Thrombosis and risk factors for thrombosis Flashcards

1
Q

Arterial thrombosis

A
  • Atherosclerosis of the vessel wall, followed by rupture of atheromatous plaques
  • Associated with endothelial injury
  • Risk factors: smoking, hypertension, diabetes, obesity
  • Treatment: antiplatelet drugs e.g. aspirin
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2
Q

Venous thrombosis

A
  • Venous stasis – abnormal flow
  • Hypercoagulable states – abnormalities cause it to become more clottable
  • Thrombi - composed of fibrin clots with a lesser role for platelet accumulation and aggregation
  • Treatment: anticoagulant drugs
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3
Q

DVT

A
  • Most common venous thrombus
  • 80% of DVTs are clinically silent
  • swelling and pain in the leg; often with dusky cynotic changes, temperature raised
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4
Q

VTE (venous thromboembolism)

A
  • Piece of clot moves off to the lung – present with sudden death (20% of PE)
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5
Q

Risk factors for VTE

A
  • Active cancer/treatment
  • Age>60
  • Dehydration
  • Medical comorbidities
  • BMI>30
  • Surgery, major trauma
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6
Q

VTE and coagulant proteins

A
  • VTE occurs when the balance of pro-coagulant proteins and anti-coagulants is tipped (Loss of AC’s)
  • Anticoagulant proteins = protein C, protein S, anti-thrombin III, fibrinolytic system
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7
Q

VTE – prophylaxis

A
  • Injection of LMW heparin or compression stockings
  • Do not treat if they have risk of bleeding
  • Oral anti-coagulants - direct inhibitors = Rivaroxaban, Apixaban.
    Dabigatran (following ortha surgery)
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8
Q

Low dose LMWH

A
  • indirect anticoagulants, most common in hospitals – anti-Xa and anti-thrombin (IIa) activity – e.g. Tinzaparin
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9
Q

Diagnosis of VTE

A
  • Exclusion tests - clinical assessment + blood tests
  • Wells score + D dimer
  • Ultrasound scanning
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10
Q

Wells score

A
  • Combines risk factors, symptoms and signs
  • Low Wells score, negative D-dimer test = no PE or VTE
  • Intermediate Wells score or positive D-dimer test = further imaging
  • Elevated D dimer = coagulation process is active and clot is being broken down
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11
Q

Ultrasound scanning

A
  • Looking for non-compressibility of vein
  • CT pulmonary angiogram (spiral CT) = chest contrast to look at blood vessels: filling defects in PE patient
  • VQ (ventilation perfusion) scan = compares radio isotopic imaging of vent and perf - look for mismatch present in VTE
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12
Q

Management of VTE

A
  • First episode of proximal DVT or PE - treat for 3-6 months, For warfarin target INR = 2.5
  • Recurrent VTE on therapeutic anticoagulation - increase target INR to 3.5 for warfarin
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13
Q

Thrombophilia

A
  • Familial or acquired disorders of the haemostatic mechanisms which are likely to predispose to thrombosis
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14
Q

Heritable types of Thrombophilia

A
  • Antithrombin deficiency
  • Protein C deficiency
  • Protein S deficiency
  • Activated protein C deficiency/FV Leiden – common genetic polymorphism
  • Dysfibrinogenaemia – dysfunctional fibrinogen molecule
  • Prothrombin 20210A – gene variant; common polymorphism
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15
Q

Acquired thrombophilia

A
  • Antiphospholipid syndrome

- Some blood count abnormalities e.g. myeloproliferative disorders

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16
Q

Antithrombin

A

works against factor Xa and thrombin

17
Q

Factor V Leiden

A
  • Epidemiology = 4-5%
  • most common familial thrombophilia
  • Factor V Leiden means that the protein is resistant to protein C and can’t be broken down by it
  • Heterozygotes – 3-5-fold risk of VTE.
  • Homozygotes – 40-50-fold risk of VTE
18
Q

Prothrombin 20210A

A
  • Point mutation = increased prothrombin levels
  • 3 fold increase in VTE
  • Very rare, 1% in UK
19
Q

Antiphospholipid syndrome

A
  • most common acquired thrombophilia
  • Presence of antiphospholipid antibodies = higher risk of thrombosis
  • Associated with venous thrombosis, arterial thrombosis and recurrent foetal loss
  • Look for lupus anticoagulant in clotting test
20
Q

Heparin

A
  • IV anticoagulant
  • activates antithrombin and inactivates FXa and FIIa (thrombin)
  • risk of heparin-induced thrombocytopenia, antidote is protamine sulphate
21
Q

thrombocytopenia

A

Thrombocytopenia is a condition characterized by abnormally low levels of platelets in the blood