Primary and secondary hemostasis Flashcards

1
Q

Main goal of primary hemostasis is to

A

form a platelet plug

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2
Q

Steps in primary hemostasis

A
  1. Vasoconstriction
  2. PLatelet adhesion
  3. Platelet activation
  4. Platelet aggregation
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3
Q

How does vasoconstriction occur

A
  1. Nerve reflexes tell smooth muscle of blood vessels to contract
  2. Endothelin from endothelial cells counteracts action of nitric oxide, a vasodilator and prostacyclin
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4
Q

How does platelet adhesion occur

A

platelets adhere to the site of injury using von willebrand factor as the glue.

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5
Q

What does von willebrand factor do

A

Glue that attaches platelets to blood vessel wall

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6
Q

Why do platelets not initially attach to vessel wall surface

A

Prescence of prostacyclin and nitric oxide preven this from happening

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7
Q

Source of von willebrand factor

A

Blood

Endothelial cells

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8
Q

How does von willebrand factor bind platelets to vessel wall

A

vWf bind to subendothelial collagen of damaged vessel wall and GP1b receptor on platelets

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9
Q

What happens in platelet activation

A

The platelet changes shape

Inactive GP2b/3a platelet receptors are made active by platelet activation and changes its shape

Degranulation occurs

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10
Q

What is involved in degranulation

A

Release of granules in platelets into blood

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11
Q

Types of granules released and what they do

A

Alpha granules- contain fibrinogen, useful for secondary hemostasis

Dense/ Delta granules - secrete serotonin, Adenosine diphosphate and calcium

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12
Q

Function of serotonin

A

Vasoconstriction

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13
Q

Function of adenosinediphosphate

A

Promotes platelet aggregation

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14
Q

Function of calcium

A

Stabilizes the clot formed in secondary hemostasis

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15
Q

Platelet aggregation is primarily mediated by

A

GP2b/3a

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16
Q

What happens in platelet aggregation

A

Platelet activation causes GP2b/3a to be activated and change shape–>GP2b/3a binds to fibrinogen—> fibrinogen binds to many other GP2b/3a receptors on other platelets—. clumping and formation of platelet plug

17
Q

Goal of secondary hemostasis

A

Formation of fibrin mesh to stabilize platelet plug produced in primary hemostasis through a coagulation cascade

18
Q

What is involved in the coagulation cascade

A

A series of events that convert inactive enzymes to active enzymes

19
Q

Coagulation cascade is triggered by

A

Vessel wall injury

20
Q

Factors involved in intrinsic pathway in coagulation cascade

A

I,II,XII,XI,IX,VIII. It is activated by internal trauma i.e trauma to blood cells directly/ exposure of blood to collagen

21
Q

What activates extrinsic pathway

A

vessel wall injury

injury to tissues

22
Q

Factors involved in extrinsic pathway

A

factor VII

23
Q

Both intrinsic and extrinsic pathway lead to

A

Common pathway which involves activation of factor X

24
Q

Function of factor X

A

Conversion of prothrombin to thrombin

25
Q

Thrombin converts

A

Fibrinogen to fibrin clot

26
Q

Fibrinolysis

A

A process that leads to the breakdown of clots in order to prevent them from growing

27
Q

Fibrin is lysed into

A

fibrin degradation products or D dimers

28
Q

Fibrinolysis process

A

At the site of clot formation, plasminogen is activated and converted to plasmin to limit it to the site of clot formation.

Plasmin will cause the dissolution of fibrin meshwork

29
Q

This substances enhances activity of plasminogen

A

Tissue plasminogen activator

Factor XIa and factor XIIa

30
Q

Plasmin is inhibited by

A

alpha antiplasmin

alpha macroglobulin