Cardiovascular Flashcards
(26 cards)
Nitroglycerin
Nitrovasodilator, nitric oxide donor
Uses: angina, acute coronary syndrome
Toxicity: tachycardia, orthostatic hypotension, headache
Sublingual for acute angina (rapid onset, short duration), oral for prophylactic (slow onset, longer duration), venodilation at low doses (decreased venous return), arteriodilation at high doses (decreased afterload)
Sildenafil
Phosphodiesterase type 5 inhibitor (elevated cGMP levels, vasodilation)
Uses: angina, erectile dysfunction
Toxicity: tachycardia, hypotension, vision disturbances (yellow halos)
Contraindicated with nitrovasodilators, rapid onset with long duration
Propranolol
Non-selective beta antagonist (decreased cardiac output, RAAS, O2 demand)
Uses: hypertension, congestive heart failure, angina, arrhythmias
Toxicity: bradycardia, AV block, bronchospasm, CNS sedation
Contraindicated in asthma, also used for performance anxiety and migraine, crosses BBB
Metoprolol
Selective beta1 antagonist (decreased cardiac output, RAAS, O2 demand)
Uses: angina, congestive heart failure, hypertension
Toxicity: bradycardia, AV block, CNS sedation
Reduces mortality in heart failure patients, widely used for stage I/II hypertension, crosses BBB
Verapamil
Cardioselective L-type Ca2+ channel blocker (decreased force and rate of cardiomyocyte contraction, decrease cardiac output)
Uses: hypertension, angina, arrhythmias
Toxicity: hypotension, excessive cardiac depression, constipation
Strong cardiac blocking effect, weak vascular smooth muscle blocking effect
Nifedipine
Vascular selective L-type Ca2+ channel blocker (decreased total peripheral resistance)
Uses: hypertension, prophylactic for angina, arrhythmias
Toxicity: hypotension, flushing, dizziness
Strong vascular smooth muscle blocking effect, weak cardiac blocking effect
Ranolazine
Late Na+ channel current modulator (decreased Na+ influx during AP, decreased Ca2+ overload)
Uses: chronic angina
Toxicity: constipation, dizziness
Avoid use in patients with long QT syndrome, drug-drug interactions due to CYP3A4/2D6 metabolism
Digoxin
Cardiac glycoside
Na/K ATPase inhibitor (increased intracellular Na+ inhibits Na+/Ca2+ exchanger and more Ca2+ is retained in the cell)
Uses: congestive heart failure, arrhythmias
Toxicity: arrhythmogenic, nausea, malaise, diarrhea, vision problems (yellow halos)
Only approved oral inotropic agent for CHF, increased [Ca2+], increased stroke volume, no net effect on CHF mortality, low therapeutic index
Metoprolol
Selective beta1 antagonist (affects cardiac and renal receptors, decreased cardiac remodeling and afterload/TPR)
Uses: congestive heart failure, hypertension
Toxicity: bradycardia, AV block, CNS sedation
Reduces mortality in heart failure patients, used for stage I/II hypertension, less bronchial effects
Carvedilol
Mixed alpha1 and beta1 antagonist (decreased afterload/TPR and cardiac remodeling)
Uses: congestive heart failure, hypertension
Toxicity: bradycardia, AV block, CNS sedation, less bronchospasm
Reduces mortality in heart failure patients
Captopril
ACE inhibitor
Uses: stage I/II hypertension, congestive heart failure, diabetic renal disease
Admin: oral
Toxicity: bradykinin cough reflex, hyperkalemia, teratogenic
First line therapy for CHF, reduces morbidity and mortality, effective for up to 12 hours
Losartan
Angiotensin II type I receptor antagonist (decreased TPR and BP)
Uses: stage I/II hypertension, congestive heart failure
Admin: oral
Toxicity: hyperkalemia, teratogenic, severe hypotension, acute renal failure
No cough reflex, first line therapy for CHF
Furosemide
NKCC2 cotransporter inhibitor in thick ascending limb of Henle (loop diuretic)
Uses: edema (due to CHF, cirrhosis, nephrotic syndrome), hypertension, hypercalcemia
Toxicity: hypokalemic metabolic alkalosis, ototoxicity, dehydration
“High ceiling” diuretic, rapid onset of action, enhanced urinary Ca2+ loss
Hydrochlorothiazide
NCC cotransporter inhibitor in distal convoluted tubule (thiazide diuretic)
Uses: hypertension, CHF, idiopathic hypercalciuria
Toxicity: hypokalemic metabolic alkalosis, hyponatremia, hyperlipidemia, hyperuricemia, hypercalcemia
“Low ceiling” diuretic, component of many combination therapies
Spironolactone
Competitive aldosterone receptor antagonist (K-sparing diuretic)
Uses: hyperaldosteronism, CHF, hypertension
Toxicity: hyperkalemia, endocrine effects (gynecomastia)
Used in combination with loop or thiazides to prevent hypokalemia, eplerenone lacks anti-androgen effects
Amrinone
Phosphodiesterase-3 inhibitor (elevated cAMP levels, increased cardiac output, vasodilation) Uses: acute decompensated heart failure Admin: IV Toxicity: arrhythmia Short duration
Dobutamine
Sympathomimetic Beta1 agonist (increased cardiac output) Uses: acute decompensated heart failure Admin: IV Toxicity: arrhythmia Short duration, positive inotrope
Nitroprusside
Nitrovasodilator, nitric oxide donor Uses: acute decompensated heart failure Admin: IV Toxicity: tachycardia, excessive hypotension Short duration
Hydralazine + isosorbide dinitrate
Hydralazine: vascular K+ channel opener
Isosorbide dinitrate: nitric oxide donor, nitrovasodilator
Uses: congestive heart failure unresponsive to diuretics/ACE-I/ARB, angina
Admin: oral
Toxicity: tachycardia, excessive hypotension, headache
Long duration
Amiloride
ENaC Na+ channel inhibitor in cortical collecting duct (K-sparing diuretic)
Uses: congestive heart failure, hypertension, hypokalemia
Toxicity: hyperkalemia
Aliskiren
Renin inhibitor (decreased ATII production)
Uses: hypertension secondary to renal failure or diabetes
Toxicity: angioedema, renal impairment
Labetalol
Mixed alpha1 and beta1 antagonist (decreased cardiac output and TPR)
Uses: pregnancy-induced hypertension, hypertensive crisis
Toxicity: bradycardia, AV block, CNS sedation
Composed of 4 stereoisomers
Prazosin
Alpha1 antagonist (decreased TPR) Uses: benign prostatic hypertrophy, hypertension Toxicity: orthostatic hypotension, reflex tachycardia Used in hypertension patients unresponsive to diuretics/Ca2+ channel blockers
Clonidine
Alpha2 agonist (decreased NE release)
Uses: ADHD, hypertension
Toxicity: severe withdrawal, sedation
Penetrates CNS and acts on sympathetic nerve terminal