Haematology - Venous Thrombosis Flashcards

1
Q

What makes up Virchow’s Triad?

A
  • Vessel Wall (endothelial injury)
  • Blood (hypercoagulability)
  • Flow (stasis of blood flow)
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2
Q

What is the escalation of investigations based off different Well’s scores?

A

Low Wells Score:
- Consider other diagnosis

Intermediate Wells Score:
- D-dimer
- IF high = USS/CTPA
- IF low = rule out

High Wells Score:
- USS affected limb for DVT/CTPA for PE

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3
Q

What are some inherited causes that increase VTE risk?

A
  • Antithrombin deficiency
  • Protein C deficiency
  • Protein S deficiency
  • Factor V Leiden
  • Lupus anticoagulant
  • Coagulation Excess
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4
Q

What are some acquired causes tht increase VTE risk?

A
  • Age
  • Obesity
  • Prev. DVT/PE
  • Immobilisation
  • Major surgery
  • Long distance travel
  • Malignancy
  • Pregnancy, COCP, HRT
  • APLS
  • Polycythaemia
  • Thrombocythaemia
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5
Q

What cause is the hgihest risk of a fatal thrombotic event?

A

Antithrombin deficiency

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6
Q

What is the mode of inheritance of protein C/S deficiency, its associations, diagnosis + management?

A

Autosomal Dominant

  • A/w: Warfarin-induced skin necrosis (initial pro-coagulant state)
  • Dx: Protein C/S assay

Tx: Long-term anticoagulation with argatroban

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7
Q

What are the different indications for warfarin reversal?

A
  • INR <= 5: Lower/omit next dose
  • INR 5-9: Omit next dose/Oral Vitamin K
  • INR >9: Omit next dose + Oral Vitamin K

Any bleeding = omit next dose + vitamin K + PCC/FFP

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8
Q

What is used for DVT prophylaxis?

A
  • Daily SC LMWH (prophylactic dose)
  • TED stockings
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9
Q

What is the treatment for a DVT/PE?

A
  • LMWH (treatment dose) followed by Warfarin or DOAC (apixaban, rivaroxaban, edoxaban)
  • LMWH stopped once INR = 2-3
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10
Q

Why is LMWH continued whilst Warfarin is started in DVT/PE Tx?

A

Warfarin affects Protein C/S + leads to procoagulant sstate in first few days before anticoagulant effect

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11
Q

What is the minimum treatment duration for VTE?

A

3 months

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12
Q

What is the action of heparin?

A

Potentiates antithrombin III which inactivates thrombin + Fx IX, X, XII

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13
Q

When is LMWH given + its monitoring requirements?

A
  • SC once daily
  • No monitoring (excep tin late pregnancy, renal failure&raquo_space; monitor anti-Xa levels)
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14
Q

When is unfractionated heparin given + its monitoring requirements?

A

IF renal impairment
- IV loading dose then infusion
- Monitor APTT (or anti-Xa/heparin levels)

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15
Q

What is given to reverse the effects of heparin?

A

Protamine sulphate

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16
Q

What are some side effects of heparin?

A
  • Bleeding
  • Heparin-induced thrombocytopenia
  • Osteoporosis (with long-term use)
17
Q

What is the mechanism of action of warfarin?

A

Inhibits reductase enzyme responsible for regenerating the active form of vitamin K so inhibits the synthesis of Factors II, VII, IX, X + proteins C, S + Z

18
Q

What is given to reverse the effects of warfarin?

A
  • IV Vitamin K (6hrs)
  • Prothrombin complec concentrate (30mins)
19
Q

What are some risks associated with Warfarin?

A

Teratogenicity

20
Q

What are the target INRs and which indications do they have?

A
  • 2.5: 1st episode DVT/PE atrial fibrillation (2-3)
  • 3.5: Recurrent DVT/PE, mechanical prosthetic valve (2.5-3.5)
21
Q

What are some pros of DOACs?

A
  • Oral
  • Immediate effects (peak 3-4hrs)
  • Short half-life (~12hrs) = useful longterm = no monitoring
22
Q

What are the suffixes for DOACs mechanisms of action?

A

-oxaban: Anti- Xa
-gatran: Anti-IIa