Anticoagulation Flashcards

(50 cards)

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
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8
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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
most commonly used DOACs:
1. Apixaban (Eliquis) 2. Rivaroxaban (Xarelto):
26
Apixaban (Eliquis) Dosing: Stroke prophylaxis: ___ mg PO BID Tx of DVT/PE: ____ mg PO BID x 7 days, then ___ mg PO BID
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
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
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
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
DOACs
29
Why is Edoxaban not used often? Betrixaban?
Edoxaban: Small CrCl window so not used much Betrixaban: expensive + long duration 35-42 days
30
Do DOACs require frequent monitoring for efficacy? What should you monitor in DOACs?
No frequent monitoring (patient prefer these) Monitor: Hgb, Hct, SCr, LFTs q 3-6mos.
31
Which patients benefit from DOACs?
Active GI bleed, no bridging, renal dz, CAD: use Apixaban Noncompliant pt: Rivaroxaban (once daily dosing)
32
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 _____ ______ , ______
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
ORAL Direct Thrombin Inhibitor:
Dabigatran (Pradax)
34
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
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
Does Dabigatran (Direct thrombin inhibitor) require frequent monitoring for efficacy?
No frequent monitoring
36
Which oral anticoagulant has the highest risk GI bleeding?
Dabigatran (Pradax)
37
Who should Dabigatran avoided in? Avoid in active _____, pts w/ _____ _____ _____ Warning: Pts receiving _____ anesthesia (epidural/spinal) or _____ puncture → increased risk of _______;
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
Side effects of Dabigatran: (3)
Side effects of Dabigatran: 1. Dyspepsia 2. gastritis-like symptoms 3. bleeding (GI)
39
What should you monitor in patient receiving dabigatran?
Monitor: Hgb, Hct, Scr
40
A patient has elevated aPTT, PT/INR while on Dabigatran, what is your concern?
Dabigatran can falsely increase aPTT, PT/INR. This is not a red flag.
41
Dabigatran antidote
Antidote: idarucizumab (Praxbind)
42
How should Dabigatran be stored? Protect from _____; dispense in _____ container + discard after __ mos of opening.
Protect from moisture; dispense in original container + discard after 4 mos of opening.
43
WHICH ANTICOAGULANT? Active GI bleed, no bridging, renal dz, CAD: use Apixaban
Apixaban
44
WHICH ANTICOAGULANT? Noncompliant pt:
Rivaroxaban (once daily dosing) or warfarin
45
Pt has an elevated aPTT and INR on DOACs (apixaban/rivaroxaban) what is your concern?
Falsely elevates aPTT and INR → not a red flag just a s/e
46
Antidote for Apixaban/rivaroxaban?
ANTIDOTE: Andexxa very expensive
47
why shouldn't DOACs be prematurely discontinued?
increase risk of thrombotic events
48
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50
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: ______, _____
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