey

- Degranulation

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9
Q

Alternate name for Factor XII?

A

Hageman Factor

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10
Q

Alternate name for Factor IX?

A

Christmas Factor

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11
Q

Alternate name for Factor X?

A

Stuart Factor

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12
Q

What factor is Tissue Factor?

A

Factor III

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13
Q

What Factor is Prothrombin?

A

Factor II

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14
Q

What Factor is Fibrinogen?

A

Factor I

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15
Q

What Factor is Ca2+

A

Factor IV

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16
Q

How does the extrinsic pathway get quickly inactivated?

A

After production of a small amount of Xa, TFPI inhibits the TF-VIIa-Ca2+ complex

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17
Q

What is a blood clot?

A

Mass composed platelets & fibrin, with erythrocytes leukocytes, and serum entrapped in fibrin

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18
Q

What is a thrombus?

A

Intravascular blood clot (cannot be used interchangeably with “blood clot”)

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19
Q

What are the anticoagulant factors?

A

Tissue Factor Pathway Inhibitor (TFPI)
Antithrombin III
Thrombomodulin
Protein C (With Protein S as a cofactor)

20
Q

What is the half-life of free Factor VIII and VIII-vWF?

A

Free factor VIII: 2.4 hours

VIII-vWF: 12 hours

21
Q

Describe Hemophilia A

A
  • Mutation in Factor VIII gene
  • X linked Recessive Trait (affects males and homozygous females)
  • Prolonged PTT
  • Normal PT and bleeding time
22
Q

Describe Hemophilia B

A
  • Mutation if Factor IX gene
  • X linked Recessive Trait (affects males and homozygous females)
  • Prolonged PTT
  • Normal PT and bleeding time
23
Q

Where is the Factor VIII gene located?

Where is the Factor IX gene located?

A

VIII: Tip of long arm of X chromosome Xq28
IX: Tip of long arm of X chromosome Xq27.1

24
Q

What is bleeding time?

A

Test done to asses platelet function; measure time from start of bleeding to platelet plug formation

25
Q

What does the Partial Thromboplastin Time Assay test for?

A

Intrinsic Pathway function

XII, XI, IX, X, V, II, I

26
Q

What does the Prothrombin Time assay test for?

A

Extrinsic Pathway function

VII, X, V, II, I

27
Q

What are the 3 main abnormalities that are part of thrombus formation?

A
  • Endothelial Injury
  • Stasis or Turbulent blood flow
  • Hypercoagulability
28
Q

What are 4 things that can happen to a thrombus?

A
  • Propagation
  • Embolization
  • Dissolution
  • Organization/Recanalization
29
Q

Where is a DVT most likely to occur?

A

In the deep veins at or above the knee

-Femoral, popliteal, iliac veins

30
Q

What is the most important activator of Factor X?

31
Q

Type I vWD?

A
  • Autosomal dominant; 70% of all cases
  • Incomplete penetrance; variable expressivity
  • Decreased maturation of increased clearance from plasma
32
Q

Type 2A vWD?

A

Decreased formation vWF multimers

33
Q

Type 2B vWD?

A

defective vWF has enhanced binding to GpIb (spontaneous binding);–>increased clearance

34
Q

Type 2M vWD?

A

Decreased binding capacity to GpIb

35
Q

Type 2N (Normandy) vWD?

A

Decreased binding capacity to factor VIII; mutation in Factor VIII binding domain

36
Q

What are the 5 sources of arterial supply for medial and lateral nasal cavity walls?

A
  • Anterior ethmoidal artery
  • Posterior Ethmoidal artery
  • Sphenopalatine Artery
  • Greater palatine artery
  • Septal bran of superior labial artery
37
Q

Where do the 5 arteries anastomose?

A

Keisselbach area (highly vascular)

38
Q

What factor and proteins use Vitamin K as a cofactor?

A

Factors: II, VII, IX, X
Proteins: C &S

39
Q

What is the name of vitamin K1 and what are its sources?

A

Phylloquinone

Leafy green vegetables (cabbage, kale, spinach)

40
Q

What is the name of vitamin K2 and what are its sources?

A

Menaquinone

Eggs, liver, fermented food, gut bacterial

41
Q

Where does our major source of vitamin K come from?

A

K2; Gut bacteria

42
Q

What form of vitamin K is used as a cofactor?

What enzyme is vitamin K a cofactor for?

A
  • Dihydroquinone/Hydroquinone vitamin K

- gamma-glutamyl carboxylase

43
Q

What enzyme reduces epoxide vitamin K to quinone vitamin K?

A

Vitamin K epoxide reductase (enzyme action is inhibited by warfarin)

44
Q

Why heparin before warfarin?

A
  • Heparin is taken first to decrease thrombin levels
  • Warfarin has to be administered second because it initially stimulates coagulation by fast inhibition of protein C & S
45
Q

What is a saddle embolus?

A

Embolism in main pulmonary artery bifurcation (will cause instant death)

46
Q

Why are extended bed rest and immobilization considered risk factors for DVT?

A

There is reduced milking action of the veins by the leg muscles, which causes stasis/pooling/decreased washout of factors and decreased venous return

47
Q

What does thrombin do?

A

activates factors V, VIII, IX, XI, XIII
Activates protein C
binds to PAR-1 on platelet ➡️ increase platelet activation
converts fibrinogen to fibrin