VTE Flashcards

1
Q

UFH dose for VTE prophylaxis

A

5000 units sq q8h

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2
Q

UFH contraindications

A

history of HIT

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3
Q

when is UFH preferred

A

its lack of renal clearance makes it ideal for patients with AKI or CrCL <30 mL/min

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4
Q

enoxaparin dose for VTE prophylaxis

A

40 mg sq q24h or 30 mg sq q12h

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5
Q

renal dose adjustment enoxaparin for VTE prophylaxis

A

30 mg sq q24h

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6
Q

enoxaparin contraindications

A

AKI, HIT

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7
Q

dalteparin VTE prophylaxis dose

A

5000 units sq q24h

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8
Q

dalteparin contraindications

A

AKI, HIT

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9
Q

fondaparinux VTE prophylaxis dose

A

2.5 mg sq q24h

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10
Q

fondaparinux contraindications

A

CrCL <30 mL/min

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11
Q

when is fondaparinux preferred

A

patient with history of HIT

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12
Q

apixaban VTE prophylaxis dose for total hip arthroplasty

A

2.5 mg bid x 35 days

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13
Q

apixaban VTE prophylaxis dose for total knee arthroplasty

A

2.5 mg bid x 14 days

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14
Q

dabigatran VTE prophylaxis dose for total hip arthroplasty

A

110 mg once, then 220 mg daily x 35 days

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15
Q

rivaroxaban VTE prophylaxis dose in acute medical illness or total hip arthroplasty

A

10 mg daily x 35 days

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16
Q

rivaroxaban VTE prophylaxis dose for total knee arthroplasty

A

10 mg daily x 14 days

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17
Q

instances to avoid DOACs for VTE treatment

A

renal insufficiency, moderate to severe liver disease, significant drug-drug interactions (CYP3A4 inducers), CrCL < 30 mL/min)

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18
Q

apixaban dose for VTE treatment

A

10 mg bid x 7 days, then 5 mg bid x 3-6 months

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19
Q

dabigatran dose for VTE treatment

A

> 5 days of parenteral anticoagulation, then 150 mg bid x 3-6 months

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20
Q

edoxaban dose for VTE treatment

A

> 5 days of parenteral anticoagulation, then 60 mg daily x 3-6 months

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21
Q

rivaroxaban dose for VTE treatment

A

15 mg bid x 21 days, then 20 mg daily x 3-6 months

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22
Q

which DOACs require parenteral anticoagulation first for VTE treatment

A

dabigatran and edoxaban

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23
Q

UFH dose for VTE treatment

A

80 units/kg IV bolus, then 18 units/kg/hr initial rate titrated to aPTT or anti-Xa

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24
Q

enoxaparin dose for VTE treatment

A

1 mg/kg q12h (reduced to q24h if CrCL<30 mL/min)

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25
dalteparin dose for VTE treatment
100 units/kg q12h
26
fondaparinux dose for VTE treatment, <50 kg
5 mg daily
27
fondaparinux dose for VTE treatment, 50-100 kg
7.5 mg daily
28
fondaparinux dose for VTE treatment, >100 kg
10 mg daily
29
which DOAC must be taken with food to facilitate absorption
rivaroxaban
30
____ is the risk calculator used for medical patients
padua score
31
____ is the risk calculator used for surgical patients
caprini score
32
non-pharm VTE prophylaxis options
early ambulation, graduated compression stockings, intermittent pneumatic compression device, inferior vena cava (IVC) filters
33
for high bleed risk patients, use ____ prophylaxis
mechanical
34
when using pharm VTE prophylaxis, opt for ___
low dose
35
for medical patients when pharm prophylaxis is used, ____ is preferred
LMWH
36
for orthopedic surgery patients when pharm prophylaxis is used, _____ is preferred
DOAC
37
for other major surgery patients when pharm prophylaxis is used, _____ is preferred
UFH or LMWH
38
lab findings in DVT diagnosis
D-dimer elevation
39
D-dimer is a product of _____
fibrin degradation
40
non-invasive testing for DVT diagnosis
doppler ultrasonography
41
invasive testing for DVT diagnosis
contrast venography
42
lab findings in PE diagnosis
d-dimer elevation
43
other ways to diagnose PE
ECG, chest xray, echo
44
invasive testing for PE diagnosis
CT pulmonary angiography, ventilation/perfusion scan
45
PE subtypes describe ____
the effect on the body, not the size of the clot
46
massive PE
high risk, hemodynamic compromise, hypotension (SBP <90), may be candidates for thrombolytic therapy
47
submassive PE
intermediate risk, without hemodynamic stability, evidence of right ventricular strain, positive cardiac biomarkers (troponin, BNP)
48
non-massive PE
low risk
49
for uncomplicated DVT and low-risk PE, what is preferred
outpatient, DOAC
50
good DOAC candidates
clinically stable, CrCL>30 mL/min, no drug-drug interactions
51
not good DOAC candidates
renal insufficiency, moderate to severe liver disease, significant drug interactions (CYP3A4 inducers)
52
for limb-threatening DVT and intermediate to high risk PE, _____ is preferred
hospital admission and parenteral therapy
53
advantages for DOACs in VTE
avoids parenteral therapy, predictable PK/PD effects, fixed dosing, similar or better efficacy with less major bleeding
54
how to bridge to warfarin from parenteral anticoagulation
bridge until INR >2 on 2 consecutive readings 24 hours apart, minimum total overlap of 5 days
55
how to bridge to DOAC from UFH
may discontinue infusion and give oral med simultaneously
56
how to bridge to DOAC from LMWH or fondaparinux
give the oral dose when the next injection would have been due
57
when is warfarin actually preferred
patients with renal insufficiency or antiphospholipid antibody syndromes
58
why does warfarin have a delayed anticoagulation effect
it doesn't influence existing clotting factors, its onset is limited by decreased production of new clotting factors
59
things to note when using warfarin for VTE
frequent monitoring is required, goal INR 2-3 for most, drug/food interactions influence dose
60
VTE treatment duration
3-6 months unprovoked, indefinite for unprovoked
61
apixaban dose for ongoing secondary prevention/risk reduction
2.5 mg bid
62
rivaroxaban dose for secondary prevention/risk reduction
10 mg daily