Hemostasis Flashcards

1
Q

What is hemostasis

A

the process of forming clots in the walls of damaged blood vessels and preventing blood loss

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2
Q

What occurs initially in response to an injury during hemostasis

A

constriction of the vessel and formation of a temporary hemostatic plug of platelets

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3
Q

loose aggregation of platelets in the temporary plug is bound together and converted into the definitive clot by

A

fibrin

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4
Q

In fibrin, the formation of covalent cross-linkages to a dense, tight aggregate is catalyzed by which factor

A

factor XIII and requires Ca2+

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5
Q

The conversion of fibrinogen to fibrin is catalyzed by

A

thrombin

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6
Q

Prothrombin is converted to thrombin by

A

Factor X

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7
Q

high-molecular-weight kininogen and kallikrein catalyzes which reaction

A

conversion of inactive factor XII to active factor XII (XIIa)

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8
Q

What facilitates the binding of Antithrombin III to serine proteases in the coagulation system

A

Heparin

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9
Q

All endothelial cells except those in the _________ microcirculation produce thrombomodulin

A

cerebral

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10
Q

Is thrombin an anti or pro- coagulant

A

A procoagulant

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11
Q

Thrombin becomes an anticoagulant when it binds to which molecule

A

thrombomodulin

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12
Q

Function of plasmin

A

lyses fibrin and fibrinogen

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13
Q

What is a natural anticoagulant

A

Heparin

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14
Q

Which agents can bind to Ca2+ to prevent blood clotting

A

Chelating

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15
Q

What are the anti-thrombotic properties of endothelial cells

A

Antiplatelet effects - prostacyclin (PGI2) and nitric oxide, adenosine diphosphatase that degrades ADP

Thrombomodulin

Protein C and protein S

Heparin like molecule

Fibrinolytic effects

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16
Q

What are the pro-thrombotic properties of endothelial cells

A

Platelet effects: von Willebrand factor (vWF)

Procoagulant effects

Antifibrinolytic effects

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17
Q

What is the hemostatic sequence in injured vessels?

A

Arteriolar vasoconstriction

Primary hemostasis (formation of platelet plug)

Secondary hemostasis

Clot stabilization and resolution

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18
Q

What steps occur during primary hemostasis

A

von Willebrand factor (vWF) and collagen binds to subendothelial collagen

Activation of platelets + release of secretory granules

Platelet aggregation to form a primary hemostatic plug

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19
Q

What steps occur during secondary hemostasis

A

Tissue factor binds and activates factor VII
Activation of coagulation cascade
formation of fibrin meshwork

20
Q

What is the function of the von Willebrand factor

A

acts as a bridge between the platelet surface glycoprotein(GpIb) and exposed collagen

21
Q

What is the role of platelets during hemostasis

A

formation of primary hemostatic plug

they change in shape which increases surface area

they secrete granules

22
Q

What are the two types of granules released by platelets during hemostasis

A

Alpha and dense granules

23
Q

Which molecule causes platelet aggregation and vasoconstriction

A

Thromboxane A2

24
Q

Which molecule causes platelet aggregation and change in GpIIb-IIIa configuration for fibrinogen bridging

25
what is Glanzmann thrombosthenia
the deficiency of GpIIb-IIIa, involved in platelet aggregation
26
What is Bernard-Soulier syndrome
the defect in GpIb (binds to Willebrand factor)
27
What molecule activates the coagulation cascade (extrinsically)
factor VII
28
What is the ultimate purpose of the coagulation cascade
To turn fibrinogen into its active for fibrin so clot stabilization can occur.
29
What is the other name for tissue factor II
Prothrombin
30
what is the other name for tissue factor IIa
thrombin
31
What are the proteins in the extrinsic pathway
factors VII, X, II, V, and fibrinogen
32
what does a PT assay do
assesses the function of the proteins in the extrinsic pathway
33
Which measurements are used to assess the anticoagulant effect of warfarin
PT and INR(International normalized ratio)
34
what does a PTT assay do
Screens for the function of the proteins in the intrinsic pathway
35
What are the proteins in the intrinsic pathway
factors XII, XI, IX, VIII, X, V, II, and fibrinogen
36
Define thrombin time
Ability to convert fibrinogen to fibrin clot( Measure of circulating fibrinogen)
37
Which molecule breaks down fibrin
plastin
38
What is the fibrinolytic cascade
it moderates the size of the clot
39
Examples of tissue plasminogen activator
Urokinase-like PA (u-PA) Streptokinase
40
Examples of Sudden massive bleeding disorders
Aortic dissection in Marfan’s syndrome Ventricular rupture following MI
41
Examples of Mild bleeding disorders
von Willebrands disease Coagulation factor deficiencies
42
Examples of Generalized defects involve blood vessels
Ecchymosis Palpable purpura Hematoma Vasculitidis
43
Examples of Defects of secondary hemostasis
Coagulation factor deficiencies Bleeding into soft tissues and joints Hemarthrosis Intracranial hemorrhage
44
Defects of primary hemostasis
``` Platelet or VWD Small bleeds in skin and mucous membranes Petechiae ( 1-3mm) Purpura ( 3mm) Bleeding in mucous membranes Menorrhagia Epistaxis Intracranial and gastrointestinal bleeding ```
45
What is Disseminated intravascular coagulation (DIC)
Complications of large number of conditions associated with systemic activation of thrombin OR Sudden or insidious onset of widespread fibrin thrombi in the microcirculation
46
What causes Disseminated intravascular coagulation (DIC)
Obstetric complications Advanced malignancy
47
What is the pathogenesis of Disseminated intravascular coagulation (DIC)
Release of tissue factor and widespread endothelial injury