Venous thrombosis Flashcards

1
Q

Describe the characteristics of venous thrombosis?

A

low pressure system
platelets not activated
activated coagulation cascade so clots rich in fibrin

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2
Q

How do you treat venous thrombosis? (3)

A

heparin
Warfarin
new oral anticoagulants
these interfere with secondary haemostasis

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3
Q

clinical signs of:

  • DVT?
  • PE?
A

-limb feels hot, swollen, tender
pitting oedema

-Pulmonary infarction causing pleuritic chest pain
CV collapse and death
hypoxia
R heart strain

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4
Q

What are the risk factors for venous thromboembolism?

-what is hypercoagulability associated with?

A

changes in: stasis, vessel wall, hypercoaguability

Age
Marked obesity
Pregnancy
puerperium
Oestrogen therapy
Previous DVT/PE
Trauma/surgery
malignancy 
Paralysis
Infection
Thrombophilia

-release of tissue factor, raised vWF and factor VIII

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5
Q

Thrombophilia

  • what is it?
  • give the potential mechanisms by which this occurs?
A

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

-inc coagulation activity: platelet plug formation and fibrin clot formation
Dec fibrinolytic activity
Dec anticoagulant activity (most common) e.g. deficiency in antithrombin protein C & protein S

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6
Q

Hereditary thrombophilias

  • what are they?
  • name 5
  • when should screening be considered?
  • management
A

-group of genetic defects in which affected individuals have an inc tendency codevelop premature, unusual and recurrent thromboses

-Factoe V Leiden
Prothrombin 20210 mutation
antithrombin deficiency 
protein C deficiency 
Protein S deficiency 
*dont increase risk of venous thrombosis*
-VT <45 
recurrent VT
unusual VT
Fam hx of venous thrombosis
Fam hx of thrombophilia 

-advice on avoiding risk
short term prophylaxis
short term anticoagulation
long term anticoagulation if recurrent events

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7
Q

How do you asses the need for long term anticoagulation?

  • first episode?
  • second?
  • how do you asses risk of recurrent thrombosis?
A

Risk of recurrent thrombosis balanced with
Risk of serious haemorrhage

  • anticoagulate for 6 months
  • lifelong anticoagulation

-Hx prev thrombosis
spontaneous= greater risk than acquired
family hx
Thrombophilia screen

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8
Q

Acquired thrombophilia: antiphospholipid antibody syndrome

  • features?
  • describe the pathogenesis?
  • name the antibodies involved and their effect on the APTT?
  • associated with which conditions?
  • treatment?
A

-recurrent thromboses at young age
Arterial & venous
recurrent foetal loss
Mild thrombocytopenia

  • antibodies lead to conformational change in Bets 2 glycoprotein 1 which leads to activation of both primary and secondary haemostasis and vessel wall abnormalities
  • autoantibodies with specificity for anionic phospholipids and which prolong phospholipid dependant coagulation tests in vitro- lupus anticoagulants
  • Autoimmune, Lymphoproliferative disorders, Viral infections, drugs, primary

-Give treatment depending on thrombotic events
Aspirin- arterial
warfarin- venous

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