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Hemostasis and Coagulation Flashcards

1
Q

About how long can clot dissolution occur after it has formed?

A
  • minutes to days later
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2
Q

Coagulation proteins are typically found in what form?

A
  • inactivated form
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3
Q

What are two reason why clotting factors do not to the endothelium of the vessel?

A
  • Endothelium is smooth
  • Undamaged endothelium doesn’t expresstissue factor or collagen
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4
Q

If the endothelium becomes damage or is injured what does that cause?

A
  • platelet and coagulation process are activated
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5
Q

What are the three layer of a blood vessel?

A
  • Intima → endothelial layer
  • Media → subendothelial layer (middle)
  • Adventitia → outer layer
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6
Q

Which clotting factors belong to the intima (endothelial) layer?

A
  • VWF
  • Tissue factor
  • Prostacyclin
  • Nitric oxide
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7
Q

Which clotting factors belong to the Media (subendothelial) layer?

A
  • Collagen
  • Fibronectin
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8
Q

How do the endothelial cells of the intima modulate hemostasis?

A

Synthesize and secrete:
* Procoagulants (initiators of coagulation)
* Anticoagulants (inhibitors of coagulation)
* Fibrinolytics (to dissolve the clot)

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9
Q

Which two vascular mediators are release by the Intima endothelial cells?

A
  • Vasoconstrictors
  • Vasodilators
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10
Q

What jobs do vWF and Tissue Factor(TF) perform on the endothelial layer?

A
  • vWF → help platelets adhere to subendothelial layer
  • TF → activates clotting cascade when vessel is injured
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11
Q

Which mediators that are released by the endothelial cells cause vasoconstriction? Which cause vasodilation?

A
  • Constrict → thromboxane A2 and ADP
  • Dilate → NO prostacylin
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12
Q

What are the functions of the following Procoagulants:
* Coagulation factors
* Collagen
* vWF
* Fibronectin
* Thrombomodulin

A
  • Coagulation factors → coagulation
  • Collagen → tensile strength
  • vWF → adhesion
  • Fibronectin → mediate cell adhesion
  • Thrombomodulin → regulate anticoagulation path
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13
Q

What are the functions of the following Anticoagulants:
* Antithrombin IlI
* Tissue pathway factor inhibitor(TFPI)

A
  • Antithrombin IlI →Degrades factors XII XI X IX II
  • TFPI →Inhibits TF
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14
Q

What are the functions of the following Fibrinolytics:
* Plasminogen
* tPA
* Urokinase

A
  • Plasminogen →Converts to plasmin
  • tPA →Activates plasmin
  • Urokinase →Activates plasmin
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15
Q

Besides vasodilation what other function does Prostacyclin provide?

A
  • inhibit aggregation
  • VSM relaxation (duh)
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16
Q

Which layer of a blood vessel isextremely thrombogenic and very active?

A
  • Media (subendothelial)
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17
Q

Which two substances does the media contain that play important roles in clotting? What does each substance do?

A
  • Collagen → potent stimulus for platlet attachement to vessel wall
  • Fibronectin → Facilitate anchoring of fibrin during hemostatic plug formation
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18
Q

How does the adventitia control blood flow?

A
  • Influences the degree of vessel contraction via NO and prostacyclin
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19
Q

How does vasodilation of the adventitia limit the activity of procoagulant mediators?

A
  • ↑ BF washes the procoagulants away
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20
Q

Briefly explain how NO enables vasodilation?

A
  • Nitro Oxide Synthaze converts L-arginine to NO
  • NO diffuses into VSM and activates soluble guanylate cyclase (sGC)
  • sGC activate cGMP which then causes VSM relaxation
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21
Q

What are Eicosanoids?

A
  • PGs and other compounds such as:
  • Prostacyclin
  • Leukotriene
  • Thromboxane
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22
Q

What are the 4 phases of Hemostasis and Coagulation?

A
  • Vascular phase (Vascular spasm)
  • Primary hemostasis (Formation of platelet plug)
  • Secondary hemostasis (Coagulation and formation of fibrin)
  • Fibrinolysis (Lysis of clot)
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23
Q

What happens during theVascular Phaseof hemostasis and coagulation?

A
  • Damaged blood vessels cause vascular spasm of smooth muscle in vessel wall
  • Localized to the injured area
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24
Q

What are the primary hormones involved in the Vascular Phase of hemostasis and coagulation? What do they do?

A
  • Endothelins → stimulate VSM and cell division of endothelial smooth muscle and fibroblast cells which help repair damaged site
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25
Vasospasm MAY slow down/stop bleeding depending on what?
* BP
26
What phase occurs after vascular contraction causes tamponade?
* Primary hemostasis
27
What two things occur during Primary Hemostasis?
* Injured blood vessel attracts platelets * Initiates the phases of platelet formation
28
What are the three phases of platelet formation?
* Adherence * Activation * Aggregation
29
What effect causes the platelet circulating in the blood to be positioned near the vessel wall?
* Platelets are smaller than RBCs/WBCs and get pushed to the sides of the vessel
30
What shape do platelets have that allow them to circulate freely in the blood?
* They are round and disk-like
31
Where are platelets formed?
* in the bone marrow from megakaryocytes
32
According to our class what is the normal concentration of platelets in the blood? How long do they live?
* 150000 to 300000 /mm3 * 1-2 wk lifespan
33
Which 2 systems clears old platelets from the blood? How much of the circulating platelets are stored in the spleen?
* Macrophages in the reticuloendothelial system * Spleen * Spleen holds about 1/3 of circulating platelets for later use
34
In general what do the glycoproteins on the external membrane of the platelet do? What about GpIb and GpIIb-IIIa?
* Adheres to injured endothelium collagen and fibrinogen * GPIb → attaches platelet to vWF * GPIIb-IIIa → links activated platelets together to form plug
35
What do the phospholipids on the surface of the platelet do?
* Substrates to PG synthesis * Produce TXA2 which activates platelet
36
Which platelet surface glycoprotein doesn't have a lot of options to reverse its effects?
* GPIIb-IIIa
37
What are the 5 platelet surface receptors for antiplatelet therapy?
* ADP * GP1b * GPIIb-IIIa * Thrombin * TXA2
38
Describe the role of each of the following substances/structures found inside a platelet: * Actin and myosin * ADP * Calcium * Fibrin-stabilizing factor * Growth factor * Serotonin * Thrombosthenin
* Actin and myosin → Contraction to form the PLT plug * ADP → PLT activation and aggregation * Calcium → Plays a role in the coagulation cascade * Fibrin-stabilizing factor → Cross links fibrin * Growth factor → Repairs damaged vessel walls * Serotonin → Activates nearby PLT * Thrombosthenin → PLT contraction
39
Explain the process by which platelets adhere to each other?
* vWF released from endothelial cells onto the endothelial lining * GPIb receptors emerge from platelet surface * GPIb binds to vWF and this process attracts other platelets
40
What change does the presence of TF cause to the platelet?
* Platelet has conformational change and is activated * GPIIb-IIIa projects outward from platelets and links them to each other → purpose is to create a platelet plug * Seal it and heal it...
41
During aggregation which mediators are released from the platelets themselves (when they are activated)?
* alpha and dense granules * contractile granules * thrombin
42
During aggregation what is the role of the mediators released from the activated platelets?
* Promote procoagulant activity * Form a primary unstable clot
43
What is the difference between a primary clot and a secondary clot?
* Small injury → primary clot (or plug) is enough to provide hemostasis * Large injury → clotting cascade must be activated to create/stabilize secondary clot for hemostasis
44
During secondary hemostasis fibrin production requires which clotting factors in order to proceed?
* all of them
45
Which protein is probably the single most important protein in the clotting cascade?
* Fibrin
46
What is a very general explanation of the clotting cascade?
* A series of enzymatic reactions (clotting cascade) that ultimately activate prothrombin to thrombin which then converts soluble fibrinogen to fibrin
47
What are the 2 paths of the clotting cascade? They ultimately join together to form...?
* Intrinsic * Extrinsic * Common path
48
What are the Vitamin K dependent clotting factors?
* Factors II, VII, IX, X
49
What is the name and source of factor I? Is it Vitamin K dependent?
* Name: Fibrinogen * Source: Liver * Vit K: no
50
What is the name and source of factor III? Is it Vitamin K dependent?
* Name: Tissue Factor (TF) or Thromboplastin * Source: vascular wall/extracellular membrane/released from injured cells * Vit K: Yes
51
What is the name and source of factor II? Is it Vitamin K dependent?
* Name: Prothrombin * Source: Liver * Vit K: n/a
52
What is the name and source of factor IV? Is it Vitamin K dependent?
* Name: Calcium * Source: Diet * Vit K: n/a
53
What is the name and source of factor V? Is it Vitamin K dependent?
* Name: Proaccelerin * Source: Liver * Vit K: No
54
What is the name and source of factor VII? Is it Vitamin K dependent?
* Name: Proconvertin * Source: Liver * Vit K: Yes
55
What is the name and source of factor VIII:C? Is it Vitamin K dependent?
* Name: Antihemophiliac factor * Source: Liver * Vit K: No
56
What is the name and source of factor VIII:vWF? Is it Vitamin K dependent?
* Name: vonWillibrand Factor * Source: Vascular endothelial cells * Vit K: n/a
57
How can we compensate for vWF deficiency?
* DDAVP infusion
58
What is the name and source of factor IX? Is it Vitamin K dependent?
* Name: Christmas Factor * Source: Liver and other tissues * Vit K: Yes
59
What is the name and source of factor X? Is it Vitamin K dependent?
* Name: Stuart-Prower Factor * Source: Liver * Vit K: Yes
60
What is the name and source of factor XI? Is it Vitamin K dependent?
* Name: Plasma thromboplastin antecedent * Source: Liver * Vit K: No
61
What is the name and source of factor XII? Is it Vitamin K dependent?
* Name: Hageman Factor * Source: Liver * Vit K: No
62
What is the name and source of factor XIII? Is it Vitamin K dependent?
* Name: Fibrin Stabilizing Factor * Source: Liver * Vit K: No
63
Which clotting factors come from the liver?
* All of them except III IV and vWF (VIII:vWF)
64
Explain how the Extrinsic pathway works up to the common path.
*For 37 cents you can purchase the extrinsic pathway* * TF released from subendothelium during injury →  TF or factor 7 activates extrinsic path * TF activates factor 7 * Factor 7 activates factor X in the presence of factor 4 (Ca++) * Prothrombin activator and platelet phospholipids activate factor 2 (thrombin) → this leads to common path * Note: Factor 5 ↑ the production of prothromin activator (+ feedback)
65
If the patient is low on Ca++ how will this effect the extrinisic path of the clotting cascade?
* It won't work as well
66
How long does it take a clot to form via the extrinsic path?
* 12 to 15 sec
67
Explain how the Intrinsic pathway works up to the common path.
*If you can't buy the intrinsic pathway for $12 you can buy it for $11.98.* * Blood trauma or exposure to Collagen → activates factor XII * Factor XIIa activates factor XI → this step needs HMW kininogen and accelerated by prekalllikrein * Factor XIa activates factor IX * Factor IXa and VIII activate factor X * Prothromin activator and phospholipids activate factor IIa (thrombin) → leads to common path
68
Which pathologies will prevent factor X from being activated in the intrinsic path?
* Hemophilia A → Factor VIII missing * Thrombocytopenia → Platelets (phospholipids) missing
69
How long does it take to creat a clot via the intrinsic path?
* 6 minutes
70
Explain how the Common pathway works.
The final common pathway can be purchased at the five(V) and dime(X) for 1(I) or 2(II) dollars on the 13th (XIII) of the month * Prothrombin activator changes prothrombin (II) to thrombin (lla) * Prothrombin changes fibrinogen to fibrin in the presence of Ca++ * Fibrin is added to platelet plug * Activated fibrin-stabilizing factor (XIlla) cross-links fibrin-fibers to complete the clot
71
When the clotting cascade gets activated what else does the body activate?
* Fibrinolysis
72
What is fibrinolysis?
* Prevents clotting from going out of control (+ feedback loop) * Precent excessive deposition of fibrin
73
What is the primary mechanism that begins Fibrinolysis? What is a secondary activator?
* tPA released by damaged endothelial cells * urokinase
74
Where is urokinase produced and what is its purpose?
* Produced by kidneys → helps prevent small clots from cloggin up kidneys
75
What are two fibrinogenic factors involved in fibrinolysis? What do they do?
* Kallikrein * Neutrophil elastase * Convert plasminogen to plasmin → plasmin breaks down fibrin
76
Explain how fibrinolysis works?
* Plasminogen is converted to Plasmin via tPA and UPA * Plasmin degrades fibrin into "split" products
77
What is a normal platelet values for our class?
* 150,000 to 300,000/mm3
78
What is a normal bleeding time (BT) for our class?
* BT = 3-10 min
79
What is a normal PT for our class?
* PT = 12-14 sec
80
What is a normal aPTT for our class?
* aPTT = 25-35 sec
81
What is a normal thrombin time (TT) for our class?
* TT = 30 secs
82
What is a normal activated clotting time (ACT) for our class?
* ACT = 80-150 secs
83
What is a normal fibrinogen level for our class?
* Fibrinogen ≥ 150 mg/dL

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