Haemostasis Flashcards

1
Q

what is haemostasis

A

process of blood clot formation at the site of vessel injury

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2
Q

what is the response of a vessel to injury

A

vasoconstriction – reduced blood flow to the injured area

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3
Q

what happens in primary haemostasis

A

formation of the platelet plug

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4
Q

what happens in secondary haemostasis

A

formation of the fibrin clot

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5
Q

components of normal haemostatic system

A

formation of platelet plug (primary)
formation of fibrin clot (secondary)
fibrinolysis
anticoagulant defences

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6
Q

how are platelets formed

A

budding from megakaryocytes in the bone marrow

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7
Q

platelet lifespan

A

7-10 days

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8
Q

how is the platelet plug formed

A

endothelial (vessel wall) damage exposes collagen and releases Von Willebrand Factor (VWF)
Platelet membrane receptor glycoprotein Ib (Gplb) has VWF receptors
Platelet adhesion at the site of injury
there is then secretion of chemicals from the platelets which leads to aggregation of platelets at the site of injury

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9
Q

what do platelets release at the site of injury

A

ADP
serotonin
thromboxane A2
fibrinogen

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10
Q

why might formation of a platelet plug fail

A

vascular
- loss of collagen in vessel walls makes it easier for them to break down

platelets

  • reduced numbers
  • reduced function

VWF
- reduced levels or not functioning

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11
Q

consequences of failure platelet plug formation

A

spontaneous bruising + purpura

mucosal bleeding

  • epistaxis
  • GI
  • Conjunctival
  • menorrhagia

intracranial haemorrhage

retinal haemorrhage

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12
Q

when is menorrhagia a key presenting complaint

A

von willebrand problems

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13
Q

screening test for primary haemostasis

A

platelet count

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14
Q

what 3 things are needed for formation of a platelet plug

A

platelets
VWF
collagen in vessel wall

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15
Q

how is a fibrin clot formed

A
  1. tissue factor is released from damaged vessel walls
    this binds the first clotting factor – factor 7
  2. this then activates clotting factors 5 and 10
  3. factors 5 and 10 turn prothrombin into thrombin
  4. thrombin then turns fibrinogen into fibrin
  5. thrombin also activates fact 8 and 9
  6. they then activate more clotting factor 5 and 10
  7. feedback loop established
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16
Q

what step in fibrin clot formation is called initiation

A

when TF is released and activates factor 7

17
Q

what step in fibrin clot formation is called is called propagation

A

clotting factor 5 and 10 converting prothrombin into thrombin

18
Q

what step in fibrin clot formation is called amplification

A

thrombin activation factor 8 and 9 which go on to activate more 5 and 10

19
Q

causes of fibrin clot failure

A

single clotting factor deficiency
- e.g. haemophilia (factor 8 deficiency)

multiple clotting factor deficiency
- e.g. disseminated intravascular coagulation

increased fibrinolysis
- part of complex coagulopathy

20
Q

how does fibrinolysis occur

A

plasminogen converted to plasmin by tissue plasminogen activator (tPA)

plasmin converts fibrin to fibrin degradation products (FDP)

21
Q

how is FDP measured

A

d-Dimers

22
Q

screening tests for fibrin clot formation

A

prothrombin time (PT)

activated partial thromboplastin time (APTT)

23
Q

what does prolonged PT suggest

A

problem with TF or factor 7

24
Q

what drug can increase PT time

A

warfarin

25
Q

what does prolonged APTT suggest

A

problem with factor 8 or 9

26
Q

what drug can increase APTT time

A

heparin

27
Q

how does anti-coagulation occur

A

anti-thrombin 3 binds to thrombin + switched off TF, factor 7, factor 5 and 10, factor 8 and 9

28
Q

what is protein C and protein S

A

co factors activated by thrombin that switched off factor 5, 10 and 8