7 Haemostasis, Fibrinolysis and Wound Repair Flashcards

1
Q

Haemostasis

A

Blood coagulation and prevention of blood loss

coagulation = clotting

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2
Q

Coagulation cascade

A

Factors
Mechanisms
Inhibitors

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3
Q

stages of wound repair

A
  1. Haemostasis
  2. Coagulation cascade
  3. Fibrinolytic cascade
  4. Wound repair§
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4
Q

Fibrinolysis

A

removal of clots, prevention of clotting

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5
Q

what is haemostasis needed for

A
  1. Mechanism is needed to reduce blood loss after vascular injury - prevention of bleeding
  2. Blood must also remain fluid during normal function - prevention of coagulation (thrombosis)
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6
Q

what does haemostasis require

A
  • Requires a balance of haemostatic and fibrinolytic processes
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7
Q

what does haemostasis result in

A

Results in great complexity

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8
Q

why are haemostasis of great medical interests

A
  • Prevention of blood loss
  • Wound repair and recovery from surgery
  • Prevention of circulatory disease (anticoagulants, antithrombotics and “clot busters”)
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9
Q

Haemostasis: Sequence of events

A
  1. Injury, involving vascular damage
  2. Inflammation (Triple response) exudate
  3. immune response
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10
Q

what does coagulation generate

A

Generation of a thrombus (clot) at a site of vascular injury

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11
Q

Thrombus

A

fibrin plug + platelets

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12
Q

what does thrombus limit

A

blood loss

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13
Q

what does thrombus initiate

A

tissue repair

fibrinolysis

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14
Q

where is fibrinogen synthesised

A

liver

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15
Q

where is fibrinogen

A

Constantly present in blood

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16
Q

what is thrombin

A
  • Enzyme

- Active form of prothrombin

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17
Q

when is thrombin formed

A

Final element of coagulation cascade

18
Q

Coagulation: fibrin

A

formed by polymerisation of fibrinogen

19
Q

fibrin in solution

A

Too large to remain in solution

20
Q

what stabilises fibrin

A

Stabilised by Fibrinoligase (Factor XIII)

21
Q

what does fibrin bind

A
  • Binds platelets
  • Binds fibronectin
  • Binds fibrinolytic factors
22
Q

Factors II, VII, IX, X

A

Group of similar molecules, arising from gene duplication

23
Q

what do factors II, VII, IX, X need for synthesis in liver

A

Synthesis by liver requires vitamin K

24
Q

what are factors II, VII, IX, X

A

Some slow-acting anticoagulants work by antagonising Vitamin K in liver

25
what do Factors II, VII, IX, X lead to
progressive haemophilia and eventual death
26
what are Factors II, VII, IX, X useful for
anti-thrombotics in human medicine
27
Factor VIII
Antihaemophilic globulin
28
Inability to synthesise Factor VIII
Haemophilia
29
what is Haemophilia
Hereditary disorder | Inability to control bleeding, often from minor injuries to skin or gut
30
who expresses haemophilia
Expressed in males only: X-linked recessive gene (carrier females may have lower Factor VIII but are asymptomatic)
31
Von Willebrand factor importance
Not strictly part of the coagulation cascade but important to coagulation
32
where is Von Willebrand factor
Circulates in plasma bound to Factor VIII
33
Von Willebrand factor effect
Stabilises Factor VIII and extends its half-life. Factor VIII ineffective in absence of vWF
34
what does Von Willebrand factor enhance
platelet binding to damaged tissue
35
Fibronlysis
Breakdown of thrombus and initiation of wound repair | Degradation of Fibrin by Plasmin
36
Re-epithelialization
Resurfacing of the wound site: Regrowth of epithelium
37
where is re-epithelialization
Sweat glands, hair follicles and nerves reform, except in scar tissue
38
ECM remodelling and scar tissue - collagen types
Collagen Type III | Collagen Type I
39
Collagen Type III
rapidly produced, short strands, limited strength
40
what is collagen type III replaced by
Collagen Type I
41
Collagen Type I
slowly produced, long strands, greater strength