Heart Drugs Flashcards

1
Q

Loop diuretics

A

Furosemide- most common
Act on the ascending loop of Henle.
Decreases the re-absorption of sodium and chloride and increases excretion of potassium.
Increase the renal excretion of water, sodium, chloride, calcium, magnesium, hydrogen, ammonium, and bicarbonate.

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2
Q

Furosemide

A
2-4mg/kg
Q1-8hrs
CRI: 0.1mg/kg/hr
Watch for:
Electrolyte disturbances (K, Ca, Na).
Severe dehydration
Decline in renal functions
Hypotension due to hypovolemia
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3
Q

Spironolactone

A
Potassium-sparing diuretic 
Aldosterone receptor blocker
Slow onset (2-3 days)- long term treatment 
2-4mg/kg/day PO
Hyperkalemia - watch kidney functions
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4
Q

What are examples of Thiazide diuretics and what do they do?

A

Hydrochlorothiazide
Chlorothiazide
Inhibit sodium reabsorption and promote potassium excretion
Decreases renal blood flow - do not administer to azotemic animals

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5
Q

Positive inotropes

A
Increases strength of contraction of the myocardial muscle=increases cardiac output 
4 groups:
Sympathomimetic amines
Phosphodiesterase inhibitors
Calcium sensitiser 
Digitalis glycosides
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6
Q

Name two sympathomimetic amines used for heart failure

A

Dopamine
Dobutamine
Stimulates beta-adrenergic receptor sites and increases calcium availability
Short half lives and must be CRIs

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7
Q

Dobutamine

A

Increases myocardial contractility and stroke volume = increased cardiac output
5-20mcg/kg/min
Counteracts effects of beta blockers

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8
Q

Dopamine

A

Precursor of norepinephrine
Dose related:
*Low dose (1-5mcg/kg/min)common
- vasodilation do renal, mesentric, cerebrovasucular and coronary
arteries by acting on dopamine receptors
High dose (6-10mcg/kg/min)
- generalized systemic arteriolar vasoconstriction
-increases afterload
-decrease cardiac output
-acting on beta receptors
Higher than 10mcg/kg/min
-acting on the alpha cells that stimulate catecholamines and leads to
vasoconstriction
*Watch for: nausea, anorexia, tachycardia and arrhythmias
: phlebitis and tissue necrosis if extravasated

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9
Q

Give examples of phosphodiesterase inhibitors

A

*Milrinone
: 50mcg/kg/min and then 0.375-0.75mcg/kg/min CRI
*Amrinone
: 1-3mcg/kg/min and then 10-100mcg/kg/min
Short half-life = CRI
*Sildenafil
:5 phosphodiesterase
: potentially be able to reduces left ventricular afterload (seen in
humans)
* Pimobendan
: phosphodiesterase inhibitors
: calcium sensitization
= positive inotropic effects and vasodilation
: long term medication PO for CHF
: potent inhibitor of platelet aggregation (watch for bleeding)

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10
Q

Digitalis glycosides

A
Improves cardiac performance
Normalizing neurohormonal aberrations
Reduce fluid retention 
Abolishing supraventricular tachyarrhythmias 
Lowers heart rate
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11
Q

Name two types of digitalis glycosides

A

1)Digoxin
-more prevalent
-only form that can be used in cats
-used in dogs with renal dysfunction
: <20kg. 0.005-0.008mg/kg PO q12
-cats
: 0.006-0.007 mg/kg PO Q48
2)Digitoxin
-dogs. 0.01-0.03mg/kg Q8

  • Must monitor for digitalis toxicity
  • cardiac arrhythmias = worsening heart disease
  • gastro upset
  • anorexia
  • weight loss
  • diarrhea
  • Drug interactions
  • antacids
  • cimetidine
  • Metoclopramide
  • oral neomycin
  • chemotherapeutic agents will decrease amount of digitalis absorbed from the GIT
  • Drugs that enhances toxic effects of digitalis:
  • diazepam
  • quinidine
  • anticholinergics
  • succinylcholine
  • verapamil
  • tetracycline
  • erythromycin
  • Diuretics or other drugs that deplete body of potassium may predispose to toxicity
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12
Q

Vasodilators

A

Classified as:

1) Arteriolar dilators
- decrease afterload (resistance of left ventricle ejection of blood)
- used in dilated cardiomyopathy, mitral valve regurge, intracardiac or vascular shunts
- Hydralazine : must watch for sodium and water retention and GI signs
2) Venodilators
- reduces preload (vol of blood in the left ventricle just before it contracts)
- used in the same situation as diuretics
- Nitroglycerin ointment
- Monitor for hypotension
3) both

  • Nitroprusside is both
  • must be CRI
  • 0.5-10 mcg/kg/min
  • Closely monitor HR and BP due to dilation effects
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13
Q

ACE I

A

Blocks the conversion of angiotensin I to II (vasoconstrictor)

  • Promotes renal sodium and water excretion
  • Slow or every reverse the progression of pump dysfunction and pathological remodeling of heart failure
  • Used in hypertension, CHF secondary to valvular disease and dilated cardiomyopathy dogs and hypertrophic cardiomyopathy in cats
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14
Q

Examples of ACE I drugs

A
  • Enalapril
  • Imidapril
  • Ramipril
  • Benazepril
  • Adverse side effects: vomiting, diarrhea, hypotension, renal dysfunction and hyperkalemia
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15
Q

Calcium channel blockers

A
Another type of vasodilator 
2 types:
1) Dihydripyridine 
-arteriolar vasodilator 
-Amlodipine: 
     -prevents cardiac output
     -used in hypotension
     -0.2mg/kg PO Q24
2) Non-dihydripyridine 
-negative inotropic drugs
-less potent vasodilators 
-negative chronotropic drugs (slows conduction through AV node)
-Dilitiazem 
    :controls supraventricular tachycardia or artrial fibrillation and hyperthrophic cardiomyopathy 
    : 0.5-2.0mg/kg PO q8 
*Adverse effects: GIT disturbances, hypotension, conduction block, CNS effects, peripheral or pulmonary edema, rashes or altered liver function
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16
Q

Amlodipine

A
  • Primary dihydropyridine calcium channel blocker
  • minimal myocardial depression
  • preserves cardiac output
  • used for systemic hypertension
  • monitor for renal insufficiency, hypotension and vomiting
17
Q

Non-dihydropyridine calcium channel blockers

A
  • negative inotropic drugs
  • depresses cardiac contractility allowing myocardial relaxation
  • less potent vasodilators
18
Q

Negative chronotropic drugs

A

Slows conduction through AV node

19
Q

Diltiazem

A
  • Most common non-dihydropyridine calcium channel blocker

* controls or terminates supraventricular tachycardia or atrial fibrillation and hypertrophic cardiomyopathy

20
Q

What are the adverse side effects of non-dihydropyridine calcium channel block Dilitiazem?

A

Gastrointestinal disturbances, hypotension, conduction block or other rhythm disturbances, CNS effects, peripheral or pulmonary edema, rashes, altered liver function

21
Q

Beta-adrenergic blockers

A
  • Binds to beta receptors of sympathetic nervous system (fight or flight) located in vascular system, heart and bronchioles
  • 2 types: beta-1 and beta-2
22
Q

What does the stimulation of beta-1 receptors cause?

A

*Increase in HR, AV nodal conduction velocity, increase in strength of myocardial contraction

23
Q

What does the stimulation of beta-2 receptors cause?

A

*vasodilation of skeletal muscle and bronchodilation in the airways

24
Q

What are the most common beta-blockers?

A

Propranolol, Atenolol, Metoprolol, and Esmolol

25
Q

Propranolol

A
  • Beta-1 and 2 blocker
  • Decrease HR, slower conduction through AV node, decreased myocardial contractility = decrease cardiac output
  • Bronchial constriction
26
Q

Atenolol and metoprolol

A
  • Selectively blocks beta-1 receptor sites
  • Blocks beta-2 receptor sites at very high doses
  • Act as negative inotropic and negative chronotropic drug
  • Causes: decreased myocardial oxygen demands, and reduces blood pressure
  • No respiratory effects
27
Q

Why are atenolol and metoprolol better than Proponolol for respiratory compromised patients?

A

They do not cause bronchoconstriction

28
Q

What beta blockers causes prolongation of hypoglycemic effects of insulin?

A

Atenolol and propranolol

29
Q

Esmolol

A
  • Ultrashort acting beta-1 blocker
  • only injectable
  • similar to atenolol
  • used as test drug
  • infusion for short term Tx of supraventricular tachyarrhythmias
30
Q

What are the adverse effects of esmolol?

A

Hypotension and bradycardia

  • *Increase serum digoxin levels
  • Morhpine Patients need to have lower doses of esmolol
31
Q

Angiotensin II

A

Potent vasodilator