cvs - drugs for HF, IHD, HTN Flashcards

1
Q

name 5 1st line anti-hypertensives

A
  • ACE-inhibitors
  • Ang II type 1 (AT1) blockers
  • Beta-blockers
  • Ca2+ channel blockers
  • Diuretics - loop, thiazide
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2
Q

name 3 2nd line anti-hypertensives

A
  • Hydralazine
  • Potassium-sparing diuretics
  • Alpha-adrenergic antagonists
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3
Q

name 9 classes of drugs used in HF

A
  • ACE-I
  • Angiotensin II type 1 (AT1) blockers
  • Beta-blockers
  • Sacubitril-Valsartan
  • Diuretics - thiazides, potassium-sparing
  • Hydralazine
  • Ivabradine
  • Nitrates
  • Cardiac glycosides
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4
Q

name 4 classes of drugs for IHD

A
  • Nitrates
  • Ca2+ channel blockers
  • Beta-blockers
  • Ivabradine
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5
Q

name 4 beta blockers used in HF

A
  1. carvedilol (non-selective)
  2. bisoprolol (β1)
  3. metoprolol XL (β1)
  4. nebivolol (mixed)
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6
Q

name 6 beta blockers used in HTN and IHD

A
  1. carvedilol (non-selective)
  2. propanolol (non-selective)
  3. bisoprolol (β1)
  4. metoprolol XL (β1)
  5. atenolol (β1)
  6. nebivolol (mixed)
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7
Q

moa of beta blockers

A
  • β1 blockade →↓ conversion of ATP to cAMP →↓PKA →↓Ca2+ channel activation →↓ heart contractility
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8
Q

moa of carvedilol

A
  • blocks α1 receptors → reduce peripheral resistance
  • antioxidative
  • anti-ischaemic
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9
Q

moa of nebivolol

A
  • β1 selective in low dose/fast metab
  • non-selective in high dose/slow metab
  • vasodilatory effects through increase NO release
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10
Q

how do beta blockers lower bp?

A

↓ CO + inhibit renin release → ↓ bp

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11
Q

how do beta blockers work in HF?

A

↓ HR and myocardial contractility → ↓ O2 demand

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12
Q

clinical uses of beta-blockers

A
  1. hypertension
  2. cardiac failure
  3. post-MI
  4. arrhythmia
  5. anxiety disorders
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13
Q

adverse effects of beta-blockers

A
  1. hypotension
  2. bradycardia
  3. reduced exercise capacity
  4. AV nodal block
  5. bronchoconstriction (esp in asthmatics)
  6. vivid dreams, depression
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14
Q

contraindications for beta-blockers

A
  1. asthma
  2. diabetes
  3. severe bradycardia
  4. advanced heart block
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15
Q

name 3 ACE-I

A
  1. lisinopril
  2. captopril
  3. enalapril
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16
Q

clinical uses of ACE-I

A
  1. hypertension
  2. cardiac failure
  3. post-MI
  4. renal insufficiency
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17
Q

adverse effects of ACE-I

A
  1. severe hypotension
  2. acute renal failure
  3. hyperkalemia
  4. angioedema
  5. dry cough (common)
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18
Q

contraindications for ACE-I

A

pregnancy (causes fetal harm)

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19
Q

name 2 ang II type 1 blocker

A
  1. valsartan
  2. losartan
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20
Q

contraindications for ang II type I blocker

A

pregnancy

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21
Q

benefit of AT1 over ACE-I

A

less/no dry cough (as bradykinin pathway not affected)

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22
Q

moa of sacubitril-valsartan

A
  • sacubitril is a neprilysin inhibitor → prolong BNP effects → promote vasodilation, natriuresis, diuresis, antagonise RAAS
  • valsartan is an Ang II receptor blocker (since neprilysin also breaks down Ang II, sacubitril prolongs Ang II effects → HF progression → need valsartan to counter effects)
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23
Q

indication for sacubitril-valsartan

A

HFrEF

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24
Q

adverse effects of sacubitril-valsartan

A
  • hypotension
  • hyperkalemia
  • renal failure
  • cough
  • angioedema
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25
Q

general effect of diuretics

A

reduce blood vol → decrease CO

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26
Q

moa of loop diuretics

A
  • selectively inhibit Na+/K+/2Cl- transporter in loop of Henle
  • increase Mg2+ and Ca2+ excretion
  • increase renal blood flow (furosemide)
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27
Q

name 3 eg. of loop diuretics

A
  1. furosemide
  2. bumetanide
  3. ethacrynic acid
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28
Q

clinical uses of loop diuretics

A
  • hypertension
  • acute pulmonary oedema and other oedema
  • acute hyperkalemia
  • acute renal failure
  • anion overdose
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29
Q

adverse effects of loop diuretics

A
  • hypokalemic metabolic alkalosis
  • ototoxicity
  • hyperuricemia
  • hypomagnesemia
30
Q

what drugs should be avoided w loop diuretics

A
  • aminoglycosides (ototoxicity)
  • NSAIDs (inhibit prostaglandin synthesis)
31
Q

name 4 eg. of potassium-sparing diuretics

A
  1. spironolactone
  2. triamterene
  3. amiloride
  4. eplerenone
32
Q

moa of potassium-sparing diuretics

A
  • spironolactone and eplerenone block aldosterone receptor
  • triamterene and amiloride block Na+ channels
    ⇒ prevent Na+ and water retention → ↓ bp
33
Q

clinical uses of potassium-sparing diuretics

A
  • hypertension (2nd line)
  • hyperaldosteronism
34
Q

adverse effects of potassium-sparing diuretics

A
  • hyperkalemia
  • metabolic acidosis
  • gynecomastia (spironolactone)
  • acute renal failure (triamterene, indomethacin)
  • kidney stones (triamterene)
35
Q

moa of thiazide

A
  • inhibit NaCl reabsorption by blocking Na+/Cl- transporter → diuresis and reduced blood vol
  • enhance Ca2+ reabsorption in distal convoluted tubule
36
Q

name 2 thiazides

A
  1. hydrochlorothiazide
  2. indapamide
37
Q

4 clinical uses of thiazides

A
  • hypertension
  • congestive HF
  • nephrolithiasis due to hypercalciuria
  • nephrogenic diabetes insipidus
38
Q

adverse effects of thiazides

A
  • hypokalemic metabolic alkalosis
  • hyponatraemia
  • hyperuricemia
  • hyperglycemia
  • hyperlipidemia
  • hypercalcemia
39
Q

contraindication for thiazide

A

NSAIDs (reduces renal prostaglandin synthesis → interfere w antihypertensive action)

40
Q

name 2 non-DHP calcium channel blockers

A
  1. verapamil
  2. diltiazem
41
Q

name 2 DHP calcium channel blockers

A
  1. nifedipine
  2. amlodipine
42
Q

diff btwn DHP and non-DHP

A
  • DHP: primarily causes vasodilation
  • non-DHP: also affect HR and force of contraction
43
Q

moa of calcium channel blockers

A

inhibit L-type calcium channels → ↓ intracellular calcium → vasodilation

44
Q

clinical uses of non-DHP calcium channel blockers

A
  • arrhythmia
  • angina
45
Q

clinical uses of DHP calcium channel blockers

A
  • hypertension
  • angina
  • ↓ risk of MI/stroke
  • Raynaud’s phenomenon
46
Q

adverse effect of calcium channel blockers

A

cardiac depression - bradycardia, AV block, HF

47
Q

adverse effects of DHP calcium channel blockers

A
  • hypotension
  • HF
  • MI
  • peripheral oedema
48
Q

adverse effects of non-DHP calcium channel blockers

A
  • constipation
49
Q

contraindications for calcium channel blockers

A
  • congestive HF
  • severe hypotension
  • heart block
  • HFrEF
50
Q

moa of hydralazine

A
  • direct arteriole vasodilator → decreases afterload
  • inhibit IP3-induced release of Ca2+ from smooth muscle cells sarcoplasmic reticulum
  • reduces peripheral resistance → compensatory release of epinephrine/NE → increase VR and CO
51
Q

clinical uses of hydralazine

A
  • HFrEF
  • essential hypertension
  • acute-onset, severe peripartum/post-partum hypertension
52
Q

adverse effects of hydralazine

A
  • reflex tachycardia
  • hypotension
  • hydralazine-induced lupus syndrome
53
Q

contraindications for hydralazine

A

coronary artery disease

54
Q

moa of isosorbide mononitrate/dinitrate

A
  • vasodilators that release NO → dilation of coronary vessels
  • at low dose, ↓ preload
  • at high dose, ↓ preload and afterload → reduce myocardial O2 demand
55
Q

clinical use of isosorbide mononitrate/dinitrate

A

prophylaxis for angina pectoris

56
Q

adverse effect of isosorbide mononitrate/dinitrate

A
  • dizziness
  • postural hypotension
57
Q

contraindication for isosorbide mononitrate/dinitrate

A

concurrent use w phosphodiesterase inhibitors

58
Q

moa of ivabradine

A

reduces HR by inhibiting I(f) current in SA node

59
Q

unique ft of ivabradine

A

targets HR wo affecting BP or myocardial contractility

60
Q

2 clinical uses of ivabradine

A
  • stable angina pectoris
  • chronic HF w systolic dysfunc
61
Q

adverse effects of ivabradine

A
  • luminous phenomena
  • bradycardia → dizziness, hypotension
62
Q

moa of digoxin

A
  • inhibit Na+/K+ exchanger → intracellular [Na+] increase → less Ca2+ efflux → stronger systolic contraction
63
Q

2 clinical uses of digoxin

A
  • systolic dysfunc
  • atrial fibrillation
64
Q

adverse effects of digoxin

A
  • severe dysrhythmia (AV block, afib, vfib)
  • nausea, vomiting
  • headache, confusion, blurred vision
65
Q

risk of digoxin

A

narrow therapeutic window and toxicity

66
Q

toxic effects of digoxin

A
  • automaticity
  • tachycardia
  • extrasystoles
  • fibrilation
67
Q

treatment of digoxin toxicity

A
  • discontinue cardiac glycoside therapy
  • correct K+/Mg2+ deficiency
  • anti-arrhythmic drugs
  • digoxin Ab
68
Q

name 2 alpha blockers

A
  • phenoxybenzamine (non-selective)
  • prazosin (α1)
69
Q

moa of alpha blockers

A

block α1 → vasodilation → ↓ peripheral vascular resistance → ↓ bp

70
Q

2 clinical uses of alpha blockers

A
  • hypertension (2nd line)
  • benign prostatic hyperplasia
71
Q

adverse effects of alpha blockers

A
  • reflex tachycardia
  • postural hypotension
  • urinary frequency
  • depression