Thrombotic disorders Flashcards

1
Q

Contrast arterial and venous thrombi

A

arterial thrombi: platelet rich white clots formed under high shear stress, generally occlusive and lead to infarction

venous thrombi: fibrin rich red clots that occur in areas of venous stasis and lead to edema, swelling, pain, and inflammation

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2
Q

What is a paradoxical embolus?

A

embolus originating in a vein that bypasses the lung and enters the arterial circulation via a patent ductus arteriosis or atrial septal defect

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3
Q

In the formation of arterial atherosclerotic plaques, increased endothelial expression of VCAM has three major effects:

A
  1. recruits inflammatory cells
  2. stimulates cytokine release, lipid oxidation, uptake by macrophages
  3. stimulates SMC proliferation
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4
Q

List risk factors for both venous and arterial thrombosis

A

hyperhomocysteinemia, heparin-induced thrombocytopenia, and antiphospholipid syndrome/lupus anticoagulants

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5
Q

List the three factors in Virchow’s triad (risks for venous thrombi)

A
  • venous stasis
  • endothelial abnormalities
  • intrinsic hypercoagulability of blood (ex factor V Leiden, AT3 deficeincey, SLE, DIC)
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6
Q

Lupus anticoagulants are phospholipid-dependent antibodies that inhibit
in vitro coagulation but are associated with ______ in vitro

A

arterial and venous thrombi- NOT bleeding

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7
Q

List two examples of targets of anti-phospholipid antibodies:

A

cardiolipin, B2 glycoprotein I

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8
Q

Describe antiphospholipid syndrome

A

the presence of persistent antiphospholipid antibodies in association with a syndrome of arterial and/or venous thrombosis, recurrent fetal wastage, and autoimmune thrombocytopenia

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9
Q

Describe the mechanism of HIT

A

moderate to severe, late
onset thrombocytopenia due to development of a heparin-dependent antibody that is associated with an increased risk of thrombosis

mechanism: PF4 binds heparin, forming neoantigens that cause Fc dependent platelet activation and release of platelet granules

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10
Q

What is appropriate treatment of HIT?

A

stop all heparin

give fondaparinux or argatroban

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11
Q

List five genetic syndromes associated with increased risk of VTE

A
  • AT3 deficiency
  • Protein C deficiency
  • Protein S deficiency
  • Factor V Leiden- most common
  • Prothrombin G20210A polymorphism (autosomal dominant, increased levels of prothrombin antigen in plasma)
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12
Q

Increased levels of _______ is a risk factor for both arterial and venous thrombosis

A

homocysteine

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13
Q

What is standard therapy for uncomplicated DVT/PE?

A

5 days of heparin, transition to warfarin (or alternatively oral thrombin or Xa inhibitors)
3-6 months of therapy

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14
Q

Patients with ______ DVT are treated for longer periods of time due to increased risk of recurrence

A

idiopathic

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15
Q

List some therapies used for prophylaxis of VTE (as in hospitalized patients)

A

heparins
dabigatran, rivaroxaban
mechanical prophylaxis- compression stockings etc

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