Anticoagulation Flashcards

1
Q

Which anticoagulants can be used in the setting of HIT?

A

Argatobran/Bivalirudin (direct thrombin inhibitors IV)

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2
Q

Signs of Heparin-induced thrombocytopenia → sudden drop in _____ by > ___ %)

confirm with serology and antibodies & list on patient’s allergy list!!!

A

Signs of Heparin-induced thrombocytopenia → sudden drop in platelets by > 50%

confirm with serology and antibodies &
list on patient’s allergy list!!!

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3
Q

CHADS-VASc:
risk stratification scale to determine patient’s risk of developing _____ and/or ____

> /=2 is moderate to high risk patient → start ______ for these patients

A

CHADS-VASc:
risk stratification scale to determine patient’s risk of developing embolism and/or stoke

> /=2 is moderate to high risk patient → start anticoagulation for these patients

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4
Q

HAS-BLED:
Bleeding risk scale; scored from 0 to 5 (__ is the highest → >/ = ___% annual bleeding risk)

Disadvantage: does not take into consideration _____

A

HAS-BLED:
Bleeding risk scale; scored from 0 to 5 (5 is the highest → >/ = 10% annual bleeding risk)

Disadvantage: does not take into consideration falls

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5
Q
A
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6
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7
Q
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8
Q
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9
Q
A
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10
Q

Length of VTE therapy:

Long-term therapy = _ months (most common)

Extended therapy = > _ months (weigh bleeding risk vs benefit) only for pts w/ ____ bleeding risk

A

Length of VTE therapy:

Long-term therapy = 3 months (most common)

Extended therapy = > 3 months (weigh bleeding risk vs benefit) only for pts w/ low bleeding risk

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11
Q

Duration of VTE therapy:

Consider:
_____ risk stratification (___-____score) and risk factors

A

Duration of VTE therapy:

Consider:
bleeding risk stratification (HAS-BLED score) and risk factors

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12
Q

Provoked VTE: no ______ event

Unprovoked status: precipitated by surgery, pregnancy, estrogen therapy, reduced mobility > ___ days, hospital admission

A

Provoked VTE: no identifiable event

Unprovoked status: surgery, pregnancy, estrogen therapy, reduced mobility >3 days, hospital admission

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13
Q

Non-cancer vs cancer patient: DOAC > VKA (warfarin) > LMWH (no cancer); LMWH > VKA (warfarin) > DOAC (cancer pt)

A
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14
Q

provoked VTE therapy duration:

A

long-term: 3 months

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15
Q

unprovoked VTE therapy depends on _____ risk

A

depends on bleeding risk:

  1. Low/moderate bleeding risk = extended therapy > 3 months
  2. High bleeding risk = 3 months
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16
Q

Warfarin dose

___ mg PO x2 days then __ mg PO daily

Elderly/frail: ___-___mg PO daily

A

Warfarin dose

10 mg PO x2 days then 5 mg PO daily

Elderly/frail: 2.5-5mg PO daily

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17
Q

Warfarin is most beneficial for which patients?

A

noncompliant pts

Mechanical heart valves

CAD

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18
Q

Warfarin MOA:

Inhibits factors ___, ___, ___, ___ (contact activation pathway best for _______ heart valves)

A

Inhibits factors II, VII, IX, X (contact activation pathway best for mechanical heart valves)

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19
Q

Cons of Warfarin:

Various interactions w/ food + meds (d/t polymorphisms CYP2C9 & VKORC1)

A

Cons of Warfarin:

Various interactions w/ food + meds (d/t polymorphisms CYP2C9 & VKORC1)

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20
Q

Factors that increase/decrease warfarin (3)

A

Dietary vitamin K increase –> decrease warfarin

Alcohol increase –> increase warfarin

Smoking increase
–> decrease warfarin

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21
Q

Side effects of warfarin (3):

A

Side effects of warfarin (3):

  1. bleeding
  2. skin necrosis
  3. purple toe syndrome
22
Q

Warfarin INR Goals:

VTE + afib: ___ to ___

Mechanical heart valve: ____ to ___

A

Warfarin INR Goals:

VTE + afib: 2-3

Mechanical heart valve: 2.5-3.5

23
Q

Warfarin reversal

24
Q

Warfarin requires or does not require bridging with Lovenox?

A

Bridging with Lovenox required for a min. of 5 days in VTE indication b/c full therapeutic effects seen 5-7 days of initiation or dose changes

25
Q

most commonly used DOACs:

A
  1. Apixaban (Eliquis)
  2. Rivaroxaban (Xarelto):
26
Q

Apixaban (Eliquis) Dosing:

Stroke prophylaxis:
___ mg PO BID

Tx of DVT/PE:
____ mg PO BID x 7 days, then ___ mg PO BID

A

Apixaban (Eliquis) Dosing:

Stroke prophylaxis:
5 mg PO BID

Tx of DVT/PE:
10 mg PO BID x 7 days, then 5 mg PO BID

27
Q

Rivaroxaban (Xarelto) Dosing:

Stroke prophylaxis:
CrCl > 50mL/min
____ mg PO daily w. Evening meal

Tx of DVT/PE:
___ mg PO BID x ___ days, then ___ mg PO daily;

CrCl < 30mL/min avoid use

A

Rivaroxaban (Xarelto) Dosing:

Stroke prophylaxis:
CrCl > 50mL/min 20 mg PO daily w. Evening meal

Tx of DVT/PE:
15 mg PO BID x 21 days, then 20 mg PO daily;

CrCl < 30mL/min avoid use

28
Q

WHICH ANTICOAGULANT AM I?

Dose: renally adjusted + has an induction period for tx of DVT/VTE (high recurrence)

Falsely elevates aPTT and INR → not a red flag just a s/e

ANTIDOTE: Andexxa very expensive

Premature discontinuation increase risk of thrombotic events

29
Q

Why is Edoxaban not used often? Betrixaban?

A

Edoxaban: Small CrCl window so not used much

Betrixaban: expensive + long duration 35-42 days

30
Q

Do DOACs require frequent monitoring for efficacy? What should you monitor in DOACs?

A

No frequent monitoring (patient prefer these)

Monitor: Hgb, Hct, SCr, LFTs q 3-6mos.

31
Q

Which patients benefit from DOACs?

A

Active GI bleed, no bridging, renal dz, CAD: use Apixaban

Noncompliant pt: Rivaroxaban (once daily dosing)

32
Q

When should DOACs not be used?

Not recommended w/ _____ ______ _____

Avoid in pts w/ severe _____ impairment

Warning: pt receiving ______ anesthesia (epidural, spinal) or ______ puncture → risk of _____
______ , ______

A

Not recommended w/ prosthetic heart valves

Avoid in pts w/ severe hepatic impairment

Warning: pt receiving neuraxial anesthesia (epidural, spinal) or spinal puncture → risk of hematomas
bleeding , anemia

33
Q

ORAL Direct Thrombin Inhibitor:

A

Dabigatran (Pradax)

34
Q

Dabigatran (Pradax) Dose:

Stroke prophylaxis:
___ mg BID or
___ mg BID for CrCL 15-30mL/min

Tx of DVT/PE:
___ mg BID after 5-10 days of parenteral anticoagulation

A

Dabigatran (Pradax) Dose:

Stroke prophylaxis:
150 mg BID or
75 mg BID for CrCL 15-30mL/min

Tx of DVT/PE:
150 mg BID after 5-10 days of parenteral anticoagulation

35
Q

Does Dabigatran (Direct thrombin inhibitor) require frequent monitoring for efficacy?

A

No frequent monitoring

36
Q

Which oral anticoagulant has the highest risk GI bleeding?

A

Dabigatran (Pradax)

37
Q

Who should Dabigatran avoided in?

Avoid in active _____, pts w/ _____ _____ _____

Warning: Pts receiving _____ anesthesia (epidural/spinal) or _____ puncture → increased risk of _______;

A

Avoid in active bleeding, pts w/ mechanical prosthetic heart valves

Warning: Pts receiving neuraxial anesthesia (epidural/spinal) or spinal puncture → increased risk of hematoma;

38
Q

Side effects of Dabigatran: (3)

A

Side effects of Dabigatran:

  1. Dyspepsia
  2. gastritis-like symptoms
  3. bleeding (GI)
39
Q

What should you monitor in patient receiving dabigatran?

A

Monitor: Hgb, Hct, Scr

40
Q

A patient has elevated aPTT, PT/INR while on Dabigatran, what is your concern?

A

Dabigatran can falsely increase aPTT, PT/INR. This is not a red flag.

41
Q

Dabigatran antidote

A

Antidote: idarucizumab (Praxbind)

42
Q

How should Dabigatran be stored?

Protect from _____; dispense in _____ container + discard after __ mos of opening.

A

Protect from moisture; dispense in original container + discard after 4 mos of opening.

43
Q

WHICH ANTICOAGULANT? Active GI bleed, no bridging, renal dz, CAD: use Apixaban

44
Q

WHICH ANTICOAGULANT? Noncompliant pt:

A

Rivaroxaban (once daily dosing) or warfarin

45
Q

Pt has an elevated aPTT and INR on DOACs (apixaban/rivaroxaban) what is your concern?

A

Falsely elevates aPTT and INR → not a red flag just a s/e

46
Q

Antidote for Apixaban/rivaroxaban?

A

ANTIDOTE: Andexxa very expensive

47
Q

why shouldn’t DOACs be prematurely discontinued?

A

increase risk of thrombotic events

50
Q

Cancer, Liver disease, coagulopathy, pregnancy: ____

Avoid Bridging/Parenteral: _______

Low compliance (once daily dosing): _____, ____ (has long half-life), ______ (downside: has low CrCl window)

Renal disease+CAD: _____, _____

GI bleed: ______

Thrombolytic therapy use: IV ____

CAD: ______, _____

A

Cancer, Liver disease, coagulopathy, pregnancy: LMWH

Avoid Bridging/Parenteral: DOACs (rivaroxaban or apixaban)

Low compliance (once daily dosing): rivaroxaban, warfarin (has long half-life),
edoxaban (downside: has low CrCl window)

Renal disease + CAD: warfarin, apixaban

GI bleed: apixaban

Thrombolytic therapy use: IV heparin