11 - Hypercoagulable States Flashcards

1
Q

If you suspect that your patient has a deep vein thrombosis in their lower leg, what would be your next stop in her management?

A

Ultrasound of the lower extremity to evaluate for thrombosis.

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2
Q

Your patient with a DVT is given enoxiparin for anticoagulation. She is transitioned for apixaban and treated for 3 mo. Three years after her initial presentation she begins to experience SOB, difficulty climbing stairs, and chest pain. In the ED, her CT shows a PE. What hemetologic deficiencies could contribute to this presentation?

A
  • Factor V Leiden
  • Anti-phospholipid antibody syndrome
  • Protein S deficiency
  • Anti-thrombin deficiency
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3
Q

What is Factor V Leiden?

A

A polymirphism in factor V that causes resistance to degradation by activated protein C (normally factor C degrades factor 5 but in this disease it cannot.)

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4
Q

People with low levels of what are at risk of warfarin related skin necrosis?

A

Protein C and S.

This is because warfarin decreases vitamin K and protein C and S are vitamin K dependent and thus their levels will DECREASE when you give warfarin. Decreased levels of C and S result in hypercoagulability (even though technically warfarin is anti-coagulating).

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5
Q

Antithrombin reacts with what two things to inhibit their activity?

A

Thrombin and activated factor X are inhibited by antithrombin.

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6
Q

If you have a patient who you suspect has a clot, would you want to know her Factor V Leiden status? What is the single biggest risk factor for clotting?

A

NO! Factor V leiden only predicts your initial risk of clotting, not the chance of reoccurence.

The single biggest risk factor for clotting is age. So a young person with a clot is a lot more concerning for reoccurence than an old person with a clot.

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7
Q

What are the risk factors for venous thrombosis?

A

Virchow’s Triad!:

  • Circulatory stasis
  • Endothelial injury
  • Hypercoagulable state
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8
Q

What does diagnosis of DVT and PE require?

A

The combined use of pretest probability tools (Wells score) plus lab (D-dimer) and imaging (usually ultrasound but sometimes CT or MRI).

The Well’s score is used to predict the probability of clotting.

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9
Q

What anticoagulants work by inhibiting factor Xa (there are 6)? How is each given?

A
  • Rivaroxaban - oral
  • Apixaban - oral
  • Edoxaban - oral
  • Fondaparinux - parenteral
  • LMW Heparin - parenteral
  • Unfractionated Heparin - parenteral
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10
Q

What anticoagulants work by inhibiting factor IIa (there are 5)? How is each given?

A
  • Dabigatran - oral
  • Unfractionated Heparin - parenteral
  • Argatroban - parenteral
  • Lepirudin - parenteral
  • Bivalirudin - parenteral
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11
Q

Describe the following as it pertains to warfarin:

  • Onset
  • Food interactions
  • Drug interactions
  • Is the drug reaction predictable?
  • Is there an antidote?
A

Onset: slow

Food interactions: significant (leafy greens)

Drug interactions: many!

Is the drug reaction predictable?: No

Is there an antidote?: Yes

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12
Q

Describe the following as it pertains to DOACs?:

  • Onset
  • Food interactions
  • Drug interactions
  • Is the drug reaction predictable?
  • Is there an antidote?
A

Onset: Rapid!

Food interactions: Minimal

Drug interactions: Few

Is the drug reaction predictable?: Yes

Is there an antidote?: Yes, but it’s expensive and less available.

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13
Q

What is the most common known inherited thrombophilia? What population is the gene relatively common in?

A

INHERITED RESISTANCE to activated PRotein C (APC) and Factor V Leiden.

Approximately 5-6% of caucasians are heterozygous for the factor V leiden mutation.

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14
Q

What is the cause of Factor V Leiden?

A

A point mutation in the factor V gene that results in an Argining > Glutamine translocation at amino acid 506 (FV-R506Q).

Position 506 is the initial site of cleavage of Factor Va by activated protein C. Therefore, factor Va is relatively resistance to inactivation.

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15
Q

If your patient is pregnant and has thrombocytopenia, what test would you want to do?

A

A peripheral blood smear! THIS IS THE HEME UNIT PEOPLE.

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16
Q

You order a peripheral blood smear on your pregnant with thrombocytopenia and it looks like the attached image. What is the mechanism accountable for the patient’s peripheral blood smear?

A

A mechanical shearing of RBCs with consumption of platelets.

17
Q

What is the function of ADAMTS13? What does it mean if it’s low?

A

It chops up vWF.

If it’s low, platelets stick to the large vWF.

18
Q

What is the pentad of clinical manifestations of thrombotic thrombocytopenic purpura (TTP) - microvascular inarction?

A
  • Microangiopathic hemolytic anemia (schistocytes/RBC fragments)
  • Thrombocytopenia
  • CNS or mental status changes
  • Fever
  • Renal insufficiency
19
Q

If your patient is pregnant and has thrombocytopenia and the labs as shown below, what is your diagnosis and why?

A

Throbotic thrombocytopenia purpura (TTP) because their ADAMTS13 is low.

20
Q

How would you treat a patient with Thrombotic Thronbocytopenic purpura (TTP)?

A

They need an emergency plasma exchange to give them the ADAMTS13 that they are missing.

21
Q

What can a factor V leiden test tell you about the present or absence of a clot?

A

NOTHING - I repeat - NOTHING!

It is NOT a helpful diagnostic took to determine if something has a clot or not.

22
Q

What does elevated D-dimer indicate?

A

Suggests recent activity of thrombosis and fibrinolysis causing fibrin degradation.

23
Q

When you first start warfarin you are ________, because of a decrease in ______.

A

Hypercoagulable due to a decrease in protein C.

This is why they need heparin bridge (ie to reduce coagulability) until their INR becomes therapeutic.

24
Q

What (bad thing) can occur during a heparin bridge for a patient trying to reach therapeutic warfarin levels?

A

Heparin induced thrombocytopenia. IE a drug-induced antibody mediated platelet destruction with consumption.

(your body makes an auto-antibody to heparin)

25
Q

What are the four indications of heparin induced thrombocytopenia?

A

4T’s!

Thrombocytopenia: moderate (rarely <20,000)

Timing: 5-10 days after initial heparin exposure

Thrombosis: associated with thrombotic events; increases risk for thrombosis 20-40 fold.

No other causes (???? this is not a T?????)

26
Q

What is the treatment for heparin induced thrombocytopenia?

A

Maybe this is the fourth T????? Treatment?

  • Stop all heparin therapy
  • Do not start low molecular weight heparin (enoxaparin) or warfarin.
  • Begin alternative anticoagulation (direct thrombin inhibitor (DTI): argatroban or bivalirudin
27
Q

How would you test to see if your patient has heparin induced thrombocytopenia?

A

Do an ELISA for factor-4 heparin antibody.

28
Q

What is the pathophysiolocy behind heparin induced thrombocytopenia?

A
  1. PF-4 binds to the surface of platelet following activation.
  2. Complexes of heparin (GAG) and PF-4 molecules form.
  3. IgG binds to the PF-4 heparin complex.
  4. Fc stimulation leads to the gerneration of procoagulant-rish microparticles.
  5. IgG/PF4/heparin complex activates via the Fc receptor.