Hemostasis and Coagulation Flashcards

1
Q

What type of hemostasis consists in the formation of the platelet plug?

A

The primary homeostasis.

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2
Q

Platelets are fragments of…

A

Megakaryocytes

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3
Q

What is the normal platelet range?

A

150.000 - 400.000 microliters(

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4
Q

What two components binds GPIb-V-IX?

A

vWF and platelets (this GP is found in the membrane of platelets).

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5
Q

What two components binds GPVI?

A

Collagen and platelets (stabilizes the adhesion)

Factor found in the membrane of platelets.

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6
Q

Where are Von Willebrand Factors stored?

A

In the Weibel-Palade bodies (endothelium) and alpha granules (platelets)

Produced by endothelial cells and Megakyrocytes (precursor of Platelets)

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7
Q

In Thrombotic Thrombocytopenia purpura the autoantibodies attack…

A

AdamTS133

No degradation of vWF which causes and increase in adherence.

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8
Q

What shape is present in activated platelets?

What causes this change of shape (activation)?

A

A spherical shape with numerous pseudopods.

The increase of Ca+ caused by the interaction of vWf and GPIb-V-IX.

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9
Q

What does thrombin cause?

A

It causes an increase of intraplatelet Ca2+ and therebefore, platelet activation.

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10
Q

Aspirin effects can last 7 days as it’s a…

A

irreversible COX inhibitor.

COX transforms Arachidonic acid into Prostaglandin G2 and H2.

No generation of TXA2 and no vasoconstriciton.

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11
Q

What protein is binded to platelets through GPIIb/IIIa?

A

Fribrinogen

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12
Q

Which procoagulant factors need vitamin K?

A

Factors FII, FIV, FIX and FX.

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13
Q

What is more predominant in blood procoagulants or anticoagulants?

A

Anticoagulants.

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14
Q

The extrinsic and intrinsic pathway will both converge in the formation of…

A

Prothrombin Activator Complex

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15
Q

What is the other sinonym for tissue factor?

A

Tissue Thromboplastin

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16
Q

By what is formed the prothrombin activator complex?

A

FX + FV + Tissue Factor+ Calcium

17
Q

What is the main function of prothrombin activator complex?

A

Convert Prothrombin into thrombin.

Thrombin will convert fibrinogen to fibrin.

18
Q

What step is common in the extrinsic and intrinsic pathways?

A

The conversion of prothrombin into thrombin.

The formation of the prothrombin activator complex.

19
Q

What factor sufferes a defficiency in Hemophilia A?

A

Favtor VIII

Justo el que protege vWF.

Vidas del gato tras el zapatazo por el campesino.

20
Q

What factor sufferes a defficiency in Hemophilia B?

A

Factor IX

El gato está sano, con sus nueve vidas.

21
Q

What ion do we need in both pathways to activate Factor X?

A

Ca2+

22
Q

APTT ( Activated Partial Thromboplastin Time) on what pathway focuses?

A

On the intrinsic pathway.

Playing Table Tennis (PTT)

23
Q

PT ( Prothrombin Time) on what pathway focuses?

A

The extrinsic pathway.

Playing Tennis.

24
Q

What causes the presence of lupus anticoagulant?

A

Will produce Clots in vivo (it’s a coagulant).

In Vitro will produce an elongated time in the Mixed Coagulation test.

25
Q

What factors does Protein C degrade?

A

Degrades factors V and VIII.

El gato con 8 vidas ocupa el último sitio del tren. Solo quedan 5 sitios

El revisor que es como un comecocos (C) le intenta comer.

26
Q

What does Heparin enhance?

A

The action of antithrombin which degrades F IX, X, XI and XII.

27
Q

What test will I make to monitor patients treated with Worfarin and Sintrom Anticoagulants?

A

PT (Prothrombin Time)

S & W cause Vit. K defficiency. F II, VII, IX and X depend on K+.

Factor VII is from the extrinsic pahtway and PT measures factors in the extrinsic pathway.