5 exca Physiology, Coagulation Pathways Flashcards

1
Q

Cascade of events that leads to homeostasis

A

The coagulation pathway

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2
Q

Two paths of coagulation

A

Intrinsic and extrinsic

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3
Q

T/F: the purpose of coagulation is to ultimately stabilize the platelet plug with a fibrin mesh

A

True

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4
Q

Function of coagulation pathway is to keep _____ which is the blockage of a bleeding or hemorrhage

A

Homeostasis

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5
Q

_____ homeostasis is an aggregation of platelets forming a plug at the damaged site of exposed endothelial cells

A

Primary homeostasis

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6
Q

_____hemostasis includes the two main coagulation pathways, intrinsic and extrinsic, that meet up at a point to form the common pathway.

A

Secondary

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7
Q

The common pathway ultimately activates _________into fibrin

A

Fibrinogen

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8
Q

Does fibrin subunits have an affinity for each other to combine into fibrin strands that bind the platelets together, stabilizing the platelet plug?

A

Yes

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9
Q

The intrinsic pathway consists of factors

A

Factor I, II, IX, X, XI, and XII

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10
Q

Name of factor 1

A

Fibrinogen

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11
Q

Name of factor 2

A

Prothrombin

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12
Q

Name of factor 9

A

Christmas factor or plasma thromboplastin component (PTA)

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13
Q

Name of factor 10

A

Stuart prower factor

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14
Q

Name of factor 11

A

Plasma thromboplastin antecedent (PTA)

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15
Q

Name of factor 12

A

Hageman factor

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16
Q

Factor 7 is called?

A

Stable factor

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17
Q

Common pathway consists of

A

Factor I, II, V, VIII, X

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18
Q

The factors circulate through the bloodstream as zymogens and are activated into

A

Serine proteases

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19
Q

These serine proteases act as a catalyst to cleave the next zymogen into more serine proteases and ultimately activate

A

Fibrinogen

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20
Q

Factors that has serine protease

A

Factor II, VII, IX, X, XI and XII

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21
Q

Factors has no serine proteases

A

Factor V, VIII, XIII

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22
Q

The intrinsic pathway is activated through

A

Exposed endothelial collagen

23
Q

extrinsic pathway is activated through ________released by endothelial cells after external damage.

A

Tissue factor

24
Q

First factor that will activate in intrinsic pathway

A

Factor XII (inactivated serine protease)

25
Factor XIIA acts as a catalyst to activate?
Factor IX into Factor XIA
26
This factor is activated by either intrinsic or extrinsic pathway
Factor I
27
Patient can actually clot well without factor?
Factor XII
28
The intrinsic pathway is clinically measured as the?
Partial thromboplastin time (PTT)
29
Once the damage to the vessel is done, the endothelial cells release _______ which goes on to activate factor VII to factor VIIa.
Tissue factor
30
This is the point where both extrinsic and intrinsic pathways become one
Factor X
31
The extrinsic pathway is clinically measured as the
Prothrombin time (PT)
32
Common pathway begins at
Factor X
33
the complex that cleaves factor X into factor Xa
Tenase
34
Two forms of tenase
Extrinsic: factor VII, III and Ca2+ Intrinsic: cofactor factor VIII, XIA, phospholipid and Ca2+.
35
Once activated to factor Xa, it goes on to activate factor II (prothrombin) into factor IIa (thrombin).
.
36
factor Xa requires factor __ as a cofactor to cleave prothrombin into thrombin.
V
37
Factor IIa (thrombin) goes on to activate fibrinogen into
Fibrin
38
As thrombin acts as a procoagulant, it also acts as a __________ by activating __________to plasmin and stimulating the production of ________
Negative feedback, plasminogen, antithrombin
39
acts directly on the fibrin mesh and breaks it down
Plasmin
40
T/F: Thrombin decreases the production of thrombin from prothrombin and decreases the amount of activated factor X.
False: Antithrombin
41
Protein C and S also act to prevent coagulation, mainly by inactivating factors
V and VIII
42
Organs involved in coagulation cascade
Liver , vascular endothelium
43
Lack of coagulation can lead to?
Hemorrhage
44
Coagulopathy in liver disease is treated with
Fresh frozen plasma
45
Hemophilia A is a deficiency in factor___ whereas; in hemophilia B is a deficiency in factor__?
Factor VIII, Factor IX
46
Factor V Leiden is a genetic mutation more prevalent in people European descent. This defect causes a state of
Hypercoagulability
47
Deficiencies in protein C and S also can lead to _________ states due to an inability to appropriately inhibit factors V and VIII respectively.
Hypercoagulable
48
Example of factor inhibitor
Lupus anticoagulant
49
Defeciency can lead to elevated PT and PTT. It can present as hemarthrosis
Vitamin K
50
an anticoagulant used in hospital settings for deep venous thrombosis prophylaxis
Heparin
51
T/F: Heparin binds and activates AT. AT goes on to inactivate thrombin and factor Xa.
True
52
used for long-term therapy in patients with atrial fibrillation to prevent a thrombus from forming in the left atrium. It acts by inhibiting epoxide reductase.
Warfarin
53
a critical component in coagulation factor production because it helps recycle Vitamin K. Without vitamin K more coagulation factors cannot be produced by the liver.
Epixode reductase