12 HF 3 Flashcards

1
Q
A

C

Lets do an ARB instead
* ARNI is also CI now

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2
Q
A

A

systolic HF = HFrEF

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3
Q
A

C

pregnant

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4
Q
A

D

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5
Q
A

B

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6
Q

Aldosterone receptor antagonists (AA) = MRA

aldosterone elevated in HF leads to:
- continued ___ activation
- ___ inhibition
- cardiac and vascular ___

___ (non-selective) and ___ (selective) block aldosterone effects independent of the effects of ACEis or ARBs
- decrease ___ and ___ losses: may protect against ___
- decrease ___ retention: decrease ___ retention
- decreases ___ stimulation
- blocks direct ___ action on myocardium

A
  • sympathetic
  • parasympathetic
  • remodeling
  • spironolactone, eplerenone
  • K, Mg, arrhythmias
  • Na, fluid
  • sympathetoc
  • fibrotic
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7
Q

AA

Spironolactone
- ___ agent, structurally similar to ___
- inhibits the effects of ___ at the receptor site and increases the peripheral conversion of ___ into ___
- AE: gynecomastia, impotence, menstrual irregularities

A

non-selectice, progesterone
dihydrotestosterone, testosterone, estradiol

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8
Q

AA

eplerenone
- ___ agent with a 100-1000x lower affinity for ___ , ___ , and ___ receptors than spironolactone
- no antiandrogenic effects
- substrate of ___

A
  • selective
  • androgen, glucocorticoid, progesterone
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9
Q

AA dosing

eplerenone
eCrCl ≥ 50
initial dose: ___ mg ___
maintenance: ___ mg ___

only if K ≤ 5

A
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10
Q

AA dosing

eplerenone
eCrCl 30-49
initial dose: ___ mg ___
maintenance: ___ mg ___

only if K ≤ 5

A

25, every other day
25, daily

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11
Q

AA dosing

spironolactone
eCrCl ≥ 50
initial dose: ___ - ___ mg ___
maintenance: ___ mg ___

only if K ≤ 5

A

12.5-25, daily
25, daily

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12
Q

AA dosing

spironolactone
eCrCl 30-49
initial dose: ___ mg ___ or___
maintenance: ___ - ___mg ___

only if K ≤ 5

A

12.5, daily, every other day
12.5-25, daily

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13
Q

AA dosing/administration

should be added to ACEi/ARB/ARNi and BB therapy

Avoid:
- SCr > ___ (men) or > ___ mg/dL (women)
- K > ___ mEq/L
- CrCl < ___ mL/min
- Hx of severe ___ kalemia or recent worsening of ___ function

concomitant use of K sparing diuretics or supplements should be avoided (unless hypokalemia K < ___ mEq/L)

A

2.5, 2
5
30
hyperkalemia, renal
4

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14
Q

AA monitoring

monitor renal function and K within ___ days - ___ week after any change or addition, diseases, or acute illnesses that may influence K concentrations
- then once a ___ for 3 months
- then every ___ - ___ months
- monitor these things when ACEi/ARB increase/change

avoid ___ substitutes

A

3 days, 1 week
month
3-4
salt

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15
Q

Consensus recommendations for AA

Stage B: No recs

Stage C
- patients with NYHA ___ - ___ and ___ with eGFR > ___ and K < ___
- careful maintenance of ___ , renal function, and diuretic dosing is essential
- patients taking AAs in which K cant be maintained ( < ___ ) should be D/C to avoid life threatening hyperkalemia

A

II-IV, HFrEF, 30, 5
K
5.5

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16
Q
A

D

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17
Q
A

C

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18
Q

SGLT2i

  • SGLT2i cause renal afferent arteriolar ___ (cause diuresis, natriuresis, glycosuria, decreased proteinuria)
  • ___ preload = decrease ___ wall stress
  • ___ afterload
  • decrease myocardial ___
A
  • constriction
  • decrease, LV
  • decrease
  • energetics
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19
Q

SGLT2i

  • unclear benefit in HF
  • osmotic ___ and ___
  • decreased arterial ___ and ___
  • preload and afterload ___
  • associated reduction in hypertrophy and fibrosis ( ___ )
A
  • diuresis, natriuresis
  • pressure, stiffness
  • reduction
  • remodeling
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20
Q

SGLT2i

indications: reduce the risk of CV ___ or ___ for HFrEF patients with NYHA class ___ - ___
dapagliflozin and empagliflozin are both ___ mg ___
- dapa: eGFR > ___
- empa: eGFR > ___

AE
- volume depletion
- ___ in DM, ___ glycemia, infection risk ( ___ )

A

death, hospitalization, II-IV
10, daily
30
20
DKA, hypoglycemia, UTIs

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21
Q

SGLT2i summary

recommended for patients with ___ chronic ___ with or without ___ to reduce ___ and CV ___

if the meet renal requirements, they should be on these for life

A

symptomatic, HFrEF, DM, hospitalizations, death

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23
Q

initiation: titration strategies

24
Q

initiation: titration strategies

ARNi and MRA: inititate at low doses, titrate in ___ weeks as tolerated

BB: initiate at low doses, titrate in ___ week as tolerated

SGLT2: initiate, continue

25
# initiation: titration strategies after 42 days - maintenance or additional titration of the big 4: ___ , ___ , ___ , ___ - consideration of EP device or transcatheter ___ valve repair - consideration of add-on medications - manage comorbidities
RASi, AA, BB, SGLT2 mitral
26
# ISDN/Hydralazine combo produces balanced vasodilator effects, causing reductions in both ___ and ___ - less effective than ACEi - ___ indicated for the treatment of HF in ___ patients as an ___ to standard therapy Nasty AE profile - headache, nausea, flushing, dizziness, tachycardia, ___ -like syndrome, hypotension, myocardial ischemia, fluid retention
preload, afterload BiDil, black, adjunct lupus
27
# ISDN/hydralazine hydralazine principle site of action: ___ vasodilation initial: ___ mg ___ / ___ target: ___ mg ___ max: ____ mg ___
arteriolar 25, TID/QD 75, TID 100, TID
28
# ISDN/hydralazine ISDN principle site of action: ___ vasodilation initial: ___ mg ___ / ___ target: ___ mg ___ max: ___ mg ___
venous 20, TID/QD 40, TID 80, TID
29
# ISDN/hydralazine ISDN/hydralazine (BiDil) initital: ___ / ___ mg ___ target: ___ / ___ mg ___
20/37.5, TID 40/75, TID
30
# Consensus recommendations for ISDN/hydralazine Stage B: no recommendations Stage C: - in ___ patients with NYHA ___ - ___ receiving optimal medical therapy to imporve symptoms and reduce mortality - patients with symptoms or previous symptoms who cant receive ARNi, ACEi, or ARB due to drug tolerance or ___ insufficiency might be considered
black, III-IV renal
31
32
# Other therapies (after GDMT optimization) NYHA II-III; HFrEF; NSR - HR > 70 bpm - on max tolerated BB
Ivabradine | Corlanor
33
# Other therapies (after GDMT optimization) NYHA II-IV; LVEF < 45% - recent HFH - IV diuretics - elevated NP levels
Vericiguat
34
# Other therapies (after GDMT optimization) symptomatic HFrEF
digoxin
35
# Other therapies (after GDMT optimization) NYHA II-IV
PUFA
36
# Other therapies (after GDMT optimization) patients with HF with hyperkalemia while taking RAASi
potassium binders
37
# Ivabradine indications: reduce the risk of ___ for symptomatic HF, EF < ___ % (HFrEF) in ___ with rHR > ___ bpm in max tolerated BB or with BB CI dosing: ___ - ___ mg ___, adjust every 2 weeks based on ___ max: ___ mg ___
hospitalization, 35%, NSR< 70 2.5-5, BID, HR 7.5, BID
38
# Ivabradine dosing adjustments - HR > 60: ___ - ___ mg ___, up to max: ___ mg ___ - HR: 50-60: maintain dose - HR < 50 or s/s of bradycardia: decrease dose by ___ mg (given ___ ); if thats current dose, D/C
- 2.5-5, BID, 7.5, BID - 2.5, BID
39
# Ivabradine AE - ___ toxicity - ___ fibriliation - ___ and conduction disturbances CYP ___ substrate - ___ CI, avoid ___ and ___ , no grapefruit juice
- fetal - atrial - bradycardia - CYP3A4 - ketoconazole, diltiazem, verapamil | cost > $6,000
40
# Digoxin/digitalis glycosides MOA 1) - decreases ___ pump - ___ Ca2+ - ___ force MOA 2: - ___ vagal activity - ___ AV conduction - ___ rate
- Na/K-ATPase - increases - increases - increase - decrease - decrease
41
# Digoxin/digitalis glycosides benefits are due to ___ modulation effects - increases ___ activity - reduces ___ - re-sensitization of ___ inhibits ___ which alters excitiation-contraction coupling - increase in intracellular __ , enhancing ___ of contraction - relatively mild ___ inotrope
neurohormonal - parasympathetic - HR - baroreceptors - Na-K-ATPase - Ca, force - positive
42
# Place of Digoxin in HF treatment efficacy in HF with ___ is well established - reduces ___ , not mortality consider in patients with symptomatic HFrEF despite optimized GDMT
Afib, hospitalizations
43
# Digoxin Dosing ___ - ___ mg ___ - ___ mg will be used in majority of patients - ___ - ___ ng/mL is the goal serum digoxin concentration (SDC) - lower doses in > ___ years, impaired ___ function, low weight name 5 drugs that increase SDC
0.125-0.25 0.125 0.5-0.9 70, renal - amiodarone, quinidine, verapamil, itraconazole, ketoconazole
44
# Digoxin AE and s/s of toxicity CNS - anorexia, N/V, abdominal pain - ___ , photophobia, altered color perception - fatigue, weakness, HA, neuralgias, confusion, delirium, psychosis Cardiac - ventricular: PVCs, bigeminy, trigeminy, VT, VF - AV ___ - AV junctional escape rhythms, junctional tachycardia - atrial ___ with slowed AV conduction or block - ___ brady cardia
halos block arrhythmias sinus
45
B
46
B
47
# Vericiguat (Verquvo) soluble ___ stimulator reduces CV death and hospitalization - ___ mg daily, up to ___ mg daily CI: ___ AE: ___ and ___ most common consider in selected high risk pateints with recent worsening with symptomatic HFrEF despite optimized GDMT | just know it exists
guanylate cyclase - 2.5, 10 - pregnancy - hypotension, anemia
48
# MSC topis PUFA = ___ - reduce risk in HF II-IV antiplatelets - long term ___ ___ mg therapy is recommended in patients with HF and ___
omega-3 polyunsaturated fatty acids - ASA, 81, IHD/CAD/ASCVD
49
# MSC topics anticoagulants - recommended in HF if ___ - or in patients with other indications like pulmonary embolism - ___ anticoagulation is not recommended CCB - ___ , ___ , and ___ should not be routinely used - ___ and ___ may be useful in managing angina/HTN if not effectively managed with HF therapies
- Afib - routine - diltiazem, verapamil, nifedipine - felodipine, amlodipine
50
# Non-PCOL ICD - LVEF < 35%, at least 40 days post-MI, NYHA ___ - ___ - LVEF < 30%, at least 40 days post-MI, NYHA ___ Cardiac resynchronization therapy - NYHA II-III-IV pts on optimal medical therapy - ___ duration greater than ___ ms and LVEF less than ___ % | know it exists
II-III I QRS, 150, 35
51
HFrEF ___ dysfunction: decreased ___ - EF < ___ - ___ % HFpEF ___ dysfunction: impairment in ventricular ___ / ___ - EF > ___ %
systolic, contractility - 35-40% diastolic, relaxation/filling - 50%
52
# summary of HFpEF treatment - SBP/DBP should be controlled - ___ should be used for relief of ___ due to volume overload (no mortality benefits) - management of AFib can improve symptomatic HF - ___ may reduce hospitalizations and CV mortality - the use of ARBs, ARNis, ACEi, and MRAs may ben considered to decrease hospitalizations
diuretics, symptoms SGLT2s
53
# summary of HFpEF treatment - ACEi and ARBs have not been shown to reduce mortality, but they do reduce ___ - MRA may improve ___ function and reduce ___ - ___ has no affect on mortality or hospitalizations - nitrates should be limited to use in patients with HFpEF who may need treatment for symptomatic ___ - CCBs may be useful to treat HTN
- hospitalizations - diastolic, remodeling - digoxin - CAD