Coagulation Flashcards

1
Q

What are the common pathway defects?

A

V, X (X marks the spot for PTT and PT and the V fits into the X)
II (prothrombin)
I (fibrinogen
*Just remember that these are the bills under 10

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2
Q

Function of thrombin

A

Convert fibrinogen to fibrin

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3
Q

Factor in PT pathway

A

7 (lucky number 7 activates factor X)

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4
Q

Factors in PTT

A

8,9,11,
*12

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5
Q

Pathognomic feature of acquired hemophilia on a mixing study

A
  • after incubation, on second read out, re-prolongs (PTT is even longer) (autoantibodies take longer to inhibit)
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6
Q

When is bethesda titer positive?

A

Any time you have an inhibitor
- congenital complicated by an inhibitor
- acquired hemophilia

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7
Q

What conditions are associated with prolonged closure time with a PFA-100?2

A

1) platelet defects
2) VWF
*plt count <100 or hematocrit <30 will also lead to prolonged time

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8
Q

Condition associated with FX deficiency

A

Amyloidosis (amyloid protein binds to it and removes it from circulation)

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9
Q

DVT in obesity

A

BMI 40-50 - NOACs okay
BMI >50 - No NOAC, lovenox

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10
Q

how do P2Y12 inhibitors work (clopidogel, prasugrel, ticagrelor, cangrelor)

A

Inhibit platelet surface receptor activation (block interaction with fibrinogen)

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11
Q

What are the GPIIb/IIIa inhibitors?

A

abciximab
*tirofiban
*eptifibatide

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12
Q

Aspirin mechanism

A

Irreversible COX inhibitor in platelets

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13
Q

What are the GPIIb/IIIa inhibitors?

A
  • abciximab
  • tirofiban
  • eptifibatide
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14
Q

Difference between 3 factor and 4 factor PCC

A

The 3-factor-PCC contains factors II, IX, X, and little or no factor VII.

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