Thrombotic disorders Flashcards

1
Q

What are the 3 elements of haemostasis?

A
  1. Primary haemostasis - Formation of primary platelet plug through primary haemostasis mechanisms
  2. Blood coagulation - coagulation factor activation leads to fibrin clot deposition. Fibrin cross-linking occurs to form a stable clot. This subsequently triggers the fibrinolytic pathways
  3. Fibrinolysis - clot degradation
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2
Q

What 3 things happen in the primary haemostasis stage?

A
  • Vasoconstriction - Primary haemostasis is triggered by tissue damage which leads to vasoconstriction at the site of endothelial insult.
  • Platelet adhesion - damage to the endothelial lining results in exposure of subendothelial collagen. Platelets bind do this.
  • Platelet aggregation - platelets clump together
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3
Q

What happens in Fibrinolysis?

A

Fibrin is broken down into fibrinogen and fibrin degradation products

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4
Q
  1. Which enzyme is responsible for breaking down the fibrin network?
  2. What is the name of the inactive precursor of that enzyme?
A
  1. Plasmin
  2. Plasminogen
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5
Q

What 4 things activate Plasminogen converting it into plasmin?

A
  • Urokinase
  • Activation factors:
    • FXIIa
    • FXIa
  • Tissue plamsinogen activator - tPA
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6
Q

Virchow’s triad

A
  • Stasis - bed rest or travel
  • Hypercoagulability - pregnancy or trauma
  • Vessel wall damage - atherosclerosis
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7
Q

What are the 3 main types of thrombosis?

A
  • Arterial
  • Venous
  • Microvascular
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8
Q

Examples of arterial thromboembolism

A
  • Coronary thrombosis:
    • Myocardial Infarction
    • Unstable angina
  • Cerebrovascular thromboembolism:
    • Stroke
    • Transient ischaemia
  • Peripheral embolism
    • Acute limb ischaemia
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9
Q

Look

A

Arterial thrombus - platelets and fibrin

Venous thrombus - red cells and fibrin

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10
Q

Risk factors for venous thrombosis

A
  • Age
  • Pregnancy
  • Surgery
  • Obesity
  • Systemic disease - cancer, autoimmune disease like IBD or SLE
  • Hormonal therapy - combined pill and hormone therapy
  • Tissue trauma
  • Immonility
  • FH
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11
Q

What risk scoring tools are there for DVT? (2)

A

Wells score

Geneva score

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12
Q

If you have a low probability score which further lab test would you do to completely rule out a serious DVT/clot?

A

D-dimer - levels will be high if you have serious DVT - d-dimer is a fibrin degradation product which present in the blood after fibrinolysis.

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13
Q

Which imaging is used to look for DVT?

A

DVT:

  • Doppler ultrasound scan - for upper and lower limb veins
  • Contrast venography, CT, MRA

PE:

  • CT pulmonary angiogram - ‘gold standard’ for PE
  • Ventilation perfusion scan (V/Q lung) - mainly used for suspected PE
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14
Q

Aims of management with venous thrombosis

A

Prevention!!

  • Prevent inital clot from propagating
  • Prevent clot embolisation
  • Prevent clot recurrence in the long term - in high risk patients
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15
Q

Treatment of venothromboembolism

A

Anticoagulants - act on the coagulation cascade before fibrin generation so prevent inital clot from extending but do not break down the clot:

  • LMWH
  • Coumarins (Warfarin)
  • DOACs - direct oral anti-coagulants

Thrombolysis only in selected cases - these work in the fibrinolytic pathways - used for massive PE

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16
Q

What are some hereditary thrombophilias? (group of conditions where you have an imbalance in naturally occurring blood-clotting proteins, or clotting factors)

A

Common:

  • Factor V Leiden mutation
  • Prothrombin G20210A mutation

Rare

  • Antithrombin deficiency
  • Protein C and S deficiency
17
Q

Describe the physiology behind the Factor V Leiden mutation seen in hereditary thrombophilia

A
  • In the presence of thrombin, protein C is activated and this is promoted by thrombomodulin.
  • Protein C is a natural anti-coagulant
  • So in a person without the Factor V Leiden mutation, activation of protein c subsequently inhibits factor 5 and prevents the thrombin formation.
  • With the factor V Leiden mutation the actions of activated protein C are blocked and so there is no inhibiting factor on factor 5. Because of this you have an ongoing drive to thrombin generation and fibrin clot formation.
18
Q

What are protein c, protein s and anti-thrombin?

A

Naturally occuring anti-coagulants

19
Q

Microvascular thrombus

A
  • Platelets and/or fibrin involved
  • Results in diffuse ischaemia
  • Principally in Disseminated Intravascular Coagulation [DIC] - unwell patients
20
Q

What is disseminated intravascular coagulation?

A

Diffuse systemic coagulation activation

Seen in very unwell patients such as:

  • Sepsis
  • Malignancy
  • Eclampsia

It causes tissue ischaemia so you can get gangrene and multi-organ failure

  • Whilst you are forming your clots there is consumption of platelets and clotting factors which leads to thrombocytopaenia
  • Activation of coagulation leading to microvascular thrombosis deposition
  • Present with haemorrhagic phenotype and thrombotic phenotype at the same time