11. Haematology Flashcards

1
Q

Complication of venous thromboembolism?

A
  • Embolus, causing pulmonary embolism (90% PE cases due to thrombus in leg)  sudden death
  • Haemodynamic abnormalities
    o Abnormal venous circulation, venous hypertension, post thrombotic syndrome
    o Venous eczema
    o Dependent oedema, pain, chronic ulcers
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2
Q

Risk factors for a VTE

A

3 broad risk factors predispose people to VTE (aka Virchow’s triad):

  • Stagnation of blood flow (venous stasis)
  • Enhanced coagulation (hypercoagubility)
  • Vascular damage (endothelial injury)
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3
Q

Treatment of VTE

A

Possible approach to treatment is warfarin + LMWH ‘bridging’

- LMWH used in conjunction with warfarin as it counteracts the hypercoagulation when warfarin first started

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4
Q

Monitoring warfarin

A
  • heparin is continued until anticoagulant effect of warfarin is confirmed by checking INR, target range 2-3
  • LMWH ceased when INR is in range for 2 consecutive days (usually 5-10 days of LMWH)
  • Dietary precautions: beetroot, green leafy veg
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5
Q

What are NOACS

A

Novel oral anticoagulant = NOAC
Eg. Apixaban, dabigatran, rivaroxaban

  • Currently only approved for TKR or THR pts
  • Same recommendations as LMWH with these pts
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6
Q

What is enoxaparin

A

Enoxaparin is a low molecular weight heparin (LMWH) and the most commonly used pharmacological approach to VTE prophylaxis

  • Replace unfractionated heparin (UFH) for VTE prophylaxis as they are more convenient and effective in high risk cases
  • Used in VTE treatment as it has immediate anticoagulant effect and counteracts the hypercoagulation when warfarin is first started
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7
Q

What is heparin?

A

impairment

- Also cheaper than LMWH

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8
Q

Limitations of Warfarin

A
  • slow onset and offset of action
  • narrow therapeutic index
  • food and dug interaction
  • reduce synthesis of all vitamin K dependent prroteins
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9
Q

What are the clinical implications of warfarin/

A
  • need for bridging with rapidly acting anticoagulant
  • varabilitity in dosing requirements
  • need for routine coagulation monitoring
  • risk of skin necrosis
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10
Q

Advantages of NAOCs

A
  • rapid onset of action
  • predicable anticoagulant effect
  • spectific coagulation enzyme target
  • low potential for food interactions and drug interactions
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11
Q

Clinical implications of NAOCs

A
  • no need for bridging
  • no need for routine coagulation monitoring
  • low risk of off target adverse effects
  • no dietary precautions
  • few drug restrictions
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