Haematology - SPAF Flashcards

1
Q

Describe the pathophysiology of Stroke in AF.

A

Irregular contraction of the left ventricle creates turbulent flow that results in the accumulation of clotting factors in the left atrial appendage. This may precipitate thrombus formation. The thrombus may embolise to the cerebral circulation manifesting in stroke.

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2
Q

What is the first thing to determine w AF?

A

If pt has mod-severe mitral stenosis or mechanical valves.

If yes, DOACs CI –> use VKA (warfarin)

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3
Q

What are the goals of SPAF?

A
  • Re-est vascularisation to brain
  • Avoid risk of haemorrhagic conversion (manage BP)
  • Prevent systemic embolism
  • Balance anticoagulation and avoiding major bleeding
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4
Q

How do we determine whether to anticoagulate?

A

CHA2DS2-VASc criteria
0: No need to anticoagulate.
1: Watch and wait till another risk factor develops. May consider anticoagulation.
2: Start anticoagulation.

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5
Q

What is the CHA2DS2-VASc criteria?

A

C: CHF
H: HTN
A2: Age >=75y.o.
D: DM
S2: Hx of stroke
V: Vascular disease
A: Age >=65y.o.
Sc: Gender (F) - often left off

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6
Q

What is the point of HASBLED criteria?

A

It helps to profile bleeding risk so we can mitigate modifiable risk factors. It is validated for AF pts.

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7
Q

What is the HASBLED criteria?

A

H: Uncontrolled HTN (SBP>160 mm Hg)
A:
- Abnormal renal fn: HD/PD, renal transplant, SCr >200 micromol/L
- Abnormal LFT: cirrhosis, ASP, AST, ALP >3ULN, bilirubin>2ULN
S: Hx of stroke
B: Bleeding predisposition, Hx
L: Labile INR
E: Elderly (age >65y.o.) or extreme frailty
D: Drugs (antithrombotics, NSAIDs) and alc (M>14units, F>7units)

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8
Q

What are the anticoagulation options in SPAF?

A

Dabigatran, Rivaroxaban, Apixaban, Edoxaban, Warfarin

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9
Q

Are antiplatelets used in SPAF?

A

NO. “ILLEGAL”

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10
Q

Describe the renal dosing adjustments for the DOACs.

A

Dabigatran:
- Adjustments start from <30mL/min: CI , [FDA]15-30mL/min: 75mg BD

Rivaroxaban:
- Adjustment starts from 30-50mL/min, [FDA] 15-49 mL/min: 15mg per day, 15-30mL/min: Use w caution, <15mL/min: CI

Apixaban:
- 5mg BD (normal)
- CrCL> 30mL/min look at criteria - Min 2 criteria: Age >=80y.o., Body wt <60kg, SCr >1.5mg/dL or 133micromol/L –> 2.5mg BD
- Adjustment starts from <30mL/min: 2.5 mg BD, <15mL/min
- HD pts not well studied, not incl in clinical trials

Edoxaban:
- 60 mg per day (normal)
- If any of the following - CrCL 30-50mL/min, wt <=60kgm, concomitant verapamil, quinidine, dronedarone –> 30 mg per day
- CrCL <15-30mL/min: 30mg per day, CrCL<15 mL/min: Not reco

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11
Q

For estimating renal dose adjustments in SPAF what considerations are there?

A

Use Cockcroft-Gault eqn

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12
Q

What special dosing remarks are there for the DOACs?

A

Dabigatran & rivaroxaban dosing is NOT based on criteria (js CrCL) while apixaban and edoxaban are criteria based (Scr, wt, age)

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13
Q

What to do if pt has high bleeding risk HASBLED >=3?

A
  1. Assess risk of stroke bleeding
  2. ID & treat other comorbidities
  3. ID cause of prev bleeding
    If unknown, untreatable, irreversible: no treatment, LAA occlusion (filter to catch embolus)
    If known & treatable: restart OAC (DOAC >VKA)
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14
Q

What are the principles of anticoagulation selection?

A

VKA decreases risk of stroke by 64% & death by 26% in pts w AF.
DOACs further decrease risk of AIS by 19% and risk of ICH by 50% vs VKA (warfarin)

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15
Q

When are DOACs preferred over VKA for SPAF?

A

Always, except in mod-severe mitral stenosis, prosthetic heart valves, antiphospholipid syndrome.

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16
Q

What are the considerations in elderly?

A

Dementia and compliance
Frailty and falls
- Age NEVER a CI for SPAF anticoagulation
- Apix performs bettern than other DOACs for elderly (Dabi & Edox for stroke and embolism better than VKA as well)

17
Q

What are the dosing considerations wrt BW?

A

Normal: 60-120kg
Lower BW accounted for w apix & edox
Higher BW limited data suggests rivarox (winder indication ranges incl ACS) & apix (easier to use)

18
Q

How may we swap between warfarin and DOACs?

A

DOAC–>Warfarin
- Dont need to hold of on DOACs: Immediately switch to overlapping regimen
- Dont load too high, cld lead to vv high INR
- Give flat dose, monitor INR day 3-5

Warfarin–>DOACs
- Hold warfarin off for 3d + INR <2.0
(Warfarin long t1/2 vs DOAC shorter t1/2)

19
Q

When we disrupt DOACs, what must we consider?

A

Take into acc DOACs, t1/2, CrCL
Pt charac:
- Age
- Stroke risk, bleeding risk
- Recent (3mo) CV event
- Comorbidities
- Meds

Dabi more dep on renal fn > Xa inhib (may req to hold off longer