HF pt 4 Flashcards

sowinski pg 106-145 (BB, MRA, SGLT2i)

1
Q

what is the rationale behind BB usage in HF?

A

decreases ventricular arrythmias
cardiac hypertrophy and cardiac cell death
VC and HR
cardiac remodeling

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2
Q

what pts should receive BB but cautiously?

A

in pts with bronchospastic disease and asymptomatic bradycardia
while initiating BB in hospitalized pts

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3
Q

what is the dosing of bisoprolol?

A

initial: 1.25 mg daily
targeT: 10 mg daily

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4
Q

what is the dosing of carvedilol?

A

initial: 3.125 mg BID
target: 25-50mg BID

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5
Q

when should 25 or 50 mg BID be targeted in carvedilol?

A

if pt under 85 kg, 25 mg
if pt over 85 kg, 50 mg

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6
Q

what is the dosing of carvedilol CR?

A

initial: 10 mg daily
target: 80 mg daily

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7
Q

what is the dosing of metoprolol succinate?

A

initial: 12.5-25 mg daily
target: 200 mg daily

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8
Q

how should BB be titrated?

A

double the dose every 2 weeks
monitor closely vital signs and symptoms (if get worse, then maybe change diuretic dose instead of BB)

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9
Q

how long after initiation should the target dose be achieved?

A

aim for in 8-12 weeks or highest dose

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10
Q

what is the conversion between carvedilol and carvedilol CR?

A

3.125 mg BID = 10 mg QD
6.25 mg BID = 20 mg QD
12.5 mg BID = 40 mg QD
25 mg BID = 80 mg QD

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11
Q

what are the core monitoring parameters of BB?

A

BP (and symptomatic hypotension)
HR (no goal)

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12
Q

when should a reduction of BB dose be considered?

A

if pt is on a slow titrate and is experiencing symptomatic hypotension, bradycardia, and dizziness –> reduce dose by 50%
if hypotension only, reduce other drugs like diuretics first

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13
Q

what are other monitoring parameters of BB?

A

edema and fluid retention
weight
fatigue or weakness

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14
Q

in what stage should BB be recommended?

A

stage B and stage C unless CI

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15
Q

what is angioedema?

A

notable swelling of the face, lips, and tongue

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16
Q

when aldosterone is elevated in HF, what does it lead to?

A

continued sympathetic activation
parasympathetic inhibition
cardiac and vascular remodeling
BAD THINGS

17
Q

how does selectivity vary in MRAs?

A

spironolactone is non-selective
eplerenone is selective

18
Q

what are the main effects of MRAs?

A

decrease K and Mg losses
decrease sodium retention
decrease sympathetic simulation
block direct fibrotic action on myocardium

19
Q

why is it important that MRAs decrease K/Mg losses?

A

may protect against arrhythmias

20
Q

why is it important MRAs decrease Na retention?

A

decrease fluid retention

22
Q

what are the AE unique to spironolactone?

A

gynecomastia
impotence
menstrual irregularities

23
Q

why is eplerenone not preferred over spironolactone?

A

usually comes down to $$
also a substrate of CYP3A4 so need to avoid interactions with KTZ

23
Q

what is the dosing of eplerenone if eCrCl is over 50?

A

initial: 25 mg QD
maintenance: 50 mg QD

24
Q

what is the dosing of eplerenone if eCrCL is between 30-49?

A

initial: 25 mg QOD
maintenance: 25mg QD

25
Q

what is the dosing of spironolactone if eCrCl over 50?

A

initial: 12.5-25mg QD
maintenance: 25 mg QD

26
Q

what is the dosing of spironolactone if eCrCl is between 30-49?

A

initial: 12.5 mg QD or QOD
maintenance: 12.5-25mg QD

27
Q

when should MRAs be avoided?

A

if SeCr is over 2.5 in males or 2.0 in females
if SeK is over 5
if CrCl is under 30
hx of severe hyperkalemia or recent worsening kidney function

28
Q

what concomitant usage should be avoided with MRAs?

A

K sparing diuretics or supplements (unless hypokalemia of under 4)
NSAIDs
triple therapy of ACEi/ARB/MRA
caution with high dose of ACEi/ARB

29
Q

what should be monitored with MRAs?

A

renal function and K
within 3 days-1 week after any change or addition, disease, or acute illnesses that may influence K concentrations, then every 3 months, then every 3-4 months and with increase ACEi or ARB restart

30
Q

what is important counseling of MRAs?

A

avoidance of salt substitutes (due to K being in most of them – use Mrs. Dash instead)
close questioning for all other sources of K

31
Q

what stage is MRA recommended?

A

Stage C only if eGFR over 30 and K under 5

32
Q

when should MRAs be d/c?

A

if K cannot be maintained to under 5.5 then needs to avoid life threatening hyperkalemia

33
Q

what are the benefits of SGLT2i?

A

osmotic diuresis and natriuresis
decreased arterial pressure and stiffness
preload/afterload reduction and associated reduction in hypertrophy and fibrosis (reduced myocardial remodeling)

34
Q

what is the dosing of SGLT2i?

35
Q

under what eGFR should SGLT2 be not used?

A

under 30 for dapagliflozin
under 20 for empagliflozin

36
Q

what are the AE of SGLT2i?

A

volume depletion
KTA in DM, hypoglycemia, infection risk (UTI/PN, NFP, mycotic)

37
Q

when are SGLT2i recommended?

A

in pts with symptomatic chronic HFEF w/wo DM to reduce hospitalization and CV mortality
stage C