Venous Thrombosis Flashcards

1
Q

What are examples of arterial thrombotic events?

A

Coronary
Cerebral
Peripheral

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2
Q

What are venous thrombotic events?

A

DVT
Pulmonary embolism

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3
Q

Why does arterial thrombosis occur?

A

High pressure system
Atherosclerosis
Platelet rich thrombus

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4
Q

How do we treat arterial thrombosis?

A

Aspirin and other anti-platelet drugs
Modify risk factors for atherosclerosis

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5
Q

How does venous thrombosis occur?

A

Low pressure system
Platelets not activated
Activates coagulation cascade - rich in fibrin clot

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6
Q

What is Virchow’s triad in venous thrombosis?

A

Blood stasis
Vessel wall damage
Hypercoagulability

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7
Q

How can we treat venous thrombosis?

A

Heparin
Warfarin
New oral anticoagulants

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8
Q

What are signs of DVT?

A

Hot, swollen, painful limb
Pitting oedema

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9
Q

What are signs of pulmonary embolism?

A

Pulmonary infarction
Pleuritic chest pain
CV collapse / death
Hypoxia
Right heart strain

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10
Q

What are risk factors for venous thromboembolism?

A

Age
Obesity
Pregnancy
Oestrogen therapy
Previous DVT or PE
Trauma / Surgery
Malignancy
Paralysis
Infection
Thrombophilia
Puerperium

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11
Q

What factors make you more hyper coagulable?

A

Age
Pregnancy
Oestrogen therapy
Trauma / Surgery
Malignancy
Infection
Thrombophilia

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12
Q

Age, pregnancy, oestrogen therapy, trauma / surgery, malignancy and infection are associated with what which can lead to hyper coagulability?

A

Associated with release of tissue factor, raised VWF and factor VIII

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13
Q

What is thrombophilia?

A

Familial or acquired disorders of the haemostatic mechanism which are likely to predispose to thrombosis

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14
Q

What are potential mechanisms of thrombophilia?

A

Increased coagulation activity (platelet plug formation; fibrin clot formation)

Decreased fibrinolytic activity
Decreased anticoagulation activity

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15
Q

What are hereditary thrombophilias?

A

A group of genetic defects in which affected individuals have an increased tendency to develop premature, unusual and recurrent thromboses

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16
Q

What are the main hereditary thrombophilias?

A

Factor V leiden
Prothrombin 20210 mutation
Antithrombin deficiency
Protein C deficiency
Protein S deficiency

17
Q

When do we consider thrombophilia screening?

A

Venous thrombosis <45 years old
Recurrent venus thrombosis
Unusual venous thrombosis
FH of venous thrombosis
FH of thrombophilia

18
Q

How do we manage hereditary thrombophilia?

A

Advice on avoiding risk
Short term prophylaxis - to prevent thrombotic events during periods of known risk
Short term anticoagulation - to treat thrombotic events
Long term anticoagulation - if recurrent thrombotic evens

19
Q

What history findings are important to assess risk of recurrent thrombosis?

A

Hx of previous thrombosis
Sponantenous thrombosis rather than acquired transient risk factor (e.g. immobility or surgery)
FH
Thrombophilia screen results

20
Q

What are causes of acquired thrombophilia?

A

Antiphospholipid antibody syndrome

Stronger risk factor for thrombosis than the hereditary thrombophilias

21
Q

What are features of antiphospholipid syndrome?

A

Recurrent thromboses - arterial (including TIAs), venous

Recurrent fetal loss
Mild thrombocytopenia

22
Q

What is the pathogenesis of antiphospholipid syndrome?

A

Antibodies lead to a conformational change in beta2 glycoprotein 1 (a protein with unknown function in health) which leads to activation of both primary and secondary haemostasis and vessel wall abnormalities

23
Q

What are antiphospholipid antibodies?

A

Autoantibodies which have specificity for anionic phospholipids and which prolong phospholipid dependent coagulation tests in vitro

Also known as lupus anticoagulants

24
Q

What are conditions associated with antiphospholipid antibodies?

A

Autoimmune disorders
Lymphoproliferative disorders
Viral infections
Drugs
Primary

25
Q

How do we treat antiphospholipid syndrome?

A

Activation of both primary and secondary haemostasis; arterial and Venus thrombosis

Thus we need to treat with both aspirin + warfarin